Welcome to the Cure MFM13 Podcast, a series dedicated to raising awareness and sharing critical information about MFM13 Myopathy. This podcast is designed for individuals and families affected by this rare neuromuscular condition, as well as clinicians and researchers working to make a difference.

In each episode, we focus on one key topic related to MFM13 Myopathy — whether it’s the latest advancements in research, genetic testing, diagnosis, management strategies, or insights from the rare disease space. We’ll discuss recent publications, dive deep into important clinical topics, and explore the latest findings in the field. Episodes will sometimes feature journal club discussions, where we summarize and analyze key publications in the HSPB8 space, helping to make complex research more accessible.

Our goal is to inform, connect, and empower the MFM13 community, while providing resources that will support families, clinicians, and researchers alike. Together, we can build a stronger, more informed community as we work towards a life free from MFM13 Myopathy.

This podcast is generated with the support of AI, NotebookLM. We do everything in our power to ensure accuracy and clarity, but we welcome your feedback. If you spot anything that needs correction or want to contribute, please reach out to us at ania@curemfm13.org.

Funzionalità

Risorse

Podcasts

Cure MFM13 - The Podcast (previously Cure HSPB8)