Greetings!

A Foundation Building Strength (AFBS) for Nemaline Myopathy is dedicated to fostering a healthier future through collaboration within the NM patient and family community, as well as partnerships with clinicians and scientists. To support this mission, AFBS seeks to understand your unique perspective as someone living with NM or caring for someone who has/had NM. If there are 2 or more in your family with NM, you may complete the survey separately for each person to provide the individual's experience and medical history.
After your response, click the "NEXT" button at the bottom of the page to proceed.

Question Title

* 1. Do you or a family member have a form of congenital nemaline myopathy (NM)?

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