Foltzy’s Story

Site created on July 2, 2018

Welcome to our CaringBridge website. We are using it to keep family and friends updated in one place. We appreciate your support and words of hope and encouragement. Thank you for visiting.


As many of you know Foltzy was diagnosed with Acute Lymphoblastic Leukemia also known as ALL. We were fortunate enough to go to an amazing pediatrician who while assessing his belly felt his spleen during his 4 month well visit. We then decided to come back in a week to reassess. She again could feel his spleen and stated that it was even harder and larger then the week before. We immediately went to INOVA Fairfax for blood work and an ultrasound of Foltzy's belly. The next day we learned that his blood showed some possibility of having leukemia cells and we needed to have a biopsy of his bone marrow to make sure.  We were able to again get in with INOVA Fairfax in order to have the procedure done. We found out the next day that he did in fact have Pre-B cell ALL. We immediately transferred to Children's Hospital and were admitted that night. 

We are so lucky to have such a strong and happy boy. Each day with him is a blessing and he has forever changed our lives for the better. Even in his short few months on this earth he has shown us what it is like to live life to the fullest and no matter what to always have a smile on our face. We know with your prayers he will make it through this tough time. Thank you all for thinking of us and visiting our site. 

Newest Update

Journal entry by Alexis Foltz

We started maintenance a week or two ago...I am loosing track of time. So far so good. Today though is another huge deal. During his dressing change on Monday we were able to take a picture and send it to our nurse practitioner. I have been saying for a few weeks now that the cuff, the "balloon" that holds his line in was basically out. It was hard to tell when his dressing was on and so finally I got proof. She emailed it to the line NP and and she said that the line had to come out immediately. We have been hoping for a port for sometime now and he didn't weigh enough. Even though he still did not weigh enough he was able to have a port placed today anyways! This is nice in so many ways. 1. He doesn't have tubes coming out of his chest. 2. I don't have to flush is every day. 3. The risk of infection is less due to the fact that I don't have to change his dressing or caps weekly. Also its not always accessed. 4. He can have a normal bath without covering it or worrying about it getting wet. 5. I don't have to worry about his tubes dragging on the floor or him pulling it out. Since he doesn't have a dressing his skin won't get irritated with the summer heat. Bottom line this is a major deal in my eyes and will make everyones life easier. The downside is that in order to use it the nurses have to stick a needle in his chest. Good thing we have a tough guy and lidocaine cream so hopefully all will be good. We also get to go swimming this summer! Wahoo!!! Thank you for all the continued thoughts and prayers! We really appreciate it all!
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