Do you really have ALS?
A diagnosis of ALS or any other motor neuron disease (PLS, PMA, PBP, MMN) is made “by exclusion” (no higher probability presents itself) and by published criteria, most critically symptoms and muscle/nerve tests.
Doctors may legitimately differ on whether you have...
http://hub.jhu.edu/2015/09/23/als-dementia-research
The research shows that the most common known risk factor for ALS and frontotemporal dementia, or FTD—a gene mutation known as C9orf72—causes cellular highways to jam, impairing brain functions. However, in tests with human and fly cells, the...
Hi, everyone :) I'm Laura, & my mom has ALS. She was officially diagnosed with Bulbar ALS just a year ago but has had symptoms for 2-3 years. Her disease has progressed rapidly; we started with hospice yesterday. I'm one of 5 children/stepchildren, but the only daughter and most local to mom and...
Woukldnt it be nice if we were the last generation to die of this disease? Piss me off big time but nice.
Scientists identify new drug target to treat ALS
Scientists identify new drug target to treat ALS
Blue is the nucleus, cyan is hUPF1, green is TDP43, red is the cell body in this image...
I have had pin and prick and insect crawling symptoms a couple of years back. I have had difficulty swallowing a few years and burping and chest pain. My right side of the body feel weak have chest (specially on the right).. have attributed them in GERD/gastro type of problem for years (feels...
als
als?
arm
back
brain
bulbar
burping
choking
dementia
emg
fibromyalgia
go away
healing
mri
muscle
pain
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swallowing
symptoms
test
tests
twitching
voice
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worries
wrong
My wife, 47, has had a diagnosis of Upper Motor Neuron Disease, along with dementia, and parkinsonism. As her caregiver for the last 18 months, I was stretched to the max. I had a heart attack 2weeks ago, and had to put my wife in a nursing home.
During a family mtg. (at the nursing home) to...
Which is the most common cause of FALS, also found in a percentage of SALS and in isolated FTD as well as ALS/FTD
They have finally developed a c9 mouse which is huge both for research and at least in the past the FDA was reluctant to accept therapies that were only tested in IPS derived cells...
I know at some point it will be very obvious that I have something very wrong going on. For the time being it is mostly my hands that are affected so I'm able to get by in most situations without people noticing. We've told our closest friends but have not gone public.
Also, we've still not...
So this may be a bit long, I apologize. My mom is currently in a hospital on a ventilator right now and we've yet to really yet to get a diagnosis. She's been through multiple doctors over the last few years, some have said ALS or MS and some have ruled it out. So I'm hoping to get some answers...
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battery
concerned
dementia
diagnosis
diaphragm
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fell
fingers
hospice
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insurance
muscle
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research
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story
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tests
therapy
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wanted
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I recently had an EMG and at the end of the test the neurologist told me I had varaint of als she also is sending me to a als specialist whom I am booked to see in 2 months. 4 years ago my left foot went numb then I lost the use of everything below my left knee. I was able to keep working with a...