HCLTech – Romania’s Post

Sickle Cell Awareness Day: Together We Can Make a Difference 🎗️ Today, we at Shinon Healthcare join the global community in raising awareness for Sickle Cell Disease (SCD). This inherited blood disorder affects millions, causing severe pain, fatigue, and other serious health complications. How You Can Help: •Educate: Increase your understanding of SCD and spread the word. •Support: Donate to research organizations working towards better treatments and a cure. •Get Involved: Engage in community events and online campaigns to show your support. By coming together, we can improve the lives of those living with SCD and push for advancements in research and care. Let's stand united in our efforts to bring hope and support to the Sickle Cell community. #SickleCellAwareness #ShinonHealthcare #SickleCellDisease #HealthcareAdvocacy #HopeForACure #SickleCellWarriors #ShinonHealthcare #ShinonGlobal #bridgeofhope #committedtoexcellence #trustedpartner

Reading this article is more than worth the effort - it also includes audio option Warm Regards Steve Ps Michael is living proof that an approach that dismantles the diagnosis, also dismantles the power that cancer has over you! #beatingcancer #EmpoweredPatient #Cholangiocarcinoma#Cholangio#CholangioChallenger#CholangioInspiration#BileDuctCancer#CholangiocarcinomaAustralia#CholangiocarcinomaAwareness#LightAustraliaGreen

Throughout this month, Next Generation Initiative will be spreading awareness about sickle Cell, the disease, warriors and everything in between. Be sure to follow them and you will definitely learn a thing or two

September is Sickle Cell Awareness Month! As we raise awareness, let's take a moment to acknowledge the resilience and strength of individuals living with sickle cell disease around the world. At Save the Sicklers, we’re dedicated to advancing solutions that improve the quality of life for those impacted by this condition. Through projects like ThermoSoothe™, we're working to provide innovative ways to manage painful crises and empower individuals with sickle cell disease to live healthier, fuller lives. But this fight requires all of us. Whether through advocacy, education, or simply lending a supportive hand, you can make a difference in the lives of those affected. Join us in spreading awareness and fostering hope. Together, we can build a future where the challenges of sickle cell disease are better understood, and innovative solutions lead the way for positive change. #SickleCellAwarenessMonth #SaveTheSicklers

💡 Did you know that a quarter of the world’s population lives with #NCDs including heart disease, high blood pressure, diabetes, cancer, and dementia? Yet, #NCDs are the most underfunded global health issue.   That’s why during this Global Week for Action on NCDs, Panorama Strategy is excited to promote a new funding opportunity from The Type 1 Diabetes Community Fund. Eligible community-based organizations supporting people living with type 1 #diabetes in low- and middle-income countries are invited to apply for grant funding to support their critical programming.   Our team is proud to lead capacity-strengthening efforts for The Type 1 Diabetes (T1D) Community Fund. We encourage all to share this opportunity with your networks and make sure funding reaches more community-based organizations supporting people living with this complex chronic disease.   The application is open now until December 9, 2024. Learn more and apply: https://bit.ly/4esd6jN   We stand together with everyone around the world living with #NCDs. #ActOnNCDs this Global Week for Action on NCDs!   NCD Alliance Panorama Global   #LeadOnNCDs

Huntington’s disease (HD) runs deep in families for generations. My family has been and is affected with grandparents, fathers, mothers aunties, uncles, nephews who have or had HD. It is a disease of the brain that is passed down from parent to child. HD is not evident at birth and symptoms will usually not appear until a person is between 35 and 55 years of age. From the onset of symptoms, people with HD have a life expectancy of 10 to 25 years. There is currently no cure for HD but treatments that can help ease certain symptoms are available. As a genetically acquired disease, you are only at risk of developing the disease if one or both of your parents also has the disease. You cannot “catch” Huntington’s disease and it cannot skip a generation. This means many people like me can have many family members with HD within each generation. If you want find out more about HD check out HD Australia and help raise awareness or even run a fund-raising event check out hd Australia's social media🫶🏽

