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Calling all LATISSE® users… It's time to show and tell us all about your lash journey. You can submit your own Before & After pictures or share your experiences with the product — and you may even be featured in future LATISSE® communications. Once you submit your entries, we'll review them for potential inclusion in future materials.

Give us your best shots.

Upload one “before“ photo (week 0 or pre-treatment) and one “after“ photo (taken at week 16 or later). We want to see your real results, so no mascara or eye makeup! And be sure to fill out the fields below. If you've submitted before, please use the same email address you used the last time.


"Before" Photos (Week 0)

"After" Photos (Week 16)

need help taking before & after pictures? see our photo tips for inspiration.
  • Choose close-up photographs that are well lit and in focus, so your lashes stand out.
  • Be sure to not wear eye makeup or mascara. We want to see your real results.
  • Photograph your lashes from the same angle each time. Try a frontal view with your eyes open or a
    superior view with your eyes closed. (See examples below.)
  • Don’t worry if you’re not an expert photographer; just share the photos that show off your lash growth.
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* I have read and agree to the Terms & Conditions and grant Allergan permission to use my submitted information to be featured in future LATISSE® communications.

Consent Form for Patient Testimonials Hide Terms & Conditions
What is the purpose of this consent form?

From time to time, Allergan, Inc. (Allergan) solicits actual (real life) patient experiences with its products, for purposes of including some of that information in its advertising, promotion, training or market research evaluation programs. By submitting your photographs and information, you may be selected as a possible candidate for providing an actual patient testimonial about your use of Allergan’s product, LATISSE®. However, there is a chance your submission may not be used.

What am I consenting to by checking this box?

By checking this consent box, you are giving Allergan, its affiliates, and other business partners working with Allergan on its products, programs and services, the right to use, copyright, license, publish, broadcast, display, reproduce, and distribute in any manner, in color or otherwise, your name, personal information, or personal experiences that you provide to Allergan, in connection with your use of LATISSE®.

What am I representing to Allergan by checking this box?

You are representing that any statements and information that you have provided to Allergan are accurate, and reflect your true and honest opinion of your experiences.

What can Allergan do with my photos or personal information if I consent?

If you provide consent to Allergan, you may have your testimony, along with some of your medical information relating to your personal experiences with LATISSE® published, circulated or presented in any way in any media (e.g., internet, printed advertisements, television or radio ads, annual reports and training programs) for distribution to the public at-large. Allergan can use your information by itself or combine it with other written, printed, graphic, or audio matter, for members of the medical, nursing, pharmaceutical and related healthcare professions, as well as to other patients and consumers.

Will Allergan share my information with any other parties?

Allergan may share your information with its affiliated companies and other business partners for purposes relating to advertising, promotion, training or market research programs that relate to Allergan products, programs or services. These parties will only be allowed to use your information consistent with this consent form, and will not be permitted to use your information for their own separate use. The business partners who may receive your information includes advertising agencies and public relations firms working with Allergan on its advertising and promotional activities.

Will Allergan or its business partners contact me?

In some situations, business partners may contact you to discuss your experience with LATISSE®, for the purpose of evaluating appropriate candidates for testimonials.

Am I entitled to any payments or ongoing compensation from the use of my photos or information?

No. There is no compensation or reimbursement for participation in this program.

Can I withdraw my consent?

Yes, you can withdraw your consent at any time by sending a written request to withdraw to Allergan, Inc., Attention: Corporate Communications, P.O. Box 19534, Irvine, CA 92623. Please allow 30 days from receipt of your request for processing. If you withdraw your consent, it will apply to new uses of your information, but will not apply to any use of your information that is already initiated, such as advertising or promotional materials that have already been prepared for use. Allergan, Inc. does not have an obligation to cease using promotional materials that have already been prepared with your information.

What am I releasing by checking this box?

By checking this box, you understand that you are releasing Allergan from any legal claims arising out of the use of your photographs or information by Allergan, its affiliates and its business partners, consistent with the allowable uses provided in this consent form.

