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Thanks, This seems like a good place. I also belong to an MSN group called

CysticFibrosis2Chat many people there have CF and many are parents of CFers. I

think maybe 1 or 2 who have CF and have kids with CF too. Well, I hope to get

good info here too. Maybe I can even help some people :)

, new member!

Welcome aboard to perhaps the most interesting and supportive place

in cyber space for those with children with cf and those with cf; I fall in

both categories. I think you will really find this list very rewarding. It

is

as good as it is because people like you join us. Thank you,

n Rojas, wcf, CFRD, mom of 3 adults,. youngest wcf, too

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