The good days
Have you ever heard the phrase “It’s a good day.” said by someone who has health issues? Many people with chronic illness know what good days and bad days are. For me, a good day with lupus means I can move relatively free without pain, I think clearly, and I can do many of the (sometimes simplest) things on my to-do list.
Sounds easy enough, right? Well, if you’ve read my previous blog post, “Flares and bad days,” you can ...Continue Reading →
A hesitant beginning to a happy commitment
2012 began for me with the Lupus Foundation of Minnesota asking me to be an ambassador for their organization. I was initially hesitant for a couple reasons. One was the lengthy flare I had been dealing with from the recent, and very sad, death of my father – I wasn’t sure if I would be able to follow through. The second reason was my ongoing, on-and-off lupus diagnosis – I wasn’t convinced that I would be a very good ...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 →
Lupus patients invited to Biovid Corp. survey
Biovid Corp. would like to invite patients to participate in a 20-minute online survey discussing experiences and attitudes toward the management of your lupus condition. The survey is strictly for market research purposes; there will be absolutely no sales or promotional activities in conjunction with this survey. Your responses are completely confidential. Qualified participants will receive a check at the end of the study for $50. If you are interested in participating in this survey, please email Dusten Brennan at Biovid ...Continue Reading →