Copyright 2007-2011 Kimberley Woodhouse

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No Safe Haven Book Trailer

Friday, July 25, 2008

Extreme Makeover: Home Edition

Our episode of EM:HE will air again this Sunday, July 27, 2008 on ABC.

I'd like to take a moment to thank all of the thousands of wonderful people who nominated us over the years for the show. When we heard about the nominations, tears flowed... abundantly.

God is so good. Through Josh's life and death hopitalizations. Through Kayla's trials and triumphs with her disorder. Through her brain surgery and recovery. And through the day to day challenges we've faced, God is so good. And He will continue to be.

This experience has changed our lives in many, many ways. Kayla's health has skyrocketed in the time we've been in our new home, and Josh hasn't had one incident with his asthma. I don't have to take Kayla's temp all the time inside our home. And as we are in the hot months, spending time inside is never boring. :)

Thank you to our wonderful community, Colorado Springs. Thank you to Premier Homes. Thank you to all of you who gave of your time, money, effort, gifts, products - the list could go on forever. We are so very grateful to all of you.

I've received cards, notes, and emails from thousands of people - telling me that this experience changed their lives. Let me say, that we feel so very blessed by all of YOU. And we want to thank YOU.

David Phelps - performs my favorite song - THAT'S WHAT LOVE IS - on our episode. His generosity and love never cease to amaze me. He is an incredible person - I hope you all check out the page on this website about him, and go to his website as well!

Heat Relief Depot - provides the cooling vests that you see Kayla wearing, and have made it possible for her to get out of the house occasionally. Their information is on the Kayla's Story page, as well as the Links page.

Gift of Pain - is the foundation that has helped our family numerous times over the years. Gabby's parents are the ones who started the foundation, and their hope is to help all the families out there who deal with this very rare disorder on a day to day basis. Thank you for your support - and to all of you who have given over the years to help provide for the medical needs. Their info is also on the Kayla's Story page and the Links page.

Thank you. Thank you. Thank you. And praise God from Whom all blessings flow.

God Bless You All!