Disclaimers

ACADEMY DISCLAIMER

ACADEMY POLICY FOR Training Days EDUCATIONAL PURPOSE & LIMITATION OF RESPONSIBILITY All courses, training, and materials provided by Snatch & Glow Clinic and Training Academy are delivered strictly for educational purposes only. We accept no responsibility or liability for how the Student applies, implements, misuses, commercialises, or relies upon the training after completion. The Student is solely responsible for ensuring that their personal use of the training complies with all applicable laws, regulations, insurance requirements, professional standards, and local licensing rules within their chosen place of practice. RELOCATION, JURISDICTIONAL RESTRICTIONS & PERSONAL CIRCUMSTANCES If the Student chooses to relocate, emigrate, change country of residence, or practise in a different jurisdiction, the Academy accepts no responsibility for whether the training, certification, or content is recognised, permitted, insurable, or usable in that location. Any restriction, prohibition, licensing requirement, or regulatory limitation arising in the Student’s present or future location does not constitute grounds for refund, cancellation, compensation, or repeat training. Any personal circumstance, future change in law, employment status, immigration status, health condition, pregnancy, lifestyle, or availability that was not disclosed prior to purchase remains the sole responsibility of the Student and does not invalidate the contract. ONE-YEAR VALIDITY, EXPIRY & RENEWAL All courses, training days, coursework access, and associated entitlements must be fully utilised within twelve (12) months from the original purchase date, unless otherwise stated in writing. Any unused training, coursework, or practical elements remaining after twelve (12) months shall automatically expire without refund. Where reactivation, renewal, or extension is permitted, this shall be chargeable at the Academy’s prevailing renewal rate at the time of request. Renewal is discretionary and not guaranteed. TRAINING ATTENDANCE, RESCHEDULING & NO-SHOW POLICY All training dates are confirmed strictly in writing by email, booking confirmation, or official onboarding documentation. If the Student fails to attend a confirmed training day for any reason, this shall be treated as a no-show and the training day shall be deemed fully delivered and forfeited with no entitlement to refund, replacement, or credit. Where rescheduling is permitted at the Academy’s sole discretion, a mandatory £300 rescheduling fee per training day shall apply and must be paid in full before a new date is issued. Failure to pay the rescheduling fee shall result in permanent forfeiture of the missed training day with no further obligation owed by the Academy. COURSEWORK COMPLETION, CERTIFICATION & TIME LAPSE RESPONSIBILITY Certification is issued strictly subject to full completion of all mandatory coursework, assessments, practical requirements, hygiene protocols, and competency standards. Where the Student fails, delays, or chooses not to complete required coursework or assessments, no certificate shall be issued under any circumstances. If certification is not achieved due to the Student’s delay, inactivity, lack of engagement, or failure to complete coursework within the course validity period, this shall be deemed a personal choice and responsibility of the Student and shall not entitle the Student to a refund; repeat training; free reassessment; or fee-free certification at a later date. NON-USE, DELAY & STUDENT CHOICE The Academy accepts no liability where a Student chooses not to attend; delays participation; postpones coursework; allows access to expire; or otherwise fails to engage with the training provided. Non-use of the course, for any reason whatsoever, including personal, medical, professional, financial, relocation, or lifestyle reasons, does not constitute grounds for refund, compensation, replacement training, or extension beyond the stated validity period.

LUNCH, REFRESHMENTS & ONSITE AMENITIES Where lunch or refreshments are provided, such provisions are offered as a courtesy and are subject to change without notice. The Academy does not guarantee specific lunch options, dietary accommodations, or availability of any particular food or beverage. Changes to lunch, refreshments, or amenities do not affect the validity of the Student’s course, shall not constitute a breach of contract, and shall not entitle the Student to a refund, compensation, or rescheduling. SCRUBS, UNIFORMS & DRESS CODE Where the Academy provides scrubs, uniforms, or protective clothing for training days, such items are provided subject to availability, sizing, and hygiene requirements. The Academy does not guarantee specific sizes, colours, or styles of scrubs. The Student is responsible for attending training in professional attire suitable for clinical and practical environments. Unavailability of scrubs or uniform items does not entitle the Student to a refund, compensation, or rescheduling. ACADEMY DISCLAIMER

ACADEMY POLICY FOR Training Days PHOTOGRAPHS, PORTFOLIO IMAGES & MEDIA CONTENT Any photographs, videos, or portfolio images taken during training are provided strictly as a courtesy and are subject to availability, lighting, model suitability, consent, staff capacity, and operational conditions. The Academy does not guarantee the provision of a minimum number of images; the quality, style, or format of images; the suitability of images for marketing or professional use; or the ability to photograph every model treated on the day. The availability or quality of photographs does not affect the validity of the Student’s course and shall not constitute grounds for refund, compensation, additional training, or repeat sessions.

PRICE VARIATION, SALES & INDIVIDUAL DISCOUNTS Course fees may vary over time, and prices may differ between Students due to sales, promotions, limited-time offers, early-bird pricing, negotiated arrangements, upgrades, or instructor-specific pricing. The Student acknowledges and agrees that another Student receiving a different price, discount, or promotional offer has no bearing on the Student’s contract; the Student is not itled to a refund, adjustment, compensation, or price match due to future or past pricing changes; promotional prices are time-bound and do not create any entitlement to retrospective application; and the price paid at the time of purchase is final. Price variation is normal in the commercial provision of training services and does not invalidate the Student’s contract or constitute unfair treatment. UAE / DUBAI GOVERNING LAW & JURISDICTION Where training, services, coursework, or digital access is delivered in the United Arab Emirates, including but not limited to Dubai, these Terms shall be governed by and construed in accordance with the laws of the Emirate of Dubai and the applicable federal laws of the United Arab Emirates. Any disputes arising in connection with UAE-based services shall be subject to the exclusive jurisdiction of the courts of Dubai. Where KHDA approvals or local regulatory permissions apply, the Student acknowledges that such approvals relate solely to licensing status and do not constitute a guarantee of results, income, competency, or commercial success. CROSS-BORDER LEGAL SEPARATION (UK & UAE OPERATIONS) Snatch & Glow operates across multiple jurisdictions. The legal entity responsible for the Student’s training, services, and contractual rights is the entity specified on the Student’s invoice and booking confirmation. UK-based purchases are governed by UK consumer law. UAE-based purchases are governed by UAE law. The Student expressly agrees that consumer protections, refund rights, enforcement procedures, and dispute resolution mechanisms vary by jurisdiction. No automatic right of refund, transfer, or legal enforcement shall arise between jurisdictions unless expressly required by law. TRAINING DAYS – STRICT LIMITATION OF ENTITLEMENT The number of training days included within any course, package, programme, or promotion is strictly limited to the number of days expressly advertised and confirmed in the Student’s onboarding confirmation and/or invoice. The Student acknowledges and agrees that: No additional training days, repeat sessions, refreshers, reassessments, shadowing, model practice, mentoring days, or extensions are included unless expressly purchased in writing; Dissatisfaction with confidence, speed, ability, results, or performance does not entitle the Student to additional training days; Failure to attend, late arrival, early departure, illness, or personal circumstances does not entitle the Student to replacement days; The Academy does not owe any training, compensation, repeat sessions, or additional support outside of the expressly contracted training days. NO IMPLIED EXTENSIONS, ADD-ONS OR UPGRADES No verbal statements, marketing materials, social media content, staff commentary, testimonials, or third-party platform listings shall be deemed to create any entitlement to training beyond that expressly stated in the Student’s confirmed package. Only written upgrades issued by Snatch & Glow and paid in full shall create any additional entitlement.

MODELS, PRACTICE & CLINICAL EXPOSURE – NO GUARANTEE OF VOLUME Where training involves models, live clients, or practical exposure, the Academy does not guarantee a specific number of models, a minimum number of treatments performed, or a minimum number of completed case studies. Model attendance is subject to external availability, cancellations, suitability, medical exclusions, consent, and safety requirements. This shall not constitute grounds for refund, additional training days, or compensation.

NO ACADEMIC OR PRACTICAL FAILURE ENTITLEMENT Where a Student does not meet minimum practical, safety, hygiene, conduct, or competence standards during training, the Academy reserves the right to withhold certification; restrict participation; require paid refresher training; or (d) terminate training without refund. Failure to pass, qualify, perform, or complete practical requirements does not create any right to refund, repeat training, or compensation. CONSUMER CANCELLATION RIGHTS (COOLING-OFF PERIOD) In accordance with the Consumer Contracts (Information, Cancellation and Additional Charges) Regulations 2013, where the Student is a consumer, the Student has the legal right to cancel a contract for services or digital content within fourteen (14) calendar days from the date of purchase (“Cooling-Off Period”), save where an exemption applies. Where the Student expressly requests immediate access to any digital content, online platform, learning portal, downloadable materials, recordings, or coursework within the Cooling-Off Period, the Student expressly acknowledges and agrees that their statutory right to cancel shall be lost upon access being granted. Where any in-person training, live practical session, classroom-based teaching, or supervised treatment begins within the Cooling-Off Period, the Student’s right to cancel is extinguished immediately upon commencement of services. Cancellation requests must be submitted in writing to info@snatchandglow.co.uk within the Cooling-Off Period. No verbal cancellations shall be accepted. ACADEMY DISCLAIMER

ACADEMY POLICY FOR Training Days DIGITAL CONTENT – STATUTORY WAIVER & FINALITY OF SALE By purchasing any digital coursework, online training, e-learning materials, portals, libraries, videos, written content, or downloadable products, the Student expressly consents to immediate delivery of digital content and expressly waives the statutory fourteen (14) day right to cancel once access has been granted. All sales of digital content are strictly final and non-refundable once access has been issued, regardless of whether the content has been viewed, completed, partially accessed, or unused. No refunds, chargebacks, reversals, or credit notes shall be issued for any digital content under any circumstances, including but not limited to dissatisfaction, inability to complete, technical issues, scheduling conflicts, or personal circumstances. FINANCE AGREEMENTS, FCA COMPLIANCE & SECTION 75 Where training or courses are funded in whole or in part through a third-party lender or finance provider, the Student enters into a separate, independent and legally binding agreement with the lender. Snatch & Glow Clinic and Training Academy is not the lender and accepts no responsibility for lending decisions; approval outcomes; credit assessments; interest rates; repayment schedules; default consequences; or credit reporting. All cancellation, refund and dispute requests must comply with both these Terms and the lender’s terms and conditions. Where digital content access or practical training has commenced, no refund shall be due under any finance agreement, save where mandated by law under Section 75 Consumer Credit Act 1974 (where applicable). Dissatisfaction with outcomes, non-attendance, or change of personal circumstances shall not invalidate any finance agreement. PROMOTIONAL, DISCOUNTED & CAMPAIGN PRICING – FINALITY OF SALE All purchases made at discounted, promotional, flash sale, seasonal, negotiated, bespoke, influencer, marketing- campaign, limited-time, or early-bird pricing are strictly final and non-refundable. By accepting a discounted or promotional price, the Student acknowledges that the reduced price reflects a binding commitment to proceed; no future price matching, re-pricing or refund shall be permitted; and dissatisfaction, delay, or personal circumstances shall not entitle the Student to a refund. Promotional pricing does not affect statutory consumer rights but overrides any discretionary or goodwill-based refund considerations.

COMPLAINTS PROCEDURE All complaints must be submitted strictly in writing to info@snatchandglow.co.uk within seven (7) days of the matter arising. All complaints shall be acknowledged within five (5) working days and a written response shall be provided within twenty-eight (28) working days. Complaints relating to finance agreements must be directed to the applicable lender in accordance with FCA dispute resolution procedures. FORCE MAJEURE We shall not be liable for any delay, postponement, rescheduling or cancellation caused by circumstances beyond our reasonable control, including but not limited to illness, pandemics, staff unavailability, venue closure, supply failure, governmental action, extreme weather, or acts of God. Where Force Majeure applies, training may be rescheduled without refund, compensation or liability. VULNERABLE CUSTOMER PROTECTION The Student must notify us in writing prior to purchase if they consider themselves to be a vulnerable consumer due to financial hardship, medical condition, learning difficulty, mental health condition, or other relevant vulnerability. Failure to disclose vulnerability prior to entering into a contract shall not invalidate the contract nor create an automatic right to refund. OUTCOMES, PERFORMANCE & EARNINGS DISCLAIMER All training is provided for educational purposes only. No guarantees are given in respect of income, commercial success, skill mastery, business performance, qualification outcome, client acquisition, or professional competency. Any illustrative earnings, business examples or marketing projections are provided for guidance only and do not constitute a guarantee. CHARGEBACKS, PAYMENT DISPUTES & RECOVERY Any chargeback or payment dispute raised in breach of these Terms shall constitute a contractual breach. We reserve the right to immediately suspend access to all services and certification; withhold course completion documentation; recover associated losses, fees and administrative costs; and submit full transaction evidence to banks, finance companies, card issuers, regulators, and legal authorities. ACADEMY DISCLAIMER

ACADEMY POLICY FOR Training Days COURSE STRUCTURE, FEES & ALLOCATION OF VALUE The Student acknowledges and agrees that the course fee is paid primarily for access to educational content, including but not limited to digital coursework, theoretical instruction, learning materials, assessments, and structured curriculum design (“Coursework”). Access to coursework is provided immediately upon purchase or enrolment and constitutes delivery of the core paid service. Any in-person practical training days, supervised practical sessions, face-to-face study, model practice, clinical observation, use of training models, supervision, consumables, facilities, equipment, staff oversight, refreshments, and ancillary support are provided at no additional cost and are included on a complimentary basis to support the educational experience. The provision, scheduling, or availability of complimentary practical elements does not alter the value allocation of the course fee and does not create any separate contractual entitlement or refund right. Where practical training is delayed, rescheduled, reduced, or unavailable due to operational, safety, regulatory, staffing, or model-availability reasons, this shall not constitute a failure of service, breach of contract, or grounds for refund, as the paid coursework has already been delivered. The Student expressly acknowledges that they are not purchasing individual training days, models, or practical sessions as standalone paid services, and that no refund, compensation, or price reduction shall be due in relation to complimentary practical components.

