I started off this year trying not to talk about family camp much with the kids. After last years anticipation turned into such a fiasco, I didn't want to get their hopes up this year and then have the same thing happen. This was our third year attending the Hemophilia Foundation of Northern California's family camp. The first year I went with just Scarlett and we had an amazing time. It was emotional, overwhelming, educational, eye opening and one of the first events I felt truly inspired and welcomed by my local bleeding disorder community. The second year, my son Walker who was 3 got to go. He had been anxiously awaiting getting to go since we returned from the first trip and was heartbroken to get sick, literally on the way to camp. Our weekend was cut short after spending the first 16 hours hauled up in the cabin with the stomach flu. So it wasn't until we were pulling into the now familiar driveway of Taylor Family Foundations Camp Arroyo that I let the exciteme...
We are here to share our story and spread awareness of this rare bleeding disorder called PLATELET STORAGE POOL DISORDER . . . . .