3/19/2024 *UPDATE*

First off, thank you to everyone who’s been supporting us! Jaxon had his transplant on January 15, 2024. Zoe did great and is fully recovered. Jaxon is 2 months post transplant, and while it’s been a bumpy ride, he is doing well in recovery. Jaxon’s DNA is officially 100% Zoe’s! The transplant was a success.

Financially this has been a nightmare, but thanks to you all the burden has been lighter. When we first started this journey we were so nervous about leaving home, but here we are on day 64 DOING IT! We have 40 ish days left in Nashville. I want to be specific with our needs and fully transparent with the “why” behind this gofund me. Jaxon will need a full time caregiver for the next 2-3 months, even as we transition home, as he will have multiple doctor visits and a new normal to adjust to. This fund is being used for our mortgage, gas, groceries, bills in general because I’m not working.

Thank you to everyone who has donated. It means the world to us. If you want to follow along with Jaxon’s journey- he has a prayer page called “Prayers for Jaxon” on Facebook :)

Jaxon and his family (Tiffany, Jacob, Zoe and Parker) are in need of our help. As many of you know, Jaxon has relapsed and has been diagnosed with T-cell ALL once again. He had his central line and first dose of intrathecal chemo today. This is just the start of a long journey in his treatment plan. If you’ve been along since the beginning, you know he was diagnosed with this same cancer at 5 years old. Then, at 9 years old, he went through treatment for a salivary mass. Jaxon has been through so much and has been so strong. We know he can beat this again!

His mom, Tiffany will have to be off work for an unknown amount of time on unpaid leave to take him to multiple appointments and hospital stays. A bone marrow transplant will be needed at some point and that will include traveling to another hospital. With two other children at home, Tiffany and Jacob can use all the help we can give!

here is the most recent post from Tiffany: Well, here we are. My baby has relapsed. Jaxon’s leukemia is back. My soul feels beaten.

What I thought was typical teen problems, like pulled a muscle playing basketball and coughing from allergies was actually my worst nightmare coming back to life.

It’s all moving fast. Jaxon has a chest tube in right now to drain fluid. He gets his port placed in the morning. He needs a bone marrow transplant. Chemo and spinal tap tomorrow. My minds running wild!

I plan to update as we go along again, but right now I just don’t have anymore words. I wanted to make this post because I know some others have and news is spreading fast. Jaxon had so many prayer warriors and good Lord, I hope y’all are still there because we need them now.

My hope is in God and his plans for our future, not to harm us. Plans for good. I’m clinging to Jeremiah 29 tight. I’m proud of my boy. Jaxon is strong. He’s got this.

Y’all pray for us ️

*UPDATE* Jaxon is finally in remission and eligible for the bone marrow transplant. Transplant will take place in Nashville where Jaxon and his mom will stay for a minimum of 100 days. For the next couple weeks Jaxon will be doing bridge chemo, in Knoxville, before they leave to maintain remission. On December 18 the family will need to stay in Nashville for 3 days so that Jaxon and Zoe can get work ups to make sure they are healthy enough for transplant. The 100 day stay will start January 1, 2024. Thank you for the continued support during this trying time