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SARKO
Patient organisation

SARKO

AdultsImmune system disorders

About the organisation

Polskie Stowarzyszenie Chorych na Sarkoidozę (Polish Sarcoidosis Patients Association), known as "Sarko Stowarzyszenie," was established in 2010 by patients themselves, driven by the need to create a supportive network for others living with sarcoidosis. The core mission of the association is to connect Polish patients with sarcoidosis and their families, fostering a vital space for the exchange of experiences and knowledge.

Areas of specialisation

Where this organisation focuses its support

Diseases & conditions
Age groups served
Adults

Organisations in the same therapeutic area Partners active in Immune system disorders

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On this site, “treatment” means an investigational medicine being studied in a clinical trial. Its safety and efficacy for the use being studied have not yet been confirmed, some participants may receive a placebo or a comparator medicine, and taking part does not guarantee any health benefit. The decision to take part is made by the doctor at the research site. This site is for information only and does not replace medical advice.

This service is not affiliated with the European Commission, the EMA, or the official CTIS system. Most information comes from publicly available international clinical-trial registries, supplemented by data from academic sites, national regulators and commercial sponsors. On this site, “treatment” and “therapy” mean a medicine being tested in a clinical trial. Its safety and effectiveness in the use being studied are not yet confirmed, some participants may receive a placebo or a comparator, and taking part does not guarantee a health benefit. The doctor at the research site decides who can take part. This site provides information, not medical advice. Certain content and visual elements on this website have been generated or enhanced using artificial intelligence (AI).