Podcasts about epilepsy awareness month

On this episode of Talk About It, we break out the Gold Jacket to chat with Alan Faneca, retired NFL offensive lineman and NFL Hall of Fame Inductee! Alan and Greg have become friends through advocacy for epilepsy awareness over the years, because Alan was diagnosed with epilepsy when he was a teenager and played at the highest levels of football with the condition. He also has a daughter with a rare form of epilepsy, so this cause is really close to his heart. Ironically, Nick also has a connection to Alan through his time with the Pittsburgh Steelers and hosting events together, so this is really a friend reunion show! They discuss his diagnosis, how his family helps him deal with the condition, going through the process again with his daughter, and - of course - his induction into the NFL Hall of Fame in Canton, OH. This is an episode that you are seriously not going to want to miss! The Talk About It podcast is excited to be sponsored in part by Neurelis. The Talk About It podcast is excited to also be sponsored in part by Seizures Are Signs — dedicated to educating families on the importance of early and specific diagnosis by providing an assessment to help get the conversation started, educational information, stories from families who have found a diagnosis, links to advocacy groups, and more. For more information, go to SeizuresAreSigns.com. Seizures are Signs is made available by Jazz Pharmaceuticals.

In V.E. Shwab's bestselling novel, A Conjuring of Light, she wrote, "Kings need not raise their voices to be heard." But on this episode of Talk About It, Greg talks to a King who is being heard not by raising his voice, but by writing a book of his own! That book is called Be There When I Return, and it is out NOW everywhere books are sold. Michael King seemed to have everything going his way as a young bartender in 1980's Los Angeles until his friends began to notice a bizarre quirk in his behavior, but he is not aware of it happening. After the closest people in his life convince him to see a doctor, he is hit with the reality of an epilepsy diagnosis and drags through years of not being able to control his seizures. He ends up becoming a candidate for an experimental surgery, but his family doesn't know if he will remember them when he wakes up. We'll let Michael fill in the rest of this story, but you don't want to miss this episode!  The Talk About It podcast is excited to be sponsored in part by Neurelis. The Talk About It podcast is excited to also be sponsored in part by Seizures Are Signs — dedicated to educating families on the importance of early and specific diagnosis by providing an assessment to help get the conversation started, educational information, stories from families who have found a diagnosis, links to advocacy groups, and more. For more information, go to SeizuresAreSigns.com. Seizures are Signs is made available by Jazz Pharmaceuticals.

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This major social media influencer is talking about it in a HUGE WAY! Jamie Simpson is not afraid of showing it all when it comes to her epilepsy -- and she is encouraging all of us to be bold when sharing our story. From dating, to having seizures in public places and showing us, to her incredible service dog Echo, Jamie lays it all on the line to help others understand the world of epilepsy, from the point of view of someone who has the condition. All in this episode of TALK ABOUT IT with Greg Grunberg. The Talk About It podcast is excited to be sponsored in part by Neurelis. The Talk About It podcast is excited to also be sponsored in part by Seizures Are Signs — dedicated to educating families on the importance of early and specific diagnosis by providing an assessment to help get the conversation started, educational information, stories from families who have found a diagnosis, links to advocacy groups, and more. For more information, go to SeizuresAreSigns.com. Seizures are Signs is made available by Jazz Pharmaceuticals.

March is Epilepsy Queensland’s annual fundraising and awareness month. CEO of Epilepsy Queensland, Sandi Rodiger, told Gary Hardgrave on 4BC Drive, "Epilepsy affects far more people than what is probably known. We say roughly 1 in 25 people will be diagnosed with epilepsy in their lifetime, and that's roughly about 270,000 people in Australia currently living with epilepsy and around 40 odd thousand in Queensland, so it is very prevalent." Mum of a young athlete who has epilepsy, Natalie Sandow added, "Aamira did not allow epilepsy to stand in her way at all." "Once she got the clearance, she just went full force on that sporting field. She has, focal seizures, so she has awareness when she has seizures and is quite capable to play her sports because of that," Ms Sandow continued. See omnystudio.com/listener for privacy information.

Ahhh, it's that time of the year! Pitchers and catchers report, spring training is underway, we buy hotdogs and beer from a guy yelling up the stairs, it's just perfection! Nobody loves the feeling of the start of baseball season more than Greg, maybe with the exception of this episode's guest. Greg sits down in studio with Joey Hanley, a former college player who has now devoted his life to coaching and training young-and-promising baseball players to achieve their dreams of playing in college and beyond. This success didn't come without struggle, however, but luckily Joey had the right mindset to take it head on. Joey was diagnosed with epilepsy after he hit his head in the bathroom following a seizure when he was younger, and he battled through this diagnosis to achieve success on and off the diamond. He isn't going to let epilepsy slow him down from anything that he wants to do, and neither should you. Don't miss this episode! The Talk About It podcast is excited to be sponsored in part by Neurelis. The Talk About It podcast is excited to sponsored in part by Seizures Are Signs — dedicated to educating families on the importance of early and specific diagnosis by providing an assessment to help get the conversation started, educational information, stories from families who have found a diagnosis, links to advocacy groups, and more. For more information, go to SeizuresAreSigns.com. Seizures are Signs is made available by Jazz Pharmaceuticals.

Join Ritika and Esha in this powerful episode in honor of Epilepsy Awareness Month (sorry we are a little late, but desi standard time?) as they sit down with Dr. Amee Shah, a successful dentist, mother, and wife living with epilepsy. Dr. Shah shares her personal journey of being diagnosed with a seizure disorder and navigating life with invisible challenges. Together, they explore how she works to combat the stigma surrounding epilepsy in the South Asian community. Key Topics Discussed: Dr. Shah's diagnosis and understanding of her seizure disorder The challenges of living with an invisible disability and the impact of cultural stigma How her Indian identity shaped her experiences and attitudes towards epilepsy The importance of advocacy and sharing personal health stories Dr. Shah's ongoing efforts to raise awareness and support others with epilepsy Tune in to hear Dr. Shah's inspiring story of resilience and advocacy. Learn how she uses her platform to educate and support the community while breaking down barriers and misconceptions about neurological disorders. Join the Conversation: Follow us on Instagram @brownwomenhealth and on Twitter @brownwomenhlth to stay updated on our latest content, learn more about health topics, and engage with our community. Don't forget to subscribe and share this episode with your friends and family to help spread awareness!

