I made and maintain this site for children and parents living with cf.
There are hundreds of sites on the internet about cf , however , many are not written for kids and use a lot of medical terms.
I try to avoid that on this site.
Cystic Fibrosis patients are prone to transmit bacteria among each other.
Which was the reason to cancel nearly all social meetings like summer camps and get togethers.
The risk of getting a serious and dangerous bacteria is quite high when meeting person to person and the internet is a safe and great place to keep contact with each other.
Many children with cf might feel they are alone with this disease.
By means of this site i try to show them they aren't alone , as a matter of fact there are around 65.000 cfers world wide.
On this site you can find several pages to communication with other cfers.
Pictures can be send and will be placed on the picture pages , the secret page is a place to vent anger about having cf , or to talk about hidden fears.
Take a tour around this site and have fun.