You are welcome. One of my board members and I both have epilepsy and we feel there is not enough educational information on epilepsy for those living with it. Please subscribe to our channel because we are researching and putting a lot of great information on the channel about epilepsy. If you have any questions, you can email me at info@defeatingepilepsy.org.
Very good video. 2 1/2 years ago I had an inner ear infection that traveled to my Left Temporal Lobe, forming a large abscess . Usually immediate surgery is required, but mine was deemed inoperable and I spent 2 months on IV antibiotics at home; three different antibiotics. My Infectious Diseases Physician said I was only her second patient to survive without surgery. This left me with TLE. My Neurosurgeon got me in to see a Neurologist who’s entire practice is Epilepsy and other seizure disorders. He is one of the best in the country and has many patients come in from other places in the country. It normally takes 6 months to see him but he took me immediately as he was a friend of my Neurosurgeon. God sent me to this man!! He is aggressive and won’t take no for an answer. He brought me to a point where I felt I could live with it. His response was “No, that’s not acceptable. I don’t want you to live with it. We’re going to stop it!!” Gotta love a Doctor like that! I’m on a strong dose of Lamotrigine. , and I haven’t had a known seizure in over a year! I have auras, but they stop at that. Friends, find a good Neurologist who knows what the Hell he/she is doing. My short term memory and other symptoms exist. Those I will live with for life, but there is hope for finding how to minimize this disease!! I’m a new subscriber to this fine channel.
Hi Mara, I'm glad that you are happy and can advocate for yourself. Any type of epilepsy is challenging to live with. I have been battling epilepsy for 41 years now, most of my life. I can relate to feeling that I could never describe what I am feeling to others. Stay strong.
I stated having seizures in my 20s so over 25 years now. I'm currently weaning off of my third and final seizure medication! I've started having seizures again however I'd rather use CBD than put up with the brain fog and anxiety of being on meds! Take care!
I have simple partial, complex partial, and grand mal seizures although simple partial seizures are what I have most often. It's like a very short, very intense panic attack where my stomach rises into my chest and then falls 40 stories down.
I have had all three types in my lifetime as well. The tonic-clonic and complex partial, I never remember anything, I just regain consciousness with a migraine and get sick. The simple partial ones are scary. I use to have the ones like you, but last year I had a few where I couldn't feel the lower part of my body, like my torso was detaching and I was floating over the table. Felt like an out of body experience. There were a couple where for a few moments, all I could see was white, it was like being blind for a moment. Those ones scared me big time. Even though the simple partial ones are brief, they can be very scary.
Hellow im just letting you know that this is Great information to Read + look at also listening too ,/ Good Advice for people suffering from Long time with Epilepsy ..💫 .
Thank you so much Brendon. That is exactly what I want it to be. Please check out our other videos as well. If you have any questions, please email us at info@defeatingepilepsy.org and we are happy to help.
I have been having episodes where i get twitching in my wrists and feel confused or scared and have extreme sweating like soaking through layers of clothing in minutes and leaving a puddle during that i am told i am unaware of whats going on stare into space and seem very confused and its obvious in my eyes that im not there. After its over i feel completely exhausted and have severe fatigue and am emotional the next day... Dose this sound like a seizure? It appears to happens when my body is run down, sick, or near my cycle
I'm sorry that your son is not doing well. Please email me at nboehm@defeatingepilepsy.org and I can see if I can find you some journal articles going more into detail about the condition and treatment. Right now here is a link for an article on abdominal epilepsy: www.mayoclinicproceedings.org/article/S0025-6196(11)62437-3/fulltext
The aura is like a warning sign telling you a seizure is going to come it's like you does forgot how your body feels when it's normal it's a scary feeling
Im still battling this epelipsy since 14 and I'm 24 now. I had all of the above symptoms once I went to college from the stop and I don't remember how I reach the place.. Couldn't imagine how do I avoid cars and bikes on that particular day. One time I was taking a test in the exam hall and i think this seizure hits me.. The only thing I remember is that my teacher woke me up and told me to go to the principal's office and it seems like I've been sleeping on the desk and haven't written anything yet and that was when I realised something is wrong with me. I took the several test and it was in the pandemic time the doctor found out that it was this epilepsy.. Since then I took medication and of course I gain alot of weight but looks like these drugs couldn't help me much 😢 anxiety's hitting hard these days could you tell how do I stop all these worries because I could not go anywhere. Couldn't make it through college, unemployed and so many this. My whole family's always worried about. Couldn't go anywhere without taking anyone with me
I'm so sorry you are going through all of this. It took my doctors a long time before they found a combination of medication to get my seizures under control. I had a seizure in college as well in class so I can empathize on how painful and frustrating that is. The weight gain is very common and very frustrating. I hope in time, they can find the right combination of medication or something like a device can help. If you have been diagnosed with drug-resistant epilepsy, see if there are other options for you. Please be proactive and advocate for yourself. I found the more I learned about what I was dealing with, the more I got my health and well-being under control.
