When Try Guys member Zach Kornfeld announced he has Ankylosing Spondylitis (AS) in September 2017 I was so relieved.
I know what you’re thinking. Relief sounds super self-centered, so let me say right now that I was also really sad for Zach’s diagnosis; I wouldn’t wish Ankylosing Spondylitis on my worst enemy. But when you live with a common-but-unknown disease, awareness is what you live for.
Well, it’s what I live for anyway. And when a celebrity makes an announcement a lot of people pay attention.
Zach’s video marked the second “Ankylosing Spondylitis coming out” by a celebrity figure in two years (Dan Reynolds announced his in 2015) and it made a big splash in the AS community. Spondylitis Twitter was buzzing. Spondylitis Facebook and Instagram were buzzing, etc etc. It was exciting to see someone talking frankly about AS to a really large audience (as of April 27, 2018 the video had nearly 4.9 million views). Zach was telling all our stories by telling his own and we clung to this moment as a chance to be seen and heard.
Here, let me lay this out for you better.
Ankylosing Spondylitis is an immune-mediated inflammatory disease that can progressively damage joints in the body, especially in the spine, and in some cases cause the spine to fuse into a column of rigid bone. Additionally, AS is a systemic, or whole-body, disease; so it can cause fatigue, cognitive impairment, sleep impairment, and damage multiple organs in the body. There is no cure, so the goal for treatment is to reduce inflammation to slow the progression of the disease and manage symptoms.
Many of us who have AS had never even heard of the disease before a doctor sat us down and opened their mouth to a flood of slow motion gibberish, “You have A n k y l o s a u r a s d i n o s a u r S p o o n d a c t y l a u r u s B l i b b i d y B l o p p i d y B o o.”
Then, as if our disease isn’t hard enough to pronounce, our own friends and family struggle to even understand what we’re experiencing and that it’s serious. And a lot of general practitioners have already forgotten the one paragraph about AS they read during medical school. There are even rheumatologists (the specialists who treat AS) who refuse to diagnose women. More about that another time.
And yet AS affects so many people. Ankylosing Spondylitis falls under an umbrella of diseases called Spondyloarthritis, which affects an estimated 2.7 million people in the USA alone. That’s more than Amyotrophic Lateral Sclerosis (ALS)/Lou Gherig’s Disease, Multiple Sclerosis, and Rheumatoid Arthritis combined. Estimates vary regarding the number of people specifically with AS in the US, but it is the most prevalent type of Spondyloarthritis. That’s a LOT of people.
There are more people with ankylosing spondylitis in the USA than there are Episcopalians.
Just, fyi.#spotspondy #spondywhat
— BeingCharis (@BeingCharisBlog) April 26, 2018
I wish nobody had AS, but since a lot of us do and we largely suffer in silence, Zach’s video was cause for celebration – not for his being diagnosed, but for his willingness to talk about it in front of millions of people.
When I saw his video I knew I wanted to help his story reach more people. I knew I wanted to talk to him.
So six months later I reached out to him about a chronic disease documentary I’m in (shameless plug) and it turned into a Skype interview.
And we ended up covering so much material I decided to make this a two-part blog post.
First of all, during the call it was quickly apparent that Zach had already mastered the pronunciation of the word ‘ankylosing,’ so half my job had already been done for me.
By the way, here’s the correct pronunciation:
Second of all, in real life he’s the same as he appears on video: animated, sociable, witty, and, well, he jokes around a lot. I mean, a lot. He’s a Try Guy for real, it’s not just a character he plays. Well, I guess he plays himself. And while I came prepared with the questions I thought I wanted to ask we ended up relaxing into a conversation about both our journeys.
I just want to say, as an Ankylosing Spondylitis writer and advocate I’ve interviewed one other person about AS – Dan Reynolds – and in that situation I was a journalist; my story was the reason I was there but my having AS was nothing more than a side story. With Zach, though, we spent considerable time comparing our experiences and learning from each other – Zach’s not even a year into his diagnosis, so he had a lot of questions for me too.
Zach’s Story’s Impact
You can best learn about Zach’s diagnosis story from his vlog announcement. I hope you’ll watch it (10 minutes) so the rest of this post will make sense.
It’s helpful at this point to understand a common theme in The Try Guys’ work. The way Zach describes it:
“People can watch our videos and be like, ‘Oh, these are just guys who do crazy shit,’ but, the crux to what we’re doing is we’re trying to connect to people’s identities and their passions… We do things that are real to real people’s lives and either help people see themselves or help people reach out and communicate ‘This is who I am,’ by inviting us in and allowing us to experience their lives with them.”
He continued, “We had been wanting to try the vlog format [to] break down the barriers and reach out directly to the audience and let them into our lives a little more directly.”
