let’s talk about trauma

DSC_0106

trauma: 1. an emotional wound or shock often having long-lasting effects. 2. any physical damage to the body caused by violence or accident or fracture etc.

Big, powerful word. It summons up thoughts of war, genocide, violence. Veterans who come home with the invisible wounds of PTSD after having fought in wars. It makes me think about my grandparents who were Holocaust survivors and what they carried deep inside them from what they had lived, from all they had lost. It makes me think about friends who have battled cancer, friends who have lost spouses, friends who – like me – have lost babies. It makes me think about all of the ways life can turn on its head in an instant, when we least expect it, and change us forever – change us down to our very cells.

Did you know that our cells carry our traumas?

I’ve been thinking about trauma lately, naming it, recognizing it inside myself. I’ve been looking at the trauma I still carry – even now, when I am feeling so much better – from the years I felt like such crap because of the auto-immune illness I live with. From the years I was so sick and struggling so completely to feel just a little bit better.

I have spent years – literally years – guided by my primitive/ancient/reptilian brain, living in fight-or-flight mode. I have spent years being cautious, fearful, and so completely careful about every bite of food I took, worried about how each bite would affect my body, frustrated to the point of rebellion that I couldn’t just fucking eat. I developed a superpower during these years: It’s an internal radar that allows me to find a bathroom – anywhere, anytime – within minutes if not seconds. I learned how to manage my condition in often obsessive ways that allowed me to trust my body just a little bit while taking away my ability to ever completely relax.

I developed other superpowers living as a sick person with a hidden illness: I got really, really good at managing my medical care, managing medical paperwork, getting reimbursements. I am the master of customer service calls, especially to health insurance companies. I got really good at researching EVERYTHING and taking what I had learned and the many resulting questions to my doctors. I got really good at developing supportive relationships with those doctors.

Do you see the theme, here, though? I am a fighter, a survivor. If shit hits the fan, I’m exactly the kind of person you want on your team. I fight. I’m persistent. I’m smart. I think 10 steps ahead at all times. I consider all possibilities in advance and I’m always prepared for anything.

But this is a crazy exhausting way to live. Especially when I was already feeling physically unwell. And especially now when I am feeling better.

(Do I even dare write “now that I am feeling better?” Am I really truly feeling better, for real? Can I trust that to be true?)

It’s a difficult lifestyle to unlearn because the trauma is still there – all the way down into my cells.

I was first diagnosed with this condition 19 years ago, after several years of other body challenges. I’ve had years of terrible illness and years with no symptoms at all and no need for meds. I’ve been surprised repeatedly when the symptoms returned, until eventually I came to expect they always would at some point – at least that’s what doctors tell you when you have a chronic condition. I’ve wrestled with whether or not to go on medication, felt frustrated when medication didn’t work or stopped working, and felt tremendous fear at how the medication might be hurting more than it helps.

I am so accustomed to living in a constant state of alert!-caution!-prevention!-attention! that it’s really difficult to turn off. To relax.

To trust my body. To trust that I am well.

The irony: Stress worsens my symptoms. That has always felt like a cruel joke. Just relax and you’ll feel better, I’ve been told, usually by people who are not living with an illness. I ate paleo – gluten free – grain free – vegan – raw – macrobiotic – (whatever) and healed! Try it, it will heal you too! This never helps me, just makes me feel like I’m chasing rainbows. Like I am never doing enough. And it makes me even more terrified of food. And I really enjoy food, a lot. And it’s not like I can just stop eating. Another cruel joke.

So how do we do it – how do we unlearn the fight-or-flight response once it is so familiar, so deeply ingrained in us? Is it possible to release, to heal some of the trauma, to lighten our load?

This is how I start: By writing these words. By naming it. Calling it by its name.

I think we all hold trauma in some form – big or small. I think when we keep it to ourselves, inside ourselves, we allow it to grow bigger, big enough to overwhelm us and drag us down. We are all fractured in some way, aren’t we? We are all imperfect and vulnerable. There is no shame in that. No need to hide our cracks, our scars, our wounds. Our traumas.

