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Re: Is this Lhermitte's Sign? MS?

Posted: Sun Jun 27, 2010 11:34 pm
by NHE
Hi Eugene,
Welcome to ThisIsMS.
shinbet2002 wrote:Whenever I look down and touch my chin to chest I get a really light barely noticeable buzzing in my right foot that lasts seconds.
I wanna be sure. Does it sound like lhermittes to you?
What you are describing seems consistent with what I have read about Lhermitte's though I don't have any personal experience with it myself.

NHE

Posted: Sun Jun 27, 2010 11:38 pm
by Algis
"my" Lhermitte's are tingling/electric needles/difficult to describe in the extremities of little fingers; starting from tip and if I slowly bend more my chin to my thorax it goes up to my hand (same fingers)

Difficult to clearly describe; sorry if it sounds confusing 8)

Posted: Mon Jun 28, 2010 4:02 am
by jimmylegs
heya, sorry you're having a rough time with the docs :(

i have had l'hermitte's and it sound like that's what you've got. mine was from basically a whole slew of vitamin and mineral deficiencies, from being very very diet restricted for a lot of years. the main thing was b12. it took a while with lots of changes to my diet and lifestyle and i do have permanent damage it seems, but it's a long slow climb and i have not had l'hermitte's in ages now.

hth,

jimmylegs

Posted: Mon Jun 28, 2010 6:40 am
by tzootsi
Sounds like it could be l'hermitte's. My wife had it until she was treated for CCSVI. For her, it was an electric shock feeling down her legs. You may or may not have a very mild case of ms, but it could be many other things. Jimmylegs suggestion of making some diet changes and taking some supplements sounds like the first thing to try.

Re: Lhermitte's Sign? MS?

Posted: Mon Jun 28, 2010 11:38 pm
by NHE
shinbet2002 wrote: I just read an interview by Dr Mark Freedman in which he says that early treatment (2nd CIS attack) is really too late to start interferon therapy. He said that its critical to start treatment if you even think you have ms i.e super early. presumably before a relapse.

This statement by Freedman is preposterous! Considering the side effects of Ifn-B (as well as the cost), one would want to be damn certain that they had MS before starting.


NHE

FIGHT

Posted: Tue Jun 29, 2010 7:20 am
by leetz
fight for the proper diagnosis...spinal tap? Mri? lesions?

Posted: Tue Jun 29, 2010 7:31 am
by Drury
I agree with NHE.

These drugs are horrible and only to be taken if necessary - there is still no proof that they actually work. In fact the recent UK study is proving otherwise from what I gather.

A proper diagnosis is critical with MRI as a start.

Good luck,
Drury

Posted: Wed Jun 30, 2010 1:03 pm
by Drury
shinbet2002

Look up MS drug trial "A Fiasco" - there are numerous other headlines but I have no idea about cutting and pasting or I would have put it on here for you.

I just want you to be informed and then you can form your own conclusions - that is when you know where you stand. Main thing is you have as much info as you can get because our experience is (our family that is) that you really have to be your own advocate.

Very best of luck.

Drury