CWL05_A Conversation with Tanisha Davis| Lupus Nephritis Patient and Advocate - a podcast by Hetlena Johnson, The Lupus Lia

Conversations with Lupus: An Interview with Lupus Patient Tanisha Davis-SmallsHow does a mother of three, diagnosed with lupus nephritis live a full life while living with lupus? Watch this interview with Tanisha as she describes how it feels to be fighting for life and happy at the same time. Lupus is a life altering and challenging disease to live with. Lupus is a chronic, autoimmune disease that can damage any part of the body to include, but is not limited to skin, joints and/or life organs. According to the Lupus Foundation of America, Inc.* about 1.5 million people, worldwide, have a form of Lupus.----Host Note: From the heart of experience, I am well aware of the related difficulties that come with living with Lupus. I was diagnosed with Lupus at the age of 16. At this time, Lupus was still a very curious disease. I was told that I would not live more than ten years after being diagnosed. Yet, life trials and errors prove that I am not dead yet! I am currently in the process of writing a memoir about combating Lupus. More research has enabled many Lupus patients to live fulfilling lives. ========================================­===Learning to live successfully with lupus.========================================­===**Click Below to SUBSCRIBE for More Videos:https://www.youtube.com/user/LupusLiar========================================­===**Click Below to Sign up for the FREE living with lupus tips via email:https://goo.gl/li06i0**FOLLOW, LIKE, TWEET, SHARE**Twitter: http://www.Twitter.com/TheLupusLiarFacebook: https://www.facebook.com/TheLupusLiarInstagram: http://www.Instagram/thelupusliarPinterest: http://www.Pinterest.com/thelupusliarWebsite: http://www.TheLupusLiar.com

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