been a while for diagnosed i thought it was MS never heard of ALS untill a posting on MS site lady said possible MS.. but wait and see, ive had twitching since aug or earlier of 10* and has gotton worst, alsoo had lower back spasms which thught i hurt at wrk blew EVRYTHING OFF.. i mean what...
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In response to a post:
Your newest batch of symptoms sound more like fibromyalgia than anything else. ALS isn't going to cause pain in early stages. LOSS OF USE is what usually sends those with ALS to the doctor. They suddenly can't do something--for me, it was I couldn't push the buttons to...
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Hello Everyone,
I have had a rough 6 months. I still don't know what I have, but I do have something. I have not been to a neurologist yet, but I will be going soon. I was wondering whether these symptoms might be symptoms of ALS. I have read a lot of posts on this forum. What is unclear...
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I really need some help! My GP is useless (I am in the process of getting a second opinion). Sorry if this whole list reads like a novel but I need some objective answers from the real people that know and can point me in the direction I need to go, whether that be a neurologist (dr wont refer...
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Hi All,
I have a question regarding one (of many) of the symptoms I am currently experiencing. I have had a nearly constant tightness/light pain on the right side of my face/top of head for 3 months now. It has been accompanied by a slight loss of balance to that side as well. The...
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Hi everyone. You all have big hearts and I appreciate the time and help. I wrote in a different thread, under "husband," but this is a specific question; when the doctor asks if you feel fatigue at the end of the day, how on earth can you separate exhaustion because you're not sleeping at night...
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Hi all. Some of you may remember me. For 5 months I have been having migratory pains that will hit one area for a few seconds to hours then move to another spot. They feel like deep toothache pains and usually affect my ankles, toes, fingers, hands, spine. A wk after the onset of this I noticed...
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I joined this group in October and have been reading your posts, almost daily, since then. This is my first post. Due to the fact that the medical community seems to have so few answers I find the antecdotal information on this site very helpful.
This is my story:
In the middle of August, 2006...
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Hello everyone,
Seeing how we're new to this disease (husband diagnosed in June '06), we still find where we have many new questions each and every day. Or, at least I do. My husband says he feels like he's under a microscope because I'm always watching him and everything he does. I keep...
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