Dialogue & Dinner about Lupus
Who We Are
Marlene’s Kaleidoscope foundation was founded in 2017 by the Kansas City own La Tanya M. Lipprand. It was formed to Bring awareness about Lupus and help individuals, as well as the families and caregivers who support those suffering from the Devastating Disease that has "1000 faces" called Lupus and other related autoimmune diseases.
Upcoming Events
Thu, Oct 06Westin Crown Center
Marlene's Kaleidoscope
Turning a conversation Into Action for Lupus.
Dedicated to improving the lives of people affected by all forms of Lupus. We strive to empower people by providing information about Lupus and offering support so that their voices can be heard in service of creating a better quality of life through research, public awareness, advocacy, and education.
Lupus & Coronavirus (Covid-19)
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What We Do
Turning a conversation Into Action for Lupus.
Dedicated to improving the lives of people affected by all forms of Lupus. We strive to empower people by providing information about Lupus and offering support so that their voices can be heard in service of creating a better quality of life through research, public awareness, advocacy, and education.
DO YOU KNOW THE SIGNS OF LUPUS
Butterfly-shaped rash
Raised red patches on your skin
You're sensitive to light
Ulcers in your mouth or nose
Arthritis in two or more joints, plus swelling or tenderness
Inflammation in the lining of your heart or lungs
Seizures or other nerve problems
Too much protein in your urine
Low blood cell counts
Certain antibodies in your blood
Results from a blood test called an ANA test suggest you may have too many "antinuclear" antibodies
If you think you or someone you know is displaying at least four of these symptoms, it’s time to talk to a medical provider about your concerns. Your primary care provider can examine you and your health history and refer you to a rheumatology specialist for further diagnosis.