Hi, I am Danni-Lea Sandland, mom of Clay Bishop.

Clay has a condition called Stat-1 Gain of Function Mutation, only 660 people in the world diagnosed.

He has to go through so much medical treatments, tests, and appointment which for an 8 year old is an awful thing to have to go through all the time.

We recently found out he needs a surgical line fitted for a treatment lasting 4-8 weeks. He has an extreme phobia of needles and every appointment is traumatic for him.

Im setting this up, suggested by someone, to get him some treats and presents for being such a brave strong boy. I don’t know how to write these and I hate asking for anything but I’m just trying for my little boy.