It's only me again.
I had a pulmonary function test at Mayo three months ago and one at U of F (Shands) this week. Mayo didn't include the raw data and Dr. Pulley wanted to do one of his own. It looks like U of F doesn't do specific tests of respiratory muscle strength and Mayo does...
hello all.
Not sure what to make of what is going on here. first twitching started in my calves and spread all over my body in a matter of days didn't think anything of it but went into the doctor to have it checked out went through several blood tests including lime and vitamin levels and...
Like many here, I come seeking advice. I have read all of the stickies and tried my best to "research" what I can about ALS. (I am a junior high science teacher, and the lack of answers and knowledge about the pathogenesis, etc. is baffling to me. But I should keep this short). Sorry).
About...
als
arm
atrophy
back
breathing problems
bulbar
bulbar onset
clean emg
clonus
crying
depressed
early
emg
exercise
fasciculations
muscles
nose
onset
pneumonia
research
shoulder
story
swallowing
swelling
symptoms
test
twitching
weakness
My husband just got some lab results back and of course it is Saturday so we cannot call the doctor. I did some research and if I am reading correctly the results have to do with heart disease and renal failure depending on the site. It reads BUN/Creatinine Ratio 8 . Flag low. His ldl...
im taking a medicine that is new and not approved, it hasnt been thru clinical trials yet. its called RCH4 Peptide and ive been on it for 9 months. my als has not progressed and im a bit improved. my fingers are moving more (i realize 'more' is a subjective term. in march when my hands were at...
There is a SOD1 gene blocking trial getting ready to enroll. You do not have to be SOD1 FALS to enroll. Apparently research has shown in the lab that lowering sod1 levels in SALS seems to be helpful!
https://clinicaltrials.gov/ct2/show/NCT02623699?term=Amyotrophic&recr=Open&cntry1=NA%3AUS&rank=2
**Sorry for the length, I didn't realize how long it got until I hit preview.**
I have read thru the sticky's and know that what I am experiencing is likely something different, and I really hope I am in the wrong place. I have been reading posts for the last week and finally got up the courage...
arm
brain
breathing
chair
emg
fingers
hope
immediately
info
kids
motor neuron disease
mri
muscles
neurologist
neurology
night
physical therapy
questions
reading
reflex
research
story
swallowing
test
tests
twitching
veteran
wrong
It is time for me to move from do I have als/mnd to another forum however I do not have a specific diagnosis as of yet, to explain which I am confident most or all of you will understand my 4 emg's and clinical exam cannot be denied.
I went in November 18 th for a fourth emg it is always an...
Hello everybody,
My name is Olly and I’m currently a PhD Researcher at Edge Hill University in Ormskirk, Lancashire (UK). I have a specific research interest in young people who help care for family members who have ALS, and also those young people who are bereaved due to the disease. I have...