Stryder is a ten year old boy that has MANY rare diagnoses, many don’t even have names. He has been to some of the best specialists in the world to get more answers, only to be told “We don’t know.”
Ruled out: hEDS, vEDS, POTS, SVT, OI and other autonomic dysfunction. Possible clEDS (per genetic variation), ROHHAD Syndrome and Mitochondrial Disease. Whole Exome Sequencing (WES) showed 56 variations of unknown significance, meaning we don’t know if they are disease causing or not without more in depth testing.