Why I fall down a lot

Or The Story of How I Developed, Suffered From, Wondered About, Was Diagnosed and Learned to Cope With Postural Orthostatic Tachycardia Syndrome.

Reblogged from earlier this year

Or The Story of How I Developed, Suffered From, Wondered About, Was Diagnosed and Learned to Cope With Postural Orthostatic Tachycardia Syndrome.

After my daughter was born in 2009, I started to notice that when I stood up from sitting or laying down, I’d be so dizzy I’d have lean on something to keep from falling down. This happens to everyone sometimes, maybe when dehydrated, hung over or ill. For me however, it gradually snowballed from every once in a while to every time I stood up. I drank more water and was careful when standing.

Then I noticed that I would get so tired standing up during hair appointments. It felt like I’d just run a marathon and all I’d done was stand and clip hair. I would get so hot during my appointments that I started wearing black tank tops under all my black shirts so that, mid hair cut, I could divest myself of the extra layers to keep myself from what felt like heat stroke.

Sometime after I’d gotten adjusted to this new weirdness, I noticed that when standing my heart would just start pounding in my ears. It would beat loud and fast and I’d feel lightheaded and the room would be blindingly bright and the world would spin.

Things got worse and I went from being lightheaded to actually passing out. Upon standing up and after standing for a not so extended period of time (something like 30-45 minutes).

At the same time I was also experiencing other symptoms (that eventually led to other diagnoses). I couldn’t stay awake, I slept all the time, my headaches were getting worse, I had horrible flu like body pain everyday, I had a prolonged panic attack where I pulled out all of my eyelashes and scratched my arms till they bled. I was confused, disoriented, forgetful, and making mistakes I would normally never make.

I finally decided I needed to take some time off to figure out what the hell was going on. I made a doctor’s appoint. And another. And another. And another.

Luckily, the first doctor I went to this time actually listened instead of writing me off because I have Bipolar Disorder. (I’d been trying to figure out more minor presentations of these symptoms for the 3 years since my daughter was born). He believed me, which in my experience is pretty damn impressive.

He diagnosed me with some things and more importantly, for what he didn’t  understand, referred me to specialists that could help me figure it out.

Unfortunately, none of them were able to figure out why I was falling down.

I didn’t go back to work. I couldn’t.

It was about a year later, that I just so happened to be reading an article about rare specialty clinics around the United States. I read about the Faint and Fall Clinic at the University of Utah hospital (mere minutes from where I lived at the time) which was one of two of it’s kind that existed in the U.S.

I was like, for sure these dudes could help me out. That’s exactly what I was doing. I was fainting and falling. If they couldn’t help, who could? What luck that there was a specialty clinic right where I live?

As a reminder, it had been 4 years since these symptoms had started and a year that they’d been keeping me from working.

I went to clinic and they told me about POTS. Postural Orthostatic Tachycardia Syndrome. Basically standing up from lying down fucks my whole shit up. My heart rate and blood pressure can’t keep it together when my posture changes so my body goes nuts. My heart rate shoots up to anywhere from 160 to 200 and my blood pressure drops so I black out. Just from standing up.

They said this is what I have. Except some of it doesn’t make sense.

They still don’t know why I get lightheaded even when I’m sitting down. They don’t know why my body goes nuts and gets so hot after standing for 20 mins when that’s not quite what POTS does.

They gave me a diagnosis and that is pretty awesome. Just knowing what part of it is takes away some of the burden of being sick. (Also makes applying for federal disability a more realistic prospect – they don’t like being told, uh, I fall down but don’t know why).

They also said there’s really not much they can do in the way of treatment other than giving me ginormous salt pills. I’m not kidding, they are like 5 grams of salt in pill form and the hardest thing I’ve ever had to swallow. I also have to drink a lot of water. So basically my treatment is salt, water and not doing the things that cause me to fall down ie. standing up.

The nice thing is that for me, it’s somewhat episodic. I’ll have periods of time where I can hardly stand at all without passing out. But then I’ll have some pretty good days where I might be able to walk around a fairly bench laden mall.

But I don’t do a lot of things anymore. I can’t take my kids for a walk around the block. (I make an exception for Halloween but even so, there have been years I’ve only made it to 3 houses before I had to go back home).

On a trip last summer I took my husband and kids to the Omaha Zoo. I graduated high school in a suburb outside of Omaha Nebraska, near the Air Force Base my dad was stationed at. Going to the zoo was one of my best memories of that time. If you’ve never been to the Omaha Zoo (and why would you unless you actually live in Omaha), it’s the best zoo ever. It’s amazing! Look it up, I’ll spare you a detailed explanation aside from four words. Indiana Jones Rope Bridge.

I was having a particularly bad day that day, but it was the only day we would be in Omaha. So I sat in a wheel chair. I was 34 years old. And I sat in a wheelchair walking around a zoo with my 3 and 7 year old kids.

Does that sound like a big deal? I can’t decide. Sometimes it feels to me like my life is unfair. I should be able to do these things like a normal parent. I should be able to walk and play with my kids.

Then again sometimes I think, well, it could be a lot worse. I can do my own standing at times and that’s something to be pretty damn thankful for. So suck it up, buttercup.

On the bright side, I was surprised how fun it was rolling myself around in a wheelchair. I also was surprised how quickly I caught on to how to maneuver myself in that thing. It was fun and interesting and slightly humiliating.

I made this diagram of a disabled person the other day. I think the idea of it had been kind of nagging at my brain since I sat down in that wheelchair last year. I made it to show how invisible illness can affect a person, in ways that are hard to understand.

Because you get some pretty funny looks when you are young, tattooed, and healthy looking rolling around a zoo in a wheel chair. You get especially funny looks when you get up from said wheelchair to grab your 3 year old down from a railing he shouldn’t be climbing on. Some people even say things. Some to your face. Some just to their buddies.

Because you look like a total asshole.

But I’m not a total asshole. I’m just disabled in a way that isn’t obvious. Invisible, you might say.

2017-04-23 18.42.56

Advertisements

Leave a Reply

Fill in your details below or click an icon to log in:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out / Change )

Twitter picture

You are commenting using your Twitter account. Log Out / Change )

Facebook photo

You are commenting using your Facebook account. Log Out / Change )

Google+ photo

You are commenting using your Google+ account. Log Out / Change )

Connecting to %s