LGMD 2A FUNDRAISER!

Siblings Michele Good, Shelley Tudin and John Kormos were diagnosed with LGMD 2A in their early teens. LGMD 2A (Calpainopathy) is autosomal recessive. Each parent passes on a defective gene to give the diagnosis of LGMD 2A. There is a 25% chance of having a 2nd child with this rare disease.
The Kormos family was and may still be the only reported family in Canada with this subtype of LGMD!