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in Lifestyle &middot September 23, 2014

Five Unexpected Things I Learned As a Medical School Wife

Hi Kate the Almost Great readers! I’m Olya, and I blog over at The Siberian American. My husband is currently in his last year of medical school. When he first started medical school, I had no idea what to expect. It was fun being a total newbie to the medical field and starting this adventure with him.
There is nothing better than watching your significant other work towards his passion. The past three years have been rewarding, crazy, sleepless, interesting, exciting, and, sometimes, just plain hard. 
Today, I wanted to share the five unexpected things I have learned as a medical school wife.
One
People ask me about their health problems: 
I knew people would come up to Chris and ask him medical questions, but I had no idea that people would ask me for advice. I am an editor. Unless it is a health problem that Chris and I happened to have discussed, I can’t help. Shocking, I know.
Two
My husband’s computer is off-limits:  
This is for my sake rather than his. Recently, Chris and I were sitting next to each other on the couch so I looked over to see what he was doing. Oh, you know, just watching an open-heart surgery on YouTube. Fantastic for him, disgusting for me. Lesson learned: never look at his screen without asking first.
Three
People often think we’re super rich: 
Honestly, I can’t even begin to describe how crazy this makes me. I hear it all the time. “You are so lucky your husband is a doctor. He must make a lot.” Or someone will joke “Wow, did you marry your husband for his money?” My husband is a medical student, and after that he will be a resident. He is still a long way from making a doctor’s salary, and even then, it’s a weird conversation starter.
Four
Residency match is complicated: 
I assumed residency programs are like colleges, where you apply, get accepted, and then get to pick the program you want. Silly me. The match is much more complicated than that. I’m not going to get into the whole process right now, but residency match is nothing like I thought it was going to be. First, Chris has to do an intern year before he starts a residency in his specialty so we might have to move twice. (What?!)
Five
The schedule constantly changes: 
I knew Chris would have a crazy schedule, but I thought it would be consistent. I couldn’t have been more wrong. Sometimes he’s at the hospital for 48 hours, and other days it feels like he has a normal 8-5 job. One day he’ll wake me up at 2 a.m. (coming home or leaving, it depends) and the next day he might get up at 6 a.m. The hard part is that you can’t get used to a schedule when there isn’t one.  
So far I’ve learned that med school wife = crazy life, but it’s an adventure that I wouldn’t trade, and I am eagerly looking forward to the next step in the journey. 

Kate Mitchell

Kate Mitchell is a blogger, chronic illness patient, and advocate who helps people understand chronic illness and helps chronic illness patients live their best lives.

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Comments

  1. Kristen says

    September 23, 2014 at 2:26 pm

    oh my goodness, i can't believe people ask you health questions or money questions – rude! my husband is a teacher and i have had people say the opposite to me 'well you better make more money than him one day' or 'how do you afford to travel when he's a teacher?' like wtf people!

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  2. The Girl who Loved to Write says

    September 23, 2014 at 3:30 pm

    Haha I've learned to steer clear of my husbands computer too! There are some medical things I just don't ever need to see.

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  3. Alissa says

    September 24, 2014 at 8:56 am

    Hi Olga! I'm working in a medical field too and I find this relatable.. It's hard being with someone who works at the hospital knowing how crazy their schedule is but I'm glad you're working that out. 🙂

    http://thewallflowersecrets.com

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  4. Lynsey @ Eternally Wanderlyn says

    September 25, 2014 at 12:25 pm

    I have a couple of friends in medical school. It's crazy! And I almost signed up for that life, but I'm so glad that I decided to pass. I would much rather spend my time traveling than studying or camping out in the hospital. 🙂

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There are a lot of medical advancements that I'm g There are a lot of medical advancements that I'm grateful for, but one of them is the ability to do IVIG at home. ⁣
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I'm on IVIG - or, in my case, subcutaneous immunoglobulin replacement therapy - because I have to kill the better part of my immune system. There are, in fact, some parts of my immune system that don't attack me, which is why we add them back in. This helps reduce my chance of serious infection and also made my rheumatologist feel comfortable enough to increase my Rituxan dose. ⁣
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This is a weekly treatment that I do, but it's so much better that I can do it at home than going into the hospital. It takes around 2.5 hours from taking my pre-meds to tossing my needles into a Sharps container. While it's another thing that I have to do, because I do it at home, I don't have to risk exposure to infections at the hospital or deal with Boston traffic, which would add another hour to the process. ⁣
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I can finish my treatment and then go about my day, which I'm very grateful for.⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣
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#IVIG #ChronicallyIll #RheumatoidArthritis #Autoimmune #AutoimmuneDisease
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1️⃣ New glasses! I really like having multiple pairs so I can switch them as I want.
2️⃣ One of my current projects. I got this standing hoop for my birthday and I’m working on an alphabet (uppercase and lower, although I’m still working on the lower) with extra floss.
3️⃣ Infusion time! I got my higher dose so hopefully my symptoms improve a lot in the upcoming weeks🤞🏻

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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣⁣

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IDs: 
1️⃣ Kate takes a selfie. Her new glasses are thin silver circles
2️⃣ An in-progress cross-stitched alphabet in a special hoop stand that Kate is sitting on.
3️⃣ Kate takes a selfie in an infusion chair.

#ChronicallyIll #RheumatoidArthritis #AutoimmuneDisease #CrossStitcher
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5️⃣ Kate’s mom smiling in a restaurant 
6️⃣ Kate with Harley again 

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While these are not my treatments, they have made my life better in some ways. ⁣
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What lifestyle changes have you made, for RA or another condition?⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣
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IDs: ⁣
A series of pictures. Each has a text box on them related to the picture. ⁣
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1️⃣ Lifestyle changes I made for my rheumatoid arthritis⁣
2️⃣ Wearing a mask⁣
3️⃣ Using a cane⁣
4️⃣ Changing my diet⁣
5️⃣ Working from home⁣
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▪ Cut myself slack ⁣
▪ Get Harley hugs⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣
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ID: Kate and Harley the golden retriever hugging. Kate is a redheaded white woman wearing a black dress, pink sweater, and round pink glasses.⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.

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1️⃣ A completed cross-stitch project, which shows 2 bears walking past a lake, trees, and mountains.
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May is Arthritis Awareness Month. Like, comment, and share to spread awareness 💖⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣
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ID: Fact or Fiction? Let's Check! ⁣
Fiction⁣
You only have rheumatoid arthritis if your rheumatoid factor tests positive.⁣
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Things are tough (all over pain, heat with POTS, i Things are tough (all over pain, heat with POTS, in a walking cast waiting to see if I need my 6th foot surgery), but so am I.⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣
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1️⃣ IVIG + Kindle reading 
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.

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IDs: 
1️⃣ Infusion tubes coming out from under her shirt. There’s a Kindle on her lap.
2️⃣ An almost-finished cross-stitch project

#IVIG #ChronicallyIll #CrossStitcher #CrossStitchersOfInstagram
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