In the company of misery
Today I sat around a patio table with four of my very good friends. Of the 5 of us, it just so happens that 3 of us have pretty serious health challenges.
One of my friends has Cushing’s Disease, which is likely going to require brain surgery soon. Another has a heart problem. And I have a crazy screwed up brain. When you sit down and think about it, the odds of the three of us being in the same program at the same time are practically impossibly small.
And today we three anomalies sat and talked for a while.
We talked about the reality of life with disease.
We talked about all the stupid little things we do to try to find control in our lives and how often they totally backfire.
We talked about how hard it is to get up and keep going when things seem like they cannot possibly get worse or seem like they’re never on track to be better.
We talked about how draining this life is. How exhausting it is just to live with pain, with disease.
We sat, a group of 3 people facing completely different challenges, and we shared a bond. Tears were shed, truths that had been long hidden were shared.
For the first time in a long time, I didn’t feel alone.
It’s hard to describe how isolating disease and pain can be. There’s the very obvious missing out on life component that’s easy to understand and to imagine. But there’s a secondary isolation. Sometimes it’s literally your absence from events that you could attend but choose not to, other times it’s more subtle. It’s physically being somewhere, but being detached. It’s the feeling of being completely alone in a room full of people.
Today’s conversation reminded me of the saying that misery loves company. But I don’t think it’s really that simple.
I don’t think I’ve ever wanted other people to be miserable or sick or in pain just because I am. Frankly, I don’t wish chronic pain or disease on anyone (okay, very occasionally, in my head, I do). But on days like today where I am surrounded in my misery with others who understand it, I realize that I have missed company. That I do really love it.
I really think that essentially we’re all bearing our own burdens. Even if we can’t admit it to anyone else, we’re all fighting our own misery.
And maybe the key to winning is finding allies who share in those fights, in those experiences. Finding people who provide you company in the face of misery.








Welcome! I'm Katie, a 28 year old, full-time graduate student who just happened to have brain surgery in November of 2007 to give my ginormous brain a little more space. This blog chronicles my daily life, from relentless headaches to being a doctor's wife. Sit down, get comfortable and stay for a while.











Loved this heartfelt post, especially the last line.
[Reply]
Great post. I’ve had some chronic pain–still do–but gah, my hips/lower back/neck stuff seems minor in comparison to your brain stuff.
Loads of sympathy.
*HUGS*
[Reply]
Sometimes misery really does love company, but it’s not always for the negative connotations most people attach to the saying. There’s just something comforting about having people you can turn to who know what you are going through. I have to say that if you are not living with chronic pain or illness, no matter how lovingly intended your actions, words and thoughts are, you just can’t fully understand it unless you’ve been there yourself. That cathartic experience of being able to identify with someone else and say ‘hey, that’s exactly how I feel’ is one of the very reasons I follow your blog. Your words are like a release for me. Sometimes I just point to the computer screen and have my fiancee read what you have written because it’s everything I want to say but can’t. Your words help more than you know. Thank you again ox
[Reply]
This is a very beautiful post, and a great introduction to your blog.
[Reply]
Finding others at work and online who share some of my struggles has been incredibly liberating for me. To have this pool of resources, even if it’s just someone who *understands* has been a huge help. I’m glad you found some of that connection and camaraderie, too.
[Reply]
UGH!! I hate that this (your head pain and struggles) is currently your life! I want so badly for this to just go away, like a stain one finally scrubs out of the carpet (I still have hope). In the meantime–how wonderful it is that you have found community, and that you offer it to others. So many people would have missed out on an amazing gift: your friendship. I’m glad to see you can also focus on the blessings.
[Reply]
A little off topic: most people say they wouldn’t wish their chronic pain on their worst enemy. But I do. Not just my worst enemy but I wish this on the people who scoff at me and tell me to “shake it off”. I wish it on doctors who blow me off. And I definitely wish this on my former boss who made my life hell after I got sick. Not that I think they deserve this any more than I do…but think of the wholesale cultural changes that would be made if “normals” knew what chronic pain feels like!
Just my two cents. And thank you for the beautiful post.
[Reply]
Katie Reply:
April 16th, 2010 at 4:56 pm
I have, on occasion, wished that people like that could experience, just for a little while, what this life is like.
But I also know that they would complain even more than I do. So it’s sort of a punishment for me too.
[Reply]
Lovely post; and I agree, that sometimes it is comforting to know that others understand (on at least some level) what you are going through.
[Reply]
My Sister has chronic health issues also so it great that we have each other to bitch to.
[Reply]
K, I don’t think its really missery loves company, it’s just easier to talk and be open and honest when you know someone understands what you are going through. Having friends that understand, have been there, know the challenges only makes it easier to be open and talk about what’s really going on. I am glad that you had that time with your friends, and have people who understand whole heartedly what you are going through on a daily basis. I have my own health issues, nothing near what you do, but I understand what it;s like to be there, but not be there, to feel alone, and to want to share how you are feeling but know what has to be going through everyone else mind. I am glad you are so open and honest on your blog on your daily struggles. Yyou are so full o strenth and inspiration. Hugs to you.
[Reply]
For me the hardest part of walking this journey is making plans in advance of any knowledge about what my reality may be when that day come. It’s very difficult to plan anything with confidence.
i really don’t like that part very much.
[Reply]
SueG Reply:
April 18th, 2010 at 8:20 pm
Yeah, you read it right…when that day come. I just got a new netbook because I am going crazy in Chicago without a computer…and half the buttons I hit don’t translate into actual letters and spaces. Argggh.
[Reply]
I’m so glad that you have experienced what you wrote about. It must be so comforting to REALLY know that you are not alone. May this truth bring you much comfort in the days ahead.
[Reply]