I had tonic-clonic seizures also known as grand mal seizures for 15 years. They can greatly impact someone's life. I'm sorry you have been dealing with this for a couple of years now. Stay strong and take care of yourself.
@@DefeatingEpilepsyFoundation I've not been this bad with my fits since I was a teenager my epilepsy has nearly cost me my own life before a number of times
@@Addy2023X it's the same with me. I'm sorry you are going through all of this. A lot of people do not understand the impact epilepsy has on someone's body.
Think I have this but I'm worried that nobody will believe me because they think I'm just crazy. :( I have strange episodes of super intense dejavu, depersonalization, and a sense of impending doom washes over me. My stomach usually hurts. I'm really tired.
I would seek medical attention and find a doctor to help you. I don't think anyone will think you are crazy. Before my seizures were controlled, I would become extremely frightened and have the same feeling of doom. After the seizure, my stomach hurt and I would get sick, then go to sleep. I'm not a physician, but from my own personal experience, it sounds like a seizure.
@@DefeatingEpilepsyFoundation I wish I didn't have so much stuff going on with me. Thanks for replying though. I will bring this up to a Dr. I'm in between Dr right now.
@@echastee you are very welcome. If you have any questions, please feel free to email me at info@defeatingepilepsy.org. I'm happy to help in any way that I can.
I am currently struggling with the same dilemma. I have bipolar disorder and as a result have also endured some emotional trauma, so when I had a strange and intense experience where I lost partial consciousness while driving about a year ago, they just said I had been under extreme stress and was extremely dissociated. But I have grown up with on and off depersonalization my whole life and something about this episode really bothered me. It still bothers me because I had a visual aura as one would have before a migraine, and my balance and sense of direction was impaired, things I have not experienced with depersonalization. I have since had another, less intense incident. They could be depersonalization episodes but they were so intense and different, plus I had lapses in my memory for days after each. When I looked up some of my experiences 'temporal lobe epilepsy' popped up and a lot of the symptoms were familiar, like the "zoning out" and the deja vu and the random feeling of your stomach dropping. I don't know I just feel like I should've gotten it looked into further but am afraid they will take one look at my file and see "Bipolar 1" and write it off.
@@hannahhansen2785 there are people who are bipolar and also have seizures. Working with both a neurologist and psychiatrist in the past was a frustrating experience I admit. I have epilepsy and PTSD and the nurse practitioner tried to convince me I was bipolar when I knew I was not. I have had a couple of traumatic experiences which led to me having PTSD. I find the problem a lot of times is the lack of communication between the doctors, that was my experience at least. I would try to find a good neurologist to see if they can rule things out or if they are seizures, do something to help. Keep a journal of what you are experiencing so the doctor has some information to work with.
Temporal lobe epilepsy is when people have seizures in that area of the brain. Temporal lobe psychosis is caused by grey and white brain matter deficits in the temporal lobe. Here is a link from an article explaining it in more detail: pubmed.ncbi.nlm.nih.gov/21119155/. Hope this helps.
@@DefeatingEpilepsyFoundation Hellow im just letting ya Know that there's a Difference Between them because i had them on both Sides of my Head the One on the Left was, Bigger than the One on the Right So they Do ne the Surgery on the Left Side Cut half The Skull and and a lot Better know .. The Right Side was Smaller in the size Still there..
I have TLE and I've had psychotic episodes but I've been diagnosed with bipolar 1 as well, which was diagnosed about ten years after I developed seizures so the seizures came first.
I had sonething like this when i was 17~20 but now im 23 and it didnt happen for 3 years now so idk if one day it will reappear or is it gone for good? I never talked to a doctor about it
It may not happen again or it can happen in the future. I have had epilepsy for 41 years now and I haven't lost consciousness in years. However, since having long-haul covid I started to have auras again and I am much more sensitive to my triggers compared to before covid. As we get older, so many things can affect us that could cause seizure activity to start again.
