Living with Flair on the Set of THE SALON

There are good days and bad days with when you live with Lupus. But, I wasn’t going to let anything or anyone stand in my way of having a great time working on the set of the new digital series- THE SALON. I have been consulting on this project for nearly a year. The premise

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Upgrading to a new level of protection.

This weekend, I will be “walking” in the Lupus Foundation of America’s Los Angeles “Walk with Us to End Lupus Now”. If you know me, you know I will be donning my purple “LA Lupus Lady” cape to harness my “flair” to transform into a patient advocate/activist that shares “Lupus Awareness is fun.  Lupus is

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“Sharing is Caring.”

My way of managing Lupus symptoms is what many would call “alternative” or “holistic”, but it is not conventional.  Each person is unique–and Lupus patients are especially so.  Unlike some diseases,  there is no protocol that works for the majority of patients.  I learned from my mother how to ask questions and make informed choices

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