B12 INJECTION DISCLAIMER

TREATMENT POLICY FOR B12 INJECTION

PATIENT CONSENT

This is an informed consent form that has been prepared to help inform you of the potential benefits and risks of vitamin B12 injection. It is important that you read this information carefully and discuss fully with your practitioner before proceeding with treatment. It is also important that you take as much time as you need to consider the treatment carefully, weighing up all your options before reaching an informed decision. It is essential that you are aware of your right to have a second opinion and you are encouraged to ask any questions that come to mind throughout the entirety of the process. Vitamin B12 is also known as Cobalamin, it is a water-soluble vitamin essential for both fatty acid and amino metabolism as well as DNA synthesis. It is vital for the normal functioning of the nervous system, myelin sheath production and red blood cell maturation and development. Vitamin B12 deficiency has a broad presentation including fatigue, anemia, multiple neurological and psychiatric signs and symptoms. Replacement of vitamin B12 is in the form of Hydroxocobalamin given by intramuscular injection. The prophylactic dose for prevention of B12 deficiency is 1mg every 2-3 months by intramuscular injection. The other form of B12 injection is called (MIC-B12) which is vitamin B12 combined with Methionine, Inositol and Choline, given as a combination injection intramuscular. The MIC-B12 combination is targeted to try and facilitate weight loss together with a healthy diet and regular physical exercise. An intramuscular injection of B12 is given into the Deltoid muscle in the side of the upper arm. The procedure is very quick, you may feel a short, sharp pain during the injection. It is important that you see your doctor/GP if you suspect or display symptoms of B12 deficiency. It is important also to not exceed the recommended doses of B12. If your B12 injector is from a non-medical background, then your B12 injection must be prescribed by a doctor or prescribing nurse practitioner on a separate consultation appointment. B12 INJECTION DISCLAIMER

TREATMENT POLICY FOR B12 INJECTION

A blood test to check your blood B12 level can be taken by your doctor/GP, the prescribing clinician may want to know your B12 level before going ahead with B12 prescription for you. If you have a known vitamin B12 deficiency, then investigation of the cause and replacement should be conducted by your doctor/GP only.

RISKS AND SIDE EFFECTS: You must be aware of the following side effects of intramuscular vitamin B12 injection before commencing treatment. You must fully discuss any questions with your practitioner and prescriber before proceeding. I understand the common side effects are pain during injection, redness, swelling and soreness around the injection site lasting up to a few days. You may also experience some bruising around the injection site also. Some people can faint or feel faint with needles and injections, it is important to tell your practitioner as soon as possible if you feel unwell during or after the injection. Uncommon side effects include dizziness, headache, nausea, vomiting, hot flushes, skin reactions, chills,tremor, insomnia. Rare side effects include cardiac arrhythmias, thrombocytosis, hypokalemia (low blood potassium level). There is also a rare risk of allergic reaction or anaphylactic reaction to the B12 injection. In the event of anaphylaxis or any serious side effects, you would require emergency medical attention. I have been advised of the relevant information associated with this treatment and I confirm that I fully understand this advice. This includes advice about: - the aims/motivations for having the procedure and the desired outcome - the risks inherent in the procedure - the risks inherent in refusing the procedure - the risks specific to me - the expected benefits of the treatment - the potential disadvantages of the treatment - alternative procedures and their pros and cons - including the option of no treatment at all - any uncertainties about and the likelihood of success of the procedure - any follow-up treatment that may be required I request treatment with B12 or MIC-B12. The injection of B12 or MICB12 has been explained to me and my questions regarding such treatment have been answered to my satisfaction. The information given to me has been in clear terms and I understand the risks, benefits, possible side effects and complications of the treatment.I certify that I am in good health. I have read the information about the B-12 injection. I have been asked what information I want and would need in order to make an informed decision. B12 INJECTION DISCLAIMER

TREATMENT POLICY FOR B12 INJECTION I have been given the opportunity to discuss my desired outcome fully in order for me to make an informed decision. I certify that I have read the above consent and that I fully understand it. I have been given ample opportunity for discussion and all my questions have been answered to my satisfaction. No new information has become available that affects my decision to have the treatment or my decision to consent. I hereby consent to this procedure. This constitutes the full disclosure and supersedes any previous verbal or written disclosures.

BOTOX DISCLAIMER

TREATMENT POLICY FOR Botox This is an informed consent document that has been prepared to help inform you concerning Anti- wrinkle injections and the risks involved. It is important that you read this information carefully and completely. Please complete each section, indicating that you have read the page and sign the consent at the bottom prior to your treatment.

INTRODUCTION

Anti-Wrinkle injections involve a series of small injections in order to weaken the chosen muscles. The weakening of the injected muscles begins to be apparent after 2–3 days, with the peak effect being reached after 10–14 days. Results can last 3–6 months. The procedure can be repeated after 3 months; however, injections given at less than 3-month intervals may reduce the efficacy of the injections.

RISKS OF ANTI-WRINKLE INJECTIONS

Every procedure involves a certain amount of risk, and it is important that you understand the risks involved. An individual's choice to undergo a procedure is based on the comparison of the risk to potential benefit. Although the majority of patients do not experience these complications, you should discuss each of them with your practitioner to make sure you understand the risks, potential complications, and consequences of Anti-Wrinkle injections: Bleeding Bruising/Swelling Infection Unsatisfactory Outcome Temporary loss of function of nearby muscles

PUBLICITY MATERIALS I authorize the taking of clinical photographs and videos. I understand that photographs and video may be taken of me for educational and marketing purposes. I hold the practitioner harmless for any liability resulting from this production. I waive my rights to any royalties, fees and to inspect the finished production as well as advertising materials in conjunction with these photographs. BOTOX DISCLAIMER

TREATMENT POLICY FOR Botox CONSENT

You certify by signing this form that you have read the information in this document and completely understand it. You choose to proceed based entirely on the information provided in this informed consent document. You have been given all the necessary opportunities for discussion and all your questions regarding anti-wrinkle injections have been answered. You therefore and hereby consent to the care or treatment described herein. Any discrepancies must be taken up with the practitioner within 1 month of treatment.

BUM FILLER DISCLAIMER

TREATMENT POLICY FOR BUM FILLER The purpose of this procedure is to add volume and shape to the buttocks using injectable fillers. This is a cosmetic procedure intended to improve the appearance of the buttocks.

BUM FILLER TREATMENT PACKAGES – FINALITY OF SALE All Bum Filler / Non-Surgical BBL treatment packages are strictly non-refundable once any deposit or payment has been made. By paying a deposit or instalment toward a Bum Filler package, the Client enters into a binding agreement for the full package value. No refunds, partial refunds, credits, chargebacks, or cancellations shall be permitted under any circumstances once payment has been taken.

NO PARTIAL USE, OPT-OUT OR BALANCE REFUNDS Bum Filler packages are sold as a bundled treatment plan and are not divisible. Where a Client elects to proceed with only part of a package (for example, receiving 300ml of a 600ml package), this shall be deemed the Client’s informed choice. There is no option to opt out of the remainder of a package; convert unused product value into a refund or credit; or reclaim any unused balance. The full package price remains payable and final regardless of how much product is ultimately administered.

COMPLICATIONS, RESPONSE & NO-REFUND POSITION The Client acknowledges that individual response to Bum Filler varies and that risks may include, but are not limited to, swelling, bruising, firmness, nodules, infection, asymmetry, migration, uneven texture, reduced longevity, or need for further treatment. Such outcomes are recognised risks of treatment and do not constitute grounds for a refund, compensation, partial refund, free correction, or package cancellation. Longevity of filler varies between individuals and is not guaranteed. Reduced duration or faster breakdown of product is not a valid basis for complaint or refund.

TIME-LIMITED AFTERCARE & GOODWILL ONLY Any concerns, questions, or aftercare queries relating to Bum Filler treatment must be raised within four (4) weeks of the most recent treatment session. After four (4) weeks, the Clinic is under no obligation to provide further assessment, review, corrective treatment, or assistance. Any support, review, advice, or intervention offered after this period shall be provided strictly as a gesture of goodwill only and shall not create a legal obligation; constitute an admission of fault; or entitle the Client to a refund, compensation, or further treatment.

NO GUARANTEE, NO COMPENSATION The Client expressly acknowledges that cosmetic outcomes are subjective and that Bum Filler treatments are elective. Dissatisfaction with appearance, volume, shape, symmetry, longevity, or comparison to other clients, marketing images, or social media results does not entitle the Client to any form of refund, compensation, or remedial treatment.

SUBJECTIVE AESTHETICS & LIMITATION OF CONTROL The Client expressly acknowledges that there is no single, universal, or objectively “correct” aesthetic outcome for Bum Filler or Non-Surgical BBL treatments. Aesthetic preferences vary between individuals, cultures, practitioners, and trends, and satisfaction is inherently subjective. Differences in opinion regarding what constitutes a desirable result do not constitute a defect, failure of service, or grounds for complaint, refund, compensation, or remedial treatment. Once a product has been injected, the Clinic cannot control how the product behaves within the Client’s body. Factors including, but not limited to, metabolism, circulation, tissue composition, immune response, physical activity, pressure, aftercare compliance, and individual biology influence the way filler settles, integrates, migrates, or breaks down. The Clinic does not and cannot guarantee uniform behaviour, symmetry, longevity, or aesthetic outcome once the product is inside the body, and such biological variability does not constitute negligence, breach of contract, or clinical fault. ELECTIVE TREATMENT, MEDICAL DISCLOSURE & EMERGENCY CARE The Client acknowledges that Bum Filler / Non-Surgical BBL is an elective cosmetic treatment and is not medically necessary. The Client confirms that they have fully and accurately disclosed all relevant medical history prior to treatment, including but not limited to allergies (including lidocaine or other local anaesthetics); sensitivities or adverse reactions; medical conditions; current or recent medications; self-medication, supplements, or recreational substances; and previous cosmetic or medical procedures. Failure to disclose complete and accurate medical information releases the Clinic from liability for any adverse reaction, complication, or outcome arising from such non-disclosure. Any reaction, complication, or outcome resulting from undisclosed information shall be the sole responsibility of the Client. The Clinic is an aesthetic clinic and not a hospital, emergency department and has limited means to assist outside of opening hours. Outside of clinic operating hours, the Client is responsible for seeking appropriate emergency medical care through NHS 111, A&E, or emergency services where required. The Clinic is not responsible for delays in seeking emergency care, third-party medical intervention, or outcomes resulting from failure to follow emergency guidance. BUM FILLER DISCLAIMER

