Re: Re: No Worse??/ Jan, Christi?

May 6, 2008

Jan, Christi,

I'm not sure you are the one who mentioned about being on the CPAP

machine but if so, please contact me at margaretbadner@...>.

I have been on my machine for 1 1/2 weeks now and it is nothing but

trouble for me, Every time the last few nights, it is ramping up

fine and I start to fall asleep I feel as if I am being suffocated.

When I called about it I was told that I am just probably breathing

through my mouth. I know I'm not - I am still awake! Someone is

supposed to come this afternoon to check the machine and I need to

know what to talk to them about. The last 2 days I have been in

terrible shape all morning but am a lot better by afternoon. Last

night I decided to not use the CPAP machine and I slept until 6 a.m.

and then had the same problem whenever I tried to fall back asleep

even without the machine.

Thanks so much, Margaret B

> oHMYGOSH--Chest pains..heart attack symptoms..God Bless You and what

> you went through!

>

> I read where websites all over say that Fibro usually doesn't

> worsen..but..I believe we are all living proof, that it is incorrect.

>>> I've got proper meds and I'm on the Cpac for sleep apnea. I think

>>> that has helped me a lot.

>>> I don't know why they think it can't get worse. A flare up

>> can

>>> include new spots for me. A flare up is also almost paralizing. I

>> can

>>> hardly move. Everyone is different though.

>>> Good luck, Jan

>>>

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