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Hello, my name is Becca. My goal for this podcast is to share my epilepsy story. Educate people more about it as well. I hope y'all enjoy!
I wanted to start a podcast for awhile now. I'm excited to start this. I hope you'll join me on this journey!
Dear Epilepsy,
I don’t get it. Why do people stare at me now? I know I look weird when I get muscle spasms but I can’t change that. Why do people stare at me like I’m some zoo exhibit? I hate it and I hate you!
I’m bitter today; I don’t know why and I don’t really care. It seems like everything bad comes my way, even though I know that isn’t true.
My mum tells me to look at the good things and not the negative, but everytime I find a good thing you take it away. I did figure skating, it was the only sport I enjoyed and now I can’t. I did drawing and now my hand jerks too much to do it. I used to write, now I forget my ideas.
I’m having a bad day today. I really hate you right now.
Sincerely,
A lost girl.
Layla needs your help. Her condition is getting worse. If you can help, please let me know and Ill put you in touch with the family. Repost please. #HelpLayla #epilepsy #epilepsyawareness #epilepsyproblems #epilepsyfighters #epilepsysupport #epilepsydisorder #medical #medicalhelpneeded #doctor
It's kinda weird that this thing is in my head. It has been a little over 3 months since I've had the RNS device implaned. After a month I got it turned on. My neurologist and techs have been making some changes with the settings. Hopefully soon they will find the perfect settings for me to be seizure free!