The Adult Sickle Cell Quality of Life Measurement Information System, or ASCQ-Me, is a patient-reported outcome measurement system that assesses the physical, social, and emotional impact of Sickle Cell Disease (SCD). ASCQ-Me asks adults with SCD questions based on in-depth interviews and focus groups with patients. ...
Since 2007, the MTSS Center has been a national leader in supporting states, districts, and schools across the country in implementing tiered support systems that address students’ academic, behavioral, social, and emotional needs.