Friday, August 19, 2011


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. is up to the parents, family, friends and people living with Cystic Fibrosis to fund this research. 

What can I do? 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

Otherwise, send your birthday cards on over to the Big Island

Caleb Meyer
PO Box 383173
Waikoloa, HI  96738


  1. Hi Missa
    I am also a mother of a 3 years old CF boy, Alon. I noticed in one of your posts you mentioned that your boys get Pulmozyme. Our doctor wants Alon to start taking it, but I read a lot against it. Through your blog I get the impression that you really look into things, so could you please share with me the pros and cons that eventually led you to treat you boys with Pulmozyme?
    Thank you so much for sharing all you do,

  2. Hello Noa,
    I would love to talk, just e-mail me