When I was 2 I had a febrile seizure I stopped breathing and turned blue my mom gave me mouth to mouth and by the time the EMTS arrived I stopped seizing. As i grew from baby to toddler my parents began to see that i was delayed. So i started early intervention at 3 years old I had occupational therapy and PT . In pre k I would get angry and punch any thing that was in front of me after my parents had been observing me in a pre k class and talking to the pre k teachers it was suggested that my parents should take me to a therapist to rule out any behavior issues. he took one look at me and said that I was having seizures he then referred me to a neurologist. At the at the age of 5, I was diagnosed with childhood absence epilepsy but I 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 and then it becomes a pill, no pun intended. My triggers are flashing lights, the transition from the out doors to inside a classroom getting too hot and recently sleep deprivation. When i have an absent my pupils will go from normal to pin point that is the only physical sign the eye can lasts My seizures last one second and happened every minute to every minute and a half. So there are 60 seconds in a minute and 24 hours in a day then I was having seizures every 1440 minutes or 86400 seconds so in total I would have 86400 seizures per day with meds. 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 . I am in collage as you can infer I was not expected to do much of what I just mentioned The effects of my seizures is that I have Aspie like tendencies due to my epilepsy which I know is difficult to understand to put it in simple terms as a result of my seizures my brain compensated and rewired itself i also have severe deficits in Processing Speed, Perceptual Reasoning, and Working Memory, Upper Limb Coordination, Breath Support for speech language, Manual Dexterity, Fine Motor Skills, Hand Strength, Visual Perceptual Skills, and understanding meaning. When was 19 my father died, and 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 . When I was thirteen I had EEG and my seizures showed up 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 for me an absent seizure lasts one-second with is rare but these flurries can last 5-10 minutes.
All the information provided by Medical Education for Visual Learners and associated videos are strictly for informational purposes only. It is not intended as a substitute for medical advice from your health care provider or physician. It should not be used to overrule the advice of a qualified healthcare provider, nor to provide advice for emergency medical treatment. If you think that you or someone that you know may be suffering from a medical condition, then please consult your physician or seek immediate medical attention.
Thank you for this I have petit Mel epilepsy and I tried to talk to my doctor the other day as I think I'm having more frequent seizures and he asked of I bite my tongue, have incontinence or black out and I was sure those questions were related to grand mal seizures not petit mal (aka absence seizures)
@@Med4VL both phenytoin and ethosuximide are Ca Na channel inhibitors.. But etho alone used as therapeutic in case of absent seizures.. But not phenytoin?why?
@@agathiyana3851 Ethosuximide can prevent seizures, while Phenytoin can worsen the them. Other drugs that should also be avoided include carbamazepine, vigabatrin, and gabapentin. Other effective options - for patients who fail or do not tolerate first-line therapy- include valproate or lamotrigine.
Interesting! I have developed these but exercise is a trigger, along with stress, but it's more the stress on my body rather than the breathing.
When I was 2 I had a febrile seizure I stopped breathing and turned blue my mom gave me mouth to mouth and by the time the EMTS arrived I stopped seizing. As i grew from baby to toddler my parents began to see that i was delayed. So i started early intervention at 3 years old I had occupational therapy and PT . In pre k I would get angry and punch any thing that was in front of me after my parents had been observing me in a pre k class and talking to the pre k teachers it was suggested that my parents should take me to a therapist to rule out any behavior issues. he took one look at me and said that I was having seizures he then referred me to a neurologist.
At the at the age of 5, I was diagnosed with childhood absence epilepsy but I 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 and then it becomes a pill, no pun intended. My triggers are flashing lights, the transition from the out doors to inside a classroom getting too hot and recently sleep deprivation. When i have an absent my pupils will go from normal to pin point that is the only physical sign the eye can lasts My seizures last one second and happened every minute to every minute and a half. So there are 60 seconds in a minute and 24 hours in a day then I was having seizures every 1440 minutes or 86400 seconds so in total I would have 86400 seizures per day with meds. 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 . I am in collage as you can infer I was not expected to do much of what I just mentioned
The effects of my seizures is that I have Aspie like tendencies due to my epilepsy which I know is difficult to understand to put it in simple terms as a result of my seizures my brain compensated and rewired itself i also have severe deficits in Processing Speed, Perceptual Reasoning, and Working Memory, Upper Limb Coordination, Breath Support for speech language, Manual Dexterity, Fine Motor Skills, Hand Strength, Visual Perceptual Skills, and understanding meaning.
When was 19 my father died, and 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 . When I was thirteen I had EEG and my seizures showed up 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 for me an absent seizure lasts one-second with is rare but these flurries can last 5-10 minutes.
All the information provided by Medical Education for Visual Learners and associated videos are strictly for informational purposes only. It is not intended as a substitute for medical advice from your health care provider or physician. It should not be used to overrule the advice of a qualified healthcare provider, nor to provide advice for emergency medical treatment. If you think that you or someone that you know may be suffering from a medical condition, then please consult your physician or seek immediate medical attention.
Thank you for this I have petit Mel epilepsy and I tried to talk to my doctor the other day as I think I'm having more frequent seizures and he asked of I bite my tongue, have incontinence or black out and I was sure those questions were related to grand mal seizures not petit mal (aka absence seizures)
Why phenytoin is contraindicated in absence seizures??
Phenytoin has the potential to aggravate absence seizures in patients with childhood absence epilepsy.
@@Med4VL both phenytoin and ethosuximide are Ca Na channel inhibitors.. But etho alone used as therapeutic in case of absent seizures.. But not phenytoin?why?
@@agathiyana3851 Ethosuximide can prevent seizures, while Phenytoin can worsen the them. Other drugs that should also be avoided include carbamazepine, vigabatrin, and gabapentin. Other effective options - for patients who fail or do not tolerate first-line therapy- include valproate or lamotrigine.
@@Med4VL u r ri8 mate... But what i want to know is how phenytoin worsen the absent seizures?...
@@agathiyana3851 The mechanisms underlying that are poorly understood.