Geli had her appointment on Tuesday for this week’s dose of chemotherapy.
Not surprising her counts were low enough to score her a free bag of platelets. In fact, she was actually too low to receive the intra-muscular injections BUT………there seems to be WAY TOO MANY BUTS recently……..they were out of platelets and had to have some brought in from an outside source.
They did end up giving her the injection anyway and had her hold bags of ice on her thighs to help her blood clot. (Platelets help your blood to clot and when they are low you are more susceptible to nose bleeds and other uncontrolled bleeding from cuts or bad bruising.) After the injections, they have to observe Angelica for 3 hours to make certain that she doesn’t have a serious allergic reaction and so if they had waited for a couple of hours until the platelets came in and then gave the platelets over an hours time period and then gave the intra-muscular injections and then watched her for the 3 hours…..well, they wouldn’t have been able to leave the hospital until after 7:30pm. This way, they were able to leave and get home by 6pm. So, it cut a few hours off the day, which was nice.
Angelica felt pretty good on Tuesday during the day, but started to feel a bit off by the time they got home…..She ate about half of her dinner and then started to really struggle with nausea. She tried valiantly to not barf but about 10:30pm she just couldn’t fight anymore. It was not pretty and it was the start of a very long, very nasty night.
We were up ALL night with her barfing and barfing and barfing and nothing was helping.
Finally she fell asleep around 5am and slept until the next “episode” at 7am. She managed to eat a tiny bit of breakfast, took her meds and around 10:30am was having a hard time keeping her eyes open or being able to sit up and so I sent her off to bed. She slept hard, only waking for me to give her some more anti-nausea meds at 11am and then slept until 2pm.
When she woke up, she ate some soup and crackers and seemed to look and act a little perkier than she had been. She seemed to be acting like she might be on the mend in the afternoon. Although, she was still pretty tired; she tried to eat some dinner and then when the other kids went to bed around 8pm….she did too.
I had planned on going to an exercise class with my sister and so I dragged myself off to the class and although it wasn’t my best class, for having next to no sleep, it wasn’t too bad.
I wondered how the night would go for us, but aside from our two littlest men tag teaming each other and managing to wake us every other hour, it was a pretty quiet night.
This morning, I was so tired, I couldn’t get up and so Jon got the kids up and off to school and I was surprised to hear that Geli had been up and at ’em like nothing was wrong…..AWESOME!
Her and Jon headed off to a BC BioMedical Lab to get her blood work done to see if she’d need another transfusion tomorrow and then they came home.
I asked Geli if she’d like to make some buns or bread with me and she was quite excited by the idea. If Geli was excited…..Siah was ECSTATIC! He LOVES to cook and bake. I’m not usually so excited as he makes quite a mess and making buns is already quite a messy endeavor, but I figured we could try to make it work.
Here is Siah, excited by his little bit of dough. (We were at “waiting for it to rise” stage)
In this next picture you can the “mess” a bit clearer…..Siah really “gets into” his baking.
I told Geli that this could be a “Home Ec.” class and that part of the Home Ec. mark always included the clean up.
We waited for the dough to rise and then punched it down, then it rose again and we punched it down again and then broke the dough up to make Cinnamon Buns, Coconut Buns, Cheese Buns and Plain Buns. The Coconut Buns are baking, but here are the rest of the buns still rising.
Angelica and Jon have gone to the High School to meet with her teachers. Based on her number today, she will be able to attend school on Monday. (They are trending upward, and should be okay for Monday.) She has more chemo on Tuesday, but should be good to go for Wednesday through the following Monday. Then she starts the Third Round of her treatment on Tuesday September 21st and that stage requires her to be admitted for 3-4 days every 2 weeks.
We are praying that Angelica would remain healthy and be able to attend school over this next week and a bit and that she would totally enjoy her school time and be able to feel integrated in with all her other class mates. Also that our other kids would remain healthy and not pick up any illness from the other kids in their school.