****

And you? Is there a wound you hold that you’d like to name, to diffuse a little, even to release? How do you do it?

 

 

the myth of perfect, or: you are not alone

GalFlying

I sat down to write yesterday, laptop on a pillow on my lap, in the armchair in my office space off the kitchen. The house was quiet and the birds sang to the spring outside. It took about 3 minutes before I surrendered and let my eyes close, because that is all they wanted to do. I wasn’t completely asleep, but I wasn’t completely awake either. Catnapping with my reading glasses on, laptop now closed on its pillow, half aware of how good it felt to just rest, half aware that I should be doing more with my precious time. I dozed for about 15 minutes, then went to take a walk around the block. That will wake me up, I thought. As I walked, I wondered why I was so tired at 11 o’clock in the morning. No answer came except, Just tired, no reason. No need to figure it out.

I’m going to be 44 in a month and a half. Not much different psychologically than 43, I am still officially middle aged. But I am aware of the process of aging in a way I don’t think I have been at other times in my life. The grays in my hair and the tiny lines around my eyes are not new, but their presence is in sharper focus, consistent. Sometimes I still get pimples, which feels like a cosmic joke, my body saying, Hey, at least you’re still a little bit of an adolescent. But what’s different at almost-44 is this: I don’t really trip out about it all very much anymore, not in the way I used to.

A wise friend who is now in his mid-seventies once told me – as I bemoaned the auto-immune challenges I have lived with for 20 years – that it is an illusion to think that it’s possible to attain perfect health while occupying a physical and very human body. Think about that: There is no such thing as perfect health. Bodies are machines, and machines get old and slow down and start acting up. And some act up long before they are supposed to – like my Tikva’s fragile little body that struggled so hard simply to get enough breath; like my friends who have courageously battled cancer in their thirties and forties.

It’s liberating, though, the idea that I don’t need to get to perfection because perfection doesn’t exist. Liberating to accept that I can still feel good – even thrive – within the container of an imperfect, fragile and slightly beat down body. I look at my 11-year-old daughter and see myself at her age, before the regular beat down of life had begun and I never even thought of the state of my health because it simply was. I think of that time and realize just how lucky I am that I could take for granted what is not always guaranteed – healthy and abundant food, warm clothing, shelter, safety, community, friends, family, love. Health.

****

I used to search for solutions, grasp at ways to heal from all that ailed me, ways to achieve the mysterious perfect, radiant health I was convinced everyone else around me had attained. I haven’t given up on the idea of radiance, the idea of thriving. But I’ve let go of perfect. And I no longer attach my wellbeing to a specific way of eating-being-living. I get annoyed, now, at the thousands of messages all around that promise complete healing of fill in the blank if only you eat fill in the blankavoid fill in the blank and do fill in the blank every day, because if it worked for fill in the blank it will definitely work for you and me, guaranteed. I don’t trust it anymore, not simply because I’ve tried it all, but more because the only thing that’s been consistent for me no matter what magic bullet I’ve tried is that I get neurotic and obsessive and end up feel deprived because I can’t enjoy the things I love. I used to follow a doctor and author on Facebook who wrote about hormones and health for women. Once she posted on her feed the five things to stay away from in order to feel great and be healthy. They were: sugar, caffeine, gluten, dairy and alcohol. I had to laugh because… Really? Honestly, what is the point of life if you can’t enjoy chocolate and cheese? I stopped following her feed.

I can’t help but be in awe of just how fragile we are in these temporary vessels; how incredibly miraculous it is that so much works when it works; how impossibly difficult it can be when it doesn’t; and how every single one of us – when we are truly honest with ourselves and with each other – struggles with something. There have been stories out there lately, brave coming out stories where people of all ages write about their struggles with illness, sharing on Buzzfeed or HuffPost or Salon about what they have always kept private because they thought they were the only ones struggling – because we can feel so much shame about being sick. The thing is, there is no failure in struggling in our bodies or with our emotions, and there should be no shame. Our culture is afraid terrified of death, and so we shy away from looking illness straight-on. We deny it, we chase after the illusion of perfect health – the magic cure that will bring perfection – and we feel like failures when we don’t achieve it. We keep our illnesses to ourselves, we feel alone. Until one brave young woman posts a picture of her colostomy bag on Instagram, leading hundreds of other young people to come out publicly as courageously as she did; and hopefully some of the shame dissolves and we feel less alone in our fragility. Did you see them, those posts? I couldn’t take my eyes off them – these gorgeous young people who have struggled, some since childhood, with irritable bowel disease, a lifetime of hiding their shame and their challenges with a hidden illness while they struggled to simply feel well. And did you see the incredibly badass pictures of women baring their mastectomy scars; turning society’s shame on its ass, turning it into pride, into strength?

