Guest guest Posted December 29, 2006 Report Share Posted December 29, 2006 Hi, I was so happy today, cause I read yours welcomes. I'm a female too. I have 27 years. I live in Swietochlowice, its South Poland. I've got MS Relapsing-remitting. Right now, I don't have any symptoms. Sometimes I'm fatigue. When I've got a relaps, I have a paresis usually. Nice to meet you too! - (everybody:)) Beata > Hi Beata, > My name is , I am a female, and I live in Florida. I have MS. Nice > to > meet you. > > Hi, I'm new to this group. I would like to meet people with MS from all > the > world. I have MS since 1999, right now I feel well. My english language > isn't very well so I beg you for understanding > love Beata Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 29, 2006 Report Share Posted December 29, 2006 Hi, I still am limited to what I can do with my left hand but I always try. --- Beata Pladzyk wrote: > > Hi, > My every paresis was for my right side. It wasn't > funny for me cause I > couldn't do anything > Beata > > > > Hi, > > > > My name is Colleen and I'm 29 years old, I was > > diagnosed with MS in 2005. I have many different > > symptoms on my left side that prevent me from > doing > > many things but I'm still hanging in there. > > --- Beata Pladzyk wrote: > > > >> Hi, > >> I was so happy today, cause I read yours > welcomes. > >> I'm a female too. I have 27 years. I live in > >> Swietochlowice, its South > >> Poland. I've got MS > >> Relapsing-remitting. Right now, I don't have any > >> symptoms. Sometimes I'm > >> fatigue. When I've got a relaps, I have a paresis > >> usually. > >> Nice to meet you too! - (everybody:)) > >> Beata > >> > >> > Hi Beata, > >> > My name is , I am a female, and I live in > >> Florida. I have MS. Nice > >> > to > >> > meet you. > >> > > >> > >> > Hi, I'm new to this group. I would like to meet > >> people with MS from all > >> > the > >> > world. I have MS since 1999, right now I feel > >> well. My english language > >> > isn't very well so I beg you for understanding > > >> > love Beata > >> > >> > > > > > > __________________________________________________ > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 29, 2006 Report Share Posted December 29, 2006 what do you do? I do exercise. I just brought some yoga tapes and I'm going to try that. --- Colleen Mack wrote: > Hi, > > I still am limited to what I can do with my left > hand > but I always try. > --- Beata Pladzyk wrote: > > > > > Hi, > > My every paresis was for my right side. It wasn't > > funny for me cause I > > couldn't do anything > > Beata > > > > > > > Hi, > > > > > > My name is Colleen and I'm 29 years old, I was > > > diagnosed with MS in 2005. I have many different > > > symptoms on my left side that prevent me from > > doing > > > many things but I'm still hanging in there. > > > --- Beata Pladzyk wrote: > > > > > >> Hi, > > >> I was so happy today, cause I read yours > > welcomes. > > >> I'm a female too. I have 27 years. I live in > > >> Swietochlowice, its South > > >> Poland. I've got MS > > >> Relapsing-remitting. Right now, I don't have > any > > >> symptoms. Sometimes I'm > > >> fatigue. When I've got a relaps, I have a > paresis > > >> usually. > > >> Nice to meet you too! - (everybody:)) > > >> Beata > > >> > > >> > Hi Beata, > > >> > My name is , I am a female, and I live > in > > >> Florida. I have MS. Nice > > >> > to > > >> > meet you. > > >> > > > >> > > >> > Hi, I'm new to this group. I would like to > meet > > >> people with MS from all > > >> > the > > >> > world. I have MS since 1999, right now I feel > > >> well. My english language > > >> > isn't very well so I beg you for > understanding > > > > >> > love Beata > > >> > > >> > > > > > > > > > > __________________________________________________ > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 29, 2006 Report Share Posted December 29, 2006 Hello Beata My Names Kaveena. and I have Ben helping my close and best friend for years she Ben ill like 20 years . and good new we are going to The Mayo clinic to find out what Beverly got if she has Lime . We do live about 30 miles from Lime Connecticut where it Got its name . but there doing milen replacement therapy at the Mayo clinic. The Nightmare could be over and with Gods grace we will see .the mayo Clinic is like 750 Mile's In Minasota .up by canada and the grate Lakes . I have to find the best transportation bev cant have any magnets near her so Flying mite be hard we where thinking of a nice trane ride like a days traval. will keep eveyone posted I cant belive that there taking her we have had such bad luck out here in conneticut . Beverly being a RN P Most the dr I have sean dont know Much and thats not good so It will be gould to see some people that care. I think a cure is here now and being workek on. was told could be in three years so to every one that has some naro problems this is real good news. some of the things I have read about here have helpet . and people are like snowflakes no to are the same. something work for some some do not. But I hope to do something to help out. MY aunt had MS when I was young in the 1960s and shes 86 now. Re: Beata Pladzyk Hi, My every paresis was for my right side. It wasn't funny for me cause I couldn't do anything Beata > Hi, > > My name is Colleen and I'm 29 years old, I was > diagnosed with MS in 2005. I have many different > symptoms on my left side that prevent me from doing > many things but I'm still hanging in there. > --- Beata Pladzyk <sevillatlen (DOT) pl> wrote: > >> Hi, >> I was so happy today, cause I read yours welcomes. >> I'm a female too. I have 27 years. I live in >> Swietochlowice, its South >> Poland. I've got MS >> Relapsing-remitting . Right now, I don't have any >> symptoms. Sometimes I'm >> fatigue. When I've got a relaps, I have a paresis >> usually. >> Nice to meet you too! - (everybody:) ) >> Beata >> >> > Hi Beata, >> > My name is , I am a female, and I live in >> Florida. I have MS. Nice >> > to >> > meet you. >> > >> >> > Hi, I'm new to this group. I would like to meet >> people with MS from all >> > the >> > world. I have MS since 1999, right now I feel >> well. My english language >> > isn't very well so I beg you for understanding >> > love Beata >> >> > > > ____________ _________ _________ _________ _________ __ > Quote Link to comment Share on other sites More sharing options...
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