Muscular dystrophy Medical equipment

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  1. Detect MD provides sponsored genetic testing for patients suspected of having MD. Forms of muscular dystrophy have overlapping clinical features making diagnosis difficul
  2. Serving The Community Since 2002. Authorized Distributor for leading brands. America's Medical & Sanitary Superstore
  3. Equipment Assistance. As neuromuscular diseases progress, MDA Care Center team members are prepared to recommend and prescribe various types of medical equipment that can increase independence and quality of life. When such equipment is needed, MDA offers assistance in locating prescribed items through referrals to community resources

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  1. Depending on the type of muscular dystrophy, your doctor may recommend orthotic devices to help with mobility. An orthotic device is a brace made to support weakened muscles. Braces can help keep the muscles flexible, which aids in slowing the progression of contractures, which occur when a muscle and its tendon shorten and reduce flexibility
  2. This Durable Medical Equipment (DME) Guide has been developed to provide families and caregivers with a comprehensive resource of equipment beneficial for individuals living with Duchenne. As the progression of this disease begins to rob individuals of muscle strength and ambulation, mobility equipment can offer realistic means with which to.
  3. Muscular Dystrophy Complete Home Medical Equipment Decatur, GA (404) 292-652
  4. Muscular Dystrophy Association National Office. 161 N. Clark, Suite 3550. Chicago, Illinois 60601. 800-572-1717 | ResourceCenter@mdausa.or
  5. Muscular Dystrophy Combined Home Medical Equipment Lawton, OK (888) 882-1999 (580) 250-1999 2504 SW Lee Blvd , Lawton , OK 7350
  6. utes ago by Danielle Dani Liptak. I received a bill from Numotion for my Corpus M3 powerchair, and it was $1200. To say I was shocked was an understatement. A month or so ago, I was told that I could use new casters and, with the age of my.
  7. Mobility Devices Muscular dystrophy is a group of genetic conditions characterized by progressive muscle wasting and loss of muscle function. Different muscle types may be affected by different types of muscular dystrophy. How muscular dystrophy affects mobilit

Muscular Dystrophy News is strictly a news and information website about the disease. It does not provide medical advice, diagnosis or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment The freedom to walk, to talk, to run and play. To laugh, to hug, to eat — even breathe. Each day these freedoms are taken away from kids and adults with muscular dystrophy, ALS and related diseases that weaken muscle strength and limit mobility

Duchenne muscular dystrophy is a multisystem disorder affecting all body systems. Treatment often includes a variety of medical supports and equipment. Duchenne affects your muscles—including those important for breathing. Lung muscles will get weaker as you grow older Medical Management. Thanks to advances in many areas of medicine, such as cardiology and pulmonology, people with Duchenne muscular dystrophy (DMD) in the 21st century are living longer than in previous decades, often well into adulthood What you need to know about traveling with medical equipment. Bye Bye, Betty: Things I Learned on my First Trip With Medical Equipment - Muscular Dystrophy Association When I was 25, I took an unlikely job as an editor at a travel magazine Adaptive Techniques and Devices for Duchenne Muscular Dystrophy While nearly everyone with Duchenne will eventually need to use a wheelchair, other devices and therapies can help with mobility both.. Assisting families affected by Duchenne muscular dystrophy in purchasing vital medical and accessibility equipment. Learn More. Camp Promise. A free, week-long camp for kids, teens, and adults with neuromuscular disorders. Learn more. JeTT foundation News. Blog. Jul 1, 2021

Respiratory management of the patient with Duchenne muscular dystrophy. Pediatrics , 142 (Suppl 2), S62-S71. Retrieved March 30, 2020, from https://pubmed.ncbi.nlm.nih.gov/30275250 Muscular Dystrophy Canada has relied upon a medical professional's recommendation in agreeing to consider a financial . contribution to enable you to acquire the equipment described herein. By signing this Application you acknowledge and agree that Muscular Dystrophy Canada has no liability whatsoever wit These tests are used to check heart function, especially in people diagnosed with myotonic muscular dystrophy. Lung-monitoring tests. These tests are used to check lung function. Electromyography. An electrode needle is inserted into the muscle to be tested. Electrical activity is measured as you relax and as you gently tighten the muscle Osteopathic medical specialists can help patients with muscular dystrophy manage the function and structure of their body through manipulations which can help the muscles heal themselves, or at least, get better. An osteopath can also serve as a counselor for people with muscular dystrophy, particularly children

