Re: Viral link to ME/CFS & Australia's Blood Service

[Guest guest]

Has anyone heard of cfs/me being heriditary or genetic?

I wondered about the same with fibro/cfs.

Often my daughter will call me on a cool/cold damp day and complain

of the same symptoms I'll be having at home that very day.

The next day will be sunny and both will be fine. She's 35 and doesn't

want to admit the fact it's possible she may have fibro, but has SO MUCH

pain. Doesn't have good insurance so

isn't able to see a specialist.

Now obama has made it so I'm unable to get two of my meds that help the

most and I have to ask my

physcian to figure something out another meds. I know, at least I have

something.

I'm thankfull for that.

fluff

[Guest guest]

It seems odd to assume that whatever contaminant ME

people might have, will disappear " when we recover fully. "

- B.

[Guest guest]

They don't know for a fact but say it does run in families....Lynn

>

>

>

> Has anyone heard of cfs/me being heriditary or genetic?

> I wondered about the same with fibro/cfs.

>

> Often my daughter will call me on a cool/cold damp day and complain

> of the same symptoms I'll be having at home that very day.

>

> The next day will be sunny and both will be fine. She's 35 and doesn't

> want to admit the fact it's possible she may have fibro, but has SO MUCH

> pain. Doesn't have good insurance so

> isn't able to see a specialist.

>

> Now obama has made it so I'm unable to get two of my meds that help the

> most and I have to ask my

> physcian to figure something out another meds. I know, at least I have

> something.

>

> I'm thankfull for that.

>

> fluff

>

[Guest guest]

I have a sister that also has it. she's still in denial and pushing herself to

the limit. She was addicted to narcotics and has ben clean 5 months and she is

afraid they cant help her!

DebbieG

________________________________

They don't know for a fact but say it does run in families.... Lynn