I think I had a focal onset impaired awareness seizure for the first time according to my discharge paperwork. I was found unconscious with my arms extended and my hands clenched and shaking a bit, but I don't see that symptom mentioned in any of the videos I am watching. Is that possible with this type of seizure? Or does that mean it became a general seizure or something? I will ask my neuro but it's a while to my appointment and just curious in the meantime
I'm not a doctor so I cannot diagnose but what you are describing sounds like a tonic seizure or tonic-clonic seizure. Tonic seizures you become stiff and then tonic-clonic you become first stiff and then start to shake. We have videos on both of them. Tonic and tonic-clonic seizures are generalized seizures. I would discuss it with the doctor because he or she would know and would know what approach to take. I hope this helps.
In the last six weeks I’ve had the following experience 3 different times. I get a strong odd smell, I have an intense feeling of Deja Vu regarding what seems to be a dream I’ve had previously (I can actually see the dream somehow, & the sense of familiarity is overwhelming), it lasts about 30 seconds. I them feel disoriented for a couple of minutes. I’ve also had issues with short term memory (names especially) for years. Multiple times a day I can’t recall peoples names that I work with, or unknowingly call people by the wrong name. I’M WORRIED, WHERE DO I GO FROM HERE??
Have you seen a neurologist or epileptologist? I would see one and have them run some tests. Write down what you have been experiencing and let them know. It would be good to start keeping a journal to see if there is a pattern, if they are happening in a certain situation. They can do an EEG to see if there is seizure activity and an MRI to see if there is anything that can be causing this. That would be the first step I would take.
Thank you so much! It’s reassuring to know that other people share similar experiences. I’ve been taking methadone for 16 years, & I’d always assumed that my issues with memory were related to my medication 💊 but after the intensity of this last episode, I think it’s time to get checked out.
@@mattsheezy5469 you are very welcome! I hope things go well. Please feel free to reach out to us at info@defeatingepilepsy.org if you need help with anything.
My memory is effected aswel and straight after a seizure I don't know where I am or what I'm doing, like it wipes my memory for a few minutes. It's pretty scary
@@elishadoyle8191 it is scary. That's how I was when I had tonic-clonic and complex partial seizures. A lot of people do not understand the effect having a seizure has on the body and how it affects us.
I don't have family history of epilepsy but I getting déjà vu many times but I also think that's my anxiety because one day I get déjà vu then I research about déjà vu and I also know about epilepsy then I saw a "real" video of temporal lobe seizure then I scared to get seizure then I getting déjà vu like feeling for some nanoseconds everyday like 2 to 3 times a day. I am scared because I also have anxiety disorder and Is anxiety can cause seizure? And sometimes I feel déjà vu like feeling continuously like about 2 min even what I am thinking that also! I am really scared
High levels of anxiety and stress can trigger seizures. Stress is a trigger of mine and I exercise and meditate to keep my stress levels down. I would keep a journal of what is happening and see if you can find a pattern of things that cause you to feel like this. Once you do, find ways to reduce your stress and anxiety. You can always email us at info@defeatingepilepsy.org if you have any questions.
I'm reading a book on temporal lobe epilepsy and it says that half of people with focal seizures aren't diagnosed so they could be seizures! See a neurologist if you can or your family Dr. anyway!
Epilepsy can be a nightmare in someone's life. That is why we need to work to not only advocate for more people to understand what epilepsy is, but to work towards improving the quality of life for people battling epilepsy. That is why I am working to educate people who do not have epilepsy about it, especially in the workforce.
Thank you for your comment! We created another video on this topic with updated information in November of 2022 in which we address the temporal lobe's role in long-term memory: th-cam.com/video/i6Bxpckv_d4/w-d-xo.html
After years of inexplicable experiences, I can't believe that i finally learned what's wrong with me. Thanks for this video
You are welcome. One of my board members and I both have epilepsy and we feel there is not enough educational information on epilepsy for those living with it. Please subscribe to our channel because we are researching and putting a lot of great information on the channel about epilepsy. If you have any questions, you can email me at info@defeatingepilepsy.org.
@@DefeatingEpilepsyFoundation sure will! Thank you
What experiences did you have?
Please, share some experiences!
We’re u diagnosed or prompted to search further?
