Living with epilepsy - Introduce yourself & meet others
Welcome to the Epilepsy group on Mayo Clinic Connect.
Having seizures, or being told you have epilepsy, affects people in different ways. Let's learn from each other and share stories about living well with epilepsy, coping with the bumps and offering tips.
I'm Colleen, and I'm the moderator of this group, and Community Director of Connect. You're likely to also meet fellow member and volunteer patient Mentor, Dawn (@dawn_giacabazi), when you post to this group. Learn more about Moderators and Mentors on Connect.
We look forward to welcoming you and introducing you to other members. Feel free to browse the topics or start a new one. Grab a cup of tea, or beverage of you choice, and let's chat. Why not start by introducing yourself?
Interested in more discussions like this? Go to the Epilepsy & Seizures Support Group.
Hi, @nadinen, and welcome to Mayo Clinic Connect. I can imagine that would be quite a change from having no seizures in 5 years to now having them three times in one day.
You'll notice I have moved your message to this existing discussion, "Living with epilepsy - Introduce yourself & meet others" in the Epilepsy & Seizures group. I did this so that you could talk with the members in this conversation who've had experience with epilepsy. If you click VIEW & REPLY in the email notification, you can scroll back through the past and recent posts.
Members like @dawn_giacabazi @jakedduck1 @isalenamom@debvat @aroman @techi and others may have some thoughts on experiencing the auras you mentioned. They also might have input on your sense that the feeling you've described before having a seizure might be interpreted by your doctor as anxiety.
You mentioned being sick of living life in fear. What would you say is making you most fearful at present?
Well yes it was an outburst of 3 in one day then it never happened again but had so much auras since.. its frustrating because u take extra precaution of having a seizure for no reason so you feel fear and worry all the time
Ive googled a million things and became too obsessed with trying new diets or cutting things out so i can see if it makes any difference but it all just comes back every few days anyways... i kept a diary of everything and i see no pattern. Its hard not knowing what causes these shocks ...mainly when i first wake or in the afternoon..
Im trying to stay positive now because i dont want epilepsy to take over my life anymore. I worry more than having the actual seizure which shows its become too much..
@nadinen I had a seizure when I was 21. No more after this. I was having auras thereafter, although for many years doctors always told me this sounds just like anxiety and I wasn’t aware I was actually experiencing auras. Finally I discovered Mayo in Rochester MN. They were able to capture these experiences with an eeg and told me they were auras. After about a year of trial and error with meds and tons of frustration on my part, and them as well, I was put on Keppra, right after it first came out, and haven’t ever had an aura since. Sometimes it just takes time.
The problem is i have had mri and eeg and no results..ever.. nothing ever shows..
I even did a sleep deprived eeg.
I am worried to do these again and be told i am just hallucinating or have anxiety..
I am tegratol i think it is controlling the seizures very well but the auras.. maybe i should change my drug? However i am too scared to try this
Did they tell u a aura is a seizure... or could these be side affects from medications.. i am very lost, i just want answers 🙁
@nadinen
I was working on a reply to you but wanted to say a little something regarding your fear.
But first I have had over 13,300 seizures in my life. You absolutely cannot live your life in fear of the next one. YOU CAN’T! Fear can be very destructive, don’t allow it to be. It’s a total waste of time and effort to worry about things you have NO control over. Besides, what good does it do? Let me answer that for you, IT DOES NO GOOD. Did you ever think of the harm your worrying may do? It’s even possible your may be causing some of your own seizures. That theory isn’t as far fetched as you May be thinking right now. Fear, worry, stress, anxiety have been proven to be major seizure triggers. You need to enjoy your life. Live your life with gusto.
Sure you need to be cautious of certain things. If you have Tonic clonic Seizures you shouldn’t take a bath without someone with you. In the shower you should have a thermostat installed so you don’t accidentally scald yourself. Always have someone with you when swimming. Using elevators instead of stairs. Just go out there and live your life like every day is the first day of the rest of you life and if you have a seizure so be it. Shake it off and move on.
Yes i understand. When i was in my teenage years if i was to have a seizure i would only have one in that day and thats it!
I believe when i had 3 in one day the last two were from shock and fear! Auras got so heavy and i believe i literally tricked myself to have a seizure. It was traumatizing. So now definitely i have learned to stay positive because like u said it does no good to be fearful.
Me too. I had years of these same tests with no results, I understand how you are feeling. I was so angry with the medical world.
Is there something that you know will cause these auras?
When I was at Mayo, they listened to everything I was saying, hooked me up to an eeg 24/7 and recreated situations best they could to bring on an aura or seizure. Took a couple of days. That’s how they were able to capture it.
They said an aura is essentially a warning that a seizure might occur. It is not a seizure in itself.
Have you gone elsewhere to get another opinion? I actually went to Mayo for a long time without ever discovering anything and being told I had anxiety. I kept pushing them and they finally set up appointments with neurologists that found out what was happening. You have to be your own advocate, be strong and positive. They aren’t experiencing what you are and rely on tests to disprove you. I actually broke down crying in the doctors office one time with both the doctor and nurse in there. I told them I felt this would never be solved; the nurse told me they wouldn’t stop until it was solved. That was the turning point for me.
I also have heart problems, a very fast heart rate. Just a couple years ago I was in a cardiologists office with him telling me that it was anxiety. The next day I went back and told him I wanted another opinion. He relented and sent me to a doctor specializing in fast heart rates. That doctor confirmed what I was telling him, treated me for a fast heart rate which is still under control today.
Sorry for the long response. Just sayin that being your own advocate helps.
Im really not sure the triggers.. did u know your triggers and what is your aura?
I tried avoiding certain foods but nothing workes..im pretty sure im underweight now from being paranoid to certain things ( thanks to google)
Most people with Epilepsy who have an EEG many don’t have activity during their test so it comes out normal. Mine are always abnormal. I haven’t had a lot of Focal Aware Seizures and the ones I had were never a precursor to a Tonic Clonic. I never knew of any triggers. Had seizures in in every conceivable place and every imaginable situation.
Congratulations on your positive attitude, a definite plus. Overcoming fear can be a difficult challenge but as you found out its possible to conquer.
You may ask your Neuro if Depakote is a viable option to control the Focal Aware Seizures.
Best of luck to you,
Jake
My focal aware/aura is the beginning of the tonic clonic..thats why it is frustrating
It can vary to all day for a few days then go away slowly or not come for a few days or even just a few times in the afternoon or even when i wake..i feel them in my sleep sometimes.. i used to wake up to a seizure into a tonic clonic aseell..
Anyways what makes you suggest depakote
Have you tried this?