Jill McNaughton
Last checked 28/04/2008
Jill McNaughton aged 46
The word epilepsy has a power beyond belief.
When I was diagnosed eleven years ago, my life changed completely.
I now had something shameful, something to be kept secret, something not mentioned, let alone discussed. I was alone with this thing and very frightened. I lost my job and there was no one to talk to. The only “advice” I got was a nurse who casually informed me that having children was now obviously out of the question; a woman with epilepsy would not be allowed to look after a baby. I believed her.
Thankfully some progress has been made, but myths still abound. My hope is the British Epilepsy Association’s vision – acceptance and understanding, fact not fiction.
Epilepsy advice and information
- What is epilepsy?
- Children
- Depression
- Disability Discrimination Act (UK)
- Driving
- Education
- Employment
- Epilepsy in later life
- Getting a diagnosis
- Health care and welfare benefits
- Inheritance
- Learning disabilities
- Me and my dad
- Memory
- Men and epilepsy
- Mobile phones and epilepsy
- Osteoporosis, osteomalacia and epilepsy
- Photosensitive epilepsy
- Relationships and epilepsy
- Safety
- Seizures
- Sports and leisure
- Stress and epilepsy
- Sudden Unexpected Death in Epilepsy (SUDEP)
- Syndromes
- Travel abroad
- Treatment
- Women and epilepsy
- Young people and epilepsy
Epilepsy Helpline
- UK freephone 0808 800 5050
- International +44 113 210 8850
- Online Tuesdays 1900-2100
- Email: helpline@epilepsy.org.uk
- Txt msg: 07797 805 390 info
Epilepsy Action blog
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