Very good video. 2 1/2 years ago I had an inner ear infection that traveled to my Left Temporal Lobe, forming a large abscess . Usually immediate surgery is required, but mine was deemed inoperable and I spent 2 months on IV antibiotics at home; three different antibiotics. My Infectious Diseases Physician said I was only her second patient to survive without surgery. This left me with TLE. My Neurosurgeon got me in to see a Neurologist who’s entire practice is Epilepsy and other seizure disorders. He is one of the best in the country and has many patients come in from other places in the country. It normally takes 6 months to see him but he took me immediately as he was a friend of my Neurosurgeon. God sent me to this man!! He is aggressive and won’t take no for an answer. He brought me to a point where I felt I could live with it. His response was “No, that’s not acceptable. I don’t want you to live with it. We’re going to stop it!!” Gotta love a Doctor like that! I’m on a strong dose of Lamotrigine. , and I haven’t had a known seizure in over a year! I have auras, but they stop at that. Friends, find a good Neurologist who knows what the Hell he/she is doing. My short term memory and other symptoms exist. Those I will live with for life, but there is hope for finding how to minimize this disease!! I’m a new subscriber to this fine channel.
I had this all my life. I am 40 now.
I never knew how to describe my feelings .
I am so happy that now I know
Hi Mara, I'm glad that you are happy and can advocate for yourself. Any type of epilepsy is challenging to live with. I have been battling epilepsy for 41 years now, most of my life. I can relate to feeling that I could never describe what I am feeling to others. Stay strong.
I stated having seizures in my 20s so over 25 years now. I'm currently weaning off of my third and final seizure medication! I've started having seizures again however I'd rather use CBD than put up with the brain fog and anxiety of being on meds! Take care!
I have simple partial, complex partial, and grand mal seizures although simple partial seizures are what I have most often. It's like a very short, very intense panic attack where my stomach rises into my chest and then falls 40 stories down.
I have had all three types in my lifetime as well. The tonic-clonic and complex partial, I never remember anything, I just regain consciousness with a migraine and get sick. The simple partial ones are scary. I use to have the ones like you, but last year I had a few where I couldn't feel the lower part of my body, like my torso was detaching and I was floating over the table. Felt like an out of body experience. There were a couple where for a few moments, all I could see was white, it was like being blind for a moment. Those ones scared me big time. Even though the simple partial ones are brief, they can be very scary.
Hellow im just letting you know that this is Great information to Read + look at also listening too ,/ Good Advice for people suffering from Long time with Epilepsy ..💫
.
Thank you so much Brendon. That is exactly what I want it to be. Please check out our other videos as well. If you have any questions, please email us at info@defeatingepilepsy.org and we are happy to help.
I have been having episodes where i get twitching in my wrists and feel confused or scared and have extreme sweating like soaking through layers of clothing in minutes and leaving a puddle during that i am told i am unaware of whats going on stare into space and seem very confused and its obvious in my eyes that im not there. After its over i feel completely exhausted and have severe fatigue and am emotional the next day... Dose this sound like a seizure? It appears to happens when my body is run down, sick, or near my cycle
Madam can u explain about abdominal seizures my son is suffering from that? No treatment helped him
I'm sorry that your son is not doing well. Please email me at nboehm@defeatingepilepsy.org and I can see if I can find you some journal articles going more into detail about the condition and treatment. Right now here is a link for an article on abdominal epilepsy: www.mayoclinicproceedings.org/article/S0025-6196(11)62437-3/fulltext
I should add that the infection left me with a large infarction and much scarring in my LTL.
The aura is like a warning sign telling you a seizure is going to come it's like you does forgot how your body feels when it's normal it's a scary feeling
For me yes. I become very frightened before having a seizure.
