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    On my way to being diagnosed...

    Thanks for the reply. I did forget to mention that the only EMG I had was of my right arm/hand, which was where they found the ulnar fibs/denervation and no conduction blocks. They didn't test anywhere else but I suspect they would find things elsewhere. I would obviously expect the ALS clinic...
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    On my way to being diagnosed...

    Here is my most recent thread from March, which is closed for replies. I had made another one probably 8 years earlier or so, shortly after things first started happening. I was told by several doctors and people on here I did not have ALS...
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    Years later...symptoms still slowly progressing

    Thanks for the reply. I guess I didn't have a specific question...was moreso seeing if anyone had any particular thoughts based on what my symptoms are and the slow progression of them (very first symptom began in 2010). I know I need to go see a neuro again but while I set up that figured I...
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    Years later...symptoms still slowly progressing

    Hi. I posted here for the first time about 10 years ago. While the very slow progression of my symptoms has me hopeful that it may not be MND, I really am at a loss and this is beginning to engulf me again, especially now that I have a son. One call out, I have not had a recent EMG...I had a...
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    hand.jpg

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    Still worried about ALS

    Yes I last posted on that ID probably two years ago and had no idea what username or password I had used...sorry for the multiple IDs. Thanks for the response.
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    Still worried about ALS

    I am a 27 yr old male. My first symptom began just over 4 years ago, when I began to be unable to take a full breath. I now get out of breath easily and cannot take a deep breath even from a sitting position or when I yawn, and when I do things like blowing out candles or singing or anything...
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