It is with the heaviest of hearts that I recently learned of the loss of a young, athletic lady, taken by complications of her disease activity. I really don’t believe there is anything that grabs the attention more of those afflicted with lupus, than the unexpected death of a fellow lupus fighter. My deepest sympathy and heartfelt wishes to the McHale family as they mourn the loss of their 23 year-old daughter, Sasha.
Straight-up, lupus is cruel. It doesn’t distinguish between ...Continue Reading →
Choosing How I Want to Use My Energy
Today I was fortunate enough to come home from work early and take a nap. I work full time and even though my job is protected through FMLA, I can only use so much of that during a month. Some days I don’t feel bad enough to stay home, but I don’t feel good enough to work all day either. Plus I know that pushing myself can sometimes be detrimental and cause a flare.
For me, having lupus is an everyday ...Continue Reading →
Introducing Kim, Lupus Ambassador
Hello everyone! I’m Kim, one of the 2012 Lupus Ambassadors for LFM. We may have even met at the Twin Cities, Rochester and Duluth Lupus Walks for Hope, or at the Lupus Night at Target Field this past year.
For those of us living with lupus, 2012 has been an exciting year filled with hope, amazing awareness efforts, breakthroughs in research and increased public donations to find a cure. I’ve seen this on a national level, but quite extensively here in ...Continue Reading →
Introducting Gwen, Lupus Ambassador
My name is Gwen Alexander and I’ve been diagnosed with lupus since 2006. I’m pretty confident I’ve been living with it most of my life but just not knowing. I’m a divorced mother of a 16-year-old dancer, wannabe actress/model/chef/beautician. I’ve been dating the same man for about 10 years and for now I’m working full time and I am currently the Ambassador for the Lupus Foundation of Minnesota (LFM). I’ve spent most of this year raising awareness and monies for ...Continue Reading →