Wicked, Wicked, WICKED! Everyone is talking about Wicked! Well, do we here at Talk About It have news for you... there is a brand new musical playing in Los Angeles that is all the rage in the epilepsy community, and it will make you forget all about good witches or bad witches. That musical is "It's All Your Fault, Tyler Price" and it tells the story of a middle school boy whose younger sister has epilepsy and is being bullied, shining a light on the high and low moments of a family dealing with epilepsy, how it affects the parent, and the challenges they are forced to overcome. It's a fresh, honest perspective and a wonderful opportunity to highlight epilepsy awareness on the stage! Greg sits down with the show's creators, Emmy award-winning composer and songwriter Ben Decter and Tony-nominated director Kristin Hanggi, to tell the story of what inspired Ben to start writing this show, how he and Kristin developed the final iteration of the musical, and so, SO much more! Plus! You'll get a sneak peek of one of the numbers that they shot a music video for. This episode is so much fun, you do NOT want to miss it! The Talk About It podcast is sponsored by Seizures Are Signs — dedicated to educating families on the importance of early and specific diagnosis by providing an assessment to help get the conversation started, educational information, stories from families who have found a diagnosis, links to advocacy groups, and more. For more information, go to SeizuresAreSigns.com. Seizures are Signs is made available by Jazz Pharmaceuticals

2024 DSF Biennial Family & Professional Conference June 20th to June 22nd. This three-day gathering united all those committed to improving the lives of individuals with Dravet syndrome – including families, caregivers, clinicians, researchers, and biopharmaceutical professionals. It provided a platform for fostering new relationships and collaborations among families and professionals alike. Recorded sessions from the conference can be accessed on demand by both virtual and in-person registrants through December 31, 2024.  conference@dravetfoundation.org

Today's episode is a look into a condition that affects millions every day, epilepsy. While it's impact and triggers can be overwhelming, the latest advancements in medicine offer much hope for patients and their families alike. Host:Willard ShepardAward-Winning JournalistExperts:Dr. Pooja Patel, M.D.Neurologist Director of the epilepsy monitoring unit at Marcus Neuroscience InstituteDr. Luis Felipe Tornes, M.D.NeurologistDirector of the epilepsy program at Baptist Health Miami Neuroscience Institute

Do you feel confident recognizing status epilepticus? When a seizure doesn't stop on its own, knowing the signs of this high-stakes emergency is the first step to preventing complications and even death. This episode breaks everything you need to know about status epilepticus — the warning signs, critical action steps, and the interventions that save lives.In this deep dive for Epilepsy Awareness Month, Sarah unpacks the role of nurses to take quick action and advocate for patients in status epilepticus. From what happens in the brain during prolonged seizures to proper use of benzodiazepines and anti-epileptic drugs, we get into the nitty gritty of managing this life-threatening condition. Topics discussed in this episode:Status epilepticus case studyDefining status epilepticus and its pathophysiologyHow to recognize the signs of status epilepticusIntervention tools and best practicesMedication use and managementPrevention and identification of underlying causesMentioned in this episode:Rapid Response and Rescue Intro CourseCONNECT

In observance of Epilepsy Awareness Month, we speak with Victor and Libby Boyce - whose son Cameron was a gifted child actor who was part of a couple of Disney programs. Cameron contended with epilepsy the last four years of his life before dying from epilepsy-related complications at the age of 20. His parents created the Cameron Boyce Foundation in his memory.

Group Chat News is back with a special episode for Epilepsy Awareness Month. Anand and his wife Amanda brought their friends Kate and Colleen, who also have children with Epilepsy. They have decided to make a difference for their own families and to help as many other families as possible. Today, they dive into many topics, sharing their unique stories and spreading awareness on Epilepsy and how you can help.    Here are some of their project to support:   https://bravebearsclub.com   https://electric-love.org   https://www.gofundme.com/f/fundraiser-for-mav?utm_campaign=fp_sharesheet&utm_medium=customer&utm_source=copy_link    

This month on Talk About It, we are cooling off the summer heat with some refreshing and delicious lemonade! Greg hosts three different interviews with people who are taking the sourest of lemons that life hands them and squeezing out incredible creative initiatives that make the world a much, MUCH better place. Up first is Landis Wiedner who developed epilepsy after a traumatic brain surgery to remove a tumor. She was disrupted by this sudden change in her adult life and realized that there weren't enough resources to help her deal with the struggles of "adulting" with epilepsy, so she started a podcast! The What the EF Podcast she started has now been on for five seasons and aims to be an outlet for those everyday conversations that aren't as accessible for adults in her situation. Way to go Landis! Then, Greg has some very special guests to the studio - his son Jake's girlfriend Morgan, and her incredible mom Karen and brother Kyle! Kyle was born with cerebral palsy, but Karen never let his condition affect his ability to play sports and enjoy recreational activities. In fact, she came on board the AYSO VIP Program for kids and helped to expand it to now host hundreds of special needs participants, from 4-year-olds to 40-year-olds! From basketball to soccer, Karen is leading the way to establish communities and provide a safe environment for individuals like Kyle to learn and grow through playing sports. Greg and Nick headed out to watch the basketball program in action, and we get a full recap of how incredible that experience was that is sure to pull on your heart strings! Finally, Greg talks with Sue Seserman, a writer and new author that harnesses her conditions and turns them into superpowers! Sue has epilepsy and type 1 diabetes, and has such a brilliant creative vision on how to use them for good. She has now released her new graphic novel Epilectra that centers around a woman who becomes a superhero by converting the electricity in her brain that causes seizures and uses them for super electric abilities! She is joined by a cast of characters - Team SEEZ - who all have a disability, but use them as “superabilities” to change the circumstances of their adversaries and save the day. She is a visionary, and we are so excited that this novel is finally here! Plus, we recap Greg's trip to the Epilepsy Walk at the Rose Bowl with some familiar faces and some new friends! Don't miss this episode! The Talk About It podcast is sponsored by Seizures Are Signs — dedicated to educating families on the importance of early and specific diagnosis by providing an assessment to help get the conversation started, educational information, stories from families who have found a diagnosis, links to advocacy groups, and more. For more information, go to SeizuresAreSigns.com. Seizures are Signs is made available by Jazz Pharmaceuticals

