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Incredibly stressed about the whole chemo treatment that I am probably going to be doing. I have an appointment with the Cleveland Clinic March 17th so I am hoping they will ease my mind a bit. Never did I think chemotherapy was a treatment option for MS, as im sure no one else has heard of it either unless they experienced it. I try to be positive always but I will tell you what, it has been hard the last couple days with all of this new info. We found a doc on the clinics site which isnt exactly the same dosage as what my doc mentioned (she mentioned one treatment a month, this doc is for a week straight) but if you want to be depressed please do read, it worked well to depress me but if the Clinic thinks its what I should do instead then we will see what happens. Just don't freak out, like I did, because hopefully I only need once a month not 5 days straight... http://www.clevelandclinic.org/health/health-info/docs/0300/0378.asp