Jett Foundation, a 501 (c)3 nonprofit, established Jett Giving Fund to assist families affected by Duchenne muscular dystrophy in purchasing unaffordable, but vital medical and accessibility equipment that is often not covered by insurance. This includes accessible vans, van conversions, stair lifts, rotating beds and more

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For Just $19 a Month, You Can Be a Champion for Kids & Adults with Neuromuscular Disease. Your Monthly Gift Can Fuel Life-Changing Treatments and Programs Year-Round. Donate Today Muscular dystrophy (MD) is a group of inherited muscle diseases in which muscle fibers are unusually susceptible to damage. Muscles, primarily voluntary mu MedPlus Medical Equipment Health Issues :: Muscular Dystrophy

Muscular dystrophy (MD) is a group of inherited muscle diseases in which muscle fibers are unusually susceptible to damage. Muscles, primarily voluntary mu Johns Hopkins Respiratory, Home Medical Equipment and Enteral Nu Becker-type muscular dystrophy - Like Duchenne dystrophy, Becker-type muscular dystrophy is linked to the X chromosome, affects dystrophin production, and occurs in males. However, the illness is about 10 times rarer than Duchenne, and it produces milder symptoms In addition to a medical history review and physical examination, your doctor may rely on the following in diagnosing muscular dystrophy: Blood tests. Damaged muscles release enzymes, such as creatine kinase (CK), into your blood. High blood levels of CK suggest a muscle disease, such as muscular dystrophy. Electromyography Muscular dystrophy (MD) is a group of inherited muscle diseases in which muscle fibers are unusually susceptible to damage. Muscles, primarily voluntary mu Baird Respiratory & Medical Equipment Health Issues :: Muscular

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Muscular Dystrophy Association of Idaho Muscular Dystrophy Association of Idaho, Muscular Dystrophy Association... Suggest an Edit MDA has a durable medical equipment loan closet, where we repair and lend out equipment. MDA also runs a week long summer camp for children age 6-17 who have a neuromuscular disease Update. 2019 The #LIUG4MD Campaign has Grown Exponentially. Once again we have acquired Proclamation's (49 states and approx 11 cities) declaring August Muscular Dystrophy Awareness/Light it Up Green for MD Month. Illuminating Landmarks Across the US and Canada with Individuals cities in Australia, London and Ireland (see list below) Many children are able to live full lives with muscular dystrophy but may need specialist equipment, support at home and school and frequent medical appointments. There is a lot of support and advice available from Muscular Dystrophy UK, including helpful factsheets especially designed for families Muscular Dystrophy Association Purpose MDA's comprehensive services program includes diagnostic and follow-up medical consultations, flu shots, support groups, MDA summer camps for youngsters, a national medical equipment program, assistance with equipment repairs and modifications, and resource referrals Finding Medical Care for Duchenne Muscular Dystrophy MDA Care Centers MDA helps oversee more than 150 MDA Care Centers throughout the United States, located at top healthcare institutions

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The Muscular Dystrophy Association provides lightly used medical equipment such as wheelchairs and lifts to qualifying patients with neuromuscular disease. The equipment is provided by local chapters, and the MDA website offers a local chapter locator [ 8 ] As reviewed in this article, rehabilitation teams should include physicians, physical and occupational therapists, speech language pathologists, orthotists and providers of durable medical equipment. This team works to collaborate with the other subspecialty members of the Duchenne care team (i.e., neuromuscular specialist, cardiologist. Limb-girdle muscular dystrophies are a large group of genetic diseases in which there is muscle weakness and wasting (muscular dystrophy). In most cases, both parents must pass on the non-working (defective) gene for a child to have the disease (autosomal recessive inheritance) Structural modifications and equipment for better accessibility: Because of trouble with movement, patients with muscular dystrophy, as mentioned earlier, utilize equipment such as strollers, walkers, crutches, wheelchairs, and braces to allow for better mobility. Some places around the world have also passed ordinances, deeming it a. Muscular dystrophy is a hereditary condition that causes loss of muscle mass and progressive weakness. The mutation or the abnormal genes prevents the production of proteins in our body. Some of the symptoms may begin as early as childhood mostly in boys, some may lose the ability to walk eventually. Some people who have muscular dystrophy will.

