Showing posts with label phlebotomist. Show all posts
Showing posts with label phlebotomist. Show all posts

Wednesday, June 25, 2014

Draw time and the difficulty with flow

Samantha had a blood draw today. We picked her up from camp and handed her a full water bottle with the instructions to drink. She had the 30 minute drive to the lab to get in as much as she could.

Samantha's never been a good bleeder, even as a baby. She's learned that the more the drinks the easier the draw. Now that she's 9, we don't have to argue about it--she equates more water with less pokes.

But today, Samantha wasn't a good bleeder. She drank a lot of water, but had expended most of it at camp. She tried to drink a lot until she felt too full to drink more.

I typically sit in the lobby of the lab while she goes back in the chair by herself. We've come to know our phlebotomist well. Samantha likes to do it by herself--it makes her feel grown up. While we were sitting in the lobby today, Samantha and the phlebotomist were giggling. They were laughing because the draw started out well and blood was flowing and the moment they mentioned it the flow stopped. It happened twice.

I'm so glad that it isn't a negative thing, these blood draws. And that Samantha can find humor in a somewhat sucky situation.

When she was a baby and I had to hold her down because she was screaming and squiggling during a heel stick. I never thought this would get any better, but it has. It has been at least two years since Samantha last cried at a draw. And now she takes it like a champ.

~ ~ ~

In May, when our school had an open house, Samantha had her autobiography displayed on the the third-grade wall. It said: "My name is Samantha. I was born in Gilroy. I was born without a thyroid. My parents were so happy that I was their daughter . . ." Of course we are!

Sunday, May 18, 2014

The Big Day

August 2012

Tuesday we have our first appointment at Lucile Packard Children's Hospital. Mind you we've been part of their clinics since Bug was born in 2005, but for some reason this is the "big deal."

I wanted to go double check the name of the doctor we are asking to see (recommend by the pediatrician) and I found a "Kids" page on their website. Then came the tears . . . my tears.

Bug doesn't know this is any different than any other appointment we've ever had, but for me it's pivotal. She's not normal even among the congenital hypothyroid set--and the doctors' are continually baffled by her test results. It doesn't make it any easier that despite my constant monitoring of the CH parents' page on the Magic Foundation FB page, I still feel alone.

Sometimes it makes me sad to think she's so different even among her CH peers. The other kids don't fluctuate so drastically with the medication needs.

And then I read on about how around 11 many kids don't want to take their pill anymore because they don't want to be different. And I cry.

You'd think after 7 years I'd be used to this. But that is not the case and I'm sure it never will be. I worry about what happens with puberty around the corner and when she becomes a pre-teen and thinks that taking a pill is abnormal.

Today Bug had a blood draw before our Tuesday appointment and the phlebotomist had a hard time finding the vein in her left arm because of the scarring due to the past draws. She's 7! What does that mean for the future?