Lymes disease

[Guest guest]

Seen the news today that the US gov have addmitted

they have Lymes disease as a biological weapon.if they

also have MS as a weopon they must know what the cure

is! Xx

--- mscured

wrote:

> Kaveena,

> She is seeing a " Lyme Literate " doctor, right?

>

>

> -- Re: Beata Pladzyk

>

> 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

> >>

> >>

> >

> >

> > ____________ _________ _________ _________

_________ __

> >