May is Lupus Awareness Month. It is so wonderful that many of us are now taking notice of a complicated and perplexed disease such as lupus. I am so proud of everyone and anyone who has taken it upon themselves to support friends, family, and the community by...
Sometimes, what you don’t know can not only hurt you, but hurt others as well. Sandra Raymond, President and CEO of the Lupus Foundation of America, Inc., thank you for being so poised in your response to the Judge Judy
When the journey seems long and the weight you are carrying gets a little heavier, a song can loosen the grip you held on the pain!
What a humbling and informative presentation. All illnesses are heartfelt, experienced, and seen differently in the heart of the beholder. But I must admit, many Lupus patients feel this way when the pain has no definite source, keeps moving to
Below is a copy of the email I received advocating support for Lupus awareness during the 2013 National LUPUS Summit. I ‘took action’ by submitting my letter to request support of more funding for Lupus research to my local representative.
Let me first explain that the title of this post is in no way a reference to a diagnosis of any sort. I was on my travel route and had an interesting encounter. I thought, at first, that maybe I