Research vs Social Welfare in Ireland — A 30 Minute Life

Yesterday I had the honour of being a keynote speaker at a conference which focused on including patients in research. By this I mean people who live with illnesses should be equal members of the research team, deciding what will be researched and how the research is conducted. The phrase we often use is:

Nothing about us, without us.

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Having lived with chronic illness for more than a quarter of a century I am now sharing my experiences. I post on www.a30minutelife.com, Facebook and Twitter

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Robert Joyce

Robert Joyce

Having lived with chronic illness for more than a quarter of a century I am now sharing my experiences. I post on www.a30minutelife.com, Facebook and Twitter

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