TREATMENT POLICY FOR BUM FILLER THIRD-PARTY INTERVENTION & CONTINUITY OF CARE Where the Client seeks, receives, or undergoes any third-party medical or aesthetic intervention following treatment at the Clinic, including but not limited to treatment by another clinic, practitioner, hospital, emergency department, or self- administered intervention, the Clinic shall no longer be able to safely continue treatment or provide further aesthetic services. Once third-party intervention has occurred, the Clinic can no longer verify the nature or extent of substances introduced; the volume, depth, or location of any product; any medication administered; any procedures performed; or any alterations to the treated area. For reasons of patient safety, clinical governance, and professional responsibility, the Clinic reserves the absolute right to decline further assessment, review, correction, or treatment once third-party intervention has taken place. Such refusal shall not constitute a breach of contract, negligence, or failure of aftercare, and shall not give rise to any entitlement to a refund, compensation, or continued treatment. VOLUME RECOMMENDATIONS, VARIABILITY & NO GUARANTEE OF OUTCOME Any recommendation given prior to treatment regarding the volume of filler required is an estimate only and is provided for guidance purposes. The Client acknowledges that until product is placed, it is not possible to determine precisely how the filler will integrate, settle, or appear within the body. As such, volume recommendations may change during or after treatment based on anatomical response, tissue behaviour, safety considerations, and professional judgment. Individual aesthetic goals, expectations, and reference images may require differing amounts of product to achieve a desired appearance. The same volume of filler can produce markedly different results between individuals. The Clinic does not guarantee that any specific volume will achieve a particular look, size, shape, projection, symmetry, or outcome. No guarantee is given in respect of results, longevity, or satisfaction. The need for additional product or further treatment to approach a desired aesthetic outcome does not constitute a failure of service and is chargeable separately where applicable. PROMOTIONAL OFFERS, SPECIAL PRICING & VARIATION IN COSTS Where a treatment or package is purchased at a discounted, promotional, campaign, flash-sale, negotiated, or special offer price (“Promotional Offer”), such pricing is strictly limited to the specific treatment, volume, practitioner, and appointment confirmed at the time of purchase. The Client acknowledges and agrees that Promotional Offers are time-limited and non-repeatable and do not create any entitlement to the same price for future appointments, repeat treatments, or follow-up sessions; The Clinic is under no obligation o honour a previous Promotional Offer if the Client returns at a later date, requests further treatment, or seeks to rebook after completion or non-attendance; Any additional treatment, extra volume, supplementary procedure, or extension requested on the day of treatment is chargeable at the prevailing standard rate and is not included within the Promotional Offer unless expressly confirmed in writing; Where the Client requests to change practitioner, the applicable fees may differ. Promotional pricing is practitioner-specific and cannot be exchanged, transferred, or honoured across different practitioners; Promotional treatments and packages are non-transferable and may not be assigned, gifted, shared, or used by another individual; Promotional Offers cannot be extended, rolled over, exchanged, or partially applied to future appointments, whether within the same course of treatment or otherwise. PROMOTIONAL PURCHASES, PRODUCT ORDERING & NO REFUNDS Where a treatment or package is purchased under a Promotional Offer, the Client acknowledges that products and clinical resources may be allocated or ordered immediately upon purchase. In accordance with consumer protection regulations, any applicable statutory cooling-off rights are extinguished once treatment has commenced or where the Client has expressly requested immediate delivery of services or products. All Promotional Offer purchases are strictly non-refundable and non-exchangeable once any payment has been made, regardless of whether the full treatment has been utilised. This does not affect the Client’s statutory rights but excludes any discretionary, goodwill, or promotional-based refunds. FAIR PRICING & FCA-ALIGNED DISCLOSURE The Clinic operates transparent and fair pricing in line with applicable consumer protection and FCA principles. Price variation between Clients, appointments, practitioners, or time periods is a normal and lawful commercial practice and does not constitute unfair treatment, misrepresentation, or grounds for complaint. The price paid at the time of purchase reflects the terms, conditions, and availability applicable at that point in time and is final. REVIEWS, FOLLOW-UPS & GOODWILL GESTURES Where the Clinic requests or facilitates a review, feedback, or testimonial, this shall be limited to one post-treatment review only, unless expressly agreed otherwise in writing. Any additional reviews, follow-up feedback requests, check-ins, progress assessments, photographs, or communications requested or provided outside of this initial review are offered strictly as a gesture of goodwill. The Clinic is under no obligation to: request further reviews; provide ongoing follow-ups; assess results months after treatment; respond to delayed feedback; or engage in post-treatment review discussions beyond the initial review period. Any goodwill review, follow-up, response, or engagement provided after the initial review does not: create a contractual obligation; extend aftercare or liability periods; constitute acceptance of responsibility; or entitle the Client to further reviews, treatment, refunds, or compensation. Absence of follow-up reviews or engagement does not affect the validity of the treatment provided and does not constitute a failure of service. BUM FILLER DISCLAIMER

TREATMENT POLICY FOR BUM FILLER FILLER PURCHASES – VALIDITY & EXPIRY Any dermal filler product purchased from the Clinic, whether as a standalone purchase, part of a treatment, or included within a package, is valid for use for a period of twelve (12) months from the date of purchase only. Where filler is not administered within this twelve (12) month period for any reason, including but not limited to non- attendance, pregnancy, relocation, change of mind, medical reasons, or personal circumstances, the unused filler value shall automatically expire without refund, credit, or compensation. Expired filler purchases cannot be refunded; exchanged; transferred to another person; or extended beyond the validity period. Any rebooking, renewal, or re-purchase after expiry shall be chargeable at the Clinic’s prevailing rates at the time of booking. This clause does not affect the Client’s statutory rights where applicable.

PERSONAL CIRCUMSTANCES AFTER BOOKING Once a Bum Filler treatment appointment has been booked and the Client has expressly requested the service to be scheduled and prepared, any subsequent change in personal circumstances shall not give rise to a right to cancel, refund, exchange, or credit. This includes, but is not limited to: pregnancy (whether known or discovered after booking); relocation or intention to move country; change of mind or altered aesthetic preference; changes in lifestyle, work, travel, or availability; or any other personal, medical, or practical circumstance arising after booking. Where a treatment cannot proceed due to pregnancy or other personal circumstances, the booking shall be treated in accordance with the Clinic’s rescheduling or no-show policy, and no refund shall be due. Such circumstances do not affect the validity of the booking, the loss of any applicable cooling-off rights following booking and preparation, or the Client’s payment obligations. This clause does not affect the Client’s statutory rights where applicable.

FINANCE AGREEMENTS, FCA COMPLIANCE & SECTION 75 (BUM FILLER TREATMENTS) Where Bum Filler or Non-Surgical BBL treatments are paid for in whole or in part through a third-party lender or finance provider, the Client enters into a separate, independent and legally binding credit agreement directly with the lender. Snatch & Glow Clinic is not the lender and accepts no responsibility for lending or approval decisions; credit assessments; interest rates or charges; repayment schedules; defaults or arrears; or credit reporting or lender enforcement action. All cancellations, refunds, disputes, or complaints must comply with both, these Clinic Treatment Terms; and the lender’s terms and conditions. Where Bum Filler treatment has commenced, products have been opened, prepared, or injected, or the Client has expressly requested immediate performance of the service, no refund shall be due under any finance agreement, save where mandated by law under Section 75 of the Consumer Credit Act 1974 (where applicable). Dissatisfaction with aesthetic outcomes, longevity, volume, non-attendance, or changes in personal circumstances shall not invalidate any finance agreement.

PROMOTIONAL, DISCOUNTED & CAMPAIGN PRICING – FINALITY OF SALE (BUM FILLER) All Bum Filler treatments or packages purchased at discounted, promotional, flash-sale, campaign, negotiated, influencer, limited-time, or early-bird pricing are strictly final, non-refundable, and non-exchangeable. By accepting a promotional or discounted price, the Client acknowledges that the reduced price reflects a binding commitment to proceed with treatment; no future price matching, re-pricing, extension, or refund shall be permitted; and pregnancy, relocation, change of mind, dissatisfaction with results, or inability to attend shall not entitle the Client to a refund. Promotional pricing does not affect statutory consumer rights but excludes any discretionary or goodwill-based refunds, credits, or exchanges.

COMPLAINTS PROCEDURE (TREATMENT-RELATED) Any complaint relating to Bum Filler treatment must be submitted strictly in writing to info@snatchandglow.co.uk within seven (7) days of the matter arising. Complaints shall be acknowledged within five (5) working days and a written response provided within twenty-eight (28) working days. Complaints relating to finance agreements must be directed to the relevant lender in accordance with FCA dispute resolution procedures. Late complaints, unsupported allegations, or complaints raised months after treatment may not be accepted. FORCE MAJEURE (CLINIC TREATMENTS) The Clinic shall not be liable for any delay, postponement, rescheduling, or cancellation of Bum Filler treatments caused by circumstances beyond its reasonable control, including but not limited to illness, practitioner unavailability, emergencies, supply disruption, venue closure, governmental action, or acts of God. Where Force Majeure applies, appointments may be rescheduled without refund, compensation, or liability. VULNERABLE CLIENT PROTECTION Clients who consider themselves vulnerable due to financial hardship, medical conditions, mental health concerns, learning difficulties, or other relevant vulnerabilities must notify the Clinic in writing prior to booking or payment. Failure to disclose vulnerability prior to entering into a treatment agreement shall not invalidate the contract nor create any automatic right to cancellation, refund, or compensation. BUM FILLER DISCLAIMER

TREATMENT POLICY FOR BUM FILLER OUTCOMES, RESULTS & AESTHETIC DISCLAIMER (BUM FILLER) Bum Filler and Non-Surgical BBL treatments are elective cosmetic procedures. No guarantees are given in respect of: aesthetic outcome; size, shape, lift, projection, or symmetry; longevity of filler; or satisfaction with results. Any before-and-after images, examples, or testimonials are illustrative only and do not constitute a promise or guarantee of outcome.

CHARGEBACKS, PAYMENT DISPUTES & RECOVERY (TREATMENTS) Any chargeback or payment dispute raised in breach of these Treatment Terms shall constitute a contractual breach. The Clinic reserves the right to: immediately suspend further appointments or aftercare; refuse future treatment; recover losses, chargeback fees, and administrative costs; and submit full transaction, consent, medical, and treatment records to banks, finance providers, card issuers, regulators, and legal authorities.

CHECMICAL PEEL DISCLAIMER

TREATMENT POLICY FOR CHEMICAL PEEL This is an informed consent form that has been prepared to help inform you of the potential benefits and risks of chemical peel. It is important that you read this information carefully and discuss fully with your practitioner before proceeding with treatment. It is also important that you take as much time as you need to consider the treatment carefully, weighing up all your options before reaching an informed decision. It is essential that you are aware of your right to have a second opinion and you are encouraged to ask any questions that come to mind throughout the entirety of the process.

WHAT IS A CHEMICAL PEEL? A chemical peel involves the application of a chemical solution to the skin which acts to remove the top layers of the skin. The skin that regrows is smoother with improved cosmetic appearance. A chemical peel can be used to improve the appearance of: Lines and wrinkles Tired skin Fine scars Acne Areas of skin pigmentation There are 3 different types of chemical peels: light, medium, and deep. These relate to the different depths of skin layer removal: Deeper peels take longer to heal but provide more significant results. Light peels are gentler and may need to be done more frequently. A deep chemical peel should only be done once, as repetition can damage the skin. Multiple treatments for lighter peels are often required to obtain optimal results, spaced apart. Due to variables such as age, skin condition, sun damage, smoking, skincare use, lifestyle, and general health, no guarantees or warranties are provided regarding results. Healing time is up to 14 days. Repeat peels should be done only after 4–6 weeks.

RISKS AND SIDE EFFECTS As with any procedure, there are risks and complications involved. I am aware of the following: Common Side Effects: Mild to moderate discomfort or pain Slight redness or swelling Increased sun sensitivity General increased skin sensitivity These can last up to 14 days. Occasionally, redness may persist longer. CHECMICAL PEEL DISCLAIMER

TREATMENT POLICY FOR CHEMICAL PEEL This is an informed consent form that has been prepared to help inform you of the potential benefits and risks of chemical peel. It is important that you read this information carefully and discuss fully with your practitioner before proceeding with treatment. It is also important that you take as much time as you need to consider the treatment carefully, weighing up all your options before reaching an informed decision. It is essential that you are aware of your right to have a second opinion and you are encouraged to ask any questions that come to mind throughout the entirety of the process.

WHAT IS A CHEMICAL PEEL? A chemical peel involves the application of a chemical solution to the skin which acts to remove the top layers of the skin. The skin that regrows is smoother with improved cosmetic appearance. A chemical peel can be used to improve the appearance of: Lines and wrinkles Tired skin Fine scars Acne Areas of skin pigmentation There are 3 different types of chemical peels: light, medium, and deep. These relate to the different depths of skin layer removal: Deeper peels take longer to heal but provide more significant results. Light peels are gentler and may need to be done more frequently. A deep chemical peel should only be done once, as repetition can damage the skin. Multiple treatments for lighter peels are often required to obtain optimal results, spaced apart. Due to variables such as age, skin condition, sun damage, smoking, skincare use, lifestyle, and general health, no guarantees or warranties are provided regarding results. Healing time is up to 14 days. Repeat peels should be done only after 4–6 weeks.

RISKS AND SIDE EFFECTS As with any procedure, there are risks and complications involved. I am aware of the following: Common Side Effects: Mild to moderate discomfort or pain Slight redness or swelling Increased sun sensitivity General increased skin sensitivity These can last up to 14 days. Occasionally, redness may persist longer. CHECMICAL PEEL DISCLAIMER

TREATMENT POLICY FOR CHEMICAL PEEL Less Common Risks: Pigment changes (lightening or darkening of the skin) Some pigment changes may be permanent Rare Complications: Allergic reaction to the chemical product (including possible anaphylaxis) Bacterial infection (e.g., cellulitis) Reactivation of herpes virus Permanent scarring I understand that the treatment may involve risks of complication or injury from both known and unknown causes, and I freely assume those risks.

DISCLOSURE AND UNDERSTANDING

Before receiving treatment, I have disclosed all relevant medical conditions that may affect this procedure. I have been advised of all relevant information and I fully understand this advice, including: Aims and motivations for treatment Inherent risks of the procedure and of refusing it Risks specific to me Expected benefits and possible disadvantages Alternatives, including no treatment Uncertainties and likelihood of success Possible need for follow-up treatment

CLINICAL PHOTOS AND VIDEOS I agree to and authorise the taking of clinical photographs and videos. I understand that these will form part of my confidential medical records.

FINAL CONSENT I have been asked what information I need to make an informed decision. I have had the opportunity to discuss my desired outcome and ask all questions to my satisfaction. I certify that I have read and fully understand the consent. I have been given ample opportunity for discussion. No new information has become available that affects my decision. I hereby consent to this procedure. This constitutes full disclosure and supersedes all prior disclosures.

