I agree on the exposing Cf kids to germs etc. BUT......Reece has a very severe case. His doctors are very concerned & are looking out for his well being! His CT scans, PFTs, charts & X Rays are being sent to UNC for them to look over to see what can be done next. Every CFer is DIFFERENT. Reece lungs well, his one lung that is halfway functioning needs to stay as healthy as possible! So if that means keeping him home to be homeschooled thats what we are gonna do!
Yes, I want him to have a "normal" childhood, but I also want him around to be able to enjoy his childhood. Reece is my world, I am gonna do what I think is right for him. Ive seen it one here before, it is sooooo different when you are a parent to a CFer! You see things in a different light.
Emily, how is going to school "good for him" if hes in the hospital every 1-2 months? Thats NOT normal. And you cant compare to what you did & didnt do to todays Cfers. Germs are different, the kids are different etc. So what worked 15 years ago isnt gonna always work today.
PS~ For the record I am NOT saying any of these things in an ugly tone, just standing up for what I believe. Just like Emily & the others think is their opinion.
Yes, I want him to have a "normal" childhood, but I also want him around to be able to enjoy his childhood. Reece is my world, I am gonna do what I think is right for him. Ive seen it one here before, it is sooooo different when you are a parent to a CFer! You see things in a different light.
Emily, how is going to school "good for him" if hes in the hospital every 1-2 months? Thats NOT normal. And you cant compare to what you did & didnt do to todays Cfers. Germs are different, the kids are different etc. So what worked 15 years ago isnt gonna always work today.
PS~ For the record I am NOT saying any of these things in an ugly tone, just standing up for what I believe. Just like Emily & the others think is their opinion.