Im still battling this epelipsy since 14 and I'm 24 now. I had all of the above symptoms once I went to college from the stop and I don't remember how I reach the place.. Couldn't imagine how do I avoid cars and bikes on that particular day. One time I was taking a test in the exam hall and i think this seizure hits me.. The only thing I remember is that my teacher woke me up and told me to go to the principal's office and it seems like I've been sleeping on the desk and haven't written anything yet and that was when I realised something is wrong with me. I took the several test and it was in the pandemic time the doctor found out that it was this epilepsy.. Since then I took medication and of course I gain alot of weight but looks like these drugs couldn't help me much 😢 anxiety's hitting hard these days could you tell how do I stop all these worries because I could not go anywhere. Couldn't make it through college, unemployed and so many this. My whole family's always worried about. Couldn't go anywhere without taking anyone with me
I'm so sorry you are going through all of this. It took my doctors a long time before they found a combination of medication to get my seizures under control. I had a seizure in college as well in class so I can empathize on how painful and frustrating that is. The weight gain is very common and very frustrating. I hope in time, they can find the right combination of medication or something like a device can help. If you have been diagnosed with drug-resistant epilepsy, see if there are other options for you. Please be proactive and advocate for yourself. I found the more I learned about what I was dealing with, the more I got my health and well-being under control.
I have grand mal fits , they do my head in and recently over the last couple of years , it has affected my daily life.
I had tonic-clonic seizures also known as grand mal seizures for 15 years. They can greatly impact someone's life. I'm sorry you have been dealing with this for a couple of years now. Stay strong and take care of yourself.
@@DefeatingEpilepsyFoundation I've not been this bad with my fits since I was a teenager my epilepsy has nearly cost me my own life before a number of times
@@Addy2023X it's the same with me. I'm sorry you are going through all of this. A lot of people do not understand the impact epilepsy has on someone's body.
Think I have this but I'm worried that nobody will believe me because they think I'm just crazy. :( I have strange episodes of super intense dejavu, depersonalization, and a sense of impending doom washes over me. My stomach usually hurts. I'm really tired.
I would seek medical attention and find a doctor to help you. I don't think anyone will think you are crazy. Before my seizures were controlled, I would become extremely frightened and have the same feeling of doom. After the seizure, my stomach hurt and I would get sick, then go to sleep. I'm not a physician, but from my own personal experience, it sounds like a seizure.
@@DefeatingEpilepsyFoundation I wish I didn't have so much stuff going on with me. Thanks for replying though. I will bring this up to a Dr. I'm in between Dr right now.
@@echastee you are very welcome. If you have any questions, please feel free to email me at info@defeatingepilepsy.org. I'm happy to help in any way that I can.
I am currently struggling with the same dilemma. I have bipolar disorder and as a result have also endured some emotional trauma, so when I had a strange and intense experience where I lost partial consciousness while driving about a year ago, they just said I had been under extreme stress and was extremely dissociated. But I have grown up with on and off depersonalization my whole life and something about this episode really bothered me. It still bothers me because I had a visual aura as one would have before a migraine, and my balance and sense of direction was impaired, things I have not experienced with depersonalization. I have since had another, less intense incident. They could be depersonalization episodes but they were so intense and different, plus I had lapses in my memory for days after each. When I looked up some of my experiences 'temporal lobe epilepsy' popped up and a lot of the symptoms were familiar, like the "zoning out" and the deja vu and the random feeling of your stomach dropping. I don't know I just feel like I should've gotten it looked into further but am afraid they will take one look at my file and see "Bipolar 1" and write it off.
@@hannahhansen2785 there are people who are bipolar and also have seizures. Working with both a neurologist and psychiatrist in the past was a frustrating experience I admit. I have epilepsy and PTSD and the nurse practitioner tried to convince me I was bipolar when I knew I was not. I have had a couple of traumatic experiences which led to me having PTSD. I find the problem a lot of times is the lack of communication between the doctors, that was my experience at least. I would try to find a good neurologist to see if they can rule things out or if they are seizures, do something to help. Keep a journal of what you are experiencing so the doctor has some information to work with.
Is there a difference between temporal lobe epilepsy and temporal lobe psychosis?
Temporal lobe epilepsy is when people have seizures in that area of the brain. Temporal lobe psychosis is caused by grey and white brain matter deficits in the temporal lobe. Here is a link from an article explaining it in more detail: pubmed.ncbi.nlm.nih.gov/21119155/. Hope this helps.
@@DefeatingEpilepsyFoundation Hellow im just letting ya Know that there's a Difference Between them because i had them on both Sides of my Head the One on the Left was, Bigger than the One on the Right So they Do
ne the Surgery on the Left Side Cut half
The Skull and and a lot Better know ..
The Right Side was Smaller in the size
Still there..
@@brendonschliebs3839 thank you for letting me know.
I have TLE and I've had psychotic episodes but I've been diagnosed with bipolar 1 as well, which was diagnosed about ten years after I developed seizures so the seizures came first.
