Good Life Project - How to Live with Invisible Pain | Samira Rajabi
Episode Date: July 15, 2024Ever felt weighed down by invisible pain or chronic illness nobody else can see? In this powerful conversation, trauma specialist Samira Rajabi gets refreshingly candid about her own decade-long journ...ey navigating conditions like a benign brain tumor, headaches, and hearing loss.Drawing from her book All My Friends Live in My Computer: Trauma, Tactical Media, and Meaning, Samira shares coping strategies for the daily struggle of invisible suffering. Discover mindset shifts, tactics for reducing stigma, and insights into radical presence despite inescapable pain.You can find Samira at: Website | Instagram | Episode TranscriptIf you LOVED this episode you’ll also love the conversations we had with Sean Mackey about the science of pain.Check out our offerings & partners: Join My New Writing Project: Awake at the WheelVisit Our Sponsor Page For Great Resources & Discount Codes Hosted on Acast. See acast.com/privacy for more information.
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We pathologize things and we narrate things as like good things or bad things.
And pain is a bad thing.
But like by narrating it as bad, we disallow ourselves from like just letting it be, just letting it be there.
The pain is not forever, just like nothing is forever.
And like maybe it'll get worse, but maybe it'll get better. And that maybe, that little bit of like possibility that like, or maybe I'll just get better at letting it be.
And that's the thing that happened.
I got better at letting it be.
And it's like, it just feels like magic.
So have you ever felt like you were carrying around an invisible weight, pain, discomfort, or struggle that no one
else could see. Something that made even the simplest daily tasks feel overwhelming at times.
For many of us, the experience of invisible pain, it's all too familiar. Yet it often goes unspoken.
We put on a brave face and power through hiding our suffering from the world. What if there was another way,
a path to make that invisible pain more visible, even if just to yourself or to those closest to
you, or a way to navigate it and experience it with more ease, even if no one else knew what
you were moving through. My guest today is also a dear friend, Samira Rajavi. She's a PhD in
researcher in media studies with a specialty in
trauma, digital media, and meaning making. A professor and author of the award-winning book,
All My Friends Live in My Computer, Trauma, Tactical Media, and Meaning. And she's also
a public speaker who helps others find a lot of light in life's darkest moments.
But here's the other part of Samira's story, the one you won't often see. She has been
walking a path of chronic pain, debilitating headaches, and an eventual diagnosis of a benign
brain tumor that's led to multiple surgeries, hearing loss, and a range of physical pain
that exists to this day, all invisible to the unknowing eye. And yet it's a part of her existence,
something she dances with every day, even as she
raises a young daughter, teaches her students, speaks, conducts research, and writes. In today's
deeply vulnerable and real conversation, we explore what it's like to live with invisible pain.
How, when, and why to maybe make the invisible visible. We talk about embracing the uncertainties
of life and finding presence even in the midst of
persistent pain. And Samira opens up about the pressures that often come to appear high
functioning despite a lot of inner turmoil and suffering and how she's consciously created
spaces for herself and for others to show up as their full authentic selves and to stop hiding struggles and all.
And I share a bit of my own journey with my own invisible pain along the way.
So get ready to explore what it really means to live a good life when invisible pain is a part of your daily reality.
So excited to share this conversation with you.
I'm Jonathan Fields, and this is Good Life Project.
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Mayday, mayday. We've been compromised.
The pilot's a hitman.
I knew you were going to be fun.
January 24th.
Tell me how to fly this thing.
Mark Wahlberg.
You know what the difference between me and you is? You're going to die.
Don't shoot him. We need him.
Y'all need a pilot?
Flight risk.
You and I first met years ago at this point, and we were actually out in Boulder, I think living in New York back then, traveled out here, recorded some conversations. I had caught you on the TEDx stage
in Boulder, I think a couple of years earlier, and was kind of mesmerized and blown away by you and
your story and wanted to go deeper with you. And we have since become good friends. And we were
talking recently about this experience that I think
so many people have, especially if you're fortunate enough to sort of like move into
more seasons of your life, we go through changes. And some of those changes are awesome.
And some of those changes also, they hit us in different ways. And I was recently having a
conversation actually with Sean Mackey, who's one of the
head pain researchers at Stanford, who's also now one of our recent guests on the podcast.
And we went into a lot of the ideas around pain, what it is, what is the circuitry of
pain, what's the psychology around pain, what happens in the body, and also this sort of
a, I guess what he would describe as a
multimodal approach to it.
And the conversation, I think, was really valuable to me in understanding it because
at my age in this season of life, I feel it, and really understanding what's going on,
what's not going on, and how to think about it.
But there was this sort of question that there was a thought bubble that was building in
my mind as we were having the conversation that I never got around to asking.
And it's something you and I have talked about a little bit, but it's also something that I know that you have had a lot of experience really trying to understand and navigate and walk through on a day-to-day basis.
And that's this experience that I also would imagine a lot of our listeners deal with on a daily basis too.
And it's this notion of, I don't know exactly how to describe it other than calling it something
like this experience of discomfort in our minds, in our bodies, hearts and souls, sometimes
all at once, that we feel maybe on a chronic level, maybe it varies on a day-to-day basis,
but it's pain that we feel that is not observable from the outside in.
And maybe in part because we keep it from being observable from the outside in.
And that's probably a part of the conversation we'll want to have.
And I've been thinking about it more and more and how prevalent this is.
And when I start to just ask friends about it, they're like, oh, yeah, yeah, me too. And like, but we never talk about it. We never go there. We never understand like,
what are you living with? What are we living through? What are you walking with? And what's
really going on? And I think because of that also, we never share both the experience of it.
We also never share how we move with it. So we were talking about this recently. I said,
let's have an open conversation about this because this has been a real part of your life experience for a solid
chunk of years now. So before we kind of get into the details of that, I think it'd be really helpful
for you to share, if you're okay, the sort of like the story of what you've been navigating for the last five,
six, seven, eight years and how it's changed you.
