I'm so computer illterate!!! I hope I do this correctly.

Thank you for the welcome!

Anyway, I am having trouble with shots in my arms. The medicine doesn't seem to want to inject into my arm?? Does anyone have any idea why this would happen? It's a pretty new auto-injector and works fine for my other shot areas.

Thanks in advance for any ideas or tips!:confused:

http://i489.photobucket.com/albums/r...allwelcome.gif

Hi, and welcome to the MS forum. Sorry I can't give you advice on your arms--I'm on Tysabri and can't remember having problems with my arms when I was on the injectibles.

Good luck to you. Don't give up! :hug:

Hello....I'm a newby
 

Hello to you all!

I've been browsing this site for a couple of weeks now and felt a bit less lonesome, so thought I'd join. I'm amazed at the amount of support and compassion here.

In a nut shell, my condition started five months ago...was hospitalized for uncontrolled headache, double vision and seizures, within 7 days tremors started and by the time they discharged me, I couldn't walk properly. I've encountered various new symptoms such as spasms, pulsing nerve pain, tingling in the past months.

At first they diagnosed me with something called conversion disorder, but the psychologist I've been seeing is certain I have a neurological disorder. Back when I was hospitalized, the LP, Brain Mri/Mra were all negative. I've been in agressive PT for five months and my walking has gotten better, but still not normal...drop foot, tremors increased with physical exertion. Cognitively, I seem to be fine. I have been referred to the Mayo Clinic for testing and leaving in a few days. I'm scared, but anxious. Looking for the answers so that I can stare this monster in the face and tell him where to go. LOL! Really just needing answers so that I know what I am facing and can find reason in the things my body is doing. So happy to be amongst you people that are supportive and understand!

Welcome to NeuroTalk Butter. Nice to meet you. Please do join us anywhere. You will find a lot of support and friendship here.:)

New Member
 

Hi Everyone,

Was browsing the internet looking for information on painful injections (after a painful Betaseron injection) and came across this Board. Looked good, so I joined, and here I am! :winky:

I'm currently unemployed, a victim of the banking crisis, looking for my next position. My kids (2 girls, 7 and 9) call me a "clumser" when I stumble, lose my balance, or bang my head on something (clumser, as in one who is clumsy).; When I saw the "Stumble Inn", I knew I was home!

I was diagnosed with PPMS 18 months ago, but suspect I've had MS for about 40 of my 47 years. I'm looking forward to posting more, meeting all of you, and learning from everyone's experiences.

Hi Clumser and welcome to NeuroTalk! :welcome_sign: Sorry for the reasons you're here but you found the right place! Join right in, ask questions, share your ups and downs, give advice and just enjoy the company of friendly folks who share the same annoying disease. Hope to see you around the forums! :)

Welcome, Clumser..:) Yep you sound like you'll fit right in at the Stumble Inn.:p

Come on in and join us anywhere. Sometimes peeps are a little forgetful to come to this thread, but don't let that make you feel unwelcome, because you're Family now..:hug:

Hi Clumser,
Welcome! We love new members. We all understand your nickname, it's part of us too. Sorry to hear that you lost your banking position.

We're glad you found us. This is really a great place, lots of friendly people who learn from each other.

The Stumble Inn is for anything you want to talk about. A place where you can sit down, put your feet up and relax.
Nice to meet you.:)

Hi Im Jeannie, I am From Boston Ma but recently relocated to Florida :) Nice to meet you all <3

Hi Jeannie,
Welcome to NeuroTalk. I'm glad you found us. How do you like living in Florida after living in Boston? It's a big weather change.

Do you have any medical problems you would like to discuss with us. We are a very friendly group of people. :)

This part of NT is the MS forum. Do you have MS?- or being tested? You could tell us a little about yourself if you want, we love new people.

We have lots of new people, and some of us have been on here for years. Let us know if we can help you, or if you just want to talk.
Nice to meet you.