I first want to say how sorry I am for those of you who have been diagnosed with this horrible disease and those of you who are facing possibilities of having it. This is a horrible thing and I know it is very terrifying. Even if I do NOT have this disease I want to become a supporter and do...
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Is clonus a common MND symptom?
For those who might not know what clonus means it is: from Greek for "violent, confused motion" - a series of involuntary muscular contractions due to sudden stretching of the muscle.
My husband has had clonus in both feet/ankles for a long time now...
A previous post brought this thought to my attention. I did not want to take away from their post and submit my own concerns regarding my mother. Therefore, I have started a separate post.
My maternal great-grandmother was diagnosed with ALS many years ago. She lived with ALS for 5 years...
It was either this or do the taxes. Hopefully somebody will find this useful.
List of Bulbar-onset ALS symptoms over 3 years.
? means I’m not sure it’s connected to ALS or FTD.
** means it’s still continuing.
These are not in accurate sequence, but generally by year.
Not sure about the...
My husband was diagnosed with ALS at the end of August, 2008. Since then, I've taken comfort from your posts ... your information, your honesty and your humor. I guess we've both just been lurking up until now, happy to know you are out there. In the past few months, I have noticed increasing...
I had an EEG (I keep spelling it EEK for some reason ... maybe when I get the report, I will know why :shock: ) yesterday. It was supposed to be a "waking/sleeping" EEG to try to find an explanation for 5 seizures I've had in the last six months, all happening when I was in deep sleep. (The...
I've been registered for a long time, but have never posted much. I just want to say that my heart goes out to everyone who has lost someone - recently and not so recently - to ALS. I wish I could just hug each of you!
I lost my darling husband Kenny on April 29. He fought ALS for 6 1/2...
Hi, all ... an update on my third clinic visit at UCLA yesterday (as opposed to my trial visits).
My "gross" strength is still good, hasn't changed much since my first visit in June, but left leg and arm are slightly weaker.
The neuro did not seem impressed by my improvement in speech and hand...
Well, it’s time for me to unload again about my husband. This will be long. Sorry.
For anybody who remembers, last summer, he developed new symptoms ... collapsing suddenly two or three times a week, being unable to stand or walk (those were the days when I was dragging him around the house on...
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Hi, all ...
I'm the PALS, but I need to get a wheelchair for my husband ASAP, and I have no idea what to look for. I assume it would be good to get something I can use down the line.
Background: You don't have to read all this, as it doesn't relate to ALS. But I think my husband has MS ... his...
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