If you're taking your meds, getting your sleep, minding your triggers, and still having seizures, you're doing wonderfully. We're proud of your effort. #Epilepsy isn't your fault. #EpilepsyAwareness
A dark start to my Fifty Miles in February. I am walking fifty miles accompanied by my epilepsy to raise money for @epilepsyaction I hope to help in the fight to stop the #stigma many people with epilepsy endure.
.@cannabillsful Most of my life I've fought off epilepsy. Since was 8. Now I have to fight off epilepsy and Trump's idiocy? Hell if I can fight off epilepsy I can fight off idiot Trump.
Anyone know if there is a badge, endorsement or award for employers who welcome and work positively with #epilepsy. I have been fortunate with my employer, over 10 years of support. I have had some shockers. Nice to have a positive. #nostigma@epilepsyaction@epilepsysociety
Good news! I am no longer feeling overwhelmed. Wonderful work place, colleagues and family help me put the building blocks in place to make my recover swifter @epilepsyaction#wpilepsy
Even after 43 years this is a journey of discovery. I have discovered the word ‘overwhelmed’. It really describes how I feel some mornings / days. Once I lose that feeling I power on #epilepsy won’t beat me @epilepsysociety@epilepsysociety @Richardrh_1967
@Richardrh_1967 Totally get that. I journal like mad when #epilepsy is taking up too much space in my mind. Journaling loads at the moment 😩. One of those phases when I want an angel to tell me everything I need to do and make all my decision making for me
Help us to encourage change.
People with epilepsy are struggling to get access to their medication and this is unacceptable.
We urge everyone who can to send this letter to their local MP, https://t.co/x0YBHz570F Action
https://t.co/FEfutLlGSo