Lizzie's Journey

Thursday, August 27, 2009

The waiting game is over,,,,, or so we thought

I never know what to expect with Boo. If anything, I’ve learned to expect the unexpected, but sometimes you’re still blind-sided. It just happens, and today was no exception. We were anticipating excellent test results from Lizzie’s most recent blood work. She’s been infection free for a while, and the initial testing was optimistic. Both of her doctors seemed pretty confident that the results would be good, and we had immunology just about crossed off of our list when… we got the curve ball.

Lizzie’s immunoglobulin numbers look good, which is great. Her T cells and B cells are both making cells and responding to some infections, but apparently her T cells are not functioning as well as we had hoped. Once again Lizzie is odd man out. Her T cells are not making any response to Candida, which is highly unusual without the presence of certain conditions (which she doesn’t have). This would explain the thrush and yeast infections, but we still aren’t sure why it would be happening outside of those conditions. Chalk it up to another 2% that Lizzie is a proud member of! Lol! So our first step is to have some more testing done next week to see if we can find some more definitive answers. The last test was done with cells in a petri dish, so this time, they will test her skin directly, and she will receive a “patch” that she has to wear for 3 days. This will test how the cells in her body actually respond to the candida. She will also have yet another blood panel to retest her latest results. After that we will move on to the vaccination titers which I am still not happy about, but I am now at least comfortable doing because I know that they are necessary.

So how do I feel about it all? Not really sure yet. On one hand, I’m excited to have a wonderful doctor that listens, explains it all and is willing to look for answers. I can’t say enough about how important that is. I’ve always felt like all of Lizzie’s issues are connected, and I think this is one more step in connecting them all. I truly feel like one day we will find the answer. On the other hand, I’m so frustrated. I’m really tired of taking my baby to be a pin cushion. I’m tired of doctors not having answers. I’ve talked to dozens of doctors, done literally hundreds of hours of research, and I know less now than I did when she was 6 weeks old. I’m tired of my baby being “special”. I’d give anything for her to be boring, dull even….

And then I’m reminded of how blessed I am. I have 2 amazing children, both of whom are happy and very healthy considering. No matter how frustrated I am, that’s a pretty big wake up call. It’s like a dear friend of mine said tonight “You’re entitled to the pity party every now and then, you even deserve it. Just don’t ever let it cloud your blessings”. What encouraging words. I do get tired of being the rock, I won’t lie about that. Sometimes it helps just to say “this sucks”. Cause guess what? It does. It’s not fun to see your little one go through so much. But then you pick yourself up, say a big fat thank you that it’s not worse, and move on. If it ends up being a true immune deficiency, Lizzie will be put on another medication to control it. Not our favorite option, but yeah we’re pretty thankful to have the option. Modern medicine is both amazing and frustrating. My goal? To find a balance between the two. Yeah, God’s definitely determined to teach me patience.

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Wednesday, August 12, 2009

Good News and Good Docs

Today Lizzie saw her new pediatric immunologist, and I'm glad to report that the visit went really well. I never know what to expect from a new doctor, and let's be honest, it doesn't always make for a good day. We've had some initial test results for a while now, with no clear explanation of what they mean. For those of you who know me, you know that it's been driving me nuts!!! Super crazy, so I was really hoping for a good doctor who doesn't mind 1000+ questions. Instead, I got 2 great doctors that welcomed the questions. Thank you Lord for teaching hospitals! lol!

The doctors didn't get copies of all the right labs, but if I've learned anything along our journey, it's to be over-prepared... so I had a copy for them. :) They went through the labs with me item by item, and explained what each one meant. The good news, is that because she is growing and developing so well they feel like her immune system just needs some time to "catch-up". She has spent so much time on antibiotics and anti-fungals, that her system is just overworked. We are pretty convinced that this is what is making her T cell numbers low, and not an actual deficiency, but we are doing a few more tests to be sure.

Speaking of tests, more good news... I think we made the right decision in waiting to do the vax titers. We are redoing the original labs to see if the numbers are still low, but since she has been off of all medication for 8 weeks now (which also means she has been thrush free for 8 wks! woo-hoo!) we may see a rise in her numbers. They are also doing some kind of test to check the actual function of the T cells. As long as the T cells are functioning well, it doesn't matter if they are lower than normal as long as they are not significantly lower. If this test comes back with good function, than we don't have to do the titers at all, which would mean no extra vax'es. Which makes me one happy momma!

So overall great news. It's not definitive and really not anything we hadn't heard, but now I understand it and feel comfortable about where we are going. Sometimes that's just as important as the answer. It certainly takes a lot of the worry out of it. We get the test results in 2 weeks, and hopefully we can take immunology back of the list. This will also mean that we are doctor free until December! You heard me right, NO visits scheduled until December, when we see urology again to discuss the take down of her vesicostomy. It will be a nice break before she starts testing again, and I'd say she deserves it. ;)

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Lizzie's Journey

Name: Wen

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