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The latest news, views and opinions from Epilepsy Society.

Aimee smiling
15 January 2014

More and more people with epilepsy are blogging about their experience of living with the condition.  Aimee Haines is a regular blogger - here is what she has to say! 

18 October 2013

Katrina Gerity, events and challenges fundraising officer at Epilepsy Society describes how trekking the Inca Trail in Peru was one of the most amazing experiences.

Two university students walking  around campus.
23 September 2013

When  Alan Kirton moved 200 miles away from home to go to university, he did his best to ignore his epilepsy. But here he explains how his seizures kept catching up him out.

12 September 2013

Epilepsy Society's Christine Brock and Sarah Vibert explain why people with epilepsy need fairer work capability assessments.

9 September 2013

Fiona MacColl celebrates her son Connal's achievement of going off to college and leading an independent student life.

21 August 2013

Katy Norris from Epilepsy Society's Chalfont Centre celebrates Learning Disability Week with a blog about her superhero mum, Joan.

Waving the flag for 66 Epilepsy Society cyclists at Wimbledon
5 August 2013

Bridget Gardiner, director of fundraising and marketing at Epilepsy Society, celebrates the  66 cyclists who took part in RideLondon100 to support people with epilepsy.

Jasmine Smith on holiday in Croatia
26 June 2013

Jasmine Smith, 22, explains why she will never let epilepsy stop her from following her dreams, including travelling alone and cliff jumping.

Mike Reed of Care Quality Commission
20 June 2013

Mike Reed of Care Quality Commission looks at what standards you can expect across all NHS and private health services.

Sarah Vibert, head of development and policy at Epilepsy Society
23 May 2013

Sarah Vibert  at Epilepsy Society explains why charities want the Department of Health to change  ordinary residence rules.


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