Caleb is doing well, praise the Lord! We are so very thankful for all the prayers and thoughts from so many people for our precious little boy!
Thankfully our worst fears of leukemia were ruled out once we got the blood work done. Unfortunately, when we had the blood work done we saw a new doctor, different from the one we usually see or the one we had seen before (the one mentioned in the previous post that could really tell something was wrong with Caleb). While the previous doctor had mentioned mono as a possibility, the new doctor didn't test for it (I think he was mostly concerned with ruling out leukemia). Since we didn't want to put Caleb through more testing, and there really isn't much to be done for mono, we didn't worry about testing him for it. However, just a couple of weeks ago I found out a friend's son, close in age to Caleb, has had mono, and we recently received a prayer request for another 6 year old boy here locally that has had mono. These other cases of mono in young boys here locally (and we live in a small town, not a big city) make me think mono is all the more of a possibility for Caleb. His symptoms certainly fit.
Regardless of whether it was/is mono, bad allergies, or something else altogether, the important thing is that he is feeling better. When he went for his first allergy shots they were concerned about how sick he was (the way he had been for so many weeks) so they gave him a breathing treatment and put him on prednisone. They warned me about the side-affects of being on prednisone, but for him it was a wonder drug. For the first time in many weeks Caleb finally had energy! Even when he had been on antibiotics for a couple of weeks, while some of his symptoms seemed to improve, he had never really had much energy. While his wild energy can be hard to keep up with (his daddy calls him the "blond tornado"), it was much harder to see him so lethargic.
Although Caleb hasn't felt well the past couple of days, overall he has been much better. He is still not completely back to his normal level of energy, but he has at least been playing a significant portion of the days lately. However, he has had a VERY hard time adjusting to the allergy shots. He goes twice each week for his shots and gets one in each arm every time he goes. While they are supposed to be subcutaneous shots, on his skinny little arms they are going much deeper. He bleeds after the shots, his arms get bruised, and they stay sore for days. Often when he gets his shots he still has bruises on his arms from the last TWO times he went in for shots, meaning not just the time a couple of days before but even the time a whole week ago. His arms are always sore - before they start feeling better he gets more shots. Sometimes the injection itself really burns, like last week due to the pollen count. I have to hold him for the shots (he doesn't fight, he just wants the comfort of my lap), and he always cries. Since I had allergy shots myself I never expected it to be this bad for him. I asked if they could use a smaller needle but they said they wouldn't. It's very hard to see him hurting so much!
Here is a recent picture of him. You can see how much better he looks. It's amazing how much the prednisone helped him! This was on the day he lost his first top tooth (he had already lost 4 on the bottom). It had been loose for awhile, but it just wouldn't come out. It was really causing him a lot of discomfort, and because of the way it was sticking out it really looked bad also. We just couldn't get it to come out. It ended up getting knocked out while Caleb was riding on a zip-line in a friend's backyard. It really shocked him at first, but I was so glad to finally have that tooth out!