The other day I opened up my Yogi tea bag at work and draped
the paper tag over the lip of my cup. I love tea tag quotes, and I was excited
to get my daily dose of optimism alongside my steaming mug of ginger brew. What
I read, however, was thoroughly disappointing.
“You are unlimited,” my tea tag read. I laughed and might
have actually replied aloud that I begged to differ.
I expected wisdom from my tea bag, but found what I was
searching for the in the transcription of the 1912 meeting of the HomeopathicSociety of Ohio (wahoo history!). Dr. E. H. Pratt of Chicago contributed this
poetic wisdom to a discussion of the importance of considering nervous
disorders in surgical cases:
It is opposition
that helps people. A bird cannot fly without the resistance of the air; a fish
cannot swim without the opposition of the water; an engine cannot pull a train
up grade without sand on the track; a violinist cannot make a sweet sound on
his violin without rosin on his bow, and the things that we call trouble are
the stuff out of which the steps of the Golden Stairs are made.
I am limited, and (how do I put this
gently?) so are you. Resistance
and opposition lend movement, beauty, and meaning to our existence. Our bodies
are limited, are brains are limited, our lives are limited, and this reality is
at the beautiful heart of being human.
This weekend, Marissa and Christine will fight to overcome
the resistance of their bodies, to see whether their limit lies after the 31.07
mile marker. Pushing our limits is an act of faith and hope, faith in our
ability to leave the known world behind, and hope that what we find past the
borders of comfort will be worth the struggle of the journey.
Some limits we push past alone; others we defy together.
Take the fundraiser- certainly $10,000 was past the limit of what my immediate
family could scrap together, and we know your pocketbooks certainly have their
limits imposed by income, need, and the many other excellent causes you
support. We set an optimistic goal of $10,000. I am so proud that the $12,010
that we’ve raised has been spread over 134 donors, rather than one donor with
unlimited coffers.
Lymphedema is an unceasing reminder of my limitations. My
skin itches, my bandages and garments chafe, and my tissue aches with the
burden of unrelieved pressure. If I stay too long on my feet, small sores open
up on my legs, releasing extra lymphatic fluid. My condition forces me to pause in the pursuit of my goals and put my legs up instead. While I’m resting, I often find myself enjoying the
time it affords me to look back at how far I’ve made it and plan where I want
to go next.
My lymphedema, my limitation, is both my rose and my thorn.
Knowing my body and my life are limited spurs me to work for the change I want
to see in the world, to overcome the challenges of today and get to work on
tomorrow.
There is such sweetness in limitation, too. My daily
reminder of what I cannot do also reminds me of all the capabilities I took for
granted when I thought I was unlimited. What a miracle a body is! To walk, to
run, to laugh and jump—not everyone can do these things, and for all of us they
are the gift of just a lifetime, too short a time to be taken for granted.
Perhaps best of all, knowing and embracing my limitations encourages
me to lean on others for support. Christine's shoes bear donors' names to power her up the trail.As Marissa shared in her last post, thinking of someone she loves for every mile of a race turns the pressure of distance markers into welcome meditations on the people who share her joy and struggles. Like Dr. Pratt’s bird, we needed the
resistance of the air to fly, but you have joined our flock and shared the
work, and together we have covered more distance than we ever thought possible.
Thank you for joining our team- for the love and for the message of hope. The
limitations of lymphedema won’t disappear after this weekend, but thanks to
your support, the search for a cure will press on. We won’t run from our obstacles
but towards them, relishing the chance they provide us to grow, learn, love,
and live fully.
I really really appreciate what you guys did with this run. I have lymphedema myself and it is SO hard because no one knows what it is, even doctors for that matter! I've struggled with showing my stockings, sometimes I do, sometimes I don't but every time someone catches a glimps of it there are always stares and questions. and "ohhh, I'm sorry, that's really strange".
ReplyDeleteWhile it won't kill us, it's still not the best thing to have. It's nice to see a young woman like myself putting her face out there. If you guys ever do this down south in LA I will be sure to be there :)
Thanks for the kind thoughts! We're so happy to be increasing awareness and raising funds to we don't get so many blank / confused stares when we mention lymphedema.
ReplyDeleteI go down to LA sometimes and wear my stocking with my shorts -- maybe we'll bump into each other and have a lymphedema moment! Wouldn't hurt if we could get them to make skin color look a little less like dead flesh :)
Also, if you get an event together down there, keep us in the loop!