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Nov 18, 2025 - Follow these tips to save money in your budget when you’re balancing health and disability-related expenses.

When it comes to caregiving for someone with Duchenne muscular dystrophy, a little knowledge can go a long way.

Being a caregiver for a child with DMD can be challenging, but making a daily routine, focusing on family, and finding support can help.

Nov 18, 2025 - Four family caregivers share the everyday ways they incorporate self-care into their lives, so they can care for their loved ones.

Learn how Duchenne muscular dystrophy affects oral health and explore tips for daily care, dental visits, and preventing common mouth issues.

Jan 19, 2021 - What is muscular dystrophy? Most forms of muscular dystrophy appear in infancy or childhood, while others may not develop until later. It’s more likely to...

There is no cure for muscular dystrophy, (MD) but the right treatment approach can ease symptoms for people with these rare genetic disorders.

Jan 31, 2025 - Quest is the largest adaptive lifestyle content platform for the neuromuscular disease community and the disability community at large. Quest includes...

Corticosteroids can slow DMD progression. Understand their benefits, side effects, and how timing impacts long-term treatment outcomes.

For DMD caregivers and people with Duchenne, knowing the early signs and next steps can improve self-care and help manage a child’s care.

Jul 14, 2023 - Learn the symptoms, causes, risks and more of Duchenne muscular dystrophy, a genetic condition causes the muscles to weaken over time.

Aug 18, 2025 - Learn about neuromuscular disorders—their causes, types, symptoms, diagnosis, and treatment options in Canada—in this helpful overview.

It is important to help pediatricians, other physicians, and nonphysician clinicians to diagnose and provide high standards of care for individuals with Du

MDA is the #1 health nonprofit advancing research, care and advocacy for people living with muscular dystrophy, ALS, and related neuromuscular diseases.

Sep 8, 2025 - Our MDA Ambassadors shared some of their favorite products, then looked high and low to find even more fantastic items that celebrate universal use.

Learning life skills to handle Duchenne muscular dystrophy can include health management, working with caregivers, and self-advocacy.

MDA is the #1 health nonprofit advancing research, care and advocacy for people living with muscular dystrophy, ALS, and related neuromuscular diseases.

Sep 13, 2025 - Discover how research and lived experience are driving breakthroughs in neuromuscular care, powered by community, donors, and collaboration

Jan 6, 2023 - Quest is the largest adaptive lifestyle content platform for the neuromuscular disease community and the disability community at large. Quest includes...

Mar 24, 2025 - Doctoral candidate Justin Moy was born with the specific type of muscular dystrophy he’s now studying in the lab at BU.

The NIH funding will propel research into the leading adult-onset form of the condition.

Capricor Therapeutics Inc. (CAPR:NASDAQ) could receive a PDUFA date for its cell therapy as early as spring 2026 if it follows the FDA-outlined path forward,...

Nov 18, 2025 - With accessible cooking and hosting hacks, holiday gift lists, travel advice, tips and tricks for managing stress and coping with loneliness, ideas for...

Nov 14, 2025 - Q&A with an expert on spinal-bulbar muscular atrophy (SBMA), or Kennedy’s disease

Nov 28, 2025 - Make a holiday donation this year to Muscular Dystrophy Canada and help break down barriers to timely diagnosis, care, and support. 

Dec 3, 2025 - Make a holiday donation this year to Muscular Dystrophy Canada and help break down barriers to timely diagnosis, care, and support. 

Managing osteoporosis, which increases the risk of bone fractures, is important for people with Duchenne muscular dystrophy.

Nov 28, 2025 - Make a holiday donation this year to Muscular Dystrophy Canada and help break down barriers to timely diagnosis, care, and support. 

MDA is the #1 health nonprofit advancing research, care and advocacy for people living with muscular dystrophy, ALS, and related neuromuscular diseases.

Muscular dystrophy causes vary depending on the disease type. There are more than 30, including the two most common, Duchenne and Becker.

Interabled relationships are full of challenges, but columnist Leah Leilani believes that adversity brings her closer to her boyfriend, Will.

Duchenne muscular dystrophy can increase the risk of pressure sores, but practical strategies can help in preventing skin breakdown.

MDA is the #1 health nonprofit advancing research, care and advocacy for people living with muscular dystrophy, ALS, and related neuromuscular diseases.

Nov 7, 2024 - Cardiovascular disease is a leading cause of death for patients with Duchenne muscular dystrophy (DMD), but age at mortality widely differs.

Practical pain relief strategies for people with DMD and their caregivers, covering daily care, medications, and emotional support.

Nov 10, 2025 - You are not alone. Muscular Dystrophy Canada is here to support individuals and families living with neuromuscular disorders.

Nov 10, 2025 - Get involved with the neuromuscular community by donating, partnering, volunteering or participating in event. Every action makes a difference.

Sep 18, 2025 - Occupational therapists can help people with DMD maintain strength, mobility, and independence longer.

