Thank you Coriell Institute for Medical Research for sharing our family’s story and why we are so passionate about working towards change in our #raredisease community! “Advocacy can give patient families – families who have been dealt an often life-changing diagnosis – an opportunity to take charge of their situation, participate in research, and focus…
Carrie Ostrea
Article: Steps to Take After Receiving a Rare Diagnosis
As a rare parent advocate, one of the questions I get asked most by newly diagnosed families is “What do I do next? How will I manage this?” My good friend and colleague, Anne Bruns, and I co-authored this article for Exceptional Parents Magazine’s annual “Navigating Special Needs Resources” magazine tackling just this topic. Click…