“And will you succeed?
Yes! You will, indeed!
(98 and 3/4 percent guaranteed.)
Reflecting back to my status from a year ago. I had this on my personal facebook status before Caleb was diagnosed. 11 days before to be exact. And a friend reminded me of that status when Caleb was dx. A year later, it still is one of my favorite Dr. Seuss quotes.
He did get the OK to go back to baseball as long as he was up for it. And since it's outdoors and not really sharing or touching the same equipment.... I was ok with that too. So on Friday he was excited to be attending his first "real" baseball game ( as he puts it ). When he showed up his coach and teammates were all happy to see him and he had a huge smile on his face ready to play. I was so nervous hoping he knew what to do when playing..... I took him outside earlier in the day to let him practice hitting and we talked about hitting the ball, dropping the bat and running for first base. So my lefty went up to bat and did awesome during the first inning. He made it to second base & ended up getting out. (Who knew these kids were so competitive during T Ball?!?) He plays short stop, so while out on the field he gets a lot of action. He got the ball a few times and threw it back to the "pitcher mound". He did great. Then during the next inning I was expecting him to be up to hit again.... but was asked by the parent in charge to come to the dugout. Caleb said he was too exhausted to keep playing.
Earlier in the day he laid down and I knew it was the steroid pulse kicking in.I even suggested we maybe wait till next week for ball and he told me "NO! The Dr said it's OK!" He never wants to "nap" - actually to get him to rest is hard at times. He is always full of energy, but when he's on steroids he's easily worn out. So we left his game early last night. It's like you finally feel some sort of "normal" and bam it's a slap in the face of your reality. I hate that my child doesn't have energy to finish a baseball game or play like normal kids do. It breaks my heart to see him so tired and worn out, yet he wants to push himself and do what the other kids are doing.
So we wait another week for counts. He just has to go in to clinic and get labs to check. Last week he had IV Chemo (that wasn't count dependent). Dr Levy said his monocytes are high so those should be turning into neutrophils and in turn increasing his ANC. His ANC has to be 750 and his Platelets need to be 75K before resuming oral chemo. His platelets jumped to 60K, in the 6 days so that is a good sign too. We will know more on Thursday.
This week he will still be resting. He has another game on Tuesday, so we will see how he is doing that day and if he will make it. Hoping that since it's towards the end of his steroid pulse he will be less tired.
Shirts will be available in the next few weeks supporting "Kickin it with Caleb" if anyone is interested. From Kids to 2XL. There will also be a fundraiser in South Amboy NJ at Costa Verde . That will be on March 19th! If you mention the flyer 15% of your bill will be donated! Thank you so much to all who set this up and who are planning to attend! It means so much to us!
Also there is Pampered Chef party online till March 10th on FACEBOOK. Please find the link off of Caleb's FB Page. Bella's Mom is holding it for Caleb! THANK YOU Cori! :)
Thank You for your continued love, support and prayers!
Love,
Caleb's Mama
Thank You Give Hope Foundation for the gift basket!
My silly boy at APH
Trying to steal Pluto's bone!
Waiting for his labs to come back
Playing Mario Party at home with Mama
Practicing his batting
Walk On
U2
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