Progressive muscle weakness is one of the hallmark signs of muscular dystrophy, but other early MD symptoms are fatigue and cognitive issues.

Accessible transportation tips for people with DMD, from paratransit and rideshares to wheelchair vans and long-distance travel options.

Duchenne muscular dystrophy can make school tricky to navigate, but good communication, accessibility, and assistive technology can help.

Sep 4, 2025 - Muscular Dystrophy Canada together with the Neuromuscular Disease Network for Canada (NMD4C) are excited to announce the recipients of the 2025 Clinical...

Apr 23, 2023 - Learn more about this rare genetic disease that first causes symptoms in early childhood and results in muscle weakness and a shortened life span.

Self-care for DMD caregivers involves coping with stress by creating a routine and connecting with professionals and support groups.

Jan 9, 2025 - Donate Bitcoin to nonprofits like Kindness Over Muscular Dystrophy (KOMD) who accept cryptocurrency, crypto donations are tax deductible.

Mar 17, 2025 - Conquering Duchenne Muscular Dystrophy

Clinicians may use a number of tests, including blood work, electromyography, and MRI, to make an accurate muscular dystrophy diagnosis.

Adaptive clothing for Duchenne muscular dystrophy offers comfort, ease, and independence for those with muscle weakness and limited mobility.

The care plan for people with Duchenne muscular dystrophy should be adjusted as symptoms change and the disease progresses.

Nov 18, 2025 - Learn expert-backed strategies for family caregivers to prevent injuries, protect their well-being, and care for their loved one safely.

Nov 26, 2025 - This document presents a selection of FSHD research news stories from the past year (ongoing studies and clinical trials, scientific and medical...

Sep 22, 2025 - Duchenne muscular dystrophy is inherited through the X chromosome. Males typically develop DMD, while females become carriers.

Assistive technology for Duchenne muscular dystrophy includes adaptive aids and modifications that help with independent living.

Sep 17, 2025 - Treatments such as corticosteroids, physical therapy, and surgery can help manage DMD symptoms and improve quality of life.

Learning how to talk to doctors about Duchenne muscular dystrophy can help support you in your role as a caregiver for someone with DMD.

MDA is the #1 health nonprofit advancing research, care and advocacy for people living with muscular dystrophy, ALS, and related neuromuscular diseases.

Myths about Duchenne muscular dystrophy (DMD) can be countered with facts about the progressive muscle-weakening condition.

The diagnosis of Duchenne muscular dystrophy, a genetic condition, impacts both the person affected and their family.

When three of Betty's children were diagnosed with DMD, her family faced many challenges, but the diagnosis also brought them closer together.

Home adaptations for Duchenne muscular dystrophy can support safety and independence with adjustable furniture and smart technology.

Many Duchenne muscular dystrophy support groups and resources are available, from education to financial assistance.

Treating Duchenne symptoms involves different approaches. From physical therapy to home adaptations, here’s how four people manage their DMD.

Aug 1, 2025 - You’re not alone. Explore Muscular Dystrophy Canada’s support and services for people affected by neuromuscular disorders in Canada.

Sep 17, 2025 - The life expectancy for people with Duchenne muscular dystrophy has increased over time as a result of advances in treatment.

May 19, 2025 - Genethon unveiled the 2-year follow-up data from its GNT0004 gene therapy clinical trial for Duchenne muscular dystrophy, at the American Society of Gene and...

Nov 18, 2025 - People living with neuromuscular diseases shared their meaningful moments in the Quest Media photo contest. Here are this year’s winner and three runners-up.

In this video series, caregivers and Duchenne patients offer practical advice for managing treatment compliance challenges at all ages.

MDA is the #1 health nonprofit advancing research, care and advocacy for people living with muscular dystrophy, ALS, and related neuromuscular diseases.

MDA is the #1 health nonprofit advancing research, care and advocacy for people living with muscular dystrophy, ALS, and related neuromuscular diseases.

Oct 10, 2025 - Sarepta says it has what could be the first gene therapy for limb girdle muscular dystrophy. But getting through the FDA may be tough.

Discover what’s new in muscular dystrophy care, from early genetic diagnosis and newborn screening to emerging gene therapies, steroid options and...

Muscular Dystrophy Association (MDA) has been at the center of progress for people living with muscular dystrophy, ALS, and over 300 other neuromuscular...

MDA is the #1 health nonprofit advancing research, care and advocacy for people living with muscular dystrophy, ALS, and related neuromuscular diseases.

MDA is the #1 health nonprofit advancing research, care and advocacy for people living with muscular dystrophy, ALS, and related neuromuscular diseases.

Raising a child with DMD can be difficult, but there are many steps a parent or caregiver can take to help them enjoy a happy and full life.

A number of strategies can help to ensure adequate joint care to best manage joint pain and stiffness in Duchenne muscular dystrophy (DMD).