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Patients seek consultations for various reasons. However, there is a new common factor that influences people’s decision to get a cosmetic treatment: social media. A person with social media dysmorphia (SMD), or selfie or Snapchat dysmorphia, may have a body dysmorphic disorder (BDD) that can be triggered or worsened by social media.
Many social media users are accustomed to sharing selfies that have been altered with filters to erase imperfections. Constant exposure to this enhanced version of oneself—combined with the positive feedback in the form of likes, shares, and follows—can make people feel their unedited selves aren’t enough. Some potential patients may even present a modified selfie to demonstrate aesthetic goals, regardless of whether or not they are realistic.
While social media dysmorphia isn’t a recognized diagnosis per the DSM-5, the term still reflects the way that social media can impact someone with BDD. A person with BDD is usually obsessed with self-perceived flaws that others likely do not notice. Too often, this psychological disorder is mis- or undiagnosed.
While social media doesn’t cause BDD, it can trigger or worsen it. Teenagers and influencers are often at higher risk for developing BDD because of their excessive use. Influencers may perceive their market value to directly correlate to the number and quality of their social media interactions.
There is a clear connection between social media use and demand for cosmetic enhancements. In fact, more than half of aesthetic surgeons say they’ve seen an increase in the number of patients who want treatments specifically to improve their selfies. However, it’s important to screen prospective patients for SMD and BDD for a number of reasons:
Researchers estimate that up to 15% of patients seeking cosmetic enhancement procedures have BDD, the majority of whom are women. Because SMD is a relatively new development, however, it isn’t clear yet how many people have it.
Symptoms of BDD include:
While it can be difficult to determine whether a patient’s perception of his or her flaws is warranted, medical aesthetic experts should screen clients for possible mental health concerns prior to administering treatment. One survey found that 84% of aesthetic practitioners had treated a person they considered an appropriate candidate and later determined that the recipient had BDD.
To better identify patients who may have BDD and/or social media dysmorphia, pay attention to their concerns. If someone presents edited selfies during a consultation, ask how much the pictures been edited. Be clear and firm about what aesthetic treatment can and can’t do. You can also ask a candidate to identify flaws in a mirror. This could help you get a better sense of his or her self-perception.
Another way to screen for BDD is to use a questionnaire that lists common symptoms. Have patients rate the severity of distress for each one. If a person has symptoms of BDD, you can then refer them to a mental health specialist.
Before treating any patient, you should address these questions:
With social media playing an ever-increasing role in people’s lives, it is imperative to keep BDD and SMD in mind during each consultation. To avoid dramatic surgical outcomes that may not be reversible, consider providing non-invasive solutions to better serve your patients.
Venus Concept offers an extensive lineup of cutting-edge, non-invasive medical aesthetic devices and post-sales support services. Contact us today for more information or download our report, “Filters and Fillers: The Growing Incidence of Social Media Dysmorphia in the Medical Aesthetics Space.”
For more information call: (888) 907-0115 // info@venusconcept.com // 235 Yorkland Blvd., Suite 900, Toronto, ON, M2J 4Y8 Canada
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Venus Bliss™ is 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 licensed by Health Canada for temporary increase of skin tightening, temporary circumferential reduction, and temporary cellulite reduction.
Venus Versa™ is licensed by Health Canada as a multi-application device intended to be used in aesthetic and cosmetic procedures. The SR515 and SR580 applicators are licensed by Health Canada 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 licensed by Health Canada 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 licensed by Health Canada for the treatment of acne vulgaris. The DiamondPolar™ applicator is licensed by Health Canada 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 for temporary body contouring via skin tightening, circumferential reduction, and cellulite reduction. The NanoFractional RF™ (Viva) applicator is licensed by Health Canada for dermatological procedures requiring ablation and resurfacing of the skin.
NeoGraft® is licensed by Health Canada 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 licensed by Health Canada 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 licensed by Health Canada for the temporary increase of skin tightening, temporary circumferential reduction, temporary cellulite reduction, and temporary wrinkle reduction.
Venus Velocity™ is licensed by Health Canada 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.
The Venus Viva™ is licensed by Health Canada as a non-invasive medical aesthetic device, intended for use in dermatologic and general surgical procedures requiring ablation and resurfacing of the skin, using the Viva™/Viva™ MD applicator, and reduction in the appearance of wrinkle and rhytides in Fitzpatrick skin types I - IV using the DiamondPolar™ applicator.
Venus Epileve™ is licensed by Health Canada 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 Freeze Plus™ 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.
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.
Venus Glow™ provides a dermal rejuvenation treatment that works to open up and deep-clean pores. Venus Concept is the exclusive distributor for Venus Glow™.
Venus Skin™ is a skin care line of various lotions and creams intended to improve different aspects of skin appearance, skin serums, and skin nourishment solutions.
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