WAKE UP AMERICA! As we wrap up Women's History Month, co-host Kerry shares about a recent panel put on by the Paul Longmore Institute On Disability Studies featuring black and brown disabled women and co-host Brian shares about March also being Epilepsy Awareness Month, started by a young girl right here in Canada. And, of course, don't forget about the upcoming solar eclipse in April. This week on Outlook it's story time and we're reading March's featured spotlight on a deaf-blind woman in history, someone we can spotlight to tell the stories of more than just Helen Keller. Thanks to Peggy Chong, The Blind History Lady, for letting us know about Helen May Martin. Believe it or not. For more fascinating stories like this one delivered directly to your inbox, email Peggy Chong: theblindhistorylady@gmail.com Check out her official website: https://theblindhistorylady.com And listen to The Blind History Lady when she joined us on Outlook back in 2020: https://podcasts.apple.com/ca/podcast/outlook-2020-08-10-interview-with-the-blind-history-lady/id1527876739?i=1000488226679

In this very special episode, we sit down with the founders of Talk About It to hear all about the past, present and future of this organization! Two of Greg's closest friends, Ken Lowenberg and Phil Gattone, are in the studio. The three co-founders tell the origin story of how Talk About It was born in a hotel ballroom. This organization is fueled by the passion for spreading awareness about epilepsy, but as we find out in this conversation, Talk About It is broadening its scope to include a variety of causes going into the future. Through the benefits of today's technology, Talk About It will now offer a mulititude of outreach channels to get people talking - talking about cancer awareness, talking about MS, talking about cerebral palsy, talking about depression, talking about the things in our lives that matter. No matter what you are going through, there is a community and an infrastructure of support ready to help, but the first step is to... you guessed it... Talk About It! The Talk About It podcast is sponsored by Seizures Are Signs — dedicated to educating families on the importance of early and specific diagnosis by providing an assessment to help get the conversation started, educational information, stories from families who have found a diagnosis, links to advocacy groups, and more. For more information, go to SeizuresAreSigns.com. Seizures are Signs is made available by Jazz Pharmaceuticals

To celebrate Epilepsy Awareness Month, Greg sits down with mother, caregiver and author Kelley Coleman to talk about navigating through scary and uncharted waters after a difficult diagnosis. Kelley is the mother of two boys, and her youngest, Aaron, developed an undiagnosed genetic syndrome in addition to epilepsy, autism, cerebral palsy, cortical vision impairment, microcephaly, and motor/ sensory disabilities. Over the years of her preparation, planning and persistence, she developed systems, lists and how-to's that she is now publishing as a practical guidebook for all parent caretakers to follow entitled Everything No One Tells You About Parenting a Disabled Child: Your Guide to the Essential Systems, Services and Supports. They also discuss motherly instincts and persistence with medical professionals, how she manages her self-care as a caretaker of others, and of course… Venus fly traps! We also get a bonus visit from a few celebrity friends who have very special messages for all caretakers this month. The Talk About It podcast is sponsored by Seizures Are Signs — dedicated to educating families on the importance of early and specific diagnosis by providing an assessment to help get the conversation started, educational information, stories from families who have found a diagnosis, links to advocacy groups, and more. For more information, go to SeizuresAreSigns.com. Seizures are Signs is made available by Jazz Pharmaceuticals

Dr. Timothy Quezada, Allegheny Health Network neurologist, joins Larry and Marty to discuss Epilepsy Awareness Month. 

Raising awareness of epilepsy amongst everyone for Epilepsy Awareness Month - through events and just chatting! With epileptologist Meriem Bensalem-Owen. ------------------------------------------

Welcome back to another impactful episode of Safety Shorts, where Libby welcomes Jason Epstein, NSSGA's Director of Membership, to delve into the significance of Epilepsy Awareness Month and explore Jason's own personal journey living with epilepsy. In this engaging conversation, they discuss the importance of dispelling myths about epilepsy, offer practical tips for assisting someone having a seizure, and highlight the broader impact of raising awareness about this neurological condition. As you listen in today, you are encouraged to remember that your knowledge can make a difference in someone's life, so stay informed, stay safe, and help raise awareness during Epilepsy Awareness Month. Episode Highlights: The significance of Epilepsy Awareness Month and its impact on millions of lives Jason's personal journey with epilepsy and his dedication to raising awareness Practical steps for assisting someone having a seizure Dispelling common myths about epilepsy The story behind the creation of the Epilepsy Alliance for Young Adults The importance of spreading knowledge about epilepsy for a safer world Toolbox Talk Discussion Questions: In this episode, Jason shares some things everyone can know about epilepsy as well as some common myths about the disorder. Have you ever heard any of these myths? After listening to this episode, do you feel like you have the information necessary to assist someone experiencing a seizure? Does anyone have a story about a time where they witnessed a seizure?   Quotes: "I was diagnosed with epilepsy when I was eight years old. I was bullied by other students, treated differently by school administrators and teachers. I felt compelled to educate others so kids today wouldn't go through what I did." "Everyone has a safety story; you don't have to be a safety health professional to have a safety story." "You never know when someone will have a seizure, and it's good to know what to do. The more people know, the safer we all are." "Dispelling myths about people swallowing their tongue or putting something between their teeth is crucial." "You took it into your hands to do something you are passionate about, to help other people, and make the world a safer place." "From 2010 until this year, I founded and ran the Epilepsy Alliance for Young Adults, a local support group in the DC area that held small local events for those with the disorder and promoted epilepsy education." "Never put anything in their mouth and never hold them down. Time the seizure and remain calm. Stay with this person until their seizure has ended and they've regained consciousness." Links: National Stone, Sand & Gravel Association website National Epilepsy Awareness Month Epilepsy Alliance for Young Adults  

March is Epilepsy Awareness Month, a great time to raise awareness, challenge myths, and help dismantle the stigma of epilepsy.Chris Kullman is the president of the board of directors for the Epilepsy and Seizure Association of Manitoba. He was also diagnosed with epilepsy at 12 years old. Today on Connections, Chris shares his journey with epilepsy. He'll also share the importance of drawing awareness to this neurological disorder. See omnystudio.com/listener for privacy information.

Did you know there is a direct correlation to cholesterol and gall stones? Painful gall stones and even gall bladder removal can be prevented, mostly from diet. Listen as Dr. Scott Bloemendal, General Surgeon at Texas Health Harris Methodist Hospital Fort Worth, discusses how to take better care of this important, and often overlooked, organ in our body. November is Epilepsy Awareness Month and we are joined by Dr. Scott Perry, Head of Neurosciences at Cook Children's to discuss this disease that affects 1 in 26 Americans, on average.

November is Epilepsy Awareness Month. Val 'the Voice' Johnson speaks with digital compositor and entertainment consultant Karla Braithwaite about her challenges and breakthroughs with the neurological disorder, epilepsy. Karla shares why she started a daily fundraising walk on her Instagram account to help increase epilepsy awareness.

