The Lupus Foundation of America just introduced a new tool to help those living with Lupus. It’s called SELF and it has been designed to “manage lupus symptoms, manage stress, manage medications, and work with your health care team.” Check it out HERE. I’ve joined and I hope you will, too! Please let me know …
A new tool to help live your best life with Lupus! Read More »
The Lupus Foundation of America is holding a nation-wide Zoom meeting which will focus on lupus and the kidneys. Check out more information on the LFA site here.
We all want to live long, healthy lives. We don’t want to take medication full of side effects, have chronic pain, or experience days, weeks or even months where we are too ill to get out of bed. We want to see our children grow up, and hold our grandchildren in our arms. I want …
I was reading this article about new research on lupus, genes and why it seems to afflict more men than women: https://www.statnews.com/2018/01/29/lupus-women-genetics/ So interesting! I know I have genes that make me more susceptible to lupus and other autoimmune issues. I’m going to have to do more research of my own on this. Have you had …
I wake up and the first thought in my head is that my ankles hurt. My ankles. I haven’t done any running in days and I didn’t overdo anything yesterday. I even ate pretty healthily. But, there it is. My ankles hurt. I start to move to sit up and my shoulder joints hurt. …
I can hardly believe it! My little boys are 1! We had their birthday party last weekend… Cowboy-themed, obviously. I think everyone had a good time, including the boys, which was extremely important to me. SO much planning went into that day, but I had fun doing it. 🙂 Their birthday was on Thursday …
