Cure MFM13
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Blog & News

7/1/2026

Cure MFM13 Launches Patient Registry for MFM13 - Registration Now Open

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6/9/2026

Thank You, VoLo Foundation: A Generous Gift Toward an MFM13 Treatment

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4/30/2026

A Comprehensive Review of MFM13

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1/5/2026

2025 Update: A Year of Growth, Collaboration, and Real Progress

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10/17/2025

Summary - Tedesco

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10/15/2025

From Gene to Diagnosis: Cure HSPB8 is now Cure MFM13!

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7/2/2025

Summary of a recently published review on HSPB8 Associated Neuromuscular Disorders

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6/8/2025

VoLo Foundation Renews Support for Cure HSPB8

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5/26/2025

Cure HSPB8 at World Orphan Drug Congress USA 2025: Accelerating the Path to a Cure

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5/21/2025

Launching the Cure HSPB8 Podcast: A Resource for the HSPB8 Myopathy Community

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3/14/2025

HSPB8 Myopathy is now officially MFM13

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12/19/2024

A year it all started – reflecting on 2024 at Cure HSPB8

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9/9/2024

Unlocking Hope for the Ultra-Rare Conference in Warsaw

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6/25/2024

Cure HSPB8 and Everlum Bio Announce Strategic Collaboration to Accelerate Research

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5/16/2024

Cure HSPB8 Receives Generous Funding from VoLo Foundation: A Boost for Research and Support

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5/15/2024

Cure HSPB8 Joins Global Genes Alliance: Strengthening the Fight Against Rare Diseases

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4/2/2024

Establishing Cure HSPB8: A New Hope for Those Affected by HSPB8 Myopathy

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