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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.
May 5
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A MyEpilepsyTeam Member

Susana, I was diagnosed in 2020 and am 65 now
Based on things I’ve learned here, I’m sure I went undiagnosed for a long time though

Take care

May 5 (edited)
MyEpilepsyTeam

What a wonderful question — and what a journey you've been on since 2014! You are absolutely not alone in living with epilepsy for many years at 64.

Many people live with epilepsy long-term, and plenty of MyEpilepsyTeam members are in similar situations — managing the same diagnosis over many years, adjusting medications Show Full Answer

What a wonderful question — and what a journey you've been on since 2014! You are absolutely not alone in living with epilepsy for many years at 64.

Many people live with epilepsy long-term, and plenty of MyEpilepsyTeam members are in similar situations — managing the same diagnosis over many years, adjusting medications, and finding their "new normal."

One MyEpilepsyTeam member shared: "I was diagnosed in 2008 — I was 18 years old at the time. It was the hardest transition I had to deal with in my life!" — showing just how long people carry this diagnosis. Living with epilepsy long-term often means learning what works best for you over time. Some things that many long-term members focus on include:

- Identifying personal triggers (stress is a very common one)
- Staying consistent with medications
- Building a strong support network
- Working closely with a neurologist

The community on MyEpilepsyTeam is full of people who truly understand the long road, and your positivity and gratitude are a wonderful gift to everyone around you! 💙

May 5
A MyEpilepsyTeam Member

Diagnosed in 2018 at age 62. It definitely wasn't on my bingo card.

May 6
A MyEpilepsyTeam Member

My diagnosis hasn’t it change Since I was 2yrs old. I’m now 51

May 5
A MyEpilepsyTeam Member

Thank you Vince

May 5

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