ever since i was little, i've experienced what they call, i guess, partial seizures, and/or chronic partial seizures. i did'nt even discover what was going on with me til about 4 yrs ago, when i had a convulsion seizure, and further got evaluated. ever since...

child with mitochondrial disorder & seizure disorder.Has mutiple issues.On a journey for answers ,treatment & wishing for a cure.

30 years living and laughing with the big E. 42 years young but still right height weight and fit. Loves outdoors and adventures. Into all sports, coffee and things that are bad for me. Live in three storey house with balcony :-) Like to travel and live my...

This is the journey of Abigail Nicole Thornsberry's life with epilepsy. The obstacles of daily life for Abigail, her parents, and her siblings dealing with Abigail's epilepsy since birth and her recent diagnosis of Lennox Gastaut Syndrome.

43 yr old male living with epilepsy and surviving on Tegretol

hi i'm Aimee and i've had seizures for almost 17 years. I just learned about this website and i think it rox. Anyway, hope you don't get too bored. Laterz.

Reading some peoples' experiences here, makes me realise my situation is not so bad after all. I had a cerebral abcess at the age of 11. and surgery to remove it resulted in my suffering from seizures. I still have 5 holes in my head where they drilled to...

im still here

What ever is on my mind at the moment

MY NAME IS ASHLEY-MONIQUE HALSELL, I AM A BRITE AND LOVING YOUNG WOMAN WITH EPILEPSY. I HAVE A TWIN SISTER NAME ARIYANNA WHOM DOES NOT HAVE EPILEPSY. I AM IN MY SENIOR YEAR AT WAYNE STATE UNIVERSITY, AND IN MY SENIOR YEAR AT ORLANDO CULINARY ACADEMY. I AM...

The first few pages cover my general life history and how I arrived at this point. Now it's a mixture of old writing, journals, poems etc and newer writing that I hope will help or at least make others understand that despite being seizure free for just over...

hey everyone. i have a project due in my computer apps class. we're suppose to come up with something that isn't on the market yet. i was tryin to think of something that had to do with epilepsy and seizures. something that would help out with them or something....

This is my life with epilepsy. Things that have happened whether I like it or not. This blog is dedicated to the memory of my father who passed away on my birthday in 2006.

call this a kind of journal if you will just because its nice to share things with someone.

Who knows? I'm totally lost with this and other problems, so who knows what might show up here?

I went without seizure meds for WAY too long. I am still paying the price...the last 4 seizures did severe muscle and Kidney damage, and I'm lucky I didn't fracture my skull. I will ALWAYS take my sz meds from now on, and make sure I follow up with a neurologist....

When i was 18 months old i suffers a convulsion & i had a high tempture and the quacks dident know if it was menigites that i had anyway my mum said the gave me a lumber puncture and this i think caused scaring on my left & possible right Tempole lobe....

Bob Sutton—Old Fool with a Big Heart From the start, Bob had ideas that pointed him in directions that veered from the ordinary. Born in 1952, he first wanted to be an astronaut. Discouraged about the long wait before he could soar through space, he...

I was just diagnosed with epilepsy in the beginning of last year. I know very little about epilepsy. I thought epilepsy was when a person passes out. But that is not the case. Recently, I would wake up in the middle of the night and I can feel like my soul...

I've had the big E for 40 yrs. Very few siezures per year,often going for up 2 yrs between szs. I had a sz in 1991...stayed sz-free until June 2003 (all while on carbatrol. On June 7, 2003 I felt waht wassdlike a lighting bolt run thr the left side of my body....

Well this blog is about a little boy and how he develops into a young adult and is told by doctors that he is cured and that he no longer has to take medicine or have annual check ups. Then one day during mid-life a double whammy hits in the middle of the night!

my expierinences , frustrations, trials and tribulations (yes there are some) , and lastly opinions on trying to live with epilepsy.

the very frist time i came on this site i thought i would only use it the once. but this site has become my life line for when i cant talk to anyone in person or wen somet else goes wrong in my life or wen i just need support or a general chat. the people...

I will provide you with info not only about my life and how it has been affected with seizures, but my successes also in life.

Mother,Wife Daughter,Friend and prisoner of my own body.

Grand mal

The feeble fumblings of a flippant friend.

My sons newly diagnois!!

Here is how it was for me when I was growing up, and later on in life with epilepsy. How I was treated how ppl reacted.

This blog will contain how I feel being a mother of a child who has Epilepsy. The changes that I see my daughter going through and how I am dealing with it all. I feel that sometimes people forget what the parents are dealing with. Here you can write me back...

I had a right temporal lobectomy in 1983. Went fine- seizure free until car accident 1987. Brain damage, memory loss, visual memory loss, seizure returned. I'm unable to work due to memory loss, despite a Master's in Social Work. A "selah" is a pause- that's...

Since all this started 15 months ago nothing about my now 6 1/2 is the same. We now have a new attitude and new behaviors. Brennan has complex partial seizures while sleeping. We was started off on Tegretol and when it was decided that it alone was doing...

My Blog

Been dealing with grand-mal seizures since I was 14, I'm now 33 and it still controls my life. Any relations out there to this? How do u cope? Email me at: blueyes73@comcast.net

I was just a fifth grader and not aware of epilepsy at the time that I began to notice that something was a little different about me. It was just about a week before school was to let out for the summer-time and I was helping a friend of mine carry a TV...

I am a classical musician (clarinetist) in my late twenties, and have been living with epilepsy since I was 13. Boudica was an ancient Celtic Warrior-Queen, and she is my "user-name-sake" because it has truly been a battle to get through school, and to work...

Trying to get some feedback from other parents who are dealing with epilepsy in their teens. I would love some direction!

Just a bit about my world over the rainbow.

The journey of a mother and father trying to find out what is wrong with there son... and then handling the results appropriately.