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Patient and public perspectives

Ben Stecher et al: Research into Parkinson’s Disease needs reform

March 13, 2018

As Parkinson’s Disease (PD) patients and research advocates, we remain hopeful that the whirlwind of research and translational studies which flood the pages of journals around the world will result […]

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Patient and public perspectives0 Comments

Sharon Roman: My doctors, my placebo effect

February 27, 2018

An excellent patient-doctor relationship is capable of doing much good, even when medicine no longer can […]

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Patient and public perspectives, Sharon Roman0 Comments

Anya de Iongh: Are patients and carers healthcare’s untapped workforce?

February 23, 2018

On Wednesday 31 January, the dark and cold weather was a contrast to the warmth, passion, and dynamism of the contributions to The BMJ’s first Twitter chat of 2018. 800 plus […]

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Anya de Iongh, Patient and public perspectives0 Comments

Dawn P Richards: The patient as a person

February 14, 2018

We need to recognise individuals as more than simply a patient […]

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Patient and public perspectives0 Comments

Humanising birth: Does the language we use matter?

February 8, 2018

Language matters as a way of respecting women’s views and ensuring that they are empowered to make decisions […]

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Guest writers, Patient and public perspectives0 Comments

Elizabeth Jameson: “I wish my health provider knew…”

January 22, 2018

As a person living with the progressive illness of Multiple Sclerosis, I visit my waiting room often. This experience can be stressful and isolating not only for visitors who are […]

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Patient and public perspectives6 Comments

Jeremy Taylor: There are reasons for patients to welcome Hunt’s return to the Department of Health and Social Care

January 17, 2018

What, as patients, are we to make of the re-appointment of Jeremy Hunt, yet again, to the government’s health brief? […]

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NHS, Patient and public perspectives0 Comments

Kirsty Gadsby on delayed diagnosis: “I felt validated after years of feeling a fraud”

January 16, 2018

Listening to patients and thinking outside the box can make the difference between diagnosis and dismissal, says Kirsty Gadsby […]

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Patient and public perspectives0 Comments

Anya de Iongh: Patients need to be activated, but so do clinicians and the system

January 9, 2018

It has been three and half years since The King’s Fund published a report on Patient Activation, and since then patient activation is increasingly on people’s radars. Patient activation is […]

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Anya de Iongh, Patient and public perspectives1 Comment

Annette McKinnon: Patients need equal access to information

January 5, 2018

I was diagnosed with rheumatoid arthritis in the days before the internet, so I had to rely on magazines and newspaper articles as a back-up to the sparse information that […]

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Patient and public perspectives3 Comments
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