Despite the needs of patients increasing around the world, healthcare continues to be inaccessible and too expensive for many people. New technology is beginning to change this but must be evaluated properly.
Success! The National Organization of People Living with Hepatitis B campaigns for the inclusion of Hepatitis B in Uganda’s health budget.
BioMed Central have established a new, open access journal called Research Involvement and Engagement. Patients and the public are invited to take part in developing and reviewing the journal.
Sophie Paterson, Communications Manager from MSIF, explores why access for people with MS is so important this World MS Day on 27 May 2015.
WHO: Is it sufficient to treat an illness without knowing and addressing the conditions that cause or contribute to individuals becoming sick in the first place?
Why should health professionals know about the conditions in which you live? By Sir Michael Marmot, Director of the UCL Institute of Health Equity and President-Elect of the World Medical Association
The Governing Board of the International Alliance of Patients’ Organizations ( IAPO ) has announced the appointment of Mr Kawaldip Sehmi as the new Chief Executive Officer of IAPO .
We thank Rebecca Johnson, Partnerships Manager, and Stephen McMahon, Interim Chief Executive Officer, for their contributions to IAPO. We also welcome Ziede Mesonyte as our new Operations Coordinator and Rose de Mendonça as our new Senior Membership Officer.
The bursary process to attend the 7th Global Patients Congress (2016) opens soon.
The World Health Organization (WHO) made it unambiguously clear today that researchers have an ethical imperative to make results from all clinical trials – including past trials – publicly available.