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If you’re looking for a hair loss treatment for women, you’re not alone—it’s estimated that a third of women will experience hair loss at some point in their life.1 Learn more about the causes and how you can get help with a solution that will restore fuller, more natural-looking hair.
HHair loss affects 30 million women in the United States alone2—and those are just the cases that are reported. Because thick, healthy hair is often associated with femininity and beauty, many women are often too embarrassed to talk about their loss. That’s why along with the impact on physical appearance, hair loss can also have strong emotional and psychological effects for women.
Female hair loss can be triggered by a variety of reasons, including short-term events like hormonal imbalances after childbirth or menopause, changes in diet, high stress, or as a side effect from certain medications. Other causes of female hair loss and thinning include impairment of hair’s natural growth cycles (typically associated with chemotherapy), tight hairstyles that damage the hair follicles, and hair loss due to the excessive production of androgens (male hormones). However, the most common cause of long-term hair loss in women is genetics. Genetic female pattern baldness, or androgenetic alopecia, is characterized by a thinning of hair follicles on the sides or top of the scalp. Most women experience this type of hair loss after the age of 50, but it can happen as early as in their 20s and 30s. Understanding the cause of your hair loss is important, as it will help to determine the best female hair loss treatment for you.
People often assume that hair restoration procedures are only for men; however, these procedures can also be a suitable solution for women who want to restore natural-looking hair. The current gold standard and highest demanded procedure in hair restoration for women is Follicular Unit Extraction (FUE), where the treatment provider extracts individual hair follicles from the back or sides of the head using a specialized device and then implants them in the area where more hair growth is desired. Unlike traditional female hair transplant procedures that involve surgically removing a strip from the back of the patient’s scalp, FUE procedures are minimally invasive, enable a faster recovery process, and leave no linear scarring.
At Venus Concept, we offer cutting-edge hair restoration solutions that utilize advanced technology to achieve discreet, natural-looking results. To find out if you are a good candidate for hair transplant for women or thinning hair treatment for women, connect with one of our certified hair restoration providers, who will customize a solution that's perfect for you!
Venus Concept’s hair restoration solutions are ideally suited to address female hair loss. Powered by advanced extraction and implantation technology, the procedures work by relocating your own healthy hair follicles to achieve a fuller, natural-looking hairline.
What you need to know about female hair loss
The best way for women to get optimal hair regrowth is by properly diagnosing the cause of their hair loss and developing a targeted treatment plan with a certified provider. Book a consultation as soon as you notice your hair loss can help to prevent further damage to hair follicles and allow for optimal regrowth when possible.
Options for treating hair loss for women may include oral medications, topical solutions, laser therapies, and hair transplant. Specific treatments should be prescribed by your doctor after a consultation.
Women can certainly be candidates for hair transplantation. Your doctor will determine if you’re a candidate for a hair transplant procedure by assessing your hair loss pattern.
FUE, or Follicular Unit Extraction, is a minimally invasive hair transplant method that works by removing individual follicles from your donor area without a scalpel incision or stitches, and then re-implanting them where you need more coverage. The procedure is minimally invasive and leaves no linear scar.
The FUE method can be done by shaving small areas, which can be covered up by the longer hair that’s left behind.
The newly grafted hair will stay in place for about two to three weeks before shedding, which is normal and an important part of the new growth process. After shedding, the new growth will begin in three to four months, after which your hair should continue to grow. However, individual results and timelines may vary for each patient.
Hair loss may not necessarily stop after transplantation, especially depending on the cause. Some women may need further sessions for continued maintenance. Your doctor will be able to assess your treatment options and discuss the results you can expect during your consultation.
Extraordinary results speak for themselves
Address thinning on the top and front of the scalp—the most common problem areas for women—by restoring thicker, fuller, and healthier-looking hair.
