LA Lupus Lady
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
TO CBD OR NOT TO CBD? If you have read any online content regarding CBD (the term for cannabidiol),), you will know that the messaging can be confusing and/or overwhelming with facts and information and lots of pros and cons. Therefore, as a person who is in the “thick” of medical issues, I think it
While most of North America slept, 100,000 or so people were partying in Indio, California Saturday night. Even more, like me, watched online as Lady Gaga performed her first (of two) Coachella 2017 sets. If you were sleeping and missed it – Lady Gaga debuted a nice song, “The Cure”, last night at Coachella mixed
Here is a post I wrote for the Personal Connected Health Alliance on Virtual Reality and Patient Care. http://www.himssconference.org/updates/open-yourself-future-personal-connected-health
Kindness Plays for the Born This Way Foundation.
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
Source: Being safe when you travel
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
Sharing “Lupus Awareness is Fun” on The Wendy Williams Show today! Happy Lupus Awareness Month!
Amanda Greene 