Many of you have been posting your pictures of all the fun parades and activities you had on your Independance Day. Well I didn't go to our annual town parade (on the 3rd of July) because I volunteered to stay home with Sam who had started running a fever the night before. He continued to be sick the entire weekened following and it turned into quite an event. So any lack of pictures I am going to blame on this. Let me share with you the entire story.
Upon our return from Bear Lake, where we went for a family reunion (you can read about this on my sister Erin's blog or sis-in law Anna's blog- or when I finally get to blogging about it) we had a couple days to recover before Sam came down with a fever. I considered this typical and just waited for it to pass. The 4th of July was day 3 of fever with not sign of improvement. I had to keep him on Tylenol and Motrin around the clock. At night he would cry and wake up because he was burning up and he needed more medicine and a drink of water. Every night. So when there was no letting up I figured it could be something more and went to urgent care on the 4th. The Dr did the typical examinations for things that could be causing fever. There was nothing showing us how it could be viral, still sometimes it is and you never see the reason, so he sent us home to wait it out a couple more days.
It continued to be difficult and I sensed it was not normal so I called the On- call Dr the next day and she said she would definitely get a white blood cell count on him considering the length of time and lack of symptoms. Well I momentarily thought he was on his way to getting better and so I waited until the next day when it was clear he was not. We were now on Sunday--5 days and counting with fever. This time the kids urgent care with peditricians was open and that made me feel good. This lady Dr did take blood to check his white blood cell count, which she found to be elevated indicating infection warranting antibiotic injections. After the blood draw he was already mad about, he had to withstand an injection in each leg of antibiotics --which they tell me really burns. He was NOT happy.
After this all I am thinkng we are finally done and that he will be better and it will be all behind us. However the Dr sait that even though he would probably be fine by the next day that we still needed to follow up with his regular pediatrician. She said if for some reason things aren't better he may need another injection of antibiotic. So we went in the next day (Monday.) Our regular Dr was not in until Tuesday, so we saw a very new, young, nice female Dr. She was worried that Sam was not better after the prior days injections and that he wasn't showing us any reason for infection. We didn't know what was wrong with him and that wasn't good. It didn't appear that was even getting better. Yes -he was still running a fever of about the same tempurature as always- maybe just slightly lower. The antibiotic they gave him was strong and they had given him a lot of it, so it should have done something... So the Dr ran even more blood tests on him, the whole slew for anything it could be. In the end we didn't have a lot of results back yet but we did know that his white blood cell count had come down and that was proof that the antibiotic was helping. So she gave him another injection (just one this time) and told us to go home and we were sure things would be fine and we would move on. Sam HATED the Dr by now especially since it seemed we were going in every day of his life and sticking him with needles. I should also mention that with this young female Dr I mentioned to her that Sam didn't seem to be able to move his neck very well and she examined him and said he was okay for not having meningitis. If they can't move their head up and down that is a sign of meningitis and his problem was with side to side movements. We did however discover he had very large lymph nodes and that was what was hurting and making him not want to turn his head. I made the comment that they were humongous --they really were, it looked like Frankenstein- like big golf balls inside his neck on either side! I made the comment that he must be really trying to fight whatever he has and she just said "yeah" and we moved on. I wish I had gotten a picture to show now, but that is just not what I was thinking of or worried about when my son was feeling so crappy and truthfully I was about in tears throughout some of it.
Well the next day I got a call from our regular Dr who was back (mind you I thought we were already done with Dr's and he was fine) and after looking at Sam's blood work, said it came back abnormal and he wanted to see him. So we go in for our 4th visit to the Dr in 5 days. I took Ed this time so that I wouldn't turn on the tears and be as worried as I was alone the day before (the lady was talking about admitting him and ruling out some serious stuff.) The blood work was abnormal what did that mean? Well the numbers that measure inflamation were 90 and the upper level for normal is 15. We head in and Sam is doing much better the fever is down and he is happier,-- except for the face that he is at the Dr, which he definitely NOT happy about. The Dr seeing that he has been traumatized decides that we still don't have a reason he is sick and that isn't good but he is getting better and is about to say that we should go home and keep in touch about how things go, when we mention how large his lymph nodes are. Well-- he then tells us what important information that is. I tell him I had told the Dr the day before. I mean if she doesn't react at all to that, why would think it was so important? Anyway its a good thing we did mention it because we found a cause for the infection and after all this run around it ended up being fairly simple. His lymph nodes were infected-- the cause of all the problems! Sometimes they help fight infection and sometimes they are what becomes infected. He is at a common age for this infection. The Dr put him on an oral round of a fairly aggressive antibiotic and now he is fine. Hooray! If we hadn't taken care of this the lymph nodes can eventually rupture and then he would've needed a CAT-scan and surgery to drain them. I tell you this in case you ever have to deal with anything like this! The fact that he could actually turn his head as difficult as it was, was a good thing, because when they rupture it makes it so you really can't turn it at all from side to side. I had never heard of this and then all of a sudden I get a call from my brother and his daughter has got it too! Too weird. Where is all of this stuff in the What to Expect Books???
Thursday, July 24, 2008
4th of July fun
Posted by Alisa at 11:09 PM
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5 comments:
Poor Sammy! I'm glad he is better, I didn't know that's what Isla had too. Sounds like a fun way to spend the 4th. Mine was spent with just Logan and Adam since Billy was at scout camp, no fun post here about the 4th, we just took a picnic to the park and I let Adam stay up and watch the fireworks outside. They do them at the lake by our house and you could see them from our front yard. I promised him next year we'd actually go to the lake when Billy is here and Logan is a year older and can stay up that late.
PS--"what to expect", they aren't as thorough as they'd like to think
!
That is so scary that Sam and you had to go to so many doctors to figure out what was wrong! I'm glad someone finally did and it was taken care of. I hate it when the little ones are sick!
I have never heard of this before. How scarey! I had it when the doctors have no answers and to have him so sick for so long. It sounds like you handled it much better than I would have. I'm so glad he's better. That's crazy that after all those doctor's, it was your own regular physicial who figured it all out. Wow! I'd stick with him! Hope the rest of your summer is very uneventful in the sickness department. What a brave little boy! And mommy!!!!
Scary! I'm so sorry Alisa! Your poor little Sam, I'm so glad he's on the mend.
Alisa! That must have made you so worried. I'm so sorry. I'mglad he is doing better now. I know how it feels to have a million tests done! It is miserable. Especailly when you don't feel like you are any closer to knowing exactly what is wrong! I'm glad you got it all figured out.
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