Together for a brighter future

LGMD2i, or Limb-Girdle Muscular Dystrophy type 2i, is a rare genetic disorder that primarily affects muscle strength and function. It is characterized by progressive muscle weakness, particularly in the limbs, and is caused by mutations in the genes responsible for muscle health.

You can support Cure LGMD2i Canada by donating, participating in fundraising events, or volunteering your time. Every contribution helps us raise awareness and fund critical research for treatment development for LGMD2i.

Our primary goals include advocating for patients and families affected by LGMD2i, raising awareness about this ultra-rare condition, and funding clinical research to develop effective treatments. We aim to create a supportive community for those impacted by this disorder.

You can get involved by joining our events, following us on social media, and sharing our mission with others. Engaging with our community helps spread awareness and fosters support for families affected by LGMD2i.

Cure LGMD2i Canada provides various resources for families, including informational materials about LGMD2i, access to support groups, and updates on research developments. We aim to empower families with knowledge and community support.

You can stay updated on research by subscribing to our newsletter, following our social media channels, and visiting our website regularly for the latest news and developments in LGMD2i research.