Overwatch Seizure Detection

💡 Ever Wondered Why Sleep Is So Important for Epilepsy Management?

Getting enough restful sleep plays a vital role in maintaining overall health and can significantly impact seizure control. Here's why:

1️⃣ Seizure Threshold: Sleep deprivation can lower the seizure threshold, making individuals with epilepsy more susceptible to seizures. Prioritizing consistent sleep routines can help maintain a more stable seizure threshold.
2️⃣ Recovery & Brain Health: Sleep is essential for the brain's recovery and overall health. A well-rested brain is better equipped to handle daily challenges and potential seizure triggers.
3️⃣ Mood & Emotional Well-being: Quality sleep contributes to better emotional resilience, improved mood, and reduced stress, which are all beneficial for managing epilepsy.

Let's support one another on our sleep journey. 🌙 Share your best sleep tips in the comments below!

Hey Overwatch fam, Are you a parent of a school-aged child and need help with Individual Education Plans, Seizure Action Plans, etc? Epilepsy Foundation of America has a 24/7 helpline we find very valuable. See below for details...

As children of all ages return to school, know that we are here to help you prepare. Call our 24/7 Helpline if you have any questions about your child's back-to-school needs, like Individualized Educational Plan (IEP) for epilepsy, seizure action plans, or seizure rescue medications.

Today, let’s talk about something crucial – creating a Seizure Action Plan. 🧠

⭐ Why is it important? ⭐

1️⃣ Safety First: With a plan in place, caregivers know exactly what to do when a seizure occurs. A plan can help prevent injuries, provide comfort, and offer immediate support.
2️⃣ Empowerment: Having a plan gives confidence and reduces anxiety for both the person with seizures and those around them. Knowledge is power!
3️⃣ Faster Response: By knowing the warning signs and appropriate steps, caregivers can act swiftly.

⭐ What to include in a Seizure Action Plan ⭐

✔️ Emergency Contacts: List phone numbers of family, friends, or doctors who should be notified during a seizure.
✔️ Triggers and Warning Signs: Identify potential triggers or signals that indicate a seizure might happen.
✔️ First Aid: List the proper first aid steps, such as keeping the person safe, staying calm, and timing the seizure.
✔️ Medication Details: Include information about the person's medications and dosage.
✔️ Post-Seizure Care: Outline what to do after the seizure, like staying with them or contacting the person’s family/friend.
✔️Regular Updates: Review and update the plan as needed, especially if there are changes in medication or health status.

Remember, creating a Seizure Action Plan can significantly impact someone's life during a seizure.

*For a user-friendly template visit:https://www.epilepsy.com/sites/default/files/atoms/files/GENERAL%20Seizure%20Action%20Plan%202020-April7_FILLABLE.pdf

🌟 Importance of Receiving Care During a Convulsive Seizure 🌟

Hey, Overwatch community! Today, We want to talk about something really important - the significance of receiving proper care during a convulsive seizure.

Seizures can be a challenging experience for individuals who live with epilepsy or other seizure disorders. During a convulsive seizure, the person may jerk uncontrollably, lose consciousness, and exhibit various symptoms that can be alarming.

It is crucial for everyone to understand the importance of offering immediate care and support when witnessing someone having a convulsive seizure. Here are a few reasons why:

1️⃣ Safety: The person having the seizure is at risk of injury due to uncontrolled movements. Ensuring their safety by placing something soft under their head, turning them on their side, and moving objects away will help minimize potential harm.

2️⃣ Comfort and Reassurance: Before and after a seizure, individuals may feel disoriented, confused, and scared. Providing a calm and supportive environment can help reduce their anxiety and bring a sense of comfort.

3️⃣ Protecting the Airway: Seizures can sometimes cause difficulties in breathing. Turning the person on their side and clearing the area around them can prevent any obstruction to their airway and minimize risk. Reminder! Never place anything into their mouth.
4️⃣ Timing: The duration of a seizure can vary, but if it lasts longer than 5 minutes or the person doesn't regain consciousness after the seizure ends, it could be a medical emergency. Recognizing these signs and seeking immediate medical attention can be life-saving.

