Hello ALS community, my name is Bill. First I would like to say how saddening it is to read people's stories and how brave they are fighting the various symptoms of ALS or other MND's. Good luck and God bless to all of you.
My symptoms actually started about 8 months ago wo even knowing it, I...
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I went for my clinic visit a couple weeks ago and the neurologist suggested hospice. I've lost 18 lbs in 3 months. I knew I lost some weight but not that much. My FVC was 39, down from 41 three months ago. Both my husband question the accuracy of this reading as we've both noticed a...
Hello all,
My name is Ashley I'm a 27 y/o nurse.
I posted my concerns in 10/2016. I had had a normal emg as per my neuro with some polyphasic potentials on my right side. I had a new emg done in 7/2017 which my neuro stated was still normal and those same polyphasic potentials on my right side...
Dear all,
Thanks to a wonderfully useful website to those who are affected by this horrendous disease. I do wonder if anyone who has been diagnosed with ALS has had the following course of events which I'm currently going through.
My current situation is as follows:
I am a 29 year old male who...
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Hi,
I was diagnosed with BFS 2 years ago now. I have continued to have twitching all over my body.. mostly in my calves. I was told by doctors that it was probably caused by anxiety. I tend to be a worrier about it and lately have had some feeling of small twitches in my tongue. I also feel...
Hi all, I have been reading this forum for a few months now to try to soothe my fears, but I have never posted. Lately my concerns have grown greatly so even though the very last thing I want to do is waste your time when you have concerns far greater than my anxiety, I felt compelled to bring...
Hello everyone,
I posted in this forum earlier this year in February about my symptoms, which I thought resembled the early stages of ALS. Specifically, I felt a sensation of weakness in my left hand that seemed like it was spreading to my right hand (I'm right-handed). My voice wasn't working...
Im sure you guys see this all of the time but I really wanted to hear from people who actually have als. In june my tongue started twitching.. not once or twice, but 24/7 literally it never ever stops. I cant feel it twitching & i only found it because my tongue went numb. Ive seen three neuros...
Hi everyone,
I have received an unofficial diagnosis and am losing my speech quickly, along with lots of respiratory weakness and breathing issues. My voice appears to be going first (especially tongue weakness) and I was wondering how long it took those who have lost the ability to swallow to...
Dear all, please excuse me if I’m bothering you, I need an advice! So in january, it will be 3 and a half years since i started twitching.I twitch all over, even the places I don’t have atrophy. Since than I teitch 24/7. From the very beggining i noticed that some minor atrophy is developing and...