Hello,
Thank you everyone who is willing to give me any feedback on my current situation. I have been reading a lot of posts on this site for the last couple of months and I have felt that the people on this forum have been extremely helpful and educating. I was hoping not to have to post, but...
I posted here in 2021 about fasciculations all over my body. I did not have any noticeable weakness at the time.
In the ensuing years I have felt fine. Fasciculations continued and I assumed I had BFS and moved on.
I’m a little concerned again because I have definite clumsiness in my right...
Hi
I am a previous poster (previous threads here and here) looking for some advice. Approx 7 months ago I began with widespread fasciculation, mainly concentrated in my calves and feet. I also suffered mild cramps in my feet. Long story short, after much delays I finally saw a nuero 3 months...
I have a new home health aide who is a firm believer in the gait belt. She's quite good with it, but it's hard to figure out where to put it -- between breasts and feeding tube? I can cram it in there, if you're patient. I currently have a dangler but am hoping to get Enfit button in a few days...
My PALS, Tom, started Riluzole in August 2022 at the time of his dx. He has been declining each month. In February he was barely conscious, weak and drowsy all the time. I thought I would lose him fairly soon.
I called the neurologist to discuss stopping the Riluzole. Are we getting only...
A year ago I started feeling numbness and tingling in my leg and burning sensation in my head
I did a brain MRI which showed corticospinal tract hyperintensities which are biomarkers of Als. Neurologists said no Als and related my symptoms to anxiety but symptoms exacerbated a lot.later I began...
als
anxiety
arm
brain
breakdown
breathing
burning
clinical
crying
diagnosis
emg
fear
mri
muscles
slurred speech
speech
swallowing
symptoms
symptoms of als
tongue
weakness
Well for starters I found this website in a state of my panic and have read others threads about similar symptoms in a search for reassurance. I have been very apprehensive about posting here because I know a lot of people are probably just overexcited or scared and have convinced themselves...
I recently came across this article and I'm freaking out now:
https://www.ncbi.nlm.nih.gov/pubmed/11464925
Everything I've read on here says that widespread twitching is not indicative of ALS, but this article states otherwise.
The worst part is that I had an emg last year that the neuro...
First off, my heart goes out to all of you. You are so incredibly brave and generous with sharing your time, experience and support.
My husband walked into a neurologist's office with symmetrical muscle weakness and walked out with a diagnosis of ALS.
Some background -
My husband is 51 and...
2nd opinion
als
brain
death
diagnosis
dying
emg
family
family history
family member
father
heart
lead
mri
muscle
neurologist
night
stress
stroke
support
symptoms
test
twitches
wanted
weakness
Good evening, everyone,
First off, I have been constantly amazed at the grace and promptness with which questions from anxious people here are answered, and in my time lurking over the last couple months these replies and stickied threads have been a huge resource. So thank you!
I'm just...
als
atrophy
back
bed
clinical
cramping
emg
family
family history
grace
holiday
hope
hyperreflexia
leg pain
neurologist
questions
running
shoulder
symptom
symptoms
twitch
twitches
twitching
weakness
worried