Hi Everyone
I am very new to this forum, but I thought that writing about my current difficulties on here would be a cathartic experience. From reading previous posts on here, it does not seem that my experience is a unique one.
Let me please give you first some background, which will...
February 20th I noticed a twitch/spasm where my arm meets my shoulder, which was on and off for the next few hours. I was laying in bed when I first became aware of the situation, went to the mall to distract myself and it sorta worked but the spasm/twitches where still present. I figured it...
One year ago, I noticed fasciculations in my calves, which then spread throughout my body! My legs would cramp up, I felt like I was getting weaker, would constantly search for atrophy, my anexity went through the roof, people close to me thought I was having a breakdown! I seen a bunch of...
15 weeks ago has noticed I slurred a few times. This when was I talking a word here and there. then again a few weeks later-not anymore that I recall . No one has mentioned it to me.
Then 10-11 weeks ago I began to have stiffness arms and calves.
It went away in a few weeks. I have felt off...
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Well. Where do I start?
I came here one year ago, almost to the day, whilst awaiting a firm diagnosis of PLS. 6 months later, I received that diagnosis. I was very happy to have an answer, though it never really sat right with me. I had done too much reading, too much research and asked lots of...
I know someone whose family is affected by FALS. They have a running team that raises money for ALS Research and are running a half this weekend in my father's memory. I keep wondering how I can I make a difference/feel like I'm doing something positive myself.
My running skills are really bad...
I am new to this. My sister was diagnosed with ALS November 2014. She has the bulbar type. Her first symptom was tiredness, then her speech was slurred and now she has no speech at all.
Is there any research in New Zealand that she could be a part of? Her anywhere in the world for that...
Dear ALS Community,
I've been having trouble with my index finger and thumb for about six months so I recently went to see a hand doctor. To my extreme surprise, she said my issues are likely related to the central nervous system and that I need to see a neurologist. Of course I was shocked as...
Hello all and thanks for being there. I was diagnosed two days ago.
My particular mystery is that i had the beginnings of ALS symptoms concurrently with an ependymoma tumor in my lumbar spinal cord and also crooked neck bones and a herniated disk in my neck. I am 59.
Neurologists had a hard time...
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Hi, I am new to this forum. I was told last Wednesday that I have ALS but believe I have been misdiagnosed. My story.
I began having spasms in my right hand of the ring finger and pinky finger in August 2014. At that time I did notice difficulty in walking but attributed it to the fact I had...
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