Hey ashes

Just to say I'm here for you..Try and take one step at a time. I think sometimes the not knowing is worse. If and when you know then you go from there. There is help and support here..and from your doctors..
Hang in there, let me know

Not knowing is worse I think. At least is was for me. I did have a period of relief, followed by a mourning period. Just know that we're here to support you.

Knowing will be a relief then you will know how to proceed. Just remember we are here for you!Annie

i always new in my gut it was MS but when the doctor confirmed it i started tearing up. good luck and just know were all here for you.

We're here for you.

Before I was diagnosed, I kept saying that I want to know what I have, if I have anything. I would say that I would deal with it if doctors would just ler me know what's going on with my body. If you get diagnosed, there are many medicines to help, so, don't be scared. I wish you luck for tomorrow, and stay strong!

What u see here is a collective that can't be found anywhere else. We are MS. We have the real thing. Sit down, go through your emotions, collect your thoughts. Then enter into the community where u are welcome. Cruise the
pages and bios to learn whose here and what their disabilities are.

Know that whatever the outcome, you are welcome here. Best wishes, Steve

Ashes,

My heart goes out to you - I think where you are is the hardest part. I was just diagnosed in August and I remember those days - I would cry worrying about the future. I just started treatment yesterday - shot didn't even bother me which was a surprise. I feel more optimistic than I have in months b/c I know I'm doing what I can about it. Try to let your husband be there for you - he's probably as scared as you are and you can comfort eachother. Hang in there! -Diane

Hi ... please know that there is a large group of people here that were in your shoes at one point. We are here and will send prayers and angels with you as you get your results.