Epsy Health

Epsy Health The #1 app for people living with epilepsy and seizures. ๐Ÿ’œ

Free app | iOS and Android

๐ŸŽพ As the US Open Tennis Championships gets underway, meet British tennis player Melissa Boyden.Diagnosed with epilepsy a...
09/01/2026

๐ŸŽพ As the US Open Tennis Championships gets underway, meet British tennis player Melissa Boyden.

Diagnosed with epilepsy at 15, she underwent brain tumor surgery - and is still pursuing her dream of reaching the worldโ€™s top 100. ๐Ÿ’ช

Read her story. ๐Ÿ‘‡

07/27/2026

Dating with epilepsy: navigating it with humour ๐Ÿ’œ

From Hinge to real life, Hattie and her partner share their experience of dating, talking about epilepsy, and building a relationship through honesty, understanding, and humour.

What advice would you give to someone about dating with epilepsy?

Comment your tips below. โฌ‡๏ธ

07/10/2026

Hundreds of seizures a day before 9am. ๐Ÿง 

That was Holly's reality. ๐Ÿ’ก

Living with hundreds of absence seizures each day meant that seizures shaped every part of her day-to-day life. Today, she's sharing her story of resilience, hope, and finding a path forward. ๐Ÿ’œ

Read more community stories here: https://www.epsyhealth.com/seizure-epilepsy-blog-subcategories/inspirational-stories

From her first seizure in a classroom at 16 to becoming an advocate, Emmiโ€™s journey is one of resilience. ๐Ÿ’œLiving with e...
06/29/2026

From her first seizure in a classroom at 16 to becoming an advocate, Emmiโ€™s journey is one of resilience. ๐Ÿ’œ

Living with epilepsy has shown her that โ€œitโ€™s more than just flashing lights,โ€ and that finding your voice matters - โ€œadvocate for yourself and take it one step at a time.โ€ ๐Ÿง 

Read Emmi's full story here: https://www.epsyhealth.com/seizure-epilepsy-blog/living-with-catamenial-epilepsy-emmis-story

Today is International Dravet Syndrome Day ๐Ÿ’œ  ๐Ÿงฌ Dravet Syndrome is a rare, severe form of epilepsy often linked to mutat...
06/23/2026

Today is International Dravet Syndrome Day ๐Ÿ’œ

๐Ÿงฌ Dravet Syndrome is a rare, severe form of epilepsy often linked to mutations in the SCN1A gene.

It begins in infancy with prolonged seizures and can lead to developmental delays and other health challenges.

This month, we raise awareness and stand in support of families affected around the world. ๐Ÿ’œ

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