Yeah, it maybe even starts a little bit before that because thinking about pain, especially physical pain, which as we know, walks alongside the emotional, spiritual,
other pain.
I started feeling it really routinely when I was about 15 or 16
in what they thought at the time were migraines. And so they diagnosed me with migraines and gave
me medications for migraines. And I'd gotten an MRI at the time. And what we found out 10 years
later was that the brain tumor that I ended up getting treated for, which was a benign brain
tumor that grew off my hearing and balance nerves was there. It was just
small and it was missed. And so that's probably what was causing the nerves to misfire and cause
all this pain. And so that's why the treatments weren't working. And that's why every day around
2 p.m. in French class, when my nerves would start to get taxed from listening and balancing and
moving through the world, trying to act like I wasn't feeling a
little wonky. I would just come down with these like debilitating headaches and my teachers knew
and they would let me put my head down on the desk or go to the nurse's office.
So it started when I was young, but I didn't understand it. So I just learned to medicalize
it really efficiently, to throw more medicines at it, to try to solve it,
to try to fix it rather than try to figure out the problems were to either solve them or learn
how to kind of like cohere with them and live with them. So fast forward 10 years later, I was 26,
fell down on my way to class. I was in grad school and literally thought someone shoved me, turned
around ready to like throw punches. I was like, and you are, and then ended up getting an MRI,
getting all these tests on finding out that I did have like a pretty large at that point tumor and
ended up getting surgery. I had 10 craniotomies in the next four years. So I had spinal fluid
leaks that was chronic. They're not even sure if they've
fixed it now, but we've just decided like, that's fine. We're going to, we're going to
stop cutting my head open and lived with really severe chronic pain probably until about two and
a half years ago. And now it's still chronic, but less severe. So I've lived with physical pain.
And alongside that comes anxiety and stress and all
these other things. And it's chicken and the egg, what's causing what at any moment, we're not
really sure, but that's kind of my pain history, right? As I remember when we first started batting
around the idea of having this conversation, it was funny because it was a text thread and it felt
like you were pretty lit up
about actually like, can we have this conversation in a public way? Because of what you've been
through, it's taken a lot of both bandwidth, but also you've had years now to really explore like,
what is this? What isn't it? How does it affect me? And what do we do with this? Which is,
I think, unusual. Yeah, I think I am lit up about it
because one of my favorite disability scholars is this person, Simi Linton, and they say that
the disabled body is asked to be, I'll never forget these two words that they use, plucky
and resolute, right? Plucky and resolute. And I think I'm just so tired. And some days when I
think about what I'm exhausted about at the end of the
day, it's not the work. It's not taking care of my 15 month old. It's not taking care of
graduate students at work. It's not the writing. It's holding it together to perform like I'm
fine the whole day through being plucky and resolute. Even when I'm somebody who doesn't really believe
we need to do that, we do it all the time. And so I am lit up about it because even just before
we started recording, when we ask each other how we're doing, we're both like, yeah, we're good.
Good. Fine. Right. Where it's like, why aren't we, why aren't we saying like, I'm working on good.
I want to tell you that I'm good.
But I woke up and my shoulders were glued to my ears and they were tense and crunchy in my bones.
And it made me feel sad, but I'm so glad to be here with you anyway.
Yeah, it's such an important conversation that we just don't normally have.
I want to round back to sort of your story and explore these ideas more.
But I'm also curious because, as you mentioned,
so you teach at the university and mostly grad students from what I remember.
But you've been teaching for, you know, like enough time now.
And you've also seen sort of like how students have navigated the last chunk of years.
What are you seeing showing up in sort of a younger generation around these experiences?
You know, I see a mix.
I had the privilege of teaching all of our freshmen at our media college right after
COVID.
And so that's 300 students.
So you don't often get to know a lot.
But the ones you do get to know are the ones that either come to you and say, like, I have these things going on in my life and I need accommodation.
So here's my letter and here's the support I need.
And they're super open about it and they're super comfortable with themselves and what they need.
And then on the flip side, the ones you meet are the ones that are trying to perform past any kind of help or support that they need. And when you actually get through to them and start
talking to them, you realize that they're deeply anxious about showing any kind of weakness.
And so we are seeing like a little bit of a shift in people being more comfortable,
but we're also seeing this sort of quick return back to hiding away any kind of weakness or
illness or sickness or disability or need for
help. That's just causing people to be super anxious. I had a student come to me and say,
Hey, I, I'm a soccer player and, and I got hit really hard in a game and I have a concussion.
And she was in person talking to me at the beginning of class. And I was like,
why are you here? Yeah. What are you doing? Why are we having this conversation face to face?
I didn't want you to think that I was bad.
Not a bad student, not a lazy student,
not all of these things we might ascribe to that.
I just didn't want you to think I was bad.
And I was like, why would I think that you're bad
for taking care of yourself?
Well, because you calculate attendance. And I was like,
I mean, kind of, but not for what? No, we don't let ourselves be human. We feel like we have to
be these endless productivity machines. And I was like, go home. And with tears in her eyes,
she was shaking. She's like, but I can't. I'm a good student. And I was like, I'm not sending
you home because you're a bad student. I'm sending you home because you're a beautiful person that
deserves to rest when your body is asking for rest. And that conversation for me has stuck with
me because it's like, even in a generation that's so much better about bodily self-awareness and care, we are seeing students
come up and say like, my value is based on how I show up and how I perform. And so even when
something legitimate has taken my ability to do that, I refuse to let that show. And I just want
people to like be in the space. You're not going to learn anything if you're sitting there with a concussion anyway.
Like live your best version of yourself when you are able.
Yeah.
Where do you think that this standard, and you're describing it in the context of, you know, like an undergrad student in college.