DERMAL FILLER DISCLAIMER

TREATMENT POLICY FOR DERMAL FILLER This informed consent form is to provide written information regarding the risks, benefits and alternatives of the procedure you are about to undertake. This material serves as a supplement to the discussion you have with your doctor/healthcare/medical provider. It is important that you fully understand this information, so please read this document thoroughly. If you have any questions regarding the procedure, ask your doctor/healthcare professional prior to signing the consent form. Dermal filler treatment with dermal fillers can smooth out facial folds and wrinkles, add volume to the lips, and contour facial features that have lost their volume and fullness due to ageing, sun exposure, illness, etc.

RISKS AND COMPLICATIONS Understanding the risks is essential. No procedure is completely risk-free. The following risks may occur, but there may be unforeseen risks and risks that are not included on this list. Some of these risks, if they occur, may necessitate hospitalisation, and/or extended outpatient therapy to permit adequate treatment. It has been explained to me that there are certain inherent and potential risks and side effects in any invasive procedure and in this specific instance such risks include but are not limited to: 1. Post treatment discomfort, swelling, redness, bruising, and discolouration 2. Post treatment infection associated with any transcutaneous injection 3. Allergic reaction 4. Reactivation of herpes (cold sores) 5. Lumpiness, visible yellow or white patches 6. Granuloma formation 7. Localised necrosis and/or sloughing, with scab and/or without scab if blood vessel occlusion occurs

PUBLICITY MATERIALS I authorise the taking of clinical photographs and videos. I understand that photographs and video may be taken of me for educational and marketing purposes. I hold the practitioner harmless for any liability resulting from this production. I waive my rights to any royalties, fees and to inspect the finished production as well as advertising materials in conjunction with these photographs. DERMAL FILLER DISCLAIMER

TREATMENT POLICY FOR DERMAL FILLER

RESULTS Dermal fillers have been shown to be safe and effective when compared to collagen skin implants and related products to fill in wrinkles, lines and folds in the skin on the face. Its effect can last up to 12 months. However, there is no guarantee that you will be completely satisfied. There is no guarantee that you will not require additional treatment to achieve the results you seek. The dermal filler procedure is temporary and additional treatments will be required periodically, generally within 4-8 months. I am aware that follow-up treatments will be needed to maintain the full effects. I am aware the duration of treatment is dependent on many factors. I have been instructed in and understand the post-treatment instructions. The results may need a downtime period of up to 2-4 weeks of recovery.

RIGHT TO DISCONTINUE TREATMENT I understand that I have the right to discontinue treatment at any time & I understand payment will still have to be made in full.

PAYMENT I understand that this is an ‘elective’ procedure and that payment is my responsibility and is expected at the time of treatment. I understand this is an elective procedure & the procedure has been fully explained to me. I have read the above and understand it. My questions have been answered satisfactorily. I accept the risks and complications of the procedure and I understand that no guarantees are implied as to the outcome of the procedure. I also certify that if I have any changes in my medical history I will notify the doctor/healthcare professional who treated me immediately. I also state that I read and write in English. I certify by signing this form that you have read the information in this document and completely understand it. I choose to proceed based entirely on the information provided in this informed consent document. You have been given all necessary opportunities for discussion and all your questions regarding dermal fillers have been answered. I therefore and hereby consent to the care or treatment described herein. Any discrepancies must be taken up with practitioner within 1 month of treatment.

FAT DISSOLVING DISCLAIMER

TREATMENT POLICY FOR FAT DISSOLVING

BACKGROUND AQUALYX was developed by the renowned aesthetic surgeon Prof. Pasquale Motolese in 2002 and has been used for many years in different countries of the European Community and abroad. The manufacturer Marllor states sales of two million vials in two years. No major side effects occurred and the treatment was well-tolerated and successful.

FORMULATION AQUALYX is an injectable, hydrous, micro-gelantuous solution, which is biocompatible and biodegradable. It causes the dissolution of fat cells, after which the body then expels the released fatty acids naturally. AQUALYX™ is a complex containing detergent from the desoxycholate family that has been physically modified in order to reduce the biological half-life and the sugar-based slow release system results in minimal side effects. Ingredients include: Polymer from 3,6-Anhydro-L-Galactose and D-Galactose Buffer systems Sodium salt of (3α, 5β, 12α) - 3,12-dihydroxy-5-cholan-24-acid Water for injection Sodium chloride During intralipotherapy, AQUALYX™ is injected directly into the subcutaneous fat tissue using very thin, sharp cannulas. In the following weeks, the treated fat cells are gradually dissolved. The metabolism in the treated area is increased. Note: Intralipotherapy is not for weight loss but is used to improve and alter the contour of the body. It is intended for patients with localised adipose tissue not responding to diet or physical activity. Results cannot be compared to liposuction. The procedure takes time to reach full effect. Long-term results have shown relevance even seven years post-treatment. The patient must bear all expenses as this is generally not covered by health insurance.

THERAPY Intralipotherapy can serve as a moderate fat reduction method or as treatment against benign adipomas in patients avoiding surgery. Anaesthesia: Generally not required Safety: No recorded cases of overdose or toxication Treatment intervals: 3 to 4 weeks Total sessions: 2 to 8 sessions depending on treatment area Ultrasound therapy: Optional, not essential A minimum of two treatments is required. About 1% of patients experience minimal to no effects. FAT DISSOLVING DISCLAIMER

TREATMENT POLICY FOR FAT DISSOLVING

ADVERSE EFFECTS General risks: Permanent nerve or tissue damage Inflammatory reactions Infections Irreversible scarring Expected effects: Swelling and heat in the injected area Haematoma Pressure sensitivity Moderate pain and itching Possible effects: Persistent redness Permanent tissue lumping or firmness Area denting due to uneven fat reduction Vegetative disorders Temporary circulatory weakness (stay well hydrated) Increased sweating Nausea or diarrhoea (uncommon) Menstrual irregularities Allergic reactions (very rare): hives, bronchial asthma, shock symptoms Hyperpigmentation (can last several months)

ALTERNATIVES & CLINICAL CONTROL I have been informed about alternatives including: Diet and exercise Surgical procedures (e.g., liposuction) I am not considering these alternatives. Follow-up: A clinical review will be carried out after all sessions and scheduled intervals.

POST-TREATMENT CARE I understand: No cosmetics should be applied to treated area for 12 hours Avoid heat exposure (sunlight, UV, sauna) for a few days Avoid laser, cryolipolysis, or radiofrequency post-AQUALYX No strenuous physical activity for 7 days FAT DISSOLVING DISCLAIMER

TREATMENT POLICY FOR FAT DISSOLVING

CONSENT I have read this informed consent and certify that I understand its contents fully. I have been given a copy of this form My consent is voluntary I understand the nature and risks of the procedure No guarantees have been given regarding outcomes I have had time to consider and am sufficiently advised I hereby give my consent to intralipotherapy with AQUALYX and possible ultrasound treatment I have been asked to sign this form after discussing it with my physician.

HYALURONIDASE DISCLAIMER

TREATMENT POLICY FOR HYALURONIDASE

PATIENT CONSENT This is an informed consent form that has been prepared to help inform you of the potential benefits and risks of hyaluronidase filler dissolving injections. It is important that you read this information carefully and discuss fully with your practitioner before proceeding with treatment. It is also important that you take as much time as you need to consider the treatment carefully, weighing up all your options before reaching an informed decision. It is essential that you are aware of your right to have a second opinion and you are encouraged to ask any questions that come to mind throughout the entirety of the process.

ABOUT HYALURONIDASE Hyaluronidase (Hyalase) is an enzyme that breaks down the hyaluronic acid component of dermal fillers. It is more commonly known as filler dissolving treatment and it is used for the removal of fillers. Hyalase will break dermal filler down into a liquid which the body can then naturally resorb. There are many reasons why dermal filler may want to be removed. Common routine reasons include: Filler migration Filler nodules Tyndall effect Unsightly filler Poor cosmetic outcomes Hyaluronidase is also used in an emergency to reverse vascular occlusion caused by intravascular injection of dermal filler. Emergency reversal is vital because if left untreated it can lead to skin necrosis, which may require reconstructive surgery.

ADDITIONAL TREATMENTS

The possibility of treatment failure has been discussed with me as well as the possibility of requiring a second filler dissolving procedure. This is more likely in cases involving: Large filler volumes Large areas of migration Stubborn filler pockets Thick fillers more resistant to dissolving I understand that several appointments may be necessary to produce optimal results, and I will be notified in advance of each session regarding location and practitioner. I understand I can change my mind at any point. HYALURONIDASE DISCLAIMER

TREATMENT POLICY FOR HYALURONIDASE

PATIENT CONSENT This is an informed consent form that has been prepared to help inform you of the potential benefits and risks of hyaluronidase filler dissolving injections. It is important that you read this information carefully and discuss fully with your practitioner before proceeding with treatment. It is also important that you take as much time as you need to consider the treatment carefully, weighing up all your options before reaching an informed decision. It is essential that you are aware of your right to have a second opinion and you are encouraged to ask any questions that come to mind throughout the entirety of the process.

ABOUT HYALURONIDASE Hyaluronidase (Hyalase) is an enzyme that breaks down the hyaluronic acid component of dermal fillers. It is more commonly known as filler dissolving treatment and it is used for the removal of fillers. Hyalase will break dermal filler down into a liquid which the body can then naturally resorb. There are many reasons why dermal filler may want to be removed. Common routine reasons include: Filler migration Filler nodules Tyndall effect Unsightly filler Poor cosmetic outcomes Hyaluronidase is also used in an emergency to reverse vascular occlusion caused by intravascular injection of dermal filler. Emergency reversal is vital because if left untreated it can lead to skin necrosis, which may require reconstructive surgery.

ADDITIONAL TREATMENTS

The possibility of treatment failure has been discussed with me as well as the possibility of requiring a second filler dissolving procedure. This is more likely in cases involving: Large filler volumes Large areas of migration Stubborn filler pockets Thick fillers more resistant to dissolving I understand that several appointments may be necessary to produce optimal results, and I will be notified in advance of each session regarding location and practitioner. I understand I can change my mind at any point. HYALURONIDASE DISCLAIMER

TREATMENT POLICY FOR HYALURONIDASE

RISKS AND SIDE EFFECTS Common side effects: Stinging pain on injection Tenderness post-injection Bleeding and bruising Swelling (typically mild, may occasionally be significant) Most swelling improves within 48 hours. Follow all aftercare advice and maintain contact with your practitioner. Tell your practitioner immediately if you feel unwell during treatment. Uncommon complications: Infection at injection site Mild allergic reactions Tissue thinning and volume loss (Hyalase may break down natural connective tissues) Risk increases with excessive or very frequent use (except in emergencies) Rare complications: Severe allergic reaction Anaphylaxis (requires emergency care) I agree to wait for 30 minutes after Hyaluronidase administration so I can be monitored for allergic reaction symptoms.

PATCH TEST CONSENT

I consent to a patch test before elective use of Hyalase to identify potential allergic risk. This involves a small injection into the forearm. Risks (uncommon) include: Pain Redness Localised rash Infection Bruising For emergency use, I agree to proceed without a patch test due to urgency. Risk/benefit has been explained and accepted. HYALURONIDASE DISCLAIMER

TREATMENT POLICY FOR HYALURONIDASE

INFORMATION RECEIVED I have been advised of and understand: Aims/motivations for the procedure Risks inherent in the procedure and in refusing treatment Risks specific to me Expected benefits Potential disadvantages Alternatives (including no treatment) Likelihood of success Any follow-up treatments that may be required

CLINICAL PHOTOS AND VIDEOS I agree to and authorise the taking of clinical photographs and videos. I understand these will be stored with my confidential medical records.

FINAL CONSENT I have been asked what information I want and need to make an informed decision. I have been given the opportunity to fully discuss my desired outcome. I certify that: I have read and fully understand this consent I’ve had sufficient opportunity for discussion All questions have been answered No new information has changed my decision I hereby consent to this procedure. This constitutes full disclosure and supersedes any previous verbal or written disclosures.

IV THERAPY DISCLAIMER

TREATMENT POLICY FOR IV THERAPY

PATIENT CONSENT This is an informed consent form that has been prepared to help inform you of the potential benefits and risks of IV infusion therapy. It is important that you read this information carefully and discuss fully with your practitioner before proceeding with treatment. It is also important that you take as much time as you need to consider the treatment carefully, weighing up all your options before reaching an informed decision. It is essential that you are aware of your right to have a second opinion and you are encouraged to ask any questions that come to mind throughout the entirety of the process.

ABOUT IV THERAPY IV infusion therapy involves the insertion of a venous cannula into a vein in your hand or arm. A bag of IV fluid is then infused into your bloodstream via the cannula. The fluid is based on sodium chloride with various preparations available, usually with multivitamin combinations. The infusion fluid you receive must be prescribed by a medical doctor or prescribing nurse. You must inform the practitioner of any known allergies, current medications, or medical conditions. The infusion fluid of choice will be decided after discussion with your practitioner and prescriber. Alternatives to IV therapy include oral supplements and/or dietary and lifestyle changes. Note: IV infusion therapy and any claims made are not intended to diagnose, treat, cure, or prevent any medical disease. These IV infusions are not a substitute for medical care. The main benefits are rehydration and vitamin/mineral supplementation.

