If you’re in an underrepresented group or have an “invisible” illness, you may be particularly prone to medical gaslighting.
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“If I’ve learned anything about the chronic illness community (and myself) since my initial onset of symptoms and diagnosis years ago, it’s this: We are strong, we are creative, and we are resilient.”
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A nurse practitioner and RA warrior shares tried-and-true tips for managing flares and improving quality of life. Learn more.
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A new report examines market trends and explains why most patients won’t reap the financial benefits of biosimilars in the near future.
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You may notice changes such as higher costs of testing and treatments, while some policies will remain the same.
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Researchers examine yet another negative health consequence of discrimination: increased inflammation and a higher risk for inflammatory diseases like rheumatoid arthritis and lupus.
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The Global Healthy Living Foundation will be following tools like ChatGPT and Bard closely to determine how this technology can best help our patient community.
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Experts are striving to simplify the COVID-19 vaccination approach, aimed at ensuring all future COVID-19 vaccines are interchangeable and potentially offering the convenience of an annual shot.
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Tien Sydnor-Campbell uses her book and background in psychotherapy and bodywork to help inspire others with chronic illness to accept their pain and advocate for better care.
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Christele Felix doesn’t apologize for having lupus. She doesn’t run from it either. Instead, she rises to the challenge each day and inspires others through her advocacy work with LupusChat.
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