In Support of Jackson Schimmel
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Jackson Schimmel is one in a million in our hearts, and has been diagnosed with a very rare genetic disorder that only affects about one in a million people.
This means Jackson's little body lacks the enzyme required to break down sugars at a cellular level. This explains Jackson's frequent illnesses, gross motor delays, scoliosis, craniosynostosis, etc. Left untreated, Jackson will decline cognitively. He will lose the ability to walk, the ability to speak, and more.
Jackson will be receiving a bone marrow transplant to help reverse some of the symptoms and receive the enzymes he needs in order to stop the cognitive decline. Our sweet boy will have to undergo chemo to get rid of his existing cells in order to receive the new. This will require Jackson’s family to relocate for 4-6 months so he can get the needed treatments and care.
Jackson’s family could use a little help to pay for medical bills and cover some everyday costs during this challenging time. We truly appreciate any support you can offer!
Updates
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- Created Aug 20, 2026
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Support Registry
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Words of Support
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Cynthia 3 days ago • with donation
Anonymous 4 days ago • with donation
Kelly Rukavina 4 days ago • with donation
Alicia Penniman 5 days ago • with donation
Liz Searcy 5 days ago • with donation
MARY E HENDERSON 5 days ago • with donation