Hi my name is Cody I’m making this LFEBridge for Daxton James Coffen. Daxton will be two years old on July 28th He is the only child of Cameron”Shrimp” & Abby Coffeen from Utah. Daxton was born with GM1 Gangliosis this disease happens to 1 in 100,000 new borns. Unfortunately there is no meds or treatment for this and sadly it’s rare for children to live past two years old with this. GM1 Gangliosis is a genetic disorder that progressively destroys nerve cells in the brain and spinal cord. Cameron is a friend/coworker he works for Parker Drilling on a land rig out of Alaska. Abby is a stay at home mommy to Daxton. Cameron has to come home from work early often an he hasn’t worked in a month. Sweet Daxton can’t crawl, sit up , walk or talk an it’s hard for him to eat. He has had seizures that are happening more a more in the last three weeks. He is on oxygen full time. At this point Daxton is very ill an Cameron will not return to work for some time. Please find it in your heart to help in any way that you can so dad can stay home with family in this very difficult time and they don’t have to worry about eating, lights ext. Even if you can or can’t donate anything please keep sweet Daxton and his parents in your prayers thanks in advance.
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