welcome to oneEDSvoice- a positively charged Ehlers Danlos Syndrome community.
- join today!
The ILC is a national peer-to-peer-focused charitable foundation catalyzing efforts to address the burden of Chronic Pain and Ehlers Danlos Syndrome through evidence based awareness and education.
-To inspire hope and contribute to the health and well-being of children and individuals living with chronic pain by providing a care model of health promotion and knowledge sharing partnerships through a family centered, awareness and education resource network.
-To inspire hope through participation and facilitation of Canadian Institute for Health Research Strategic Patient Oriented Research.
To help all children, adolescents, young adults and families living with chronic pain to have the best opportunity to reach their potential through a comprehensive support network and program that fosters knowledge transfer.
expertly curated content related to this topic
Ehlers-Danlos Support Group Buddy SystemThis group is for the members of the Ehl...
EDS UK (Ehlers Danlos Syndrome)This is a group created to offer help an...
Ontario Announces New Clinic for EDS, Expands Other Clinics for Rare DiseasesThe Ontario government said Monday that ...
Ehlers-Danlos Syndrome (EDS) Community (RareConnect)Ehlers-Danlos syndrome (EDS) is a geneti...
23 Things You May Not Know About My Ehlers-Danlos SyndromeWhen the media features Ehlers-Danlos sy...