Jackson developed PANS at 8 years old, but because of so few doctor's treating PANS, he went misdiagnosed for 2 years and his condition became severe.  He is on medications now that are helping him with the symptoms, but they are just 'bandaids'.  The real treatment is out of reach because it is so expensive and insurance won't cover it.  Jennifer, Jackson's mom, is on the board of SEPPA and hoping to bring change for the children affected by this awful illness.  It has completely changed Jackon's life, and we want to help him get it back.  Please donate today for Jackson, and so many other children who need treatment.