Day: June 22, 2011

Winding Down for the Evening

Jon and Geli are settled in their room and getting ready to wind down for the evening. There was talk of a movie and possibly some snacks and a midnight run of antibiotics.

She’s feeling and acting a lot better after receiving two bags of red blood cells. She’s not feeling 100% but definitely better than earlier today. We are going to head in to the hospital tomorrow and hang with them a bit. Probably have lunch with them……or maybe dinner….or both? Who knows?

We just spoke with Jon and Geli on Skype and now I’ve kicked Xandra and Jeremy up to bed. I’ve got to go and “encourage them” to actually shut the lights out and go to sleep and then I’m headed to bed myself. It was a LOOOOOOONG night last night and solo parenting is not easy and I’m not sure how long I’ll be at it. So I gotta sleep when I can….and unfortunately, I don’t do daytime naps as easy as I’d like.

Fortunately, my parents are AMAZING, and they’ve kept Siah overnight. They had him last night (which was a blessing) and they are keeping him again tonight. He still wakes up in the middle of the night and climbs into our bed. It’s not that big of a deal, but typically him and Judah tag team each other and only one of them is up at a time……..which means that if they are both here…..I don’t get hardly any sleep. The worst thing….when he sleeps at my mom’s house….Siah stays in his own bed. What is up with that? Oh well, I just keep telling myself that this is not a forever thing. One day I’ll wish for cuddles….I will try to enjoy and appreciate every one I can get right now.

Thanks for all your prayer and support. We really appreciate it.

Excuse the stupid sound that I make with my mouth. Judah was doing that and I was trying to capture it on video cause he was doing it ALL DAY! But when I turned my iPhone on so that he could see himself in the camera he got so excited and stopped doing it. But his little happiness and laughter is so contagious…….It’s too good to keep to myself. Sometimes I wish I could bottle it up and give it away. The world would be a better place……

May your evening be peaceful and full of rest.

Magic Numbers

We got the results back from a few of Geli’s blood tests.

Her White Blood Count was at a .2
Her Hemoglobin was at a 77
Her Platelets were are a 35

This means that everything is down a bit from yesterday. This is not good news. Geli will get platelets and red blood.

Her temperature continued to hover around 37.8F and they started the platelets and while the platelets were running, her temperature spiked up to a 38.3F and then in another half an hour it made it all the way up to 38.6F. They have given her some Tylenol to bring the fever down and to make her feel a bit more comfortable.

Not Feeling Great

chillin’ in the clinic

The platelets have finished running and they have started her on a dose of antibiotics.

After the antibiotics is finished running then she will get some red blood.

They are scheduled to be in a room up on 3B on the Oncology Ward and we are happy about that. It really sucks to be on a ward where you don’t know anyone and where they don’t know the typical protocol for oncology kids. I mean, it sucks to be in the hospital at all but at least having the staff that you know and being in familiar surroundings is a definite bonus.

There is another test that they did on her blood that can indicate whether an infection might be brewing and it didn’t seem to indicate that she had a raging infection. It’s well within the “normal range” for that test but until the blood is cultured, we won’t know for sure if anything is growing (bacteria) or if this is a neutropenic fever or if it’s a virus.

And so we wait some more.

I HATE waiting.

I know that this phase is almost over and that her counts are not expected to be this low again, but it sucks. It sucks that Angelica is not feeling 100%. It sucks that we are split up, as a family. There is just a lot to this situation that sucks.

I had a bit of a moment this morning, where I just wanted to throw a temperature tantrum. I wanted to scream and kick my feet and fall of the floor and yell, “This isn’t fair! Why did my daughter have to get cancer? Why did she get sick and not someone else? Why is our family going through this?”

I wouldn’t wish this on anyone else.

I know that life is not fair. I don’t even expect it to be. I just hate that this is happening to us.

Down This Road

We talked with our nurse at the clinic around 10am and after talking through what Geli looks like, is feeling like and acting like – the decision was made to go into the clinic, run a CBC (Complete Blood Count) and a few other blood tests.

Based on the results of those tests we should know a bit more about what we are dealing with.

It could be that the elevated temperature, dizziness, the pressure in her chest, the tiredness…..they could all be symptoms of low red blood or……they could also be an infection.

Jon and Geli are at the hospital right now and she’s had her blood drawn so at this point we are just waiting for the results of her blood draws to come back.

I HATE waiting. Unless her red blood cells are amazing, she’ll probably get red blood today which combined with her almost non-existent White Blood Count could mean a fever and admission.

I’m trying to resign myself that they are there for sure until the weekend. And that sucks!

Overnight Update

We took Angelica’s temp every two hours last night and it hovered between 37.4F and 37.8F.

It’s up but it hasn’t crossed the 38F critical marker. At about 4am, we called into the hospital because we really don’t want to play around with this. We’d rather error on the side of caution and take her in early and catch an infection in the early stage as opposed to waiting it out and having it be a full blown problem.

She’s tired from having an interrupted sleep, and so she’s upstairs sleeping right now.

We will take her next temperature reading around 9:30-10am and will call into the clinic then to talk to our nurse.

Until then, we wait and pray.