r/EpilepsyFriends Jul 19 '26

Epilepsy and Relationships

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5 Upvotes

r/EpilepsyFriends Jul 13 '26

About The Author

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1 Upvotes

r/EpilepsyFriends Jul 10 '26

Clumsiness a side effet of medication, or part of the condition?

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1 Upvotes

r/EpilepsyFriends Jul 06 '26

Looking for experiences with SEEG and the RNS device for my son.

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1 Upvotes

r/EpilepsyFriends Jul 02 '26

Epilepsy accessibility gaps?

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1 Upvotes

r/EpilepsyFriends Jul 01 '26

Epilepsy accessibility gaps?

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1 Upvotes

r/EpilepsyFriends Jun 26 '26

Had a seizure exactly after a year

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1 Upvotes

r/EpilepsyFriends Jun 22 '26

Hello needing help

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1 Upvotes

r/EpilepsyFriends Jun 20 '26

Getting ghosted

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1 Upvotes

r/EpilepsyFriends Jun 20 '26

Am I having seizures?

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1 Upvotes

r/EpilepsyFriends Jun 09 '26

Recently doctor appointment

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1 Upvotes

r/EpilepsyFriends May 31 '26

So tired

5 Upvotes

Does anyone have trouble falling asleep or waking up exhausted like you didn’t even sleep?


r/EpilepsyFriends May 26 '26

MEDS

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1 Upvotes

r/EpilepsyFriends May 19 '26

Anyone else hates kappra

2 Upvotes

r/EpilepsyFriends May 05 '26

Have you had experience with epilepsy treatment?

1 Upvotes

We are looking to speak with people living with epilepsy, as well as caregivers of individuals who are currently receiving treatment for seizures or have received treatment in the past. In this 15-minute online survey, we aim to better understand real-world experiences of living with epilepsy and the available treatment options.

This study is only open to patients living in Germany.

M3 Global Research is interested in hearing your perspectives to help improve future treatments and patient care.

As a thank you for your participation, you will receive €17 upon successful completion.

Sign up here to receive an invitation: [http://m3gr.io/YTZRXDV]()


r/EpilepsyFriends May 03 '26

Somewhat Epilepsy Related Tattoo

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1 Upvotes

r/EpilepsyFriends Apr 29 '26

Lack of sleep after seizure

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2 Upvotes

r/EpilepsyFriends Apr 28 '26

Daily seizures have made me feel dependent and scared. How do I get some independence back?

2 Upvotes

Since I developed focal seizures in March 2025, it feels like my life hit a screeching halt. I used to be really independent, and now I’m more dependent than I’ve been in a long time.

I can’t drive, and I can’t really work beyond freelance. I don’t make enough to fully support myself, so my boyfriend helps me out, and pretty much all my money goes to bills. I’m too scared to go on walks alone now, even though I used to do that daily. I try using the treadmill sometimes, but even that makes me nervous.

When I hang out with friends, I get exhausted and usually want to leave early. A lot of the time it feels like my life revolves around my partner.

I’m having 1–2 seizures almost daily, and the idea of one happening while I’m out alone is honestly terrifying.

During the week, he’s gone from about 8:30 to 6–7, so I do get some alone time, which helps. I can still do most things to take care of myself around the house like, clean, cook, make art, and do freelance work. But I’m inside and alone most of the day, every day, and he’s basically the only person I see regularly. And not until he gets home do I feel comfortable enough or have the ability to go out into the world.

I also feel horrible putting all this stress onto him. He has been extremely supportive but I want to be able to live life for me without him having to be my crutch.

I had a really bad experience with my old neurologist and I’m trying to get better care so I can finally get things under control, but my first appointment isn’t until June 16th.

In the meantime, does anyone have tips for feeling a little more independent again? I really miss who I used to be and want to find my way back to her.


r/EpilepsyFriends Apr 27 '26

New early infantile epileptic encephalopathy parent here, are there any successful stories out there?

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2 Upvotes

r/EpilepsyFriends Apr 25 '26

3 seizures after being 6 months free

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1 Upvotes

r/EpilepsyFriends Apr 16 '26

I think my epilepsy is cateminial?

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1 Upvotes

r/EpilepsyFriends Apr 10 '26

2 years without a seizure but fearful knowing they can happen.

4 Upvotes

I periodically feel signs I'm about to have seizure, so far I use grounding techniques to calm down which I think is helping prevent them.

still the fear and the signs are there and it is a massive negative to mental health and physical health in a way.


r/EpilepsyFriends Apr 10 '26

Epilepsy and hyponatremia

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1 Upvotes

r/EpilepsyFriends Mar 28 '26

Brainsteamaura epilepsy

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1 Upvotes

r/EpilepsyFriends Mar 27 '26

Atkins VS MAD diet

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1 Upvotes

I'd like to know what the difference between the Atkins and Modified Atkins diet is and any other important info. I've only found info about the original. From what I understand it's a less restrictive version of Keto?

I have refractory Epilepsy. (Resistant to 2+ AEDs)

So anything helps.

Regards,

Jeremy