May is National ALS Awareness Month, a time dedicated to raising awareness about this disease and the people affected by it. ALS is a neurodegenerative disease that affects nerve cells in the brain and spinal cord, gradually leading to the loss of muscle control and function. It affects people of all ages and backgrounds, and its impact reverberates not only through the lives of patients but also their families, friends, and caregivers. Here are a few ways to contribute during ALS Awareness Month: 1. Share informative posts, articles, and resources about ALS on your social media channels. 2. Engage with organizations and institutions working to find a cure for ALS. Consider making a donation or volunteering your time to help fund scientific studies and clinical trials aimed at better understanding the disease and developing effective treatments. 3. Participate in online events organized by ALS associations, advocacy groups, and research organizations. Webinars, panel discussions, and fundraisers provide opportunities to learn, share experiences, and contribute to the cause. #ALSAwarenessMonth #ALS #LouGehrigsDisease #Community #Advocacy #Research #Support

Over 400 million people around the world are affected by rare diseases. Approximately half are undiagnosed, and receiving a diagnosis takes an average of five years. (Submit your Solution) NGOs and nonprofits have an important role to play in improving the experience and wellbeing of patients with rare diseases. How can nonprofits use innovation to improve the journey for patients with rare diseases, from diagnosis to treatment and holistic care? (Submit your Solution) https://lnkd.in/dqNJQ3Wc

Welcome to September! A month dedicated to awareness, advocacy, and action! September is here, and it's a month full of important causes and awareness events! This September is the National Spinal Cord Injury Awareness Month and the National Childhood Cancer Awareness Month. These are powerful reminders of the challenges faced by those living with spinal cord injuries (SCI) and childhood cancer, as well as the importance of supporting ongoing research and innovation to improve lives. We at Diverse Health Initiative will be raising awareness about key health and social issues this month. Every year, thousands of lives are impacted by SCI, leading to significant physical, emotional, and financial challenges. Similarly, childhood cancer affects many young lives and families, emphasising the need for continued research and support. At Diverse Health Initiative, we believe in the power of community, awareness, and research to drive change. Here’s how you can help: - Share this post to spread awareness about SCI and childhood cancer. - Engage with us by following our updates throughout September on key world events that matter. - Support research initiatives to improve treatments, rehabilitation, and care for those affected. But that’s not all! This month is packed with important global observances that promote health, safety, and human rights. Stay tuned and follow us for valuable insights and updates on each of these days: September Awareness Days: Sept 4: World Sexual Health Day Sept 5: International Day of Charity Sept 8: International Literacy Day Sept 10: World Suicide Prevention Day Sept 12: World First Aid Day Sept 15: World Lymphoma Awareness Day Sept 15: International Day of Democracy Sept 16: International Day for the Preservation of the Ozone Layer Sept 17: World Patient Safety Day Sept 18: International Equal Pay Day Sept 21: World Alzheimer's Day & International Day of Peace Sept 22: World Rheumatic Disease Day Sept 23: International Day of Sign Languages Sept 25: World Dream Day Sept 28: World Rabies Day Sept 29: World Heart Day Join us in spreading awareness, supporting research, and advocating for change! Follow us across our social media platforms for more updates, resources, and ways to get involved. Let’s make a difference together! Contact us at +2348066690096. #DiverseHealthInitiative #SCIAwarenessMonth #ChildhoodCancerAwareness #SupportSCI #SupportChildhoodCancerResearch #HealthForAll #InclusionMatters #ResearchForChange #SeptemberAwareness

📢 Raising Awareness for The Fight Against ALS (Maladie de Charcot) Imagine losing control over the simplest movements: lifting a cup, tying your shoes, or even breathing. This is the harsh reality faced by individuals with Amyotrophic Lateral Sclerosis (ALS), also known as Maladie de Charcot. This rare neurodegenerative disease progressively destroys motor neurons, paralyzing the body while leaving the mind fully intact. For many, life expectancy after diagnosis is tragically short—only 3 to 5 years. Yet, amidst this struggle, there is a call for hope and support. While there is no cure for ALS today, treatments like riluzole can slow its progression, and multidisciplinary care helps patients retain some independence. However, the battle against ALS extends beyond medical treatments—it requires collective action: Awareness: Educating others about ALS helps foster understanding and compassion. Research: Advancements depend on continued funding and scientific innovation. Support: Standing beside those affected—patients and their families—eases their burden. Let’s join hands to spread awareness, encourage research, and support the ALS community. Together, we can make a difference. #charcot #als #illness