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Re: a cf mom-you are not alone

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I know how you feel. You are strong, cope well and are positive but at times

chronic life just gets to you. For some reason the strong aren't allowed

time to " crash " we must go on! Its tough. We take care of everyone and I think

burn ourselves out. Emotionally CF is draining. Especially now as kids get

older and ask more intense questions.

You are not alone. I have never been in a Chat room. If you figure it out

tell me!

Rosemary in NY with 3 children (13, 10.6 and 6.6)

with CF. I have a dog named TOBI and have

coined the phrase " BREATHE DAMMIT "

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there is a very friendly chat room at <A

HREF= " http://groups.msn.com/CysticFibrosis2chat/messageboard " >

http://groups.msn.com/CysticFibrosis2chat/messageboard</A>

This is an MSN group that is very helpful and inviting as well and they have

two scheduled chat times per day. They are very easy to talk to and seem very

informative as well. I havent been on there except when the baby was in the

hospital cause i just dont have a lot of time to chat but I know they are there

if I want to talk.

Marie, mom of 3 youngest wcf

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