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Showing posts from December, 2011
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On the way to granting Hawke's wish. Thanks rainbow connection!

Hydrocephalus faces

Hawke is in the running to be the "Face of hydrocephalus". Drawing is early January. Neat to see all the faces submitted, just a sample of all the children and families effected! http://www.hydrocephaluskids.org/images/theboys.html Sent on the Sprint® Now Network from my BlackBerry®

Rainbow connection

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Hawke has been granted a wish to Disney World. Praying he continues to have good days as the trip is nearing. No flying, we don't want to take any chances with pressure on his head as many have complained of this. We get to stay in a village for children with life threatening conditions. This trip is such a blessing particularly after a year with 9 brain surgeries. Praising God for all things and thanking the rainbow connection! Tomorrow is not a guarantee or entitlement, every day is a gift.

Prayer

Please pray for Willow, our friends daughter whom is fighting hydrocephalus some of her recent posts: Spending the last hour of my birthday in ER Thinking it is still ear infection but doc said to go in They are going to order a CT scan to make sure it is not shunt related her ventricles are slightly enlarged from her mri a month ago. We are going to be admitted here tonight, her temp has also gone up. :( Sent on the Sprint® Now Network from my BlackBerry®

Loven's

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