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An online community for children and adults with brain inflammation diseases, like myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). People can share their stories, symptoms, life events, and donate samples for research.

Provides support groups and clear information on postural orthostatic tachycardia syndrome (POTS) and other types of dysautonomia associated with Long COVID. These health problems affect things the body does automatically, like breathing and heart rate.

Long COVID Alliance is a group of patient advocates, scientists, disease experts, and drug developers. They work together to teach policy leaders and help us understand diseases that happen after viruses.

Long Covid Families helps children and families affected by diseases that spread from one person to another (infectious diseases).

Long COVID Kids represents and supports children and young people living with Long COVID and similar diseases. This group also supports the parents and caregivers that look after them.

The COVID-19 Longhauler Advocacy Project helps people understand Long COVID and similar diseases. The group supports people with Long COVID and their families through advocacy, education, and research.

Marked By COVID is a movement for pandemic justice and to remember those affected by the pandemic. It is led by COVID-19 survivors.

MaskBloc.org lists active Mask Blocs around the world. Mask Blocs provide masks, COVID-19 tests, and other equipment to communities for free.

Mask Together America is an organization that shares ways to prevent COVID-19 and advocates for families who have had COVID-19 and lost loved ones to COVID-19 and people with Long COVID.

The Patient-Led Research Collaborative is a group of Long COVID patients and people with similar diseases, like myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and post-orthostatic tachycardia syndrome (POTS), who also do research.