We continue to hold the Nord family in our hearts and prayers. Ann and Jeremy Nord along with their daughter Hannah (Caleb's sister) are champions in the advocacy for Caleb's recovery. His ability to rebound to the extent he has is testimony to the amazing ability his parents have in understanding this very complex and complicated illness and therefore making the best decisions for Caleb going forward.
Happy 7th anniversary through trying times for Ann and Jeremy Nord.
Two year old little boys deserve to be healthy and read to their dogs like Caleb is doing right here. So let's keep up those prayers and believe in the power of prayer in helping Caleb through this new treatment....
This 2 year-old boy, Caleb Nord, is still receiving chemotherapy and steroid treatments to enable his body to go into remission.
Caleb's Mommy, Ann Nord, does a fantastic job updating on www.caringbridge.org/visit/calebnord but she has been sick and isolated from the family for about a week. She is slowly regaining her strength from a bad flu and will update the site soon.
Please include Ann in your prayers for her recovery and regaining of her strength.
There is a foundation organized by parents of HLH children called Liam’s Lighthouse at LiamsLighthouseFoundation.org and on Facebook. Since February is Rare Disease Month over 100 parents and volunteers of Liam’s Lighthouse Foundation will be outside the Today’s Show in NYC on next Tuesday, Feb 28th, 2011 publicizing awareness for HLH. This organization will be holding a picture of Caleb along with many other children affected by HLH.....
A very sick 2 year boy named Caleb Nord
Posted - Feb 17 2011 : 4:35:19 PM
