Pages

Showing posts with label bravery. Show all posts
Showing posts with label bravery. Show all posts

Tuesday, February 21, 2017

You are only one, but you are not the only one.


Life is powerful. It can be
powerfully destructive:
tearing babes from mothers' chests
ripping through dead rain forests like a dragon
breathing fire
sucking dry
the oceans that feed us,
spreading famine of
tears that make us beating hearts;
spilling blood
on unholy ground
as the dying rivers cry
their songs of weariness--

But we
who rise from the ashes 
over and over again, 
dawning like a phoenix flecked with gold
after choking on the dust, after 
breaking every limb; 
climbing the spines of our own backs 
up again
and again
and again
racing our hearts to beat
faster, live longer,
love deeper.
 
We are the beauty of this world. 
We can 
claim that for ourselves and 
be beautiful and free, 
in spite of the slavery.

Wash yourself. Again and again.
Be beautiful.
Build your life
as if it were a work of art.
You fall, get back up. Be brave.
Tell your truth. Live.
This is what beauty is.
And you are a part of it.

Tuesday, December 13, 2016

full moon got me like...

Maaaaan, this full moon cycle is hitting me really hard. Not sleeping well, and the waning hours of daylight are heavy and depressing. Lethargy is pulling my body around my house while I wait for something to lift. Depression isn't just mental, it's deeply physical. Mostly in my stomach. Body aches. Disembodiment cloud of fog. I am here.

Just last week I got great news from my transplant doctor: basically I'm doing really well physically. I've stopped my immuno-suppressant drug; which I have been on for over three years. It was what was keeping my new immune system at bay until it got used to living inside my body, a foreigner. I'm lucky that I am able to get off of this drug- any other type of transplant, you have to be on anti-rejection drugs for the rest of your life and you will always be immuno-suppressed. Mine's a special case: since I got my immune system replaced, there is a chance that I would be able to get off the drug eventually. And, hooray. It's happened. It is no small thing. I've been off of it for a couple months now, and none of my organs are shutting down.  It is no small thing.

I'm grateful. My doctor actually smiled at me, told me: "You don't need us anymore" and then gave me a hug. It is no small thing. As I hugged him in his white coat; I said "thank you" and it felt like I was actually thanking him for saving my life, for the first time. I didn't need to say anything else. I couldn't, really. Just "thank you."

I just performed in a movement piece a couple weekends back- after devising the show for two months. It was incredible to be in my body for the first time and feel like it somewhat belonged to me. It's been a long time since I've felt that way. I loved performing. It is no small thing. I really didn't know, until now, that I love performing. That I need to do that.

I performed a heartbreaking physical theatre show four times in a single night: cried through most of it as I embodied a girl growing up, getting caught up into sex trafficking and drugs, having an internal war with herself and finally finding an arm up, which was from inside her. It doesn't end happily. It ends hopeful, I guess. But it was where the real work began. The end was the beginning.

Getting to the point of embodying the headspace of trauma was not what was difficult. I have a well to draw from. We all do. The hardest part was that exact realization. There is no other. We all embody trauma. The woman I embodied was me. It was you. Your daughter. Your sister. My sister.

I was overcome after creating this work (and discovered even more while performing it) of the strength once again of human beings. This woman, this one story we told through movement, is the story of strength. It isn't the story of pity, or the story of weakness. It is the story of bravery. No one is immune to trauma- internal and external. What amazed me was embodying this woman who went through most of her life hating herself, disembodying, disassociating. But in the end, her liberation came from within her. She had to choose to get out. She made the move to do it. Every single time we got to the end of the show, there is a reveal- and even though I knew- actor-brain-wise what was going to be revealed... I was shocked every single time. Honestly, earnestly and authentically. I didn't feel I was acting. I was embodying. I've never had this experience before. Not like this.

So here I am, approaching the end of 2016: job searching, a totaled car, lethargy and depression steeping in me like earl grey. And yet. This time last year I had recently been released from the hospital after one of the most dehumanizing experiences of my life; depressed and entering the literal darkness of this time of year. I am not her anymore. I am a year older, wiser. I see what is happening to me- the full moon or whatever it is, and I can call it out on its' shit. I see you, depression. You are not me. You are not who I am. You try to own me sometimes, but you don't. And that is no small thing.

Approaching this new year with a curiosity. I have almost no idea what will happen in the future. Job searching is lonely and difficult, but I am also just curious. What WILL happen?