If there’s one thing I’ve learned it’s this: The moment I have honestly and compassionately shared my own struggles with another person, I’ve let that person know that it is safe, acceptable and normal if they are struggling too. I’ve let them know that struggle is easier when you aren’t going through it alone. I’ve let them know that shame has no place where there is compassion.

****

I am not an athlete. I’ve tried many things, some for extended periods of time – boxing, rock climbing, dance, pilates, yoga, resistance training, running – but I’m not someone who craves exercise and keeping at it is not where I am most disciplined. In spite of this, though, I still feel active. At 5’5″ and 118 pounds, I can lift my 28 pound son up and down the stairs with one arm, full laundry basket in the other. Don’t get me wrong. I am entirely capable of tripping myself out with plenty of I should exercise more, my legs are flabby, I should eat more leafy greens, the pimples are hormonal and I need to get my hormones in balance and eat less chocolate, I’m scared of what the medications I take might do to my body long-term, etc. etc. etc. All that goes along with the house is dirty and I need to mop, I should be writing every day instead of a few times a week, tomorrow I will be more patient when my children are whiny, I need to make more time to be outside, there’s nothing in the fridge for dinner, etc. etc. etc. I’m human and the nag of perfection still whispers in my ears too.

I try to be gentle, though – something I hear myself asking my friends on a regular basis: Are you being gentle with yourself? What did you do today that is good for you? I try to remember to praise myself for all I do, for all I am. I try to express gratitude for my health even when it feels tenuous. I thank my (flabby) legs for carrying me (and my son) up and down the stairs, for walking me around the block. I try to let myself nap in my chair if that is what my body needs, and I enjoy a cup of coffee on those mornings when my son decides to wake up and stay awake at 4:30am.

To my friends and those I don’t know who are struggling, who want nothing more than to feel better in your bodies, who are fighting for your lives, who are feeling in a deep place all the pain that is everywhere around us:

I honor you.

I honor your struggle.

I honor your wellbeing.

I honor your good days and your shitty ones.

I honor the shame you long to release.

I honor your deep desire to feel better.

I honor your perfect imperfection.

seventy-five percent: on nourishment and fear

Nourish

Image source: Nourish Raleigh

Do you like kale? I mean really truly love it? Kale is one of those foods that has two staunchly opposing camps – the kale camp and the anti-kale camp – I have yet to meet someone who is neutral about kale, who could take it or leave it. You either love it or you can’t stand even the thought of it. I’m in the kale camp, but not because I totally and completely adore the taste and texture of kale in my mouth, or its bitter flavor before I drench it in salt, pepper and lemon and saute it in coconut oil. What I like about it is the color and what that dark green (or purple) tells me: I am really good for you. If it’s cooked well, I can even enjoy the chewy grittiness of it. I like the sensation of literally chewing on and swallowing iron and the other nutrients that come in dark leafy greens. And I love kale chips for the salt and pepper and crunch they are vehicles for. But would I eat as much kale if it had the nutritional value of iceberg lettuce? If the experience didn’t come with a message of nourishment? I’m not so sure.

This is the thing, though. I read recently that eating raw kale is not good for you. Raw kale can inhibit the uptake of iodine needed by the thyroid gland, which can lead to hypothyroidism. And it is high in oxalic acid, which binds with minerals in the body and makes them crystalize. These crystals can damage tissues and cause inflammation. So it’s best to cook your kale before eating it.

Okay, I can do that.

