Emily and I set off on quite the adventure
the IDF FAMILY CONFERENCE in Baltimore (Immune Deficiency Foundation)
Emily couldn't wait to get on the plane!
the IDF FAMILY CONFERENCE in Baltimore (Immune Deficiency Foundation)
Emily couldn't wait to get on the plane!
The first day we had the amazing opportunity to attend Advocacy Day on Capital Hill.
We met with the office staff of Representative Jason Chaffetz, Senator Hatch and Senator Lee.
Emily and Ryan Berger both have SCID and talked about their treatments. Sydney is Ryan's adorable sister!
A HUGE highlight of the trip was spending the day with the amazing family in DC.
Monica and her girls Sophie and Hannah. Hannah has ADA SCIDS also. We met at the conference in Arizona a few years ago. They will be FOREVER FRIENDS!!
There are some people you meet that you automatically bond and connect with....this is one of those friendships! We had a total blast!
Note the picture of Emily at the Lincoln monument. The girls were so tough all day, they even ran up the stairs to see Mr. Lincoln...Emily wasn't too impressed!
The girls loved going to the museums together. The day ended WAY too soon ;(
This is the view from our hotel...I could run on the treadmill and watch a game every night!
The Conference was good I was able to see old friends and make new ones. It's so great to talk with other families who have and are going through the same things.
Emily enjoyed the kiddie corp only because she had Ryan and Sydney to hang out with but she got to see Iggy, one of her favorite stuffed animals in real life! :)
Emily's stuffed animals got to share 1/2 of our bed...lucky me!
2 comments:
I'm so glad you had such a great time! I can't wait for the SCID conference next summer!
I may always be jealous of that view. :). I didn't realize you got to hit some of DC. Cool!
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