Welcome back to the Boneyard Podcast, where 3 ECU Alumni, Jared Shafit, Artie Brower, and Courtney Layton sit around, drink beer and talk about ECU sports. This week the boys are back doing their thing for Episode 125 of the Boneyard Podcast! This episode of the Boneyard Podcast is Presented by Manscaped, use promo code Boneyard20 for 20% off your entire order + FREE SHIPPING at manscaped.com Former ECU Softball Star and Longtime Friend Of The Podcast, Courtney Layton joins to discuss Epilepsy Awareness Month and is along for the whole show Recap from ECU's embarrassing loss against Houston on Senior Day Kevin Copp, Temple's Radio Play by Play voice joins to preview the cougars Bowl Projections Twitter Questions ECU Basketball Walk The Plank Betting Lines We hope you enjoy this episode of the Boneyard Podcast! Make sure to follow us on Twitter and on Instagram @BoneyardPodcast, and subscribe to the podcast wherever you listen to your favorite podcasts, and also please rate us and let us know what you think! Become a #FriendOfThePodcast by leaving us a 5 STAR Review! Want to hear your voice on the Boneyard Podcast?! Leave us a message! --- Send in a voice message: https://anchor.fm/boneyard-podcast/message

Tuesday November 22, 2022 - Guests: Greg Grunberg & Chris Jacobs Announcement: the 2022 Purist Group toy drive will be at GVBC again Friday, December 2, 2022. This is also the day before Nicole's birthday. She requests in place of any gifts for her, to please bring toys to the toy drive! Sean Lee will be there in a new NISSAN to collect in person. Thank you! Now, on with the show... Chris Jacobs & Greg Grunberg are LIVE in Studio 11 to talk their new Zero to 60 podcast and Greg's absolute nightmare of new (old) Porsche ownership. Disaster! He needs help!! Chris bought a new (old) car as well and we find out if it went any better than Greg's... Progressing on to "The Caretaker" series, Epilepsy Awareness Month, Hagerty Ride Share & Mecum Auctions • PLUS: Jay Leno comes home and Conan O'Brien buys a BMW today on the #EastCoastFeed • THANK YOU for being with us #happythanksgiving

Meghan Kennedy, Executive Director of Epilepsy Education Everywhere, discusses Epilepsy Awareness Month. 

Welcome to the newest episode of Let's Talk To...! This is our show where we have a conversation with an interesting guest! This week we talk to the late Cameron Boyce's father, Victor Boyce. The Disney Channel star died in July after suffering a seizure in his sleep because of epilepsy. November is Epilepsy Awareness Month and Victor talks to us about "The Cameron Boyce Foundation (TCBF), created in Cameron's memory. He's changing the face of Epilepsy and their message for the medical community. All that and more on today's episode of Let's Talk To...! #BetterThanRadio If you enjoy daily ad-free content, subscribe to The BS at www.podcastthebs.com --- Send in a voice message: https://anchor.fm/the-bailey-show/message

November is Epilepsy Awareness Month, so NHBR editors Jeff Feingold and Amanda Andrews speak with representatives from the Epilepsy Foundation of New England - Amy Mahoney, Executive Director, and Bill Murphy, Director of Advocacy and Public Policy - to learn more about what their organization advocates for here in New Hampshire.

Epilepsy is a neurologic central nervous system disorder in which brain activity becomes abnormal, causing seizures or periods of unusual behavior, sensations and sometimes loss of awareness.Seizure symptoms can vary widely. Some people with epilepsy simply stare blankly for a few seconds during a seizure, while others repeatedly twitch their arms or legs. Having a single seizure doesn't mean you have epilepsy. At least two seizures without a known trigger (unprovoked seizures) that happen at least 24 hours apart are generally required for an epilepsy diagnosis.Anyone can develop epilepsy. Epilepsy affects both males and females of all races, ethnic backgrounds and ages. When a child is diagnosed with epilepsy, families may need support to adjust to this new diagnosis. Parents and schools can partner with the medical team to help."One of the things that's really important for families to remember is they are not fighting this battle on your own," explains Dr. Elaine Wirrell, a pediatric neurologist and chair of Child and Adolescent Neurology at Mayo Clinic Children's Center. "You need to share the diagnosis and inform those who are caring for your child — teachers, daycare, coaches — so they are prepared to help." Medication is generally the first course of treatment for epilepsy. Finding the right medication or combination of medications, and the optimal dosages, can be complex. Many children with epilepsy who aren't experiencing epilepsy symptoms can eventually discontinue medications and live a seizure-free life.For some children with drug-resistant epilepsy, surgery is an option. Epilepsy surgery, which is considered when at least two anti-seizure medications have failed to work, removes or alters an area of the brain where seizures originate.Experts at Mayo Clinic Children's Center also are studying neurostimulation treatments for epilepsy, an alternative treatment for children with severe epilepsy or for those who cannot have surgery. This treatment applies electricity to the central nervous system with the goal of reducing seizure frequency and severity.On this Ask the Mayo Mom edition of the Mayo Clinic Q&A podcast, host Dr. Angela Mattke is joined by Dr. Wirrell for a discussion on epilepsy in children.Related articles: "Consumer Health: Treating children with epilepsy." "Mayo Clinic Q&A podcast: Epilepsy Awareness Month."

Ken talks with Pro Football Hall of Famer, Alan FanecaSee omnystudio.com/listener for privacy information.

Ken is joined by Dr. John Bunka Epilepsy Specialist at the Bronson Neuroscience CenterSee omnystudio.com/listener for privacy information.

Join Tony Dinges, Chris Tucker, and Zeb Wever with special guest Jason Dinges of Lost Rhetoric and Dr. Donut and the Dingus podcasts. We discuss epilepsy its effects, causes, and how millions of people are affected by this in their daily lives. We wanted to bring awareness and me, Tony, as I am epileptic because we feel this is not discussed enough and people, are not educated on epilepsy as so many people have epilepsy or have probably experienced someone having a seizure and did not know what to do to help them in the event of one. Also, this November is Epilepsy Awareness Month so take the time to educate yourself and wear purple in support.website: brotherswithopinions.comlostrheteric.com

Monday March 28th - Epilepsy Awareness Month by VOCM

If you've seen a lot of purple around lately, it might be because March is Epilepsy Awareness Month. The month is dedicated to educating and dispelling myths about a condition that affects over 10,000 people in Newfoundland alone. Epilepsy NL has been hard at work to keep the conversation going the past few weeks.

