Cherished Mom’s Post

🎗𝗬𝗼𝘂 can help strengthen the resiliency of patients like Yazmine, their siblings, and caregivers through healthy coping strategies. Your donation of $𝟮𝟱𝟬 or more 𝗽𝗮𝘆𝘀 𝗳𝗼𝗿 𝗮 𝗺𝗼𝗻𝘁𝗵 𝗼𝗳 𝗰𝗼𝘂𝗻𝘀𝗲𝗹𝗶𝗻𝗴, 𝗴𝗶𝘃𝗶𝗻𝗴 𝗳𝗮𝗺𝗶𝗹𝗶𝗲𝘀 𝘁𝗵𝗲 𝗲𝗺𝗼𝘁𝗶𝗼𝗻𝗮𝗹 𝘀𝘂𝗽𝗽𝗼𝗿𝘁 𝘁𝗵𝗲𝘆 𝗻𝗲𝗲𝗱.   𝗣𝗹𝗲𝗮𝘀𝗲 𝗗𝗼𝗻𝗮𝘁𝗲 𝗮𝘁: https://lnkd.in/dUHfSRWf 🎗   #Keatons | #ChildCancerAwareness | #BigDayofGiving | #childcancer | #ChildCancerSupport | #MakeADifference 

If you would like to support Franky and Epilepsy Action, please visit the ‘Just Giving’ page here: https://lnkd.in/e-AnrAc5 We're incredibly proud of our team member Franky Wooders who is taking on an extraordinary challenge for our company charity of the year, Epilepsy Action. Starting January 1st, 2025, he will be running 10KM EVERY DAY in January while carrying a 22lb weighted vest - that's an incredible 310KM total! This showcase of dedication, discipline, and mental strength. Why Epilepsy Action? Because epilepsy affects 1 in 100 people in the UK yet remains widely misunderstood. It's an unpredictable and potentially life-changing condition. Join us in supporting Franky's journey and help create a better world for those affected by epilepsy. Together, we can make a difference. 💪 #310km #EpilepsyAwareness #CorporateSocialResponsibility #RelianceHighTech #EpilepsyAction #Charity

🎗𝗬𝗼𝘂 can help strengthen the resiliency of patients like Yazmine, their siblings, and caregivers through healthy coping strategies. Your donation of $𝟮𝟱𝟬 or more 𝗽𝗮𝘆𝘀 𝗳𝗼𝗿 𝗮 𝗺𝗼𝗻𝘁𝗵 𝗼𝗳 𝗰𝗼𝘂𝗻𝘀𝗲𝗹𝗶𝗻𝗴, 𝗴𝗶𝘃𝗶𝗻𝗴 𝗳𝗮𝗺𝗶𝗹𝗶𝗲𝘀 𝘁𝗵𝗲 𝗲𝗺𝗼𝘁𝗶𝗼𝗻𝗮𝗹 𝘀𝘂𝗽𝗽𝗼𝗿𝘁 𝘁𝗵𝗲𝘆 𝗻𝗲𝗲𝗱. 𝗣𝗹𝗲𝗮𝘀𝗲 𝗗𝗼𝗻𝗮𝘁𝗲 𝗮𝘁: https://lnkd.in/g-q7guai 🎗 #Keatons | #ChildCancerAwareness | #BigDayofGiving | #childcancer | #ChildCancerSupport | #MakeADifference

🌟 Announcing Willow Rebloom: A Groundbreaking Solution for Maternal Mental Health 🌟 We are proud to share our mission at Willow Rebloom: establishing the first-ever Mother-Baby Unit (MBU) in the United States, right here in Arizona. This specialized inpatient facility will provide life-changing care for mothers experiencing severe perinatal mood and anxiety disorders (PMADs) — without separating them from their babies. 🤝 Why Willow Rebloom Matters: Maternal mental health is the leading cause of pregnancy-related deaths in Arizona. Up to 1 in 5 women experience PMADs, yet too many go undiagnosed and untreated. Currently, there are no dedicated perinatal psychiatric facilities in the U.S. that allow mothers and babies to stay together during treatment. Willow Rebloom is here to change that. With your support, we can create a compassionate, secure environment where mothers and their babies heal together. 💡 How You Can Help: Your donation helps us open and sustain this vital facility, ensuring mothers get the care they need while strengthening the bond with their babies. 👉 Click here to donate: https://lnkd.in/gWVcPxv8 Every contribution brings us closer to building a future where no mother faces a mental health crisis alone. Together, we can transform maternal mental health care in the U.S. 💙 #MaternalMentalHealth #PerinatalCare #PMADs #WillowRebloom #MotherBabyUnit #Nonprofit #DonateNow

