I'm sure the sensor hunt is only a temporary fix. At some point she will realize if she doesn't actually find the stuff it draws out the time before it's inserted. She is a bright kid...I'm sure it won't be long. :-) But, for now, we will enjoy our successful and witty approach to a common Type 1 problem--the pain of site and sensor change days. Enjoy the pics!
~Hmmm where to start my hunt?

~Ah-ha! The sensor hiding by mom and dad's bed. Too easy!

~The CGM inserter~ Show those muscles. :-)

~The spoils of her Sensor Hunt.

~Showing the camera the big ole needle that just inserted her CGM--or sensor. (See no tears!)

~The inserted CGM.

~The new home for her insulin site...It gets a new home every 3 days.

~2 thumbs up for a successful change day!! Yay!
10 comments:
Oh good girl Sydney!!! You are so brave. What a beautiful smile! :) Shamae, you are so lucky to only have to change every 3 days. We have to change Tristan every 2 days. :( At first we were doing the 3 day thing but they came to the conclusion that on the third day, his numbers were always higher so they made us switch to 2 days.
Keep up the great work guys! :)
WOO HOO!!!! Way to go Team Sydney :)
Funny...we're watching Little Mermaid over here too!!!!
LOL! Funny! And hooray for Sydney!! You go girl!!
I know what a drag those sensors are. I feel for you!
What an amazing little girl!!! I like how she went for a hunt to find her equipment that was cute!! Way to go Sydney
Smart of you to make it a game. I would just pretend like I can't find it. I am sure she will figure it out soon. What a brave little girl.
everytime i see this pictures i just want to cry it's so sad to see what she has to go through what a tought little girl. I also wanted to let you guys know that we are moving to wy this friday. I hope we can see you guys one more time but if we can't it was so good to get to know you guys. I'm so greatfull we had a chance to learn from you guys wonderfull example and testimonies. hope you guys have a gonderfull day hope to see you soon
Blasi :)
way to go Syd!
Wow, my daughter is T1 and I love your idea of the hunt:) We are starting to think about getting her a CGM...do you like Sydney's? Kennedy was diagnosed in August of this year and is 3 years old.
Very clever making it a game. . .
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