Today is World Scleroderma Day which highlights the need to increase awareness of scleroderma and to advocate for those affected by this life-threatening disease. It's a day to recognize the bravery of those who live with scleroderma, and to demand equal treatment and equal care. Learn more here: https://hubs.li/Q02D2Jt20
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What does 50 years of impact look like for those affected by Crohn’s disease and ulcerative colitis? It’s Crohn’s and Colitis Canada’s 50th anniversary! Learn more about the difference we’ve made – together: bit.ly/50yearsimpact
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No one should have to stop their treatment due to cost—but for many with psoriatic disease, this is the harsh reality. The time to act is now. The psoriatic disease community needs better care and resources today. Your gift can make an immediate difference, breaking down barriers and ensuring that millions can treat their disease without delay. on #InternationalDayofCharity give the gift of hope: https://ow.ly/ZRui50T3nZz
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The preparation of a UVB home phototherapy device represents a prudent approach to mitigating treatment costs for individuals affected by psoriasis. #psoriasis #Skincurex #UVBtherapy
No one should have to stop their treatment due to cost—but for many with psoriatic disease, this is the harsh reality. The time to act is now. The psoriatic disease community needs better care and resources today. Your gift can make an immediate difference, breaking down barriers and ensuring that millions can treat their disease without delay. on #InternationalDayofCharity give the gift of hope: https://ow.ly/ZRui50T3nZz
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Today on #RareDiseaseDay, we raise awareness for the nearly 30 million people in the United States living with a rare disease, along with their families and caretakers who make up the rare disease community. At HealthDyne, we know the importance of supporting patients with life-changing medications to combat the complexity of rare diseases. #RareDiseases #CareAboutRare #showyourstripes
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May is ALS Awareness Month! 🎗️ It's a time when we strive to shed light on this rare yet devastating disease, known as Lou Gehrig's disease. Let's use this time to raise awareness, advocate for research 🧪and support those living with ALS. 🤝#FightALS #CureALS #ALSAwarenessMonth #VisitingAngels
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Never lose hope! You're not crazy—it's not in your head. After 27 years of undiagnosed Lyme, I became a practitioner who can help you find answers and healing. Don't give up; the solution may be just around the corner.
🌿 How do you talk to yourself? Sometimes, the fight is invisible. May is Lyme Disease Awareness Month, and it's time to shed light on the silent struggles many face every day. Those affected by Lyme disease might not show it outwardly, but are fighting hard internally. 🍃 Go to my website. The link is in my bio to learn more💚 #LymeDiseaseAwareness #InvisibleIllness #FightLyme #LymeWarrior #TickTalk #HealthAwareness #SpreadAwareness #LymeSupport #TickPrevention #thelymeboss #thereishope #youarenotalone
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April 11 is World Parkinson’s Day; a day to raise awareness for this debilitating disease and share resources to help those affected. It’s no easy thing to live with this disease, nor to watch a loved one go through it. However, there are resources available to learn more about Parkinson’s and to assist with the care and treatment of those who live with it. Read our Beginner’s Guide as one such resource: https://brnw.ch/21wIHJO #ParkinsonsDisease #ParkinsonsAwareness #WorldParkinsonsDay #ResourcesforParkinsons
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Demand Generation Manager at UBEO Business Services | Business Technology Assessment | Digital Document Solutions | Study- Based Organization | Application and Workflow Driven Solutions
A topic near/dear to my heart! Take a moment to read more about how you can help and on #rarediseaseday
"Having any disease can be frightening but having a rare disease is not only traumatic and scary, but also isolating. You can feel as if no one in the world would ever understand what you might be going through. For better awareness, more accessible support, and better treatments, we must all play our role and lift up these communities so they may also be in the light and know that they are cared for and that they matter." - Lisa Butler, Executive Director To read more visit: https://lnkd.in/ege43xHv
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As medical students, we are taught to keep a "rare disease" diagnosis at the bottom of the list of differentials. During my professional journey as a Clinical Geneticist, I have realised that the adjective "Rare" restricts due attention from healthcare providers, researchers, and policymakers. Awareness, support, and sensitivity on these fronts will definitely bring hope in the lives of millions of individuals affected with #raredisease worldwide. Bringing comprehensive care for #raredisease under one roof @ Yashoda Hospital & Research Centre, Nehru Nagar, Ghaziabad, Genestring Lab, Seeds of Innocens IVF & Fertility Centres #rarediseaseawareness #rarediseaseday2024
On this Rare Disease Day, we are raising awareness among the people and committed to provide quality care to our patients and help the families to navigate the disease complexities and problems. #rarediseaseday2024
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👋 “Hi, I'm Simoni, and I have type 3 von Willebrand disease (VWD), the most severe and rarest form of the disease.” 👧 Simoni tells her personal story of growing up with type 3 (severe) VWD - the challenges of injuries and periods and learning to manage her own prophylaxis treatment. 👉 https://lnkd.in/gFhEPpv7 #BDAM24
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