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Be a part of the world’s largest network of patients, families, clinicians, researchers, and friends advocating for FSH muscular dystrophy.
Sign up to receive the latest word on clinical trials, how to live strong, and connect to our remarkable community. Your personal information will be kept strictly confidential.
When you join our community you will also have the opportunity to become a part of our patient contact registry.
If you want to know more about this and why it is so important, learn more HERE
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Do you have family members with FSHD? Let them know we'd love them to join us, too!
Even if you have been a member of the FSHD Society for many years, or personally know our staff, the fact that you are a patient may not be recorded in our database. We have also added additional questions and we'd love to have full and correct information.
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