Health Matters: Muscular dystrophy research breakthroughs
2:38
Global News
Health Matters: Muscular dystrophy research breakthroughs
Health Matters March 1: A University of Alberta researcher is coming up with ground-breaking new treatments for Duchenne muscular dystrophy, thanks to the support of a family with a personal connection to the disease. Su-Ling Goh reports.
Mar 2, 2022
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U of M muscular dystrophy research gives patients hope
U of M muscular dystrophy research gives patients hope
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Advancements & Challenges in Muscular Dystrophy Treatment | AJMC
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💥 We’ve invested £2 million in new research – thanks to your support. This marks our third consecutive year of increased funding, backing 13 pioneering projects that aim to deepen understanding, improve care, and explore new treatments for people living with muscle wasting and weakening conditions. This year’s projects include: 🔬 Our first-ever investment in VCP multisystem proteinopathy type 1, a rare and often overlooked condition 🎓 Double the support for PhD students, helping train the nex
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💥 We’ve invested £2 million in new research – thanks to your support. This marks our third consecutive year of increased funding, backing 13 pioneering projects that aim to deepen understanding, improve care, and explore new treatments for people living with muscle wasting and weakening conditions. This year’s projects include: 🔬 Our first-ever investment in VCP multisystem proteinopathy type 1, a rare and often overlooked condition 🎓 Double the support for PhD students, helping train the nex
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U of M muscular dystrophy research gives patients hope
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💥 We’ve invested £2 million in new research – thanks to your support. This marks our third consecutive year of increased funding, backing 13 pioneering projects that aim to deepen understanding, improve care, and explore new treatments for people living with muscle wasting and weakening conditions. This year’s projects include: 🔬 Our first-ever investment in VCP multisystem proteinopathy type 1, a rare and often overlooked condition 🎓 Double the support for PhD students, helping train the nex
0:57
💥 We’ve invested £2 million in new research – thanks to your support. This marks our third consecutive year of increased funding, backing 13 pioneering projects that aim to deepen understanding, improve care, and explore new treatments for people living with muscle wasting and weakening conditions. This year’s projects include: 🔬 Our first-ever investment in VCP multisystem proteinopathy type 1, a rare and often overlooked condition 🎓 Double the support for PhD students, helping train the nex
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Muscular Dystrophy research at A&M gets FDA approval for human clinical trials
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We’re celebrating 75 years of progress! 🎉 The Muscular Dystrophy Association has been at the forefront of breakthroughs in research, care, and advocacy for neuromuscular diseases since 1950. 💙💛 Watch our new PSA, Legacy. Impact. Momentum. – and see how YOU have been part of this incredible journey. Together, we can create a future without neuromuscular disease. Visit MDA75.org to learn more. https://www.mda.org/press-releases/2025/mda-launches-75th-anniversary-campaign-and-premieres-new-psa-t
1:01
We’re celebrating 75 years of progress! 🎉 The Muscular Dystrophy Association has been at the forefront of breakthroughs in research, care, and advocacy for neuromuscular diseases since 1950. 💙💛 Watch our new PSA, Legacy. Impact. Momentum. – and see how YOU have been part of this incredible journey. Together, we can create a future without neuromuscular disease. Visit MDA75.org to learn more. https://www.mda.org/press-releases/2025/mda-launches-75th-anniversary-campaign-and-premieres-new-psa-t
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FacebookMuscular Dystrophy Association
Duchenne muscular dystrophy (DMD) is a devastating genetic condition that results in progressive muscle weakness, spinal deformities, heart failure and early mortality. While genetic therapies are being explored, current treatments only alleviate symptoms. However, MCW’s Dr. Brian Lin and his lab are researching a promising approach that examines a calcium channel which becomes hyperactive in DMD and how inhibiting that channel could counteract the leading cause of death in DMD patients. Learn m
1:49
Duchenne muscular dystrophy (DMD) is a devastating genetic condition that results in progressive muscle weakness, spinal deformities, heart failure and early mortality. While genetic therapies are being explored, current treatments only alleviate symptoms. However, MCW’s Dr. Brian Lin and his lab are researching a promising approach that examines a calcium channel which becomes hyperactive in DMD and how inhibiting that channel could counteract the leading cause of death in DMD patients. Learn m
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FacebookMedical College of Wisconsin
Today, on World Health Day, the Muscular Dystrophy Association reaffirms our commitment to ensuring that every person we serve who lives with a neuromuscular disease—has equitable access to healthcare. We believe that access to lifesaving treatments, specialized care, and groundbreaking research is not a privilege but a right. Together, we are driving real change, but there is more work to be done. Join us in making a difference: MDA.org/Advocacy | Muscular Dystrophy Association
0:37
Today, on World Health Day, the Muscular Dystrophy Association reaffirms our commitment to ensuring that every person we serve who lives with a neuromuscular disease—has equitable access to healthcare. We believe that access to lifesaving treatments, specialized care, and groundbreaking research is not a privilege but a right. Together, we are driving real change, but there is more work to be done. Join us in making a difference: MDA.org/Advocacy | Muscular Dystrophy Association
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MDA is at the forefront of ALS research, identifying over 50 ALS-linked genes and pushing for advancements in clinical research, early detection, and treatment development. Our efforts include improving diagnosis methods and patient care, highlighted by the recent approval of groundbreaking treatments like tofersen. We're also committed to nurturing the next generation of ALS researchers, ensuring a sustained fight against ALS. With each discovery, we're moving closer to a future free from ALS.
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New study alert 🔬 🚨 On Nov 14, 2025 Esper et al. (a group out of 🇨🇦) published in Nature Communications that dystrophin loss in Duchenne muscular dystrophy (DMD) doesn’t just hit after birth — it actually disrupts muscle stem cell function during fetal (secondary) muscle devrlopment 🤰 They found fewer progenitors, smaller fibers, and mis-polarized cells in DMD mouse embryos 🐭 Even cooler: deleting AAK1 (a kinase) rescued that polarity and helped restore development ❗️ This reveals a fetal
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