Let me begin by saying; I do appreciate anyone who is taking the time to read this. I also realize you are not doctors but individuals w/ unique experiences through this evil disease. I respect each of you and all you have to say.
1/ When you started having symptoms•concerns who did you speak...
Hi i was pointed here by Nikkij . The Introduction link should be top of the page IMHO.
I left the Fire service here in the UK aged 50 in 2012 I had enough in my pension pot to get by on and I had a sweating problem, I thought this might be due to job stresses and would clear up when I...
Hello to everyone, this is my first post, after spending a lot of time browsing the forums. It seems like a very supportive place.
I've noticed in these groups as well as in the local ALSA support group we go to, that some people are dealing with the stress and demands of a fairly rapid...
I am a 61 year old female diagnosed in May 2018. Not a fan. Most of my issues are with my legs at this point and I am hoping to return to work (working from home though). Been to the ALS clinic here in Toronto and they were really supportive and helpful. Doing physio. Getting a foot brace for my...
Hello all,
I never in a million years thought I would be joining a group here, but turns out it is looking like this is the next phase of my life. I started noticing a little weakness in my right leg, especially getting into a vehicle for ie. Also around the same time, I kept wondering if...
2nd opinion
advice
age
atrophy
back
brain
denial
diagnosis
emg
falling
footfoot drop
grief
hip
insurance
lead
life
lyme
mnd
muscle
research
stress
symptoms
weakness
wes
Hi I’ve posted twice before but the threads have closed!
I’m still having problems with my speech which is my main concern nobody has mentioned it to me but during conversation I can see them screwing up there face as if to say what are you on about! My nose feels constantly blocked but no...
My brother died last year 10/31/2017, from ALS w/FTD he was 56. His ALS started in 2012 with a small fasciculation in his upper arm. At the time he was a airline pilot, he went to the Dr. and was told it was stress related. The FTD was more of a problem than the ALS and he eventually lost his...
Hey all,
I'm hoping you all can help me.
About a month and a half ago I was laying down for bed and my face went numb. It stayed numb off and on for 3 days. I went to the doctor and he said he thought it was anxiety due to me going thru a stressul time at the time. He done an MRI and...
als
ankle
anxiety
atrophy
back
balance
bed
cramps
family
foot
mri
please help
speech
symptoms
symptoms of als
tongue
twitches
twitching
work
worried
young
Last year about this time, I started feeling like I had ALS. Some twitching, trouble swallowing, feeling weak. The symptoms went away for a while, but now I feel like they are back. I have twitching in both hands sometimes, even when hands are at rest, my hands shake when I lift a heavy pitcher...
Before I ask my question I will give a little background info on my situation. I was injured in the military and have two discs pushing on nerves which causes extreme pain down to left foot. The VA wants to do disc replacement surgery but I have been holding off as long as possible. I was...