Botox®, Dysport, & Xeomin are 3 brands of a neurotoxin produced by the bacterium Clostridium A. that can relax the muscles on areas of the face and neck that cause wrinkles associated with facial expressions. Treatment with Botox can cause your facial expression lines or wrinkles to essentially disappear. Areas most frequently treated are: a) glabellar area of frown lines, located between the eyes; b) crow’s feet (lateral areas of the eyes); and c) forehead wrinkles. Other areas considered Off-label may also be treated, which I consent to by signing this document below. Botox is diluted to a very controlled solution and when injected into the muscles with a very thin needle, it is almost painless. Clients may feel a slight burning sensation while the solution is being injected. The procedure takes about 15-20 minutes and the results last 3-6 months. With repeated treatments and correct number of units, the results may tend to last longer.

RISKS & COMPLICATIONS

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, and bruising, 2) Post treatment bacterial, viral, and/or fungal infection requiring further treatment, 3) Allergic reaction, 4) Minor temporary drop of eyelid(s) in approximately <1% of injections, this usually lasts 2-3 weeks, 5) Occasional numbness of the forehead lasting up to 2-3 weeks, 6) Transient headache, and 7) Flu-like symptoms may occur. 8) Difficulty swallowing, 9) Blurred vision, & 10) Dry mouth.

PREGNANCY, ALLERGIES & NEUROLOGIC DISEASE

I am not aware that I am pregnant, have any significant Neurologic disease, or have any allergies to the toxin ingredients, or to human albumin.

RESULTS

I am aware that when small amounts of purified botulinum (“BOTOX®”, DYSPORT, or XEOMIN) are injected into a muscle it causes weakness or paralysis of that muscle. This appears in 3-4 days and usually lasts 3-6 months but can be shorter or longer. In a very small number of individuals, the injection does not work as satisfactorily or for as long as usual. I understand that I will not be able to move the treated muscles while the injection is effective but that this will reverse after a period of months at which time re-treatment is appropriate. I understand that I must stay in the erect posture and that I must not manipulate the area of the injection for the four hours post-injection period.

I hereby voluntarily consent to treatment with Botulinum Toxin Type A injection for the condition known as: Facial Dynamic Wrinkles. The procedure has been 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 understand that no guarantees are implied as to the outcome of the procedure. I consent that payment is due in full at the time of service and that there are no refunds under any circumstances. I also certify that if I have any changes in my medical history I will notify the injector immediately. By signing below I accept full liability for the procedure & I will not hold the providers or Natural Injections liable of any adverse event or unfavorable outcome.

This is an informed consent document which has been prepared to help inform you concerning Hyaluronic Acid Filler such as Restylane®, Juvaderm, & Belotero. (Non-Animal Stabilized Hyaluronic Acid) tissue filler injection therapy, its risks, and alternative treatments. As well as Radiesse , a sterile, latex-free, non-pyrogenic, semi-solid, cohesive subdermal, injectable implant, whose principal component is synthetic calcium hydroxylapatite, a biocompatible material with over 20 years of use in medicine, approved for use in hands, cheeks, and pre-jowel sulcus. Hyaluronic acid is a naturally occurring substance that is found within all mammals. It is a material that is contained in various soft tissues. Hyaluronic acid can be synthetically produced from a process of bacterial fermentation, chemically stabilized, and purified for use as an injectable soft tissue filler (non-animal, stabilized hyaluronic acid The hyaluronic acid in Dermal-Fillers is biocompatible and is a totally non-animal product; there is little risk of animal-based disease transmission or allergic reaction. Dermal-fillers can be performed in areas involving the face, eyebrows, temples, undereyes, nose, jaw, chin, jowels, cheeks, hands, forehead, and lips, just to name a few and some areas are considered Off-Label use, not FDA approved areas. Dermal-Filler injections contain local anesthetic in the syringe to diminish discomfort. Continuing treatments are necessary in order to maintain the effect of Fillers over time, they do not stop the aging process. Once injected, dermal-fillers will be slowly absorbed by the body. The length of effect for fillers injections is variable and depends on the person.

Alternative forms of management include not treating the skin wrinkles or soft tissue depressions by any means. Improvement of skin wrinkles and soft tissue depressions may be accomplished by other treatments: laser treatments, chemical skin-peels, other skin procedures, or alternative types of tissue fillers.

