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This dove  will always be  a part of this web site as a remembrance for those who lost the battle with cf .
- - - Welcome to Cystic Fibrosis for KIDS !!! :) - - -


I am your host my name is William. 

Just like you I have Cystic Fibrosis. 

I know that much of Cystic Fibrosis that all the people I know call me Dr.Bob .

On the next pages I'm going to tell you everything I know about Cystic Fibrosis.

The good thing is , I'm not going to give you shots, IV's or anything so come along and follow me.

Dr.Bob has many, many friends on the internet, and 3 nurses that help me with everything i don't know (even a doctor doesn't know everything).

I'm William and I live in The Netherlands.

That country is located between Germany and Belgium, look on a world map for that .

I'm a 39 years old man and have 1 brother with Cystic Fibrosis and 1 sister without it.

Sometimes I really wish I didn't have Cystic Fibrosis and I bet you feel the same.

Still I know it will never go away, no matter how hard I wish.

WELCOME TO YOUR OWN WEBSITE , CLICK ON THE BUTTONS BELOW.





email dr bob Go to the Funstuff chapter Go to the support  chapter Go the the Cystic Fibrosis Chapter


Site updated 29-01-2004








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