Uniting for a common purpose
We recently finished the Lupus Walk for Hope and 5K in Plymouth on September 14, Rochester on September 28, and the last event in Duluth on October 5. Time has flown by, as it seems like it was just last week we were in Duluth. I’m grateful to have participated in all three Walk/5Ks and even more grateful my body decided to cooperate with me through the weather, travel, and excitement of it all.
As Ambassador, I’ve had the pleasure of ...Continue Reading →
Surviving the first trimester with lupus
I can imagine that the first trimester for every pregnant woman is nerve-racking. The first trimester with lupus is even more so. It’s nerve-racking, overwhelming, exciting and scary all at once. Not only do you have to worry about taking care of yourself AND a baby, you also have to worry about miscarriages and how your lupus is going to affect your pregnancy (and your baby).
With lupus I was at a higher risk of miscarriage. I have talked to a ...Continue Reading →
The biggest decision I’ve made with lupus
Hi, my name is Kristie Bauer. I was diagnosed with lupus at the age of 17. I am now 26 and have been through so much. Sometimes I like to look at lupus as an adventure. It keeps life interesting. Usually when you least expect it. Lupus has affected me in many ways including my heart, lungs, kidneys, joints, muscles and more.
Since being diagnosed with lupus, I have graduated high school, moved away to college, graduated college, got my first ...Continue Reading →
Support comes in all forms
Lupus is a chronic disease which means it’s something that is life-long with no cure. I am doing well today, but that does not mean that’s true tomorrow. I knew I would be dealing with lupus for the rest of my life. Given that, I quickly realized I would have to rely on, and ask for support, from those around me. For someone who is fiercely independent and rather “Type A,” this is very humbling. Asking for help used to ...Continue Reading →
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 →
Flares and bad days
When you have lupus, you have periods of disease remission and flares. Remission may seem like the disease is gone, but the reality is it never goes away; it’s just quiet. A lupus flare is a period of heightened disease activity which for me, ranges from mild to moderate and to severe. I’ve had both remission and flares all in the same day. Lupus turns on me that fast. After being diagnosed, I’ve become very aware of how I am ...Continue Reading →
Confirming my future direction
Before the start of this fellowship, I was contemplating whether I wanted to go into medicine, research, or both. Upon talking to many mentors, I was leaning towards going into practicing medicine, but finding a way to also stay involved with research. However, although I have had a passion and interest in both for quite a while now, I wanted to experience more before I made the decision.
After the first several weeks of the fellowship under Dr. Peterson, I ...Continue Reading →
Channeling My Passion
I have had a passion for medicine and research since mid-high school. However, I was not sure about whether I would pursue one, the other, both, or the integration of the two as my future career.
At the start of my undergraduate career, I was set on trying to get into the M.D., Ph.D. program to integrate the two fields, as well as apply myself in both settings, as I always loved biology and medicine and had experience with clinical and ...Continue Reading →
My “New Normal”
As I’m thinking of ideas to blog about, it occurred to me to talk about some of the topics I find myself discussing with friends and family. Most people have heard of lupus but many don’t really know how life-altering it is. I sure didn’t.Continue Reading →
When I was diagnosed nearly three years ago, I knew very little about lupus. I knew it’s an autoimmune disease meaning that my body is basically attacking itself. I knew of people who got ...
Introducing 2013 Lupus Ambassador Chris Cronick
My name is Chris Cronick and I’m honored to have been chosen as the 2013 Lupus Ambassador for the Lupus Foundation of Minnesota (LFM). I’m 37 and I was diagnosed with lupus in 2010. Prior to my diagnosis, I was in and out of the hospital for six months. It was a very scary time, not knowing what was wrong. I was tested for everything, but eventually was diagnosed with lupus SLE.
I have found that many times those ...Continue Reading →