Maurissa Tancharoen Instagram – “But you don’t look sick!” Those words, though well-intentioned, sometimes make me want to punch a wall, depending on the kind of day I’m having… 😆 While lupus affects millions of people around the world, the general public knows little to nothing about the disease. Those suffering with #lupus often don’t appear unwell. The following is my feeble attempt to convey what #LivingWithLupus looks like in just ten photos. May is #LupusAwarenessMonth, so to amplify awareness, I’m sharing some personal moments from my life in surviving this chronic, often debilitating disease. I’ve lived with lupus for decades, and over the years I’ve been hospitalized for flares of the lungs, kidneys and central nervous system. But I’m still here and thriving thanks to the care of my stellar medical team, innovative drug treatments, stress and wellness management, and the love and support of my incredible husband and daughter, family and friends. 💜
Navigating this disease has been a lifelong journey, which is why my work with @lupusla is deeply important to me. At #LupusLA we are committed to finding a cure, while providing support, services, and hope to all who suffer from lupus. Through fundraising events, community support, and advocacy, we aim to raise awareness and improve the lives of those affected by this autoimmune disease, both in Los Angeles and around the world. For more information, or if you’d like to donate to our cause, please go to www.lupusla.org. Thank you!
p.s. Shoutout to @selashiloni and @_beautybygg_ for making me look good even when I wasn’t feeling my best. 📸✨ | Posted on 14/May/2024 01:43:57