But I wonder what the raw food people would say to that. What does that mean for all those amazing “massaged kale” salad recipes out there? What does it mean for the big world of green juices and smoothies? Seems like it is impossible to win if all of a sudden a leafy green vegetable, which even my children’s mainstream pediatrician promotes, is suspect. This is the thing, and the reason I’m thinking about kale at eight o’clock in the morning:

There is always going to be something out there that’s not good for us. 

There will always be a hundred different theories about whether that thing is really bad for us, good for us or benign, and another hundred theories about why. Back in the early eighties when tofu was relatively new to the American grocery scene, pre-Whole Foods when it wasn’t in every store and instead a rare ingredient found in Asian restaurants, it became the new greatest thing, the healthier option to replace meat. At the small health food store in our town, you could find soy products in a hundred forms, but no meat. It was around the advent of soy in our home that the fried steaks and breaded filets of sole my French mom was so good at cooking disappeared and were replaced by spanakopita that was made with ground tofu instead of ricotta, and whole wheat crust instead of filo dough. I actually liked it, though it was definitely not true spanakopita like my Sephardic grandmother made.

But we know now that all that soy is actually not good for you because of the way soy mimics estrogen hormones and confuses the body. The paleo camp has soy at the top of its do not eat list for this and a dozen other reasons, and the paleo diet has in its presentation and coolness factor replaced vegetarianism and veganism as the new hot health trend. In the same way that all the “healthy people” in Hollywood used to be vegetarians, now they are paleo. Please rest assured I am pointing this out for its irony, not because I believe there is any one way for all people to be healthy. I’ve done the paleo thing and I like it for the most part, but for me it’s too much meat – I’m a 3-4 times a week carnivore, not 3-4 times a day. And I actually feel better when I eat some grains on a daily basis. And I love dairy and the goat milk yogurt I make myself is one of the most nourishing things I love most in the world, filled with good, fresh probiotics. And this: I’m not convinced that just because we’ve only been eating grains and dairy as a species for 10,000 years and before that we ate just meat, vegetables and fruits, nuts and seeds for millions of years… well, I’m not convinced that 10,000 years isn’t enough time for our bodies to adjust to consuming grains and dairy. But mostly this: I am incredibly resistant to the idea that ALL OF A PARTICULAR THING IS TOTALLY AND COMPLETELY BAD FOR ME. (Except maybe a Twinkie, but there is a big difference between a fluffy yellow thing filled with white stuff of dubious origin with a half-life of a million years and a bowl of homemade yogurt.)

It makes me want to say, Prove it! Prove it for MY body. Prove it beyond a shadow of a doubt that YOUR way will bring me complete healing and consistently radiant health. Forever.

It’s hard to keep up, and I can assure you that I have tried. But not toward a blind goal of generally wanting to feel “better” or do the “right” thing, but to address an auto immune condition in my gut that has been an on-and-off challenge for 20 years. People will ask me, Oh, you’re not eating that, is it because you’re gluten free? To which I once replied, Sort of, about 90 percent of the time. I think it helps, but I’m not 100 percent sure. It’s been literally years since I’ve eaten a sandwich so I’m not sure what would happen if I did. A sandwich. Years. The food I pretty much lived on for the entire 17 years of elementary school (when I wasn’t sent to school with a slice of tofu spanakopita), middle school and high school, and much of college – though by then I had become a vegetarian and incorporated bagels, burritos and pizza to my healthy collegiate diet.

****

At some point early in our marriage, probably around the time we had our first child, my husband and I incorporated what we call The 75% Rule. Mostly it applies to what we eat, what we clean our house with, what we clean our bodies with. It also applies to how we parent and to bigger life decisions. I think it’s a very kind and gentle approach to ourselves – guided by the idea that perfection is a trap, an endless black hole that has no end, and if we can aim for doing our best 75 percent of the time, that’s pretty great.

