GlobalSkin

🌟 #FollowFriday Spotlight 🌟 This week: @RdcEczema4128 Eczema RDC—supporting people living with #eczema and raising awareness in #Congo. ➡️ Builds community & visibility ➡️ Shares patient resources ➡️ Advocates for skin health Follow: FB: facebook.com/profile.php?id… IG:

Last chance to submit your written input in the #GlobalSkin #RegionalEngagement Series. Share your insights by March 22. Your input helps ensure our regional reports fully capture lived experiences of skin patients. Check your email for details. #Dermatology #Survey

Members, join the April 1 Coffee Chat with our Board Directors to learn what serving on the GlobalSkin Board is really like and how it supports patient leadership. Check your email for the registration link. #GlobalSkin #CoffeeChat #BoardElection #Dermatology

🌟 #FollowFriday Spotlight: Dansk Forening for Albinisme (Danish Association for #Albinism)! Supporting people with #albinism and their families across #Denmark through guidance, resources, and community. 🌐 Learn more and connect: albinisme.dk/en/home

#GlobalSkin Members — Every perspective helps us better understand what #skinpatients are experiencing in each region. If you couldn’t attend the Regional Engagement #Workshop or haven’t shared your insights yet, submit your input by March 22, 2026. See your email for details.

🌍 Join GlobalSkin at WCRSD 2026 in Versailles, France (July 1–3)! We're offering 14 Travel Bursaries for RareDERM Community members. ✈️ Apply: 9 Mar – 12 PM ET ⏳ Deadline: 20 Mar – 12 PM ET At the event: 🔹 Patient Symposium 🔹 #GlobalSkin Booth 🔹 #RareDERM Member Meeting

🌟 #FollowFriday Spotlight 🌟 Flying for Lily supports people affected by Congenital Melanocytic #Naevus Syndrome (#CMN) in #Belgium. They raise awareness, share trusted information, and connect families worldwide. 🌐 flyingforlily.weebly.com 👍 facebook.com/flyingforlily/ #Congen

Calling all #GlobalSkin Members — Missed the Regional Engagement #Workshops or have more to share? Submit your written input by March 22 and help ensure the realities of #skinpatients in your country are reflected in our regional reports. Details in your inbox. #Dermatology

Thank you to everyone who took part in #RareDiseaseDay 2026 💜 By sharing your story, posting, or standing in solidarity, you helped break stigma and amplify the #MySkinisRare Campaign & our #RareDERM voice. More people are learning & supporting because of you!

On #RareDiseaseDay, we stand with 6.8M people living with 800+ rare skin diseases. Many face delayed diagnosis & limited care. Join our #MySkinIsRare campaign to raise awareness, amplify #RareDERM voices & drive change worldwide. – Jennifer Austin, GlobalSkin CEO #GlobalSkin

🌍 On #RareDiseaseDay 2026, we raise awareness and honor those living with rare dermatological diseases. In 2025, the World Health Assembly recognized skin diseases as a global public health priority. Share your story: globalskin.org/RDD2026 #RareDERM #MySkinIsRare

🌟 #FollowFriday Spotlight 🌟 This week we’re highlighting the Skin of Color Society, advancing skin of color dermatology through research, education & advocacy in the #UnitedStates & globally. 🔗 skinofcolorsociety.org

GlobalSkin CEO Jennifer Austin spoke at the European Parliament in Brussels on advancing the #WHA Resolution on Skin Diseases. Encouraged by engaged MEPs & grateful to EADV, @ILDSDerm & European patient advocates for ensuring the patient voice was heard. #GlobalSkin #SkinHealth

The February 2026 Members Matter Bulletin is out now! Members, check your inbox to read it. Not a GlobalSkin Member yet? Learn how you can become one: globalskin.org/member-communi… #GlobalSkin #MembersMatter #PatientAdvocacy #Dermatology #HealthPolicy

💜 On #RareDiseaseDay (Feb 28, 2026), we’re spotlighting people living with rare dermatological diseases and the movement supporting them. 🌍 💬 Share your story: globalskin.org/RDD2026 Every story drives awareness & change. Together, we lift #RareDERM voices. 🤝 #GlobalSkin

🌟 #FollowFriday Spotlight 🌟 Highlighting Fundación Piel de Luna Albinos de #México A.C., dedicated to improving life for people with #albinism. They provide support, advocacy, education & #skincancer prevention. 🔗 fundacionpieldeluna.com

February is Ectodermal Dysplasias Awareness Month - a time to amplify voices, share stories & raise awareness of these rare conditions. 💙 Join this year’s theme: “Blue Out for #EctodermalDysplasias” by wearing blue all month! Learn more & get involved: nfed.org/get-involved/r…

Four of six #GlobalSkin Regional Engagement #Workshops are complete. On, Feb 19, we meet with our European Members, followed by North America on Feb 24. Your insights will help shape regional reports and strengthen patient-led advocacy worldwide. Check your inbox to register.

GlobalSkin Members, Skin Sri Lanka, has launched a powerful Sinhala song tackling drug-resistant #tine - using music to fight stigma, misuse of treatments & delayed care. Watch & share: youtube.com/watch?v=8i32in… #GlobalSkinMembers #AntifungalResistance #RareDERM #SkinHealthForAll

💜 This #RareDiseaseDay (Feb 28, 2026), share your story of living with a rare skin condition. Your experience helps raise awareness, build understanding, and support others who may feel alone. Submit: globalskin.org/RDD2026 Share & repost! #RareDerm #MySkinIsRare