So here it is, the long awaited blog for Noah's Noggin. This is THE place (in fact the only place) to go for information on our lil'fighter. Want to know how he's doing? Come to the blog! Want to know how the family is doing? Come to the blog? Want to know the latest in Epilepsy? Come to our house or come to the blog. Want to know the latest on the race? Come to the blog. Want to know how many calories are in a Whopper w/cheese? Go to Burgerking.com or google it. This is all Noah all the time. This is actually a Blog that is all about our family: G, Amy, Owen and Noah.
This blog will give all our friends the latest not just Noah and Epilepsy, it will also chronicle how each of us is dealing with it. Right now, we are committed to building up Team Noah's Noggin for the Epilepsy Northwest Foundation's Walk For A Cure. Want to join our team? Just pop over to this link:
https://www.kintera.org/faf/search/searchTeamPart.asp?ievent=307541&lis=1&kntae307541=9BBC1AC53CBD4389B2D47E1071B1ABAB&supId=255156944&team=3399646
Just follow the directions. This is a Run/Walk so feel free to do both. I was going to gallup but then i decided to just sprint, before remembering that I cant, so now I am just going to jog. Our family has been so touched by the outpouring of support we have received from our family and friends since Noah's diagnosis. It has been a tough time for all of us but now we have to buckle down and focus on doing what we can for him. One way to start, is to donate to organizations that are actively looking for a cure and more effective side-effect-free medicines. Thank you in advance for signing up and/or your contribution. Words cant express our thanks but...thank you.
Until next time!
G
Love the name..."Noah's Noggin". Very cute. I look forward to hearing all about your triumphs and struggles...hoping the triumphs greatly outway the struggles. I am so impressed with my now all grown up cousin, and how she is taking this all in stride...at least, outwardly.
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