myslonmmgusjourney wordpress.com

myslonmmgusjourney

My SLONM MGUS journey! June 26, 2015. June 27, 2015. The muscle biopsy finally happened in late April, 2014. The pathologists examining the biopsy tissue sample discovered that I had Nemaline Myopathy NM, a form of Muscular Dystrophy, as rod-shaped protein deposits were found in the muscle tissues, rendering the muscles weak and performing way below standard. I seemed to be getting worse by the week! My neurologist contacted an oncologist at Princess Margaret Hospital in Toronto, the preeminent cancer .

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nemalinetreatment

21 My Half Year Report. 20 Five Months or So. 18 Three Months after the Transplant.

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My SLONM MGUS journey! June 26, 2015. June 27, 2015. The muscle biopsy finally happened in late April, 2014. The pathologists examining the biopsy tissue sample discovered that I had Nemaline Myopathy NM, a form of Muscular Dystrophy, as rod-shaped protein deposits were found in the muscle tissues, rendering the muscles weak and performing way below standard. I seemed to be getting worse by the week! My neurologist contacted an oncologist at Princess Margaret Hospital in Toronto, the preeminent cancer .

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The site had the following in the homepage, "My SLONM MGUS journey! June 26, 2015." I noticed that the web site stated " The muscle biopsy finally happened in late April, 2014." They also stated " The pathologists examining the biopsy tissue sample discovered that I had Nemaline Myopathy NM, a form of Muscular Dystrophy, as rod-shaped protein deposits were found in the muscle tissues, rendering the muscles weak and performing way below standard. I seemed to be getting worse by the week! My neurologist contacted an oncologist at Princess Margaret Hospital in Toronto, the preeminent cancer ."

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