NDF Talks

NDF Talks with: GNE Myopathy Patient, Amy


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“It is hard on my family, but we go on this journey together and I think it helps us. We are stronger together as a family..”

      -Amy, on her and her 3 siblings all having GNEM

About NDF: Our mission is to enhance the quality of the lives of people living with GNE Myopathy through advocacy, education, outreach, and funding critical research focused on treatments and a cure.

To learn more about GNE Myopathy visit: https://www.CureGNEM.org

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NDF TalksBy Neuromuscular Disease Foundation