Adults with absence seizures

Posted by sophiasmith01 @sophiasmith01, Jun 2, 2025

I am 21 years old and never grew out of my absence seizures like I was told I would. Is there anyone in this group who is an adult with absence seizures, or do you know anyone who is? I've never met anyone my age who has absence seizures, and I am just curious if there are people experiencing what I am.

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Profile picture for Chris Gautier, Volunteer Mentor @santosha

Hi @annestudio
So sorry to hear the ER experience your husband faced.
Since neither your husband's neurologist nor his PCP seems interested in reviewing these videos, I would encourage you to seek a second opinion.
Where are you currently located? There may be other members in our group living in the same region who could recommend an experienced neurologist in epilepsy, or an epileptologist.
Chris

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@santosha
We’re in Western MA near Springfield and Northampton. We’ve been paying a “Conceirge” PCP, thinking we’d get better care. But She is slow in responding and seems not to be proactive in our care. Maybe if you are over ninety, intervention is useless

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Profile picture for absentsenior @absentsenior

@santosha i'll apologize in advance and say I hate that question. With unaware seizures, you, of course, have no clue. Because I don't know if i'm having seizures or when i'm having seizures since I live alone.I've never felt a loss of time. I ended up coming to the clinic because I was losing long-term memory and after everybody telling me it was normal at my age. I trusted my gut and took myself to an neurologist, who advised me I had a seizure disorder.
When she retired, I applied to the clinic and thankfully, was accepted. And for the first time started getting answers.
The various medications for epilepsy have either been not effective or the side effects have been to difficult to live with.
Soon, I am being put before the committee for surgery to possibly implant a neurostimulator and will have an answer sometime in the next couple of weeks. Then I will have more decisions to make. Between the damage of the epilepsy and that of the medications, I am not the person I was and I want her back. At this moment in time, I only have to deal with social security and learning about Medicare when my epilepsy has affected my ability to learn new things. This should be a lot of fun.

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@absentsenior this must be extremely difficult to go through alone. Do you have any family or close friends who will be with you after the surgery ? of course you want your own self back.
I Meditate with a Zoom group and Meditation since to help me stay more emotionally stable through these trying and difficult medical decisions
Certainly hope modern medicine can help you. I am sending you big comforting. Hugs.

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Profile picture for annestudio @annestudio

@absentsenior this must be extremely difficult to go through alone. Do you have any family or close friends who will be with you after the surgery ? of course you want your own self back.
I Meditate with a Zoom group and Meditation since to help me stay more emotionally stable through these trying and difficult medical decisions
Certainly hope modern medicine can help you. I am sending you big comforting. Hugs.

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@annestudio i have a sister and a best friend of almost 50 years that I am very close to and have walked side by side with me through this. I definitely would not have survived without them.

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Profile picture for annestudio @annestudio

@santosha
We’re in Western MA near Springfield and Northampton. We’ve been paying a “Conceirge” PCP, thinking we’d get better care. But She is slow in responding and seems not to be proactive in our care. Maybe if you are over ninety, intervention is useless

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@annestudio age is irrelevant when it comes to service that you're paying for. If you're paying for service and not receiving it, stop paying for it. Find a different doctor and trust your gut when it comes to their service.

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Profile picture for annestudio @annestudio

@santosha our wonderful Epileptologist became the Dean of a Medical School.
We will seek someone at Mass General because our local Hospital is affiliated with it.
Thanks for the encouragement and interest

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Good Morning @annestudio
If I understood you correctly, your wonderful epileptologist is no longer seeing patients since becoming Dean of a Medical School. Even so, it might be worth reaching out to him directly to ask whether he has any recommendations at Mass General. A trusted colleague's referral from someone of his standing could open the right doors.
Wishing you the best of luck with this!
Chris

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Profile picture for absentsenior @absentsenior

@annestudio age is irrelevant when it comes to service that you're paying for. If you're paying for service and not receiving it, stop paying for it. Find a different doctor and trust your gut when it comes to their service.

