I'll Be Here At.....

When Will You Be Online?


Want to let others know when you'll be online and available to chat? Then add your time below. It would also be great if you could introduce yourself so that users will know who they're talking to.

If this works, you'll be able to show up when other MSers are actually online. I see where many of you miss each other by a few hours or days. Try being as specific as possible and add a day and time in the near future when you'll be here to chat.

Comments for I'll Be Here At.....

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Feb 05, 2015
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GOING CRAZY IN TENNESSEE
by: Mary

Hi...I'm new to all this and to MS. I was diagnosed in October 2014-scared the crap out of me... I actually had symptoms more than a year and didn't know it... I since have seen at least 5 different doctors and take a lot of meds for headaches, back, RLS (Restless Legs Syndrome), and OAB (Over Active Bladder)....

This is a nightmare come to life for me... Just recently had pins and needles to add to my attacks of hot burning sensations down my arm and and my face, finger tips, and philanges. Also have a numbing/tingling sensation.... I almost got fired from my job cuz of my vision probs.. I now wear glasses...

I guess I just need a friend to talk to who understands what the hell is happening to me...

Jan 15, 2015
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Need to Talk with Someone!
by: SarahM

Hi!
I've been diagnosed with MS, and I just knew about it two days ago. I'm freaking out and scared and I don't want to talk about what I feel with any family member or a friend. Anyone who has experience with MS or know a lot about it can chat a bit with me?
I really need it.

Thanks.

Oct 18, 2014
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need help
by: steve

I should start by saying I live with my girlfriend who has MS and would like to chat with a lady in a relationship who also has MS PLEASE Im here now

Sep 15, 2014
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New here
by: dunkyslady

Hi all I'm new to chat and getting ready to start my therapy. Problem is I'm afraid of needles does anyone know if these shots hurt?

Apr 15, 2014
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Pins, Needles and Pricking
by: Anonymous

I need help!! In 2009 I found out about my MS. I am on 3600 mg of Gabapentin a day and Aubagio. I continue to have pins and needles all over, face, feet, hands, everyplace. I can not take this any longer. Can someone help me??

Feb 11, 2014
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bordem !!!!
by: Anonymous

Hi, I'm Steve, 43 yrs, diagnosed in 2007, medically retired from work for a year soon and I am so bored. Be good to chat sometime and make new friends.



REPLY: Have you tried our social site, The Link? It's not a chat room per se, however it is a place where you can meet others who have MS. I am working on getting an actual chat room set up. In the meanwhile, here is the link - You may have better luck there. Here's the link to join - The Link
or our Facebook page if you are a member there - Life in Spite of MS - Facebook Page

Apr 10, 2013
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keep trying
by: SAMMY

I don't see anybody here in/on chat board

I'm Sam, 55 yo. Have had (MS) for almost a decade.

I USED TO BE ON AOL WHERE A REAL CHAT ROOM WAS SET UP

NOT JUST THIS BOARD

IT WAS A LIFE LINE

MY S/N IS FINDTHECURE4MS@ATT.NET

E/MAIL OR I/M IF YOU WANNA CHAT

REPLY:

Hi Sam,

Sorry you haven't found anyone here. You can try joining our network site, "The Link". You may have better luck there. Here's the link to join - The Link
or our Facebook page if you are a member there - Life in Spite of MS - Facebook Page

Dec 28, 2012
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tired
by: Emily

I was diagnosed in 2004. But I am going out of my mind staring at the 4 walls. Can't work and have nobody to talk to about it, at least someone who might understand that I am not lazy, that I do not have any energy. I would love to chat with people who might understand.

Nov 17, 2012
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Need to talk to someone that understands
by: annetta

Hi, my name is Annetta. I have MS and my world is turned upside down. I used to work as much and hard as 5 men put together. Now I can't get out of bed by myself. I stay in pain all the time.

I forget everything. My husband says my moods change all the time, but I don't see it. I feel so lazy, but I feel drained of energy. At night I can't sleep because I worry.

We have a lot of trouble with our grown children. And my husband's health is getting bad. No one in my family realizes what's up with me. I give them pamphlets to read but they don't read them.

I've tried 3 different MS medicines but I've had bad reactions to them. I'm starting a new one this week. Sorry if this was too long and for my spelling. I'm not very good with a computer and I don't know any short cuts. I don't know what the abbreviations mean. HA, HA.

I don't want anyone to feel sorry for me, after all, we're all basically in this together, I just really needed someone to talk to that understands. And I have so many questions that maybe someone can answer.

Thanks for listening.

Annetta

Sep 07, 2012
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help me with MS
by: Maureen

I'm trying to learn all I can about MS. I know very little about it and just heard my neighbor has it. What side effects does it have? How should I expect her to change now that she has it? What can I do to help her knowing she has it?

Jun 25, 2012
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THIS SUCKS
by: Annett e Roy

THIS REALLY SUCKS TODAY, I FEEL LIKE I AM GOING TO CRACK.

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