Oliver Bee RMTRegistered Massage Therapist

Massage therapy · Kitchener–WaterlooMuscular Dystrophy

Foot

What It Is

Muscular dystrophy is a group of genetic diseases in which the muscles become progressively weaker and break down over time (National Institute of Neurological Disorders and Stroke, 2026). Many people with muscular dystrophy will need to use mobility equipment, such as a wheelchair, as the muscle weakness gets worse, but how severe it is and how quickly it progresses depends on the type (NHS, 2025).

Multiple types of muscular dystrophy exist. Some types begin in early childhood, while others do not start until later in life (NHS, 2025). The most common type is Duchenne muscular dystrophy, which begins in early childhood, usually only affects boys, and progresses quickly (NHS, 2025). Some people with muscular dystrophy develop problems with swallowing and breathing (National Institute of Neurological Disorders and Stroke, 2026). Muscles and tendons around the joints can shorten, so that the joints become fixed in one position; this is known as a contracture (National Institute of Neurological Disorders and Stroke, 2026). Some types of the disease can also affect the heart, lungs and spine (NHS, 2025). Even though there isn’t a cure, treatment can help manage the symptoms, and some medicines can slow the progression of certain types (NHS, 2025).

Muscular Dystrophy Anatomy

Muscular dystrophy is a genetic muscle disease causing progressive weakness and wasting of the muscles. It is caused by an altered gene, and different genes cause different types of muscular dystrophy (NHS, 2025). The altered gene can be passed on from the parents, or a person can be born with it even if their parents do not have it (NHS, 2025). Some types, such as Duchenne muscular dystrophy, are caused by a change in a gene on the X chromosome, which is why they mainly affect boys; other types are inherited in different ways and can affect both men and women (National Institute of Neurological Disorders and Stroke, 2026).

There are more than 30 forms of muscular dystrophy, which vary in the age they start, how severe they are and which muscles are affected (National Institute of Neurological Disorders and Stroke, 2026). Many people with muscular dystrophy eventually lose the ability to walk. Some types also affect the heart, lungs, gastrointestinal (digestive) system, endocrine (hormone) glands, spine, eyes, brain or other organs (National Institute of Neurological Disorders and Stroke, 2026).

Duchenne muscular dystrophy is the most common childhood form of muscular dystrophy (National Institute of Neurological Disorders and Stroke, 2026), and one of its early signs is Gowers' sign, described below (Chabbi et al., 2026).

MD Symptoms:

Symptoms vary with the type of muscular dystrophy, but can include (NHS, 2025; National Institute of Neurological Disorders and Stroke, 2026; MedlinePlus, 2025):

  • Muscle wasting (atrophy) that is progressive
  • Poor balance
  • Difficulty walking
  • Frequent falls
  • Unusual or waddling gait
  • Spinal scoliosis (curvature of the spine)
  • Joint stiffness and contractures
  • Difficulty breathing
  • Heart problems, such as an irregular heartbeat
  • Using the hands to aid/support walking or stair climbing
  • Difficulty getting up from lying flat on the back
  • In young children, floppiness and taking longer than expected to crawl or walk
  • Gowers' sign

Gowers' Sign

Gowers' sign is difficulty getting up from the floor, and it is often seen in young children with Duchenne muscular dystrophy (Chabbi et al., 2026). In Duchenne muscular dystrophy, muscle weakness begins in the legs and pelvis (MedlinePlus, 2025). Because the muscles around the hips and thighs are weak, the child has difficulty getting up from the floor, so they learn to go onto their hands and feet and to "walk" the hands up the legs, using the arms to push the body upright.

Not a diagnosis — for more information, contact me or another trusted healthcare provider.

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