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A national equipment program that provides wheelchairs and other medical equipment to individuals with muscular dystrophy. Resources regarding government benefits for people with disabilities, state resources, publicly funded medical benefits, transportation and travel, and webinars.  Assistance in educational advocacy Muscular dystrophy (MD) is a group of inherited muscle diseases in which muscle fibers are unusually susceptible to damage. Muscles, primarily voluntary muscles, become progressively weaker. In the late stages of muscular dystrophy, fat and connective tissue often replace muscle fibers

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  1. Steadily improving management of Duchenne muscular dystrophy (DMD) continues to lead to improved physical and functional status, allowing increasingly successful transitions to independence and self-actualization in adulthood. Rehabilitation principles remain key to overall management for individuals with DMD with increasing options for ever more successful management, reflecting a changing.
  2. Becker muscular dystrophy is very similar to Duchenne muscular dystrophy, but it progresses much more slowly and is less common. It affects boys and usually is diagnosed between the ages of 11 and 25. Boys and men with Becker muscular dystrophy develop progressive weakness in the muscles of the hips, thighs, pelvis, and shoulders
  3. Muscular dystrophy (MD) is a broad term that describes a genetic (inherited) disorder of the muscles. Muscular dystrophy causes the muscles in the body to become very weak. The muscles break down and are replaced with fatty deposits over time. Other health problems commonly associated with muscular dystrophy include the following: Heart problems

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  1. Duchenne muscular dystrophy is the most common and most severe form of childhood muscular dystrophy. Depending on the type of muscular dystrophy, the damaged muscles may mean a child will lose the ability to perform certain functions, such as walking, sitting upright, breathing easily, using the hands or moving the arms and legs
  2. Duchenne muscular dystrophy is a form of muscular dystrophy.It worsens quickly. Other muscular dystrophies (including Becker muscular dystrophy) get worse much more slowly.. Duchenne muscular dystrophy is caused by a defective gene for dystrophin (a protein in the muscles). However, it often occurs in people without a known family history of the condition
  3. Myotonic muscular dystrophy (MMD) is a multisystem disorder that affects the brain, skeletal and smooth muscles, eyes, heart, gastrointestinal tract, lungs, and endocrine system. The 2 forms, type 1 and type 2, are caused by different gene mutations. Type 2 does not have a congenital or early childhood form and is not discussed further here
  4. ars to assisting families with durable medical equipment and giving kids with muscular dystrophy the best week of the year at MDA Summer Camp, MDA empowers families in hometowns across America with the help and support they need today
  5. In her role, Ms. Santillo is present at clinic each week to help connect individuals and families to the resources provided by the MDA including the loan and repair of durable medical equipment, support services, socialization opportunities and MDA Summer Camp, a free week-long residential camp for children ages 6-17 with muscular dystrophy

Shaan's story took place in 2016, but already different parts of the world are adopting adaptive equipment, including the joystick system, and other tools to help muscular dystrophy patients gain the right to drive. Connor Colhoun: England. In the UK, another 19-year-old with muscular dystrophy was recently granted the opportunity to drive 14 Diagnosis-Based Assistance Programs for Muscular Dystrophy. Provides service dogs to people with a disability or medical condition covered by the program. Provides access to integrative therapy, primary care, and other complementary services to improve health outcomes and reduce healthcare costs for persons with physical disabilities with. Muscular Dystrophy (DMD) Duchenne muscular dystrophy (DMD, or just Duchenne) is a rare genetic disease and one of more than 30 forms of muscular dystrophy. It primarily affects males, but, in rare cases, can also affect females. Duchenne causes the muscles in the body to become weak and damaged over time Medical Equipment Manufacturer. Orthopedic Service Company. Medical Supply Store. Home and Bath Solutions. Medical Company. Parrish Home Medical. Learn how genetics plays a role and if there are any risk factors that may cause muscular dystrophy. English (US) Español; Français (France Duchenne Muscular Dystrophy (DMD) Patient Assistance Programs. What is NORD? The National Organization for Rare Disorders (NORD), a 501(c)(3) organization, is an independent charity dedicated to the identification, treatment radiological exam or for durable medical equipment

