Weekend update! Matt came up on Friday after work and spent Friday and Saturday nights with Hudson so I could have a couple nights out of the hospital. There’s just something about having Daddy here - he brings the fun and energy! Clare, Kate, and my parents came Saturday afternoon after Clare’s rainy soccer game, and we had a good visit. Then they got to have a sleepover with Uncle T, Aunt Shelby, and Lily, which they LOVED. They came back for another visit this afternoon. It was so good to spend some time together this weekend.

Hudson’s admission is going well so far. He got his first two chemo meds yesterday afternoon - vincristine and methotrexate. He ended up breaking out in hives, and the team has decided it seems to be related to the vincristine. Last round of chemo he also got very rashy right away, but he had been under anesthesia from his central line placement so it was difficult to place the cause.

We could not be more grateful that our team gave us this week at home to recover before round two of chemo. Honestly, I think it was the best medicine to just be home for some time as a family. Hudson’s ANC reached 12,000 last week on Friday, so we were able to get out and about a bit, too. Hudson could not have been more thrilled to return to daycare for three days this week and spend time with his friends.

We ended up discharging today! Thank you, Jesus! We made it home around 8:30 and had a great welcoming crew! The girls got to stay up late to get some snuggles with mommy and little bro, books, and prayers.

12:00PM Update: Hudson is undergoing his pheresis right now! He is resting with the help of some Benadryl (lying still is important for better collection) and his favorite movie, Frozen. So far the procedure is going well. Hopefully we are getting a good number of stem cells. They know exactly the amount we need to complete three transplants, so after they examine what is collected today, we’ll know if another day (or more) of pheresis is needed. They primed the machine with a blood transfusion to keep him comfortable, so he didn’t experience the feeling of losing blood.

Long weekend update! I was planning to write an update last night but little guy didn’t fall asleep until 11pm so midday update it is. We’re still camped out at SLCH, waiting on his ANC. It was up to 79 yesterday but fell back to 56 today. It needs to be at least 500 to talk about going home. Today he got his third high dose of the medication which is stimulating his bone marrow for WBC production.