Congenital Hyperinsulinism International’s Post

✨️ "We support the Sweetest Cause because it has given us a community of warriors and caregivers just like us around the world. We’ve become one family." - Kiersten, HI Mom ✨️ 💙 Why do YOU support the Sweetest Cause? Let us know in the comments 💬 below! 💙 📣 We need your help to support the #SweetestCause .... help us RAISE IT NOW for awareness, support, and research at https://bit.ly/chidonate #hyperinsulinism #raredisease #congenitalhyperinsulinism #hypoglycemia ⁠

Did you know that March is #MSAwarenessMonth? 🧡 Join us in raising awareness and supporting people living with Multiple Sclerosis. 🟧 Keep watching this space for updates and insights on how you can make a difference. Together, let's make MS visible and show our solidarity! 💪 #MSSocietyUAE #MultipleSclerosis #MSawareness #LivingwithMS #MSCommunityUAE

Not everyday you get to cosy up for a cause! Today Staffscanner we don on our PJs for work in raising awareness for dementia on "Wear Your Pyjamas to Work Day." Let's show support for those affected and spark conversations about this important issue. Together, we can make a difference! 💙 #PJsForACause #DementiaAwareness #feeltheforce

#BreakTheStigma 🤝 Today, we celebrate Vitiligo Awareness Day, highlighting the beauty of diversity and promoting understanding and support for those affected by this condition. 📢 Did You Know? Vitiligo is an #autoimmune disorder that affects about 1% of the world's population, yet misconceptions and stigma persist. Out of this, 25-30% of patients are children. By sharing the experiences of individuals with #vitiligo, we can foster a more compassionate society and encourage research towards better treatments and a potential cure. #WorldVitiligoDay #VitiligoAwarenessDay #SkinDiversity #InclusionMatters #GlobalHealth #DiversityInWellness #VitiligoVisibility

𝗝𝘂𝘃𝗲𝗻𝗶𝗹𝗲 𝗔𝗿𝘁𝗵𝗿𝗶𝘁𝗶𝘀 𝗔𝘄𝗮𝗿𝗲𝗻𝗲𝘀𝘀 𝗠𝗼𝗻𝘁𝗵 - 𝗝𝘂𝗹𝘆 🌟 𝗝𝘂𝗹𝘆 𝗶𝘀 𝗱𝗲𝗱𝗶𝗰𝗮𝘁𝗲𝗱 𝘁𝗼 𝗝𝘂𝘃𝗲𝗻𝗶𝗹𝗲 𝗔𝗿𝘁𝗵𝗿𝗶𝘁𝗶𝘀 𝗔𝘄𝗮𝗿𝗲𝗻𝗲𝘀𝘀 𝗠𝗼𝗻𝘁𝗵, a crucial time to support children battling arthritis. This month aims to raise awareness about the impact of juvenile arthritis on young lives and the importance of early intervention. Juvenile arthritis can affect not only joints but also other organs, leading to swelling, stiffness, and potential permanent damage if left untreated. Educating ourselves about this condition is key to ensuring timely detection and appropriate care for affected children. 𝗝𝗼𝗶𝗻 𝘁𝗵𝗲 𝗰𝗮𝘂𝘀𝗲 𝗯𝘆 𝗹𝗲𝗮𝗿𝗻𝗶𝗻𝗴 𝗺𝗼𝗿𝗲 𝗮𝗯𝗼𝘂𝘁 𝗷𝘂𝘃𝗲𝗻𝗶𝗹𝗲 𝗮𝗿𝘁𝗵𝗿𝗶𝘁𝗶𝘀, 𝘄𝗲𝗮𝗿𝗶𝗻𝗴 𝗮 𝗯𝗹𝘂𝗲 𝗿𝗶𝗯𝗯𝗼𝗻 to show solidarity, and actively engaging in community events to spread awareness and support those affected. Let's stand together this month to make a positive impact for children with juvenile arthritis. #JuvenileArthritisAwareness #SupportChildren #EarlyIntervention #SpreadAwareness #MakeADifference #ChildHealth #RaiseAwareness #CommunitySupport #HealthEducation #SCABPharmacy

