It is time for another party...WOOT WOOT!!!!
Caleb is turning 4 in the month of September and we have a huge wish for our youngest child.
What is that wish?... you ask :)
That we will never ever, ever have to have a talk with him about his life expectancy due to having Cystic Fibrosis.
How can that happen?.. you ask :)
In order for us to never ever, ever have to have THAT talk, we NEED lots of prayer and a cure, of course! The problem is, that the government does not fund the research for that cure. So....it is up to the parents, family, friends and people living with Cystic Fibrosis to fund this research.
What can I do?....you ask:)
You can make the birthday month of September for Caleb one he will never forget. Send him a card wishing him a happy birthday and place just $1 in (more is always excepted). The card will go up on our birthday wall and the $$$ will be sent to the Cystic Fibrosis Foundation.
If you wish to donate virtually, you can go directly to the Cystic Fibrosis Foundation or you can head over to PAYPAL and enter our e-mail address firstname.lastname@example.org.
Otherwise, send your birthday cards on over to the Big Island
PO Box 383173
Waikoloa, HI 96738