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Becker Muscular Dystrophy (BMD) Becker Muscular Dystrophy (BMD) is a condition that causes progressive weakness of the skeletal muscles (the muscles that control movement). It also commonly affects heart muscle. BMD is genetic condition, meaning it is usually inherited through genes from parents Feb 12, 2016 - Explore Ginger Wilcox's board Muscular Dystrophy on Pinterest. See more ideas about muscular dystrophies, muscular, duchenne muscular dystrophy Duchenne muscular dystrophy (DMD) is the most common muscular dystrophy; despite improved screening diagnostic techniques and novel US Food and Drug Administration (FDA)-approved treatment options, DMD is not screened for at birth beyond investigational studies. Recently, 4 molecular therapies for DMD have been approved by the FDA The medical summary for young adults with DMD can be used by a provider or individuals with DMD to communicate details of their health plan, provider contacts, and medical equipment needs. It can be used in transition handoffs, when adding new providers, or when informing new nursing agencies or personal care attendants

Muscular dystrophy is a group of genetic diseases that permanently weaken and shrink your muscles. The disease is rare. However, it gets worse over time. Eventually, the muscle weakness will affect your ability to walk, swallow, and breathe. There are several types of muscular dystrophy Caring for someone with Muscular Dystrophy . Though there's no cure for MD yet, doctors are working to improve muscle and joint function, and slow muscle deterioration in people who are living with the condition. If someone is diagnosed with Muscular Dystrophy, a team of medical specialists can work with the individual and their family

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The Muscular Dystrophy Association (MDA) is an American 501(c)3 umbrella organization that works to support people with neuromuscular diseases. The association was founded in 1950 by Paul Cohen, who lived with muscular dystrophy. It works to combat neuromuscular disorders by funding research, providing medical and community services and educating health professionals and the general public Muscle Dreams provides memorable experiences for children and young people with muscular dystrophy. Dreams can include trips abroad, the chance to meet a celebrity as well as medical equipment, home adaptations or wheelchairs. Promise Dreams will consider applications from children who have already received a wish from another organisation Choosing the correct equipment to help in the care of a family member with Duchenne muscular dystrophy can be frustrating with many choices available. From the right manual wheelchair that can be later used for travel to a durable powerchair designed for the active person to looking for lifts, breathing support and personal care products the.

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The Muscular Dystrophy Clinic is sponsored by the Muscular Dystrophy Association and provides a multidisciplinary clinic serving the needs of adults and children with over 40 types of neuromuscular disorders. These disorders include all forms of muscular dystrophy, spinal muscle atrophy, and hereditary neuropathies like Charcot Marie Tooth disease Myotonic muscular dystrophy is a common multi-system disorder that affects the skeletal muscles (the muscles that move the limbs and trunk) as well as smooth muscles (the muscles that control the digestive system) and cardiac muscles of the heart. Symptoms of myotonic dystrophy might include difficulty releasing one's grip (myotonia. Muscular dystrophy refers to a group of disorders characterised by progressive muscle weakness and loss of muscle tissue. In specific forms, other muscles—including respiratory muscles, cardiac smooth muscles, facial muscles and swallowing muscles—can also be affected. Duchenne muscular dystrophy (DMD) is the most common childhood onset.

