Taylor: The holidays

Monday, December 7, 2009

The holidays

Thanksgiving Day at my Aunt Linda's

Trick or treating with his sister, best friend and his little cousin Kieden.

Sorry that it's been so long since I've posted, things have been crazy around here. Every day is getting better though. Tay went back to school a week a go today, he only goes half a day and will resume full days after Christmas break. He now sits in his chair all day. He doesn't complain of back pain hardly at all, just a little thigh and calf pain. I can't believe it's been 2 months since his surgery. I'm just glad were over the rough part, there were times I thought we would never get through it. Here are some pics from Halloween and Thanksgiving and one that was taken today.

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Taylor has Duchenne muscular dystrophy (DMD) it's a severe recessive X-linked form of muscular dystrophy characterized by rapid progression of muscle degeneration, eventually leading to loss of ambulation and death. This affliction affects one in 3500 males, making it the most prevalent of muscular dystrophies. In general, only males are afflicted, though females can be carriers. The disorder is caused by a mutation in the gene DMD, located in humans on the X chromosome (Xp21). The DMD gene codes for the protein dystrophin, an important structural component within muscle tissue. Dystrophin provides structural stability to the dystroglycan complex (DGC), located on the cell membrane. Symptoms usually appear in male children before age 6 and may be visible in early infancy. Progressive proximal muscle weakness of the legs and pelvis associated with a loss of muscle mass is observed first. Eventually this weakness spreads to the arms, neck, and other areas. Early signs may include pseudohypertrophy (enlargement of calf muscles), low endurance, and difficulties in standing unaided or inability to ascend staircases. As the condition progresses, muscle tissue experiences wasting and is eventually replaced by fat and fibrotic tissue (fibrosis). By age 10, braces may be required to aid in walking but most patients are wheelchair dependent by age 12. Later symptoms may include abnormal bone development that lead to skeletal deformities, including curvature of the spine. Due to progressive deterioration of muscle, loss of movement occurs eventually leading to paralysis. Intellectual impairment may or may not be present but if present, does not progressively worsen as the child ages. The average life expectancy for patients afflicted with DMD varies from early teens to age mid 30s. There have been reports of DMD patients surviving past the age of 40 and even 50.

Taylor

Monday, December 7, 2009

The holidays

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