My problem is that I know DS will want to play on the playground equipment and last year I entrusted DS to my MIL and SIL because I'm on the walk committee with instructions to keep him away from the playground once it became a free-for-all and they didn't. Plus the local CF clinic actually encourages interaction between CFers "not an issue because none of their patients have cepacia" is what one of the doctors told us -- reason we don't go there anymore. So I got doubly nervous when the dietician made the comment about there being a LOT of kids there and she looked worried about it.
I also think about comments Kiwilady made in the adult forum a year or so ago. Prior to her getting cepacia she attended CF events and what sticks with me is her comment about sharing food -- digging into bags of unwrapped candy.... This year we've got donuts, pizza, cookies -- things that aren't individually wrapped. I think about park shelter with limited bathroom facilities -- is everyone washing their hands...?
I am going to feel weird about DS not being there this year. But just think it's probably for the best until he's a little older. We always have a bbq afterwards with friends, family and people from our walk team at our house afterwards. So they'll all get to see DS there.
I also think about comments Kiwilady made in the adult forum a year or so ago. Prior to her getting cepacia she attended CF events and what sticks with me is her comment about sharing food -- digging into bags of unwrapped candy.... This year we've got donuts, pizza, cookies -- things that aren't individually wrapped. I think about park shelter with limited bathroom facilities -- is everyone washing their hands...?
I am going to feel weird about DS not being there this year. But just think it's probably for the best until he's a little older. We always have a bbq afterwards with friends, family and people from our walk team at our house afterwards. So they'll all get to see DS there.