Combining this knowledge and support with innovative solutions like the Overwatch Seizure Detection App can improve the overall well-being and safety of those with seizure disorders.

Today, let's shed light on tonic-clonic seizures, also known as Grand-Mal or Convulsive seizures.

These seizures are characterized by two distinct phases: the tonic phase and the clonic phase. During the tonic phase, the body becomes rigid, accompanied by potential loss of consciousness, falls, or loud cries. Subsequently, the clonic phase commences, involving rhythmic muscle jerks. Witnessing such seizures can be distressing, and providing support and understanding is crucial.

With Overwatch seizure detection’s advanced capabilities, the app identifies tonic-clonic seizures and immediately notifies caregivers. This innovative technology empowers users to gain valuable insights into seizure occurrences, facilitating better care for individuals with epilepsy. Together, let's raise awareness about tonic-clonic seizures and the instrumental role played by the Overwatch seizure detection app in supporting those affected by epilepsy.

https://www.hopkinsmedicine.org/health/conditions-and-diseases/epilepsy/tonic-clonic-grand-mal-seizures

💜🤝 Living with epilepsy can be challenging, but having a supportive community makes all the difference. It's a place where we can share our experiences, challenges, and triumphs, knowing that we are understood and accepted. 💪🤗

Whether it's through local support groups, online communities, or connecting with fellow epilepsy warriors, we create a safe space for mutual support, encouragement, and knowledge-sharing. Together, we raise awareness, combat stigma, and provide a beacon of hope for those who may feel alone. 🌍

Share your experiences about being a part of the epilepsy community and the support systems that have made a positive impact on your journey. Let's continue to build a strong and inclusive community that uplifts and empowers everyone affected by epilepsy. Together, we are unstoppable! 🤝💜

Let’s face it…EEGs are no fun, but they are a powerful tool for diagnosing and monitoring epilepsy. 🧠💜

EEGs provide valuable insights into brain activity by recording electrical signals generated by the brain. For individuals with epilepsy, these tests can help identify abnormal brain patterns and determine the type and location of seizures. 🎯 With electrodes placed on the scalp, the EEG captures brain wave patterns, allowing doctors to analyze and interpret the data. This non-invasive procedure plays a crucial role in guiding treatment plans and optimizing the management of epilepsy.

🎵🎸Happy Birthday Prince 💜🎸🎵

Hey there, music lovers! 🎶✨ Did you know that the legendary singer, songwriter, and multi-instrumentalist Prince was not only a musical genius but also an inspiring warrior who lived with epilepsy? Let's take a moment to remember this musical icon and celebrate his incredible contributions.

Behind the electrifying performances, catchy melodies, and iconic style, Prince Rogers Nelson quietly battled epilepsy throughout his life. 💪💜 Despite the challenges it presented, Prince never let this condition define him or dampen his spirit.

Prince's dedication to his craft and unwavering passion for music kept him pushing boundaries and defying expectations. His drive to create unforgettable melodies and lyrics was fueled by his determination to overcome the obstacles epilepsy posed.

Throughout his career, Prince remained remarkably private about his health struggles, choosing to focus on his musical legacy instead. Prince's resilience and talent continue to inspire individuals living with epilepsy and anyone facing adversity. His refusal to let his condition hinder his artistic expression stands as a testament to the power of perseverance and determination. ✨💪



Comment your favorite Prince song below and join us in appreciating his immeasurable impact. 💜🎶

🌟 Today, we celebrate the remarkable life and legacy of Harriet Tubman, a courageous icon in the fight against slavery. But did you know that Tubman also lived with epilepsy, a condition that did not deter her from making a permanent impact on history? 💜💪

Harriet Tubman, often referred to as the "Moses of her people," experienced seizures throughout her life. Despite the challenges posed by her condition, Tubman's spirit remained unyielding. Her determination to secure freedom for herself and others was unwavering, making her a beacon of hope for generations to come.