Thanks for sharing photos
LATISSE® (bimatoprost ophthalmic solution) 0.03% Important Information
Approved Use
Important Safety Information
If you use/used prescription products for eye pressure problems, use LATISSE® under doctor care. LATISSE® may cause increased brown pigmentation of the colored part of the eye which is likely permanent. Eyelid skin darkening may occur and may be reversible. Only apply at the base of upper lashes. DO NOT APPLY to lower lid. Hair may grow on skin that LATISSE® frequently touches. If you have eye problems/surgery, consult your doctor about use of LATISSE®. Common side effects are itchy and red eyes. If discontinued, lashes gradually return to previous appearance.

You are encouraged to report negative side effects of prescription drugs to the FDA.
Visit www.fda.gov/medwatch or call 1-800-FDA-1088.
BOTOX® Cosmetic (onabotulinumtoxinA) Important Information
BOTOX® Cosmetic is a prescription medicine that is injected into the area around the side of the eyes to improve the look of moderate to severe crow's feet lines in adults for a short period of time (temporary).

BOTOX® Cosmetic may cause serious side effects that can be life threatening. Call your doctor or get medical help right away if you have any of these problems any time (hours to weeks) after injection of BOTOX® Cosmetic:

  • Problems swallowing, speaking, or breathing, due to weakening of associated muscles, can be severe and result in loss of life. You are at the highest risk if these problems are pre-existing before injection. Swallowing problems may last for several months
  • Spread of toxin effects. The effect of botulinum toxin may affect areas away from the injection site and cause serious symptoms including: loss of strength and all-over muscle weakness, double vision, blurred vision and drooping eyelids, hoarseness or change or loss of voice (dysphonia), trouble saying words clearly (dysarthria), loss of bladder control, trouble breathing, trouble swallowing. If this happens, do not drive a car, operate machinery, or do other dangerous activities

The dose of BOTOX® Cosmetic is not the same as, or comparable to, any other botulinum toxin product.

There has not been a confirmed serious case of spread of toxin effect when BOTOX® Cosmetic has been used at the recommended dose to treat frown lines, crow's feet lines or both at the same time.

Serious and/or immediate allergic reactions have been reported. They include: itching, rash, red itchy welts, wheezing, asthma symptoms, or dizziness or feeling faint. Tell your doctor or get medical help right away if you are wheezing or have asthma symptoms, or if you become dizzy or faint.

Do not take BOTOX® Cosmetic if you: are allergic to any of the ingredients in BOTOX® Cosmetic (see Medication Guide for ingredients); had an allergic reaction to any other botulinum toxin product such as Myobloc® (rimabotulinumtoxinB), Dysport® (abobotulinumtoxinA), or Xeomin® (incobotulinumtoxinA); have a skin infection at the planned injection site.

Tell your doctor about all your muscle or nerve conditions, such as amyotrophic lateral sclerosis (ALS or Lou Gehrig's disease), myasthenia gravis, or Lambert-Eaton syndrome, as you may be at increased risk of serious side effects including severe dysphagia (difficulty swallowing) and respiratory compromise (difficulty breathing) from typical doses of BOTOX® Cosmetic.

Tell your doctor about all your medical conditions, including: plans to have surgery; had surgery on your face; weakness of forehead muscles, such as trouble raising your eyebrows; drooping eyelids; any other abnormal facial change; are pregnant or plan to become pregnant (it is not known if BOTOX® Cosmetic can harm your unborn baby); are breast-feeding or plan to breast-feed (it is not known if BOTOX® Cosmetic passes into breast milk).

Tell your doctor about all the medicines you take, including prescription and nonprescription medicines, vitamins, and herbal products. Using BOTOX® Cosmetic with certain other medicines may cause serious side effects. Do not start any new medicines until you have told your doctor that you have received BOTOX® Cosmetic in the past.

Especially tell your doctor if you: have received any other botulinum toxin product in the last 4 months; have received injections of botulinum toxin, such as Myobloc®, Dysport®, or Xeomin® in the past (be sure your doctor knows exactly which product you received); have recently received an antibiotic by injection; take muscle relaxants; take an allergy or cold medicine; take a sleep medicine; take anti-platelets (aspirin-like products) or anti-coagulants (blood thinners).