An individual’s choice to undergo this procedure is based on the comparison of the risk to potential benefit.

Normal Occurrences during Tissue Filler Injections include:

Bleeding and Swelling - Swelling (edema) is a normal occurrence following the injections. It decreases after a few days or weeks. Erythema (Skin Redness) - Erythema in the skin occurs after injections. It can be present for a few days after the procedure. Needle Marks - Visible needle marks from the injections occur normally and resolve in a few days. Acne-Like Skin Eruptions - skin eruptions can occur following the injection of tissue fillers that generally resolve within a few days. Skin Lumpiness - Lumpiness can be treated with hyaluronidase to smooth it out if necessary. Visible Tissue Filler Material - This can be resolved with hyaluronidase Asymmetry - It may not be possible to achieve or maintain exact symmetry with tissue filer injections. Pain - Discomfort associated with injections is normal and usually of short duration.

Damage to Deeper Structures - Deeper structures such as nerves and blood vessels may be damaged during the course of injection. Injury to deeper structures may be temporary or permanent. Infection – unusual, herpes outbreaks can be triggered Skin Necrosis - It is very unusual to experience death of skin and deeper soft tissues after dermal-filler injections. Skin necrosis can produce unacceptable scarring. Should this complication occur, additional treatments, or surgery may be necessary. Allergic Reactions and Hypersensitivity Scarring - Dermal-fillers maybe susceptible to keloid formation or hypertrophic scarring. Granulomas - Painful masses in the skin and deeper tissues after a dermal-filler injection are extremely rare. Should these occur, additional treatments including surgery may be necessary. Antibodies to Fillers - Presence of antibodies to hyaluronic acid tissue fillers may reduce the effectiveness of this material or produce a reaction in subsequent injections. The health significance of antibodies to hyaluronic acid tissue fillers is unknown. Accidental Intra-Arterial Injection - It is extremely rare and unpredictable Under /Over Correction - The amount of correction may be inadequate or excessive. It may not be possible to control the process of injection of tissue fillers due to factors attributable to each patient’s situation. If under correction occurs, you may be advised to consider additional injections of tissue filler materials. If over correction occurs, the use of hyaluronidase can decrease the volume. Migration of Dermal-Fillers - Dermal-fillers may migrate from its original injection site and produce visible fullness in adjacent tissue or other unintended effects. Drug and Local Anesthetic Reactions - There is the possibility that a systemic reaction could occur from the local anesthetic when tissue filler injections are performed. This would include the possibility of light-headedness, numbness, and, allergic reaction, and fainting. Medical treatment of these conditions may be necessary. Unsatisfactory Result - Dermal-filler injections alone may not produce an outcome that meets your expectations for improvement in wrinkles or soft tissue depressions. There is the possibility of a poor or inadequate response from filler injection(s

Pregnancy and Nursing Mothers - Animal reproduction studies have not been performed to determine if dermal-filler could produce fetal harm. It is not known if Restylane®, Juvaderm, or Beloter or its breakdown products can be excreted in human milk. It is not recommended that pregnant women or nursing mothers receive dermal-filler treatments. Drug Interactions - It is not known if fillers reacts with other drugs within the body.

There are many devices, medications and injectable fillers that are approved for specific use by the FDA, but some proposed use is “Off-Label”, that is not specifically approved by the FDA. It is important that you understand this proposed use is not experimental and your physician believes it to be safe and effective.

I acknowledge that I have been informed about the Off-Label FDA status & uses of dermal-fillers such as Juvaderm, Restylane,

& Belotero and I understand it is not experimental and accept its use.

I understand and agree that all services rendered to me are charged to me directly and that I am personally responsible for payment. The fees charged for this procedure do not include any potential future costs for additional procedures that you elect to have or require in order to revise, optimize, or complete your outcome. Additional costs may occur should complications develop from the injections and will also be your responsibility. In signing the consent for this procedure, you acknowledge that you have been informed about its risk and consequences and accept responsibility for the clinical decisions that were made along with the financial costs of all future treatments.

I understand and unconditionally and irrevocably accept this & that all costs are NON-REFUNDABLE

Informed consent documents should not be considered all-inclusive in defining other methods of care and risks encountered.

