Tim Pitman - writing, theatre, epilepsy and sport

It's hard work living with #epilepsy but my other hashtags make life a happy one #writing #theatre #cricket #friends #fishing #art #beautifulfamily #hockey

[Tim Pitman - writing, theatre, epilepsy and sport @tim_pitman]

Done it! Stigma sucks. Fifty miles in February #epilepsy ⁦@epilepsyaction⁩

[Tim Pitman - writing, theatre, epilepsy and sport @tim_pitman]

@BrainAblaze I agree. You are heroes!

[Brain Ablaze @BrainAblaze]

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

[Tim Pitman - writing, theatre, epilepsy and sport @tim_pitman]

Fifty miles in February, raising money and awareness of my condition for @epilepsyaction

[Tim Pitman - writing, theatre, epilepsy and sport @tim_pitman]

50 miles in February for @epilepsyaction nearly there.

[Tim Pitman - writing, theatre, epilepsy and sport @tim_pitman]

@BrainAblaze Yup. Absolutely no one in my family on either side has had #epilepsy

[Tim Pitman - writing, theatre, epilepsy and sport @tim_pitman]

@ImRobWalker @BrainAblaze Sadly I think the condescending clowns may have moved to my neighbourhood

[Tim Pitman - writing, theatre, epilepsy and sport @tim_pitman]

@Teri65902468558 @BrainAblaze Same. Good at handling my moments, not so good at hiding them

[Tim Pitman - writing, theatre, epilepsy and sport @tim_pitman]

Smashed it today. 8 miles leaving me 36 more to walk out of 50 for @epilepsyaction Check out my walk on Strava.
https://t.co/22gIn9WE7H

[Tim Pitman - writing, theatre, epilepsy and sport @tim_pitman]

Here is the route 2.44 miles done.

[Tim Pitman - writing, theatre, epilepsy and sport @tim_pitman]

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.

[Tim Pitman - writing, theatre, epilepsy and sport @tim_pitman]

@BrainAblaze Yes! Let’s start with Donald Trump

[Todd B @John_Beckham14]

.@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.

[Tim Pitman - writing, theatre, epilepsy and sport @tim_pitman]

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

[Tim Pitman - writing, theatre, epilepsy and sport @tim_pitman]

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

[Tim Pitman - writing, theatre, epilepsy and sport @tim_pitman]

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

[Tim Pitman - writing, theatre, epilepsy and sport @tim_pitman]

@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

[the_epilepsy_guy @Theeppilepyguy]

I'll never let #epilepsy define me. I'll use it as fuel to ignite my passions,my creativity and my purpose. #epilepsyawareness #seizure #seizures

[Tim Pitman - writing, theatre, epilepsy and sport @tim_pitman]

@epilepsysociety @epilepsyaction @defeatepilepsy Was really good. Opened conversations I would never normally had💜

[Tim Pitman - writing, theatre, epilepsy and sport @tim_pitman]

First day out with Invisible disability sunflower lanyard on. Just experimenting to see how I am treated. #epilepsy #invisibledisability @epilepsyaction @epilepsysociety @defeatepilepsy

[Epilepsy Action @epilepsyaction]

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