💜 Today is Purple Day, a special day dedicated to raising funds for those living with intractable epilepsy. Read more about Oliver's story.💜https://lnkd.in/gR-zX23s Join us in making a difference by supporting our fundraising campaign. https://lnkd.in/gGK34CSu Your generous donations can help provide crucial resources, support services, and research initiatives for individuals and families affected by intractable epilepsy. 💜 By donating on Purple Day, you are directly contributing to improving the lives of those living with this challenging condition. Your support can help fund vital medical treatments, access to specialized care, and advocacy efforts. 💜 Every contribution, no matter how big or small, can have a significant impact. Together, we can make a difference and provide hope to those who need it most. Let's come together as a community and show our support for individuals living with intractable epilepsy. 💜 To make a donation, visit our website https://lnkd.in/dxBxqhn3 or click the link in our bio. Your generosity will help us continue our mission of raising awareness, providing support, and advocating for better treatments. 💜 Share this post and spread the word! Together, we can create a brighter future for those affected by intractable epilepsy. Thank you for your support! 💜 #PurpleDay #EpilepsyFundraising #SupportAndEmpowerment #MakeADifference #EndEpilepsy
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This March, join us as we tell epilepsy to GET MUCKED! Sign up for the Purple Muck Challenge to spread awareness and raise funds for people living with epilepsy. Participation is easy. Simply: 1. Visit https://bit.ly/3vWrxez and create a fundraising page to share with your network, encouraging people to donate. 2. During March, film yourself pouring a bucket of purple muck over your head. An easy recipe for making purple muck can be found at https://bit.ly/482D5dk 3. Share the video on social media and nominate/tag at least three friends to participate. If they choose not to participate, they must donate to your page. 4. Continue to encourage your family, friends and colleagues to donate throughout March. Be sure to tag the Epilepsy Foundation and use the hashtags #GetMuckedEpilepsy #MuckMeForEpilepsy in all your posts. Let's Make March Purple like never before! Sign up to the Purple Muck Challenge today. #EpilepsyFoundation #Epilepsy #MakeMarchPurple #EpilepsyAwareness #EpilepsySupport #BreakTheStigma #PurpleMuckChallenge
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In Australia, every year, over 12,000 people are diagnosed with epilepsy. Shockingly, 1 in 3 won't gain control through medication alone. 😞💊 But together, we can make a difference! Get your organisation involved and join our #Spark4Epilepsy campaign this November. Help raise awareness and show your support for people living with epilepsy by sparking a conversation for Epilepsy Awareness month. 💜📸 What can you do? 1️⃣ Share our content and raise awareness. 2️⃣ Take a 'static selfie' as a team or take one yourself and update your profile picture to help spark a conversation in your network. 3️⃣ Help us continue to raise awareness but holding a fundraiser. It doesn't need to be big - gold coin donation events, purple dress ups, all help us make a difference! 4️⃣ Make a donation to Epilepsy Action Australia. Learn more: https://lnkd.in/g-aTirqf #EpilepsyAwareness #SparkAConversation #EpilepsyActionAustralia #Breakthestigma #Epilepsy
Spark4Epilepsy
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Did you know that epilepsy is a significant part of Coach Heather Binns‘s life’s journey? Epilepsy, a neurological disorder, doesn’t discriminate based on age, race, or gender. Shockingly, 1 in 10 individuals will experience a seizure, and 1 in 26 will develop epilepsy in their lifetime. Heather’s personal battle with epilepsy began in her twenties after a near-death experience, leading to simple partial and complex partial seizures. The journey was bewildering, navigating from one doctor’s office to another in search of answers to the peculiar sensations she was experiencing. In our ongoing commitment to raise awareness about epilepsy and empower individuals to support those affected by it, We’ve formed a team for the Epilepsy Walk Los Angeles on April 28th at the Rose Bowl in Pasadena. And guess what? You don’t have to be local to participate! 😁 We invite you to join Team Renov8, whether virtually or in person, for the Epilepsy Walk Los Angeles, or consider donating to the cause at https://lnkd.in/gy4VZeuY - This cause is deeply meaningful to us, and your support in spreading awareness and raising funds for this vital cause would mean the world to us. Thank you for your kindness and generosity! 🙏 Epilepsy Foundation #HeatherBinns #HeatherCPT #FindYourAthleteWithin #Renov8TheBody #Renov8TheMind #Renov8Fitness #TeamRenov8 #epilepsy #epilepsywalkla #epilepsywalklosangeles #donate #charity #fundraiser #fundraising #EpilepsyAwareness #EndEpilepsy #EpilepsyWalk #RaiseAwareness #SupportEachOther #RoseBowl #Pasadena #NeurologicalDisorder #CommunitySupport #HealthAwareness #Empowerment
