An association of patients, family members, and allies
We work to give a voice to people with Myalgic Encephalomyelitis (ME/CFS), Long COVID, and other acute-onset post-infectious syndromes (PAIS).
About us
Aliança Millions Missing is a non-profit organization that advocates for the rights of people with Myalgic Encephalomyelitis (ME/CFS), Long COVID, and other acute-onset post-infectious syndromes.
Created in 2018 and formalized in 2025, AMM operates in Portugal, Brazil, and Portuguese-speaking communities, promoting scientific research, professional training, effective public policies, and awareness campaigns.
What sets us apart: AMM is led by patients, ensuring that all decisions are based on the real experiences of those affected, in close collaboration with the scientific community.
No one chooses to have these diseases. That is why AMM ensures that all services and support are provided free of charge and universally, whether or not patients are registered as members.
Join us
AMM is open to all individuals and entities who want to contribute to its mission. You can register as a Member or as a Friend.
Learn more
Information about diseases. AMM works on several fronts to transform scientific knowledge into real impact on patients' lives.
Resources
AMM guides patients, families, professionals, and civil society to current and credible sources of clinical, scientific, and support information.
2ª CONFERÊNCIA INTERNACIONAL
Avanços Clínicos e Científicos em
ENCEFALOMIELITE MIÁLGICA e COVID Longa
SAVE
THE
DATE
NOVEMBER
12-13
2025
AT
ORDEM
DOS MÉDICOS
NO PORTO
“Every voice counts.
Together, we are stronger.”
We invite everyone to
join us.
Join our community.
You can sign up as a Member (symbolic annual fee + voting rights at the General Meeting) or as a Friend (supporting member).