I am one of the very few people to have been diagnosed with a genetic disorder called Carnitine palmitoyltransferase II Deficiency, or "CPT2 Deficiency". In between episodes, life with CPT2 is very normal. However, during an episode CPT2 patients experience muscle pain, rhabdomyolysis, myoglobinuria and other unpleasant symptoms. I will use this blog to periodically describe my experiences with CPT2 in the hopes that others with the disorder will find it useful.