Well done to those braving the cold waters to take a 'Dip for Diagnosis' on World MS Day today! Today is such an important day for raising awareness and supporting those affected by multiple sclerosis, so please do share or get involved if you can. https://www.ms-society.ie/ #msireland #dipfordiagnosis #inspirational

🌎️ Today is the International Day of Families 👩👦👨👩👧👦👨👨👧👩👩👦👨👧This day provides an opportunity to promote awareness of issues relating to families and to increase knowledge of the social, economic, and demographic processes affecting families. 📣 We’re raising awareness of hyperinsulinism with our CHI Fam – we know that living with HI affects families deeply – whether you are a caretaker, sibling, or diagnosed with HI yourself. 💙According to our HI Global Registry's Caregiver Quality of Life Survey, 1 in 5 HI caregivers feel they do not receive adequate support from family. 🔁Share this post and share something you’d like other families to know about hyperinsulinism. #hyperinsulinism #raredisease #congenitalhyperinsulinism #hypoglycemia | Hyperinsulinism | Congenital | HI | Hypoglycemia | Rare Disease

it takes a village....support is so needed on many levels

Empowering the Sickle Cell Community: The Warriors Project Initiative As a proud Sickle Cell Warrior, I understand firsthand the unique challenges that come with this journey. It’s not just about enduring physical pain; it’s about resilience, hope, and the pursuit of a full life. This is why I am thrilled to be part of the Warriors Project Initiative. The Warriors Project Initiative is more than just a cause; it is a mission dedicated to improving the lives of children living with sickle cell anemia. We aim to provide educational resources, health support, and emotional encouragement to empower these young warriors, ensuring they are not defined by their condition but by their potential. Our work is rooted in advocacy, raising awareness about sickle cell disease, and offering practical solutions to the challenges faced by warriors and their families. By fostering a supportive community, we ensure that these children feel seen, understood, and valued, helping them build confidence to chase their dreams. Through education and health initiatives, we create a brighter future for every warrior, breaking down barriers and rewriting the narrative surrounding sickle cell disease. Join me in supporting this cause, because together, we can make a difference in the lives of these warriors, one step at a time. #SickleCellAwareness #theWarriorsProject #EducationForAll #HealthcareAdvocacy #WarriorSpirit

In a heartwarming turn of events, the Parkinson’s community is celebrating a significant contribution to research and awareness, thanks to notable figures like Patrick Morrissey, who has openly shared his journey with Parkinson's Disease. As covered in a recent CNN article, his collaboration with the Michael J. Fox Foundation highlights the vital role of public figures in advancing the cause and uplifting the spirits of those affected. 🏅 Patrick Morrissey’s story is more than just a personal battle; it’s a beacon of hope for millions. 🔬 Research and Progress: The Michael J. Fox Foundation has been at the forefront of Parkinson’s research, striving to uncover new treatments and ultimately a cure. Stories like Morrissey’s help to galvanize public support and funding, which are crucial for accelerating research efforts. Seeing public figures confront Parkinson’s with such courage and openness serves as a powerful source of motivation for others dealing with the disease. It reassures people with Parkinson's and families that they are not alone in this fight and that their struggles are recognized on a global stage. Let’s use his story as a catalyst for more conversations and actions towards understanding and fighting Parkinson’s! 💬 Share Your Thoughts: How have public figures influenced your perception of Parkinson’s? Have their stories changed how you support or view the disease? Join the discussion and let us know how awareness can lead to better support and solutions for the PD community. #ParkinsonsAwareness #CelebrateAdvocacy #InspirationInAction #LightForPD #parkinsonsdisease #parkinsons #parkinsondisease #parkinsonsdiseaseawareness #parkinsonawareness #caregiver #goodnews