Join Rare Diseases Events & Webinars
If you or a loved one is living with a rare disease, it’s important to learn all you can about it. One way you can do this is by attending a patient education event. Hear from lysosomal storage diseases experts and patients on topics related to better understanding Fabry, Gaucher, MPS I and Pompe. Register now to attend an event or join us online.
Anisia
Living with
MPS I disease
Living with
MPS I disease
Join Rare Diseases Events & Webinars
If you or a loved one is living with a rare disease, it’s important to learn all you can about it. One way you can do this is by attending a patient education event. Hear from lysosomal storage diseases experts and patients on topics related to better understanding Fabry, Gaucher, MPS I and Pompe. Register now to attend an event or join us online.
Julia
Living with
Fabry disease
Living with
Fabry disease
Join Rare Diseases Events & Webinars
If you or a loved one is living with a rare disease, it’s important to learn all you can about it. One way you can do this is by attending a patient education event. Hear from lysosomal storage diseases experts and patients on topics related to better understanding Fabry, Gaucher, MPS I and Pompe. Register now to attend an event or join us online.
Hillary
Living with
Pompe disease
Living with
Pompe disease
Join Rare Diseases Events & Webinars
If you or a loved one is living with a rare disease, it’s important to learn all you can about it. One way you can do this is by attending a patient education event. Hear from lysosomal storage diseases experts and patients on topics related to better understanding Fabry, Gaucher, MPS I and Pompe. Register now to attend an event or join us online.
Francisco
Living with
Gaucher disease
Living with
Gaucher disease