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.
May is Lupus Awareness Month! Here is our fact for Day 2: Lupus affects nine times more women than men, and more women of color than white women. African-American and Latina women with no family history of lupus have about a one in 250 chance of developing the disease.
In honor of May being Lupus Awareness Month, I am sharing a fact about lupus every day in May. Please share and raise awareness about lupus and its impact on the lives of millions of people like me, and our families. Please share! Let’s raise awareness so we may find a cure!
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 …