Devices that offer hair restoration: NeoGraft®
Results after: 1 treatment
Graft Count: 1,200
Courtesy of Joseph Hunstad, MD; Bill Kortesis, MD; & Gaurav Bharti, MD
After
BeforeINDICATIONS FOR USE:
NeoGraft® is cleared by the FDA, licensed by Health Canada and has CE Mark with indication for use in suction-assisted follicular extraction and re-implantation. NeoGraft® is an auto-graft system and can be used on both male and female patients.
REFERENCES:
1. Harvard Health Publishing. Treating female pattern hair loss. (2018, November 14). Retrieved from https://www.health.harvard.edu/staying-healthy/treating-female-pattern-hair-loss
2. U.S. National Library of Medicine. Androgenetic alopecia. (n.d.). Retrieved from https://ghr.nlm.nih.gov/condition/androgenetic-alopecia#statistics
Search below to find a provider near you and to learn about our non-surgical aesthetic treatments with ARTAS®, NeoGraft®, Venus Bliss™, Venus Blilss MAX™, Venus Versa™, Venus Legacy™ Venus Versa™ Pro, Venus Velocity™, Venus Viva™ MD, and Venus Glow™.
For more information call: (888) 907-0115 // [email protected] // 235 Yorkland Blvd., Suite 900, Toronto, ON, M2J 4Y8 Canada
REGULATORY CLEARANCES [ More ]
Venus Bliss™ is cleared by the FDA and licensed by Health Canada for non-invasive lipolysis of the abdomen and flanks in individuals with a Body Mass Index (BMI) of 30 or less, with the diode laser applicators. The (MP)2 applicator is cleared by the FDA for temporary reduction in the appearance of cellulite, and licensed by Health Canada for temporary increase of skin tightening, temporary circumferential reduction, and temporary cellulite reduction. Venus Bliss™ has CE Mark as a non-invasive medical aesthetic device enabling a comprehensive approach leading to body contouring, addressing fat reduction, skin tightening, circumference reduction, and cellulite reduction.
Venus Versa™ is cleared by the FDA, licensed by Health Canada, and has CE Mark as a multi-application device intended to be used in aesthetic and cosmetic procedures. The SR515 and SR580 applicators are cleared by the FDA, licensed by Health Canada, and have CE Mark for the treatment of benign pigmented epidermal and cutaneous lesions and treatment of benign cutaneous vascular lesions. The HR650/HR650XL and HR690/HR690XL applicators are cleared by the FDA, licensed by Health Canada, and have CE Mark for the removal of unwanted hair and to effect stable long-term or permanent hair reduction for Fitzpatrick skin types I-IV. The AC Dual applicator is cleared by the FDA, licensed by Health Canada, and has CE Mark for the treatment of acne vulgaris. The DiamondPolar™ and OctiPolar™ applicators on the Venus Versa™ system are cleared by the FDA for non-invasive treatment of moderate to severe facial wrinkles and rhytides on females with Fitzpatrick skin types I-IV. The DiamondPolar™ applicator is licensed by Health Canada and has CE Mark for non-invasive treatment of moderate to severe facial wrinkles and rhytides on females with Fitzpatrick skin types I-IV. The OctiPolar™ applicator on the Venus Versa™ system is licensed by Health Canada and has CE Mark for temporary body contouring via skin tightening, circumferential reduction, and cellulite reduction. The NanoFractional RF™ (Viva) applicator is cleared by the FDA, licensed by Health Canada, and has CE Mark for dermatological procedures requiring ablation and resurfacing of the skin.
NeoGraft® is cleared by the FDA, licensed by Health Canada and has CE Mark with indication for use in suction-assisted follicular extraction and re-implantation. It is an auto-graft system and can be used on both male and female patients.
ARTAS iX™ is cleared by the FDA, licensed by Health Canada and has CE Mark with indication for use for harvesting hair follicles from the scalp in men diagnosed with androgenic alopecia (male pattern hair loss) who have black or brown straight hair. ARTAS iX™ is intended to assist physicians in identifying and extracting hair follicular units from the scalp during hair transplantation; creating recipient sites; and implanting harvested hair follicles.
