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#1
Jul 03, 2009, 03:49 PM
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I have been going through so many tests for the 3 years, finally they are concluding muscular dystrophy, but they can't tell me which form because I'm currently waiting for my appointment for a muscle biopsy.
Has anyone else had a muscle biopsy??? What does it feel like??? What are the after effects??? Does anyone have muscular dystrophy??? I'm so tired of all the testing that I'm just so glad that I will finally have an official diagnosis, but am stressed over what form it is and what it's going to do to me Help anyone???
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"Life is like photography, you use the negatives to develop"
"When the world says 'Give up,' Hope whispers 'Try it one more time'" ~ Unknown "To dwell in the here and the now does not mean you never think about the past or responsibility, plan for the future. The idea is simply not to allow yourself to get lost in regrets about past or worries about the past or worries about the future. If you are firmly in the present moment, the past can be an object of inquiry, the object of your mindfulness by looking into the past, but you are still grounded in the present moment"  Thich Nhat Hanh |
 Puffyprue
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#2
Jul 04, 2009, 11:17 AM
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 (((((((((((((hugs)))))))))))))))I don't have muscular dystrophy, I have Spina Bifida, but I DO know a fair number of people with MD. http://www.nlm.nih.gov/medlineplus/e...cle/003924.htm That tells you what will happen, I'm glad you won't have to be in pain for it! This is some good info about MD too: http://en.wikipedia.org/wiki/Muscular_dystrophy
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 dance59326
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#3
Jul 05, 2009, 04:42 PM
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Hey there
 I don't have MD but know friends that do. I am sorry for your inner pain... ((((((((((((((((Hugs))))))))))))))))  ThaCrew
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| dance59326
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