But the reality is like we all still have it.
There are very few people that I know
have fully embraced this notion that,
oh, I get to rest when I need to rest
and I get to take care of myself
when I need to take care of myself.
We still perpetually show up.
And I would imagine it actually just gets worse and worse
as most of us progress through life
because then you pile on.
It's not just the quote, I want to be a good student. I want to be a good parent. I want to be a good employee. I want to be a good leader. I want to, I'm rising up the ladder of whatever this vision of success that I had, you know, like described for myself earlier in life is, or was handed down to me. Like this is the path. So it's almost like the stakes keep raising higher and higher. And as much as you
can tell somebody, it's okay to take care of yourself. It's okay to be the way you need to be
and also share that experience when needed, because it's part of the way we take care of
ourselves. We still don't like it. And you're describing this in a young student. I would
imagine we could have a version of that exact same conversation with people we know in their 30s, 40s, 50s, 60s, 70s.
It persists, like just on and on and on.
What do you think that's about?
I think it's about so many things.
I think one of the things is I think our fear that we will get left behind kind of like this. One of my favorite, she's a feminist
disability scholar is named Rosemary Garland Thompson. And she says that one of the reasons
we fear disability so much is because it's something that's going to eventually happen
to all of us. And it's also something that reminds us of our mortality and our kind of like fallibility as humans.
And I think we're afraid to get left behind, to get left out, to be ignored, to be less than.
I think it's also kind of this like churn of late stage capitalism. learn to equate our value as people into how much we do, how much we accumulate, how much we produce,
how efficient and effective we are at doing all of that. I'm really good at telling my grad students,
especially, to put boundaries on the work and go home and rest. And I'm okay at that in theory,
right? I don't work when my spouse is not working. I make sure to be super present with my kid.
But when I put her down to bed, I'm usually met with two options, right?
Rest or clean the kitchen and vacuum the house and do all the dishes and make everything
perfect and pristine and get everything ready and don't ask for any help doing it.
And I usually pick that one.
And then if I don't, I have found myself asking my spouse, like, am I bad? Like, literally,
am I a bad mom? Am I a bad spouse? And he's like, what are you talking about? You're always telling
everybody to rest and relax. But it's so ingrained in me, this idea that like to be good, we have to
be doing good for others at all times and producing and successful and financially stable. And it's so
much pressure that something that might make us feel weak or scared or vulnerable, like pain,
we're not going to share that because that's just going to
get us cast aside. And we don't want to be cast aside.
No, that makes so much sense. You've used the word disability a couple of times and referenced
a number of disability scholars. The question in my mind, and I don't know if this is sort of like
generally accepted, do you see as being falling sort of like under that umbrella of disability? it is to be human and we should stop seeing like normal bodies and disabled bodies and things that
remove us from this ability to hold on to that construct of normal our disabilities but rather
than thinking about what that might foreclose on for us like what might that enable for us and
understanding ourselves and our humanity and our vulnerability and our ability to understand then
other people's kind of unique bodily experiences. So for
me, there's kind of like an important politics to it, but it's also about recognizing that like
normal's this made up trumped up idea that we all were told at some point in our life that we ought
to try to grapple towards, but like really that's never been real. It almost, it creates in it, like a quote in and out group.
Like there's, if there's a clear divide, it also creates a,
I don't want to use the phrase, but it's like,
I think it's the patterning that we have, like the aspirational group.
Like, you know, like that, what,
that capital N normal is the group that you should ascribe to be a part of.
Whereas like what you're describing is actually now,
like we all fall along a spectrum, ability and disability. And that spectrum, we're going to,
like, we're going to dance along all different parts of that for the entirety of our lives.
Some people in very different ways at different times. But at some point, if you're fortunate
enough to live long enough, you're going to find yourself sort of like increasingly on one side.
It's just the way things are. Like that's life. And rather than saying, oh, I've hit that point
or I've crossed the threshold and now I'm quote like disabled. What if we just looked at it as
we're all living in our bodies, doing the best we can. And that's actually okay. It is interesting.
I think people have such wonky and uncomfortable feelings around the word and the notion. But it's important which I'm now completely deaf in my right ear, right?
And they kind of used the language of disability.
I felt my whole family kind of bristle, like, oh, she's not disabled.
Look at her.
She's fine.
She's perfectly normal.
No one will ever know.
She'll move through the world.
She'll be fine.
And I had this moment where I was like, or maybe I won't be, right?
But maybe that's fine.
Maybe that's what has to be fine, right? But maybe that's fine. Maybe that's what has to be fine, right? Like one of the things
I came up against when I first got sick was that not only did I want to get better, I wanted to
have this superhuman response to it. And then I learned that there's actually a name for that,
right? Like when somebody is crippled either physically, emotionally, mentally through illness and then wants to
overcome it, not only are you being asked by society, by yourself, by your own kind
of constructs you've bought into to overcome it and go back to normal, but then overcome
even that normalcy.
And they call it the super crip, right?
Like I didn't want to just get better.
I decided like I literally Googled after I got better. I decided like, I literally Googled
after I got sick, I'm in the hospital bed Googling hardest workout on planet. That's what I Googled.
And it was like CrossFit. And I was like, all right, I'm a CrossFitter. And the doctor comes
in and I was like, all right, when am I cleared to exercise? And he was like six weeks, six weeks.
And one day I was in a CrossFit gym. Was it a mistake? Yes, it was. I got hurt. I got more surgery. But what I was trying to do was be this super crip to overcome not just the illness that made me feel vulnerable, but any kind of question that I might not be absolutely amazing in every way, rather than recognizing that like,
wow, my experience and my ability to cohere with it and the way I navigated it and the grace I
brought to myself and my family through it and the way I learned with it, that's what's incredible.
It's not being more normal or like super extra normal. I don't know.
