June 27, 2011

All Things Joshua

This past weekend, we attended the 2011 National Immune Deficiency Foundation Conference. It was IDF's 30th anniversary, and the conference just happened to be here--in Phoenix!

For the very first time, we finally were able to meet other CGD families who traveled from all around the country to be here. Remember--CGD is very rare. Only about 40 people are born with it each year.

We also had the amazing opportunity of meeting 3 doctors who are experts in the subject of CGD, and spend their entire medical career researching and helping families with this unusual disease. One of which, Dr. Stephen Holland, is now Salesi's new hero!

IDF's motto is: "When you hear hoof beats, think zebras, not horses". In medical school, many doctors learn the saying, "when you hear hoof beats, think horses, not zebras" and are taught to focus on the likeliest possibilities when making a diagnosis, not the unusual ones. However, sometimes physicians need to look for a zebra. People with primary immunodeficiency diseases are the zebras of the medical world.

So, if you happen to see us dressed up in zebra wear, a little more than the usual, you will now know why!

1 comment:

  1. I'm so glad you were able to connect with others who have gone through the same thing you guys had to face. May God bless you, the doctors who study CGD, and all others affected by it.


I have never deleted anyone's comment. (Not even the mean ones from my sisters.)