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We are all pulling for your son on this list, ! The frustrating part of

suddenly

becoming the parent of a rather ill child with cystic fibrosis is that anyone

who is

even slightly motivated wants to know it ALL NOW, but our children are unique

and

it takes time.

We learn by increments, some of us in more or less organised fashion, some more

by emotional reaction and some by both. The important thing is that we SHARE

what

we think we have learned. I happen to think that this is the place to do it.

Many of us on this list also belong to a research group,

sharktank ;

it is unmoderated, but I usually post to geo@... and that is how I joined

after

hearing about that list. You can check it out at yahoogroups and view its

criteria and

see whether you might like to join that one as well; many here have done so.

But for now, I will just put my own energy into high hopes for your little guy!

Love to all in your family, , and to you yourself!

n Rojas

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