Living in a time of great adversity, Tubman fearlessly led hundreds of enslaved individuals to freedom through the Underground Railroad. She risked her life time and again, navigating dangerous terrains and outsmarting slave catchers, all while managing her seizures. Her bravery and selflessness continue to inspire us today. 🗝️ 💜


Tubman's resilience in the face of epilepsy serves as a testament to the strength of the human spirit. She proved that physical limitations do not define one's worth or ability to effect change. 💫

Let us remember Harriet Tubman as not just a freedom fighter but also as an individual who defied societal expectations. Her story reminds us to celebrate diversity and embrace the triumphs of those who have thrived despite living with epilepsy. 🌍 💜

Hey, Overwatch fam! Today, let's shed some light on epilepsy by addressing common myths and misconceptions surrounding this neurological condition. It's time to promote understanding. 💜✨

Myth 1: Epilepsy is a mental illness.

Fact: Epilepsy is a neurological disorder, not a mental illness. It affects the brain's electrical activity, leading to recurrent seizures. People with epilepsy have varied abilities, strengths, and talents, just like anyone else.

Myth 2: Seizures are life-threatening.

Fact: While seizures can be unsettling to witness, most seizures are not life-threatening. With proper management, education, and support, many individuals with epilepsy lead full and meaningful lives.

Myth 3: Epilepsy is contagious.

Fact: Epilepsy is not contagious. It cannot be transmitted through physical contact, sharing belongings, or being near someone having a seizure.

Myth 4: Only children can develop epilepsy.

Fact: Epilepsy can develop at any age, from infancy to adulthood. While some cases may begin during childhood, many individuals are diagnosed with epilepsy later in life. It's important to recognize that epilepsy does not discriminate based on age.

By dispelling these myths and misconceptions, we can foster a more inclusive and understanding society for people living with epilepsy. 💜🌍

💜 Who is your 1 in 26? 💜

In a world where 1 in 26 people are affected by epilepsy, it's time to reflect on the individuals who make up this statistic. Behind the numbers, there are real people with unique stories and experiences.

Take a moment to think about someone you know—a family member, a friend, a colleague, or even yourself—who is living with epilepsy. They are your 1 in 26, and their journey deserves recognition and support.

Hey there, Overwatch community, we have some exciting news about “What the EF” which is one of our favorite podcasts for the epilepsy community.

Seizen (season) 2 is now live and we couldn't be more excited to listen! In Episode 1, hosts Lexi and Landis chat with Jeff Parent, the president and general manager of Gulf States Toyota AND the Chairman of the Board of Directors of the National Epilepsy Foundation. Tune in to hear Jeff talk about what it’s like when you, your dad, and two of your kids have epilepsy.

If you or someone you know has been recently diagnosed with epilepsy, it's important to know that you're not alone. Epilepsy affects millions of people around the world, and there are many resources available to help you manage your condition. Here are some helpful resources to get you started:

1. Epilepsy Foundation: The Epilepsy Foundation is a non-profit organization that provides support, education, and advocacy for people with epilepsy. Their website has a wealth of information on epilepsy, including types of seizures, treatment options, and how to manage your condition. They also have local chapters that provide support groups and events in your area.
2. Epilepsy.com: Epilepsy.com is another great resource. They offer a variety of resources, including information on seizure first aid, medication management, and coping strategies. They also have a community forum where you can connect with other people with epilepsy and share your experiences.
3. National Institute of Neurological Disorders and Stroke (NINDS): NINDS is a government agency that conducts and funds research on neurological disorders, including epilepsy. Their website has information on the latest research on epilepsy, as well as information on clinical trials that you may be eligible to participate in.
4. Citizens United for Research in Epilepsy (CURE) is a non-profit organization that funds research to find a cure for epilepsy. While they do not provide direct services or support for people with epilepsy, they do provide resources that can be helpful for people looking for information on the latest research into epilepsy and potential treatment options.
5. MyEpilepsyTeam is a social networking site that is specifically designed for people living with epilepsy. It provides a supportive community where individuals can connect with others who have similar experiences and share information, advice, and support.

