Support Groups

About

From North America to Europe to Asia, there are active communities and reliable organizations for anyone living with vitiligo. Reach out for medical news, emotional encouragement, and the shared wisdom of others who understand your journey.

Tips on Finding Local Groups

  • Facebook & Instagram Hashtags: Search #vitiligo, #vitiligosupport, or your language’s equivalent.
  • Hospital / Dermatology Clinics: They often list local support networks or patient-led groups.
  • National Health Organizations: Websites of official dermatology or health associations may link to vitiligo resources.

Your site here

Want to be added to our list? We’d love to feature your vitiligo-focused Facebook group, nonprofit, or community organization! If you’re offering helpful resources for people with vitiligo whether it’s online support, local meetups, or educational materials, please reach out to us. Just head over to our Contact Form and share your details. Let’s connect, collaborate, and grow the vitiligo support network together!


 

 

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A Chinese-language discussion forum with threads on treatments, clinical experiences, and emotional support.

https://tieba.baidu.com/f?kw=%E7%99%BD%E7%99%9C%E9%A3%8E

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A Dutch-language resource focusing on vitiligo awareness, patient stories, and medical guidance. May also reference local support groups.

https://www.vitiligo.nl/

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A dedicated Romanian website offering information on causes, treatments, and the psychological impact of vitiligo.

https://www.vitiligo.ro/

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An international discussion forum with users worldwide sharing photos, personal stories, and treatment experiences.

https://www.reddit.com/r/Vitiligo/

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A global nonprofit focusing on advancing vitiligo research, awareness campaigns, and patient education.

https://vrfoundation.org/

🌍

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Supports anyone with a visible difference, including vitiligo. Offers mental health resources, helplines, and advocacy.

https://www.changingfaces.org.uk/

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A UK-registered charity offering newsletters, webinars, and online support groups. Runs awareness campaigns and events.

https://vitiligosociety.org/

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A social network for those with vitiligo to share experiences, ask questions, and give/receive support.

https://www.myvitiligoteam.com/

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A vitiligo support group offering virtual meetings, local chapters, and mentorship programs.

https://www.vitfriends.org/

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An international consortium of physicians, researchers, and patients. Hosts annual conferences and supports research/advocacy.

https://globalvitiligofoundation.org/

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One of the longest-running online communities for vitiligo. Offers message boards, newsletters, and in-depth information on treatments.

https://www.vitiligosupport.org/

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A leading French association raising awareness, supporting research, and connecting patients to resources.

http://www.afvitiligo.com/

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A nonprofit self-help group that provides resources, organizes events, and publishes newsletters.

https://www.vitiligo-bund.de/

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