Cartesian’s COO Metin Kurtoglu recently attended the 2024 National Lupus Advocacy Summit held by the Lupus Foundation of America, Inc. The event highlighted the continued need for #lupus research and funding and we’re proud to support this important cause.
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Sales Account Executive at Howard Technology Solutions | Photographer | Advocacy Chair at The Lupus Foundation of America, SoCal Chapter.
If you have lupus or know someone with lupus. please consider becoming an advocate. Lupus advocacy helps raise awareness about the disease, fosters research for better treatments, and supports those affected by lupus. Additionally, advocacy efforts contribute to improved healthcare policies and increased funding for lupus research. Why I Advocate: For those we have lost. For those who are currently fighting. For those who have not yet been diagnosed. Lupus can affect various organs and systems in the body. Common areas of organ involvement include: Skin: Skin rashes, especially on the face (butterfly rash), and sensitivity to sunlight. Joints: Joint pain and arthritis are common lupus symptoms. Kidneys: Lupus nephritis can cause inflammation and damage to the kidneys. Heart: Lupus can affect the heart, leading to inflammation of the heart muscle or the membrane surrounding the heart. Lungs: Inflammation of the lungs can occur, causing chest pain and difficulty breathing. Brain and Central Nervous System: Lupus may cause headaches, seizures, and cognitive dysfunction. Blood: Lupus can affect blood cells, leading to anemia, leukopenia (low white blood cell count), or thrombocytopenia (low platelet count). The extent of organ involvement varies among individuals, and symptoms can range from mild to severe. Regular medical monitoring and proper management are crucial to address lupus-related complications. #slelupus #LupusAdvocacy #medicalresearch #autoimmunedisease #lupusreseach Lupus Foundation of America, Inc.
📅 Save the date for the 2024 National Lupus Advocacy Summit! We're hosting the nation's largest lupus advocacy event during Lupus Awareness Month in Washington, DC on May 19-21. 💜 Join lupus warriors from across the country as we turn Capitol Hill purple once again! Registration opens in January -- learn more here: https://bit.ly/3RB2VAq
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Hello CTAMFT Friends! Are you interested in one of the many ways in which CTAMFT Advocated for MFTs and the MH Community this session? Check out our website ctamft.org under Advocacy; Updates and you can see some of the testimonies submitted by CTAMFT Advocacy Chair, Jaime Rodriguez, this session. Here is a link! https://lnkd.in/e9mV4TWy #ctlegislation #testimony #ctamftadvocacy #ctamftadvocacymatters
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May is #LupusAwarenessMonth and we're throwing it back to sitting down with Adrienne Nicole, founder of The Lupie Fam, to talk about lupus advocacy & #clinicaltrials. Watch here: https://bit.ly/4bMqnlo #BlackHealthMatters
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https://lnkd.in/eF4uMUTP check out my latest blog post on homesteading and advocacy in Belize.
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Today is #Chromosome18Day and #InternationalDayOfPersonsWithDisabilities. Here's Sydney to explain more about her chromosome 18q- proximal deletion diagnosis journey, and how she now advocates for herself. You can follow Syndey's advocacy page on Instagram @disabilitiesunite21.
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I grow your community of Advocates. Advocacy educator. Advocacy expert. Host of the Voices In Advocacy® Podcast.
Know the steps and actions needed to reach your destination.
"The time to have a map - is before you leave on a journey." Roger Rickard, President & Fouunder, Voices in Advocacy
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Have you read the July HAEA Community Blog? This month’s HAEA Community Blog article focuses on HAEA Social Media Intern, Wessam, as he describes his journey to an HAE diagnosis as a young child, the challenges he has faced along the way, and how getting involved with advocacy has changed his perspective on his diagnosis. Check out Wessam’s blog here! https://lnkd.in/gcKpF27E #HAEA #HAE #HereditaryAngioedema #CommunityBlog #HAEAyouth #ShareYourStory
US Hereditary Angioedema Association
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Learn how to get involved in advocacy at the local level! In this training, we will go over tips and rules to remember as you advocate for your programs. Register here: https://lnkd.in/ewkqt9wU
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CEO | HIMSS | Advisor Mindforce Game Lab & DAYA | Board Member | UN Goals 3 Health | 17 Partnerships
Share your stories of patient needs, health access, clinician challenges, burnout and more. HIMSS Northern California Chapter Sign up to learn how to become an effective advocate for healthcare access! 👇🏽
Join us for two 🌟important🌟 Advocacy Events - Advocacy 101 Webinar on 4/17 at 2PM (register here: https://lnkd.in/gefpHb4t), then our in-person State HIT Day on 5/15 from 9AM - 6PM, where you can meet with legislators to help shape policy (get tickets here: https://lnkd.in/gFuQ7Ct8). Your voice matters - ensure that it is heard by registering today! #HIMSS, #HIMSSNorCal, #HIMSSSoCal Viveka Rydell-Anderson JD, MSc, Larry Ozeran, MD, FAMIA, Ian Slade, Sofia Chancey, Jeff Hawley, Emily Ly, MHA, Eugene Pozdnikov, MBA, Dipty Desai, Ph.D., Christina Morato, Suman Mishra, Carrie Murray
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