Posts Tagged 'lupus'

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 ...

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kristiebauer
kristiebauer
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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 ...

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kristiebauer
kristiebauer
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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 ...

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chriscronick
chriscronick
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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 ...

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chriscronick
chriscronick
0

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 ...

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chriscronick
chriscronick
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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 ...

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ayamamoto
ayamamoto
1

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 ...

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ayamamoto
ayamamoto
0

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.
 
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 ...

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chriscronick
chriscronick
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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 ...

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chriscronick
chriscronick
0

Local lupus study recruiting participants

SLE is an autoimmune disease capable of causing severe tissue damage in many organs. The cause of SLE is unknown, but recent research has identified infection-fighting proteins called interferons (or IFNs) which are made and released by host cells in response to the presence of pathogens such as viruses, bacteria, parasites or tumor cells. IFNs allow for communication between cells to trigger the protective defenses of the immune system that eradicate pathogens or tumors.

In this ...

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lupus_admin
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