Over 1️⃣ in 3️⃣ people are affected by neurological conditions, the leading cause of illnesses and disability worldwide*. In 2021 a study by The Lancet Neurology stated there were more than 3️⃣ billion people worldwide living with a neurological condition. In the UK alone, 1️⃣ in 6️⃣ people are affected by neurological disorders, meaning access to neuro-rehabilitation, early intervention and care and support has never been more vital than it is today. At The Rainbow Centre for Conductive Education, we provide a specialist neuro-rehabilitation called Conductive Education for those affected by neurological conditions. We work tirelessly to enable greater independence and quality of life for children and adults and to provide the support and care that they and their families so desperately need. As a Charity, we strive to provide our vital service with no government or statutory funding - our doors remain open purely down to the generosity of voluntary donations. More than ever, we need your support to help us to continue to deliver our life altering service. Together, we can make a measured impact in enabling a positive and fulfilling life for those affected by these conditions. If you can, donate today here ⬇️ https://lnkd.in/euDxnac5 #neurologicalsdisorders #neurorehabilitation #stroke #parkinsons #cerebralpalsy #multiplesclerosis #charity *World Health Organisation

🌟 Urgent Help Needed: Support Cory Lewis & His Family 🌟 Cory Lewis is a devoted stepfather and full-time caregiver for his mother, who is battling a debilitating brain disorder and bone cancer. Life’s challenges have left him in desperate need of our support. 💔 What’s Happening: Cory had to leave his job to care for his mom. He’s struggling to cover rent, medical bills, and daily expenses. His family urgently needs help to stay afloat. 💡 How Your Support Helps: ✅ Covers life-saving medical treatments. ✅ Provides housing stability. ✅ Funds essential living expenses. 🎯 Goal: $100,000 Every contribution, big or small, makes a huge difference. 🔗 Act Now: 💵 Donate today: http://spot.fund/2x86tzsc 🔄 Share this story with your network to spread the word! Together, we can give Cory and his family hope. Your kindness can create a lasting impact. 🙏 http://spot.fund/2x86tzsc

Struggling to make sense of hypermobility terminology? You’re not alone! With acronyms like EDS, HSD, and even pediatric generalised hypermobility spectrum disorder, it can feel like a bowl of alphabet soup In her Alphabet Soup blog, founder Jane Green MBE FCCT breaks down how these terms cause confusion—not just for individuals, but also for researchers, funders and charities. As a charity, we use Hypermobility as an umbrella term to keep things simple, but understanding the terminology is still important. Read more in Jane’s May 29th blog post: https://lnkd.in/eYPiAV7h... #Hypermobility #AlphabetSoup #EDS #HSD #hEDS #JH #pGJH #pgHSD #vEDS #cEDS #GJH #Neurodivergence #Pain #School #POTS #autism #brainBody #connective #BJHS

*Urgent Help Needed: Save a 2-Year-Old's Life!* I'm reaching out to my LinkedIn community with a heart-wrenching plea for help. A 2-year-old child is suffering from Spinal Muscular Atrophy Type-2 (SMA2), a rare genetic disorder. The only life-saving treatment is an injection called ONASEMNOGENE ABEPARVOBEC (XOLGENSMA), but it comes with a staggering price tag of ₹9.5 crores and is only available in the US. Time is of the essence! We need your support to raise funds for this life-saving treatment. Every contribution, big or small, counts. Let's come together to make a difference in this child's life. *Please donate generously:* *Share this post with your network:* Let's spread the word and help this child receive the treatment they deserve. Together, we can make a difference! *#SMA2 #XOLGENSMA #SaveALife #DonationAppeal #RareDisease #MedicalHelp #CommunitySupport*

Transforming SCN8A: Meet Brindle “Just because my child doesn’t have epilepsy doesn’t mean he isn’t affected. He struggles with delays, muscle issues, and so much more.” – Brindle’s mom, Rachel Brindle’s story reminds us that SCN8A’s impact reaches far beyond seizures. Every day brings new challenges, but with your support, we can provide the research and resources families like Brindle’s desperately need. Together, we can make a difference. 💜 Donate today to help children like Brindle: 👉 https://lnkd.in/gpJdVU7U #scn8a #scn8aawareness #scn8astrong #thisisscn8a #curescn8a #scn8aresearch #scn8aalliance #scn8aepilepsy #scn8asuperhero #scn8afamily #scn8aresearchroadmap #scn8afact #scn8adiversity #scn8astories