I'm lucky to have what I have. I have a body that is still alive, for better or for worse (bit of both). I have discovered what I am meant for: theatre. performance. directing. devising. writing. creating. Not everyone can say either of these things. I am lucky. It is no small thing.

So, full moon: effing bring it. I'm gonna put on my running shoes and leave the house today, even though most of me is saying no, just curl up and die. I'm gonna put on music that inspires me to be a better human. I will be unafraid to read or think things that make me cry or feel overwhelmed by the idea of the world. Beauty and Terror in everything, is everything. Because feeling these things reminds me that I am alive. And that is no small thing.

Wednesday, August 26, 2015

Day 706: human AND dancer?

10 weeks since my last post. I may do better as a writer to be more disciplined at this, but honestly, I just wait until the impetus to write starts bubbling up. And it's been bubbling for the past few weeks- and after so many things happening, I finally have a moment to sit and write it out. My friend today asked what it would be about. I answered: "I don't know yet" because I don't. This blog has been a discovery for me, nearly every time I sit down to type, I have almost no idea what I will write about, and I make discoveries about myself and my life as I write. So here goes.

[edit: Upon reflection/re-read, this is serving as a catch-up post for people interested in what I've been up to, and not necessarily all of what I've been thinking about, which is usually somewhere between crying over beauty or being crippled by existential terror. But that's always sort of thrown in I guess. There's more and more still waiting in me, but I think it shall wait for its own blog post.]

I'm sitting in an unfamiliar kitchen in Ipswich MA where I am dog/house sitting. The pooch is an adorable, loving 11 year-old chocolate lab mix, and we're best buddies now (it's my second day). I may not need a shower as I've been licked head to toe by this baby.

I'm thinking over what has been crawling through my mind these past few months- and much has happened: good and bad things; and as always, Life showing itself truthfully. I 95% moved out of my old apartment and into my new apartment this past weekend. I can't believe I've moved so many times, and each time it is so similar; too similar. First, moving is sooo fun. In addition to being anxiety-ridden and stressful, I am seemingly always the last person to leave an apartment (read: I am responsible for cleaning the entire thing). Thankfully I still have another weekend to move the rest of my stuff (HOW SO MUCH STUFF?! HOW) and to clean it all. I've been fortunate to have time to move; the usual move out/in and clean all in one day is a nightmare, and I'm pretty sure everyone has experienced this at some point.

Good news on the goal-front! I have traveled a bit. I am making it happen, sort of. I haven't mentioned it yet, but I went to Southern CA back in April, and though it was the COLDEST WEEK in recent memory (WHY, HOW), it was more cleansing than I could even understand until I got back to MA. I've not traveled too much in my life yet, but that trip- though I spent many (too) many hours in my rental car driving all across the (Southern CA) world- it was healing and just what I needed. It was a difficult winter (yes, didn't we all love it), and I was seriously getting ready to move out to CA sight-unseen, but decided to take this trip first. I now don't have the urge to move out there, at least not at the moment, but just going on a vacation (my first personal vacation! ever!) cleaned me out and refreshed me in a way I didn't know it could.

I also just got back from SCOTLAND. Yes. International traveler, me. I went to Edinburgh for the Fringe Festival and it was divine and difficult, both of which I was anticipating. Edinburgh is a very walkable city, but it is also mostly hills. This was tough for my body, and though it got easier every day, it was still pretty rough and I was almost always tired. It was also quite chilly (though apparently the week I was there we had some of the warmest days in recent memory... I guess good karma from my iceberg CA trip?) and I am a perpetually cold being now, even when it's 70.

I first went to the Fringe Fest in Edinburgh back in 2011, and I saw some work there that completely changed my life. It inspired me to start my own theatre company here in MA, and I've been longing to return ever since (on a side note: a few months before I was diagnosed, I was planning to go back that summer with my sister). So in going back, of course I wondered if I would see anything that would break me like my first time in Edinburgh.

...It happened. It took until my second-to-last day there, but it happened. I almost missed the show because while standing in queue, I suddenly got a massive coughing attack (oh yeah, I got a great chest cold about mid-way through the week. Nights full of feverish delirium. Sweet) and had to step out of line while they let everyone else in. At the literal last second, I was finally able to compose myself and climbed to the very back of the stadium seating (which actually turned out quite nicely: I was able to see the entire stage, and being a shorter person, this is not usually the case.) The show was a physical theatre piece called Institute by a UK company called Gecko. It was absolutely brilliant. I could attempt to talk about it for a while, but honestly, physical theatre and dance is always it's own, usually wordless language. I would find myself crying, not even entirely sure why.

