This website and It’s Rare For Me project is organised and funded by
Chiesi Global Rare Diseases

This website and It’s Rare For Me project is organised and funded by Chiesi Global Rare Diseases

This website and It’s Rare For Me project is organised and funded by Chiesi Global Rare Diseases

A BELIEF THAT CHANGE IS POSSIBLE

Mandie

“I’m Mandie. I’m a wife, a mother, poet, an artist […] for me sometimes breaking things means that you can put them together in a more beautiful pattern”

Despite the challenges of living with Fabry Disease, Mandie doesn’t let the condition define who she is. Mandie turned her personal experience into the strength she needed to advocate not just for herself, but for her family and the entire community.
With several family members also diagnosed, the journey hasn’t been easy but facing it together with the loved ones brings strength, understanding, and a clearer path forward.

DISEASE

Fabry Disease
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