RT @IrishVasculitis: First of 3 visits yesterday to meet MEPs as part of Rare Disease Week. Thank you @SeanKellyMEP @eurordis #rarediseasemonth @rareireland #vasculitis @_ERNRITA @fairvasc #RAIN

🐦🔗: https://n.respublicae.eu/SeanKellyMEP/status/1623363436959629313

Seán Kelly MEP (@SeanKellyMEP)

RT @IrishVasculitis: First of 3 visits yesterday to meet MEPs as part of Rare Disease Week. Thank you @SeanKellyMEP @eurordis #rarediseasem…

Nitter

It’s #RareDiseaseMonth!

This is my first year as a double rare patient — if I were a gemstone, I would be priceless ✨

Learn more about my story by watching this news feature: https://www.fox5atlanta.com/news/georgia-grad-student-defies-medical-expectations-25-years-after-devastating-diagnosis

#RareDiseaseDay #rarediseaseawareness #disability

Georgia grad student defies medical expectations, 25 years after devastating diagnosis

Linseigh Green was just 2-weeks-old when she was diagnosed with a life-threatening intestinal disease, known as necrotizing enterocolitis, or NEC. Today, the Johns Creek woman is 25 and working on her second master's degree in England.

FOX 5 Atlanta
As we approach #RareDiseaseMonth #RareDiseaseDay2023 , what topics would you like me to write about this year? 🦓