Recent content by kcw082407

Do you think this could be adapted for a child to use? Our weather here is also bad, so we don't get out to exercise as much as we should, and in school, the kids only get 1 recess, but only if the weather is good.

My Kate is 2 1/2 and 32lbs. We have the smart vest, and we really like it. Through a friend, I acquired "the vest" that she uses at my mom's house (she stays there while I work). I like the smart vest more. The Cf clinic really didn't give us settings, we just experimented with what's...

My Kate is 2 1/2 and 32lbs. We have the smart vest, and we really like it. Through a friend, I acquired "the vest" that she uses at my mom's house (she stays there while I work). I like the smart vest more. The Cf clinic really didn't give us settings, we just experimented with what's...

My Kate is 2 1/2 and 32lbs. We have the smart vest, and we really like it. Through a friend, I acquired "the vest" that she uses at my mom's house (she stays there while I work). I like the smart vest more. The Cf clinic really didn't give us settings, we just experimented with what's...

My Kate is 2 1/2 and 32lbs. We have the smart vest, and we really like it. Through a friend, I acquired "the vest" that she uses at my mom's house (she stays there while I work). I like the smart vest more. The Cf clinic really didn't give us settings, we just experimented with what's...

My Kate is 2 1/2 and 32lbs. We have the smart vest, and we really like it. Through a friend, I acquired "the vest" that she uses at my mom's house (she stays there while I work). I like the smart vest more. The Cf clinic really didn't give us settings, we just experimented with what's...

Hi! KC has deltaF508 and 4218insT mutations with a 7T/9T polyvariant. The only info I can find is that there are only 3 other people with this mutation. I am wondering if this can be correct? She has the pancreatic insuff, had bad GI issues prior to enzymes, but doesn't have any lung symptoms at...

Hi! KC has deltaF508 and 4218insT mutations with a 7T/9T polyvariant. The only info I can find is that there are only 3 other people with this mutation. I am wondering if this can be correct? She has the pancreatic insuff, had bad GI issues prior to enzymes, but doesn't have any lung symptoms at...

Hi! KC has deltaF508 and 4218insT mutations with a 7T/9T polyvariant. The only info I can find is that there are only 3 other people with this mutation. I am wondering if this can be correct? She has the pancreatic insuff, had bad GI issues prior to enzymes, but doesn't have any lung symptoms at...

Hi! KC has deltaF508 and 4218insT mutations with a 7T/9T polyvariant. The only info I can find is that there are only 3 other people with this mutation. I am wondering if this can be correct? She has the pancreatic insuff, had bad GI issues prior to enzymes, but doesn't have any lung symptoms at...

Hi! KC has deltaF508 and 4218insT mutations with a 7T/9T polyvariant. The only info I can find is that there are only 3 other people with this mutation. I am wondering if this can be correct? She has the pancreatic insuff, had bad GI issues prior to enzymes, but doesn't have any lung symptoms at...

Hi! Sorry to hear about your twins, but, as everyone else has been saying, it does get easier. My daughter was diagnosed @ 6weeks. We had no idea we were carriers, and there's no family hx of CF. My daughter would just cry for hours after eating, had poor weight gain, weird BMs. She is now a...

Hi! Sorry to hear about your twins, but, as everyone else has been saying, it does get easier. My daughter was diagnosed @ 6weeks. We had no idea we were carriers, and there's no family hx of CF. My daughter would just cry for hours after eating, had poor weight gain, weird BMs. She is now a...

Hi! Sorry to hear about your twins, but, as everyone else has been saying, it does get easier. My daughter was diagnosed @ 6weeks. We had no idea we were carriers, and there's no family hx of CF. My daughter would just cry for hours after eating, had poor weight gain, weird BMs. She is now a...

Hi! Sorry to hear about your twins, but, as everyone else has been saying, it does get easier. My daughter was diagnosed @ 6weeks. We had no idea we were carriers, and there's no family hx of CF. My daughter would just cry for hours after eating, had poor weight gain, weird BMs. She is now a...