So it means we don’t go into debt buying the $4.00/dozen grass-fed eggs at the farmers market – because even though they are really beautiful and delicious and I wish they were in the budget, our children’s 529 college savings account takes priority. It means we make sure our meat is free of added hormones and antibiotics and splurge on the local, grass-fed stuff once in a while, and we don’t eat meat every day. It means we get some of our fruits and vegetables organic – in particular the ones that are at the top of the eat only organic list – and others non-organic, again because I prefer this to credit card debt of any kind. It means the products we clean our house with are natural, except for the bottle of bleach we keep in the cabinet for unexpected totally gross messes like the dead squirrel one of our cats dragged into the basement last week. It means we don’t spray our lawn with pesticides or chemical fertilizers but will do a non-toxic spray against mosquitoes before they return in the spring. It means we keep a frozen pizza in the freezer for babysitter nights. It means there is always chocolate in the pantry because if any camp believes chocolate is bad for me, I don’t want to know.

It means we do our best without making ourselves crazy, because I know from years of experience that making myself crazy is the #1 worst possible thing for my auto immune condition. Not to mention crazy is not good for my self-esteem or my sanity, and I value my self-esteem and sanity a great deal.

There is always going to be something out there that’s not good for us.

We can spend our lives chasing after the next great thing, the surefire solution to all of our physical ailments or challenges. We can feel constantly like we are never doing enough. And the Enough Trap is in close collaboration with the Perfection Trap in conspiring against us.

Or we can do our best, follow the good feeling that leaves room for the enjoyment of all that is out there, and remember that anything we fear – even if it’s organic, grass-fed, homemade, artisanal, all-natural – as long as we fear it, it will not nourish us. I probably would be fine if I had a sandwich like the kind I used to eat back in high school – roast beef on a French roll with tomato and mayo. I probably would love it, too. Especially with really good bread and really good roast beef and a juicy organic tomato. As long as I could let myself enjoy it fearlessly, just for the purely delicious experience of savoring something good. I’m pretty sure it would taste better than a bowl of kale.

momentum

_MG_6255_med

photo: Kate Inglis

For a long time now, I have lived with a chronic illness. An auto-immune condition. What doctors like to call a disease. (I am not a fan of that.) I’ve never written it down quite like that before, that I live with a chronic illness. I don’t like that I live with a chronic illness. But I do. I’m surprised – sometimes stunned – that some unfortunate life circumstances have gotten me here. But I’m here.

I’ve written this post in my head so many times, yet shied away from writing and sharing it for so many reasons. Because it’s personal. Because who wants to hear about my auto-immune challenges? Because fixating on it doesn’t help anyone. Because I am tired of talking about it and thinking about it and dealing with it. Because I live it, and isn’t that enough attention to put on it? Because WHY?

But I wonder if maybe it could help for me to share. Not just to know I’m not alone (because I do know that) but also because I can’t possibly be the only one who struggles with something physical (and often invisible) in silence. I know I’m not, I’ve been inspired and moved when I’ve read posts and articles by friends and strangers “coming out” about their illnesses and struggles. And when I have shared my own story with friends, I’ve often gotten some form of, “I can relate!” from them.

We’re all dealing with something.

****

I am by nature an optimistic person. I don’t give up when things get hard; there is always a part of me that hopes to feel better, that believes I can. That believes in healing (which is a complicated word for me). Overall I feel good. Overall I feel better than I felt a few years ago. When doctors ask me if I have any of the long list of conditions their questionnaires usually ask about, my answer is always, “Except for this one thing, I’m actually doing well.”

There are two ways I can look at myself and I’ve learned which one works best for me within the cycle of chronic illness.

There’s the micro-lens approach, where I look at every single detail of my body and health through a telephoto zoom lens to see ALL of the ZILLIONS of things that are going WRONG. Primary issue: My gut isn’t happy. Then: My hair is thinning. I’m always cold because I can’t keep extra weight on and my thyroid is probably low. My hormones are for sure imbalanced because I’m in my forties. My adrenals are definitely tired from years of physical and emotional stress. My skin is getting thinner and drier. etc. etc. This approach sometimes involves internet research, which leads to panic and despair, or sometimes hope that attaches to something that I haven’t tried yet that might, just might work (but usually doesn’t).

