Jaxon’s Journey

Jaxon has been diagnosed with Aplastic anemia and Short Telomeres syndrome. Both very rare in young children. He is scheduled to be admitted on April 17 to begin his journey with chemotherapy and a bone marrow transplant. The red and white blood cells are unable to produce correctly, causing severe complications of anemia and premature aging of his organs with extreme effects on his physical health. The Short Telomeres syndrome is extremely rare, with no known treatment or cure available. Clinical studies are ongoing. Preliminary tests will start March 24th. Electrocardiogram and CAT scans are required to insure Jaxon is strong enough to go through with the procedure. There are two donor’s available, in case the first is unsuccessful. Jaxon will have to spend 3-6 months in a confined space to ensure his body is accepting of the new bone marrow, and can physically begin to regain his strength again.

All proceeds will go towards helping Jaxon and his family with ongoing bills, travel/accommodation expenses, babysitters for Jaxon’s baby sister Ellie, food, and the ability to allow Jaxon to enjoy this short window of time before he undergoes this difficult battle.

We are unable to find the words to express the LOVE we all have for Jaxon. Every single prayer and loving thought is truly appreciated.

Thank you all so much.

❤️❤️❤️