Spread the word! May is Celiac Disease Awareness Month, the perfect time to join up with the Celiac Disease Foundation in generating support for research for treatments and a cure. Raise or donate any time before May 31st and you'll receive King Arthur Baking gluten-free products! Check out the chart to see what you can get for your donation. https://bakewith.us/cdf
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Psoriatic arthritis isn’t just a disease – it’s a daily battle for millions like Dedra. But with your help, we can change that. NPF is leading the charge in research for psoriatic disease, funding breakthrough projects that bring hope to those in need. Dedra’s journey is proof that together, we can make a difference. Join us in the 2024 Spring Match Challenge. Your donation will be matched dollar for dollar, up to $50,000, doubling its impact! Let’s rewrite the story of psoriatic disease. Donate now and be a part of Dedra's journey towards a brighter future! https://ow.ly/NoaU50RvbNx
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Did you know that 32% of parents of children under 18 mistakenly believe that it’s fine for a child with celiac to eat gluten at special events if it only happens occasionally? 🤔 Misinformation is scary, and for those with autoimmune diseases, it can be dangerous. We’re correcting Americans’ misinformation about celiac disease that was uncovered in the 2024 Beyond Celiac/Harris Poll survey. ✅ We know that one day, we’ll have treatments and a cure! But we need your help to get there. Every dollar counts—celebrate our summer of science and make your donation today at https://hubs.li/Q02BzC560 ☀️ #celiac #celiacdisease #autoimmune #autoimmunedisease #gluten #glutenfree #glutenfreeliving #chronicillness #celiacresearch #celiacawareness
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Today is World Thalassemia Day, a significant occasion to raise awareness about this genetic blood disorder characterized by abnormal hemoglobin production. Let's support individuals living with thalassemia and emphasize the critical need for regular blood donations to aid in their treatment. Your donation can make a life-changing difference. #WorldThalassemiaDay #BloodDonation #SupportThalassemia #DigiTrendshealthcare #DigiTrends
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KNOW YOUR GENOTYPE! Genotype testing for sickle cell disease (SCD) is vital for identifying carriers and individuals with the disease, allowing Sickle Cell Warriors to learn their risk of passing on and plan for healthier kids. Knowing your genotype can also ultimately help to "Reduce the cycle of pain." Take control of your health today! Our endgame is to reduce the death rate of children below the age of 5 living with sickle cell disease form 75% to less than 10% by 2025. Our goal is to raise 30,000,000 NGN to provide essential nutrients for 2,000 children with Sickle Cell Disease (SCD). To contribute in dollars, kindly click this link: https://lnkd.in/di4F8mff For Naira donations: Account Name: Brain and Body Foundation Account Number: 0178810529 Bank: GTBank For more information about our work, please visit: https://lnkd.in/dpQpsgC
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Today is World Lupus Day! As you put on purple to support the over 50,000 North Carolinians living with lupus, please consider donating to spread awareness of this cruel disease. Your donation of $25 or more will help us provide research to ultimately find a cure, educational opportunities for those living with lupus, and spread awareness. As a nonprofit organization, the Lupus Foundation of America, North Carolina Chapter relies on the generosity of our community to support those living with lupus by: • Developing safer and more effective treatments for the multiple symptoms of lupus. • Giving those affected by lupus access to educational programs that include pertinent medical, emotional and wellness topics, many led by medical experts. • Providing access to the Lupus Foundation of America, North Carolina Chapter emergency funds for people living with lupus. Because lupus is a complex disease, it affects people's daily lives. Many cannot work and require assistance with paying for things such as durable medical equipment, utilities, housing, medications, and transportation. • Providing those living with lupus access to medical professionals specializing in lupus. We really appreciate your support and rallying with us on this important day! DONATE HERE https://ow.ly/qrWb50RfQfw