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Hi @annestudio !
I share the same view as @absentsenior. It might well be worth reaching out to your previous epileptologist to check if he has a referral to offer.
Chris

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Profile picture for Jake @jakedduck1

@sophiasmith01
It's important to be patient, as you're still young. The journey with seizures can be unpredictable, and while no one can say for certain if or when they will stop, many individuals find that absence seizures can become less frequent by late adolescence. It's worth noting that absences can start or occur at any age.
In my personal experience, my first seizures began at 14 and were tonic-clonic. Absences started later. I had mostly tonic-clonic seizures, as well as focal aware and focal impaired seizures, along with status epilepticus. I continued to experience absence seizures into my 40s. When I was young I took Zarontin which helped my absences. What medicine/s are you taking. Research suggests that around 20% of children may continue to have these seizures into adulthood. It's also possible for absence seizures to change into tonic-clonic or other types, or even coexist with them. My seizures stopped after 45 years, for the most part.
Remember, every person and journey is unique, and it’s important to live your life to the fullest and to stay hopeful.
Take care,
Jake.

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@jakedduck1 may I ask if you know the cause of your seizures?

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I am an adult with absence seizures. I have one about every 4-6 months.
Would you like to share any other information about yours, such as how long they last and if anyone has observed them, what do they say your behavior is like during one?
How is it effecting your life?
How do you feel right before one occurs?

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@msaneurysm
No, I don't know for sure what caused my seizures. Perhaps a head injury when I was a kid. I believe my friend hit me in the head with a baseball bat but I have no recollection of that incident.
I developed generalized tonic clonic seizures in my early teenage years. I started having daily tonic clonic seizures along with absences (although not often and focal aware and focal impaired seizures. At age 14 or 15 I went into Status Epilepticus for the first of many times resulting in induced comas to stop the seizures.The longest was 8 months.
I had a difficult time accepting my seizure disorder. It took me about 2 years to come to terms with my new normal. I was kicked out of school. I understand they had no choice since I was either seizing, post-ictal or asleep. I wasn't conscious long enough to be able to study or learn anything so there was no reason for me being there. When I had a seizure someone would come pick me up, take me home and I would sleep until time to go to school the next morning and then it started all over again. I went to a couple of psychiatrists
who I believe were escapees from an insane asylum. They were crazier than I was and were only guesing about the cause of my seizures. I resented them guessing. I went once to each psycho psychiatrist, and never went back.
After the first two years I accepted my epilepsy and didn't let it affect my life. I swam 5 miles a day until multiple surgeries on my shoulders interfered with range of motion and my freestyle swimming ability.
I used to have absences also along with focal awareness & impaired seizures but most frequently my seizures were tonic clonic with no warnings. Just drop and out. I had seizures lasting from about 2-3seconds with occasional 20-45 second (absences) up to 20 minute (tonic Clonic) & convulsive status epilepticus seizures.
It's very sad how many people can't come to terms with their seizures. Those people suffer unmercifully with stress, anxiety, and depression. Some say stress is the most often reported seizure trigger with anxiety and depression lowering the seizure threshold. I know a man who refuces to come out of his apartment because he doesn't want anyone to see him during a seizure. And then there is the stigma of epilepsy. It's amazing how many ignorant people there are and how they put others with epilepsy down to build themselves up. And those who make cruel remarks like, "people like that belong in a circus" and those who equate people with epilepsy with the devil, and the religious folks who invite you to church to perform an exorcism and rid you of demons that are causing your seizures. I was told by a potential employer "we don't hire cripples" she tore my application in half and threw it in the garbage. When I have a seizure, I just fall to the ground since I usually have tonic clinic seizures and shake like a fish out of water. I actually think some people enjoy watching others suffer. I've had over 13,300+ seizures in the last 60 years. My last seizures were in the spring of 2024 because my doctor refused to refill my medication so I ended up in the hospital and had six seizures. When I got out of the hospital, I went and got my medical records and believe it or not they said "patient was noncompliant with his medication. Go figure??
Anyway, I'm sorry you're having seizures and I hope the doctors get them under control. Have you tried Zarontin or Depakote for your absences. Granted they are first generation meds but just because is old doesn't mean it's not effective. I take Carbatrol and Phenobarbital that control my seizures, both first generation drugs.
What medication do you take?
Blessings,
Jake

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@msaneurysm
Sorry you asked if I wanted to share?, lol🤣
Take care,
Jake

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