It was like a weird thing to do, but it was just empty in the end.
Yeah. I would imagine it's probably not an atypical response also.
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Mayday, mayday. We've been compromised.
The pilot's a hitman.
I knew you were going to be fun.
January 24th.
Tell me how to fly this thing.
Mark Wahlberg.
You know what the difference between me and you is?
You're going to die.
Don't shoot him, we need him.
Y'all need a pilot.
Flight Risk.
It's interesting, you mentioned your family as part of their response was,
you know, like, no one will ever, like, no one knows this or no one will ever see it.
Like, it's, which brings us back to sort of like the conversation around invisibility,
you know,
because whether it's disability pain as a subset of that,
I wonder if there is a sort of a qualitative difference between something
that is where you move through life and it's observable by other people.
You don't have to announce it.
You don't have to describe it.
You don't have to say,
Hey,
this is what's going on with me.
People may still,
it may cause a whole bunch of like series of additional other challenges
or social issues and things like that.
Versus when you know internally, you're living with something, you're moving through each
day with something.
But unless you tell somebody, they'll have no idea.
When I was a kid, I was a gymnast.
I was a competitive gymnast.
And I've had, I've learned later in
life that there are things in my body that tend me towards inflammation and towards chronic pain,
especially in it. It's shown up in my joints for more or less my whole life. I also trained as a
competitive gymnast until I was about 20 years old, year round, about the worst thing I could
have been doing for the way that my body is stacked. So I was in pain nonstop.
And it got to the point where my wrists were often so painful.
But if you looked at me walking down the hall, I was in great shape.
I was a gymnast.
I was like, you would never know unless I said anything.
But it was weighing so heavily on me.
I knew I was in pain.
I knew I was carrying this.
It's funny.
This certainly just popped into my head. I started wearing, I started wrapping my wrists with ACE bandages during the day. So that, cause I couldn't figure
out as a kid how to handle the internal and like the conversation around, and I kind of wanted
people to know I was in pain, but I didn't want to go up to them and say, Hey, I'm in pain.
So I use this sort of like mechanism to make this invisible pain observable to others. And they'd be like, hey, what'd you do?
Did you hurt yourself?
I said, yeah, you know, like a gymnast, like just like blah, blah, blah, whatever it is.
There was a part of my body that was almost perpetually taped or wrapped, like almost
every day when I was a kid.
And in hindsight, I've like, I've realized I'm like, I don't really need the structural
support of those things.
What I was really doing was trying to figure out how to make this thing that I was carrying
internally observable in a way that I could somehow tell people I'm suffering without
having to tell them I'm suffering.
And this is when I'm in my teens.
I didn't have, I'm still working on the skills to be able to handle that now in my 50s.
I was completely unequipped.
And I was just trying to make up mechanisms because there's something in me that said,
I want people to know.
And I don't know how to handle this.
I don't even know what the conversation is after they do.
But maybe it'll at least resolve some tension or create some compassion or something so
that I don't have to go around telling people what's happening inside of me,
how I'm suffering. And what's interesting is later in life, even though I carry pain in
different ways, it is entirely invisible to pretty much everybody except close friends if I share
what I'm going through at the moment. So I've almost backed away from the mechanisms of being
able to create an opportunity to share this with people.
I mean, as a kid, right, it's lonely to be in pain. It's really, really lonely to be in pain.
And when we're younger, I feel like we still are okay wanting people to take care of us and like intuit what we need. And that's what you did. You gave people a cue to like, be able to intuit what you might need. And then as we grow up, we feel less and less able to be
like, Hey, someone take care of me. Like someone ask me if I'm okay. I did the same thing in my
twenties and thirties with my pain. I would start carrying ice packs around and like gingerly
placing them on my head so that someone would be like, are you okay?
So I'd be like, I'm not okay.
Thank you for asking because I felt so alone in it.
But you don't want to be the person that like breaks the rhythm of the meeting or the day or the coffee meetup by saying like, oh, hey, I'm in really horrible pain, but I'm still going to try to be here with you. Because suddenly that shifts everybody's reaction to you. And they worry in a way that
we don't learn a language of care really in our culture. And so people do their best,
but they end up making you feel out of place. And it used to make me want to remove myself
from situations. I was in a Zoom
meeting once with colleagues I've worked with for a really long time, right? Colleagues and friends.
And I got a horrible headache and I could feel it kind of like inching up my neck. And I was
kind of grabbing my neck and stretching a little bit. And it was a cameras on meeting. This was
like height of COVID, right? And so I didn't feel like I could turn my camera off. And so I tried to slyly below the camera, like get medication out and like
secretly take the medication without anybody seeing my mouth moving, all of this stuff.
When in reality, as someone who studies this stuff and teaches this stuff, I could have said,
Hey, can we take a pause? I'm in a lot of pain and I need to address it really quick and I'll be right back. Right. But I couldn't even figure out
the language to do it now. I mean, we do this to ourselves and our kids, like our culture from a
really young age. I see it with my daughter, Josephine, all the time when she cries, the
first impulse, even in me, but in grandparents and friends, it's like, oh, don't cry.
And I have to catch it.
And I say like, oh, no, cry as loud as you want.
Let me know how you feel.
Figure out how to tell me.
Tell me you're mad.
Be mad.
Get mad.
Be sad.
Feel that.
That's a real feeling.
We got to feel that.
And I feel like our inability to cohere with that discomfort of
like another person being sad or sick or unwell gets translated in our desire to sort of like
hide it away. But sometimes it's too severe. Like that suffering creates a rupture in us.
And so we do cue people like, hey, this ice pack, this ace bandage, this is my way of being like,
hey, can you please see me in my actual experience,
not the way like we feel forced to see each other all the time.
