I'm primarily on dailystrength nowadays, I have my own LDN group, http://dailystrength.org/groups/ldn and keep a SNIPS archive group there too http://dailystrength.org/groups/daily-snips-archives

My dad is on LDN 528 days and doing AWESOME, 1969 for me.

Hi Robyn and Adrian!!! Welcome to the group! There is a wonderful group of caring and knowlegeable people here so make yourself at home.

Welcome Robyn and adrian!!!

to NT, Adrian.

Cherie

Hi, I am real new to all of this and found this site while researching MS.
Long story short ( I think); Back in early spring of this year I was diagnosed w/ON. They also ordered MRI's and found several lesions. Then sent me to MS Specialist who ordered more MRI'S,Evoked potentials, and LP. He says now ( after waiting all summer) I have MS. I have to see him ( the Doc) in about 2 weeks and he said he may or maynot start me on treatment. Meanwhile, my eye is acting up again here over the weekend. I am awake here in the early wee morning hours becasue my arm and shoulder is having crazy spasms and my joints are hurting ( this is a first ). My face on the same side that my eye hurts feels tingly, kinda like how you feel when novacaine is wearing off when you get a filling (also a first). I am at my wits end with this and crying as I type because my hubby is as worried about all this as I am and even though I have a diagnosis of MS now, my Doc is unsure I should be treated cause he thinks I am early stages of this disease????? Everything we have researched points out I should be on treatment to help slow this progression. Anyway, this is probably not the best introduction I could have given, but I am having a REALLY bad night..I am sorry. On the brighter side, I did contact our local MS Society and they are going to send me info and possibly refrences for a new Doctor. UGH! Otherwise, I love spending time in my gardens, with our animals, reading, but more than any of that, with my hubby of 28 years and our grown children and their spouse ( only one is married so far). Thanks for letting me come here, sorry about the vent along with the intro. Helen

HELEN, to NeuroTalk. I am so glad you found us. We are caring fun group of MSers and here to support each other.

I'm sorry noone was here to greet you in the wee hours, when you most needed some support, but do come on in today, and join us anywhere.

I so understand your anxiety and fear of, what's to come next, with this disease and will try to be here for you..


P.S. Please break your posts up in shorter, easier to read, paragraphs...Thanks.

WELCOME ONE AND ALL! EVERYONE HERE IS VERY HELPFUL!

Howdy, it's me Que.

Hey, there! I remember you from MSW! I'm so glad you've come over here....did you have lunch with Sassy and Beth?

Welcome!!

Hi Helen2! Welcome to NeuroTalk! I'm so glad you decided to join us. We have a very large group of MSers here. Please visit us at The Stumble Inn for some fun, too! We're a pretty goofy bunch....well, some of us are goofier than others!