I hereby authorize Natural Injections and it’s trained licensed designees to perform the injection of hyaluronic acid dermal fillers such as Juvaderm, Resylane, or Belotero 1. I have received and read the INFORMED CONSENT and PRE & POST PROCEDURE INSTRUCTIONS that were explained to me & I agree to follow all instructions, to follow up as directed, and to notify the office if any problems or questions arise. 2. I recognize that during the course of the procedure and medical treatment or anesthesia, unforeseen conditions may necessitate different procedures than those above. I therefore authorize the above mentioned provider to perform such other procedures that are in the exercise of his or her professional judgment necessary and desirable. 3. I consent to the administration of such anesthetics considered necessary or advisable. I understand that all forms of anesthesia involve risk and the possibility of complications, injury, and sometimes death. 4. The nature and purpose of the treatment have been explained to me. I understand what my provider can and cannot do, and I understand there are no warranties or guarantees implied or specific about my outcome. I have had the opportunity to explain my goals and understand which desired outcomes are realistic and which are not. I have read and understand this agreement. All of my questions have been answered to my satisfaction and I consent to the terms of this agreement. Alternative methods of treatment and their risks and benefits have been explained to me. 5. I understand that I have the right to refuse treatment. By signing this form, I elect to proceed with treatment. 6. I consent to be photographed or televised before, during, and after the procedure(s) to be performed, including appropriate portions of my body, for medical, scientific or educational purposes, provided my identity is not revealed by the pictures. 7. For purposes of advancing medical education, I consent to the admittance of observers to the treatment room.

I take full liability and responsibility for any and all risks, undesired outcomes, or adverse events associated with the injections

and will not hold the providers or Natural Injections liable for any unfavorable outcome or adverse event. I release Natural Injections

LLC, owners, and medical staff from liability associated with the procedure. This consent form is freely and voluntarily executed and

shall be binding upon my spouse, relatives, legal representatives, heirs, administrators, successors and assigns.

I CONSENT TO THE TREATMENT OR PROCEDURE AND THE ABOVE LISTED ITEMS (1-7 I AM SATISFIED WITH THE EXPLANATION.

Kybella is an FDA approved cosmetic injection indicated for improvement in the appearance of submental fullness associated with submental fat in adults. Kybella may be used off label for other areas deemed appropriate by the providers and industry standard.

The results of Kybella are not immediate. At your first treatment visit you will receive a series of injections in the submental area. At the time of injection and for several days following the injections you will have swelling in the submental area. Kybella will cause the fat cells to diminish gradually over the course of the next month following your injection in the treated area. A series of treatments may be necessary to achieve optimal results and these will occur at no sooner than the one month interval. Your doctor will decide the appropriate number of treatment sessions and the amount of Kybella you will need at each session.

SIDE EFFECTS

Side effects of Kybella may include: bruising, swelling, numbness, induration, marginal mandibular nerve injury, dysphagia (difficulty swallowing), bleeding, tenderness or discomfort, tissue necrosis, hyperpigmentation, redness, or alopecia at the site of injection. Alopecia: Kybella injections could cause small patches of alopecia in the treatment area.

PRE INSTRUCTIONS

You should not be pregnant, nursing an infant, have a history of a bleeding disorder or infection of the area to be treated. The morning of your treatment you should take tylenol if you are able to tolerate this medication. Also, you should tell your physician if you take any blood thinners or aspirin or have a history of any issue with lidocaine.

POST INSTRUCTIONS

• Do not massage the injection site

• Avoid heavy exercise the day of your treatment

• Notify your practitioner if any significant, swelling, bleeding, pain, dusky discoloration, difficulty swallowing or smiling, or fever occurs.

ALTERNATIVES

As explained not all submental fullness will respond to Kybella. Other alternative treatments are liposuction to the area, a neck lift and/or platysmoplasty procedures.

You agree to have this procedure and understand the full risks & benefits and hold Natural Injections and its medical providers harmless from any liability associated with you Kybella injections

I CONSENT TO THE TREATMENT OF KYBELLA INJECTIONS AND I HAVE READ THE ABOVE LISTED ITEMS. I ATTEST IT HAS BEEN EXPLAINED THOROUGHLY WITH THE OPPORTUNITY TO ASK QUESTIONS AND I AM SATISFIED WITH THE INFORMED CONSENT PROCESS.