Re: Re: Summary of BoardRESPONSE

[Guest guest]

I agree with Jan. Also, what makes this group unique is the friendships that

have devoped. If we just wanted CF information we could go to a research

site or medical website. At this e-group we are all here for each other. We

give each support and since many of us have been on this e-group for a couple of

years the familarity makes it nicer and allows us to " Joke " . I wouldn't trade

the warmth of this group for anyother list.

If you are looking for strictly information there are many sites. I like the

people here and the mix of information, experiences, articles, research and

support.

Just me 2 cents........

Rosemary in NY with 3 children (13, 11 and 7)

with CF. I have a dog named TOBI and have

coined the phrase " BREATHE DAMMIT "