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The care of individuals with Duchenne muscular dystrophy (DMD) now extends into adulthood. Childhood to adulthood transition planning is an important aspect of care, affecting health outcomes as well as other important aspects of adult life. In this article, we address transition planning as it relates to DMD health care, education, steps toward vocations, personal care, accessing the home and. Symptoms of myotonic muscular dystrophy include: 14. Difficulty or inability to relax muscles following a sudden contraction. Weakness in the muscles in the face and the front of the neck. Haggard, hatchet face and a thin, swan-like neck. Atrophy and weakness in forearm muscles Lab Equipment; Interviews; a patented experimental protein replacement therapy for merosin-deficient congenital muscular dystrophy (MDC1A), a life-threatening, ultra-rare disease caused by a. Muscular dystrophy (MD) is a group of heredity disorders that causes the loss of muscle tissue, resulting in muscle weakness that worsens over time. There are many types of MD that can affect both children and adults. MD affects adults, but the more severe forms tend to occur in early childhood

People with Duchenne muscular dystrophy or Becker muscular dystrophy may develop a condition that prevents the heart from pumping blood efficiently, called cardiomyopathy. Arrhythmia, fatigue, shortness of breath, and swelling of the legs and feet are symptoms of cardiomyopathy that can worsen rapidly and become life threatening As muscular dystrophy progresses and muscles weaken, fixations (contractures) can develop in joints. Tendons can shorten, restricting the flexibility and mobility of joints. Contractures are uncomfortable and may affect the joints of your hands, feet, elbows, knees and hips Muscular dystrophy patients, especially those diagnosed with Duchenne muscular dystrophy, usually lose their capability to perform simple tasks like walking, sitting up, moving or even breathing. While this condition has no cure, a diet loaded with protein, supplements, and herbs could significantly help avoid weight gain that is more common in. Specialist team for muscular dystrophy. Because muscular dystrophy affects multiple muscle groups - including heart and breathing muscles - your child may need care drawn from several medical fields. Advocate Children's Hospital offers the complete range of required doctors, all with pediatric training and experience Luckily, the muscular dystrophy campaign have a guide to help people plan a holiday safely, as well as enabling people to experience the joy of worldwide travel which can be a complicated task by any means. If you have any worries about taking your ventilator or any other medical equipment, our medical advisors have made sure that this.


Muscular dystrophy refers to a group of rare diseases which progressively weaken muscles. therapies and services that can improve the condition and quality of life of people with muscular dystrophy. With good medical management, people with some types of muscular dystrophy live long and fulfilling lives. Equipment and assistive technology Anthony Kincaid, in xPharm: The Comprehensive Pharmacology Reference, 2007. Other Information - Web Sites. Muscular Dystrophy Association; MDA-This freely accessible, comprehensive web site is sponsored by the MDA, a voluntary health agency, and contains educational and health service information on the muscular dystrophies and other neuromuscular diseases for patients and health care providers Lab Equipment; Interviews researchers have found that extracellular RNA in urine may be a source of biomarkers for the two most common forms of muscular dystrophy, noninvasively providing. The Ohio State University Wexner Medical Center provides a full range of diagnostic testing for muscular dystrophy, much of which is not available at other facilities. Many individuals come to Ohio State for our state-of-the-art, specialized testing, such as genetic testing, muscle biopsy, electromyography, electrodiagnostic testing and. The Muscular Dystrophy Association Elects Renowned Medical Researcher and Scientist Donald S. Wood, PhD as President and CEO Dr. Wood will launch next chapter of scientific discoveries and.

To Parents Whose Child Was Just Diagnosed With Muscular Dystrophy. When our oldest son was 5 years old, we attended a Muscular Dystrophy Association (MDA) fundraising event. There we met a mother whose 17-year-old son has muscular dystrophy. We chatted during dinner, and as we were leaving to go home she said, I know you don't want to be. The hospital is distinguished by a high professionalism of its doctors, state-of-the-art technological equipment and the availability of the most ad. Duchenne Muscular Dystrophy Diagnosis. 3.409,00 €. Go to the program chevron_right. Diagnosis and conservative treatment of duchenne muscular dystrophy. 11.618,00 € My baby has a rare and sever form of muscular dystrophy called L-CMD. It is fatal; there are no treatments and no cure. Still, I'm trying to come up with $2 million in hopes we can find one