ABOUT IV THERAPY As with any procedure, there are potential risks. You must be aware of and discuss these with your practitioner. Common complications: Pain during cannula insertion Bruising and pain at the injection site Failed cannulation requiring multiple attempts Tissuing (fluid leaking into the skin due to dislodged cannula) – causes pain and swelling; may require cannula removal Fainting or feeling faint during treatment IV THERAPY DISCLAIMER

TREATMENT POLICY FOR IV THERAPY Uncommon complications: Skin/tissue infection (cellulitis) Vein inflammation (thrombophlebitis) Venous injury and haematoma Rare complications: Fluid overload Electrolyte imbalances Nerve or artery injury during cannula insertion Extremely rare complications: Severe allergic reaction Anaphylaxis (requires emergency medical care)

INFORMATION PROVIDED I have been advised of the relevant information associated with this treatment and I confirm that I fully understand this advice. This includes advice about: The aims/motivations for having the procedure and the desired outcome The risks inherent in the procedure The risks inherent in refusing the procedure The risks specific to me The expected benefits of the treatment The potential disadvantages of the treatment Alternative procedures and their pros and cons – including the option of no treatment at all Any uncertainties about and the likelihood of success of the procedure Any follow-up treatment that may be required

CLINICAL PHOTOS AND VIDEOS I agree to and authorise the taking of clinical photographs and videos. I understand that these clinical photographs and videos will form part of and will be kept with my confidential medical records.

FINAL CONSENT I have been asked what information I want and would need in order to make an informed decision. I have been given the opportunity to discuss my desired outcome fully in order for me to make an informed decision. I certify that I have read the above consent and that I fully understand it. I have been given ample opportunity for discussion and all my questions have been answered to my satisfaction. No new information has become available that affects my decision to have the treatment or my decision to consent. I hereby consent to this procedure. This constitutes the full disclosure and supersedes any previous verbal or written disclosures.

JALUPRO DISCLAIMER

TREATMENT POLICY FOR JALUPRO

PATIENT CONSENT This is an informed consent form that has been prepared to help inform you of the potential benefits and risks of Jalupro skin booster. It is important that you read this information carefully and discuss fully with your practitioner before proceeding with treatment. It is also important that you take as much time as you need to consider the treatment carefully, weighing up all your options before reaching an informed decision. It is essential that you are aware of your right to have a second opinion and you are encouraged to ask any questions that come to mind throughout the entirety of the process.

ABOUT JALUPRO Jalupro is an injectable dermal biorevitaliser which acts as a skin collagen booster. It is a combination of amino acids and hyaluronic acid in liquid form, injected intradermally. The product stimulates dermal collagen and elastin production, creating a skin rejuvenation effect. Jalupro can be used to treat: Fine lines and wrinkles Stretch marks Anti-aging effects on face, neck, and body Dark under-eye circles Tired skin around the eyes Note: Jalupro is rejuvenating, not volumising like dermal fillers. It will not be effective for deep wrinkles or scars. Results: Can be seen instantly but take up to 14 days to peak Recommended: 1–3 treatment courses, spaced 2–4 weeks apart Effects may last up to 6 months (can be longer or shorter) I am aware that results vary between clients and there is no guarantee of desired outcomes. Multiple treatments may be required to achieve or maintain results.

TREATMENT PLAN I understand that several appointments may be necessary. I will be informed in advance of: The location of each session The practitioner involved My progress and any changes to the plan I understand I may change my mind at any point. JALUPRO DISCLAIMER

TREATMENT POLICY FOR JALUPRO

RISKS AND SIDE EFFECTS Jalupro is a safe and low-risk procedure, but I must be aware of the following: Common side effects: Pain during injection Minor bleeding Bruising in the treatment area Swelling and redness Raised, red, swollen bumps resembling insect bites (may itch or feel warm/irritable) – Usually settles within 48 hours – Bruising may last up to 2 weeks or longer around the eyes Fainting or feeling faint (inform practitioner immediately) Uncommon side effects: Extensive bruising (haematoma) Skin infection (cellulitis), requiring medical attention Jalupro is a liquid (not a thick gel like fillers) and does not cause vascular occlusion Rare risks: Allergic reaction to Jalupro (including anaphylaxis, which requires emergency care)

INFORMATION PROVIDED I have been advised of all relevant information and confirm I fully understand it. This includes: The aims/motivations for the procedure and the desired outcome The risks inherent in the procedure The risks of refusing the procedure The risks specific to me The expected benefits Potential disadvantages Alternatives (including no treatment) Any uncertainties and the likelihood of success Possible follow-up treatments

CLINICAL PHOTOS AND VIDEOS I agree to and authorise the taking of clinical photographs and videos. These will form part of and be kept with my confidential medical records. JALUPRO DISCLAIMER

TREATMENT POLICY FOR JALUPRO

FINAL CONSENT I have been asked what information I want and need in order to make an informed decision. I have had the opportunity to fully discuss my desired outcome. I certify that: I have read and fully understand this consent I’ve had sufficient opportunity for discussion All questions have been answered No new information has changed my decision I hereby consent to this procedure. This constitutes full disclosure and supersedes any previous verbal or written disclosures.

LEMON BOTTLE DISCLAIMER

TREATMENT POLICY FOR LEMON BOTTLE

Product Information: The Lemon Bottle is an aesthetic treatment product designed specifically for fat dissolution. It involves a solution that is injected into fat pockets to facilitate fat breakdown and enhance the body’s natural fat removal processes.

Treatment Information: The treatment procedure involves the injection of the Lemon Bottle solution into specified areas of fat accumulation. It is a non-surgical procedure performed by a licensed practitioner. The procedure duration and number of sessions required may vary based on individual needs and the amount of fat to be dissolved.

Potential Risks: While the Lemon Bottle fat dissolving treatment is generally considered safe, it comes with potential risks. These may include but are not limited to: Localised pain, swelling, redness or bruising at the injection site Potential for an allergic reaction to the product Possibility of infection if aftercare instructions are not properly followed Temporary changes to skin texture or irregularities in body contour In rare instances, more serious complications may arise

Benefits: The Lemon Bottle fat dissolving treatment can offer several potential benefits including: Reduction of localised fat pockets Improvement in body contour Enhancement in overall body appearance

INFORMATION PROVIDED I have been advised of the relevant information associated with this treatment and I confirm that I fully understand this advice. This includes: The aims/motivations for having the procedure and the desired outcome The risks inherent in the procedure The risks inherent in refusing the procedure The risks specific to me The expected benefits of the treatment The potential disadvantages of the treatment Alternative procedures and their pros and cons – including the option of no treatment at all Any uncertainties about and the likelihood of success of the procedure Any follow-up treatment that may be required LEMON BOTTLE DISCLAIMER

TREATMENT POLICY FOR LEMON BOTTLE

CLINICAL PHOTOS AND VIDEOS I agree to and authorise the taking of clinical photographs and videos. I understand that these clinical photographs and videos will form part of and will be kept with my confidential medical records.

FINAL CONSENT I have been asked what information I want and would need in order to make an informed decision. I have been given the opportunity to discuss my desired outcome fully in order for me to make an informed decision. I certify that I have read the above consent and that I fully understand it. I have been given ample opportunity for discussion and all my questions have been answered to my satisfaction. No new information has become available that affects my decision to have the treatment or my decision to consent. I hereby consent to this procedure. This constitutes the full disclosure and supersedes any previous verbal or written disclosures. All deposits and booking fees are non-refundable unless agreed to with the practitioner.

LIDOCAINE DISCLAIMER

TREATMENT POLICY FOR LIDOCAINE I understand the esthetician will take every precaution to minimise or eliminate negative reactions as much as possible. I do understand that, very rarely, permanent damage occurs. I have given an accurate account of any over-the-counter or prescription medications that I use regularly, and I am not presently using (nor have I used within the last year): Isotretinoin (Accutane) Retin-A Acyclovir Tranquilisers I have not had any chemical peels, skin care procedures, laser treatments, or infections that I have not disclosed to my esthetician. I am not ingesting or using topically any other over-the-counter product or prescription medication/agent that has not been disclosed to my esthetician. I have informed my esthetician if: I am pregnant or lactating I am over the age of eighteen (18) or have written consent as a minor I have not had recent radioactive or chemotherapy treatments I do not have sunburn, windburn, or broken skin I have not recently waxed or used a depilatory on the area to be treated I do not have a history of: Keloid scarring Diabetes Any autoimmune disease Active herpes blisters Any other condition that may interfere with a positive treatment outcome

PUBLICITY MATERIALS I authorise the taking of clinical photographs and videos. I understand that photographs and video may be taken of me for educational and marketing purposes. I hold the practitioner harmless for any liability resulting from this production. I waive my rights to any royalties, fees and to inspect the finished production as well as advertising materials in conjunction with these photographs.

FINAL CONSENT I certify that I have read the above consent and I fully understand it. I have been given ample opportunity for discussion and all my questions have been answered to my satisfaction. hereby consent to this procedure. This constitutes the full disclosure and supersedes any previous verbal or written disclosures.

LUMI EYES DISCLAIMER

TREATMENT POLICY FOR LUMI EYES Dermaren Lumi Eyes is a tissue stimulator designed for needle mesotherapy treatments around the eyes and the tear valley with a filling effect, but with no side effects in the form of lymphoedema. Lumi Eyes is a high-quality product that repairs damage to the dermis with polynucleotides with a strong tissue regenerating effect. The effect of the treatment is strong hydration and rejuvenation of the tissue, as well as the reduction of symptoms of fatigue and skin blueing.

How it Works: Polynucleotide PDRN is used to: Regenerate damaged tissues Moisturise Restore volume Smooth skin PDRN is a low molecular weight complex that supports cell repair, damaged tissue regeneration, and internal homeostasis. It stimulates collagen synthesis, helps restore DNA chains, and increases elastin production. Glutathione provides antioxidant effects during the biorevitalisation procedure.

Product Description: Lumi Eyes is a high-quality injection product based on polynucleotides (from purified salmon milk DNA). It: Repairs dermal damage Destroys dark circles Moisturises Fights fine wrinkles Smooths and lifts under-eye skin Rejuvenates skin and delays aging Strengthens firmness, density, and skin quality Thanks to its rapid absorption, there is no downtime with this treatment. You can return to your normal activities immediately after the procedure.

Recommended Protocol: A perfect effect can be seen after just one treatment For enhanced results: 3 treatments at 4-week intervals, repeated twice a year Benefits: Rejuvenation Brightening Reduced bruising and fatigue Fresher, more energised appearance LUMI EYES DISCLAIMER

TREATMENT POLICY FOR LUMI EYES

CONSENT INFORMATION I have been advised of the relevant information associated with this treatment and I confirm that I fully understand this advice. This includes: The aims/motivations for having the procedure and the desired outcome The risks inherent in the procedure The risks inherent in refusing the procedure The risks specific to me The expected benefits of the treatment The potential disadvantages of the treatment Alternative procedures and their pros and cons – including the option of no treatment at all Any uncertainties about and the likelihood of success of the procedure Any follow-up treatment that may be required

CLINICAL PHOTOS AND VIDEOS I agree to and authorise the taking of clinical photographs and videos. I understand that these will form part of and be kept with my confidential medical records.

FINAL CONSENT I have been asked what information I want and would need in order to make an informed decision. I have been given the opportunity to discuss my desired outcome fully. I certify that: I have read the above consent and fully understand it I have had ample opportunity for discussion All my questions have been answered to my satisfaction No new information has come to light that affects my decision I hereby consent to this procedure. This constitutes the full disclosure and supersedes any previous verbal or written disclosures.

MICRONEEDLING DISCLAIMER

TREATMENT POLICY FOR MICRONEEDLING PATIENT CONSENT This is an informed consent form that has been prepared to help inform you of the potential benefits and risks of microneedling. It is important that you read this information carefully and discuss fully with your practitioner before proceeding with treatment. It is also important that you take as much time as you need to consider the treatment carefully, weighing up all your options before reaching an informed decision. It is essential that you are aware of your right to have a second opinion and you are encouraged to ask any questions that come to mind throughout the entirety of the process.