I had sonething like this when i was 17~20 but now im 23 and it didnt happen for 3 years now so idk if one day it will reappear or is it gone for good? I never talked to a doctor about it
It may not happen again or it can happen in the future. I have had epilepsy for 41 years now and I haven't lost consciousness in years. However, since having long-haul covid I started to have auras again and I am much more sensitive to my triggers compared to before covid. As we get older, so many things can affect us that could cause seizure activity to start again.
I think I had a focal onset impaired awareness seizure for the first time according to my discharge paperwork. I was found unconscious with my arms extended and my hands clenched and shaking a bit, but I don't see that symptom mentioned in any of the videos I am watching. Is that possible with this type of seizure? Or does that mean it became a general seizure or something? I will ask my neuro but it's a while to my appointment and just curious in the meantime
I'm not a doctor so I cannot diagnose but what you are describing sounds like a tonic seizure or tonic-clonic seizure. Tonic seizures you become stiff and then tonic-clonic you become first stiff and then start to shake. We have videos on both of them. Tonic and tonic-clonic seizures are generalized seizures. I would discuss it with the doctor because he or she would know and would know what approach to take. I hope this helps.
In the last six weeks I’ve had the following experience 3 different times. I get a strong odd smell, I have an intense feeling of Deja Vu regarding what seems to be a dream I’ve had previously (I can actually see the dream somehow, & the sense of familiarity is overwhelming), it lasts about 30 seconds. I them feel disoriented for a couple of minutes. I’ve also had issues with short term memory (names especially) for years. Multiple times a day I can’t recall peoples names that I work with, or unknowingly call people by the wrong name. I’M WORRIED, WHERE DO I GO FROM HERE??
Have you seen a neurologist or epileptologist? I would see one and have them run some tests. Write down what you have been experiencing and let them know. It would be good to start keeping a journal to see if there is a pattern, if they are happening in a certain situation. They can do an EEG to see if there is seizure activity and an MRI to see if there is anything that can be causing this. That would be the first step I would take.
Thank you so much! It’s reassuring to know that other people share similar experiences. I’ve been taking methadone for 16 years, & I’d always assumed that my issues with memory were related to my medication 💊 but after the intensity of this last episode, I think it’s time to get checked out.
@@mattsheezy5469 you are very welcome! I hope things go well. Please feel free to reach out to us at info@defeatingepilepsy.org if you need help with anything.
My memory is effected aswel and straight after a seizure I don't know where I am or what I'm doing, like it wipes my memory for a few minutes. It's pretty scary
@@elishadoyle8191 it is scary. That's how I was when I had tonic-clonic and complex partial seizures. A lot of people do not understand the effect having a seizure has on the body and how it affects us.
I don't have family history of epilepsy but I getting déjà vu many times but I also think that's my anxiety because one day I get déjà vu then I research about déjà vu and I also know about epilepsy then I saw a "real" video of temporal lobe seizure then I scared to get seizure then I getting déjà vu like feeling for some nanoseconds everyday like 2 to 3 times a day. I am scared because I also have anxiety disorder and Is anxiety can cause seizure? And sometimes I feel déjà vu like feeling continuously like about 2 min even what I am thinking that also! I am really scared
High levels of anxiety and stress can trigger seizures. Stress is a trigger of mine and I exercise and meditate to keep my stress levels down. I would keep a journal of what is happening and see if you can find a pattern of things that cause you to feel like this. Once you do, find ways to reduce your stress and anxiety. You can always email us at info@defeatingepilepsy.org if you have any questions.
I'm reading a book on temporal lobe epilepsy and it says that half of people with focal seizures aren't diagnosed so they could be seizures! See a neurologist if you can or your family Dr. anyway!
It's Great News and Good Advice for People Suffering From Epilepsy Its a NIGHTMARE ⚘⚘💫👌...Brendon..
Epilepsy can be a nightmare in someone's life. That is why we need to work to not only advocate for more people to understand what epilepsy is, but to work towards improving the quality of life for people battling epilepsy. That is why I am working to educate people who do not have epilepsy about it, especially in the workforce.
Quick question. I thought the temporal lobe (Hippocampus) has long term memory not short term. Please explain
Thank you for your comment! We created another video on this topic with updated information in November of 2022 in which we address the temporal lobe's role in long-term memory: th-cam.com/video/i6Bxpckv_d4/w-d-xo.html