Hello and thank you for taking the time to read this and giving me your opinion. About 1 month ago my left shoulder began to be in pain. Nothing major and I took little notice to it. About 2 weeks later I began having significant shoulder weakness and numbness in the deltoid region. This...
Greetings:
It is hard to say where I should start; I guess from the begenning. I have been having strange little 'issues' for several years. It seems like they have been coming and going. I generally do not have time for a doctor visit so I have been letting them go, thinking "That's what...
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Hello again.
6 7 months ago, i wrote this forum about my concern due to somehow dirty emg and fasiculations. Topic was close now. Here is link for topic: https://www.alsforums.com/forum/do-i-have-als-als/28290-got-my-emg-result-please-help-me-understand-3.html
First emg was dirty, second one is...
My first dirty EMG was back in October. I was sent to Mayo. They did another, complete with lots of needles, in December. Possible MND. The symptoms I had then were atrophy in my left arm, hand, brisk reflexes (both sides) and cramping in feet. They did a third in March and noted that there...
On 9/9 after an EMG where he found "Mild Denervation" our first Neuro diagnosed my husband with ALS (No clinical Weakness, no Hyper-reflexivity). We were sent to an ALS "Expert" Neurologist (A Dr. Barkhaus at Froedtert Hospital in Milwaukee, WI). He did an exam and found no clinical weakness...
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Let’s begin by saying I could have easily put this under the “PLS/ALS Association” thread but after much thought decided to start a new thread. As a matter of fact looking back in the pages of the PLS forum there are many threads that debate the PLS/ALS relationship question. So this is just...
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Breathe.
Ok in 2010 I reported to my doctor that my left foot twitched a lot but would stop once I'd start moving. I reported sporadic twitching throughout my body as well but not nearly as much as in the foot. I was worried about als then but for some reason I relaxed and the fear went...
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We will try to answer reasonable questions. We are not here to argue with you. If you announce that you ”know” you have ALS when the doctors say otherwise, or you have not bothered to see a doctor, your thread will be closed.
It is not our place to try to convince you you are wrong. Neither...
Last time I was here 2 years ago, I had a dirty EMG and weakness, diagnosed with ALS by the first neurologist...I went for my second EMG at a University and here's what they found...
Not sure.
Possible myotonia congenita...neuromyotonia...paramytonia.
I will be anxiously awaiting my genetic...
Hi Everyone,
I would like to introduce myself. My husband has been diagnosed with MND. I have been lurking on this site since January of this year because ever since the first dirty EMG back in August of 2012, I have been wondering if this would turn out to be ALS. Because he is so slowly...
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