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What is Sturge-Weber

Communicating Rare Diseases and Disorders in the Digital Age
Rare congenital disease that is often characterized by a port-wine stain birthmark and neurological and eye abnormalities.
Published in Chapter:
Representation of Patients With Rare Diseases in Spanish Media
Paloma López Villafranca (University of Málaga, Spain)
Copyright: © 2020 |Pages: 25
DOI: 10.4018/978-1-7998-2088-8.ch006
Abstract
There are more than 360 associations of patients with rare diseases in Spain that strive for visibility to obtain funding and encourage clinical pathologies. The Spanish Year of Rare Diseases has been a considerable effort to be part of media agenda since 2013 and a “collective voice” throughout the media has been encouraged with the international initiatives devoted to the cause. Over the past years, representation of patients with rare diseases in Spanish media has been very superficial, despite the renewed interest during the Spanish Year of Rare Diseases. Certain cases as “Paco Sanz” or “Los Padres de la Pequeña Nadia” have negatively affected this representation by using the disease to pursue economic benefit. This chapter reports on the representation of rare diseases through Spanish media and the way it evolved in the last 6 years. The findings highlight the effort that has been made by patient advocacy groups with rare diseases and their relatives and caregivers, who have been recognized and proactive to get the treatment and medication needed.
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