Hey everyone I'm new! I am 21 years old with Cystic Fibrosis,
diagnosed at birth. I have the Delta F508 mutation, I should join
the club right <img src="i/expressions/face-icon-small-smile.gif" border="0"> and also W1282X mutation. I know that the second
one is a rare mutation. Does anyone else have this one? I wanted to
tell everyone about a search engine that I came across while
reading a Self magazine a few months back. The magazine mentioned a
search engine: http://www.goodsearch.com where every time you
search the web it donates a penny to a foundation or organization
of choice. Go to the site and type in Cystic Fibrosis on the bottom
box and then click verify. There are several different Cystic
Fibrosis organizations to choose from. Then in the top box type in
your search. Every penny can go a long way. Spread the word! <img src="i/expressions/face-icon-small-smile.gif" border="0">
diagnosed at birth. I have the Delta F508 mutation, I should join
the club right <img src="i/expressions/face-icon-small-smile.gif" border="0"> and also W1282X mutation. I know that the second
one is a rare mutation. Does anyone else have this one? I wanted to
tell everyone about a search engine that I came across while
reading a Self magazine a few months back. The magazine mentioned a
search engine: http://www.goodsearch.com where every time you
search the web it donates a penny to a foundation or organization
of choice. Go to the site and type in Cystic Fibrosis on the bottom
box and then click verify. There are several different Cystic
Fibrosis organizations to choose from. Then in the top box type in
your search. Every penny can go a long way. Spread the word! <img src="i/expressions/face-icon-small-smile.gif" border="0">