Thanks for taking the time to visit my JustGiving page.
This often overlooked charity is close to our family's hearts. My younger sister was diagnosed with Type 3b GSD as a baby, through a liver biopsy. Her parents were given a very negative prognosis, ie unlikely to live past 5 yrs. Thanks to some wonderful care she has proven them wrong! She is lucky as she only has a very mild 'version' and there are others much more poorly than I've ever been. There are over 10 Types and in total only about 560 people with GSD in the UK so it is very rare. Through research there are now treatments for some of the Types but no cure and the charity urgently needs funds to continue vital support for families. Please read, sponsor and share (every little donation will help).