Yeah. I mean, you bring up another really interesting point, which is in a professional
context, I feel like this really gets like layered because if we were suffering, maybe it's a
migraine, maybe it's a headache, maybe there's some other chronic pain that you're just like, this is a part of your daily experience. And it's not that we don't
want people to know. I mean, maybe there, I think for some, there's a perception that
everything about us is being judged. And if somebody knows that we're carrying this thing,
there's a potential perception of, quote, not being up to the job or being weak, or if it's a tough job with long
hours and we're all on deadline, you're not up for it. You're not capable of it. You don't have
the stuff that you need to have in order to not just do this job or this project, but then
progress further and further and further. And the reality is that may be true. Not that you don't have the stuff,
but maybe you don't in a particular role or job or culture,
but there also may be that perception,
like that thing that you're concerned about,
people may actually be layering that onto you
if they start to see like,
oh, he's got a constant headache
or just this pain seems to really make it
so that he can only work for a couple hours at a time
and then he needs to take a break.
And part of it is this concern that's in our head
that maybe partially is fabricated,
but it's also probably partially real.
Yeah, I, for a long time at work was the,
I mean, they wouldn't call me this,
but I knew I was like the brain tumor girl.
Like I was the person with the brain tumor.
It's what I talked about.
It's what took up my time.
It's what I had to deal with.
Did I do a whole host of other really incredible work
in between all my brain surgeries?
Totally.
Is that what people saw?
Not really.
And I had to work really hard to undo that perception of me
to show that like, that's one thing, right?
I'm many things, but I have kind of a luxury and a privilege that in the kind to show that like, that's one thing, right? I'm many things, but I
have kind of a luxury and a privilege that in the kind of job I have, I can forefront it in a
particular way and not lose my job. I still have to deal with people's perception of me, which like,
I've talked to you about this. I've asked your advice about it. It's not always great. And
they're not always kind about it. And they're not always supportive about it, right? So knowing that I have to stomach that, I still make the choice to go into my classrooms
and with my grad students and with my students to be like, hey, here's the whole host of
things I bring to the table that makes being here in this space really challenging for
me.
But the reason I'm sharing it with you is because I want to offer you a space where
you can be your actual
self and not make you think that the best version of yourself has to be the version of yourself that
hides who you really are. Like in my grad class this last semester, we did check-ins at the
beginning of class, just a few minutes to tell each other how you're doing, what's going on,
who you are, so that we're not just coming into the space
pretending that we're all just like little research robots. We are going to first come in as people
and recognize that people have a lot of things that happen in their life that bring them in and
out of the space, physically, emotionally, spiritually. And then we're going to let that
sit in the space for a minute and then go into
the content. And yeah, it took like 30 to 40 minutes some days at the beginning of class.
It's a two and a half hour class worth it. I think we learned better because then the students felt
able to do their best work. So in me sort of like forefronting my vulnerabilities,
even though on sort of like the administrative institutional end,
it's caused me to be looked at in a way that has caused me a lot of harm and caused me a lot of
pain. I'm still choosing to make that choice to create a shift in the culture that I can control,
the culture of my classroom, so that people might feel safe to let their guard down for a second, because I think we do better work when we feel safe and
valued and whole. And we can't do that when we're hiding pain, when we're hiding the things that are
occupying our mind and pretending that we can just, like my mom, for example, one day I came
into class and she had gotten a PET scan and an MRI of her brain. She
has chronic breast cancer. Like a chronic breast cancer has to stay on her treatment every three
weeks for hopefully many, many years. But the scans are really scary and it had spread to her
brain and it's scary. It's catch the breath from your throat scary. And I had to go teach a class
and I knew I had to go teach a class and I knew I had to go teach a class and I
wasn't going to cancel the class because what was I going to do? Spin my wheels at home? That's not
going to be better. But I went in there and I was like, hey, today I'm dealing with a lot of hard.
So like if you're dealing with hard, you can share it here. You don't have to. If you're
dealing with joy, you can share it here, but you don't have to. But I just want you to know where I'm at so that we can walk forward from this common ground.
That makes so much sense. The experience of making the invisible visible in these contexts
is scary, I think, in a lot of different ways. And we're not taught about this.
We don't have the skills. We don't have the language because we never have this conversation.
Even though literally the experience of disability or pain
is going to be a part of all of our lives at some point,
whether chronic, whether just in moments,
and making that invisible experience visible,
I mean, the way you're describing it also,
as you step up and you say, you know what, I actually, as somebody who's convening a space, convening a group, and I'm
asking them to show up and be their best selves and do the best work to the extent that they can
on this given moment in time, that me sharing where I'm at, what I'm going through in a way
that is honest, but also safe for them. And I think that's a
really delicate and hard thing to often do in any kind of leadership or parenting or in context like
that. It makes it better for both for you and also for them. And then giving them permission
and saying, Hey, listen, if there are 25 people sitting in a room right now, like there are a
whole bunch of things that nobody else in this room can see that are going on with you. And that is causing some level
of pain or suffering. It may have been the diagnosis of a friend or family member. It may
be something going on with you personally, whatever. It may be the world. And to the extent
that we can make that invisible experience visible in the context of safety and normalize it.
It's good, not just for the individuals, but for the collective.
And yet we're so terrified of doing it the way that you just described it.
You know, imagine if leaders and organizations did this on a regular basis,
but it's so counterculture to what like adulting,
especially adult careering has always been described as that. Who's going to show up and start doing that within the context of an organization.
Like you're doing it within your organization.
You're a professor and a researcher and you're also, you know, you work for a big institution.
And like you said, it creates a great context in the room.
And at the same time, there are things, there are other like ripples of harm
that you've experienced because of it, because it makes you really different within the context of
larger institution. It's so hard to do that balance. It is really hard and it's really risky.
