Living with EDS and the fight to be taken seriously | (MIS)Treated

 

(MIS)Treated

(MIS)Treated, a TVO podcast, explores how medicine has – and still is – failing women and speaks to the people looking to make a difference. Join host… 
41 clip(s)
Loading playlist

When a story about one woman's search for care sparked a flood of messages, we began investigating Ontario's healthcare system and the possible obstacles facing people with Ehlers-Danlos syndrome (EDS), especially those with craniocervical instability (CCI).

For patients living with EDS, getting a diagnosis can take years. And when complex spinal conditions enter the picture, some patients and their families say they have been forced to look to the United States for help because they believe there is no surgeon in Canada able to provide the care they need. In this special episode of (Mis)Treated, we meet patients whose lives have been upended, families fighting for answers, and doctors who disagree about how these conditions should be treated.

Got a question or comment? Email us at: mistreatedpodcast@tvo.org

If you, or someone you know, is struggling with mental health, visit any of the following resources for support: Canada.ca/mental-health Kids Help Phone Call 1-800-668-6868 (toll-free) or text CONNECT to 686868.

In 1 playlist(s)

(MIS)Treated

(MIS)Treated, a TVO podcast, explores how medicine has – and still is – failing women and speaks to … 

Social links