Let’s Talk about Epilepsy .

Epilepsy is more than a medical condition—it’s a misunderstood reality for over 3.4 million Americans.

Epilepsy is a hidden disease, not a rare one.

We believe awareness starts with visibility.

Every item we create is designed to challenge stigma, spark conversations, and make epilepsy impossible to ignore.

And the best part? 50% of proceeds of our collection support epilepsy education, advocacy, and community programs across US. That means every purchase helps fuel real change.

Join us. Start the conversation. Break the stigma.

Epilepsy Awareness promotes four key tenets of boosting awareness for the epilepsy community: Belonging, strength, change, and impact.With more voices, we can bring hope to all of us facing the disease. Learn about other ways to show your support of the epilepsy community now. Epilepsy is a neurological disorder that causes seizures. This disorder can affect people very differently. The severity and frequency of a person’s seizures generally determine the overall impact on their life. Common causes of epilepsy include strokes, brain tumors, infections, and traumatic brain injuries. Additionally, several types of birth injuries are linked with seizures.Genetics also plays a significant role in causing epilepsy. Since the causes of epilepsy are often unknown, the condition can be difficult to treat. Therefore, living with epilepsy can be challenging for patients.

Quick Facts About Epilepsy

- 1 in 26 people will develop epilepsy during their lifetime

- 3.4 million Americans have epilepsy

- 470,000 children in the United States have epilepsy

- 150,000 people are diagnosed per year

- An epilepsy diagnosis is usually made when a person has had 2 or more seizures

- Seizures can look very different, ranging from staring spells to collapsing

- Seizures range in duration from a few seconds to a few minutes.

The Importance of Epilepsy Awareness

Doing your part to increase awareness helps bring hope to people living with epilepsy. It helps to spread the word about the serious condition, which can ultimately improve diagnosing and treating it.It's also a great opportunity to educate yourself and others about the condition to benefit the epilepsy community as a whole.

Here are some important do’s and don'ts when someone has a seizure:

DO:

- Stay calm — most seizures last only a few minutes.

- Stay with the person and place something soft under their head.

- Turn them on their side to keep airways clear.

- Keep onlookers calm and at a distance.

- Look for emergency information, like a medical bracelet.

- After the seizure, help them to a safe place and calmly explain what happened.

- Check if they know their name and offer to contact a loved one or arrange transport.

- Call 911 if the seizure lasts over 5 minutes, if they’re pregnant, or if they have multiple seizures.

DON’T:

- Don’t hold the person down.

- Don’t try to stop their movements.

- Don’t put anything in their mouth — they cannot swallow their tongue.

- Don’t attempt mouth-to-mouth — they will usually start breathing again on their own.

- Don’t try to give them food or water until they are fully alert.

Since about 1 in 10 people will have a seizure in their lifetime, you may need to help someone someday. Seizure preparedness and basic first aid can provide vital support during these challenging moments.

For me, sharing epilepsy awareness is not just advocacy ,It’s deeply personal. Living with epilepsy has taught me the importance of compassion, understanding, and visibility. Every story shared helps replace fear with knowledge, stigma with empathy, and silence with connection. By speaking openly, we give a human face to this condition, educate others on seizure first aid, and help create safer, more supportive spaces in our communities, workplaces, and schools.

Epilepsy affects millions of people around the world, yet it remains widely misunderstood. That is why I believe we must go All In for epilepsy awareness. Awareness leads to acceptance. Acceptance leads to inclusion. Supporting research brings us closer to better treatments, improved quality of life, and ultimately, a cure. Advocacy ensures that those living with epilepsy have equal access to healthcare, education, and opportunity.

When we go All In, we become part of something bigger than ourselves. We choose understanding over judgment, action over indifference, and hope over fear. Together, we can build a more informed, compassionate, and inclusive world — one where no one faces epilepsy alone.