Ryan, Cate, and I made it to Philadelphia yesterday! Cate did very good on the plane and in the car. Charlie is at home with papaw playing with her new Buzz doll and very happy.
We are staying with our friends who are here with their son too. They have an amazing story, http://www.defyingthediagnosis.com. I am so impressed with how hard they work and how far their little boy has come!
Each time we visit or send in a report to IAHP we also make a video so the experts can see her progress and the execution of her program at home. This is done every 3 months. Here is the video of Cate. I have taken out her oxygen enrichment (so no one tries it at home) and kinesiology tapping (because it is long). If you are interested in learning more about these things let me know. I also wrote a blog about the oxygen enrichment last year that may explain it better, http://www.injuredtoincredible.com/2014/07/24/respiratory-patterning-machine-and-masking.
I look forward to brining you more updates this week!