I am new to the forums (see https://www.alsforums.com/forum/newly-diagnosed/27588-steve-s-introduction.html for a bit of an introduction).
The doctors want me to start seriously considering a PEG. I have read many threads on this topic, but still have questions about how soon I should take the...
He everyone,
I would like to introduce myself. I am Steve, and was diagnosed with MND in July of this year.
First, I would like to thank all the folks that make this site such a wonderful place. I discovered this forum over a year ago and have found great value in the conversations here...
Hello all -
I've decided to stop lurking & introduce myself. I was diagnosed last Sept by Dr Stanley Appel in Houston. Like all of you - it was quite a shock for me & my husband, Jim. My symptoms had started about a year before that with left arm & hand weakness which was initially...
Hello Everyone,
I posted in the Intro section, but Nikki suggested I post here in that not everyone reads the introduction section:) I had also previously posted in the is this als? section as the neuromuscular team tried to piece together what was going on with me. Today after being in the...
als?
bed
bulbar
china
cramping
diet
dysphagia
emg
feeding
feeding tube
introduction
is this als
is this als?
medicine
muscles
pls
slurred speech
speech
symptoms
testing
tongue
I've been reading this forum for a while now. My PALS was diagnosed with Bulbar ALS in January. It's been tough watching him try to cope with the diagnosis and what ALS is doing to him. I find this forum to be helpful, and I've learned a lot. I appreciate the abundant support and caring.
I wanted to take a quick moment to reach out and say "hello" and to introduce myself. My name is Jim (60) and my wife's name is Darcey (59). Darcey is my PALS and first showed symptoms in November of 2012. Originally diagnosed and treated for CIDP for about a year,
we became concerned that...
back
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bipap
diagnosed
diagnosis
early
hope
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hoyer
hoyer lift
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life
lift
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support
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symptoms
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voice
wanted
I've been lurking for several weeks--ever since we learned that my husband, my invincible superman, has ALS. We knew something was wrong, but never even considered ALS.
Today I was finally able to say the words, "My husband has ALS", out loud without crying. I'd actually practiced it out loud...
By way of introduction I live in the Knoxville, TN area and was diagnosed with ALS in September 2013 at Vanderbilt. I am retired Air Force.
The reason I am writing is I hope I may be able to help someone else out who may have leg twitches. My twitches are often triggered by what I call...
Hello Everyone,
I'm new here and I'm interested to get update, questions, information and answers on medical treatment, doctors and clinics . I hope this forum helps me to get what I'm looking for.
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