Mitchell’s Story: Solving a Rare Undiagnosed Brain Disease 

Mitchell Herndon lived a healthy life until he was twelve years old, when he began to develop devastating symptoms due to an undiagnosed brain disease now known as Mitchell Syndrome. In pursuit of answers, Mitchell and his family were connected to Dr. Hugo Bellen and his research team at the Duncan Neurological Research Institute (Duncan NRI). Through extensive research and genetic sequencing, Dr. Bellen was able to solve the root cause of Mitchell’s disease.
There are so many children just like Mitchell who the Duncan NRI is honoring and remembering through our work. To support lifesaving research, please visit: www.texaschild....