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… Continue reading CBD for Me – One Lupus Patient’s Experience with Cannabidol. (Repost)
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… Continue reading Upgrading to a new level of protection.
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… Continue reading “Sharing is Caring.”
Sharing "Lupus Awareness is Fun" on The Wendy Williams Show today! Happy Lupus Awareness Month!