After it was over, I stumbled out of the venue, put on my sunglasses and tried not to burst out sobbing on my way back to my flat (thankfully not a far walk home). I couldn't speak. And when I finally could, it was tearfully to two girls who were in my flat, as tried to explain what I had just witnessed. They had to leave for something else, and I went to my room and lay on my bed and cried for a while. Seriously, just laid there and cried. I wasn't trying to "process it" in any real way, but rather just let the experience wash over me. And it still does.

The next day, my last day there, I went back to the venue after the show got out because I heard that the company actually comes out afterwards to chat with people, which is incredibly generous especially after giving everything on the stage! It was amazing to talk with them about their process and their different paths to finding themselves in a physical theatre company. They asked where we "went"- what the show was to us. I spoke a little bit about spending a lot of time in hospitals (there was definitely imagery resonating there), and how we all try to care for each other even though we are failing at it all the time. I was trying to not cry. One of them asked me if I was a dancer, and I sort of stuttered and managed to burp out something about missing my chance. One of the company members points to one of the quieter members and says "Chris was a firefighter in California."

For some reason this stuck with me. I have spent so many hours and days being so sad and pissed off about how my "new" body fails and constantly disappoints me. From lack of mobility for so long, my muscles atrophied, and it's taking SO MUCH LONGER to get back than I could have ever imagined. And my flexibility is so poor that usually when I try to stretch it just becomes a crying session. But seeing this company's work, and in talking with them after their show-- I have a renewed sense of vigor to build my body again. For the first time in a long long time, I feel like I actually might be capable of getting to where I want to go. I know that it will take a lot of work. Probably more than I even realize at this moment. But I want it so badly.

Before I got sick, the only real option that I was considering for continuing my education into grad school was physical theatre and/or clown school. People would chuckle after I told them, then I'd usually have to say, "no, but seriously." I don't know necessarily that clown school is in the cards for the future, but I feel this urgency--a vitality to jump start and get this body to a different place. I'm promising myself that the next six months are going to be dedicated to self-care in the form of HEALTH: building muscle and flexibility. Let's do this. I've always felt that I could have been a dancer. And now: who knows? Maybe I will be one.

Friday, September 26, 2014

Day 365: to the girl in the waiting room

Twelve days after my transplant, after I got out of the hospital and was in for my first weekly check-up, I was sitting in the 8th floor waiting room, infusion side. My parents and sister were there. A lean and pretty girl was sitting reading across from us. She had a short dark pixie cut and adorable clothes, and honestly except for her bracelet I don't think I would have known she was a patient. She sent her husband out to get some Starbucks, and I caught the front of her book: Anne Lamott. I was actually feeling pretty good that day, considering. I guess I was just so happy to be finally out of the white box that I'd spent the past two months in, and my throat sores had subsided considerably. I told her I loved Anne Lamott-- and we got to chatting. She told me she was in for her year check-up, post-transplant. I couldn't believe my eyes. She looked so good. She told me about her class (she's a middle school teacher) and that sometimes the kids ask her about the scars on her chest. She laughed. She told me that I looked pretty good for being day 12; that she was still in an Ativan haze around then. She said "It gets a lot worse before it gets better. But it is so worth it. Keep going, soul sister."

And again, I am reminded of Rilke. How could she have possibly known? Let everything happen to you: beauty and terror. Just keep going. 

It meant so much to me (more than I even knew at the time) to see her, looking so healthy and happy and strong, a year away from where I was. At the time, I couldn't imagine myself being in her place. I couldn't imagine it. I couldn't see outside of where I was. I was still so blown over, so caught up in dealing with symptoms of this deadly treatment that I couldn't imagine a time when cancer wouldn't be my life. I hadn't even really started the arduous journey of dealing with everything that cancer disrupts or takes away. I felt it's immediate stoppage, of course: I was ripped out of my life and put on a single-lane fast track labeled in big letters CANCER. It changed everything. And then later, when the solitude and mental exhaustion took its hold, I couldn’t make jokes anymore and winter and depression drove me close to losing my mind or taking my own life--I couldn't see outside of it. There were nights I didn't think I would make it, because I would cry myself to death. 

