Hi all, thank you for allowing me to join and be able to post here. I've been on this website a lot since October 2017 and I'll explain why.
My husband, who is 31 years old began getting some twitching in his muscles in or around October 2017. He went to his GP for around two visits before the...
My MIL started showing symptoms in June 2018. It started with back pain and slurred speech and progressed from there. In August she needed a cane to walk, and by September a walker. We had began seeking answers from her PCP and a Neurologist who couldn't give us any answers. The only thing...
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feeding tube
go away
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Hi all,
Just wanted to underline how grateful I am for this forum. This morning, Mum had her first really rattling experience with trouble breathing, a series of spasms that wouldn't allow her to get her breath. Because of how PALS and CALS share their experiences here, and I've been reading...
Hi everyone! First I wanted to say a huge thank you for these forums and the time you put up with a lot of people with symptoms that are in need of help.
That said, now to my condition:
My name is Felipe I'm a 30 M who lives in Brazil.
I've started with a fasciculation outbreak on my whole...
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back
bfs
diagnosis
early
emg
exercise
fasciculation
fasciculations
father
finger
ice
neurologist
paralysis
pressure
problem
reflex
scared
sensitivity
shoulder
symptom
symptoms
test
tremor
wanted
Hi ,
I wanted to say thank you. You guys provide such more accurate answers than google and are so kind along with it. Thank you Shiftkicker for helping me about a month ago.
I am 20, I still twitch about 24/7 all over. It's been about 4 months of consistent bodywide twitching. I have...
I haven't posted in a while so I wanted to update.
One of the main reasons I haven't been on here is... I'm writing a book!
Or trying to. It has nothing to do with ALS or anything autobiographical. It's a scifi/fantasy romance. I've long been an avid fantasy reader, and always had stories of...
Hello Everyone,
Let me start by saying I have been in here for a month now reading up on discussions and symptoms and I have read through the stickies as well. Just wanted to say the community here is amazing and the people diagnosed with this diseased who take time to help people with care and...
Hello, people!!!
I'm so sorry for bothering you all and taking your precious time.. One day(it's became my dream lately..) I want to discover a cure for this awful, terrible disease...
I'm a tall(1.85 m), white, 14 year old boy living in Europe. Recently I've noticed muscle twitches mainly in...
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balance
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crying
cure
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fell
happiness
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wanted
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wrists
My Pals started a downward spiral 30 days ago. Could no longer talk, appetite diminished, slept 14-15 hours at night and often a long nap in the afternoon. I asked twice if she wanted our granddaughters to come decorate for Christmas and never got a response. I had them cone out anyway and she...
Hi everyone, I wanted to share an article about my son (Ashton 10) and I (Diagnosed 9/7/17) that USC did on our story this month. I think it came out really cool!
Link to the video
Link to article inMotion Fall 2018
Shaun