Katie Bergstrom, a Genetic Counselor based in Seattle, kindly shares a guest blog discussing some important considerations for both individuals…
To mark Rare Disease Day, we have a guest blog from Mike who is kindly willing to share his experience…
Durhane Wong-Rieger, President & CEO of CORD (Canadian Organization for Rare Disorders), has kindly shared this guest blog explaining why…
In this special guest blog Katie Stevens, Executive Director of Team Telomere, shares her story of learning about telomeres, telomere…
To mark Pulmonary Fibrosis Awareness Month this September, we have a special guest blog from the Canadian Pulmonary Fibrosis Foundation…
To show our support for Pulmonary Fibrosis Awareness Month we are pleased to share a special guest blog from the…
Samantha Simmons, Coordinator of Marketing & Communications for the Pulmonary Fibrosis Foundation, shares a special guest blog explaining how you…