pmad925

KelliD,

I totally agree with you.

As much as it is the meds it is also the quality of life. I enjoy every day. . it will be five years in July when I was dx with MS, and it will be two years in August since my last flare up!!!! Knock on wood (lots and lots of wood). I have some fatigue, but I can deal and still tug along. I keep my own pace and don't keep up with anyone else but me.

It took my 1 1/2 years to accept this dx and the totally numb torso, arms and hands, and pain really was what changed me to accept this MonSter. Since then, I have change my outlook. I took control. I can finally tell people about MS and not cry. It is unbeliveable how many people know someone that has MS when I talk to them. Talking about it helps create awareness.

I have a great dr. . who listens and has a personality. I think that is a big plus for dealing also. He has allowed me to get off all meds except for Avonex. Of course, everyone is different and MS can effect everyone differently.

I am only 36 and have to much to do in my life time. . I will fight to keep me going!!!! I am don't let MS control my life. . I control of my life. I hope that people that read this will see there is hope and know that it can get better. I can see my difference which has really helped me.

Laugh loud and often and enjoy life to the fullest.

__________________
Paula (TN)