We got home last night after a long day. Analise needed her chest port butterfly needle changed out. She wasn’t too happy with the one she had and let us know it.
Anyway, we’re home and I’m logged in to catch up on some work email. Be back later with updates!
Something I found today…. http://www.brain-surgery.com/chtum2.html
Chemotherapy:- Unfortunately, chemotherapy is the hard part of brain tumor treatment. It is only required for the more aggressive tumors. As a rule, chemotherapy should be even more aggressive than the tumor itself. The trials which are imposed both on the child and parents are legion. Bravery and an unremitting attitude of hope are required by all involved.
Archive for December, 2008
12.31.08… home last night
12.30.08…counts are up and will be going home
Ana’s wbc are up from when we arrived and her platelet counts are ok. They redraw at 2pm. Since wbc are regenerating that gives us the go-ahead for home. We may stay longer today for a platelet transfusion should the 2pm draw shows a drop, but we’ll be going home today regardless.
Thank you to everyone for their support through prayers, phone calls, text messages, and emails.
For those who have or plan to donate to Analise’s benefit account THANK YOU. There is an account setup at First Midwest bank under Analise Jordan Deanching Benefit. This account is associated with a tax id#, 26-3857267.
For those who bank at Chase or live outside of First Midwest bank branch locations, we will be setting up an account with Chase using the same tax id#. I will provide more details after the account is established.
Have a good day and God Bless.
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12.29.08…fever down
Thankfully, Analise’s fever has gone down, but now they are just observing her and checking out her blood count.
12.28.08…Fever=ER visit and admittance
Well, last night was long. Melissa and her father were still recovering from their battles with the flu virus. Melissa’s mom, kept Sophia occupied until she feel asleep. I kept the monitor on in Ana’s room while I tried to sleep in the family room. Every so often Ana would cry or yell in her sleep, I’d jump up and end up seeing melissa’s mom at Ana’s door about to check her. Most of the time Ana would be looking for her bottle or needed a new diaper. This went on nearly every 1-1.5hrs. At one point I was so asleep, melissa was calling me out from our loft to wake up. Another time, I had repositioned her bottle into her hands and walked to the bathroom. Just as I was going, sure enough, Ana belted out a cry or scream.
Around 445am, melissa woke up and brought Ana to the family room to calm down and watch tv. Sometime around an hour later, I brought Ana back to bed and slept in the twin bed next to her. I want to avoid this, b/c I would probably keep her up with my snoring. Luckily, she was either really tired or I muffled my snoring enough for her to sleep.Today, Sop had a little tantrum while Analise was mostly being herself. Melissa’s mom took Sop over to Carrie’s for a sleepover.
Big thank you to Carrie and Jeff for their help with Sophia. They have been so nice to help watch and occupy Sophia’s attention.
Most of this day was uneventful, besides watching the Bears lose and not make the playoffs. Ana had her moments of crying or yelling or being restless. We noticed thrush in her mouth and started treating it with nystatin. By 8pm, we had taken normal temps via Ana’s ear several times already. She had been waking up, restless and crying, so we took her temp. She was at 101.something, so melissa and I scrambled to get our stuff together and page the oncologists. The answering service was slow to pickup and also took my mobile # wrong. Evidently, my 5′s sound like 1′s to this operator. Nearly, 15min later and a few miles from Hope/ER, I updated the answering service and the dr finally got ahold of us.
Let me say that nothing tests your will like taking care of your sick child. While I appreciate everyone saying melissa and I are strong, the fact is, for me, I’m just scared. No bravery here. A lot of wishful thinking, praying, and some denial mixed in. I’m not the model Catholic, but I’m working on it.Tonight we held ana down while 2 nurses accessed her port for cbc test samples. They got in ok but then had to fiddle with it to flush it well. They had to remove the dressing to get it flowing properly. Ana was unhappy as u can imagine and she was squirming and screaming ‘mommy’ the whole time. Endure this a few times and this will break you down. Absolute torture.
Thankfully Dawn and Kristin, nurses from the 4th floor did a great job.
We’re back on the 4th floor and in another positive pressure room. This type of room requires entry into a small room to wash hands and gown up prior to room entry. These are a little bigger than the regular rooms.We went through the routine patient background questioning (interrogation, if you ask me). And spoke with some residents and our nurse.
Ok, it’s late and I’m sure that I’ve babbled my share….
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12.27.08… flu virus!
It appears as the flu/virus that Melissa’s mom had a few days ago, has moved to it’s way to Melissa and her dad. Melissa’s mom is back to normal, after that virus held it’s ground for nearly 36hrs. Today, I must thank my parents and Jeff & Carrie for coming over with food and help throughout the day. Thanks to Jeff for putting together the girls’ petite house and kitchen etc set.