Other side effects of BOTOX® Cosmetic include: dry mouth, discomfort or pain at the injection site, tiredness, headache, neck pain, and eye problems: double vision, blurred vision, decreased eyesight, drooping eyelids, swelling of your eyelids, and dry eyes.

For more information refer to the Medication Guide or talk with your doctor.

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch or call 1-800-FDA-1088.

Please see BOTOX® Cosmetic full Product Information, including Boxed Warning and Medication Guide.

Natrelle® Breast Implants Important Information

Who may get breast implants (INDICATIONS)?

Natrelle® Breast Implants are indicated for women for the following:

  • Breast augmentation for women at least 22 years old for silicone-filled implants.
  • Breast augmentation for women at least 18 years old for saline-filled implants.
    Breast augmentation includes primary breast augmentation to increase breast size, as well as revision surgery to correct or improve the result of a primary breast augmentation surgery.
  • Breast reconstruction. Breast reconstruction includes primary reconstruction to replace breast tissue that has been removed due to cancer or trauma or that has failed to develop properly due to a severe breast abnormality. Breast reconstruction also includes revision surgery to correct or improve the result of a primary breast reconstruction surgery.


Who should NOT get breast implants (CONTRAINDICATIONS)?

  • Women with active infection anywhere in their body.
  • Women with existing cancer or pre-cancer of their breast who have not received adequate treatment for those conditions.
  • Women who are currently pregnant or nursing.

What else should I consider (WARNINGS)?

  • Breast implants are not lifetime devices, and not necessarily a one-time surgery.
  • Many of the changes to your breasts following implantation cannot be undone. If you later choose to have your implant(s) removed and not replaced, you may experience unacceptable dimpling, puckering, wrinkling, or other cosmetic changes of the breast, which may be permanent.
  • Breast implants may affect your ability to breastfeed, either by reducing or eliminating milk production.
  • Rupture of a silicone-filled breast implant is most often silent and may not be detected by you or your doctor. You should have an MRI 3 years after your surgery and then every 2 years after that for as long as you have your breast implants to determine if rupture is present. If implant rupture is noted on an MRI, you should have the implant removed, with or without replacement.
  • With breast implants, a routine screening mammography and self-examinations for breast cancer will be more difficult. Ask your doctor to help you distinguish the implant from your breast tissue. Symptoms of a ruptured implant may be hard knots or lumps surrounding the implant or in the armpit, change or loss of size or shape of the breast or implant, pain tingling, swelling, numbness, burning or hardening. Tell your doctor of these symptoms and remove ruptured implants.
  • Inform any other doctor who treats you of the presence of your implants to minimize the risk of damage to the implants.

What types of conditions require more study (PRECAUTIONS)?

Caution: Notify your doctor if you have any of the following conditions, as the risks of breast implant surgery may be higher:

  • Autoimmune diseases (for example, lupus and scleroderma).
  • A weakened immune system (for example, currently taking drugs that weaken the body’s natural resistance to disease).
  • Planned chemotherapy following breast implant placement.
  • Planned radiation therapy to the breast following breast implant placement.
  • Conditions that interfere with wound healing and blood clotting.
  • Reduced blood supply to breast tissue.
  • Clinical diagnosis of depression or other mental health disorders, including body dysmorphic disorder and eating disorders. Please discuss any history of mental health disorders with your surgeon prior to surgery. Patients with a diagnosis of depression or other mental health disorders should wait for resolution or stabilization of these conditions prior to undergoing breast implantation surgery.

What are some complications with breast implants (COMPLICATIONS)?

Key complications are reoperation, implant removal with or without replacement, implant rupture with silicone-filled implants, implant deflation with saline-filled implants, and severe capsular contracture (severe scar tissue around the implant). Other complications include asymmetry, nipple/breast/skin sensation changes, scarring or wrinkling/rippling. Talk to your doctor about other complications.

Talk to your doctor. For more information see the Patient Brochures at www.allergan.com/labeling/usa.htm or call the Allergan Product Support line at 1-800-433-8871.

To report a problem with Natrelle®, please call Allergan Product Surveillance at 1-800-624-4261.
Natrelle® Breast Implants are available by prescription only.

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