Think about it. We shouldn’t discount other illnesses. Heck there’s so many other ailments mixed in with Lupus itself.
It is not a contest of who has the most pain, who hurts worst, who requires the most medicine, who’s
Sometimes even three steps can be a mountainous feat for those with Lupus. But, I have confidence that constant exercise and physical therapy can provide support. I have some friends that are a little hesitant about joining a gym because they
Not meaning to do so, friends tend to make the sick friend ‘into’ a problem. It’s okay to be open, honest, and just plain there. And this friendship thing has to come from both sides. That means that even the
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
“Someone You Know Has LUPUS.” In effort to support LUPUS Awareness month, during my busiest travel season, (May and into the end of June) I’m wearing my purple band that sports a message! And I’m mobilizing the message! You never know where
You must be logged in to post a comment.