I don't know if this would truely help one million peope this year, but to me, in my heart and mind it would. Because any time you truely give selflessly of yourself, for no other reason than truely, "just to help" the blessings of it goes futher than you can see.If there's a way to encourage everyone to reads this to share this story with even a handfull of their friends...it could help so much.I know of two families, with sick children, who need litterally help. Prayer. Love. Compassion and mercy.

Nathan's site;www.contrerashome.us

Article about Kaylee Maze(10yrs) and her sister(8 yrs) both with cystic fibrosis..

http://www.maysville-online.com/articles/2007/06/17/local_news/2476maze.txt

Dear friends,
This is my first time in here, I just joined today. I have a son Nathan that is almost 2 and a half. He was diagnosed at 10 weeks old with cystic fibrosis. Since then, he's been hospitalized 13 times and had 4 surgeries. including having a g-tube place. (feeding tube)
He's a true miracle and blessing from God and we love him so much. He developed a oral aversoin to food due to some misinformation we received for 6 months from his medical care providers. So it's very sad because it didn't have to happen. We changed his CF team and hospital, and that first day (in Jan of '06) they were able to correct one of the biggest problems we'd had. So that was wonderful, but unfortunately damage had already been done, and as of today, he hasn't eaten /swallowed solid foods for 1 and 1/2 yrs....he gets all his nutrition from the tube feedings, and it's just incredibly sad. So one of the # one things we desperatey need it feeding therapy for him, and to be able for us to afford it consistantly. My husband works f/t and makes a middle income living which under normal circumstances would be enough. But things have been incredibly stressed, and just on May 20th, I just miscarried a baby boy. That was our 3rd miscarriage, so now at the end of July I am going in for a partial hystorectomy. So just in general please pray for our finances, mercy and help form Nathan's web site where there's a pay-pal if people want to know more about him and can donate if possible. But the #1 thing is to pray. His co-pay's just for his medicine each month is around 500, and then we owe over 50,000 in medical bills for him alone, (not to mention the miscarriages, or this up coming surgery)We need more than honestly than any one person could supply. So please share this prayer request with others...
The other link is to a woman that has two daughters with cystic fibrosis also. But one of her daughters is in a really bad situation, and now hospice is there taking care of her, and they haven't given her much time. So her family is doing an incredibly kind and thoughtful gesture for their daughter, and invited the whole community where they live in Kentucky out to celebrate little Kaylee's life. PLEASE pray for this family. Their hearts must be full of so much pain and sadness, they are trying to make the most of every day they have with her..even though they know she's going to a better place, thier hearts have got to be breaking. She's SO SWEET and SO young....this touched my heart so deeply because she has what my son has...and his is bad too, and we were told by his doctors at that time, when he was 10 months old that they didn't think Nathan would live to be 10....but we don't beleive that, and are trying to stand on the Word..honestly my husband's been better at that lately than I have been. But still I just know God is faithful.
Please pray for miracles in both our lives. Our family and sweet little Kaylee's life. If there's ANYTHING you can do to reach out to her family, rather prayer or finacially, helping them in any practical way at all...please do. Please share Nathan's web site with others, and this little article about Kaylee. CF is a terrible disease, and I know that Christ is a healer. Please pray. This is incredibly important.
I appologize for taking up so much of your time.
God bless you all deeply.