welcome

Sangamo’s purpose is to translate our groundbreaking science into therapies that transform patients’ lives. 

 

Our Patient Advocacy engagement provides us with a valuable opportunity to learn from patients and families impacted by the diseases we aim to cure. By connecting with them, we are each better equipped to understand our roles in bringing innovations to patients.

 

We thank these families for sharing their stories with us and providing a glimpse into their lives, loves, hopes, and struggles as they face their diseases.

 

I hope you take the time to read and view these stories and find the same connection and inspiration that I feel each time I visit these pages.

 

Christeen Moburg

Sr. Director Patient Advocacy

MPS I

HURLER SYNDROME

MPS II

HUNTER SYNDROME

hemophilia

TYPE A

hemophilia

TYPE B

If I woke one day and I wasn't in pain, I'd probably be dead."

- Hannah  -  14 years old

training modules

"There is often too much focus on the diagnosis instead of on the person, and helping them to become somebody."

- Erica  -  34 years old