Hello everyone!
This ended up being a very long post so I I'm going to put a tldr at the end for those of you with limited energy.
This is my first post here and as a c9 carrier I will likely be lurking around for a while as it is the most comfort I have found so far. I want to say thank you...
Hi so to start with I’m male age 26
So a few months ago I got rapid heartbeat tachycardia (I know not often a symptom of MND),
They found no cardiac explanation, then started getting muscle twitches which I still get sometimes, again no obvious explanation. I noticed a panting in my throat...
Hey everyone, thanks for reading. I am a 24 year old girl, no family history of ALS. I KNOW that I have health anxiety but I can’t seem to shake the idea that what I’m experiencing might be ALS.
So two weeks ago I was home and my finger was twitching. Naturally I panicked and googled and ALS...
Thank you to anyone taking the time to read this and giving me your thoughts and insight. Please know that it is truly appreciated. I have read the stickies, but still have some questions.
I am a 40 year old male. I began with a twitch in my left bicep in early December 2018, but the...
allergies
back
bed
bulbarbulbar onset
clinical
concerned
early
emg
family
family member
friend
muscle
neurologist
onset
problems
questions
reading
swallowing
symptoms
tremor
twitch
twitches
twitching
voice
weakness
I posted two years ago but was unable to post on that thread but it had been closed.
During the time between then and now for the most part I was able to move on from my fears of ALS. However that has changed recently as I have developed a mild slur, not noticed by normal folks but was...
als
back
breathing
bulbarbulbar symptoms
clean emg
clothes
diagnosed
finger
mnd
mri
muscle
neurologist
night
normal emg
scared
sleep
spasms
speech
symptom
symptoms
tongue
twitching
work
young
My husband has bulbar ALS .The DR has upped his dosage of Baclofen to 5 times a day.He is considerably weaker taking after taking them.Anyone else .Thank you .
Hello everyone , thank u for taking time to read my post , any and all feed back is greatly appreciated , and for all of u suffering with ALS I pray for u all and am starting a campaign to raise and donate money for ALS ! Ok so here is my story , for the past 2-3 years I have suffered with what...
als
anxiety
back
bulbarbulbar onset
burning
emg
heart
iron
medicine
mnd
money
neurologist
night
onset
scared
shortness of breath
story
swallowing
symptoms
taste
test
twitching
work
worried
My story starts in Feb 2018. During an xray for shoulder pain they discovered my left diaphragm was elevated, but they didn't bother to tell me. They gave me painkillers for shoulder bursitis.
I complained to my PCP in Sep 20108 of constipation. She ordered an abdominal CT scan that showed...
abdominal
age
als
back
bulbar
constipation
diagnosis
diaphragm
fear
fvc
insurance
life
mucus
neurologist
pain
paralyzed
saliva
shoulder
story
swallow
swallowing
symptoms
test
tests
wanted
My pALS is my mom. She is newly diagnosed with bulbar onset ALS. As of now her mobility is not impacted too much, just her speech, swallowing and breathing.
We have been discussing living arrangements as her mobility and breathing decline.
Other pALS out there, what did you decide? Did you...
artist
breathing
bulbarbulbar onset
decline
diagnosed
disability
family
hospice
insurance
medicare
mobility
newly diagnosed
onset
social security
speech
swallowing
va benefits
work
So I am back after a brief hospital stay which caused whatever I have to flair up again.
It all began in 2011
*******-------Feb 4-5th 2019-----------*********
So went back to same neuro with exasperated symptoms after a brief stay in the hospital for severe constipation.
After the hospital...
als
arm
autoimmune
back
bulbar
clinical
constipation
cramping
denervation
emg
exercise
fasciculations
immediately
media
mri
neurologist
scared
shoulder
support
symptoms
tests
tongue
weakness
worried
wrist