Skip to main content

Eager Beaver Med Students

I have blogged before about the eager beaver med students we've met who have been incredibly sweet, helpful, and interested in our case--from my polyhydraminos (extra amniotic fluid) to Abby's not swallowing, to Abby's diagnosis, to her incredible progress. 

We encountered another med student who was doing her pediatric rotation and thought Abby was pretty interesting.  I filled her in on the basics of CCMS, shared the miracles that had occured, and described my girl's personality for her (since, at that point, she was sleeping off the anesthesia!)  She came back the next day telling me she had researched CCMS further and would like to share it with the entire pediatric team at Abby's bedside, if that was okay with me.  I smiled and said that would be fine.

So, in came about 8 pediatric residents, attendings, and med students.  Two we had met, but the rest were new to us.  They all crowded in around Abby's bed (which is one of six in the large room called the Intermediate Care Unit) and the med student shared what she had learned. 

Abby, by this point, had slept 15 straight hours and was feeling really good!  She sat up playing, smiling, and signing "more" throughout the entire presentation...the little show-off!  :)  Even if the med student had wanted to paint a grim picture of Abby's diagnosis, it would be hard for any of them watching her to believe it. 

I have to say, I did feel a little like Abby was a caged lion in a circus while they were there.  After all, they were all circled around her baby jail (our affectionate term for the crib with the very high bars and plastic that can roll down to keep kids from climbing out) staring at her while she did tricks.  I almost said that she would stand up on her hind legs if they threw her a peanut, but I figured I'd better be good.  :)

All in all, the med student did a good job...and now about 8 more young doctors know what CCMS is--and they also know how well some CCMS kids can develop!!

Comments

Debbie said…
Abby, just like her mom and grandmom educating youngsters everywhere. I bet she'll grow up to be a Teacher also.

GO ABBY GO!
gail said…
It's great that you took the time to share with Residents- who knows, 10 years down the road they may be the pediatrician to a girl or boy like Abby and what hope and comfort the parents will be given when the doctor talks about Abby!

Popular posts from this blog

Cerebrocostomandibular Syndrome

If you happen to pick up the latest Reader's Digest, there is an article in there about Piper Breinholt , a four year old with CCMS.  If you've been around here a while, you'll remember wayyyyyy back when we first received Abby's diagnosis that I was able to speak to Piper's mom, Reagan.  The article is more about their story and not as much about the ins and outs of CCMS, but I think it's probably enough to get some people googling it and I'm hoping a few will end up here. Every once in a while, I give a blog post the title of Cerebrocostomandibular Syndrome so that it would show up in Google.  My ever-present hope is that people will stumble across my blog and 1) be encouraged by the hope we have in Christ, 2) feel a connection with someone in a similar situation as them, or 3) get excited over the miracles that have been performed in Abby's life!!  (a combination of all 3 is great too!)  :)   Notice that it's not to get famous and it ...

Bath Time Photos!!

As promised, here are lots of photos of Abby's first bath. Caleb was supposed to be in bed, but the bathroom is right next to his room... "I'm not too sure about this..." Once she learned how to splash, she was all smiles! Her first good hair wash! Gotta protect the trach! She really liked getting water poured on her head.  It was cute! Smiley (and bubbly) for Daddy while he dried her off. All clean!!  (Note the Lysol wipes in that last picture.  They are NEVER far away!)

Imagination Movers Photo Recap

Seriously, The Imagination Movers were so much fun!  They played lots of their own music, with some classic rock mixed in for the adults.  There were also quite a few jokes and references to Baltimore, which was kind of fun.   The whole night centered around this robot named Rock-o-Matic, or "Rocko."   This is Mover Scott, and he wears Wobble Goggles that help him see new ideas.  Caleb and Abby have a pair of goggles too.  :) There are 4 main Movers that are part of the TV show, but they have 2 extra movers to play instruments and do back-up vocals in their live tour. Abby finished up her feed before the show started so that she would be free to dance! My dancing queen did NOT want to sit in my lap.  The row in front of us was empty, and that is where she stood almost the entire show--dancing the night away. My Imagination Movers  Caleb did his share of singing and dancing too.  He knows m...