This week we welcomed Mike Miller of the Huntington’s Disease Society of America! Thank you to everyone who came to our first speaker event of the semester! instagram.com/p/B7_sF0xAWre/…
Out now! Download the official poster for #RareDiseaseDay 2020 now available via rarediseaseday.org/downloads. Share it today to show your support for the rare disease community!
Your patient experience is your expertise and the role of the FDA Patient Representative® is an equal part of the important equation. Learn more about the FDA Patient Representative Program® youtu.be/F4yxgzGVRXg
Join RareNeu at @NUafterHOURS tonight for a free musical performance by TEGA. All proceeds will be going to @SCDAAorg to support sickle cell disease! Succulent fundraiser at 7, concert at 8 🎤🎼🎉
Patient Affairs Staff works closely with #FDA medical product centers to find ways to include your voice as patients, caregivers, and advocates. #NORDSummitgo.usa.gov/xPXQD
We’ll be tabling with these adorable Valentine’s Day succulents to raise awareness for @1p36DSA tomorrow in Curry Table #1B 10am-4pm, and Wednesday 12-6pm!