Samuel’s Famous…well, almost…
November 7, 2008 | Updates
When we were in the PICU at Primary Children’s Hospital 3 1/2 years ago, we were in a room right next to a wonderful family and the cutest little boy named Parker. Parker is the kind of kid that wraps you around his finger in a heartbeat. And his family is great. Parker has one tiny extra chomosome that, in my honest opinion, makes him even cuter and more loveable than the rest of us. Parker’s mom is the managing editor at an awesome site called “5 Minutes for Special Needs” and we’ve been asked to be a guest blogger there each Friday through the month of November. Cool, huh?!
So, run on over there by clicking the button below and enjoy the first post of us introducing ourselves to them. And then take a moment to pray for little Parker or visit his site to give his family encouragement as he is right now undergoing the third surgery needed to complete his “teeny, tiny, designer hiney.” If you have no idea what I’m talking about, you’ll just have to go visit his site. He’d love to have you there!
Love,
The Jewkes
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November 7th, 2008 at 7:51 pm, Karen Says:
I stopped by from 5 minutes for special needs to say hi.
November 7th, 2008 at 9:02 pm, Caradie & Corbin Says:
I go check on Parker from time to time. He sure is a dollie.
Caradie & Corbin
November 7th, 2008 at 10:58 pm, Bobbi Says:
Hi, I found your site from five minutes for special needs. Your little boy is adorable and I am so glad that he is alive. I can’t imagine what you and your family went through. I will keep you all in my prayers. I hope you can visit my blog if you get the chance. I have a little boy named Parker who has autism. I also know who the other Parker is. I want to say that I can’t imagine going through what you are going through but I know it won’t help. Maybe as I read your blog, you could let me know what to say. Bobbi
November 9th, 2008 at 9:51 pm, Erin Amundsen Says:
Just stopped by to see how you guys were doing. I’m so sorry that Samuel has been having a hard time. I hope that something will start working for him again soon. Colby and I will keep you and your family in our prayers.
November 25th, 2008 at 1:02 pm, Suzi Searles Says:
Keep hoping to see an update. Wondering how Samuel’s seizures are doing? Have they calmed down yet? Hopefully no more Dr. visits.
Suzi Searles