Calgary P2P Resource Network Meeting
Family and Child Support Resource Brainstorming Calorie Fest
What local resources are you using to help you and your child and what resources are you looking for? Join us for our last meeting before the summer break for some special treats and a resource sharing session with local families. Hope to see you there!
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!