And yet. I am here. Somehow I have survived this long, trudged this far into the journey. I have a lot of people to thank for that. Some people would say I'm so close that I might as well finish this. I can hardly grasp that I am one year out. It doesn't feel like something that will end. It feels like it can’t end. And in some ways, I don't want it to--what I mean is, some of the changes I don't want to lose sight of. I don’t want to forget how I feel about living now, right now at least. After really experiencing fragility, and beauty and terror all together...it makes me want to live differently. It’s a part of me, and a part of my story now, and I am different. I knew this would change me; and I’m still learning what that means, and figuring out who I am now. 

Today I’m trying to claim that bravery again, finding ways to celebrate even if I don’t feel like doing it 100%. Finding way to be thankful, and trying to thank the people responsible for my still being here (the list is long). Because cancer has changed me. For one, it makes me not want to be afraid of dumb shit that’s not scary. Life is so temporary. Ask for his number! Fly to Edinburgh! Start a new job! Open a cafĂ©! Apologize! Forgive! Take risks! Ask questions! Do things! Choose Freedom! Choose Love!

The effects of cancer have outlived the cancer. And that is a mixed bag, I must say. I am not whole yet. There are effects that hurt; really hurt. I am still climbing out of this emotional wreckage, let alone the physical wreckage that is my now weird body. But I am--today, in this moment--trying to focus on the constructive effects in my life: the ways in which I am changed for the better. I am lucky to be able to do that right now, and perhaps tomorrow will not even look quite as bright. But life won’t stop being hard after this is over. Challenges will always arise, and life will seep down to the bare mundane tasks if I let it. I need to keep finding ways to live and love better. I have to trust that time heals, that days will go by, and that I have a thousand choices in each one of them. 



To the girl in the waiting room: thank you for saying that to me.

And to the other girl in the waiting room: you did it. One year down. One hundred more to go.
























Friday, June 13, 2014

Day 260: power pants vs. cancer pants

Today I had my first rounds of immunizations, as I am “starting over” you could say, with my immune system and need all my shots again. I thought perhaps it was a cocktail shot with the few that I was scheduled to receive today. NOPE. Four separate shots, two in each arm. I hate shots. I hate needles. However, all the prodding and IVs and bone marrow biopsies and LPs that have happened to me have at least helped a little in the anxiety department. I know, rationally, that I will make it through the shot. So I focus on breathing and relaxing, and it also helps to tell the nurse to push it in slowly. Perhaps the worst part of shots is that icy cold WHOOSH of the stuff flying in. So, the slower the better; and if I can’t feel the needle, it’s not as bad. It also helps to have a heated massage (let’s not get carried away here, it vibrates on two levels) chair to sit in, which they have at Dana Farber. My arms are a little sore, but it’s not too bad. Immunizations round 1 complete! #boombaby In other news, my blood/kidney/liver numbers look great, and my chimerism (the percentage of my cells to percentage of donor cells) is holding at 100% donor. #BOOMBABY

Then on the way home from Boston, in true Friday the thirteenth fashion, my car died. It was the second time this week—and thankfully in the CVS drive-through (instead of THE ROAD), but still. Really though? After finagling and praying and scraping with a wire brush, the jumper cables finally worked and I drove straight to the mechanic and got a new battery. As I sat in the little waiting room at the auto place, masked and gloved, I spoke with a woman whose tire just blew up. We chuckled about car troubles. I explained that I had a stem cell transplant, which is why I was all covered up. It made me realize that I miss being in the world, meeting new people, and even those silly and seemingly meaningless brief conversations that let you peep for a second into a strangers’ life. My nurse told me today that I can go to the grocery store at low-traffic hours, and that in general, the strict rules are starting to relax: as long as I still stay away from crowds, dirt, and mildew-y basements. I guess this calls for 9:30pm ice cream runs. I’m glad to be able to start doing things again, mentally I’m trudging through. I feel I have lost so much of the strength I had to get through this. It’s just,…a long time. It’s a lot to ask of a person. I know it’s what I need to do in order to then live the rest of my life, but sometimes it doesn’t seem like the end is in sight. I feel alone. I’ve been searching for tools to help me mentally pull through. I’m trying to reach out to people. I’m starting a new theatre project with my company, and our website will be live in a few days. And thankfully, on cue today, a tool—however small, however silly—arrived in the mail.

After the mechanic, I came home to find a package that I’ve been waiting for. Meet my Power Pants, the foil to my Cancer Pants: helping me conquer each dreary day with their stripes, every lonely long hour with their stretchiness, and my sadness with their general badassery.



ONE PANT TO RULE THEM ALL. Cancer ain't got nothin on you…
As my mom said, "must be your donor showing" (the Knight may live in the UK)



pardon me while I go shake my Brit-striped booty to some Bey—