#VFSC, LA Lupus Lady, LaLupusLady, Social Media Correspondent, Twitterati

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… Continue reading Upgrading to a new level of protection.

LaLupusLady

“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… Continue reading “Sharing is Caring.”