About Rare Disease Network of Alberta
The Rare Disease Network of Alberta (rDNA) is a non-profit corporation that was formed in 2018 to help people understand about rare diseases.
With so much to learn, from the technologies used in making the diagnosis, the new and different methods, of treatment, finding help for caregivers who need to find resources in the community and through government programs, we want to reach out to patients and their families and support them in their journey. Let’s work together for a different future.
The ghosts in our genes: Using DNA to find and treat rare diseases
rDNA will be hosting a special event on worldwide Rare Disease Day 2019 at the Patricia A. Whelan Performance Hall in the Calgary Central Library on February 28, 2019 between 12 pm – 3 pm. Visit our website at https://rdna.ca to Register. Tickets are free but registration is required to attend.