Warriors and advocates, like Charlotte Curtis, are working to fight misinformation and educate about the impact of #sicklecelldisease. By uplifting voices in the community who are dedicated to improving care and reducing stigma, we can help make meaningful change for people living with sickle cell disease and their families. This #WorldSickleCellDay, challenge yourself to learn more about the sickle cell community and the importance of supporting the diverse experiences of people living with sickle cell.
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Today is World Parkinson's Day, a day dedicated to raising awareness and supporting those affected by Parkinson's disease. Today is also about celebrating the strength, perseverance, and resilience of those living with this condition. #worldparkinsonsday #parkinsonsawareness #parkinsons #movementdisorder #parkinsonsdisease #wpd #worldparkinsonsdiseaseday #parkinsonsuk #wpd2024 #parkinsonsdiseaseday
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Did you know that ALS, also known as amyotrophic lateral sclerosis, affects nearly 30,000 people in the US alone? Let's unite to raise awareness for this disease and support those bravely fighting it. #ALS #ALSAwareness #ALSAwarenessMonth
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Today is #GlobalALSAwarenessDay. 🌎 ALS doesn't just affect individuals; it impacts entire families. After Lou Gehrig's ALS diagnosis in 1939, there is still no cure for this horrible disease. Live Like Lou is committed to leaving ALS better than we found it by supporting families affected by ALS, funding ALS research to find treatments or cures for Lou Gehrig's disease, and honoring Lou Gehrig's legacy. Learn more on how you can help make a difference: https://lnkd.in/g9PR5C4B #livelikelou #als #alsawareness
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Psoriatic disease doesn't just affect the person living with it, but also the family. This year we celebrate the importance of the family, and bring awareness to the disease's impact on their everyday life and well-being. Together we can fight and end stigma! 💪💜 For more information, click here - https://lnkd.in/d5vDCjTt #psoriaticfamily #familywellbeing #psoriaticdisease #family #psoriaticawareness #psoriaiscommunity #psoriasissupport #psoriasislife #familyimpact #psoriasis
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Did you know March Is Multiple Sclerosis Education and Awareness Month? Educating ourselves and others about this chronic disease can make a significant impact on those living with it. Join us in spreading knowledge and support for #MSAwarenessMonth! #MultipleSclerosisEducationAwareness #MSWarrior #ShareYourStory #SupportMSResearch #EndMS #FindACure
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Today we spotlight on the strength and courage of those facing rare diseases. Every individual impacted by a rare condition has their own unique journey, yet together, form a powerful community united by hope and determination. On this Rare Disease Day, we raise awareness about the challenges faced by patients and their caregivers, advocates, and families. It is a day to celebrate victories, big and small. We acknowledge the ongoing efforts in the pursuit of better treatments and cures. By continuing to spread awareness, we have the power to foster compassion, inspire reach, and drive tangible change. #RareDiseaseDay2024 #RareDiseaseAwareness #HopeForACure #RareDiseaseCommunity #Duchenne #DuchenneMuscularDystrophy #DuchenneAwareness #MuscularDystrophy #CureDuchenne #RareDiseaseCommunity #Mdawareness
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March is Multiple Sclerosis Awareness Month, a time to learn more about this debilitating disease and what you can do to help patients with treatments and improving their quality of life as we search for a cure. Read more about MS and how you can participate in raising awareness here --> https://hubs.li/Q02n2gf50 #multiplesclerosis #msawareness #chronicillness #multiplesclerosisawareness
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Are you ready to express your BIG movements and LOUD voice during the month of April for PD awareness? This April, organizations around the world join forces in raising awareness for those living with Parkinson’s Disease (PD). Learn how you can get involved: https://hubs.ly/Q02r-qJh0 #parkinsonsawareness
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Calling on all scleroderma advocates! February marks not just #RareDiseaseAwarenessMonth but also #RaynaudsAwarenessMonth. 📣 Let's work together to raise awareness about Raynaud's phenomenon and its impact on those with scleroderma. Did you know that nearly 90% of people with this disease also live with Raynaud's as a complication? Share your stories—what Raynaud's means to you, how you navigate a flare-up, or the daily impact on your life—or share the facts of Raynaud's, like its signs and symptoms. Use #RaynaudsAwareness and #SayScleroderma. We want everyone to understand what scleroderma is and does & the urgent need for research—and understanding Raynaud's is an important part of that. Looking for info to share? Visit https://lnkd.in/gmprDt8a today. When you speak up about this disease and its complications, you make a real difference in the lives of those with #scleroderma. #sclerodermaawareness #srfcure #sclerodermaresearch
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⚡ #ParkinsonsAwarenessMonth is coming to an end, a month dedicated to raising awareness for Parkinson’s Disease (PD), the people affected by it, and treatment methods. PD affects more than 1.2 million people in Europe, but many misconceptions are still prevailing – here are some popular myths about PD: https://lnkd.in/dUT9AHgb #BSCEMEA #DeepBrainStimulation #DBS
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