Opinions on ALS plus Criteria?

reneecatx

Well-known member
First of all, I saw this on mgh board from 1998. I was a little alarmed by it. I'm only asking for opinions,no bashing, please :)
I'm typing it as I saw it.

Folks the scope of criteria required for an ALS diagnosis has increased greatly. In fact, neuologists have coined a term
"ALS plus" to describe patients that have primary motor neuron degeneration symptoms along with symptoms such as the following sensory abnormalties (parathesia,dysthesias, tingling,burning, ect) gastrointestinal abnormalties, sleep disorders, autonomic nervous system disorders, various types of pain and finally, most notable dementia. It has been observed that many of the old standbys that have been used for differencial diagnosis in ALS are unreliable. For example, sensory symptoms are quite common on PALS. Many people that have been told that because they have sensory abnormalties that ALS is not a possibility. This is proven untrue. I bring this up so people will give their physicians a shove to update themselves.

Fasciculations, particularly those accompanied by other symptoms are a sign of a serious underlying disorder. This is not meant to alarm anyone, it's meant to awaken some. Not every fasciculator will develop ALS, but many will. People, please keep in mind that emg's are usually only useful in the LATE STAGES of ALS.

This post is challenging my sanity. What do you think of it? I'm alone and scared right now... I just had to talk(write) to someone.

I'm going to the neurologist for a followup appt. next Tuesday. I'm going to print it out and see what he says.

I also want to say that just because a post isn't all friendly,nice, and rosy doesn't mean it's bad or mean. It's just someone's opinion.

Renee :(
 
Renee, Renee, Renee....

Go back and read the article on BFS put out by the Mayo Clinic. The person that wrote this clearly has no reason to write it other than to scare people. You did not find it in a scholarly journal, and most likely it was written by someone with no medical knowledge or experience at all. If you look for stuff like this to scare you, you WILL find it. Take all the accumulative knowledge found on this board, all the medical journal articles written by the the experts, and none of them say, "most fasiculators will go on to develop ALS". No one here has ever, to our knowledge, gone on to develop ALS after a clean neuro exam and/or EMG. Forget this article, and get on with life. It's nonsense.

Jen :D)
 
I completely agree with Jenn. This posting is utter nonsense. Just because it's posted on the mgh board doesn't mean it's true. I could post a message there saying that Arnold Schwarzenegger is the illegitimate offspring of Mickey Mouse and Madonna but that wouldn't make it true. Also, this post is from 1998. Funny that no other published articles supporting this have surfaced over the ensuing 5 years. My advice is to forget it - rubbish like this is what keeps people so scared of bfs.

You can have a look at my story at which covers stuff like this!

David
 
a quote from Adams and Victor's Principles of Neurology, which is the number 1 neurology journal


"A simple clinical rule is that fasciculations in relaxed muscle are never (my italics) indicative of motor system disease unless there is an associated weakness, atrophy or reflex change."
 
Many people that have been told that because they have sensory abnormalties that ALS is not a possibility. This is proven untrue. I bring this up so people will give their physicians a shove to update themselves.



this is untrue, Mayo clinic, the number 2 ranked hospital in the world by U.S. news and World report



Mayo clinic obviously has the study to prove that benign twitches leads to ALS is untrue




Fasciculations, particularly those accompanied by other symptoms are a sign of a serious underlying disorder. This is not meant to alarm anyone, it's meant to awaken some. Not every fasciculator will develop ALS, but many will. People, please keep in mind that emg's are usually only useful in the LATE STAGES of ALS.


this is also false, changes in EMG will be evident in a short time after ALS starts, not years later
 
I have not been here so long I replied wrong. So I guess this was entered by a medical professional and we should all be prepared to die right. I do not know what to believe anymore. I mean I will never be free of this fear never.

Kerri
 
I had a great honeymoon and while I was there I found out that I am infact pregnant I must have taken the last test to soon or something because the doctor figures me to be 6 weeks. I was so happy but now I have a constant twitch in my left knew I mean it is going off constanly.

This scares me.

Kerri
 

Users who are viewing this thread

Back
Top