MPS Society Fundraising Letter
This is the letter that Kirsten Harkins and I wrote for the Canadian MPS Society’s Annual mailer. Click here to read the letter.
We want to hear from you! Send us your story so we can share it with the world. Every person and family battling Fabry Disease has a unique story to tell - one of bravery, resilience, and perseverance. We'll share all stories online here and on our social media feeds!
Drop over to our social media streams to keep updated on the latest rare disease news in Canada, including updates on research projects funded throughout the year. We'll also share your stories on our feeds and share news reports from throughout Canada!