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I Go On The Internet And Read As Much As I Can On A Subject That I Really Need Answers To. I Read And Read Does Anyone Else Try For Answers
service dog's you get on internet and there are state funding and sites to help, medications there are so many answers to how it might affect you. We are all different and what works for me might not work for you. How bad are your seizures, how many different types of seizures you have. how has your life changed. We can give our thoughts on things but if you really truly want answers look up studies, look up the good and bad of things and how the numbers in studies have real information. Our… read more
When I want to understand certain subjects, I do research on the Internet and, use YouTube videos and Documentaries on TV
@A MyEpilepsyTeam Member, you have some very good questions. But i'm afraid due to government regulations there won't be any answers. I always wondered why people with epilepsy have to pay for a service dog when people who are visually impaired are given the service dog free. Good luck finding your answers.
@A MyEpilepsyTeam Member
I do a lot of research over the internet to get a better understanding of how things work. If you read my story you could tell. My seizures are from a lack of oxygen at birth. The lack of oxygen killed my brain cells and caused brain damage (seizures).
I agree with Rusti. I do read up on any medication that my doctors prescribed. I have too. Hypersensitivity.
It's dif per person, but I agree with you on your comment here, I do like the site that is here where everyone else can put in from their condition, experiences, treatment, what and how it's effects from and such etc, and then share with the people here and distribute to others and so on, everyone here and their questions and answers, opinion, whatever does make a difference in our lives, I do also when not on this site, do my own research on Google and other resources, haven't found a cure for epilepsy but as for the medical field etc, I would say making progress, that is a good thing, ever little bit of advice and progression is a plus, my opinion
Two Of My Three Adult Children Developed Seizures Around 20years Old. I Did Not, But My Sister Did At 16 And Still Suffers At 62 Years Old.
How Many Of You Have Multiple Family Members With Seizures?
Loss Of Readiing
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