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I am 1 of the 5% without lesions

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    #16
    lets hope your wrong mean that lovely,i'm not trying to be offensive in anyway . i personally felt that all the responses were heart felt and truly caring . we all here seem to try to give are best reply from the experiences we have had with our ms. most of us aren't doctors no phd here. all of us I'm sure would say that we are a poor substitute for a neuro consult. we are here for support and to possible sure are experiences with this awful disease.
    I to hope that the original poster was not in anyway offended or discouraged from posting again. This is a wonderful place to go to for ms support but can't take the place of your doctor ever.
    dx.SPMS (baclofen,gabapenin,norco)
    started tecfidera 7/10/2013
    rituxan 11/13/2012 stopped due to side effect &it didn't help me (for RA and MS)
    copaxone started 4/2012 but stopped due to bad allergic reaction
    Matt.19;26 “With man this is impossible, but with God all things are possible.”

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