Calgary P2P Resource Network Meeting
Rare Disease Day Brainstorming Session - bring your ideas!
The Rare Disease Foundation is comprised of parents, caregivers and clinicians who are united in their desire to change the world of rare disease care.
We work together to see that more research goes into rare disease, and through our Parent to Parent Resource Networks we band together to share resources and navigate the world of rare disease care together.
Refreshments will be provided. New parents are always welcome!