We are a scientific, nonprofit, non-governmental organization with legal personality, officially established by a decision issued by the Bucharest Tribunal – Sector 1 on January 12, 2018, with headquarters in Bucharest, Sector 1, Târnava Street, No. 5.

SRSTL is an organization aimed at promoting knowledge and research related to lymphedema, a condition characterized by the accumulation of lymphatic fluid in tissues, often caused by surgeries, trauma, or oncological conditions. This society strives to improve the quality of life for affected patients by informing and educating both medical professionals and patients.

Objectives of the Romanian Society for the Study and Treatment of Lymphedema:

• Information and Education: Organizing conferences, seminars, and workshops to educate doctors, therapists, and patients about lymphedema, diagnostic methods, and treatment options.

• Research: Supporting scientific research in the field of lymphedema in collaboration with higher education institutions and research centers.

• Patient Support: Creating informational materials and resources for patients, ensuring they have access to accurate and useful information about managing lymphedema.

• Interdisciplinary Collaboration: Promoting collaboration between various medical specialties involved in the diagnosis and treatment of lymphedema, including oncology, surgery, infectious diseases, family medicine, physiotherapy, and dermatology.

• Representation of Patient Interests: Advocating for patients’ interests before authorities and decision-making institutions to ensure access to necessary treatments and resources.

Activities:

• Organizing regular conferences and symposiums for professionals in the field.
• Creating support groups for patients and their families.
• Publishing case studies, articles, and practice guidelines in specialty journals.
• Collaborating with international organizations to share best practices and experiences from different countries.

Benefits for Members:

By joining this society, members gain access to the latest updates and research in the field of lymphedema, can participate in specialized training, and benefit from networking opportunities with other professionals in the field.

For more information, it is recommended to visit the official SRSTL website, where you can find details about events, available resources, and the membership process.