Did you know that the Overwatch seizure detection app is always monitoring, even when you're sleeping? That's right, our advanced technology can detect generalized tonic-clonic seizures even at night, so you can rest assured that you're always protected. Sleep easy with the Overwatch app.

Today, we want to recognize a historical figure, Vincent van Gogh, one of the greatest artists of all time, who is believed to have lived with epilepsy.

Despite the challenges he faced, Van Gogh was able to channel his experiences into his art, producing some of the most iconic and moving works in the history of art. His paintings, such as "Starry Night" and "Sunflowers," continue to inspire and captivate people all over the world.

Van Gogh's life serves as a powerful reminder that epilepsy does not have to limit your creativity. He remains a symbol of the strength and resilience of those living with epilepsy and a testament to the power of art.

Do you experience auras? An aura is a warning sign that someone with epilepsy may experience before having a seizure. Research suggests that up to 65% of people with generalized epilepsy may experience auras.

Caregivers: Understanding auras can be extremely helpful in managing epilepsy and ensuring that the right care is provided in the event of a seizure. So, take some time to learn about the different types of auras that your loved ones with epilepsy may experience, it may seem like a small thing, but it could make a huge difference in their well-being and safety.

Hey Overwatch NASCAR fans!

Today, we want to take a moment to highlight the incredible journey of Matt Tifft, a talented driver who has shown courage and strength in the face of adversity. As you may know, Matt was diagnosed with epilepsy when he experienced a seizure after a race at the Chicagoland Speedway in 2016. Rather than letting this diagnosis hold him back, Matt has been an inspiration as he continues to chase his dreams on the racetrack. He has spoken out about his epilepsy diagnosis, raising awareness and showing that it's possible to overcome obstacles and achieve greatness, no matter what challenges life throws our way.

Attention Overwatch friends! Did you know that some people with epilepsy experience a sensation called a seizure aura? These can include feelings of déjà vu, sudden fear or anxiety, or a variety of other unusual sensations.

Here's a question for you: Do you think it would be helpful for people living with epilepsy to alert their caregivers when they detect an aura? Let us know your thoughts in the comments below!

Nothing makes us happier than hearing from satisfied Overwatch users. Thank you to those who share their success stories with us. If you're interested in experiencing the benefits of real-time tonic-clonic seizure monitoring and detection, sign up now for three months free!

Disability rights activist, Judy Heumann passed away earlier this month at age 75. Ms. Heumann played an instrumental role in developing and implementing multiple groundbreaking pieces of legislation, including the Americans with Disabilities Act, or ADA. Thanks in part to Judy, the ADA also protects people with epilepsy from discrimination due to health conditions.

Please read more in Laura Beretsky's essay published by NPR affiliate WBUR’s online journal, Cognoscenti:
https://www.wbur.org/cognoscenti/2023/03/29/judy-heumann-americans-with-disabilities-act-laura-beretsky?fbclid=IwAR1enQLUr4Y74oxMuaOMdX300VyBir_ICHXUU5ilKFFaT_KwZcZ6OChuwmc

The mother of the disability rights movement knew this: ‘Disabilities are not problems to be solved’ Disability rights activist Judy Heumann passed away recently, at age 75. As someone with epilepsy, writes Laura Beretsky, I am one of many who stood on Giant Judy’s shoulders when I relied on the Americans with Disabilities Act.

Did you wear purple yesterday for National Epilepsy Day? Overwatch is proud to be part of, and serve, the epilepsy community. We know that peace of mind and independence matter.

Neurologist vs Epileptologist? Although these doctors both see epilepsy patients, it's helpful to know their differences.