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Patient and public perspectives

Ceinwen Giles: Giving patients a cancer diagnosis—what we need is more time

September 21, 2017

Enabling patients to fully understand their diagnosis and treatment is something best done over a period of time, says Ceinwen Giles […]

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Patient and public perspectives0 Comments

David Gilbert: Why we need patient leaders

September 21, 2017

There’s not much point in training patient leaders unless there are meaningful opportunities for them in decision-making roles […]

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Patient and public perspectives6 Comments

Amy Price on shared medical appointments—just say no

September 18, 2017

It is premature to identify this strategy as medically helpful without clear outcomes and clinical trials, says Amy Price […]

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Patient and public perspectives4 Comments

Sharon Roman: In good hands

September 13, 2017

What are the qualities that make for a good doctor and what can patients do if they’re missing? […]

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Patient and public perspectives, Sharon Roman0 Comments

Joe Fraser: It takes more than language to make a good patient-clinician relationship

September 13, 2017

If you’re a clinician or a “Type Zero” (someone without diabetes) choosing the words to use when talking about diabetes is not straightforward. That’s true even for “Type ones” like […]

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Patient and public perspectives1 Comment

Nick Smallwood: Young cancer patients advocate for improved care

September 5, 2017

For many young cancer survivors, the impact of cancer does not stop when treatment does […]

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A collective effort is needed to encourage patient centricity in ophthalmic research

August 15, 2017

Alastair K Denniston and Xiaoxuan Liu “Why is it so hard for you guys to have us in the room?” a patient asked. Addressing an audience of leading eye researchers, UK […]

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Bernie O’Reilly: The impact of open disclosure for patients and healthcare staff

August 11, 2017

Patient advocacy was new to me when I joined Patients for Patient Safety Ireland (PFPSI) in 2015. It was established in 2013 by Margaret Murphy, External Lead Advisor at WHO […]

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David Gilbert: Asking “What matters to you?”

August 11, 2017

Asking “What matters to you?” rather than “what’s the matter?” has become a clever bit of reframing within the health service, intended as a phrase to re-imagine the relationship between […]

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Patient and public perspectives1 Comment

Wendy Mitchell: I have dementia and I take part in research. Here’s why

August 8, 2017

Wendy Mitchell, who has young onset dementia, writes about taking part in dementia research, being valued, and opportunities to change the future. Imagine being given a diagnosis of young onset […]

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