Lupus nephritis is a severe complication of systemic lupus erythematosus (SLE), an autoimmune disease, where the immune system attacks healthy tissues, including the kidneys. In lupus nephritis, inflammation affects the kidneys, leading to kidney damage and impaired function. Symptoms may include blood in the urine, proteinuria (excess protein in the urine), high blood pressure, swelling (edema), and decreased kidney function. Management involves medications to suppress the immune system, control inflammation, and protect kidney function, alongside lifestyle modifications and close monitoring by healthcare professionals.
Patients are the experts in their condition and advocacy groups provide a platform for patient voices. Working directly with these communities is the key to pushing research forward in an inclusive way.
Often underrecognized and misunderstood, Lupus Nephritis presents significant challenges for those diagnosed with it. More than half of individuals diagnosed with Systemic Lupus Erythematosus (SLE) will develop Lupus Nephritis. At Leapcure, we offer a platform with valuable resources, including links to support groups focused on providing information to individuals affected by Lupus Nephritis.
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We’ve committed to having 500,000 conversations in the next three years, to equip ourselves and our Pharma partners with the insights needed to increase predictability.
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The ever-growing investment in advocacy doesn’t appear to be slowing down, and research is certainly seeing the benefits. Which at the end of the day, means better patient care and more options for patients.
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We’re ready to keep forming links between our Advocacy friends and Pharma partners, so these fruitful relationships continue to evolve beyond the study-to-study view.
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