Diffuse large B-cell non-Hodgkin lymphoma
In late 2020, when Paula Hall should’ve been basking in the newness of motherhood, she was instead thrust into intensive treatment for a rare blood cancer.
Rheumatoid Arthritis
Linda Roy has spent the majority of her life immunocompromised. Now, from her home in a remote New Brunswick community, she’s turned her experience into a passion for helping others.
Primary Sclerosing Cholangitis
At just 16 years old, Afsana Lallani was diagnosed with a rare liver disease. Only a few short years later, she found herself in urgent need of a life-saving organ transplant.
Learn about the CIAN's position on the challenges and recommendations for achieving an equitable future for immunocompromised Canadians.
In 2020, a survey by Statistics Canada found that approximately 14% of Canadians aged 15 years or older are living with compromised immune systems. In other words, over 5,450,200 Canadians are immunocompromised.
Patient Voice spoke with nine-year-old Simon Hoskins and his mother, Becs, about Simon’s journey with Morquio syndrome, the challenges he faces, and how he continues to remain positive and resilient in the face of a rare disease.
Authentic friendships, both in-person and online, became a lifeline for me. They offered strength and allyship when I needed them most.
Bardet-Biedl syndrome (BBS) has touched nearly every aspect of Natasha Rivard’s young life. Now, as she enters adulthood, her mother, Annie, is pausing to reflect on just how far she’s come.
Industry Voice sat down with Christophe Griolet, General Manager of Gilead Sciences Canada, to discuss how he applies global learnings in a local context, his commitment to health equity, and the incredible promise of personalized medicine.