March is Epilepsy Awareness Month, a great time to raise awareness, challenge myths, and help dismantle the stigma of epilepsy. Chris Kullman is the president of the board of directors for the Epilepsy and Seizure Association of Manitoba. He was also diagnosed with epilepsy at 12 years old.  Today on Connections, Chris shares his journey with epilepsy. He'll also share the importance of drawing awareness to this neurological disorder.  See omnystudio.com/listener for privacy information.

Billie Jean Colbourne of Gander is this year's Newfoundland and Labrador ambassador for Epilepsy Awareness Month. She talks about her condition, her diagnosis, and her future.

March is allocated to educate people about Epilepsy. Here is a medical discussion with Dr. Kasun Withanage from Melbourne to mark the Epilepsy awareness month - මාර්තු මාසයට යෙදී තිබෙන අපස්මාර රෝගය පිළිබඳව දැනුවත් කිරීම වෙනුවෙන් මෙල්බන් නුවර වෛද්‍ය කසුන් විතානගේ සමගින් SBS සිංහල සේවය ගෙන එන මේ වැදගත් කරුණු ඇතුලත් කෙටි සාකච්ඡාවට සවන්දෙන්න ....

In this episode we talk to Hailey Adkisson about her daughter Juniper who has infantile spasms, a rare and catastrophic form of epilepsy. We discuss the process of making medical decisions, holding onto and losing hope, and carving out a different view of the future for your child. Check out her instagram @growing_juniper Raising awareness during Epilepsy Awareness Month, she is also hosting a fundraiser for Juniper's intensive treatments this summer. Check out the link here: https://www.bonfire.com/growing-juniper/ More Links: https://www.epilepsy.com https://www.epilepsy.com/learn/types-epilepsy-syndromes/infantile-spasms-west-syndrome https://www.cureepilepsy.org/ https://www.brainrecoveryproject.org/

Blog: riseaboveepilepsy.com Instagram: Instagram.com/tiffanykairos Twitter: twitter.com/tiffanykairos TikTok: tiffanykairosofficial Rise Above Epilepsy By the strength of God, I battle epilepsy. Even so, I refuse to give up hope and am determined to live courageously with every breath I take. --- This episode is sponsored by · Anchor: The easiest way to make a podcast. https://anchor.fm/app

November is Epilepsy Awareness Month, so in this week's podcast Doug Beacham and Tracy Reynolds interview Chris Maxwell about his personal story about a life changing experience. Do today's leaders know the needs of those who battle epilepsy—or other health issues? Do our churches and businesses creative a climate that shows deep care of those people and their struggles? Chris offers suggestions of ways today's leaders can lead others and let weaknesses become positives instead of negatives. Doug talks about how Chris became a different person through his illness and the long-term effects, while Tracy talks about this being the only Chris he knows. Tracy and Doug also talk about the many needs around them, and around us all. With the care of Jesus, we can love and lead people no matter what they struggle to overcome.

2022 is going to be supercharged. You heard it here first. Karen Rogers. Need we say more? Dave Portnoy is in the middle of something again, but what? It is behind a paywall. The Bernie Madoff of Mac N Cheese strikes again, but this time he pimps out Bieber. Not only is it Indigenous People Month, but also Epilepsy Awareness Month. @Tee_Platt@IAmRyanLacosse@TheCTZPodcastTheCTZ.com

#EpilepsyAwarenessMonth | En el marco de la campaña conforme a la sensibilización acerca de la epilepsia, tenemos como invitada a la neuropsicóloga Natalia Ariza @psinataliaariza, que nos hace un abordaje sobre qué es la epilepsia, los mitos de este trastorno neurológico y las asociaciones que tiene con el déficit cognitivo.

The month of November is Epilepsy Awareness Month. This is something dear to us since our little guy has been diagnosed with Epilepsy with onset seizures. This means they have no idea what is causing them. The day was May 29th, 2021, 3 days after he finished remote learning he started having seizures before he wakes up. Here we are in November, he's been in and out of the hospital. His last event was August 17th, 2021. This is all new to us. We're trying to bring awareness and recount our story of the last few months. between doctor visits, specialists and different overnight studies, we are glad to say he has not had one event since then. Check out our story. --- Send in a voice message: https://anchor.fm/tableforfour/message

This week, I am again joined by Kayla as we review 2 of the four new Christmas movies this week, titled Christmas in Harmony starring Ashleigh Murray and Luke James, as well as Coyote Creek Christmas starring Janel Parrish and Ryan Paevey. One theme we found occurring in both of these movies is "Sucky Parents and Misplaced Anger". Parents of the leading lady in both movies kept huge secret from their daughter and instead of being even remotely angry at the parents, she took it out on her love interest. In "Christmas in Harmony", we had a good laugh at the title, share our wish for more singing, and the disappointment that it wasn't like Sister Act movies, lol. "Coyote Christmas" was a bore. We both found the storyline just boring. The real star of the movie was Azriel Dalman who played Noah. He should definitely be in more Hallmark movies. A couple of things happened this week. Lol. Two Hallmark actors spoke publicly on their stance with GAC. Paul Campbell and Emilie Ullerup have put out statements along the lines of they will not be working for the company unless they see significant inclusion in the channel. We were also featured in a Heavy article about these very statements since these statements were prompted by Camille calling out these actors. https://heavy.com/entertainment/hallmark/hallmark-stars-speak-out-gac-family/ November is also Epilepsy Awareness Month. Kayla has epilepsy. If you want to donate to the cause, here's the link http://www.epilepsy.com Future Podcasts: Interview with Tia Streaty, star of Christmas in Harmony Christmas Promise and Christmas in Sail Review Interview with Azriel Dalman, star of Coyote Creek Christmas  

CURE Epilepsy and Epilepsy Canada recently entered into a strategic partnership to accelerate scientific progress and drive research forward to find a cure for epilepsy. To celebrate this new partnership, and in honor of Epilepsy Awareness Month in Canada, we speak with Alek and Brittany Stewart, husband and wife advocates for Epilepsy Canada. The post Community, Fatherhood, and Seizures appeared first on CURE Epilepsy.

