Thursday, September 15, 2011

First chemo

For all the time Joel and I spent thinking and worrying about Eila's first chemotherapy treatment, it actually was very straight forward (long, but straightforward). We had the usual vital sign checks (weight, length, blood pressure, temp), followed by an IV and a blood draw. The IV was probably the worst part of the day (and even the IV wasn't that bad). Since her previous hospital stay, she's getting pretty hip to the system. She knows when she's about to be pricked. Once the IV technician came in the room today, it took her, the nurse, and both Joel and I to hold Eila still and get it in.

Once that was in we meet with doctors, both hematology/oncology and surgery. Because she was getting Actinomycin-D today, they administered an anti-nausea medicine. Then came the chemo, and that turned out to the be the shortest part of the day - it couldn't have taken more than five minutes (it only lasted one book).


From Sept/Oct 2011

From Sept/Oct 2011

When the IV came out, and she was very happy to get to leave.

From Sept/Oct 2011

So far the anti-nausea medicine is working well for her. She's happily playing here at home as I type this. Even though today went well, we probably won't know how Eila is handling the chemo for a few days since most of the side effects show up after the medicine has worked its way through her system. And even then Eila's reaction to the medicines may vary day to day, and week to week.

We'll be back up to DCH on Monday when Eila will undergo a small surgery to install the portacath so she won't have to get an IV every week for the chemo and blood draw.

6 comments:

Annie Gyllen said...

Let us know if we can help. What a sweetie!

Unknown said...

I'm so encouraged reading this, but at the same time my heart aches for you all. I just can't imagine what you're going through. Please know our prayers are with you every day. You are an amazing family!!

Anonymous said...

We're all thinking about you. Will Eila be able to go out or will you be fearful of sicknesses this fall? If not, please let us know if you'd like distractions on days that you are home - e.g. playdates. We'll keep her and you all in our prayers.

Adventures with the Millam's said...

I'm so glad they're putting in the line that will make it easier in the long run and make it less traumatic on you all. Stay strong-- she's in good hands and getting the best care. Much love to you all!

Kyran said...

Glad to hear they are putting in a portocath. That will make treatment much less stressful for her, since the hard part is the prick, during the visit.
Here's hoping she'll have minimal side effects. What a brave girl, what a strong family! You are in my thoughts always.

KB in Corvallis said...

We continue to pray for all of you, and are available to help in anyway you need! I am inspired by your ability to keep the blog up to date so we know what is happening. It shows such strength and courage.