With over a decade of enjoying life with a new kidney, Rick never expected to need a second chance. But he’s determined to not let his search for another kidney transplant get him down. Read Rick’s story and how he inspires others living with kidney disease to never give up: https://ow.ly/XS2g50UatH6
DaVita Kidney Care’s Post
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Living with kidney disease isn’t easy, but it’s a journey shared by many. In a compelling exchange between KidneyTalk® host Lori Hartwell and Jennifer Cramer Miller, author of “Incurable Optimist: Living with Illness and Chronic Hope,” striking parallels emerge in their respective multiple kidney transplant experiences. So, grab a seat, relax, and tune in to their engaging discussion as they delve into the art of cultivating optimism, drawing insights from their expertise on the subject. https://ow.ly/THaU50Thty5
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Red blood cells in people living with #sicklecell disease are not very durable and break down faster than typical red blood cells, which live for about 120 days. The shortened lifespan of the red blood cells in sickle cell disease cause anemia meaning there are less working red blood cells carrying oxygen throughout the body. This causes chronic fatigue. These short-lived red blood cells cause anemia, meaning there are less working red blood cells carrying oxygen throughout the body. This as a result causes chronic fatigue.
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When you are living with chronic kidney disease or are a kidney transplant recipient, it's important to take extra care in the heat to maintain your fluid balance and protect your skin from the sun. Read our advice here https://lnkd.in/eAKf-6TZ #Heatwave #Summer
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TALK TO YOUR DOCTOR. GET YOUR KIDNEYS CHECKED. People of all races and backgrounds get kidney disease, but Black and Hispanic people are more likely to have diabetes and high blood pressure, the top two causes of kidney disease — and more likely to develop kidney failure. But kidney failure is often preventable. Talk to your doctor. Get your kidneys checked.
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If you or someone you know has liver disease, it's never too late to make healthy changes. You can help your liver heal by taking simple steps every day. Learn more at https://lnkd.in/gu868r88 #LiverHealth #LiverCancerAwareness #LiverFoundation
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Living with kidney disease isn’t easy, but it’s a journey shared by many. In a lively exchange between myself and Jennifer Cramer Miller, author of “Incurable Optimist: Living with Illness and Chronic Hope,” striking parallels emerge in our respective multiple kidney transplant experiences. So, grab a seat, relax, and tune in to this engaging discussion as we delve into the art of cultivating optimism, drawing insights from our expertise on the subject. https://ow.ly/A9bM50ThtBt
Believing in Possibilities - Renal Support Network
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October is Liver Awareness Month! It’s a time to shine a light on liver health and the importance of early detection and prevention. Educate yourself, get regular check-ups, and take steps toward a healthier lifestyle. Together, we can raise awareness and support those affected by liver disease. 🧡 #NationalLiverAwarenessMonth #LiverHealth
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National Kidney Foundation (NKF) guidelines recommend you start dialysis when your kidney function drops to 15 percent or less—or if you have severe symptoms caused by your kidney disease, like shortness of breath, fatigue, muscle cramps or nausea and vomiting. Your doctor will help you decide, based on lab tests that measure how much kidney function you have left and on your symptoms. (305) 621-8899 [email protected] http://fpdialysis.com/ #dialysis #miami #FirstPreventionDialysisCenter #kidneydisease #florida
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Peripheral artery disease is the progressive narrowing of the blood vessels. This is most often caused by atherosclerosis resulting in low blood flow to the legs which can cause muscle cramping after walking. Learn more about peripheral artery disease: https://bit.ly/3LBN2G9
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Aptly named, sickle cell disease causes red blood cells to take on a crescent shape, like a sickle. At the same time, the cells become hard and sticky, making it possible for them to block blood vessels and keep oxygen and nutrients from getting where they need to go. The results can include extreme pain, organ damage, heart problems, severe infections and even early death. #sicklecell #healthcare Read more: https://lnkd.in/g8ZPRtRt
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Kidney Watch advocates for ethical kidney care, organ donation, and equitable transplantation. We hold systems accountable, empower patients through education, and raise awareness to empower patients.
1wDaVita Kidney Care let’s talk about your post featuring someone waiting for a second transplant. Yes, second chances are incredible, but what about the thousands still waiting for theirs? Or the countless others, like me, holding out hope for a third or even fourth transplant? Where’s the recognition for them? Your post feels incomplete, cherry-picking one feel-good story while ignoring the broader reality of the transplant community. Do you realize how many of us felt unseen? How many patients felt excluded from the narrative? Instead of just sharing one story, why not use your platform to educate, advocate, and truly represent everyone on this journey? Where are the resources and information for those navigating the complex realities of multiple transplants? Social media is powerful, but you’re wasting its potential by being selective and subjective. You missed the chance to raise awareness for the real challenges facing patients waiting for a second, third, or fourth transplant. DaVita, do better. Represent the full picture. Empower the entire community. Because we deserve more than feel-good moments—we deserve accountability, advocacy, and truth.