CLF – Cutaneous lymphoma foundation
CLF’s vision is to build a life free of cutaneous lymphoma, eliminating the burden of the disease by promoting awareness, providing education, advancing patient care and fostering research.
A selection of useful links to websites of associations and research organisations providing the most updated information and advice about cutaneous lymphomas.
CLF’s vision is to build a life free of cutaneous lymphoma, eliminating the burden of the disease by promoting awareness, providing education, advancing patient care and fostering research.
Orphanet was established in France. Its focus is on rare diseases and its mission is to improve the diagnosis, care and treatment of this patients. Over the past 20 years, Orphanet has become the reference source of information on rare diseases.
EMA fosters scientific excellence in the evaluation and supervision of medicines, for the benefit of public and animal health in the European Union (EU).
EURORDIS - Rare Diseases Europe is a unique, non-profit alliance of 961 rare disease patient organisations from several countries that work together to improve the lives of people living with a rare disease in Europe. EURORDIS strengthens the patient voice and shapes research, policies and patient services.
ISCL is a non-profit, global organisation which comprises physicians, scientists, and allied healthcare professionals involved in cutaneous lymphomas.
