Vision

Formed in September 2013, the LGMD2D Foundation is a registered 501(c)3 non-profit foundation built for families living with LGMD2D - both patients and caregivers - by families with the same diagnosis. We, too, saw there was a gap in providing information and resources to those living with this rare disorder. Our mission is to expedite the development of treatments or a cure for Limb-Girdle Muscular Dystrophy, type 2D / R3 (LGMD2D).

Goals

1. 1.Build a solid infrastructure for the growth and expansion of the LGMD2D Foundation to increase consideration for patient treatment options and support.
2. 2.Engage and partner with new and existing industry stakeholders to increase consideration and development for LGMD2D treatments.
3. 3.Continue to raise awareness and advocate for LGMD2D patients.