Marta Campabadal

  • RareConnect Manager

Marta Campabadal

Marta Campabadal joined EURORDIS in 2012 as RareConnect Coordinator and is now working as RareConnect Manager.

Marta is part of the Communications team based in Barcelona and works on the RareConnect project. She develops and maintains the RareConnect communities for specific rare diseases while bringing together and engaging patient organisations and patient advocates from all over the world in order to build successful online communities.

She also works identifying the needs of rare disease patients in order to match those needs to available resources, services, patient groups and contact people.

Among other responsibilities, Marta is in charge of the social media channels of RareConnect, designing and implementing the communication and content strategy.

Previously, Marta worked for the Government of Catalonia in internal communication and promotion activities.

Marta has a degree in Advertising and Public Relations from the Pompeu Fabra University in Barcelona.

She is a native Catalan speaker and also speaks Spanish and English.

Telephone: +34 932 20 32 59
Email: marta.campabadal@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