- This page is about the 2011 National Epilepsy Week. Please visit the National Epilepsy Week 2013 page to information on what we are doing this year.
The focus of National Epilepsy Week 2011 (15-21 May 2011) was information. This is about making sure people affected by epilepsy have everything they need to make informed decisions about their health and lifestyle.
What happened during National Epilepsy Week?
- Sunday 15th: Lots of Wonga Walks happened around the UK, raising money for Epilepsy Action and raising awareness of epilepsy
- Monday 16th: There's was supplement in the Guardian newspaper [PDF file], featuring an interview with Epilepsy Action vice president Paul Maynard MP
- Tuesday 17th: The All-Party Parliamentary Group on Epilepsy met to discuss education. Epilepsy Action’s Leanne Creighton presented the issues to the assembled MPs
- Wednesday 18th: Epilepsy Action Radio Day
- Thursday and Friday 19th: The winners of this year’s Edwards awards for education were presented with their trophies.on most major networks.]
As part of National Epilepsy Week, we broadcast a 12 hour online radio day. It featured a wide range of programmes with lots of information about epilepsy, how to live with it and how it affects people.
Wake Up with Mark and Aimee
Music and chat, all along an epilepsy-theme. Includes an interview with Rabbi Lionel Blue.
Author William Fiennes shares his favourite passages from his acclaimed novel 'The Music Room' and talks about how the book has allowed him to raise awareness of epilepsy.
Epilepsy and Women
We take a look at the specific issues that affect women with epilepsy, from puberty and pregnancy to the menopause
A Man’s World
Do men talk about their epilepsy? We look at sex, relationships, fatherhood and everything else that come with being a man with epilepsy.
What are your rights when it comes to employment, benefits and social care and how can you access the right support? We explore your experiences and ask those in the know for expert advice.
Your burning questions about epilepsy: call in and talk to staff from Epilepsy Action’s helpline team
The Doctor Will See You Now
A look a health services across the UK: how will NHS reform affect services for epilepsy, what’s going on with the Service Development Directive in Wales and how good are services in Northern Ireland and Wales? We talk to clinicians and people with epilepsy about their experiences and predictions.
A young girl's world is turned upsidedown when she starts have 'funny turns' following a head injury. Follow her journey to diagnosis in Diagnose it Yourself, written by Nina Gray and performed by actors from the Ilkley Players in West Yorkshire.
Driving Epilepsy up the Agenda
Why doesn’t epilepsy have the same profile with politicians and departments of health and education as other neurological or long-term conditions? We explore the barriers to raising the profile and how we might overcome them.
What’s the Alternative?
When the drugs don’t work, what else is there? Look at the ketogenic diet, as well as less mainstream treatments such as homeopathy.
Clarrie’s Story: a Social History of Epilepsy
How attitudes to epilepsy have changed over the last 100 years, through the eyes of one fictional character.
By young people, for young people. Coping with epilepsy growing up and through your teens.
Epilepsy and Education
Achieving your potential: how can education establishments best support people with epilepsy? Pupils and students, parents, teachers and special educational needs coordinators share their views.
What are we up to? We speak to branches, volunteers and Diamond projects we have funded
How is epilepsy portrayed in film, on TV and in the news and how does this shape public opinion? And is it ever ok to make jokes about epilepsy? We talk to those involved about the issues.
The Future of Epilepsy
The research that could revoluntionise our understanding of epilepsy and whether stigma can ever be broken down.
A round-up of the day’s highlights
Final song played [mp3]: Dave Biro: 'Full Esteem Ahead'
By downloading the podcasts you are agreeing to the following terms and conditions:
- Our podcasts are designed to give people information about epilepsy-related issues. They are for information purposes only. We do not give medical advice.
- We try and make sure that our podcasts are up-to-date and as accurate as possible at the time of production. We accept no responsibility for any error or omission. We are not liable for the results of any action you take based on the information in the podcasts.
- The podcasts protected by copyright laws, and are owned by Epilepsy Action. You may download and listen to the podcasts for your own personal use. If you want to use the podcasts or the audio in the them for any other reason, you must seek Epilepsy Action's permission.
- We are not responsible for the content of websites we mention in the podcasts.
- We do not recommend any of the products mentioned in the podcasts, unless indicated. Comments and content provided by guests on the podcasts reflect their individual views and Epilepsy Action can not held accountable for them in any way. It should not be assumed that Epilepsy Action agrees with or endorses any guest just because we allow include the guest in the podcast.