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I agree with Tonya...my son is 2 and loves playing with me or dad during his vest time. I have some toys and activities that he only does while using the vest. I keep them in small bins and he usually tells me what he wants to play with. Right now he loves playdough. He's also enjoyed cutting...

I agree with Tonya...my son is 2 and loves playing with me or dad during his vest time. I have some toys and activities that he only does while using the vest. I keep them in small bins and he usually tells me what he wants to play with. Right now he loves playdough. He's also enjoyed cutting...

I agree with Tonya...my son is 2 and loves playing with me or dad during his vest time. I have some toys and activities that he only does while using the vest. I keep them in small bins and he usually tells me what he wants to play with. Right now he loves playdough. He's also enjoyed cutting...

I agree with Tonya...my son is 2 and loves playing with me or dad during his vest time. I have some toys and activities that he only does while using the vest. I keep them in small bins and he usually tells me what he wants to play with. Right now he loves playdough. He's also enjoyed cutting...

I agree with Tonya...my son is 2 and loves playing with me or dad during his vest time. I have some toys and activities that he only does while using the vest. I keep them in small bins and he usually tells me what he wants to play with. Right now he loves playdough. He's also enjoyed cutting...

Have you tried using the EMLA cream? One of my kids tried it and he didn't feel the needle at all. He was so relieved!

Have you tried using the EMLA cream? One of my kids tried it and he didn't feel the needle at all. He was so relieved!

Have you tried using the EMLA cream? One of my kids tried it and he didn't feel the needle at all. He was so relieved!

Have you tried using the EMLA cream? One of my kids tried it and he didn't feel the needle at all. He was so relieved!

Have you tried using the EMLA cream? One of my kids tried it and he didn't feel the needle at all. He was so relieved!

Lindsay, I can respond to your questions from a parent's point of view. My son is only 2 so who knows what his future will be like w/regards to cf, but right now he is PS and his only regular treatment is using the vest daily. I think everyone's issues are a bit different, so I just feel...

Lindsay, I can respond to your questions from a parent's point of view. My son is only 2 so who knows what his future will be like w/regards to cf, but right now he is PS and his only regular treatment is using the vest daily. I think everyone's issues are a bit different, so I just feel...

Lindsay, I can respond to your questions from a parent's point of view. My son is only 2 so who knows what his future will be like w/regards to cf, but right now he is PS and his only regular treatment is using the vest daily. I think everyone's issues are a bit different, so I just feel...

Lindsay, I can respond to your questions from a parent's point of view. My son is only 2 so who knows what his future will be like w/regards to cf, but right now he is PS and his only regular treatment is using the vest daily. I think everyone's issues are a bit different, so I just feel...

Lindsay, I can respond to your questions from a parent's point of view. My son is only 2 so who knows what his future will be like w/regards to cf, but right now he is PS and his only regular treatment is using the vest daily. I think everyone's issues are a bit different, so I just feel...

Lindsay, I can respond to your questions from a parent's point of view. My son is only 2 so who knows what his future will be like w/regards to cf, but right now he is PS and his only regular treatment is using the vest daily. I think everyone's issues are a bit different, so I just feel...

We were told by a genetic counselor and our cf clinic that one of our son's mutations (R117h/7T) would most likely result in mild cf symptoms. But that there is no guarantee. We reached our diagnosis through prenatal screening which is becoming more common.

We were told by a genetic counselor and our cf clinic that one of our son's mutations (R117h/7T) would most likely result in mild cf symptoms. But that there is no guarantee. We reached our diagnosis through prenatal screening which is becoming more common.

We were told by a genetic counselor and our cf clinic that one of our son's mutations (R117h/7T) would most likely result in mild cf symptoms. But that there is no guarantee. We reached our diagnosis through prenatal screening which is becoming more common.

We were told by a genetic counselor and our cf clinic that one of our son's mutations (R117h/7T) would most likely result in mild cf symptoms. But that there is no guarantee. We reached our diagnosis through prenatal screening which is becoming more common.