My name is Sam, I am 34 and was diagnosed with Pompe Disease in February 2010. From the...

A short film giving insight into different families that have a child with Pompe disease (Glycogen Storage Disease...

Haley, who has Pompe Disease, doing her "weight exercises" for Pompe disease.

Haley, who has Pompe Disease, doing her "weight exercises" for Pompe disease.

Haley, who has Pompe Disease, doing her "weight exercises" for Pompe disease.

Juans Progress on Myozyme Treatment dated June 2012. Juan is an infantile onset child living in South Africa....

Caitlin is our 3rd child. She was born a year after our 2nd child Nicole, who passed away...

I was first diagnosed in 1983, by Professor John Hopwood’s facilities at the Adelaide Children’s Hospital. My particular...

"My Special Sister" is about what it is like to have a sister with a rare disease and...

After 6 years of ERT, my daughter Wei Ling and Yen Ling are both now standard 2 and...