ABOUT MICRONEEDLING Microneedling is a skin treatment used to rejuvenate the skin and improve its surface. It can help with: Fine lines and expression lines Wrinkles Enlarged pores Acne scars Hyperpigmentation Stretch marks The device creates multiple micro-punctures in the outer layer of the skin, producing minor injuries that trigger collagen synthesis. These micro holes also allow healing serums to penetrate deeply, promoting rejuvenation. A topical anaesthetic is applied beforehand to ensure comfort. Healing gels or serums are typically used during treatment. In a vampire facial, platelet-rich plasma (PRP) from the patient's own blood is used. Duration: 30–60 minutes depending on treatment site More than one treatment may be necessary to achieve or maintain results. Initial results: 2–3 weeks Peak results: 4–6 weeks

TREATMENT PLAN & FOLLOW-UP I understand that I may need multiple sessions, and I will be informed: In advance of the treatment location and provider About my progress throughout the course of treatment That I may change my mind at any time Post-treatment: Avoid excessive sun/UV exposure and extreme cold until any initial swelling/redness resolves. MICRONEEDLING DISCLAIMER

TREATMENT POLICY FOR MICRONEEDLING RISKS AND SIDE EFFECTS Microneedling carries certain risks that must be discussed with your practitioner: Common side effects: Discomfort or pain (stinging sensation) during/after the procedure Tightness, swelling, and sensitivity of the skin Redness and sunburn-like effect (resolves within 24 hrs to 7 days) Itching, pinpoint bleeding or bruising Scabbing and darkening of treated areas Fainting or feeling faint during treatment (alert your practitioner) Uncommon side effects: Skin infection (cellulitis) Reactivation of cold sores (herpes) Hyperpigmentation or hypopigmentation (fades in 6 months, may be permanent in rare cases) Risk of pigmentation issues is higher for tanned or darker skin tones and with sun exposure To minimise pigmentation risk, avoid sun exposure for 4 weeks before and after treatment, use sunscreen/SPF, and follow pre/post-care instructions. Rare side effects: Permanent skin scarring

INFORMATION RECEIVED I have been advised of and confirm I fully understand information about: The aims/motivations for having the procedure and the desired outcome The risks inherent in the procedure The risks inherent in refusing the procedure The risks specific to me The expected benefits of the treatment The potential disadvantages of the treatment Alternative procedures and their pros and cons – including the option of no treatment Uncertainties about and the likelihood of success Any follow-up treatment that may be required

CLINICAL PHOTOS AND VIDEOS I agree to and authorise the taking of clinical photographs and videos. I understand that these will form part of and be kept with my confidential medical records. MICRONEEDLING DISCLAIMER

TREATMENT POLICY FOR MICRONEEDLING FINAL CONSENT I have been asked what information I want and need to make an informed decision. I have had the opportunity to fully discuss my desired outcome. I certify that: I have read the above consent and fully understand it I have had ample opportunity for discussion All my questions have been answered to my satisfaction No new information has come to light that affects my decision I hereby consent to this procedure. This constitutes the full disclosure and supersedes any previous verbal or written disclosures.

All deposits and booking fees are non-refundable unless agreed to with the practitioner.

MODEL DISCLAIMER

MODEL POLICY FOR Training Days Introduction This beauty Model Policy applies to all models who participate in our Training Days at Snatch & Glow (“we”, “us”, or “our”). By agreeing to participate as a model, you acknowledge and agree to be bound by the terms of this Policy.

Non-Refundable Deposit All models are required to pay a non-refundable deposit to secure their appointment for Training Days. This deposit will not be refunded under any circumstances.

Work Correction & Anti-Wrinkle Reviews Work performed during training days will be corrected at the next model day. Anti-Wrinkle reviews will not be conducted routinely; however, in some cases, models may be allowed to attend the next model day for review. Work performed during training days is supervised, safe, and offered at a lower cost but will not be corrected by main practitioners. The only exception to this can be in a medical emergency; not in the case of Aesthetic concerns.

Eligibility & Requirements MODELS MUST MEET THE FOLLOWING ELIGIBILITY REQUIREMENTS TO PARTICIPATE IN TRAINING DAYS: 1. Not pregnant or breastfeeding 2. Not taking blood thinners 3. Have eaten prior to attending the appointment 4. Consent to having photos and videos taken during the session, which may be used by 5. Snatch & Glow or students for promotional or Educational purposes. 6. Allow up to two hours after the scheduled appointment time to be seen. Training Days may experience delays due to supervision and learning requirements. If you are unable to wait, your appointment may be cancelled and your deposit will be forfeited.

Participation & Patience Please only apply to be a model if you are comfortable being worked on my trainees, as these training days are designed to improve the industry overall and teach new skills to practitioners. Trainees may require more patience due to their less experience. Appointments are non-transferable, and retained payments cannot be transferred for future appointments.

Health & Timeliness Models must be in good health and must not consume alcohol within 24 hours prior to the appointment. Please arrive on time for your appointment. If you are late, your deposit may be forfeited if we are unable to accommodate you. Low blood sugar can cause dizziness, lightheadedness, and fainting therefore, ensure you have eaten prior to attending.

Upgrading to Full Price In some cases, we may allow models to pay the difference and upgrade to a full-price treatment with a practitioner. The decision will be made at our sole discretion.

BY AGREEING TO PARTICIPATE AS A MODEL IN SNATCH & GLOW TRAINING DAYS, YOU CONFIRM THAT YOU HAVE READ, UNDERSTOOD, AND AGREED TO BE BOUND BY THIS BEAUTY MODEL POLICY FOR TRAINING DAYS.

058585 8543 Info@snatchandglow.ae SNATCHANDGLOWDUBAI SNATCHANDGLOWACADEMY

NON SURGICAL RHINOPLASTY DISCLAIMER

TREATMENT POLICY FOR Non-Surgical Rhinoplasty Disclaimer: This consent form is intended to provide written confirmation of discussions with your healthcare provider regarding your non-surgical rhinoplasty procedure, also known as a "liquid rhinoplasty" or "nose filler" treatment.

Treatment Information: Non-surgical rhinoplasty is a minimally invasive, non-permanent cosmetic procedure that modifies the contours of the nose without surgery. The process involves injecting a dermal filler, typically a hyaluronic acid derivative, into precise areas of the nose to alter shape, symmetry, or size. The procedure is typically performed under local anaesthesia (numbing cream) to minimise discomfort. A fine needle is used to inject the filler in targeted areas to: Smooth bumps Enhance symmetry Lift the nasal tip Make other aesthetic modifications Duration: 15 to 60 minutes depending on case complexity. Results: Visible immediately Final effects appear once swelling/redness subsides Effects last 6 to 18 months, depending on filler type and individual response A follow-up appointment may be scheduled to evaluate results and determine if additional treatment is necessary. Note: This procedure cannot reduce the size of the nose and may be limited by your existing nasal anatomy.

Potential Risks and Side Effects: While generally safe, non-surgical rhinoplasty may involve risks, including but not limited to: Swelling, redness, and bruising at the injection site Tenderness or discomfort at the injection site Unsatisfactory aesthetic result Allergic reaction to the filler Rare complications: infection, skin necrosis, or blindness NON SURGICAL RHINOPLASTY DISCLAIMER

TREATMENT POLICY FOR Non-Surgical Rhinoplasty INFORMATION PROVIDED I have been advised of the relevant information associated with this treatment and confirm that I fully understand this advice. This includes: The aims/motivations for having the procedure and the desired outcome The risks inherent in the procedure The risks inherent in refusing the procedure The risks specific to me The expected benefits of the treatment The potential disadvantages of the treatment Alternative procedures and their pros and cons – including the option of no treatment at all Any uncertainties about and the likelihood of success of the procedure Any follow-up treatment that may be required

CLINICAL PHOTOS AND VIDEOS I agree to and authorise the taking of clinical photographs and videos. I understand that these will form part of and be kept with my confidential medical records.

FINAL CONSENT I have been asked what information I want and would need in order to make an informed decision. I have had the opportunity to discuss my desired outcome fully. I certify that: I have read and fully understand the consent I have been given ample opportunity for discussion All my questions have been answered No new information has become available that affects my decision I hereby consent to this procedure. This constitutes the full disclosure and supersedes any previous verbal or written disclosures.

POLYNUCLEOTIDE DISCLAIMER

TREATMENT POLICY FOR POLYNUCLEOTIDE This document is a written statement that certifies that the patient, hereafter referred to as the "Client," fully understands the Polynucleotide Injection treatment, the potential risks, and benefits associated with said treatment. The Client provides their consent to be treated by the healthcare professionals associated with the "Clinic."

TREATMENT INFORMATION The term "Treatment" refers to Polynucleotide Injection, a procedure designed to: Stimulate natural collagen production Improve skin elasticity Enhance overall skin quality The procedure involves the injection of polynucleotides into specific areas of the skin.

RISKS Every medical treatment carries inherent risks. The potential risks associated with Polynucleotide Injection include, but are not limited to: Allergic reactions: Possible allergies to substances used during treatment Physical discomfort or pain: During or after the procedure Skin reactions: Redness, swelling, itching, or other types of irritation Unforeseen side effects: Any unusual reactions or complications not typically expected

RISKS Every medical treatment carries inherent risks. The potential risks associated with Polynucleotide Injection include, but are not limited to: Allergic reactions: Possible allergies to substances used during treatment Physical discomfort or pain: During or after the procedure Skin reactions: Redness, swelling, itching, or other types of irritation Unforeseen side effects: Any unusual reactions or complications not typically expected

RISKS Every medical treatment carries inherent risks. The potential risks associated with Polynucleotide Injection include, but are not limited to: Allergic reactions: Possible allergies to substances used during treatment Physical discomfort or pain: During or after the procedure Skin reactions: Redness, swelling, itching, or other types of irritation Unforeseen side effects: Any unusual reactions or complications not typically expected POLYNUCLEOTIDE DISCLAIMER

TREATMENT POLICY FOR POLYNUCLEOTIDE This document is a written statement that certifies that the patient, hereafter referred to as the "Client," fully understands the Polynucleotide Injection treatment, the potential risks, and benefits associated with said treatment. The Client provides their consent to be treated by the healthcare professionals associated with the "Clinic."

TREATMENT INFORMATION The term "Treatment" refers to Polynucleotide Injection, a procedure designed to: Stimulate natural collagen production Improve skin elasticity Enhance overall skin quality The procedure involves the injection of polynucleotides into specific areas of the skin.

RISKS Every medical treatment carries inherent risks. The potential risks associated with Polynucleotide Injection include, but are not limited to: Allergic reactions: Possible allergies to substances used during treatment Physical discomfort or pain: During or after the procedure Skin reactions: Redness, swelling, itching, or other types of irritation Unforeseen side effects: Any unusual reactions or complications not typically expected

RISKS Every medical treatment carries inherent risks. The potential risks associated with Polynucleotide Injection include, but are not limited to: Allergic reactions: Possible allergies to substances used during treatment Physical discomfort or pain: During or after the procedure Skin reactions: Redness, swelling, itching, or other types of irritation Unforeseen side effects: Any unusual reactions or complications not typically expected

BENEFITS While risks are inherent to any treatment, potential benefits of Polynucleotide Injection include: Improved skin texture: Smoother, healthier-looking skin Increased collagen production: Can improve elasticity and reduce wrinkles Enhanced aesthetic appearance: Cosmetic improvements that may boost overall appearance POLYNUCLEOTIDE DISCLAIMER

TREATMENT POLICY FOR POLYNUCLEOTIDE This document is a written statement that certifies that the patient, hereafter referred to as the "Client," fully understands the Polynucleotide Injection treatment, the potential risks, and benefits associated with said treatment. The Client provides their consent to be treated by the healthcare professionals associated with the "Clinic."

TREATMENT INFORMATION The term "Treatment" refers to Polynucleotide Injection, a procedure designed to: Stimulate natural collagen production Improve skin elasticity Enhance overall skin quality The procedure involves the injection of polynucleotides into specific areas of the skin.

RISKS Every medical treatment carries inherent risks. The potential risks associated with Polynucleotide Injection include, but are not limited to: Allergic reactions: Possible allergies to substances used during treatment Physical discomfort or pain: During or after the procedure Skin reactions: Redness, swelling, itching, or other types of irritation Unforeseen side effects: Any unusual reactions or complications not typically expected

RISKS Every medical treatment carries inherent risks. The potential risks associated with Polynucleotide Injection include, but are not limited to: Allergic reactions: Possible allergies to substances used during treatment Physical discomfort or pain: During or after the procedure Skin reactions: Redness, swelling, itching, or other types of irritation Unforeseen side effects: Any unusual reactions or complications not typically expected

BENEFITS While risks are inherent to any treatment, potential benefits of Polynucleotide Injection include: Improved skin texture: Smoother, healthier-looking skin Increased collagen production: Can improve elasticity and reduce wrinkles Enhanced aesthetic appearance: Cosmetic improvements that may boost overall appearance

PROFIHLO DISCLAIMER

TREATMENT POLICY FOR PROFIHLO PATIENT CONSENT: This is an informed consent form that has been prepared to help inform you of the potential benefits and risks of Profhilo. It is important that you read this information carefully and discuss fully with your practitioner before proceeding with treatment. It is also important that you take as much time as you need to consider the treatment carefully, weighing up all your options before reaching an informed decision. It is essential that you are aware of your right to have a second opinion and you are encouraged to ask any questions that come to mind throughout the entirety of the process. Profhilo is a skin bioremodeller consisting of high concentration hyaluronic acid. It works by stimulating skin collagen and elastin production as well as promoting increased skin hydration. Profhilo is administered in small amounts by intradermal injection using very fine needles and aims to boost, tighten, hydrate and lift your skin. Profhilo is used to treat tired, aged, lax and dehydrated skin as well as for fine lines and wrinkles. Profhilo is commonly used for skin rejuvenation on the face but can also be used on the neck and hands. Profhilo is not the treatment of choice for deep lines and scars or to add volume, it is not a dermal filler and will not produce the same results as these. You will be offered a topical anaesthetic cream before injection of Profhilo to help reduce discomfort during the procedure. Profhilo is injected on two treatment sessions 4 weeks apart; to maintain results, a further 2 treatment course is recommended every 6 months. After initial treatment, you can expect to see results gradually over a period of 4–6 weeks. Results should last 6 months on average but they can last for longer or shorter time periods. I am aware that results vary between clients and results are dependent on many individual factors. I am aware that there is no guarantee that I will achieve desired results and that more than one treatment course may be needed to achieve or maintain desired results. I understand that several appointments may be necessary to produce optimal results and I will be notified, in advance of each session of treatment, about the location where the next treatment session is going to take place and the identity of who is going to be involved in my care at each stage. I also understand that I will be kept informed of progress and that I can change my mind at any point.

