Showing posts with label Overcoming. Show all posts
Showing posts with label Overcoming. Show all posts

Monday, August 29, 2016

Body Shaming and Chronic Illness

One of the first things I heard when I started this illness journey was that my body was attacking itself.  And that rather than fighting off foreign invaders, my body was mistaking my own organs and joints as things that weren’t actually supposed to be there.

While that provides a somewhat easy explanation for a very complicated process of what’s going on, it’s a profoundly negative thing to be told.  And it sticks with you. 

We are told that our bodies are attacking themselves.  We are told that we must have done something along the way that caused this to happen. 

I’ve never been the most confident person in the world.  I’ve been self-conscious most of my life.  And THEN I got sick.    

But with all of this stuff going on, I never really had to worry about my weight.  If anything, I had to be worried about being underweight.  And then, slowly, my weight crept up.

I felt like I was stuck in a rut.  While I used to look at some pictures of me in high school and think I was chubby, I know now that I really wasn’t.  And I was so fixated on gaining the “Freshman 15” in college that I inadvertently lost 15 pounds.    

At my lowest since high school, when I first went to my rheumatologist, I weighed in at 86 pounds.  I know now that, that definitely wasn’t healthy.  And part of my lack of eating was the amount of pain I was in.  That had a lot to do with it.  It wasn’t that, that was my goal all along, to weigh 86 pounds.  And until about five years ago, I never topped out at more than 98 pounds.  Then things changed.  And the number kept going up and up.  When I went to the doctor in February, I weighed in at 121 pounds.  It was the most I have ever weighed in my whole life, and I was completely disgusted with myself.    

That number on the scale was the kick in the pants that I needed to do something about it.  And it wasn’t just the number on the scale.  It was the way I felt.  It was the fact that I could barely look in the mirror let alone consider letting another human being see me without clothes on.  No one in my life was explicitly telling me that I was fat, but I could tell by some of the looks I got that people thought I had gained weight, and I had.  This doesn’t really hit you until you start losing weight and people tell you how great you look.    

So in June, I joined Weight Watchers.  It’s not so much that I wanted to diet, as much as whatever I was doing myself – mainly eating as many carbs and as few fruits and vegetables as possible – wasn’t working.  Sure, it didn’t help that eight years ago I got sick, two years ago my dad died, eight months ago I lost my job and my boyfriend of three and a half years broke up with me, and I moved back to Michigan; jobless, boyfriend-less, and otherwise confused about where my life was headed.  Who would blame me if pizza became my go-to food? 

But I’ve had to do something, and I’ve tried to look at this whole experience as more of a lifestyle change than a diet. 

But I assure you, there is no judgment towards other people.  I know some people I have talked to have looked at me and said “I would kill to weigh what you weighed at your highest.”  But that’s not what it’s about.  It’s about the fact that I didn’t feel like I looked good, and I didn’t feel good, physically or emotionally.  That extra weight was literally and figuratively weighing me down.  

But slowly, I’m working on turning my negative self-talk into positive self-talk.  I can actually look at myself in the mirror again, and shocker, kind of like what I see.  I’ve lost almost 13 pounds, which puts me almost at the high end of my goal.  I know 13 pounds isn’t a lot, but it is for me.  It’s actually 10% of my starting weight.  But honestly, and I keep having to tell myself this – the pounds don’t matter, the percentage doesn’t matter, as much as how I feel, physically and emotionally, matters.    

I hate when my rheumatologist asks me if I’m exercising.  Because it’s not code for “are you moving enough?”  It’s code for “get off your butt and move, you fat ass”.  Trust me, I’ve known him long enough to know that, that’s exactly what he’s saying.  And rather than retort back, “And what’s your excuse?” I smile and nod, and pretend that what he said hasn’t hurt me at all, when clearly, it has. 

I don’t think I’ll ever hit below the 100 pound mark again, but who am I kidding?  I’m 31 years old.  It’s not as easy as it used to be.  Seriously, at 25, it all started going downhill. 

So from the very beginning of our illness journeys, we are fed information about our bodies that our profoundly negative.  And we are expected, despite the pain, despite the stiffness, despite the medications and their side effects, despite whatever else in life might happen besides our illnesses, to rise above, and do it with a smile and all while looking great, all like you would never know we were sick.    

Wednesday, June 18, 2014

My Rallying Cry

I just got back from a two week vacation in Michigan.  I got to spend time with my family and friends.  It was a really nice time.

It also made me realize that some of the comforts of home involve my illnesses. 

There were two and a half days in the last two weeks in which I felt really bad. 

The day after I got home, it rained all day, so that left me with a headache and totally spacey feeling.

Then we were going to a Tiger’s (baseball) game.  I woke up feeling fine, but a few hours later ended up with a pretty bad headache.  I went back to bed and told my sister to wake me up, and each time, asked for another half an hour, because every time I tried to lift my head off of the pillow, I overcome with dizziness.  Eventually, it got to the point where I didn’t have another half an hour before we needed to leave.

So I got up and dressed.

The nice thing was that my family told me I didn’t have to go to the game, if I didn’t feel up to it.  Or, I could go, and if I didn’t feel well, we could leave the game. 

It was so nice.  But I told them that I would go, that I would rally.  And I did. 

But I always struggle with trying to rally and simply waiting until I feel better to do things.  Sometimes I wonder whether I wouldn’t start to feel better just by pushing myself to get out of bed. 

However, then there are real feelings of not feeling well, that you can’t shake, no matter what.

But what was really refreshing was to have people just get it.  Who I didn’t have to explain to, and who I wouldn’t have to justify myself to if I wouldn’t have been able to rally.

And that’s a big part of what is missing in New York.  Aside from my family, of course.  I feel like I have to have an explanation for everything I don’t do.  The lifestyle in New York City is just go, go, go, do, do, do, no matter what.  And that just doesn’t work for me.    

I pride myself in my ability to rally.  Sometimes it takes an hour and I can bounce back.  Other times, it takes hours.  And other times, it doesn’t happen at all. 

But with my family, the important thing is being together.  So whether that means me being in bed and my parents being in the next room, going to a baseball game or the mall or whatever, it doesn’t matter.  Because we’re together.  And now that I live in New York, we get that time so much less often than we used to.

But that time is sacred.  And so is my health.  And when it comes to my family, those two things happen to go together.