And I know that I actually risk my livelihood sometimes with the way that I move through the
world, but I'm so invested in it because sort of the assumption is that like the people that
aren't saying it aren't experiencing it. But like you just said, everybody's experiencing something,
right? Like just because someone is a polished CEO in a fancy suit and always, you know,
has like the twinkly smile and efficient meetings doesn't mean that they don't have a whole world
and a whole life and a real human body that they exist in. And I think the safety is the key part, right? Letting people know that
there won't be a consequence to you for being honest in this space. We're respectful. We're
caring. We're compassionate. We respect the boundaries of the type of space that we're in
when we choose to share, but we still share honestly, right? Like I had a grad student who had some wild stuff happen in their family and
they just weren't in the space. They were physically there, but they were not there.
And finally, I was like, look, you should go. You should go home. And their immediate knee-jerk
response, even after dealing with me, my personality all semester was, will this count
against my participation grade? I was like, no, first of all, you're not participating. But even
if like, it's not about that right now, it's about you and what you need to take care of yourself.
And I think that safety makes people actually better, more effective workers, better, more
effective researchers, for sure, looking at
qualitative research, which is what I do. But when I put my baby girl to bed every night, when I hug
her before I put her down in her crib to figure out how to put herself to sleep, I say, you're
safe here. You are safe here. And I'll come back for you. Right? We lose that ability to feel safe. But if people at the top made it safe by also
allowing themselves to be the whole human that they actually already are, it would shift. Is it
going to happen? I don't think so. Probably not. Not anytime soon. But am I going to keep doing it?
Yeah, because I think it's worth the flack I get.
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Mayday, mayday.
We've been compromised.
The pilot's a hitman.
I knew you were going to be fun.
January 24th. Tell me how to fly this thing.
Mark Wahlberg. You know what the difference between me and you is? You're going to die.
Don't shoot him, we need him. Y'all need a pilot.
Flight risk.
If somebody's listening to this
and they're like, yeah, I'm going through stuff and I've been going through
stuff and maybe there's chronic pain in my life and all the questions you're talking about,
these are things I'm thinking about all the time. And I don't, I don't feel like I'm ready. I don't
feel like I have the agency or the power to actually make these invisible things visible.
I'm doing everything that I can to try and resolve them to the extent that I can but
Maybe a part of this is just going to be a part of me as I move forward in my life
And i'm trying to make peace with like that part of it. Also if that is part of the reality
I don't want to I don't have the ability. You're like I need this job
I'm a single parent. I'm working three jobs. I've got kids
And no matter what i'm going through right now,
no matter what pain, whether it's chronic migraines, whether it's whatever it is,
if I make this visible and if I make this a part of the experience of work, I know I'm going to
take a hit. And right now I literally can't afford to do that. And there will be many people who are
in that moment. And if they're many people who are in that moment.
And if they're not now, it may be coming.
So you're kind of left with the question then,
what can I start to think about or do or explore individually
to try and make my internal experience
as good as it can possibly be given what I'm walking with?
And I know this is a question that you've asked yourself a lot and that
you've done a lot of research around and exploring and tried a lot of
things.
Take me into your experience of this.
It's such a good question.
Cause I think sometimes we get lost in sort of like the structural
constraints that are on us that we forget that like,
there's sort of like two levels to how we move through the world,
our own individual choices and what we can control. And then the structural things that are really out of our control. Work doesn't have to always be the place we make ourselves visible and I put my bag down, it's different.
She's different, right?
And that's okay.
So one of the things I think is like, find the people where you can tell them, like,
hey, it's been really hard right now.
And I don't need solutions.
I just need solidarity, right?
Like, I just need friendship.
I just need...
Dr. Becky, the parenting expert, says, I can tolerate my own feelings if you just sit with me, right? Like I just need friendship. I just need Dr. Becky, the parenting expert says I can tolerate
my own feelings if you just sit with me, right? Like I just can't tolerate them alone.
I really believe that narrating our pain, even if it's just to ourselves,
helps us manage it and helps our brain process it. Because a lot of pain comes from,
it's signals that are sent to our brain. And one of the things that I found in lots of physical pain therapies, but also trauma therapy, and both in studying trauma therapy as well as part of my research expertise, is that when our brain sees a pain signal coming, whether that's an emotional pain signal or a physical pain signal, it kind of tries to prepare for it based on past experience, right? And so we
tend to tense up and we tend to like really think that we have to just like shut it down.
But really like that tension is part of the problem. So one of the things I do when I'm in
pain is I actually talk to myself out loud about the pain. You are dealing with a headache right now. You're dealing
with really severe neck and head pain. It hurts to stand up. It hurts to take a step.
And then I do something I learned from pain meditations and pain therapy. This pain is not
going to last forever. I don't know how long it's going to last. I don't know how long it's going to
last. But in telling my brain, cuing my brain and body that
this pain is not necessarily going to last forever, I don't know that it's not going to
last a long time, but I don't know that it's not going to last a short time. I have released my
brain from those signals that just are cuing more and more tension, more and more tension.
The metaphor that I got in a pain therapy is if we're an oak tree
in the wind, when the storm hits, our branches are going to be hit by wind and rain and hail,
and they're going to break. They're going to break as we brace ourselves against the pain.
But if we're the tall grass in the wind, if we just try to move with it, even when it hurts really bad,
it's a little bit easier. We don't break. We bend. We adapt. We cohere. And I love exercise. I just
want to be an athlete so bad, right? I just really want to. And it hurts a lot of the times. It helps
the pain a lot of the times, but it hurts a lot of the times. And people will hear me on runs saying to myself, this pain's not going to hurt me. It hurts me,
right? But this pain is not going to like destroy me. It's just going to be here with me. You're
welcome to stay here with me, right? Just learning to talk to yourself in a way where you're like,
I know that this is kind of part of my circumstance right now, and I'm working
towards solutions, but there may not be one.
And just allowing yourself to like find comfort in the uncertainty and the possibility that maybe the outcome won't be as horrible as we have decided it's going to be.