This episode won't feature an awareness section as I wanted to dedicate this episode to Epilepsy Awareness Month as March is very special to me and raising any kind of awareness for Epilepsy is very much a passion of mine.   Podcast edited by - Mustafa Ali 

Ep. 100 Gobble Gobble Write Club Welcome to the bench! We write on the bench, we snack on the bench and we procrastinate on the bench and it’s our 100th episode! It’s a writing podcast, about friendship, snacks, sometimes Bill Murray and today is our November #BENCHWRITECLUB. Come for the laughs, stay for the prompts! Thank you so much for listening, we love you.   On 11/26, Thanksgiving, we will be on FB Live, calling @butterball and showing you our turkeys!   Thank you to our #BENCHWRITECLUB November participants: Prompt: Include the following phrase: “that is not how you cook a turkey” in your 250 word story. @KaylaStorytella (Kayla #Sharpie) @bjkdrvr8  (Bret-Jordan) @HRHammer  (Stephanie #TheHammer) @BrookReadingPod (Melissa aka #MelBrook)   BENCH GIVES BACK: November is Epilepsy Awareness Month. If you want to donate our fundraiser for the Epilepsy Foundation, you still can. THANK YOU! https://epilepsyfoundation.donordrive.com/participant/30787 The Red Cross still needs blood donations: https://www.redcrossblood.org/give.html/find-drive Be sure to follow @AlltheHorror18 so you stay up to date with horror content all year long! If you want some #AlltheHorror merch so you can match us head here – all proceeds go to @ScaresThatCare   Join our #Benchlings group on Facebook! https://www.facebook.com/2girlsonabench Twitter: @2girlsonabench Instagram: https://www.instagram.com/2girlsonabench/ Support the show via Patreon: https://www.patreon.com/2girlsonabench Buy us a snack at https://ko-fi.com/benchsnack Check out our family of shows on the Podfix Network: https://podfixnetwork.com/

It's Epilepsy Awareness Month and in this episode,  I share my story on how I got epilepsy and how it has affected my life.  I got Epilepsy as a child after contracting Meningitis and Scarlet Fever. It has been difficult living with this neurological disorder; however, I have made the best of it.  Learning how to help yourself if you have it and others you may come in contact with who have seizures is important. Hopefully one day they will find a cure for epilepsy, also known as seizure disorder.  Thank you for tuning in! If you have any comments, feedback, or questions about this or any other episode, please email me at shesdifferent.me@email.com

Joyce welcomes Peggy Beem Jelley is the president & CEO of the Epilepsy Association of Western and Central PA. to the show. With November as National Epilepsy Awareness Month, Ms. Beem Jelley will talk about the programs and services of the organization to bring greater awareness to epilepsy and how to live with the condition.

Joyce welcomes Peggy Beem Jelley is the president & CEO of the Epilepsy Association of Western and Central PA. to the show. With November as National Epilepsy Awareness Month, Ms. Beem Jelley will talk about the programs and services of the organization to bring greater awareness to epilepsy and how to live with the condition.

Pamela Price currently serves as the Deputy Director for The Balm In Gilead managing the various health initiatives of the organization.  Mrs. Price holds a Bachelor’s of Science degree in Public Health and has more than 20 years of experience in public health, epidemiology, and healthcare. In addition to her role as Deputy Director, she also serves as the Director for The National Brain Health Center for African-Americans. Mrs. Price has co-developed educational curricula and trainings for the community, clinicians, nurses, & other allied healthcare professionals aimed at addressing knowledge & cultural competency gaps related to health inequities affecting African Americans. As an advocate & leader for diversity & inclusion, she provides strategic leadership to organizations on best practices related to impactful community engagement. Pamela has worked with national and government agencies to develop and implement multi-faceted programs to meet the societal and cultural needs of underserved communities.  Mrs. Price has conducted hundreds of trainings across the country on best practices related to diversity, inclusion, & equity as well as educational symposia on the impacts of socioeconomic challenges and health outcomes among communities of color.  She is passionate and purpose driven in her desire to see individuals, families, and communities living and thriving across the life span.    

November is Epilepsy Awareness Month. In this episode, Joe sits down with a close friend and they discuss their common struggle with epilepsy, podcasts/vlogging and dried meats. It's a light-hearted discussion amongst friends having a few laughs. Listen to this new content, enjoy it and maybe even learn a thing or two.  If you'd like to learn more about living with Epilepsy, please visit https://www.epilepsy.com/ and/or https://www.cureepilepsy.org/  Like our podcast? You can show us by taking a moment and going over to Apple Podcasts and giving us 5-star rating and dropping an comment or review. We really appreciate it and believe it or not it really helps the show. Thanks. Show your support at www.adarktale.com. With a small donation, you will earn an Executive Producer credit at the end of a new episode of A Dark Tale! Check out the website for more info. Thank you! Twitter/IG: @ADarkTalePod                   @Joe_TheHost                   @JamesNuzz Drews Info: IG @hikingwithepilepsy      YT Channel: Hiking with Epilepsy Original music and FX composed by @Joe_TheHost ©2020  

Epilepsy is a neurological disorder that affects the central nervous system and causes seizures. More than 3 million Americans and more than 65 million people worldwide have epilepsy - a key reason that November is recognized as National Epilepsy Awareness Month. Thankfully, treatment with medications or sometimes surgery can control seizures for most people with epilepsy. On the Mayo Clinic Q&A podcast, Dr. Joseph Sirven, a Mayo Clinic neurologist, discusses the importance of raising awareness of epilepsy to lessen the stigma, Dr. Sirven also highlights the latest in treatments and research.

Once upon a midnight dreary...Now that Eric is settling into his new house, it’s time to learn all the idiosyncrasies of his new digs. There are many. His son is convinced that a drawer in his kitchen is haunted and as a night wears on, Eric finds himself wondering if he himself may be convinced as well. The guys discuss why a child’s fears can be easily transposed onto an adult.  It’s an epilepsy awareness month. Fun is poked at the idea of reminding people suffering from a condition that they have it when they were just finally able to get over it.  Who needs awareness anyway? Please visit us at https://thetragedyacademy.com On social media, you can find us at @thetragedyacademypodcast on Instagram, The Tragedy Academy Podcast on Facebook, and @tragedy_academy on Twitter.  Don't forget to subscribe, download, rate, and review!  (00:35:40 - 00:36:50) Eric finds a ghost in the drawer.  You can support epilepsy research at the National Epilepsy Foundation at epilepsy.com  

Where are we with AHFE and what does this month mean to us. --- Support this podcast: https://anchor.fm/epileptics-hero/support

