Information for Schools

A chronic, debilitating illness like Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) can severely impact a student’s school experience and ability to participate. It is important not to mistake symptoms of the illness for laziness or avoidance of social interaction.

Information for teachers

Students with ME/CFS want to attend school and want to continue their education. Teachers can help by understanding the illness and supporting the student with accommodations like extra time on exams and assignments, or combining in-classroom instruction with home-based tutoring.

One key is to work as a team with school administrators and parents to develop an approach that works for the individual student. School Fact Sheet for Parents, Educators, and School Nurses (PDF) describes the disease and the educational implications, while School Fact Sheet: Classroom Strategies (PDF) describes accommodations and teaching strategies. More information can be found in the resources below.

Information for school nurses

School nurses can help students with ME/CFS by believing students when they need assistance and by providing a quiet place to rest during the day. They can also help by keeping track of medications and side effects, and by keeping track of day-to-day variations in condition and functioning. Please see the documents below for more information.

Note: CFIDS (Chronic Fatigue and Immune Dysfunction Syndrome) is an older name for ME/CFS.