Kidneylink’s Post

We’re proud to be helping advance early detection and intervention of retinal disease through our ability to look at a patient’s eye and assess how that translates to further disease risks. The entire process, from scanning the eyes to producing a personalized report with diagnosis and #AI-predictive analytics, takes 90 seconds. It’s because of this that we’re able to provide more accessible and affordable care. Read more as I discuss how we can make this technology scalable and what our plan to grow and scale in the US looks like, based on our proven success in Australia and Europe. https://lnkd.in/gTfMqC_g #optain #optainhealth #leadership #innovation

Today we recognize the nation’s first AMKD Awareness Day! People who are from or have ancestors from west or central Africa are at increased risk of having a mutation in one or both of the genes that causes APOL1-    mediated kidney disease (AMKD). It is estimated that 13% of Black Americans have two mutations of the APOL1 gene, and these individuals have a 1 in 5 chance of developing a rapidly progressing form of genetic kidney disease. Become #APOL1Aware by learning more about AMKD and join the American Kidney Fund in AMKD Awareness Day: kidneyfund.org/APOL1aware

The depth of emotions experienced by patients upon discovering they have a rare disease is indescribable. I have witnessed their world shatter upon receiving the news that there is no known cure for their condition. However, amidst the darkness, I have also had the privilege of witnessing the radiant spark of hope that ignites within them when a glimmer of possibility for recovery emerges. Rare Disease Day serves as a beacon of awareness, aiming to dismantle stigmas and champion improved healthcare and treatments for those navigating the complexities of rare diseases. Together, let us weave a tapestry of compassion and support, making a profound and uplifting impact on their lives. #RareDiseaseDay empowers individuals to #ShowYourRare, inspiring a brighter future for all. #innovation #management #HumanResources #digitalmarketing #technology #creativity #Future #futurism

Turning Setbacks into Progress for Rare Disease Families For many families, navigating the rare disease journey has been riddled with delays and disappointments. We are changing that narrative now. Transforming the rare disease treatment landscape, making it faster and more efficient while keeping all the data in the hands of the client and moving them towards better health is our focus. We understand the frustration of working with multiple organizations that can't seem to provide the solutions you need. That's where Everlum Bio steps in. We're laser-focused on accelerating rare disease research and guiding families like yours through the disrupting process. Our specialized expertise and technologies have given us the ability to uncover insights and multiple potential therapies much faster than traditional approaches you may have previously encountered. Don't let delays define your rare disease journey any longer. Partner with Everlum Bio and experience the difference our solutions can make. Contact us today to learn what we can provide in the breakthrough you've been searching for. #PrecisionMedicine #RareDiseaseResearch #PersonalizedMedicine #BiotechLeaders #EverlumBio

Health literacy and patient education empower individuals and families facing health challenges. Fostering understanding equips them with tools to navigate complexities, make informed decisions, adhere to treatments, and actively participate in well-being. This empowerment enhances care quality, instills control and resilience, fostering improved outcomes and the ability to cope with health challenges, irrespective of severity or duration. #healthliteracy #patienteducation #informeddecisions #rarediseaseawareness #empowerment #patientempowerment

February 29th is Rare Disease Day, a moment to shed light on the 300 million individuals worldwide battling rare diseases, alongside their dedicated families and caregivers. At CogenTech, we understand the critical importance of innovation in healthcare. We stand in solidarity with the rare disease community, leveraging our expertise to support the development of groundbreaking solutions that address unmet medical needs. In sharing this message, we reaffirm our commitment to our core values: empathy, empowerment, and collaboration. By raising awareness and fostering inclusivity, we strive to make a meaningful impact in the lives of those affected by rare diseases. Today, we salute the rare disease heroes: the individuals living with rare diseases, their families, healthcare professionals, policymakers, and industry representatives. Together, let us continue to champion innovation and collaboration to drive progress in the field of MedTech. #RareDiseaseDay #Community #Collaboration #MedTech #Innovation

Are your patients reflecting on their kidney disease journey? Their insights could be invaluable to others. Encourage your patients to make a difference by becoming a patient peer mentor. Explore resources at the ESRD NCC Kidney Hub: https://bit.ly/3RZYqzk #ESRD #Dialysis #Transplant #PeerMentoring

“Technology like ours is making care more accessible and affordable, and its portability will make it scalable.” Read more from Jeff Dunkel, CEO of Optain, as he discusses how the field of oculomics is the future of healthcare and where Optain plans to expand in the near future. #healthtech #AI #oculomics https://lnkd.in/g_f3xVb5.

Read Karen‘s story to better understand what it means living with pain associated to knee osteoarthritis

Green Minds has just completed a comprehensive study on Rare Disease Management in demanding landscapes like China and Japan. With the help of our top-notch experts, we have uncovered valuable insights that can drive healthcare advancements. Feel free to reach out if you want to leverage our experience or discuss collaborations. Together, let's conquer complexities and drive positive change! #RareDiseaseManagement #HealthcareInnovation #GreenMinds #ExpertiseInAction 🚀