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Blog

Mon, 07/25/2016 - 15:27
I was diagnosed with epilepsy 4 years ago when I was 15 and in June I started I blog where I share some of the things I've learned and my own experiences. It's quite advicey as I know how difficult it is to be a teen with epilepsy and how lost you can feel. I really hope I can help even just a few people who are currently going through this so feel free to check it out :) anepilepticgirl.blogspot.co.uk

Comments

You can reach out to me via

Submitted by Jacinda_5a467b935fe87 on Wed, 2018-03-28 - 18:29
You can reach out to me via Facebook or email if you would prefer.  My email address is jhlay@hotmail.com.  I look forward to hearing from you.

My son is 13 and has been

Submitted by thomas12 on Sun, 2018-12-02 - 03:32
My son is 13 and has been diagnosed with a rare form absence status epilepsy. His seizures show no symptoms until the seizure has lasted for hours! The only warning we had was he started acting only tired at first then gradually he started acting confused and from there for 24 hours he didn't know what year it was, where he went to school, or even what grade he was in etc. his motors skills were perfect and he talked to everyone normal the entire time, he just couldn't answer certain questions. The hospital kept him overnight and gave him fluids and in 24 hours he slowly started remembering and they said he was good and sent us home. We know now that he was having a constant seizure the ENTIRE TIME of his confusion! Almost 3 months later he begins having the same symptoms when I woke him up for his 2nd day of school. we are sent for an EEG, which revealed at 10 am he was actually having what the neurologist referred to as the worst EEG he had seen) we then were sent to a different children's hospital where they observed him until 8:00pm, all this time my son passes every test, he is talking and his motor skills are completely normal! They finally begin his EEG around 9:00pm. It reveals he is still in seizure! They are blown away. Say they have never seen an absence case like his and they quickly gave him a big dose of adavan which immediately stops the seizure and he is able to regain his memory immediately. Does anyone have a child who has these same symptoms? His neuro doctor ordered a brain glucose test, but when we went for a follow up last week they said the test had been canceled and they had no idea what happened? When I asked if they were going to draw his blood and re do the test, they said that his medicine was controlling the seizures so far so they didn't feel the need to do the test!  I need advice and some direction. I searched further; visited epilepsy websites, blogs. I find info about someone having the same symptoms. I was really determined. Fortunately for me, I stumbled on a testimony of someone who had epilepsy for several years and was cured through Herbal medication. I read awesome stories of people whose condition were worse. I was not a fan of Herbal Medication, because I once believed that they have not researched it enough. But due to numerous testimonies  I was more than willing to try it…. I contacted the doctor lawson. my son used the herbal medication. It became a miracle for my son free from rare form absence status epilepsy within 3 months. The herbal medication worked without any trace of side effects on my son…. totally free.  I decided to share my son story to tell people out there, that there is a hope for those with epilepsy using herbal medicine, and anyone who suffers from seizures can be cured. 

I began having seizures at

Submitted by Bailey18 on Sat, 2020-04-18 - 11:42
I began having seizures at the Same age. Doctors could not figure out why. Eventually a doctor discovered 2 main causes were hormones, that's why they started at that age, and aspartame, fake sugar. No birth control or diet pop.

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