Contents
What is the effect of muscular dystrophy on a person?
Muscular dystrophy is a group of diseases that cause progressive weakness and loss of muscle mass. In muscular dystrophy, abnormal genes (mutations) interfere with the production of proteins needed to form healthy muscle.
What is life like for a person with muscular dystrophy?
Until recently, children with Duchenne muscular dystrophy (DMD) did not often live beyond their teens. However, improvements in cardiac and respiratory care mean that life expectancy is increasing, with many DMD patients reaching their 30s, and some living into their 40s and 50s.
How does muscular dystrophy affect you emotionally?
Patients said their lives were at least moderately affected by such problems, as well as by difficulty with stairs, inability to run, difficulty thinking, pain, decreased satisfaction in social situations, decreased performance in social situations, and inability to do specific activities.
What organs are affected by muscular dystrophy?
Many individuals eventually lose the ability to walk. Some types of MD also affect the heart, gastrointestinal system, endocrine glands, spine, eyes, brain, and other organs. Respiratory and cardiac diseases may occur, and some people may develop a swallowing disorder.
What is the best treatment for muscular dystrophy?
What are the treatments for muscular dystrophy (MD)?
- Physical Therapy. Beginning physical therapy early can help keep muscles flexible and strong.
- Respiratory Therapy.
- Speech Therapy.
- Occupational Therapy.
- Surgery.
- Drug Therapy.
- Gene-Based Therapy.
What are the final stages of muscular dystrophy?
In the last phase of Duchenne, there is usually increased difficulty in breathing. Life-threatening heart and lung conditions are more likely. Regular heart and lung monitoring is required, medications are often necessary, and breathing support may be needed.
Does everyone with muscular dystrophy end up in a wheelchair?
The prognosis for muscular dystrophy depends on the type and the severity of symptoms. However, most individuals with muscular dystrophy do lose the ability to walk and eventually require a wheelchair.
How long does a person with muscular dystrophy live?
In its most common form, Limb-girdle muscular dystrophy causes progressive weakness that begins in the hips and moves to the shoulders, arms, and legs. Within 20 years, walking becomes difficult or impossible. Sufferers typically live to middle age to late adulthood.
How long can a person live with muscular dystrophy?
How long does someone with muscular dystrophy live?
People with Duchenne muscular dystrophy typically require a wheelchair before their teenage years. The life expectancy for those with this disease is late teens or 20s.
How does muscular dystrophy affect your daily life?
Over time, muscle weakness decreases mobility, making everyday tasks difficult. There are many kinds of muscular dystrophy, each affecting specific muscle groups, with signs and symptoms appearing at different ages, and varying in severity.
How is muscle spasm a symptom of muscular dystrophy?
Cardiac Complications: This is the most serious symptoms of muscular dystrophy as the disease also involves the cardiac muscles. 2 Muscle Spasm: The patient of muscular dystrophy also experiences muscle spasm. Difficulty Walking: Due to weakness and denegation of muscles, the patient is either unable to walk or have difficulty in walking. 2
How does Duchenne muscular dystrophy affect the body?
It is accompanied by symptoms such as stiffening of muscles and prolonged spasms. The symptoms get worse when it is cold. • Duchenne muscular dystrophy: This affects only males. It is most likely to appear between the age of 2 and 6. The muscles tend to decrease in size and grow weak with time.
How does muscular dystrophy affect the eye and throat?
• Oculopharyngeal muscular dystrophy: This affects the eye and the throat. This mostly appears in men and women post 40 years of age. It causes weakness in the eye and facial muscles. What Are The First Signs Of Muscular Dystrophy?