Tyler’s Story

Site created on January 23, 2024

Welcome to Tyler’s Journey.    Tyler was diagnosed with High Risk B-ALL, which has a very positive outlook for Ty at the end of his treatments.  We (Michelle, Chris and Tyler) are using this page to keep family and friends updated in one place. We appreciate your support and words of hope and encouragement.  We believe in the power of prayer as Tyler takes on this fight.  Throughout his journey we will be reaching out to family and friends for help with Brandon and Mason or to take a walk/talk/hang out.  In the meantime one way you can help Tyler (and so many others) is to donate blood (if you are able) with the American Red Cross (it cannot be direct to Tyler but would benefit others like him) and most importantly remember to tell your family and friends how much they mean to you each and every day.  If you click on Journal at the top, you can see how we got here, what the first phase of treatment is, and we will continue to update his progress.
 Thank you for visiting.

Newest Update

Journal entry by Michelle Lockett

Blood levels are checked/monitored every clinic day (2x/week).  Unfortunately Ty needed a platelet transfusion before the LP and blood before going home.  Due to needing all of this, he was at clinic much longer than expected.  (Nothing to eat and drink before the LP either).  

LP#2  out of 22 - Tyler did really well with this one!  The doctor was very impressed with his success and will look at trying the next one with oral meds, so he can eat that morning.  While he was laying flat for the 30 min. after it, lunch was on the way.  Moe's queso for the win!

Ty ate lunch during his blood transfusion and chemo before going home.  He was very surprised how much the blood transfusion helped his shortness of breath the next day!  We are told the transfusions will continue to be needed at times throughout the rest of his journey.

Clinic visits will continue until Day 29 with PT weekly, OT, doctor/nurse visits, nutritionist, and other staff.  So far he has done well overall with just some shortness of breath, occasional headaches, some nausea, a little tired, and the normal prednisone effects.  The doctors and nurses are so impressed with his exceeding the step goal and still remaining active when he can.  He was even able to start back to school on days when not at clinic on Wednesday, 1/17 (thanks for the 2 hour delay this made the transition a little easier!), and Thursday 1/18.  We will update again at the end of Induction.  Ty is hoping to continue with school during this phase.  

Pictures are the LP room, clinic room, and infusion.

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