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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.

Are You Ok With Say Your Condition And The Meds We Take Or Do You Think There Is A Difference Between The Two? I Think It's Ok About Equal.

A MyEpilepsyTeam Member asked a question 💭
Lakewood, CO

I kinda have gotten used to the condition I have and the meds I take, and the side effects of them, and kinda know what to expect from them, once in a while I'll have say a strange kind of dif side effect and a bad seizure, but It is more stable than before and I am ok with that, what are your thoughts?

October 1
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A MyEpilepsyTeam Member

Our condition makes us seizure along with other struggles. The medications are for helping with reducing or hope for full seizure control.

October 1
A MyEpilepsyTeam Member

My seizures did not start getting a little under control until 2022 so I am just starting to research all the medication I take but I will be finish by this year and so type of fix. I take medication for high blood pressure also.

October 5
A MyEpilepsyTeam Member

I am okay with my condition right now. I learned to deal with specific side effects and take them as they come along. My seizures are pretty well under control especially for going through the change of life. My feet fall asleep sometimes, but I try to get up and walk around. I feel like some things can be worse off.

October 5
A MyEpilepsyTeam Member

Accepting an epilepsy diagnosis and coping with medication side effects can be challenging. As shared by members on MyEpilepsyTeam, the first years after diagnosis are often filled with struggles. It takes time to find the right treatment plan. Keeping a journal to identify triggers, getting enough sleep, reducing stress read more

Accepting an epilepsy diagnosis and coping with medication side effects can be challenging. As shared by members on MyEpilepsyTeam, the first years after diagnosis are often filled with struggles. It takes time to find the right treatment plan. Keeping a journal to identify triggers, getting enough sleep, reducing stress, and finding a trustworthy doctor are all helpful strategies. The trial-and-error process of balancing medications and side effects is frustrating. However, small medication adjustments, hormone testing, or exploring alternatives like medical marijuana may provide relief for some. Stay hopeful through the ups and downs by connecting with others who understand the journey.

 This AI-generated response comes from MyEpilepsyTeam and other selected sources. It is not a substitute for medical advice. Always ask your doctor about specific health concerns.

What MyEpilepsyTeam Members Would Tell Those Who Have Just Been Diagnosed
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October 1
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A MyEpilepsyTeam Member

I’m used to it.

October 1

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Just Curious About This ❓ Below And Not Nothing Against It Or Anything Else Like That? Or On Anyone Else Here And Such Etc Or The Med Field?

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