Recent content by gocamping2

I'm no doctor and I'm still fairly new to this CF stuff but that seems really odd to me that you're on your 3rd sweat test and that was a couple of days ago and also they couldn't confirm from the first 2 tests ( unless they couldn't get enough sweat). We got my son's confirmation on the sweat...

I'm no doctor and I'm still fairly new to this CF stuff but that seems really odd to me that you're on your 3rd sweat test and that was a couple of days ago and also they couldn't confirm from the first 2 tests ( unless they couldn't get enough sweat). We got my son's confirmation on the sweat...

I'm no doctor and I'm still fairly new to this CF stuff but that seems really odd to me that you're on your 3rd sweat test and that was a couple of days ago and also they couldn't confirm from the first 2 tests ( unless they couldn't get enough sweat). We got my son's confirmation on the sweat...

I'm no doctor and I'm still fairly new to this CF stuff but that seems really odd to me that you're on your 3rd sweat test and that was a couple of days ago and also they couldn't confirm from the first 2 tests ( unless they couldn't get enough sweat). We got my son's confirmation on the sweat...

I'm no doctor and I'm still fairly new to this CF stuff but that seems really odd to me that you're on your 3rd sweat test and that was a couple of days ago and also they couldn't confirm from the first 2 tests ( unless they couldn't get enough sweat). We got my son's confirmation on the sweat...

Something similar was once said to me, but it was different because it was from a co-worker, who is mother of a cancer patient (in remission), so she lives with the same kind of fear and dread that we (CF parents) do. As rude as the comment was, I am grateful because that I know to live...

Something similar was once said to me, but it was different because it was from a co-worker, who is mother of a cancer patient (in remission), so she lives with the same kind of fear and dread that we (CF parents) do. As rude as the comment was, I am grateful because that I know to live...

Something similar was once said to me, but it was different because it was from a co-worker, who is mother of a cancer patient (in remission), so she lives with the same kind of fear and dread that we (CF parents) do. As rude as the comment was, I am grateful because that I know to live...

Something similar was once said to me, but it was different because it was from a co-worker, who is mother of a cancer patient (in remission), so she lives with the same kind of fear and dread that we (CF parents) do. As rude as the comment was, I am grateful because that I know to live...

Something similar was once said to me, but it was different because it was from a co-worker, who is mother of a cancer patient (in remission), so she lives with the same kind of fear and dread that we (CF parents) do. As rude as the comment was, I am grateful because that I know to live...

Wow! is all I can say. I found this web totally by accident looking for information on "vests" for the near future for my 16 month son that has CF (DF508/DF508). I knew that there were support sites and "groups" for CF, but who has time for that when you have a new baby and the world is now...

Wow! is all I can say. I found this web totally by accident looking for information on "vests" for the near future for my 16 month son that has CF (DF508/DF508). I knew that there were support sites and "groups" for CF, but who has time for that when you have a new baby and the world is now...

Wow! is all I can say. I found this web totally by accident looking for information on "vests" for the near future for my 16 month son that has CF (DF508/DF508). I knew that there were support sites and "groups" for CF, but who has time for that when you have a new baby and the world is now...

Wow! is all I can say. I found this web totally by accident looking for information on "vests" for the near future for my 16 month son that has CF (DF508/DF508). I knew that there were support sites and "groups" for CF, but who has time for that when you have a new baby and the world is now...

Wow! is all I can say. I found this web totally by accident looking for information on "vests" for the near future for my 16 month son that has CF (DF508/DF508). I knew that there were support sites and "groups" for CF, but who has time for that when you have a new baby and the world is now...