Zach was the first Try Guy to test the vlog idea and it turned out that sharing his personal story got to the heart of the Try Guys’ mission, evidenced by the overwhelming response to the video.
Zach said, “It’s not the most-viewed video I’ve ever done, but um, it is certainly the most impactful, …just the amount of responses. There were some who said ‘Oh my God, I found out I have Ankylosing Spondylitis because of you, so thank you.’ Hearing me describe my symptoms made them realize, ‘Wait, that’s what I have.’”
Others told him they had been living with depression and because of his video they could finally acknowledge it.
Now I, Charis, have a confession. My life is so radically centered around raising awareness of Ankylosing Spondylitis with the hope for a cure that I forget that raising awareness also means more people get diagnosed along the way. And that’s exactly what Zach’s video did – it helped countless people recognize their own symptoms and seek a diagnosis, and many of these people thanked Zach for being the reason they finally got an answer whether they were diagnosed with AS or a similar disease. One of these stories in particular stuck out to Zach and to me:
“I got this one email from this trans high schooler who was getting bullied by all of his doctors, being told to lose weight and that was the only reason that he was, um, going through pains because he just wouldn’t accept his body. And he found out he had Ankylosing Spondylitis and Lupus and it was because of the video and I just had a cry session in my apartment by myself.”
Which leads me to the next thing. What it means to be diagnosed.
Something we discussed in more detail was how validating it was for Zach to be diagnosed. Finally he knew what was wrong with his body. Having an answer was everything.
He went from this (pre-diagnosis Zach):
“I was a zombie in my own skin – like, I was like an alien guest wearing my own skin, where it’s like…a weird sleepy simulation of what it’s like to be Zach.”
“There were days where it was bad and then there were weeks where I wouldn’t feel it. So there was a lot of doubting my own reality of not being quite sure what this thing was – and I didn’t have a language for it. The pains that I was having didn’t seem to match up with anything I knew of.”
To this (post-diagnosis Zach):
“I honestly think it was the biggest relief I’ve had in my life… I don’t say that to belittle the seriousness of it. It’s just this, I thought I was crazy. For the longest time I just had this pain and I had no explanation and I couldn’t even trust myself that it was real pain. So, getting a diagnosis to me meant 1) That I was right, and I knew what was going on [in my body] and 2) Now there’s a path, right? Because before I was just in darkness, and every single direction looked the same and it all looked painful. So, the diagnosis for me meant the hope for a way out. It meant that it came with medication, it came with a set of predictable symptoms and actions I could take, it meant there are other people that are going through the same thing and I could lean on their knowledge, and yeah, it meant things like targeted physical therapy….and yeah, I guess now I’m looking for the end of the sentence. It was the difference between keeping living and not. It was the difference between having a next step and continuing to live in uncertainty forever.”
This is a common theme in the AS community – so many people feel such relief when they are diagnosed because they finally have answers and options, just as Zach said: “It was the difference between having a next step and continuing to live in uncertainty forever.”
Ankylosing Spondylitis has an average delay of diagnosis of 8-11 years. Zach and I both had symptoms starting in middle school or earlier and we were both diagnosed when we were 26. That’s 13+ years of suffering and doubting our own reality.
Here’s where my story takes a different path. For me, getting the diagnosis wasn’t a relief. My dad had AS and I grew up watching his back curve forward more each year and in the end he looked like a walking question mark – his face was horizontal to the ground and his spine was one column of inflexible bone perpetually lurching forward. Growing up I’d been told AS was a man’s disease, so I wasn’t too worried about getting my dad’s disease (we’ll talk about genetics later). So when I was diagnosed I was absolutely devastated. All I could think about was becoming just like my hunchbacked father.
FYI – AS is most definitely NOT just a man’s disease.
AS Never Goes Away
But enough about me. Back to Zach, who admitted that after beginning treatment for AS he started slacking. And it didn’t take too long for AS to remind him to pay attention:
“I was like great, I have medicine, the medicine’s working. I don’t need to learn more about this disease; I don’t really need to think about it. I just give myself a shot – done. I made that video… It was reaching people and I helped some people and I was really proud of it. But if I’m being completely honest, I stopped thinking about it. Um, and then it started getting worse.”
“The pain started coming back, you know, just like a day or two at a time. I use this metaphor where if you drop a frog in a pot of boiling water it’ll jump right out. It’ll say, ‘You’re trying to kill me!’ But if you put a frog in water and slowly increase the temperature it’ll sit there until you boil it to death. That’s what happened to me the first time and it’s what started to happen the second time.”
Now nearing his one-year anniversary with the diagnosis, Zach’s still learning about the permanence of AS and the fact that it’s always there beneath the surface even when the treatments are helping. And he’s recognizing that he has to pay attention to any changes before things get out of hand again.
