Just Popping My Head In

[Guest guest]

Um one of the other sites I was at recommended me joining you guys. Unfortunately I'm whooped! So I signed up and can't wait to get your email and by the way I am 46 years old, married 21 years with two teens and I have had CFS/ME since 1998. I no there is no cure, but something has gone desperately wrong and I feel as if I'm going to be winding up in a wheelchair like some I have heard about. Love and Blessings~~B4cjcll

[Guest guest]

Hello Beauty,

Sorry you have to be here, and I hope this group can give you some

idea of where to go with diagnosis and treatment. Obviously, from the

name of this group we have found that our cfs/me is from chronic,

severe infections. The bacteria involved actually can be found inside

white blood cells or hypernating in a cyst form that the immune system

cannot attack. Thus the immune system is overactive, you feel sick

forever, but the bacteria just continue to thrive.

If you don't mind tell us the area of the country where you live I

might be able to come up with a doctor to see who could begin to find

out what your underlying problems may be and a possible treatment

approach.

a Carnes

Las Vegas, NV

>

> Um one of the other sites I was at recommended me joining you guys.

> Unfortunately I'm whooped! So I signed up and can't wait to get your

> email and by the way I am 46 years old, married 21 years with two

teens

> and I have had CFS/ME since 1998. I no there is no cure, but

something

> has gone desperately wrong and I feel as if I'm going to be winding

up

> in a wheelchair like some I have heard about. Love and

> Blessings~~B4cjcll

>