Has anybody experienced lack of taste/changed sense of taste caused by Keppra and/or Lacosamide?
Sense of Taste: Has anybody experienced... - Encephalitis Inte...
Sense of Taste
Written by
Tuesando
To view profiles and participate in discussions please or .
Read more about...
1 Reply
•
My tastebuds changed with Kepra and are only now really returning after 2 years since I stopped taking it. I was lucky, I didn’t lose my sense of taste, just some things, like grapes or coleslaw randomly tasted horrible.
Not what you're looking for?
You may also like...
Autoimmune encephalitis
My husband was diagnosed with autoimmune limbic encephalitis in 2024 (age 52). Both GAD65 and LGI1...
Moods depression update
So far my moods are still off the the track. I hate being alone as i struggle emotionally with...
Memory, dreams and alcohol
Enc. plays fast and loose with my memory/ies these days. When I wake up I carry fragments of the...
Decision-making and being realistic
We have a visit scheduled with a psychiatric nurse this afternoon and my wife and I have been...
Can a TENS device help with mood and pain relief?
A TENS device has a pad which is attached to your body. Small electrical pulses are sent to the...
So much to learn, such good company to learn from!
Lack of family support?
Best experience of being part of the encephalitis society community?
Encephalitis of unknown origin and currently no diagnosis!
