Ariane Weinman

  • Public Affairs Senior Manager

Ariane Weinmann

Ariane Weinman joined EURORDIS in 2004 and works in the Public Affairs team.

She is involved in European public health projects where EURORDIS is leader or partner, currently the EU Joint Action for rare diseases, RD-ACTION, and the EU Joint Action for Rare Cancers, JARC. She is particularly involved in supporting the work of patient advocates in a) implementing EU integrated national plans for rare diseases, and b) in providing recommendations to integrate provisions for rare cancers in adults and paediatric cancers in all national plans for cancer control in EU member states. Ariane also supports the European Patient Groups’ Advocates (ePAGs) in the four European Reference Networks (ERNs) for, or related to rare cancers: EURACAN, ERN PaedCan, EuroBloodNet and GENTURIS.

Ariane has a broad knowledge of the international aspects of medicine, public health and scientific research which are a recurring focus in her professional experience.

She has previously worked for the French Federation of Public Hospitals and the Scientific Department of the French Embassy in China. Ariane holds a Master of Arts in International Policy Studies from the Monterey Institute of International Studies.

She speaks French, English and Mandarin Chinese.

Telephone: +33 1 56 53 52 65
Email: ariane.weinman@eurordis.org

 
 
La voz de los pacientes de enfermedades raras en EuropaEURORDIS La voz internacional de las personas que tienen enfermedades rarasRare Disease International Reuniendo a pacientes, familiares y expertos para compartir experiencias en un foro moderado en distintos idiomas. RareConnect El Programa Rare Barometer es una iniciativa de EURORDIS que realiza encuestas para transformar las experiencias de los pacientes con enfermedades raras en cifras que puedan compartirse con los responsables políticos.Rare Barometer Una campaña internacional de sensibilización que se celebra todos los años el último día de febrero, El Día de las Enfermedades Raras es una iniciativa de EURORDISRare Disease Day Únete al mayor grupo de partes interesadas en toda Europa, en la Conferencia Europea sobre Enfermedades Raras y Medicamentos Huérfanos que se celebra cada dos años. ECRD es una iniciativa de EURORDISEuropean Conference on Rare Diseases