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Although muscular dystrophy often robs people of the ability to complete normal tasks, this doesn't mean that they still can't lead a normal life. There are many options for adaptive equipment that can help many be nearly 100% independent, even with long-term symptoms in place The following are samples of Letters of Medical Necessity that Dr. Bach uses for justifying intervention, equipment and training needs. MMD - Myotonic Muscular Dystrophy. 49-Year-Old Woman (PLV-100, Oxymeter, CoughAssist Medical Equipment Supplier. Myositis Support (MyositisSupport.org) Health & Wellness Website. Flexicure. Health & Wellness Website. Todd Harrison. Entrepreneur. FindaTopDoc Muscular Dystrophy Community. Cause. Ionmyhealth. Many people think muscular dystrophy is a specific disorder, but the term actually refers to a collection of related. A local fund intended to financially complement the existing regional services program and allow for some flexibility through the local Chapter.Provides financial assistance for the purchase of medical equipment or to support such needs as medical travel, respite care, adapted recreation programs, and therapies including: Respite services for caregivers Attendan Accessing medical services can be challenging for people with muscular dystrophy during the COVID-19 pandemic, especially since it is recommended to avoid exposure and contact with others. Thanks to technology, people with muscular dystrophy can now maintain some aspects of their care through telehealth visits that are carried out virtually

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Muscular dystrophy (MD) is a group of disorders that affects voluntary muscles, mainly those around the hips and shoulders. MD can affect people at any age. The most common type seen in children is Duchenne muscular dystrophy, which affects an estimated 1 in 3,500 boys worldwide The Muscular Dystrophy Telethon is needed and inspirational. Jerry Lewis performs at the Muscular Dystrophy Association telethon in Beverly Hills, Calif., on Sept. 5, 2005, left, and Kevin Hart. Muscular dystrophy is a genetic disease that is characterised by a progressive muscular degeneration. Incidence. Muscular Dystrophy occurs in approximately 1 in 3500 male births. Medical Considerations. There are two main types of muscular dystrophy: Myotonic This type includes when the muscles cannot relax after contraction. Duchenn Commercially insured health plan members were eligible for the study if they had at least 1 medical claim with a primary or secondary diagnosis for MD (ICD-9-CM diagnosis code 359.0 [congenital hereditary muscular dystrophy] or 359.1 [hereditary progressive muscular dystrophy] between July 1, 2000, and December 31, 2009 (identification period)

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Duchenne muscular dystrophy (DMD) is a genetic disorder characterized by the progressive degeneration of muscles and their weakness. It is a rare muscle disease that largely affects men. An increase in the number of patients with Duchenne muscular dystrophy is expected to propel the global Duchenne muscular dystrophy treatment market during the. Duchenne muscular dystrophy is one of the most serious forms of muscular dystrophy as the symptoms and associated health complications tend to deteriorate rapidly. The signs and symptoms of Duchenne muscular dystrophy can be easily seen from a very early age, between 1 and 4 years of age

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Duchenne Muscular Dystrophy (DMD) is a severe muscle wasting disease that typically affects young men. There is no cure for DMD and the average life expectancy is 26. These are troubling facts that scientists at the University of Pennsylvania are hoping to change with their recent findings in Stem Cell Reports Patient access to care, services and medical equipment - Annie Kennedy, Parent Project Muscular Dystrophy: 3:00:50 8: Access to Genetic Testing and Interdisciplinary Care - Kristin Stephenson, Muscular Dystrophy Association: 3:45:48 Under our Assistive Device & Equipment Subsidy, members with muscular dystrophy were provided with subsidies for the purchase of life-saving medical equipment. This enables them to enjoy a better quality of life and to live with dignity. We also prioritise the need of providing functional motorized wheelchairs for members as this is the first. Having a child with a severe medical condition like Duchenne muscular dystrophy brings a whole new set of challenges, especially during COVID-19. That is why Team Joseph and ten other Duchenne nonprofits are working together to ease the additional challenges Duchenne families are currently facing. The Coronavirus Relief Fund is a part of the.

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HACKENSACK, N.J., June 21, 2021 /PRNewswire/ -- Parent Project Muscular Dystrophy (PPMD), a nonprofit organization leading the fight to end Duchenne muscular dystrophy (Duchenne), will host their.

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