Then there’s the macro-lens approach. This is where I step back to get the BIGGER PICTURE, looking through a very wide angle lens instead of zooming in at the details. This is what I see through this lens: I’m happy. I’m peaceful. Overall I’m feeling better than I have in a long time. I’m healthy, and I have this thing that is a challenge and that I deal with. It’s chronic but it’s not lethal. And I know for the most part how to manage it. I know how to seek out good doctors and how to work with them and advocate for myself, essentially directing my own care. I am blessed to be surrounded with abundance and love and security. I eat well and take good care of my health and the health of my family. I have access to healthy ingredients. I have access to health care.

I am safe.

Can you guess which approach works best?

****

I fluctuate between feeling acceptance and feeling frustration about my physical challenges. I’m starting to get that it is possible to feel both at the same time. For me, there is a lot of peace to be found in acceptance. I don’t like feeling as though I am trapped in my body and fighting against myself. Screaming out, “No, no, no! I don’t want to live with a chronic condition! How did I get here and how can I get out of this confining box?!” Because the thing is that I can’t get out of this body, and I don’t want to. I like it here. Very much. It’s the only body I know and it is the vehicle carrying my soul this time around. And I am nowhere near done with this time around, so this is the body I get till I’m 101 and I can go peacefully in my sleep.

My husband once pointed out to me that I have a lot of momentum invested in being sick. He’s right, and at the same time, I’m not really sure how to manage my condition without investing so much momentum in it. Because it is a lot of work managing an illness: Time in doctors’ offices, time and money spent at the pharmacy, time and money getting tests, time and money getting treatments, insurance paperwork to sort through, reimbursements to make sure I get, time reading about things that could help, the energy I spend thinking about what to eat that won’t hurt more than it helps. 

Fear. Fear is a lot of work. I don’t like fear, and most of the time I don’t live in a place of fear. The one thing I can’t quite shake, though, is the fear that I might never get better. That this is as good as it gets. And I mean better in a very broad sense, which is where acceptance comes in: For years I resisted accepting that I would need to live with taking medication (possibly for the rest of my life) to manage my illness. I was determined to get better, naturally, forever. (That was a very heavy burden to carry, a very abstract and untenable goal to reach.) Then one day, after literally years of specially tailoring and limiting my life and still feeling like crap, I surrendered. I went for the big guns and I took the heavy drugs. And I started to feel better. And I had about 9 months when I felt normal again, where it was all worth it, where I forgot I had an illness at all, where I could eat normally and go on long walks with my family. The acceptance paid off and I was able to relax for the first time in years.

Then a round of antibiotics for a sinus infection set the wheels of my illness in motion again and I’ve been trying for 9 months since to calm things down again. (Or, I’ve thought, it was all just a coincidence and the antibiotics had nothing to do with it, and the medication just stopped working; which, I’ve learned, happens.) And sometimes it feels like new things are starting that are also challenging. Sometimes it feels like I can’t eat anything without paying a heavy price later on. Sometimes I feel trapped in my house and fearful of getting in my car. Sometimes I feel like I want to tattoo my forehead with, “I have an invisible illness!” so that everyone will know and I won’t have to explain why I can’t do something or eat something.

****

Recently I was at a holiday party talking to a man in a wheelchair. He was in his late fifties or early sixties and had been paralyzed at age 20 following an accident. He also lived with his own auto-immune condition similar to mine, so we had experiences that were shared and others that were not. And that is what we talked about, about disabilities that are visible and those that aren’t. About planning every inch of your life to make sure you can get through a day feeling good and functioning in a way that is expected by others. About the many things “other people” just cannot understand. All these things we talked about juxtaposed with my awareness the entire time that I really wanted to get a chair so that I wouldn’t be towering over him as we spoke, but every chair in the room was taken by other guests. All these things we talked about while I was aware of how strong my legs felt as they held me and moved my body. All these things we talked about as I felt so grateful to be understood.

****

I think the lesson here must be about directing the momentum in another direction, harnessing all that energy towards the shift I want to create. Following the good feelings I feel and the good feelings I want to feel and calling on the rest of me – physical, emotional and spiritual – to move ahead towards those feelings. It’s a fascinating experience, learning that I can feel good amid something that is a struggle, rather than giving in to that struggle and letting it pull me under and take over.