🌍 Part 2 is here! More voices. More strength. One united message.
People with lipodystrophy from around the world continue to raise awareness for #WorldLipodystrophyDay 💙
Representation matters. Connection is powerful.
#WLD2025 #WeAreUnited #RareButGlobal #LipodsytrophyUnited #Lipodystrophy
🎥 “We know our bodies way better than anyone can guess.”
For #WorldLipodystrophyDay, Briana Steiner shares her story and the importance of being heard, understood, and connected. 💙
#WLD2025 #WeAreUnited #LipodystrophyAwareness #RareButStrong #LipodystrophyUnited #Lipodystrophy
To kick off World Lipodystrophy Day 2025, our global community comes together to say, "We are here." 💙
Watch as people living with lipodystrophy introduce themselves in their languages—because awareness has no borders.
#WorldLipodystrophyDay #LipodystrophyUnited #Lipodystrophy
🎥 Andra Stratton, co-founder of Lipodystrophy United, kicks off World Lipodystrophy Day with a
powerful message of hope, unity, and action.
💙✨
Today, we shine a light on this rare condition and the incredible strength of our community.
#WorldLipodystrophyDay #LipodystrophyAwareness #RareButStrong
A promotional flyer for the “World Lipodystrophy Day Virtual Symposium” happening on Saturday, March 29, 2025, from 11:00 AM to 2:00 PM Central Standard Time. The event features expert panelists: Dr. Elif Oral (11:30 AM - 12:00 PM), Dr. Baris Akinci (12:00 PM - 12:30 PM), and Zainab Alzoubi (1:15 PM - 1:45 PM). A special guest, Sonia, will also share her story. The flyer encourages participants to join for global updates, wellness discussions, and a live audience Q&A. Logos of Lipodystrophy United, Michigan Medicine, and Lipodystrophy Canada are at the bottom. The design includes circular headshots of the three speakers.
It’s almost here! 🎉 World Lipodystrophy Day Virtual Symposium — March 29 🌎💻
✅Global experts
✅Community stories
✅Live Q&A
Special guests: Dr. Elif Oral, Dr. Baris Akinci, Zainab Alzoubi, & Sonia! 💬
🗓️ 11 AM - 2 PM CST
👉Sign up: us06web.zoom.us/meeting/regi...
#WorldLipodystrophyDay #RareDisease
