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Updated 17 July 2014

Twitter reinforces negative perceptions of epilepsy

A study provides evidence that the perception of epilepsy is not faring well in social media, especially Twitter where 41% of seizure-related tweets are derogatory in nature.

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A revealing study published in Epilepsy & Behavior provides evidence that the perception of epilepsy is not faring well in social media. Kate McNeil and colleagues from Dalhousie University in Canada analysed data collected from Twitter to provide a snapshot of how epilepsy is portrayed within the twitter community.

Twitter, a social networking platform launched in 2006, allows its users to communicate through posting of "tweets" limited to 140 characters. Twitter has gained worldwide popularity since its inception, with approximately 110 million tweets per day from 200 million users worldwide counted in January 2011.

Twitter's role in a number of revolutions, including the 2011 Egyptian revolution and the 2010-2011 Tunisian protest, has confirmed its ability to influence culture and perceptions on a global scale.

How the study was done

In their study McNeil and colleagues analysed 10 662 tweets collected during one week in April 2011 mentioning the word "seizure" or "seizures". They found that 41% of these seizure-related tweets were considered to be derogatory in nature.

Fortunately there were a few tweets that spoke out against mocking those with seizures. For instance, "Why do people joke about epilepsy and seizures? Do they joke about cancer? Attach your brain 2 a car battery & see how funny it is!" articulates this point emphatically.

The researchers do argue, however, that the online voices of those speaking out against such negative stereotypes and disparaging remarks need to be stronger. They emphasise the need for improved epilepsy education to advance public knowledge and behaviour on the topic.

Positive attitude needed

The study concludes that although Twitter could hold the power to positively affect how epilepsy and seizures are perceived, currently an epilepsy stigma is being perpetuated instead.

"While we are well aware of the stigma faced by people with epilepsy, we were shocked to see just how pervasive the problem is in social media. It certainly emphasises a need for public campaigns to combat these negative attitudes," said Dr Brna, corresponding author of the study, based at Dalhousie University in Canada.

Dr Joseph Sirven, Professor of Neurology and Chair of the Department of Neurology at Mayo Clinic in Arizona, in an accompanying editorial wrote, "It is now time for the epilepsy community to rise up, have our own Twitter revolution, and alter the way the condition is perceived.

There is too much suffering and too great a burden for this to go unchecked...By taking charge, we can potentially change the equation and allow the silent voices of individuals with epilepsy to rise up, revolt, and finally correct the misperceptions and eliminate the stigma associated with the condition once and for all." 

(EurekAlert, February 2012)

Read more:

Epilepsy

Living with epilepsy

 

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