Originally Posted by xrayeyes
My name is Colleen, I was dx with MS in May 2007. Symptoms have gotten worse since Jan. 09. I had a relapse in Sept. 10 which resulted in me collectng disabilty from work and now SSD. I am currently doing cytoxan treatments and physical therapy. MS only effects my legs which are really stiff and require me to use a walker to get around. My family completely supports me but I still feel very alone and I am loking for people to connect with who understand how lonely MS can be.
Hi Colleen, my name is Kathy I have not been dx yet, but have alot of the systems. My nero thinks I may have ms, first mri I had a few brain lesion but spinal tap was neg. Just had another mri after five years and I have alot more lesion, not active. My biggest problem is my legs. Do you get pain in the bones in your leggs and they seem to get will stiff. It is called spascisity, I told my nero that is my worry is with my legs. How long did your legs take to progress to where they are now. I am so looking for some answers. Take Care Kathy