Update, I suck at these..

We spent Christmas and Christmas Eve in the hospital. He wasn’t feeling super awesome but seeing his sisters and family really lifted his sprints. They did finally let us take him outside and to say it was the highlight of the stay is an understatement!! After 11 days in the hospital we were finally able to go home! We were so happy to take him home to spend New Year’s Eve and New Year’s Day at home with the girls! Home health comes in once a week to check blood levels. He is responding to treatment awesome! They are now unable to trace leukemia cells in his spinal fluid, and his blasts in his blood are going down! Such fantastic news. In typical Dax nature he was being him stubborn self and started refusing his meds so unfortunately he had to have an NG tube placed and he has done awesome with it! That was Monday January 6th. Tuesday the 7th Dax wasn’t doing very well and spiked a fever. Since he is in his induction phase of treatment he has no immune system so the medical team takes fevers very serious because of risk of blood infection. Back to primary’s we went. He was admitted again to start testing, he fevered all day Wednesday and they couldn’t pinpoint the reason. He had his last fever at 11 pm on Wednesday. He was able to stay fever free and we got to go home Thursday evening. When we got home we had some friends come visit and I saw a lot of my daxon and it made my heart so happy. We take those times anytime we can get them. I’m sorry I suck at updates I will be better.  I want to thank everyone for the support we have received. I can’t put into words the amount of appreciation we have.