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Real members of MyEpilepsyTeam have posted questions and answers that support our community guidelines, and should not be taken as medical advice. Looking for the latest medically reviewed content by doctors and experts? Visit our resource section.
A MyEpilepsyTeam Member asked a question 💭

Has anyone experienced loss of words, names? Sometimes when Im talking I just can catch the words I’m trying to say.

January 20, 2023 (edited)
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A MyEpilepsyTeam Member

Yes ! Very often. It can be a word name, that I use often . All of a sudden I have a BRAIN FART ( that’s what I call them ) … it can take minutes, hours, and days , by the time it comes back to me. By that time, it’s too late.

January 22, 2023
A MyEpilepsyTeam Member

I do and I used to be very articulate. I often feel a loss for words I'm trying to say

January 22, 2023
A MyEpilepsyTeam Member

Everyday. But that is from mold, lyme disease.

January 22, 2023
A MyEpilepsyTeam Member

Yes I have it often

January 25, 2023
A MyEpilepsyTeam Member

Myself as well. Not any more.

January 23, 2023

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