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🌟🎉 Happy World Social Media Day! 🎉🌟 Today, let's harness the power of social media to make a real difference! 💪✨ Help us spread the word about the amazing work we do at The Meath Epilepsy Charity Here's how you can get involved: ✅ Share Your Story: Have you or someone you know benefited from the services at The Meath Epilepsy Charity? Share your story with us using the hashtag #MeathEpilpesyCharity. Let's celebrate the impact we’ve made! 🌈 ✅ Follow and Engage: Follow The Meath Epilepsy Charity on all our social media platforms. Like, comment, and share our posts to help increase our reach. Every click counts! 🔄❤️ ✅ Share With Your Friends: Tag your friends and encourage them to follow us. Let's see how far we can spread the love! 📲💬 ✅ Donate and Support: If you can, consider making a donation to support our Capital Campaign. Every bit helps in making a positive change. 💖🌟 https://lnkd.in/dk8fd7V ✅ Stay Informed: Keep an eye on The Meath Epilepsy Charity's updates to stay informed about our projects, events, and ways you can contribute. Knowledge is power! 📚🧠 #SupportMeath #ShareTheLove #MakeADifference #MeathEpilepsyCharity
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I want to share this post to bring an awareness about the epilepsy and HIGHLY recommend everyone to read it, comment on it and share in your network. #epilepsy #topgscrummaster
Today, I share with you something personal in hopes to raise awareness. I live with Epilepsy. It is a neurological disorder which causes recurring, unprovoked seizures. After 2 tonic clonic seizures in my teens, I have been fortunate to live seizure free with the help of medication for over 30 years. No matter the side effects, I am extremely grateful for my health. 💜 Please consider making a donation. https://lnkd.in/epjyB77J Help us find a cure. This is a long post but I am asking you to spread the word. Repost. Make a comment. 🤝💜 I understand not everyone may have the means to donate, but raising awareness is free. 5 years ago, I founded EpiPalooza as a way to raise awareness and money for Epilepsy, as well as foster an environment for others who live with Epilepsy to not feel alone. With 3.4 million people in the U.S. living with Epilepsy, it is more common than people are aware, so we must work towards a cure. You can help us make a difference. How? Please consider making a donation. https://lnkd.in/epjyB77J By giving to CURE Epilepsy you help fund critical research and advance their mission of finding a cure for epilepsy. 💜 1 out of 26 people will develop Epilepsy at some point in their life. One of those 26 is my daughter. At the age of 4, she had her first seizure. She struggled for several years with 11 seizures but now has tapered off. Spread the word. Repost. Make a comment. Send a text to a friend. Tell your friends; not just one who lives with Epilepsy. Epilepsy is more common than you think. They may have a friend or relative who lives with Epilepsy. I’ve met people who had their first seizure at the age of 40 and their lives were drastically changed within an instant. Donation: https://lnkd.in/eA5Cb-ut Thank you for reading. My daughter thanks you. 3.4 million people thank you. 💜 #epilepsy #epilepsyawareness #epipalooza #cureepilepsy #1outof26
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Imagine a big, extended family that comes together when someone is facing a life-changing condition. Some help with practical things, others examine and work out the science behind it all. Everyone is united for the common good. This is what our Christmas Appeal is all about. Every year, thousands of babies in Australia are born with Craniosynostosis, a skull deformity. Untreated, the condition can lead to developmental delays, seizures and more. Parents are left confused and anxious, not knowing what the future holds and what the diagnosis means for their child. What we do know is that each and every family desperately needs better access to immediate and individualised support, so that they are better equipped to face adversity. Like most parents, Brisbane couple Ashlea and Sean were not given any information about daughter Sienna’s condition and what to expect. “The operation was one of the hardest days of our lives, but the hard part didn’t stop there. It continued. Watching your baby go through something without being able to help them, you’d do anything to put yourself in their place. Sienna’s resilience was an inspiration to all” Ashlea says. “We had never heard of Craniosynostosis before. Craniofacial Australia provided such a safety net to our family. After the operation, Sienna received her Care Pack which put a huge smile on her face, and mine. We cannot thank Craniofacial Australia enough.” Our investment in research is critical to better informing and supporting families like Sienna’s. A current research study we are funding looks at the psychosocial supports that would benefit families following a diagnosis. Led by Prof Rachel Roberts from the University of Adelaide, they are identifying where the gaps lie, from diagnosis to post-treatment. Your donation this Christmas will help us apply these translational findings to shape the resources and services provided for families, so that in the future when a family faces this life-changing diagnosis, they know exactly where to turn to receive the support they urgently need. This Christmas, your donation will bridge the gap between patient and support. Please donate today: https://lnkd.in/grvRVqbz #craniofacialaustralia #christmasappeal #charity #notforprofit #christmas2023 #donatenow #donate
