It is going to alright katie . I have juvenile myoclonic epilepsy.. just hang on and never give up ... Let people say the negative rant about it... But never give up ... God give his hardest battles to his strongest soldiers. God bless you
Omg u are amazing at whot u do keep doibg whot u do i have. Tonic clonic seizuers. Ans i know it is not fear and. U wobt to do whot everyone els is doibg i do too but we have to take it one stop at a time and sorry if u cant read this i am trying too and. I. Am trying to get on with my life. If u look on my youtube channl u will see that i dance. And i try. And do whot everyone els is doibg or a try bit u are amzibg at whot u do. Keep doibg whot u do dobt leat probles get in the away. And. Love u so much. And agen sorry if. U cant read this
I have absence seizures. I was diagnosed at the age of 5 but have been seizure free since the age of thirteen and so was taken of meds which caused massive weight gain a hand tremor and memory loss. The point is meds are good up until a point an then it becomes a pill no pun intended. my triggers are flashing lights, specifically the transition from the out doors to inside a classroom getting too hot and recently sleep deprivation. my parents were told to treat me as a normal child and to see how fare I would develop and look at me now I have graduated high school with honors though I did hope for a regents diploma but after taking the algebra common core regent seven times starting out with a 40 and ending up with a 57 oh well. as you can infer I was not expected to do much of what I just mentioned After my father died, it seems I have had a relapse if that is possible. i still have my absence seizure but it is not enough to put me on meds . i have been getting driving lesson and have 10 -20 seizures in the drivers seat. i take omega 3 cod liver oil liquid form as i can not swallow pills this helps decrease the too -small -to -medicate -seizures i have very small seizures that show up on the EEG as misfired neurons and the Dr. called them "flurries" so here is what my flurries are typically like i will become very spacey i can not interact with my surroundings i also felt locked in to place. i am completely aware my vision becomes like a tunnel and thing start to move or vibrate on there own an absent seizure lasts 1 second but these flurries can last 5-10 minutes.
What were your meds and doseage as I have absence seizures since 19 now 37 and take 400mg epillim m/n and 50mg latimal m/n. Have a tremors in my hands and my legs and arms will finch (small ones, often but you can tell I get them) by themselves at times
Katie, what an amazing and strong young woman you are!
I was diagnosed with Epilepsy when I was 2 years old and had a Brain Tumor surgically removed when I was 8.
23 years Seizure free.
You`re amazing! Keep it up!
May the Lord bless and heal you!
It's got nothing to do with the mass cultural delusion that is religion. Medicine will help the condition. Don't insult us.
It is going to alright katie . I have juvenile myoclonic epilepsy.. just hang on and never give up ... Let people say the negative rant about it... But never give up ... God give his hardest battles to his strongest soldiers. God bless you
I think I'm the only 12 year old with RLS
Omg u are amazing at whot u do keep doibg whot u do i have. Tonic clonic seizuers. Ans i know it is not fear and. U wobt to do whot everyone els is doibg i do too but we have to take it one stop at a time and sorry if u cant read this i am trying too and. I. Am trying to get on with my life. If u look on my youtube channl u will see that i dance. And i try. And do whot everyone els is doibg or a try bit u are amzibg at whot u do. Keep doibg whot u do dobt leat probles get in the away. And. Love u so much. And agen sorry if. U cant read this
Fell sorry to Katie I have epilepsy 15 a day
Well done katie i dont have seizures but its excellent you are getting on.
Hi katie ....tel me what r epilepsi your memory los ...plz tel me
You inspire me. Thank you.
Know about CBD Oil?
I have absence seizures. I was diagnosed at the age of 5 but have been seizure free since the age of thirteen and so was taken of meds which caused massive weight gain a hand tremor and memory loss. The point is meds are good up until a point an then it becomes a pill no pun intended. my triggers are flashing lights, specifically the transition from the out doors to inside a classroom getting too hot and recently sleep deprivation. my parents were told to treat me as a normal child and to see how fare I would develop and look at me now I have graduated high school with honors though I did hope for a regents diploma but after taking the algebra common core regent seven times starting out with a 40 and ending up with a 57 oh well. as you can infer I was not expected to do much of what I just mentioned
After my father died, it seems I have had a relapse if that is possible. i still have my absence seizure but it is not enough to put me on meds . i have been getting driving lesson and have 10 -20 seizures in the drivers seat. i take omega 3 cod liver oil liquid form as i can not swallow pills this helps decrease the too -small -to -medicate -seizures i have very small seizures that show up on the EEG as misfired neurons and the Dr. called them "flurries" so here is what my flurries are typically like i will become very spacey i can not interact with my surroundings i also felt locked in to place. i am completely aware my vision becomes like a tunnel and thing start to move or vibrate on there own an absent seizure lasts 1 second but these flurries can last 5-10 minutes.
What were your meds and doseage as I have absence seizures since 19 now 37 and take 400mg epillim m/n and 50mg latimal m/n. Have a tremors in my hands and my legs and arms will finch (small ones, often but you can tell I get them) by themselves at times