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We have news! The format you loved at The Rare Fair is now available through My City Med Events. Our...
Are you ready for the only 100% virtual, worldwide event for the rare community? The Rare Fair is back,...
As a rare disease advocate for over a decade, I’ve attended some of the nation’s best rare disease conferences...
Rare Disease Brief – Pantothenate Kinase-Associated Neurodegeneration (PKAN) The team here at My City Med is proud to bring...
Angie resides in Kansas with her husband and four children. She is working towards her Bachelor’s degree in Psychology...
We are thrilled to announce the My City Med ALS Road Map is now live on our site. Visitors...
Day 2 of our amazing staff highlights… Meet Kelly, Executive Assistant on the C-Team. Kelly lives in Kansas...
Here at My City Med, we are thrilled to announce that we’re partnering with Uber to give My City...
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You’ve felt it for a while now. Your calls go unanswered; your concerns are glossed over. You don’t seem...