Tonight I watched an episode of Extreme Makeover Home Edition that aired on Sunday night. It was about a woman that helped children in need. She had the disease Myasthenia Gravis that my sister has. It was an interesting story yet sad to see how tough it was for this woman to get around in her wheel chair with the house that she had.
Myasthenia gravis is a chronic autoimmune neuromuscular disease characterized by varying degrees of weakness of the skeletal (voluntary) muscles of the body. The name myasthenia gravis, which is Latin and Greek in origin, literally means "grave muscle weakness." The hallmark of myasthenia gravis is muscle weakness that increases during periods of activity and improves after periods of rest. Certain muscles such as those that control eye and eyelid movement, facial expression, chewing, talking, and swallowing are often, but not always, involved in the disorder. The muscles that control breathing and neck and limb movements may also be affected.
The thymus gland, which lies in the upper chest area beneath the breastbone, plays an important role in the development of the immune system in early life. Its cells form a part of the body's normal immune system. The gland is somewhat large in infants, grows gradually until puberty, and then gets smaller and is replaced by fat with age. In adults with myasthenia gravis, the thymus gland is abnormal. My sister had her thymus removed as well as part of a lung with no success.
In most cases, the first noticeable symptom is weakness of the eye muscles. In others, difficulty in swallowing and slurred speech may be the first signs. The degree of muscle weakness involved in myasthenia gravis varies greatly among patients, ranging from a localized form, limited to eye muscles (ocular myasthenia), to a severe or generalized form in which many muscles - sometimes including those that control breathing - are affected. Symptoms, which vary in type and severity, may include a drooping of one or both eyelids (ptosis), blurred or double vision (diplopia) due to weakness of the muscles that control eye movements, unstable or waddling gait, weakness in arms, hands, fingers, legs, and neck, a change in facial expression, difficulty in swallowing and shortness of breath, and impaired speech (dysarthria).
I hate that my sister has to live everyday with this horrible disease.
2 comments:
Yes, but I love the way she lives with it - every day with courage and joy.
Mom
April, thanks for putting this on your blog. Really good info. I am grateful that I do not have it as bad as some. At least not yet, who know what the next 2-3 years will do to me.
Mom, thanks for the comment, it was really nice to hear!
Manda
Post a Comment