November is Epilepsy Awareness Month, a cause that is near and dear to my heart. This is mainly because someone who is near and dear to me has epilepsy. So to support her and the cause of epilepsy awareness, I could think of no one better to interview for today’s episode than my very special guest, my amazing baby sister, Lauren Boyd. In this episode, we dive DEEP into what epilepsy is and the different types of seizures those who suffer from epileptic episodes can experience. We talk about Lauren’s history with her disorder, and how she has learned to listen to her own mind and body better in an effort to outperform it. We tap into Lauren’s incredible knowledge as she dispels some of the misconceptions of epilepsy. And finally, we revisit the events of our younger years that led to her finally being properly diagnosed with epilepsy. You guys, this episode was SUCH A SPECIAL TIME for me! Not only did I get to interview my baby sister, but I got to talk with her openly about a disorder she’s lived with for more than a decade for the first time as adults. I couldn’t be more proud of the woman she’s become and her strength, resilience, wisdom, and poise continues to inspire me on a daily basis! Get ready to experience inspiration on a whole n’other level.  If you'd like to learn more about epilepsy, seizure first aid, or how to raise awareness during Epilepsy Awareness Month, visit epilepsy.com today. Be sure to follow Lauren on Instagram and check out her stomping grounds, dance company Sac Dance Lab, as well! --- This episode is sponsored by · Anchor: The easiest way to make a podcast. https://anchor.fm/app Support this podcast: https://anchor.fm/fearlessu/support

I rant about Epilepsy Awareness Month and how to help someone who is having a seizure, Santa is declared an essential worker and a town comes together to feed stranded passengers on Christmas. #goodnews #EpilepsyAwarenessMonth #seizuretips #essentialSanta #comingtogether

Listen to an American Lung Association spokesperson unpack vital details from this year's 'State of Lung Cancer' report including heartening news about survivability in Connecticut. Then we'll celebrate Epilepsy Awareness Month with the CT Epilepsy Advocate and a Yale researcher who developed important new information to help folks with drug resistant epilepsy. And we'll introduce you to VetFuel - a nonprofit whose mission is to ensure no veteran should want for a job or appropriate medical care because of a lack of transportation.

Michelle Fiacco, CMO of AHFE talks about epilepsy in the US and how it compares to other neurological conditions. --- Support this podcast: https://anchor.fm/epileptics-hero/support

Over 65 million people have epilepsy worldwide and close to 4 million in the US. Bruno Fiacco, our CEO wants to raise awareness all November long. --- Support this podcast: https://anchor.fm/epileptics-hero/support

This week host John Voket and the award-winning For the People talks with the Connecticut Epilepsy Advocate, and discusses new research findings and therapies with a local neurologist as we close out Epilepsy Awareness Month. Then we'll check in with the Aspetuck Land Trust for some great tips on winter walking, hiking, snowshoe, and recreational opportunities - and meet a UConn professor who just completed a study on the state's expanding Black Bear population. And we'll wrap with the Connecticut League of Conservation Voters - revealing high hopes for the upcoming legislative session and enhanced environmental leadership under Governor-Elect Ned Lamont.

Ever watch Jeopardy and seen a bathroom attendant be a contestant? Us neither but imagine if they were! Dave has been watching a lot of Jeopardy lately. Flexy Michelle talks Epilepsy Awareness Month (link below), and Mike Mason pops in with some NFL Picks for this weekend, and he’ll weigh in (with those calves) on the CFL West Division Final this Sunday in Calgary! Thanks for your ongoing support! Please SUBSCRIBE FOR FREE on your favorite platform! PLEASE Support the show on Patreon!WITM all over your chest! Pictures of Cats Humping Sofa'sCheck out the ‘Music News You Can Use’ Daily Playlist on iTunes and SpotifySocial Media:Franks Pizza TwitterEmail for Franks Winnipeg Jets Tickets: info@frankspizza.caBryan Lotocki – InstagramSafetyNetStudio - TwitterSafetyNetStudio - InstagramCandace Rae - InstagramDave Wheeler - InstagramDave Wheeler - TwitterDave Wheeler – YouTubeSponsors:Vernaus AutobodyMike Mason of RemaxItty Bitty Baby BoutiqueFranks PizzaHenderson Massage Health and Wellness CentresSources:Winter Driving OptionsSanctions for Crown PrinceGo Fund ThemEpilepsy Awareness MonthFlexy MichelleMusic News You Can Use:NME.comJohn Lennon - Imagine6ix9ine – GummoThe KLF – Justified and AncientClips:Top Gun – WingmanSupport the show (https://www.safetynetstudio.com/plans-pricing)

AHFE has been hard at work on a number of projects that we would like to start sharing with you as well as creating new content for Epilepsy Awareness Month which is all November long. --- Support this podcast: https://anchor.fm/epileptics-hero/support

A Hero for Epileptics describes why November is so important for Epilepsy Awareness. --- Support this podcast: https://anchor.fm/epileptics-hero/support

Making time to be around those that understand what you go through everyday is vital as these people are your main support. We also discuss plans for the remainder of the year and why November and Epilepsy Awareness Month is the best way to raise awareness and kick off #GivingTuesday and year end giving. --- Support this podcast: https://anchor.fm/epileptics-hero/support

Joyce welcomes Bob Smith, chairman of the national board of directors of the Epilepsy Foundation. To close out of National Epilepsy Awareness Month, Mr. Smith will discuss the programs and services of this organization and what is being done nationally to improve the lives of people living with epilepsy.

Listen live, weekdays from noon to 1, on Zoomer Radio!

Actor Greg Grunberg and TV Host Leeza Gibbons join us on this week's show!Greg Grunberg, who appeared in Star Wars: The Force Awakens and Heroes Reborn in late 2015, and Star Trek Beyond in 2016, is best known for his role as Matt Parkman, the mind-reading police officer on the television series Heroes. In real life, Grunberg is a hero and advocate of a different kind — serving as an advocate for people with epilepsy all over the country, including his oldest son, Jake, who was diagnosed at seven years old. Greg will share his experience as a dad and caregiver for his son and how they manage his epilepsy, and tell us about a new awareness campaign called #MyEpilepsyHero for Epilepsy Awareness Month.Caring for a loved one can be an extremely rewarding experience, but it can also be difficult and overwhelming. Many caregivers deal with guilt and worry about the amount of time they spend with a parent or family member. TV Host Leeza Gibbons is a longtime advocate for caregivers and joins us for National Caregivers Month. She will discuss improvements in senior care, share caregiving tips and offer her personal experience caring for her father.Women make approximately 80 percent of the health care decisions in their families and take the lead role in choosing health plans. So much of the burden rests on women to make health care decisions for themselves and their families this open enrollment, which is why we are talking to our next guest. She is one of the top wealth experts in the country and host of the popular radio show Renegade Millionaire, Winnie Sun. She has the results of an informative new study about working moms’ healthcare choices.Tamara Walker, RN, aka MomRN, and her expert guests share practical advice, information and support for raising a happy, healthy family.

