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Matt,My thoughts and prayers go out to you and your family - Do you have a suggestion, or preference for a Duchenne charity that I could donate to?
Matt,Is there anything that we can do to help you guys at this point on top of praying? Let us know now or in the future as needs arise.Ken
So there is still plenty of reason to pray and pray hard. The doctors are pretty confident that it is DMD but we wont know for sure until we get back the full genetic spread in three weeks.
On a positive note, there is a chance that he has the less progressive Beckers Muscular Dystrophy. It basically boils down to how damaged his X chromosome is. If he can produce no Dystrophin (a protein that helps shield muscle fibers) then he has Duchenne's, if his x chromosome is slighly less damaged, then he can produce a small amount of Dystrophin that would delay the onset of MD by several years ( for reference DMD, or Duchenne's Muscular Dystrophy) patients often lose the ability to walk by age 12 and have a life expectancy of late teens or early 20's while Beckers' MD patients can often walk into their 30s and have a lifespan that can last from 40- a near normal life span.So there is still plenty of reason to pray and pray hard. The doctors are pretty confident that it is DMD but we wont know for sure until we get back the full genetic spread in three weeks.