Like, I feel like being in pain is also like this like tacit acceptance that it's just not going to get better.
But maybe it could. Or maybe we get better at stomaching it.
I don't actually think my pain is a lot better.
When I move my body, it's just as stiff and crunchy and messed up as it was two years ago.
But I have gotten a lot better at managing it.
I mean, that makes so much sense.
It really jives with what Dr. Sean
Mackey was telling me. It's about what pain really is and isn't, and this notion that we tend to
think that pain is where we feel it in our bodies. And what he described to me is like, well, that's
part of it. Pain has this stimulus part. Something hurts, something is injured, like there's inflammation somewhere,
but that's just a signal. And like that becomes pain actually when it enters our nervous system
and our brain. It's the brain that then says this signal is pain and you're going to feel this thing
called pain, you know? So you need both parts of that to actually experience this thing called pain.
And that's why I was saying like, oftentimes you're like, when
the original injury or illness or inflammation resolves, if that circuit between like the
stimulus and the response in your brain that says this is pain has become reinforced so many times
during that window, sometimes the original insult can be gone, but your brain is still like the
circuitry is still alive. So like your brain literally itself is then generating the experience of pain.
And what you're describing is saying, okay, look, let's acknowledge that the brain is
a really big part of this.
Like our minds are a big part of it.
And that's not to blame or shame anybody and saying you're causing your own pain.
You know, but what you're saying is like the way that we process it, the way that we tell
the story about it, the way that we sort of like, as you're using your words, narrate it, is such a big part of the experience of it.
And sometimes, even if it's there with you and you're feeling it, and this is, again, something that Sean described to me.
He's like, you know, and he used the example of somebody, a patient who had a neuroma, like a nerve
inflammation, which most people often get on the bottom of their foot.
And he was, I think, a tennis player and it's excruciating.
And finally, he went to the doctor and said, like, good news, bad news.
You know, the bad news, you have this thing, like it's in your nerve, you know, like unless
we do surgery, you know, it's going to kind of be there and cause a lot of pain.
He's like, but the thing is, the pain that you're feeling,
like if you want to go and run on this,
if you want to go and play tennis on it,
you're going to feel the pain.
But the pain actually isn't going to do any damage.
You're not doing something that's causing more and more harm to you.
By doing the activity that you love to do,
that's also now causing you this experience of pain.
And that was like transformational
because the person was like, oh, I can deal with that. But it was the story that I was telling
myself about like spiraling of what is this doing to me beyond what I'm immediately feeling? What's
it going to do? And how is this going to destroy me and limit me if I keep doing it? And that
narrative was such a powerful part of the limiting experience of it in the beginning and then
the freeing experience of it, even though it was the exact same situation before and after.
And it's kind of what you're describing, I think.
Yeah. And I know that that's like a privilege and a luxury that's not available to everybody
who suffers from pain, right? But I think it's a huge thing for me. The initial reaction I had when like a physical therapist
was like, well, we can, we can probably not solve all the things in your body that have caused you
pain. Your surgeons have told you this, your doctors have told you this, but we could try
to train your brain. My initial reaction was sort of like, okay, you're the worst. The pain is not
in my head. I'm going to go to somebody who can actually fix this.
Yeah. Okay. Thanks for not solving anything. You're rude and your pain's in your head, right? But he wasn't saying like your pain is in your head. He was saying like, let's look at the
complicated thing that this body is, right? And what can we do, right? We can help your brain
figure out how to ignore those nerve signals.
I also suffer from tinnitus.
It's like this chronic ringing in my deaf ear.
I'm like, homie, you're deaf.
Why are you ringing at me?
And it's my brain literally sending these nerve signals to find the thing that used
to be there.
And it's not gone, but it's gotten better over the years as I've done work to train my brain, right?
And some of that is literal sensory exercises, talking to myself in the mirror.
And I feel so silly doing this stuff.
But I have found that talking to myself with grace and compassion and care and reminding myself that I can withstand this, that I can
survive this. The pain itself, like you said, is not causing damage. It's not causing harm. It might
be cuing us to things in our body. So we should always listen to it and do our due diligence.
But when we know sort of the causes of the pain and we know that we can't necessarily fix them,
we have to learn how to walk alongside it, right? Like this is my
companion now. Okay, let's figure that out. Let's remind us that that can't hurt me. And when it
wants to amp up, I do this thing where I imagine a circle around me and it's just a little circle,
a little safety circle. And the pain is real close to the circle, but it's just outside. You could be really close
to me, but I'm not going to allow you to just break down all of me. It's the same thing I do
when somebody says something to me that really wants to let my rage monster out in response.
I draw my little safety circle and I give myself just 10 seconds. I just count to 10 quietly to
myself. And that 10 seconds is long
enough to cue my brain that, yeah, this input is coming and it's scary and it's hard and it's
making you feel all kinds of way. And those feelings are valid and you get to have them,
you get to process them, but you don't need to react. You don't need to knee jerk react
with tension and more pain. Now that makes so much sense. I think we've talked about this also.
I've attended this also.
I've talked about it on the podcast over the years.
And my initial response was, it was absolutely brutal.
It was taking me down and in a very, very fast and dark way.
And after about three months, the doctors were like,
I don't know.
Most people just figure out a way to be okay with it.
I'm like, thank you.
That's super helpful.