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This Giving Tuesday Support the Fatty Liver Alliance – Just $18 Makes a Difference! This Giving Tuesday, we're reaching out to our global community to support the vital work of the Fatty Liver Alliance. With just an $18 donation, you can make a significant impact in the lives of those affected by fatty liver disease. Our mission is to empower patients through community education events and scientific summits, providing Primary Care professionals with the latest data on fatty liver disease. This ensures the highest standard of care for patients and their families. We're at the forefront of sharing new clinical study insights on MASLD and MASH, advocating tirelessly for patient access to essential liver health assessments. Our voice is heard not only on social media but also at international conferences, amplifying the needs and challenges faced by those with liver disease. Your donation of $18 will help us: * Host more educational events * Support ongoing liver disease research * Enhance our outreach to ensure information reaches those who need it most Together, we can make a difference. Your support allows us to continue our work, expanding our reach and impact in the fight against fatty liver disease. Please consider donating $18 today. Your contribution is more than a donation; it's a lifeline to those in need of knowledge, care, and support. Tax receipts provided for donations of $18.00 or more. https://lnkd.in/gKJuDTKt #GivingTuesday #FattyLiverAlliance #LiverHealth #CommunitySupport #ResearchMatters #MakeADifference
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These remarkable kids, with their unparalleled zest for life, remind us of the beauty in diversity and resilience. If you've had the pleasure of meeting Aidan, you'll know first-hand what I mean! ✨ Support KSF's ground-breaking research and help turn the possibility of therapeutic treatment into reality: https://bit.ly/3SXHkl4
Commemorate this special Leap + Rare Disease Day by making a donation in support of life-changing treatments. We are relentlessly pursuing brighter futures by following our strategic, 2-year, $3.5M plan - LEAP! LEAP is the roadmap to treatments for Kabuki syndrome. This rare disease has no cure nor specific treatments, but we are an active, bold, joyful community fueled by science that shows Kabuki syndrome can be treated! LEAP with us and donate today: https://lnkd.in/gH2wj4Bx
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Donor safety is key to ensuring a regular plasma donation regimen. Learn more about donor health and safety priorities >> https://lnkd.in/dBAEpHWQ
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🌟 Making Waves of Change: Supporting the Cystic Fibrosis Foundation! 🌟 As part of my selection into the 2024 class of Nashville’s Top 30 Under 30, I am excited to partner with the Cystic Fibrosis Foundation to raise crucial funds for research, advocacy, and support programs for individuals battling cystic fibrosis (CF). Cystic fibrosis is a genetic disease that affects the lungs and digestive system, posing significant challenges to those living with it and their families. But with your help, we can make a tangible difference in their lives. Here's how you can get involved: 1. Donate: Your contribution, no matter the amount, directly impacts the lives of those affected by CF. Every dollar raised brings us closer to breakthroughs in treatment and ultimately, a cure. Please consider donating to the cause via the link below. 2. Learn More: There are a number of helpful resources available to learn more about cystic fibrosis, including cff.org, which has a vast library of guides, articles, etc. 3. Spread Awareness: Share this post with your network to raise awareness about cystic fibrosis and the critical work being done by the Cystic Fibrosis Foundation. Together, we can educate others and inspire action. Thank you all for your support and commitment to making a difference!
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**6 miles in 6 days to Help End Lupus!** Join me and support the mission of the Lupus Foundation of America! My goal is to complete 6 miles in 6 days and raise critical funds for the estimated 1.5 million people living with lupus in the United States. Your donation will help me reach my personal fundraising goal and support the Foundation's efforts to improve the quality of life for all people affected by lupus! **Did you know?** - Lupus is a complex disease that is hard to define. It strikes without warning, affects each person differently, and has no known causes or cure. - While lupus mainly affects women between the ages of 15-44, men and children are not spared. - Lupus symptoms can be severe and highly unpredictable and can damage any organ or tissue, from the skin or joints to the heart or kidneys. - Only three drugs have been developed and approved by the US Food and Drug Administration specifically to treat lupus. Let's end this cycle now! By donating today, you are joining the fight against lupus! #LupusAwareness #EndLupus #LupusWarrior #SupportLupusResearch #LupusFoundation #AutoimmuneDisease #FightLupus #LupusWarrior #6Miles6Days #DonateForACause #RaiseAwareness #TogetherWeFight #HopeForLupus #LupusStrong #OnEpiphanyLane #OntheJourney
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