Ritecare Hyderabad’s Post

🟣 "Shine a Light on Epilepsy: Celebrate Purple Day!" 🌟 Join us in raising awareness for epilepsy on Purple Day! Let's come together to show support for those living with epilepsy and spread knowledge about this neurological condition. 💜 Spread Awareness: Share this flyer with friends, family, and colleagues to spread awareness about epilepsy and Purple Day. Wear purple on Purple Day to show your support and solidarity. Together, let's shine a light on epilepsy and empower those living with the condition! 💜🌟 #PurpleDay #EpilepsyAwareness

✨ 2,389,313 Steps Towards Awareness ✨ Proud to share that during the IBE's 50 Million Steps Campaign, we collectively achieved an incredible milestone of 2,389,313 steps! This campaign wasn’t just about walking – it was about stamping out the stigma around epilepsy and creating a world where those with epilepsy feel understood, accepted, and supported. Every step symbolizes unity, perseverance, and the power of community coming together for a cause bigger than ourselves. 💜 Why 50 Million Steps? The number represents the 50 million people worldwide living with epilepsy. It’s a call to action for all of us to take tangible steps—both figuratively and literally—towards raising awareness and supporting those affected. As someone who has witnessed the challenges and triumphs of living with epilepsy, this initiative holds a special place in my heart. Together, let’s continue to spread awareness, educate others, and inspire action. 💡 How can you contribute? Take a step today, whether it's spreading awareness or offering support to someone in need. Share this post to amplify the message. Let’s all unite to #StampOutStigma. Every step counts. Every voice matters. Let’s keep moving forward, together. INTERNATIONAL BUREAU FOR EPILEPSY #EpilepsyAwareness #50MillionSteps #StampOutStigma #TogetherForEpilepsy

Did You Know? The #50MillionSteps campaign serves as the starting point for International Epilepsy Day which takes place on February 10, 2025. Aligned with the overarching goal of #EpilepsyDay, #50MillionSteps seeks to: ● Raise awareness about epilepsy. ● Dispel the myths and misconceptions surrounding epilepsy. ● Improve knowledge levels about epilepsy across all sectors of society. Learn more about the campaign at: https://lnkd.in/dA6AmyY

🔮💜 Get your purple ready for tomorrow... it's Purple Day on Tuesday, March 26th! 💜🔮 Tomorrow is a special day dedicated to raising awareness about epilepsy and seizures, and we need your support! Wear your favourite shade of purple to show solidarity and spread awareness. 💜 Why is Purple Day important? Because it sheds light on a neurological disease that affects millions worldwide. It's a reminder that epilepsy isn't something to fear... it's something to understand and support each other through. Here's how you can get involved: 1️⃣ Wear purple tomorrow! Show your support visually. 2️⃣ Share a fact about epilepsy or a personal story to raise awareness. 3️⃣ Educate yourself and others about epilepsy and seizures. Knowledge is power. 4️⃣ Show compassion and empathy to those living with epilepsy. A little understanding goes a long way. Let's break the stigma surrounding epilepsy together. Together, we can make a difference. 💪💜 #PurpleDay #EpilepsyAwareness #EndTheStigma #DurhamRegion #DDSB #DCDSB

Join Our Quarterly Support Groups Living with epilepsy can be challenging, but you don’t have to navigate it alone. At South Carolina Advocates For Epilepsy, we’re here to provide a supportive community where you can share your experiences, learn from others, and find encouragement on your journey. Our Quarterly Support Groups offer a safe and welcoming space for individuals with epilepsy (ages 14 and older) to connect, learn, and grow together. What to Expect: Connection: Meet others who understand the challenges and triumphs of living with epilepsy. Education: Access valuable information and resources to help manage your condition. Support: Share your thoughts and concerns in a judgment-free environment. Who Can Join? Anyone 14 years and older living with epilepsy is invited to participate. How to Get Involved: Our meetings are held virtually for your convenience. To join the next session, email Karen@scepilepsy.org to request the Zoom link. Let’s support one another, share our stories, and create a stronger community—because together, we can make a difference!

In recognition of National Epilepsy Awareness Month (NEAM), check out the latest issue of Foundation Quarterly, which highlights the theme "Creating Change." This issue focuses on the strength, resilience, and courage of individuals within the epilepsy community. Committed to the mission that no one faces epilepsy alone, we share the powerful impact of people coming together to foster belonging and drive meaningful change. Read it here: https://lnkd.in/gX8TpdyT

For those recently diagnosed with epilepsy, know that you're not alone. Our "New to Seizures and Epilepsy" Toolkit is designed to support you on your journey. From navigating daily life to equipping yourself with the right questions for your next doctor's visit, we're here to help. Explore the toolkit today: https://bit.ly/3PqsN0I 

Check out Angels of Epilepsy July Newsletter! 💜 Get the latest news, blogs, events, & more in the epilepsy community! SUBSCRIBE to #AOENEWS Read here: https://lnkd.in/e6bWPxw6

💜 November is Epilepsy Awareness Month! ✨A time to shine a light on #epilepsy and how it impacts lives across all ages. In the early 1990s, our R&D center in Compiègne (France) discovered and developed a breakthrough anti-epileptic treatment for a rare and severe condition starting in infancy: #Dravet Syndrome. Since then, we've been committed to supporting awareness efforts on rare forms of epilepsy, working hand in hand with healthcare professionals, patients, and caregivers.🤝 💡 Why is awareness important? Dravet syndrome is often misunderstood, but raising awareness helps build understanding and provides support for those living with this condition. Every patient, every family face daily challenges—challenges that we can help ease by sharing information and showing compassion. 🌟 How can you make a difference? Learn and share trusted information about Dravet syndrome. Support organizations and initiatives focused on improving the lives of patients and families. 💪Together, we can foster a more inclusive, supportive environment for families impacted by Dravet syndrome. Every action, big or small, brings us closer to advancing knowledge and improving lives #DravetButterflyEffect.🦋 #DravetSyndrome #EpilepsyAwarenessMonth #BiocodexCares

Join Our Quarterly Support Groups Living with epilepsy can be challenging, but you don’t have to navigate it alone. At South Carolina Advocates For Epilepsy, we’re here to provide a supportive community where you can share your experiences, learn from others, and find encouragement on your journey. Our Quarterly Support Groups offer a safe and welcoming space for individuals with epilepsy (ages 14 and older) to connect, learn, and grow together. What to Expect: Connection: Meet others who understand the challenges and triumphs of living with epilepsy. Education: Access valuable information and resources to help manage your condition. Support: Share your thoughts and concerns in a judgment-free environment. Who Can Join? Anyone 14 years and older living with epilepsy is invited to participate. How to Get Involved: Our meetings are held virtually for your convenience. To join the next session, email Karen@scepilepsy.org to request the Zoom link. Let’s support one another, share our stories, and create a stronger community—because together, we can make a difference!