RISKS AND SIDE EFFECTS: As with any procedure there are potential risks and complications associated with Profhilo. You must be aware of the following possible risks before proceeding. You must fully discuss any questions with your practitioner. Common complications: Pain, bleeding and bruising at the time of injection. Tenderness in the area after injection (should not be actively painful). Bruising, which is often mild but occasionally more significant. Severe bruising can lead to haematoma. Redness and swelling, typically mild and lasting a few days, but can persist up to 14 days. PROFIHLO DISCLAIMER

TREATMENT POLICY FOR PROFIHLO Uncommon complications: Infection (cellulitis): Presents as hot, red, shiny skin; may require antibiotics. Abscess: Swollen collection requiring urgent medical attention. Cold sore reactivation. Granuloma formation: Delayed inflammatory reaction. Fainting or feeling faint during injections. Rare complications: Allergic reaction to Profhilo, including anaphylactic reaction needing emergency care. Vascular occlusion: Profhilo injected into an artery may block blood flow, leading to necrosis and possibly requiring reconstructive surgery. Emergency treatment with Hyaluronidase is required in such cases. I have been advised of the relevant information associated with this treatment and I confirm that I fully understand this advice. This includes advice about: the aims/motivations for having the procedure and the desired outcome the risks inherent in the procedure the risks inherent in refusing the procedure the risks specific to me the expected benefits of the treatment the potential disadvantages of the treatment alternative procedures and their pros and cons – including the option of no treatment at all any uncertainties about and the likelihood of success of the procedure any follow-up treatment that may be required

CLINICAL PHOTOS AND VIDEOS: I agree to and authorise the taking of clinical photographs and videos. I understand that these clinical photographs and videos will form part of and will be kept with my confidential medical records. I have been asked what information I want and would need in order to make an informed decision. I have been given the opportunity to discuss my desired outcome fully in order for me to make an informed decision. I certify that I have read the above consent and that I fully understand it. I have been given ample opportunity for discussion and all my questions have been answered to my satisfaction. No new information has become available that affects my decision to have the treatment or my decision to consent. I hereby consent to this procedure. This constitutes the full disclosure and supersedes any previous verbal or written disclosures.

PRP DISCLAIMER

TREATMENT POLICY FOR PRP PATIENT CONSENT: This is an informed consent form that has been prepared to help inform you of the potential benefits and risks of PRP (platelet rich plasma) treatment. It is important that you read this information carefully and discuss fully with your practitioner before proceeding with treatment. You should take as much time as you need to consider the treatment, weigh up your options, and understand your right to a second opinion. You are encouraged to ask any questions throughout the process. Treatment Overview: Platelet Rich Plasma (PRP) is a cosmetic skin rejuvenation procedure that involves microneedle injection of some of the client’s own blood components back into the skin. Commonly known as a “Vampire Facial,” the process includes: Drawing a blood sample from the patient’s arm. Using a centrifuge to separate blood components (Red Blood Cells, PRP, Platelet Poor Plasma, White Blood Cells). Injecting the PRP component into the skin using microneedling. Benefits of PRP: PRP is rich in growth factors that promote skin rejuvenation and can improve: Tired and aged skin Fine lines and wrinkles Enlarged pores Acne scars Hyperpigmentation Stretch marks Additional benefits include: Minimal downtime Good safety profile Short recovery time Low risk of allergic reaction due to use of autologous (self-derived) blood Treatment Notes: Procedure takes 30–60 minutes. A topical anaesthetic cream is offered for comfort. Results may appear within 2–3 weeks, peak at 4–6 weeks. Duration of results varies and is not guaranteed. Multiple sessions may be needed for optimal or maintained results. PRP does not prevent recurrence of treated conditions. PRP DISCLAIMER

TREATMENT POLICY FOR PRP RISKS AND SIDE EFFECTS Common side effects: Discomfort or pain during/after (especially over bony or thin-skinned areas) Tightness, swelling, sensitivity, redness (like sunburn), often resolving within 7 days Itching, pinpoint bleeding, bruising, scabbing, temporary darkening of treated areas Uncommon side effects: Skin infection (cellulitis) Cold sore reactivation (herpes simplex) Hyperpigmentation or hypopigmentation (typically fades in 6 months) Granuloma (scar tissue formation, very rare) Rare side effects: Permanent scarring Extremely unlikely allergic reaction Complications from phlebotomy (blood draw), such as: Pain, tenderness, bruising, or bleeding Fainting during procedure Multiple attempts if veins are hard to access Haematoma, cellulitis, thrombophlebitis, arterial puncture, or nerve injury

INFORMED CONSENT I agree to the taking of clinical photos and videos for medical records. I have been advised of all relevant information and confirm that I understand: The aims and expected outcomes The risks and alternatives The consequences of declining treatment The likelihood of success and uncertainties involved The possibility of requiring follow-up treatment

CLINICAL PHOTOS AND VIDEOS: I agree to the taking of clinical photos and videos for medical records. I have had the opportunity to ask questions and discuss my desired outcomes. All my questions have been answered to my satisfaction. I certify that I have read and understand this consent and hereby agree to the procedure. This consent supersedes any prior written or verbal disclosures.

PRP SCALP DISCLAIMER

TREATMENT POLICY FOR PRP SCALP I voluntarily consent to receive Platelet-Rich Plasma (PRP) Scalp Treatment. I understand and acknowledge the following: Purpose: The purpose of the PRP Scalp Treatment is to improve hair growth, reduce hair loss, and promote healthier, thicker hair by utilizing the patient's own platelet-rich plasma, which contains growth factors and other bioactive molecules to stimulate the hair follicles. Procedure: A trained healthcare professional will draw a small amount of blood from the patient's arm and process it in a centrifuge to separate the platelet-rich plasma. The treatment area will be cleansed, and a topical anesthetic (if necessary) will be applied to minimize discomfort. The PRP will be administered via a series of injections into the scalp, typically following a grid pattern. The number of sessions required will depend on the individual's condition and the healthcare provider's recommendation

Risks and Side Effects: While PRP Scalp Treatment is generally considered safe, some risks and side effects may occur, including but not limited to: Pain, swelling, or inflammation at the injection site Infection or hematoma Allergic reactions Temporary redness, itching, or tenderness Uneven hair growth or changes in hair texture Contraindications: PRP Scalp Treatment may be contraindicated in certain conditions, such as: Active skin infections or inflammation in the treatment area Blood clotting disorders Chronic liver disease or low platelet count Pregnancy or breastfeeding Autoimmune disorders No Guarantees: I understand that the results of PRP Scalp Treatment may vary among individuals, and there is no guarantee regarding the outcome or efficacy of the treatment. Confidentiality: I understand that my medical information will be kept confidential and will only be disclosed to appropriate healthcare professionals or as required by law. Questions and Concerns: I have discussed any questions or concerns I may have about the PRP Scalp Treatment with my healthcare provider, and I am satisfied with the information provided. PRP SCALP DISCLAIMER

TREATMENT POLICY FOR PRP SCALP

INFORMED CONSENT I have been advised of the relevant information associated with this treatment and I confirm that I fully understand this advice. This includes advice about: The aims/motivations for having the procedure and the desired outcome The risks inherent in the procedure The risks inherent in refusing the procedure The risks specific to me The expected benefits of the treatment The potential disadvantages of the treatment Alternative procedures and their pros and cons – including the option of no treatment at all Any uncertainties about and the likelihood of success of the procedure Any follow-up treatment that may be required I have been asked what information I want and would need in order to make an informed decision. I have been given the opportunity to discuss my desired outcome fully in order for me to make an informed decision. I certify that I have read the above consent and that I fully understand it. I have been given ample opportunity for discussion and all my questions have been answered to my satisfaction. No new information has become available that affects my decision to have the treatment or my decision to consent. I hereby consent to this procedure. This constitutes the full disclosure and supersedes any previous verbal or written disclosures.

PRX T33 DISCLAIMER

TREATMENT POLICY FOR PRX T33

PATIENT CONSENT: This is an informed consent form that has been prepared to help inform you of the potential benefits and risks of PRX-T33 chemical peel. It is important that you read this information carefully and discuss fully with your practitioner before proceeding with treatment. You should take the time you need to consider the treatment, weighing all options, and know you have the right to a second opinion. You are encouraged to ask any questions throughout the process. What is PRX-T33? PRX-T33 is a brand of chemical peel that contains: TCA (trichloroacetic acid) Hydrogen peroxide Kojic acid The treatment involves applying this solution to the face, where it penetrates the dermis without damaging the surface epidermis. It stimulates fibroblasts, growth factors, and new collagen formation, resulting in smoother, rejuvenated skin. Uses: PRX-T33 can help improve: Fine lines and wrinkles Tired skin Fine scars Acne Skin pigmentation Stretch marks (including on the body) Expectations and Results: Due to factors like age, skin condition, sun exposure, lifestyle, and overall health, results vary. There are no guarantees of satisfaction. Often 3–5 applications are required, spaced at least one week apart, to achieve desired results. Treatment Planning: You may need several sessions. You will be informed in advance about the location and care team for each session. You have the right to stop treatment at any point.

PATIENT CONSENT: RISKS AND SIDE EFFECTS Common side effects: Mild discomfort Redness or swelling for up to 14 days (occasionally longer) Increased sun and skin sensitivity PRX T33 DISCLAIMER

TREATMENT POLICY FOR PRX T33 Less common side effects: Pigment changes (lightening or darkening); may be permanent in rare cases Rare side effects: Allergic reactions (including possible anaphylaxis requiring emergency care) Bacterial skin infection (cellulitis) Herpes virus reactivation Permanent scarring You accept all known and unknown risks and affirm that you have disclosed all relevant health conditions.

INFORMED CONSENT I confirm that I understand the following: The aims and motivations for the treatment The risks involved The consequences of declining treatment Personal risk factors Expected benefits Disadvantages of treatment Alternatives and their pros/cons (including no treatment) Possible uncertainties and success likelihood Potential need for follow-up care

CLINICAL PHOTOS AND VIDEOS: I agree to the taking and storage of clinical photos/videos as part of my confidential medical record. I have had the chance to ask questions and discuss outcomes. I confirm I understand and consent to proceed. No new information has arisen that changes my decision. This document constitutes full disclosure and replaces any prior verbal or written agreements.

Booking Policy: All deposits and booking fees are non-refundable unless otherwise agreed with the practitioner.

SCULPTRA DISCLAIMER

TREATMENT POLICY FOR SCULPTRA

Treatment Overview: Sculptra therapy involves the injection of poly-L-lactic acid into the skin and underlying tissues to help correct: Skin depressions (creases, wrinkles, folds, scars) Hollow eye rings Degenerative skin aging Facial lipoatrophy (fat loss) Sculptra is a biocompatible, biodegradable, synthetic polymer derived from the alpha-hydroxy-acid family (fruit acids). It has been used medically for many years in dissolvable stitches and does not require allergy pre-testing. Duration and Treatment Schedule: Effects may last 1 to 2 years, but this can vary. Most areas require 2 to 4 sessions, spaced 3 to 6 weeks apart. Touch-up treatments may be needed for maintenance. Results develop gradually as new collagen forms (neocollagenesis). What to Expect: At each return visit, response to previous treatment is assessed. The therapy does not treat the underlying cause of tissue/fat loss, only its appearance.

RISKS AND SIDE EFFECTS Common and expected post-injection effects: Swelling Redness Pain Itching Discoloration Tenderness (usually resolve in 1 to 15 days) Initial swelling (edema) occurs due to the water in the injection solution and is temporary. Micro-nodules (small bumps under the skin): Often only felt, not seen Typically last 6 to 12 months Usually resolve on their own and are symptom-free SCULPTRA DISCLAIMER

TREATMENT POLICY FOR SCULPTRA

Induration (feeling of thickness): A normal inflammatory response Can be minimized by massaging the treated area 3 to 5 times a day for 3 to 5 minutes, for 3 to 5 days Rare complications: Visible granulomas (bumps with redness, tenderness, or texture changes) that may require further treatment Injection site abscess Allergic reaction Skin hypertrophy or atrophy Malaise, fatigue Extended edema Contraindications: Pregnancy or breastfeeding (must notify provider) Use of anti-inflammatory, anti-clotting drugs, or aspirin (may cause bleeding/bruising) History of herpes simplex at injection site (injection may provoke outbreak)

INFORMED CONSENT I confirm I have been informed about and fully understand: The aims and desired outcomes Risks of undergoing or refusing the procedure Personal risk factors Expected benefits and disadvantages Alternatives (including no treatment) Uncertainties and success likelihood Follow-up treatment requirements

CLINICAL PHOTOS AND VIDEOS

I consent to the taking of clinical photos/videos as part of my confidential medical record. I have had the opportunity to ask questions, receive satisfactory answers, and understand all details. I consent to proceed with treatment. This consent supersedes any previous verbal or written agreements. SCULPTRA DISCLAIMER

TREATMENT POLICY FOR SCULPTRA

Induration (feeling of thickness): A normal inflammatory response Can be minimized by massaging the treated area 3 to 5 times a day for 3 to 5 minutes, for 3 to 5 days Rare complications: Visible granulomas (bumps with redness, tenderness, or texture changes) that may require further treatment Injection site abscess Allergic reaction Skin hypertrophy or atrophy Malaise, fatigue Extended edema Contraindications: Pregnancy or breastfeeding (must notify provider) Use of anti-inflammatory, anti-clotting drugs, or aspirin (may cause bleeding/bruising) History of herpes simplex at injection site (injection may provoke outbreak)

INFORMED CONSENT I confirm I have been informed about and fully understand: The aims and desired outcomes Risks of undergoing or refusing the procedure Personal risk factors Expected benefits and disadvantages Alternatives (including no treatment) Uncertainties and success likelihood Follow-up treatment requirements

CLINICAL PHOTOS AND VIDEOS

I consent to the taking of clinical photos/videos as part of my confidential medical record. I have had the opportunity to ask questions, receive satisfactory answers, and understand all details. I consent to proceed with treatment. This consent supersedes any previous verbal or written agreements.