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🌟 Empowerment Through Knowledge 🌟 Facing childhood cancer is a journey of strength and resilience. Our latest blog explores how families can harness the power of education and advocacy to navigate this challenging path. 💛✨ 📚 Learn about treatment options 🤝 Comprehensive support for families 👥 Connect with peers and communities Explore the full blog here: https://bit.ly/3Genj3J . To view our extensive database of available supports and resources, visit the 'Resources' section of our website. Together, we can empower families and spread hope. 🌈💙 #talisfund #childhoodcancerawareness #childhoodcancerresearch #supportnonprofits #nonprofitfundraising #nonprofitorganisation #braincancer #cancerawareness #fightagainstcancer #ATRT #childhoodbraincancer
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Trainee Team Leader - Barclays Fraud | Freelance Sales and Marketing Professional | Campaign Design | Lead Acquisition & Customer Retention
The battle against Alzheimer's and other dementia-related diseases is incredibly personal to me, having recently lost both my grandad and grandpa to them. To honor their memory and contribute to the fight, I've committed to running the AJ Bell Manchester 10K for Alzheimer's Society. This isn't just about the run; it's about making every step count towards a future where Alzheimer's and dementia no longer steal our loved ones from us. To make this vision a reality, I need your support. I've set up a fundraising page where you can donate, and every penny raised will go directly towards research and support services for those affected by Alzheimer's and dementia. No amount is too small, and your generosity can make a huge difference in this fight. If you can't donate at this time, please don't underestimate the power of sharing. By sharing this post, you're helping to spread the word and increase the reach of fundraising efforts, which is just as valuable. Please consider donating through the link below. Together, we can make a significant impact. Thank you for your support, kindness, and for being part of this journey with me. Let's run towards a cure, one step at a time. #AlzheimersAwareness #DementiaSupport #Manchester10K #RunningForACause #TogetherWeCan --- https://lnkd.in/ehZi25MS
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Remember, Remember to donate to Movember 💰 This month, along with my colleagues at NordVPN, I will be helping to raise money and awareness for the fantastic charity Movember! Like many men in November, I want to break free from my beard in favour of a Freddie Mercury-style moustache to help grow awareness about mental health, suicide prevention, prostate and testicular cancer. Here are some important reasons why: Globally, on average, 1 man dies of suicide every 60 seconds. With 3 out of 4 suicides in the UK being men. More than 1.4 million men worldwide are diagnosed with prostate cancer each year and it's the most commonly diagnosed cancer in men in the UK. Testicular cancer is the most common-form of cancer from men aged 15-39. Movember fund groundbreaking projects all over the world which help educate and support men during tough times and help to accelerate change 💪 I won't just be growing a moustache, I will be putting my cardio to the test by taking on the London Landmarks Half Marathon Limited next year to help raise money for Movember. My target is to raise £2,000 🏃♂️ Please donate to support all the dads, brothers, sons and mates in our lives ⬇ #movember2023 #mentalhealthawareness #suicideprevention #testicularcancer #prostatecancer https://lnkd.in/dM9t7jXY
Jake Storer's Mo Space
uk.movember.com
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Today, we commemorate #DonateLife Blue and Green Day, a day dedicated to raising awareness about tissue and organ donation. As we reflect on this day, two crucial issues come to light regarding transplant care. First, it’s critical to acknowledge the pivotal role that caregivers play through every step of the process. Most living donations occur within families, increasing the likelihood of the donor becoming a caregiver to the recipient. Second, it's imperative to address the inequities families of color face to access the waitlist, find a suitable match, and navigate the donation process. Read NAC's Transplant Caregiving in the U.S Report to learn about how family caregivers are unrecognized, unprepared and under-resourced, and the urgent need to increase support services in the transplant system. https://lnkd.in/ePBVe8mv #BlueandGreenDay #TransplantCare
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