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New Report Release: A Guide to Nutrition for Patients with Duchenne Muscular Dystrophy

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Exclusive Report

New Report Release: A Guide to Nutrition for Patients with Duchenne Muscular Dystrophy

We’re excited to share our latest in-depth report developed in collaboration with AllMyHealth. This guide provides practical insights on how nutrition plays a vital role in managing Duchenne muscular dystrophy (DMD).

Key highlights: understanding DMD and its impact on nutrition, general dietary guidelines for people with DMD, specific nutritional needs for DMD patients, practical advice and meal planning tips (including sample meal plans and recipes).

Available in both text and audio formats - dive in today and share with your community!

View the Full Report

The report is available for free online on the AllMyHealth website.

www.allmyhealth.io/reports

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Latest Research

In their research, Jaber et al. (2025) discovered that Duchenne Muscular Dystrophy (DMD) involves significant lysosomal damage in muscle cells. They observed an increase in Galectin-3, a marker indicating lysosomal membrane damage, and changes in the number and shape of lysosomes. Current gene therapies, which introduce a shortened form of dystrophin, do not fully address this lysosomal damage.

However, when the researchers combined gene therapy with trehalose, a sugar that protects lysosomes, they saw marked improvements in muscle function and overall muscle health in DMD mice models. This suggests that addressing lysosomal damage could be a key component in developing more effective treatments for DMD. The study indicates that combining gene therapy with treatments targeting lysosomal protection may enhance the therapeutic outcomes for patients with DMD.

Community News

Muscular Dystrophy AssociationMuscular Dystrophy AssociationFeb 13, 2025

The National Institutes of Health (NIH) has implemented a harmful 15% cap on indirect costs for research grants, threatening future progress in neuromuscular disease research. Indirect costs are essential to keeping labs running, supporting clinical trials, and ensuring that progress is made toward new treatments.

40 neuromuscular advocacy organizations have united to demand the NIH immediately reverse this policy, which could catastrophically harm neuromuscular disease research, drug development, and care ecosystem. Specifically, this policy would halt research, shut down labs, and stall future medical breakthroughs that are important to the MDA community.

Muscular Dystrophy Association Post
Muscular Dystrophy UKMuscular Dystrophy UKFeb 14, 2025

💕 Love is in the air — but dating with a muscle wasting condition can bring unique challenges.

Despite the barriers, Carrie and Kiera have both found love.

Carrie has known her fiancé for 10 years, but they only started dating three years ago. She shared:

"I think dating is generally tough these days, though I’d be lying if I said my disability hasn’t made things more challenging."

Kiera and her fiancé, Andrew, have been together for 11 years, but their relationship hasn’t been free from judgment.

"There have been comments regarding how we shouldn’t consider starting a family as it’ll be too much for Andrew, or that it would be selfish if I was to pass on my condition."

"The right people will see you before your disability – and you’ll navigate a way through the complexities that come with having a muscle wasting condition."

🧡 Read the blog: https://loom.ly/BSniRis

Harrison & DuchenneHarrison & DuchenneFeb 17, 2025

Does your child have a Healtj Care Card?

If your child visits the Queensland Children’s Hospital and has a health care card please visit the travel hub on 2a and ask them about cappedparking.

At our last visit lasting 5 hours we paid no more than $6 instead os 4 to six times that.

Eternally grateful to a fellow Duchenne Mum who shared this with me.

#hospitallife#duchennemusculardystrophy#tips#parking

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