Stephanie- What a great website you have and I think it's great all of the fundraising and education you do. It helps not only your daugher, but so many kids who might not have a parent as great as you! Sarah

I have a little girl alll though she hates it when I call her that.She is 19 and till here a few mo ago we had a real hard time getting her to do like the dr.told her to do.She doesn't live at home anymore and thinks she knows all about life.She went for a dr visit and he told her that if she didn't start doing like she is supost to be doing not only is she going to kill herself but her baby to.Her father and I have been divorced for 15 years and the kids really got the raw end of the deal I feel like the reason she wasn't doing like dr said is because she wanted to have a family of her own one day and her father and everyone one on his side of the family kept telling her that she could never have a baby when she would talk to me about it I would tell her yes she could but it would be high risk and she would need to talk out all the pros and cons with her dr after she got out of school and on her own and was staying healthy.Well she got out of school ,got her own place,and was trying to be healthy because she askd her dr if she was able to have a baby and he told her the same thing that I'd been telling her all these years.So now her baby is due Nov.12.at the med in Memphis,Tn. Sorry all I talked about was my daughter but I don't know anyone else around who has a child whith C.F. that would even know the heartache, and tears that we shead for our baby for all the pain they have to go through.All my best wishes and prayers for your family. Angel

I really enjoyed reading your guys website. I hope all the best for faith. My little guy dylan is 4.5 years old and he has severe cerebral Palsy and a host of other disabilities. I have a special understanding of being a parent of a child with special needs, it changes your entire life. These little ones can be and are very inspiring to all those who come in contact with them. I wish Faith all the best and I am glad I had a chance to learn a little about her.

The dinner was great. It was nice to meet you and other moms who are going through the same things. Being new to the CF family, I really needed some reassurance! See you at the walk.

awe cool site how is she doing that is an awesome photo. i miss the family so much.well cath u on my space rrrrrrrrr