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  • Hey, I'm Zach,

  • and I'm getting worse.

  • About eight months ago, I got diagnosed with ankylosing spondylitis,

  • A.S for short.

  • But in reality, it's something that I've been dealing with for over ten years.

  • The short of it is that I have bone growing where bone shouldn't be.

  • If left untreated, I would just become one giant stiff bone body man.

  • Sounds cooler than it actually is.

  • It's an inflammatory disease that causes me a great deal of pain and, often, keeps me from sleeping at night.

  • Not sleeping leaves me fatigued and in just this constant fog.

  • Symptoms get worse any time I'm immobile for a long period of time.

  • So sitting at my desk, laying in bed.

  • Airplanes is a big one.

  • Oh, sorry, excuse me.

  • It f*cking sucks. It sucks.

  • I'm living with a baseline of pain every single day,

  • to the point that I forget what it's like to not hurt... somewhere.

  • Eight months ago, I got language to explain the chronic pain that I had been feeling.

  • But this video is not about my diagnosis.

  • It's about everything that's happened since.

  • [i'm getting worse]

  • So I started my medication and for a few months,

  • life was incredible.

  • I was able to sleep throughout the night without waking up in pain.

  • I wasn't stiff throughout the day, my body felt safe.

  • During this time I was instructed to keep up with physical activity,

  • *laughing* "Bowie!"

  • but as the months passed,

  • I got a little lax.

  • F*cking sue me, I got lazy.

  • I figured you know, I don't hurt every day anymore,

  • so maybe it's okay if I missed exercising this week to stay late and edit or you know,

  • it's okay if I spend the whole weekend on the couch being a lazy sack of sh*t cause that's what normal people do.

  • But I'm not normal.

  • Not anymore.

  • Like with any invisible illness, I look okay-

  • at least I think, I think, I think I look okay.

  • But it's a bizarre experience because it's it's just that. It's invisible.

  • You feel like you're deteriorating on the inside, but you have nothing on the outside to prove it.

  • So no one can see you getting sicker.

  • You can't see yourself getting sicker.

  • I started waking up again in the middle of the night.

  • At first confused, and then as the weeks went by, a nagging discomfort, then a pain.

  • I was distracted, I was upset.

  • I was back to where I was eight months ago.

  • I was in pain all the time,

  • but still with all that evidence screaming in my face,

  • I was back to the same old bullshit of not accepting my own reality.

  • Why? Why?

  • Why?

  • The truth is--

  • the truth is I started ignoring my disease the second I could,

  • the moment that my medicine started working.

  • I stopped paying attention to it. I stopped researching it.

  • I didn't want to know more about my A.S.

  • because the more that I would learn, the more I would have to accept that this is now a part of me.

  • This is now a part of me.

  • And that was a huge f*cking mistake.

  • Yesterday, I had the worst flare-up I've ever had in my life.

  • My neck felt swollen. I had a horrible headache, my body hurt.

  • Um, today, even worse.

  • So I'm laying on,

  • Cassie Mobis peas, Keith's Eggo waffles, and real ice.

  • I have my little setup right here.

  • [Keith] Do you feel like it's worse than yesterday?

  • Yeah, it's worse than yesterday.

  • My back is stiff,

  • my neck is stiff. I...

  • This whole week I haven't been able to sleep.

  • I'm afraid that I'm just gonna keep getting worse.

  • It's so easy to normalize the pain and just think like yeah, this is,

  • how I feel.

  • I don't want to do that anymore.

  • So it was time to go back to the doctor,

  • finally ready to accept and confront my symptoms,

  • and ready to attack this sickness head-on,

  • and-

  • he said I was fine.

  • My inflammatory markers were still low,

  • which means that the medicine was-

  • the medicine is still working, which meant that I'm okay.

  • And so I had to go home, uh,

  • wondering if it was just all in my head.

  • But then, I thought about you.

  • After my first video on A.S, I got a ton of incredible emails,

  • some people who found out that they also had A.S,

  • or some who just discovered they had a different autoimmune disease,

  • others who just had that something in their lives that they had been ignoring for far too long and decided,

  • it's time to do something about it.

  • Your emails made me realize that if I'm gonna talk the talk, I gotta walk the walk,

  • and so,

  • I decided to make my health a full-time job.

  • Physical therapy twice a week.

  • Yoga and stretching, first thing when I wake up, and last thing before I go to bed.

  • Long walks with Bowie every single day instead of letting someone else walk him for me.

  • And exercise, especially on the days that I don't want to.

  • Accepting that, sometimes, being late to work in the morning is a necessary component to my health.

  • Realizing that I need to push things to make room for physical activity in my life.

  • Learning to close the laptop at the end of the day, get off my ass, and go outside.

  • Experimenting with autoimmune diets and natural sleep aids.

  • Listening to my body, and hearing what it has to say.

  • And after all that?

  • I feel okay. *laugh*

  • I feel okay.

  • I still have a baseline of pain, most days.

  • I have days where I'm stiff. I have flare-ups.

  • Some days, I just don't sleep, and the fog is certainly not entirely gone.

  • And in truth, I don't know that I'm ever gonna fully be a hundred percent again.

  • But I am done ignoring my pain.

  • I'm sharing this all as a way to show that,

  • treatment is not an upward trajectory.

  • It goes up, and it goes down, and with luck, it goes back up again.

  • It's a bumpy f*cking road.

  • I have A.S. for life.

  • There's no day where I get to ignore my treatment or stop my physical activity.

  • This is it. This is it.

  • This is my life. But this is my responsibility.

  • And how I respond now decides the rest of my life,

  • and I decide that I'm gonna kick its f*cking ass.

  • That I'm going to continue to prioritize myself and my health.

  • That this is not going to stop me from doing the things that I love to do,

  • and it sure as hell is not gonna define me.

  • Cause also it's a stupid sounding disease. It's Ankylosing Spondylitis. It's a dumb name.

  • I'm not trying to demean it, but like...

  • I've got a lot of life to live and,

  • ain't nothing gonna hold me back.

  • So,

  • my name is Zach and,

  • I'm getting worse.

  • But I'm also getting better.

  • "Eugene, can you open this for me please?"

  • Eugene: "This does not affect your fingers."

  • (Keith laughs)

  • Eugene: "You're just making me do this cause you like-"

  • Zach: "Can you feed me?"

  • Eugene: "See?"

  • Keith: "Is the seaweed helping?"

  • Zach: "Mhm."

Hey, I'm Zach,

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