NeuroTalk Support Groups

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-   Multiple Sclerosis (https://www.neurotalk.org/multiple-sclerosis/)
-   -   Hi Newbys....Please Introduce Yourselves (https://www.neurotalk.org/multiple-sclerosis/4543-hi-newbys-please-introduce-yourselves.html)

yeahbut 05-07-2007 06:57 PM

Hi Everyone, My name is Charlotte but must folks call me Char. I was told in November 2006 that I have 4 lessions on my brain and I needed to go see a Neuro for MS. Went to see the neuro in Feb (first appointment I could get) to be told I don't have any lessions but I am pretty sure you have MS by your SX and her Neuro Exam but can't put you on any CRABS because your insurance won't pay for it and I can't say 100% because we don't have proof from the MRI. See you in a year but you can call if you get a flare or get to bad off. Here is some meds to help you get through...... I have had some rough times with ON and the winter weather here in Maine but since spring has sprung I seem to be having more good days than bad.

It is nice to be here....

SallyC 05-07-2007 07:25 PM

Welcome Char, nice to meet you.

Your Neuro needs a backbone and maybe a few more tests before He/She shoves you out of the door.:mad: What happened to the four lesions? Dissappear?

You've come to a good place for support and understanding. Looking forward to getting to know you.

:grouphug:

Aletha 05-12-2007 06:00 PM

LDN and MS/new to group
 
Hello everyone, My name is Aletha. My husband has had MS now since Sept. 2004. He was one of the lucky ones, as he had miraculous success with LDN. I would love to post his story here if everyone does not mind my doing so. It is a bit lengthy however as it is about 2 pages long. I have also created a sort of "welcome e-mail" for those wishing to know more about LDN. I would be more than happy to send that along to anyone that requests it. My e-mail is Aletha@redshift.com.

My mother went on LDN for Parkinson's about 2 months ago and she is feeling better, and has more energy. Our hope is of course that she has no more progression.

This site appears to be very positive and caring. I love that. :) Kindest of regards, Aletha

Snoopy 05-13-2007 06:34 AM

Hello Aletha and welcome to NeuroTalk.

Feel free to start a thread of your own. We like getting to know our new members:) and hearing their story.

AfterMyNap 05-17-2007 09:22 PM

Hi Aletha, how nice of you to come. This is a lovely bunch and there is a ton of great information here.:)

DM 05-18-2007 08:10 AM

Hi Aletha and Welcome.... :welcome_sign:

sloth 05-18-2007 04:36 PM

Hi
 
Hello Im not really new to boards those who used braintalk will know me as Row boat or roe.

I have been labeled prob' ms since 99' or sometime there after. Multiple brain lesions, neg lp done early on, neg emg and other stuff.

Just lots of wonky sxs mostly right sided spasms contractions, numbness or nerve pain and heavyness, fits of vertigo and walking unbalanced and a tremor of head and hands.

I have developed good sided sxs now last few years.

Anyway wanted to say hi and let everyone know who I am, just decided to reg' as sloth it suits me sooo well LOL.

Thanks for being here great forum how old is it?

:winky:

Curious 05-18-2007 04:48 PM

we were "born" 8-21-06

welcome to neurotalk sloth. :D

sloth 05-18-2007 04:51 PM

Hi curious...
 
I love your name and avatar ;) No wonder I never found the board before, its sorta new then well to me.

I wonder how it got started anything to do w/ braintalk failures?

Anyway...thanks for the board and the welcome :)

Curious 05-18-2007 04:58 PM

hey...we can hang around in some trees together. :D i'll bring the brownies.

you are correct. we started as a temp site when bt crashed. it was loved so much, docjohn (owner admin) was asked to make a permanent site.

so..whalla...here we are. :)


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