For everyone I’ve talked to, AS becomes a job for those who have it – a balancing act for the rest of their lives marked by periods of notable disease flare-ups (for many) and, for others, periods of disease inactivity. It’s important to note here that Ankylosing Spondylitis is incurable and affects everyone differently, so Zach’s AS will not be my AS will not be your AS.
And that’s where I’m going to leave the conversation for now.
Ready for part two?
That was getting really interesting, wasn’t it? I can’t wait to share more soon.
In part two, I’ll share Zach’s approach to living with AS and dive deeper into his decision to announce his diagnosis on YouTube, plus talk about what advocacy looks like to both of us. And I’ll also share his exclusive message to the AS community. Oh, and perhaps there’s a mention of Stanley Kubrick as well.
In the meantime, what’s one question you would ask Zach? Put it in the comments below.
Learn more about Ankylosing Spondylitis and Spondyloarthritis from the Spondylitis Association of America by clicking here.
Be sure to follow my blog below (keep scrolling to the bottom) so you are the first to know when I publish part two!
Please consider supporting my blog and advocacy with a Ko-Fi (Coffee): ko-fi.com/beingcharis (that’s a fancy way of asking for a $3 tip)
14 thoughts on “I talked with Zach, the Try Guy with Ankylosing Spondylitis (part I)”
My daughter is 32 she was just diagnosed about 4 years ago and has had AS since she was 19,thats when the pain started. She is such overweight and Is always in pain. I don’t know what exercises are good for her. She needs surgeries for all of her extra skin but we can’t afford it. She is on a biologic but i feel she needs more help.
Hi Judy, thanks for your comment! If your daughter would like to find more resources to help her manage AS, she can visit Spondylitis.org. There’s a plethora of information!
I have been recently diagnosed with AS I am a 48yr old woman. I have suffered for over 20 years with this disease. There have been good and bad at times with it. My kids showed me Zach’s videoes and it helped to just explain what he was experiencing. I related with so much of what he was saying. I am 1 month in with the shots. I work fulltime. I have 3 teenage kids and a disabled husband. I didn’t have time to suffer but none the less I am. This has given me hope but still scares the crap out of me. Thank you both for all you do. PS. I never leave a comment.
Carrie, I feel so honored for you to have commented on this post! Thank you for sharing some of your own story, I’m so sorry for all you’ve gone through and the difficulty I’m sure you experience as the full-time worker and supporter of your dear family. How great that your kids are a big part of your journey into understanding this disease and feeling less alone. Please keep me posted!
Thank you for all you do!! Your blogs are an encouragement to me. I realized that I have an AS Familia and it has helped me through this journey. My name is Marlen and I have an AS family. I am not alone!! Thank you Charis, Dan & Zack!
Hi Marlen, I’m so glad my blog is helpful for your journey with AS. You absolutely do have an AS familia!!
This was very inspiring. My name is Shannon and I was diagnosed with AS at the age of 16 years old. The difference with my story is now that I’m about to be 28 years old I’ve realized I been in denial of my condition because it was always listed UNKNOWN for the cause. I’ve always believe and sort of still believe it was cause by a major accident that happened in my life as a kid. For 12 years I’ve tried medication like embral, humaira and now remicade. Lately I’ve been thinking about telling my story but just don’t know how. Thanks again for this.
Shannon, thank you for sharing a piece of your story here. That’s the first step!!! The biggest thing I have learned is that no one can tell my story better than I can. I hope you’ll do some more exploring on my blog or other blogs for inspiration to begin sharing more about your journey with others. Send me an email to tell me how it’s going!!!
Thank you so much for this post, and for sharing this video. It’s just so beautiful and helpful for those of us suffering, particularly suffering without a diagnosis which is where I am. I’ve been doing a bit better lately in terms of my primary symptoms which always makes me doubt myself (again) and it is so refreshing to hear people talk about this who get it. I have an appointment in a couple weeks, one of my doctors referred me with a particularly potential diagnosis/avenue for exploration in mind, so I’m really hoping it holds answers. I really want that validation and those next steps. (Of course, the big appointment would happen at a time where I’m in less pain… because that’s how life works.)
Good luck Cole, I really hope you get answers soon! Please feel welcome to report back here when you find out –
LikeLiked by 1 person
Just wanted to update you that the appointment was a little mixed, but did seem to hold at least the beginning of a diagnosis. I quite clearly have at least Hypermobility Spectrum Disorder, and it seems less clear whether or not I have hypermobile Ehlers-Danlos (this at least explains a large subset of my symptoms). I am mostly just happy to have validation and be able to feel like I can join a community.
Thank you for all of your advocacy, your writing, your support! I have been following your blog for a while now and find it so wonderful.
How do you cope with being a public figure and having to ‘perform’ at a time and not having much control over that? I’m a musician, and there are days where studios are booked, shows are scheduled, etc. But because of the pain I have to stretch every hour.
LikeLiked by 1 person