Takeda have produced a film for Fabry awareness month this April highlighting what it is like to live with Fabry. In this video Katrina and her family discuss their symptoms, dealing with frustrations of having to withdraw from life and how they eventually discovered they had Fabry after another family member was diagnosed. For Katrina, the guilt and worry for the future of her sons has led to some low times but trials and new treatments now keeps her hopeful.
More videos
Why is my MPS child walking less and what can be done to help? By Si Santra
Research article - Pathway to diagnosis and burden of illness in MPS VII
MPS National Conference 2019 Interviews
Webinar on coronavirus (COVID-19) and living with an inherited metabolic disease (IMD) 23 March 2020
Simon's video - Fabry Awareness Month