Venus Legacy™ is cleared by the FDA for the non-invasive treatment of moderate to severe facial wrinkles and rhytides in females with Fitzpatrick skin types I-IV with the OctiPolar™ and DiamondPolar™ applicators, and temporary reduction in the appearance of cellulite with the 4D Body (LB2) and 4D Face (LF2) applicators. It is licensed by Health Canada and has CE Mark for the temporary increase of skin tightening, temporary circumferential reduction, temporary cellulite reduction, and temporary wrinkle reduction.
Venus Velocity™ is cleared by the FDA, licensed by Health Canada and has CE Mark for hair removal, permanent hair reduction (defined as the long-term stable reduction in the number of hairs re-growing when measured at 6, 9 and 12 months after the completion of a treatment regimen), and the treatment of pseudofolliculitis barbae for all Fitzpatrick skin types.
Venus Fiore™ received regulatory approval in Israel for aesthetic and functional treatment of the vagina, labia and mons pubis. Venus Fiore™ is available for sale in India, Hong Kong, and other selected Asian countries.
Venus Viva™ is cleared by the FDA, licensed by Health Canada, and has CE Mark for dermatological procedures requiring ablation and resurfacing of the skin. The DiamondPolar™ applicator is cleared by the FDA, licensed by Health Canada and has CE Mark for the treatment of moderate to severe wrinkles and rhytides in Fitzpatrick skin types I-IV.
Venus Freeze Plus™ is cleared by the FDA for the non-invasive treatment of moderate to severe facial wrinkles and rhytides in females with Fitzpatrick skin types I-IV. It is licensed by Health Canada for temporary skin tightening, and temporary reduction in the appearance of cellulite on the abdomen and flanks, using the DiamondPolar™ and OctiPolar™ applicators. The DiamondPolar™ applicator on Venus Freeze Plus™ has CE Mark for the non-invasive treatment of moderate to severe facial wrinkles and rhytides, and the increase of skin tightening, temporary circumferential reduction, and cellulite reduction with the OctiPolar™ applicator.
Venus Heal™ is licensed by Health Canada and can be used for the treatment of both acute and chronic disorders of the musculoskeletal system, such as muscle spasms, back pain, and soft tissue injuries, and results in effects such as pain relief, myorelaxation, increase of local blood circulation, and edema reduction. In the U.S., Venus Heal™ is cleared by the FDA for the relief of minor muscle aches and pain, relief of muscle spasm, and temporary improvement of local blood circulation. These indications enable the treatment of certain soft tissue injuries and conditions.
Venus Glow™ is cleared by the FDA as a Class I motorized dermabrasion device. It provides a dermal rejuvenation treatment that works to open up and deep-clean pores. Venus Concept is the exclusive distributor for Venus Glow™.
Venus Epileve™ is licensed by Health Canada and has CE Mark for hair removal, permanent hair reduction (defined as the long-term stable reduction in the number of hairs re-growing when measured at 6, 9 and 12 months after the completion of a treatment regimen), and the treatment of pseudofolliculitis barbae for all Fitzpatrick skin types. Venus Epileve™ is also CE-Marked for hirsutism.
Venus Freeze™ is cleared by the FDA for the non-invasive treatment of moderate to severe facial wrinkles and rhytides in females with Fitzpatrick skin types I-IV. It is licensed by Health Canada for temporary skin tightening, and temporary reduction in the appearance of cellulite on the abdomen and flanks, using the DiamondPolar™ and OctiPolar™ applicators. The DiamondPolar™ applicator on Venus Freeze™ has CE Mark for the non-invasive treatment of moderate to severe facial wrinkles and rhytides, and the increase of skin tightening, temporary circumferential reduction, and cellulite reduction with the OctiPolar™ applicator.
Venus Swan™ is cleared by the FDA for the non-invasive treatment of moderate to severe facial wrinkles and rhytides, and licensed by Health Canada for the non-invasive treatment of cellulite reduction, skin tightening, and temporary reduction in the appearance of stretch marks.
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