SKIN BOOSTER DISCLAIMER

TREATMENT POLICY FOR SKIN BOOSTER

RISKS AND SIDE EFFECTS: As with any procedure, there are potential risks and complications associated with Skin Booster Injections. You must be aware of the following possible risks before proceeding and discuss any concerns with your practitioner. Common complications: Pain, bleeding, and bruising at the time of injection Tenderness after the injection (should not be actively painful) Significant pain requires prompt contact with your practitioner Bruising, typically mild, but occasionally more significant, may take up to 2 weeks to fully resolve Severe bruising may cause haematoma (collection of clotted blood), needing up to 2 weeks to heal Redness and swelling at the injection site, typically mild and resolving in a couple of days, but can last up to 14 days Uncommon complications: Skin infection (cellulitis): Hot, red, shiny skin, possible systemic symptoms Abscess formation: Swollen area requiring urgent medical care Cold sore reactivation (herpes virus) Granuloma formation: Inflammatory reaction presenting months after treatment Fainting or lightheadedness: Must be reported to the practitioner immediately Rare complications: Allergic reaction, including anaphylaxis requiring emergency care Vascular occlusion: Accidental injection into an artery leading to tissue necrosis. Treated with emergency Hyaluronidase injections. If Hyaluronidase fails, urgent medical or specialist aesthetic assessment is required Your practitioner is trained in the emergency use of Hyaluronidase TREATMENT CONSIDERATIONS: Multiple sessions may be needed to achieve optimal results You will be informed in advance of each session's location and care team You may change your mind at any time

CLINICAL PHOTOS AND VIDEOS

I consent to the taking and storage of clinical photographs and videos as part of my confidential medical record. I confirm that I have had the opportunity to ask questions and discuss my desired outcome, and all my questions have been answered. I certify I understand and consent to the procedure. This document constitutes full disclosure and replaces all prior verbal or written disclosures. SKIN BOOSTER DISCLAIMER

TREATMENT POLICY FOR SKIN BOOSTER

INFORMED CONSENT I confirm that I understand and have been advised about: The purpose and expected outcomes of the treatment The inherent risks and those of refusing treatment The risks specific to me The expected benefits and potential disadvantages Alternative procedures (including doing nothing) Uncertainties regarding treatment success The need for possible follow-up treatments

Note: All deposits and booking fees are non-refundable unless otherwise agreed with the practitioner.

TEAR TROUGH DISCLAIMER

TREATMENT POLICY FOR TEAR TROUGH

TEAR TROUGH DISCLAIMER This consent form aims to provide you, the patient, with sufficient information about the tear trough treatment, its risks, benefits, and possible alternatives, so that you can make an informed decision to proceed with the treatment. Please read this form carefully, ask questions if anything is unclear, and sign at the end to indicate your understanding and agreement to proceed with the treatment.

TEAR TROUGH DISCLAIMER Tear trough treatment is a non-surgical cosmetic procedure that uses dermal fillers—typically composed of hyaluronic acid—to fill the hollows under the eyes. This helps improve: The appearance of dark circles Eye bags A sunken appearance The treatment involves injecting the filler into the targeted area using a fine needle or cannula, aiming to rejuvenate the under-eye area for a more youthful and refreshed appearance.

Risks and Side Effects: As with any cosmetic procedure, there are potential risks and side effects, which may include: Pain, swelling, bruising, redness, or itching at the injection site Asymmetry or lumps in the treated area Infection, inflammation, or allergic reaction Damage to blood vessels, nerves, or surrounding structures Migration or displacement of the dermal filler Unsatisfactory or temporary results that may require further treatment By signing this form, you acknowledge that you have been informed of and accept these risks. Alternatives to Tear Trough Treatment: Topical creams and skincare products Laser treatments or chemical peels Surgical procedures, such as lower eyelid surgery (blepharoplasty) Please discuss alternatives with your practitioner to choose the best approach for your individual needs. TEAR TROUGH DISCLAIMER

TREATMENT POLICY FOR TEAR TROUGH

INFORMED CONSENT I confirm that I fully understand: The aims and motivations behind the procedure The risks of undergoing or refusing the procedure Any personal risk factors The expected benefits and potential downsides All alternative treatments, including their pros and cons The uncertainty and likelihood of treatment success Any follow-up treatment that may be required

CLINICAL PHOTOS AND VIDEOS: I agree to the taking of clinical photographs and videos, which will be stored as part of my confidential medical record. I have been asked what information I want and need to make an informed decision. I have been given the opportunity to fully discuss my desired outcome and have had all my questions answered. I certify that I understand and consent to this procedure. This constitutes full disclosure and supersedes any previous verbal or written disclosures.

PDO and PLLA THREAD LIFT DISCLAIMER

TREATMENT POLICY FOR PDO and PLLA Thread Lift PATIENT CONSENT This is an informed consent form that has been prepared to help inform you of the potential benefits and risks of thread lift procedures. It is important that you read this information carefully and discuss fully with your practitioner before proceeding with treatment. It is also important that you take as much time as you need to consider the treatment carefully, weighing up all your options before reaching an informed decision. It is essential that you are aware of your right to have a second opinion and you are encouraged to ask any questions that come to mind throughout the entirety of the process.

ABOUT THREAD LIFTS Thread lifts are a minimally invasive alternative to a facelift using naturally resorbable suture materials. Two commonly used thread materials include PDO and PLLA. 1. PDO Threads Made of Polydioxanone Provide immediate tightening and long-term collagen stimulation Fully resorbable (degrade into CO₂ and water) Types: mono (gentle lift), cog (barbed, stronger lift), screw (volume) Choice of thread depends on treatment goal 2. PLLA Threads (e.g. Silhouette Soft) Made of Poly-L-Lactic Acid Last longer than PDO (up to 12 months) Promote collagen for extended periods Dissolve into glucose, CO₂, and water Better for volumisation than PDO Treatment Areas: Midface, cheeks, eyebrows, nose, neck, jawline.

TREATMENT PROCESS Insertion points are marked Local anaesthetic is applied Threads are inserted using a needle or blunt cannula No incisions required Threads are positioned and excess trimmed Multiple threads may be required at one insertion point. Some immediate lift is visible, but full results develop over 6 months. Results can last up to 2 years, and a top-up may be needed after 6 months. PDO and PLLA THREAD LIFT DISCLAIMER

TREATMENT POLICY FOR PDO and PLLA Thread Lift I am aware that: Results vary per client There is no guarantee of achieving desired results Multiple courses may be necessary I will be informed in advance about: Treatment sessions Practitioners involved Progress updates My right to discontinue at any time Thread lifts are not a substitute for surgical procedures like facelifts.

RISKS AND SIDE EFFECTS You must be aware of the following and comply with aftercare instructions: Common risks: Pain or discomfort Bruising, bleeding, swelling Temporary puckering, dimpling, or lumpiness Fainting or feeling faint (inform your practitioner) Uncommon risks: Extensive bruising (haematoma) Infection (cellulitis) Prolonged puckering/dimpling Thread migration, displacement, or protrusion Facial asymmetry Poor cosmetic outcome Failure of treatment Prolonged pain Rare risks: Nodule or granuloma formation Allergic reaction (to thread or anaesthetic) Anaphylaxis (requires emergency attention) Salivary gland damage Tissue necrosis Permanent scarring Sensory nerve injury (numbness or tingling) Motor nerve injury (facial weakness or paralysis) PDO and PLLA THREAD LIFT DISCLAIMER

TREATMENT POLICY FOR PDO and PLLA Thread Lift INFORMATION PROVIDED I have been advised of and fully understand: The aims/motivations for the procedure The risks inherent in the procedure The risks of refusing treatment Risks specific to me Expected benefits Potential disadvantages Alternatives (including no treatment) Likelihood of success Any required follow-up

CLINICAL PHOTOS AND VIDEOS I agree to and authorise the taking of clinical photographs and videos. These will form part of and be kept with my confidential medical records.

FINAL CONSENT I have been asked what information I want and would need in order to make an informed decision. I have had the opportunity to fully discuss my desired outcome. I certify that: I have read the above consent and fully understand it I’ve had ample opportunity for discussion All questions have been answered to my satisfaction No new information has changed my decision I hereby consent to this procedure. This constitutes the full disclosure and supersedes any previous verbal or written disclosures.

Vitamin C INJECTION DISCLAIMER

TREATMENT POLICY FOR Vitamin C Injection

PATIENT CONSENT: This is an informed consent form that has been prepared to help inform you of the potential benefits and risks of vitamin C injection. It is important that you read this information carefully and fully discuss it with your practitioner before proceeding. Take as much time as needed to consider your options and ask any questions. You have the right to seek a second opinion.

What is Vitamin C? Vitamin C (ascorbic acid) is a water-soluble vitamin and antioxidant essential for: Collagen production Wound healing Prevention of cell damage Production of neurotransmitters Supporting immune system function It is typically obtained through diet (recommended intake: 40mg/day), and deficiency is rare in the UK.

Vitamin C Injections: Used when oral supplementation is not practical or possible Often used off-label for purposes like boosting the immune system, supporting general health, aiding cancer treatment, and promoting weight loss Important: There is no medical evidence that it helps treat cancer, supports weight loss, or prevents the common cold

Medical Supervision Required: You must consult your GP if you suspect vitamin C deficiency Injections must be prescribed by a doctor or nurse prescriber If your injector is non-medical, a separate consultation is required with a prescribing clinician who will review your medical history and determine a safe dose

Injection Procedure: Administered intramuscularly into the deltoid (upper arm) A short, sharp pain may occur Vitamin C INJECTION DISCLAIMER

TREATMENT POLICY FOR Vitamin C Injection

RISKS AND SIDE EFFECTS: Common (especially at doses <1000mg/day): Pain, redness, swelling, or soreness at the injection site Bruising Feeling faint (report this to your practitioner immediately) At doses >1000mg/day: Gastrointestinal issues (abdominal pain, diarrhoea, flatulence) Rare: kidney stones or iron overload Very rare: allergic or anaphylactic reaction (requires emergency care)

INFORMED CONSENT I confirm that I understand the following: The aims and desired outcomes of the procedure The risks of proceeding and of refusing treatment The risks specific to me The expected benefits and possible disadvantages The available alternatives and their pros/cons The uncertainty and likelihood of success Any necessary follow-up treatment

I request treatment with vitamin C injection. The procedure has been explained clearly and all my questions have been answered. I understand the risks, benefits, and potential complications. I certify that I am in good health and have read and understood the information provided. I hereby consent to the treatment. This consent replaces any prior verbal or written disclosures.

VITAMIN D INJECTION DISCLAIMER

TREATMENT POLICY FOR Vitamin D Injection This consent form provides written confirmation of the discussions you have had with your healthcare provider regarding your treatment with Vitamin D injections.

Treatment Information: Vitamin D is essential for: Bone health Immune system function Overall well-being Your healthcare provider has recommended Vitamin D injections because your current levels are lower than the healthy range, and oral supplementation might not be sufficient in your case.

Potential Risks and Side Effects: Vitamin D injection is generally safe, but side effects can occur. These may include: Pain, swelling, or redness at the injection site Nausea Vomiting Constipation Fatigue Rare but serious risk: Hypercalcemia (excess calcium in the blood), which may cause: Confusion Disorientation Heart rhythm problems

INFORMED CONSENT I confirm that I fully understand the following: The aims and motivations behind the treatment The risks associated with the procedure The risks of not undergoing the procedure Personal risks specific to me The expected benefits of the injection The disadvantages and potential complications Alternatives to treatment, including the option to decline it Any uncertainties regarding success The likelihood of needing follow-up treatment VITAMIN D INJECTION DISCLAIMER

TREATMENT POLICY FOR Vitamin D Injection

CLINICAL PHOTOS AND VIDEOS: I consent to the taking and confidential storage of clinical photographs and videos as part of my medical record. I have been offered the chance to ask questions and discuss the treatment in detail. All questions have been answered to my satisfaction. No new information has emerged that would change my decision. I hereby give my consent for this procedure. This form constitutes full disclosure and overrides any previous verbal or written explanations.