And again, for anyone who doesn't understand what this is, literally,
your brain is creating a sound inside of your head. It doesn't exist outside of you that you hear. And for some people, it's mild and not a big deal. For me, it was extremely loud. And at any
given moment, if I go and look for it right now, it's still there, you know, like a dozen years
later. And for the first three to six months, my whole thing was, how do I stop this from happening? This can't be my reality
because this is devastating. I can't function. I can't think I was writing a book about uncertainty,
which actually ended up being something that was super helpful as I was diving into the research
for the book. And I started to apply it to this, but it was again, one of those things where,
okay, so it's dude, it's just a sound in
your head. You know, like whatever, like you hear sounds, I was living in New York city,
there's sound all over all day, every day. Like we literally lived on the corner on top of one
of the biggest subway stations. Like, and I heard that all day, every day, people fighting on the
street, the court, like everything. I'm totally fine with that. I could sleep through the night
easy peasy, but this high pits, like digital sound in my head was destroying me. And it was causing pain,
like very real suffering. And it took like a whole bunch of reprocessing that like you were
describing to basically eventually get to a point where I say, and as I would start to share it with
people also, everyone was like, started offering me cures and ways to fix it and miracle cures and all this
different stuff.
And eventually I was like, please, I just stopped telling anyone because I didn't want
to be offered any of those anymore.
And I got to a point where that sort of like classic Buddhist slogan, abandon hope, started
to make sense to me.
I was like, oh, I get it.
Actually, it's not fatalistic.
It's not about futility.
It's about saying, if this is me for life,
what do I do with that? How do I stop just searching for this to not be my reality
and saying, if this is my reality, how do I walk with that? Is there a way? And if I invest the
same energy in trying to deny it or make it not my reality, that if I take that energy and invest
it in, how do I walk with this? Is there a way to walk with this where I'm closer to okay on a regular basis? Like, could that help? And that
was the shift that was like the switch that got flipped for me that made a huge difference because
there were a whole bunch of things, a lot of what you just described, where like now I'm, you know,
it's still there anytime I look for it, but I'm fine, you know? And when it first happened,
it was absolutely destroying
me. And a lot of the research that brought me to that was actually research on chronic pain,
because it's the same stuff. Yeah. It's the nerves in our body telling us something,
right? Telling us something is misfiring or going sideways, but it's kind of magical, right? Because
you said twice, it's there if I go look for it, but you don't need to go
look for it. You're just allowing it, right? Just allowing it. And we pathologize things and we
narrate things as like good things or bad things. And pain is a bad thing. And I'm not saying like,
oh, go be in pain. It's so great. But like by narrating it as bad, we disallow ourselves from like just letting it be,
just letting it be there. And we come from a culture that just wants to fix everything and
fix everything and make it make sense and like make it certain. The biggest gift getting sick in my 20s gave me was like an awareness of how uncertain
things are, right?
Because it was uncertain before.
I just didn't know it.
Now it's uncertain and I know it.
And okay, how do I live in spite of that?
How do I live knowing that?
How do I make really deliberate choices in my life,
recognizing that like, I will do my best, but it's not in my control. It makes me want to do even
better in the sense that like, if it could all fall apart tomorrow, do I want to have put the
most love into it or not? Right. And so like the uncertainty to me has been a gift. And I think it's actually
the thing that helps me manage my pain. Like the pain is not forever, just like nothing is forever.
And like, maybe it'll get worse, but maybe it'll get better. And that maybe that little bit of like
possibility that like, or maybe I'll just get better at letting it be. And that's the thing that happened.
I got better at letting it be.
And it's like, it just feels like magic.
Yeah.
When you think about everything that we've talked about so far in this context, is there
anything that's been on your mind that we haven't touched on?
I mean, I think sometimes we think making things visible, right, is like I got to go on like social media and like tell everybody I've been in chronic pain or I need to share it at work.
But I think it's really just about like letting the thing that's been weighing on us breathe, like letting it out, setting it down. Sometimes that's even like journaling about it or just sharing it with
a significant other or a close friend, just letting it breathe, just like setting it down.
Let someone help with the weight of it a little bit. I think that mentally and emotionally, that
is a huge part of navigating like a physical condition in particular. And so I don't want people to walk away thinking
like, okay, so I have this horrible thing happens and I now need to announce it to the world. You
get to choose how to share your story and where and when and what feels good. But what I want
people to think about is how can I just let it breathe a little bit and maybe take some of the pressure off myself to hold it all in
and hold it all together? And that if I release some of it, release some of my attachment to also
like naming it and being in it and being someone who suffers from pain, what might that allow to
allow me space to fill in, you know?
That resonates so deeply. It's a good place for us to come full circle. So I asked you this question many years back now, but time has passed, people change, the world has changed.
In this container of good life project, if I offer up the phrase to live a good life,
what comes up?
I don't remember what I said before, but I think now to live a good life
is one where you are present in it,
like really present in it.
Even if it's just for five minutes a day,
just like allow yourself to just be in the space
that you're in, you know?
Just, I'm a new mom. She's 15 months old. The best moments are the
moments where she's looking at me and I'm looking right back at her that she didn't have to fight
for my attention. That's when I feel most alive. That's when I feel most in my world is like just sharing space with people so fully sharing space with myself so fully
being present with the hard and the good and the bad that's what it's all about for me right now
thank you hey before you leave if you love this episode safe bet you'll also love the conversation
we had with sean mackie about the science of pain you'll also love the conversation we had with Sean Mackey
about the science of pain.
You'll find a link to Sean's episode in the show notes.
This episode of Good Life Project was produced by executive producers,
Lindsay Fox and me, Jonathan Fields.
Editing help by Alejandro Ramirez, Christopher Carter,
crafted our theme music and special thanks to Shelley Adele
for her research on this episode.
And of course, if you haven't already done so, please go ahead and follow Good Life Project in your favorite listening app.
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next time, I'm Jonathan Fields, signing off for Good Life Project. Apple Watch Series 10 The Apple Watch Series 10 is here.
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Mayday, mayday.
We've been compromised.
The pilot's a hitman.
I knew you were going to be fun.
On January 24th.
Tell me how to fly this thing.
Mark Wahlberg.
You know what the difference between me and you is?
You're going to die.
Don't shoot him, we need him!
Y'all need a pilot.