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Top 10 Search Results for "treatments for focal seizures"

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Does Anyone Have Focal Awareness Seizures And How Has It Effect Your Life?
A MyEpilepsyTeam Member asked a question 💭
A MyEpilepsyTeam Member

A friend has partial complex and I met her thru a friend . We were at a deli eating dinner She pushed a salt shaker across the table she stopped talking at that time When her eyes stopped being… read more

How Many People Have Headaches That Last All Day After Aura's?
A MyEpilepsyTeam Member asked a question 💭
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A MyEpilepsyTeam Member

I had bad headaches accompanied by visual auras before my first seizure. My fingers and arm moved involuntarily before this, while sleeping I had spasms. Eventually my headache tolerance increased. I… read more

Has Anyone's Seizures Changed Over Time Mine Went From Tonic Clonic To Secondary Generalized
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A MyEpilepsyTeam Member

Mine always start as focal. Then they spread to generalized seizures

Has Anyone Experienced A Focal Seizure? Also Known As Simple Complex Seizures?
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A MyEpilepsyTeam Member

yes i have focal seizures as well as many others but latly ive only had very small focal seizures due to my vns helping me with my epilepsy

Does Anyone Talk In Their Seizure
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A MyEpilepsyTeam Member

Same here I talk but don’t make sense

Social Meetings And Awareness For Epileptic
A MyEpilepsyTeam Member asked a question 💭

Hello everyone I am a new member and would like to connect with more people who can relate to my neurological condition. I am located in Dallas, TX and if any others are interested don't hesitate to comment or message. I look forward to hearing from some of you all. And Happy Holidays!😇

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A MyEpilepsyTeam Member

Ask me any questions You would like to. I have had epilepsy for over 50 years. I have the VNS now, had this one replace the older model. I don’t like eeg’s, I have had to many. They just do not… read more

Epilepsy Diagnosis
A MyEpilepsyTeam Member asked a question 💭

When did you get it?

1950s

1960s

1970s

1980s

1990s

2000s

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A MyEpilepsyTeam Member

1959 is when I was diagnosed at age 7.

Lack Of "Event On EEG"
A MyEpilepsyTeam Member asked a question 💭

My one hour Eeg showed sharp waves over bilateral frontal lobes, more dominant on the left.

My ambulatory Eeg said that it could not rule out partial seizures but read as follows.

" intermittent and elipitform spike and sharp waves were noted in the bilateral frontal regions,more on the left. Intermittent runs of sharply contoured theta waves centropartietal head region, more on the left."

Goes on to talk about focal cortical irritability and epilipic potiential. And the clincial significance… read more

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A MyEpilepsyTeam Member

It sounds like there were some abnormal brain waves, even if you didn't have a seizure. When medication dosages are being lowered and new meds are being introduced, sometimes we don't have enough of… read more

Blackouts
A MyEpilepsyTeam Member asked a question 💭

I noticed lately lots of people on the forum are having lots of blackouts as well as seizures. Is there a common link here or medication?

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A MyEpilepsyTeam Member

The blackouts I experienced is a form of a seizure. It an also be a side effect from the medication.

Is Having Speech Difficulties Signs Of Having A Seizure? Or Is It Side-effects From Medications?
A MyEpilepsyTeam Member asked a question 💭

I had a conversation with a few people here. We all have had difficulties speaking. Getting confused, slurring words, dyslexia getting worse, not being able to put sentences together properly, etc.
If that’s a seizure, what type of seizure is it?
Or is it more likely just side-effects of medications?
Thanks.

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A MyEpilepsyTeam Member

@Pamale6
I always had trouble speaking clearly when I was having an aura, which is a warning sign for a seizure.