Actor Greg Grunberg and TV Host Leeza Gibbons join us on this week's show!Greg Grunberg, who appeared in Star Wars: The Force Awakens and Heroes Reborn in late 2015, and Star Trek Beyond in 2016, is best known for his role as Matt Parkman, the mind-reading police officer on the television series Heroes. In real life, Grunberg is a hero and advocate of a different kind — serving as an advocate for people with epilepsy all over the country, including his oldest son, Jake, who was diagnosed at seven years old. Greg will share his experience as a dad and caregiver for his son and how they manage his epilepsy, and tell us about a new awareness campaign called #MyEpilepsyHero for Epilepsy Awareness Month.Caring for a loved one can be an extremely rewarding experience, but it can also be difficult and overwhelming. Many caregivers deal with guilt and worry about the amount of time they spend with a parent or family member. TV Host Leeza Gibbons is a longtime advocate for caregivers and joins us for National Caregivers Month. She will discuss improvements in senior care, share caregiving tips and offer her personal experience caring for her father.Women make approximately 80 percent of the health care decisions in their families and take the lead role in choosing health plans. So much of the burden rests on women to make health care decisions for themselves and their families this open enrollment, which is why we are talking to our next guest. She is one of the top wealth experts in the country and host of the popular radio show Renegade Millionaire, Winnie Sun. She has the results of an informative new study about working moms’ healthcare choices.Tamara Walker, RN, aka MomRN, and her expert guests share practical advice, information and support for raising a happy, healthy family.

November is Epilepsy Awareness Month and most people may not realize that this is the fourth most common neurologic problem and can be scary if anyone has ever witnessed someone having a seizure. We'll be talking with a panel of experts about the common misperceptions about epilepsy and also reviewing the facts.

This morning, John Voket and the award-winning 'For the People' introduce an outreach specialist representing Connecticut's Vet Centers. Then we'll air a very special visit with Nelba Marquez Greene and Jimmy Green, whose Ana Grace Project is honoring the daughter they lost at Sandy Hook Elementary School by hosting a symposium for trauma responders at Western CT State University.And since November is Epilepsy Awareness Month, we'll welcome Connecticut's Epilepsy Advocate, and a representative of the LGS Foundation zeroing in on this pervasive type of epilepsy.

This morning, John Voket and the award-winning 'For the People' introduce an outreach specialist representing Connecticut's Vet Centers. Then we'll air a very special visit with Nelba Marquez Greene and Jimmy Green, whose Ana Grace Project is honoring the daughter they lost at Sandy Hook Elementary School by hosting a symposium for trauma responders at Western CT State University.And since November is Epilepsy Awareness Month, we'll welcome Connecticut's Epilepsy Advocate, and a representative of the LGS Foundation zeroing in on this pervasive type of epilepsy.

In recognition of November being National Epilepsy Awareness month, Joyce welcomes Peggy Beem-Jelly, CEO of the Epilepsy Foundation of Western/Central PA and Shannon Bursick, whose daughter died from SUDEP at the age of seven. Ms. Beem-Jelly and Ms. Bursick will discuss epilepsy and SUDEP (Sudden Unexpected Death of Someone with Epilepsy); now the leading cause of death in persons with chronic uncontrolled epilepsy.

Joining us once again, speaker, and health coach, and author of several books about natural health and wellness, Stacey Chillemi, will be back this time to talk about Epilepsy, in honor of Epilepsy Awareness Month. We will also be talking with singer songwriter Lauren Corzine on her way to Nashville.  

In continuing with Epilepsy Awareness as the topic for November, Joyce welcomes The Honorable Tony Coelho, author of the Americans with Disabilities Act and former congressman from California to the show. Mr. Coelho will discuss his journey living with epilepsy, and the progress that has been made nationally to end the stigma.

Epilepsy is a neurological disorder that affects the central nervous system and causes seizures. More than 3 million Americans and more than 65 million people worldwide have epilepsy - a key reason that November is recognized as National Epilepsy Awareness Month. Thankfully, treatment with medications or sometimes surgery can control seizures for most people with epilepsy. On the Mayo Clinic Q&A podcast, Dr. Joseph Sirven, a Mayo Clinic neurologist, discusses the importance of raising awareness of epilepsy to lessen the stigma, Dr. Sirven also highlights the latest in treatments and research. Advertising Inquiries: https://redcircle.com/brandsPrivacy & Opt-Out: https://redcircle.com/privacy

Epilepsy is a neurologic central nervous system disorder in which brain activity becomes abnormal, causing seizures or periods of unusual behavior, sensations and sometimes loss of awareness.Seizure symptoms can vary widely. Some people with epilepsy simply stare blankly for a few seconds during a seizure, while others repeatedly twitch their arms or legs. Having a single seizure doesn't mean you have epilepsy. At least two seizures without a known trigger (unprovoked seizures) that happen at least 24 hours apart are generally required for an epilepsy diagnosis.Anyone can develop epilepsy. Epilepsy affects both males and females of all races, ethnic backgrounds and ages. When a child is diagnosed with epilepsy, families may need support to adjust to this new diagnosis. Parents and schools can partner with the medical team to help."One of the things that's really important for families to remember is they are not fighting this battle on your own," explains Dr. Elaine Wirrell, a pediatric neurologist and chair of Child and Adolescent Neurology at Mayo Clinic Children's Center. "You need to share the diagnosis and inform those who are caring for your child — teachers, daycare, coaches — so they are prepared to help." Medication is generally the first course of treatment for epilepsy. Finding the right medication or combination of medications, and the optimal dosages, can be complex. Many children with epilepsy who aren't experiencing epilepsy symptoms can eventually discontinue medications and live a seizure-free life.For some children with drug-resistant epilepsy, surgery is an option. Epilepsy surgery, which is considered when at least two anti-seizure medications have failed to work, removes or alters an area of the brain where seizures originate.Experts at Mayo Clinic Children's Center also are studying neurostimulation treatments for epilepsy, an alternative treatment for children with severe epilepsy or for those who cannot have surgery. This treatment applies electricity to the central nervous system with the goal of reducing seizure frequency and severity.On this Ask the Mayo Mom edition of the Mayo Clinic Q&A podcast, host Dr. Angela Mattke is joined by Dr. Wirrell for a discussion on epilepsy in children.Related articles: "Consumer Health: Treating children with epilepsy." "Mayo Clinic Q&A podcast: Epilepsy Awareness Month." Advertising Inquiries: https://redcircle.com/brandsPrivacy & Opt-Out: https://redcircle.com/privacy