Видео

I feel like life is not fair do you have any advice for me and I have no friends people laugh at me and look at me funny and I have been made fun of all my life and my brother in law says I quit things easy . And my brother in law says that my epilepsy is a disease and that’s why no one wants to be around me

Hi Sam my name is John Barrett and my dad treated me bad growing up because I have epilepsy and cerebral palsy and he wanted me to stay inside for ever and then later in life he told me that he wanted me to live in a group home but now he doesn’t even talk to me anymore

I have cerebral palsy and epilepsy do you know of any good podcasts about epilepsy and cerebral palsy. I subscribed to your podcast last month and I just subscribed to your RUclips channel today and your podcast RUclips channel today hi my name is John Barrett

Big huga and love to you Sam ❤ I enjoyed your rant. Stay optimistic ❤

Sorry you went through this too, Sam.

I'm sorry you've made the decision to show your face, however I COMPLETELY understand how the extra burden of setting up lights just to get a good shot would influence your decision. As for you being "too pretty", Epilepsy doesn't care. We need as many faces as possible to show that Epilepsy can affect anyone. I support your decision either way. Keep up the great work!

So frustrating that these platforms just ignore our reports.

I have epilepsy too, i can relate with a lot of things you said, thank you for speading awareness and for your strenght to open up on your condition. 🙏 Have you ever been able to film one of your seizures?

Thanks so much for your support of Marcus and the Mandatory Epilepsy Training Petition.

Great interview with Trevor Gordon. Trevor works as well with Canadian Epilepsy Alliance, Epilepsy Ontario, and Epilepsy South Central Ontario. We would love to promote Epilepsy Awareness Month in Canada during the month of March.

This is great!!!