foodfoodbodybody

eat, move, think, feel

My Nights With the Mask September 9, 2016

img_7417

It’s been a few weeks of adjusting to sleeping with the CPAP mask for my sleep apnea. I’m not gonna lie. It has not been easy. I was really hoping that after a few nights of using it, I was going to feel super energetic, chipper (“genki” in Japanese) and awesome. But no. The issue is that even though I am breathing better, with fewer episodes of non-breathing, I am sleeping much more fitfully than before.

Before this diagnosis, I was sleeping straight through, long nights, but breathing terribly (which I was never really aware of). NOW, I wake up many times during the night. And I’ve got this THING on my face. Which I do not enjoy. Well, to be honest, sometimes the thing ends up on the floor. The second night I wore it, I apparently fought with it in my sleep and I woke up to find it in multiple pieces on the floor next to my bed.  (not broken, just completely disassembled!)

I took it with me on vacation. One night, I woke up and I was just so dang uncomfortable. I hated the feeling of this rubber triangle covering my nose, and straps around my head. But I thought, just hang in there. I lay there being hyper-aware of every breath and every little indentation into my skin. I was awake for hours.

But the frustrating thing was, I didn’t NEED to wear it for hours while I was awake. The thing with sleep apnea is, it only happens when you’re ASLEEP. So basically I was lying there feeling tortured, for nothing. After several hours of this I was beside myself, so I ripped it off. Then I promptly rolled over and fell dead asleep. Of course.

When I woke up, hours later, I realized that I had spent half the night awake, (with the mask on my face) and then the early morning hours asleep, without the mask. I broke into hysterical sobs. I had been trying SO hard to be compliant, to do the right thing, and ended up doing exactly the wrong thing.

I’ve had better nights since then. I’ve made it sometimes six or seven hours. When I wear the mask, I’ve had fewer than one “breath interruption” per hour, in contrast to the 37+ I was having PER HOUR before. (!!)  So that’s good.

But I’m sort of heartbroken. I feel like this beautiful relationship I used to have with sleep, and my bed, has been shattered. I used to love going to bed, and love sleeping. I was in love with sleep, and I felt so lucky to not have it be a fraught kind of thing. But now it is fraught. It is super-fraught. I dread going to bed. I dread that moment of putting the mask on my head, and trying to find a comfortable position that will allow me to sleep without letting air hiss and leak all over. I’ve found that it’s much easier to deal with if I go to bed when I’m really, really, really tired. (so I don’t have much consciousness or energy to fight it) Which means I’m going to bed super late. And waking up much later than before.

Overall, I admit I’m getting more used to it. I signed up with the website that manufactures my particular CPAP machine and it has all kinds of helpful tips and videos. One woman who appears in several videos said that it took her 3 months to adjust to her machine. Three months!! That was a bit of  shock, but it also encouraged me to not expect it to be all good right away.

One of the most moving parts of the website was a video about “Getting Used to Treatment.” It featured a Woman of a Certain Age who was worried about her relationship with her husband. She was bummed about wearing a mask every night. She was wearing flannel PJs (like me) and kind of looked like a sad elephant. But her extremely kind looking husband leaned over and tweaked her trunk-tube a little, and just looked at her in this extremely loving way (as opposed to, You look like a TOTAL FREAK) and then she felt better and was able to deal with it. My eyes actually filled up when I saw this because this is just how Mr. McBody has been dealing. He’s been very reassuring and supportive and kind. And that is why we are now going on our 28th year together. He’s just like that.

I hope that by the time I get to my 3-month mark, this will just be an automatic thing, no big deal. And that I’ll fall in love with falling asleep again.

 

 

Does Cricket Flour Bug You? April 6, 2015

Filed under: cooking,diet,eating,health,Paleo — Susan @ 10:28 pm
Tags: , , ,
Photo Credit: N@ncyN@nce/Flickr

Photo Credit: N@ncyN@nce/Flickr

Until a week or two ago, I had never heard of cricket flour. Yes. Flour made out of dehydrated, ground up crickets. But then somebody brought some cricket-flour cookies into work and they were passed around the lunch table.

cricket

Hey Mikey! I liked them!

They were actually pretty good. Chocolatey. Like… a cookie. Because the crickets had been pulverized into dust, they didn’t FEEL like crickets. (ie., I could not distinguish any little antennae or cricket-legs as I ate my cookie) There was no discernible cricket or insect like flavor. They just tasted like.. cookies. I had no idea I had stumbled onto a hot new food craze. WHO KNEW?

A company here in the Bay Area produces both these cookies and the flour they’re made of. At first I was thinking, WHYYYYY? but then today I read this article about how my newfound love, almond milk, is sending us deeper into drought-land by the minute, and how we might all end up eating dried insects if this keeps up. Or how maybe we should, anyhow.

According to Bitty’s website,

Cricket flour is a tasty source of sustainable nutrition, packed with protein, healthy fats and micronutrients. We start with sustainably raised crickets, which are slow roasted to bring out their nutty, toasted flavor. Then we mill them into a fine flour that becomes the basis of our delicious, high-protein baked goods and baking mixes.

All our products are free of grains and processed sugar, and are made with coconut oil rather than dairy products. Best of all, they taste terrific. When you’re starting with an ingredient as good as cricket flour, why would you add any of the “bad” stuff?

Crickets are also one of the most sustainable forms of protein on the planet. Last May, the United Nations Food and Agriculture Organization published an incredible report concluding that edible insects may be the key to stabilizing the global food supply.

According to the UN, if edible insects become a part of the mainstream global diet, we can reduce greenhouse gases by 18%, and lower the average cost of food globally by 33%. Check out Bitty founder Megan Miller’s TED Talk to learn more about the benefits of cricket flour.

So what do you think? Would you eat cricket flour products to save the planet?

I’m not quite ready to pop a chili-flavored insect in my mouth, feet and all, but I just… might… be able to start with flour.

 

Year of Pain, Year of Humble November 13, 2014

IMG_7202Last week, after I spoke on a panel on reproductive stigma and justice, an audience member came up to me and said, “I know you.” I looked at her. I didn’t recognize her at all – a warm smile, brown skin, dimples. I squinted and said, “Really!” She said, “You’re Foodie McBody. I follow your blog!”

I was overwhelmed by a storm of thoughts and emotion. What blog? Hahaha. I haven’t posted a thing in months. And who? Foodie McWho? That person was a person who had receded so far away from me. I’d changed my Twitter handle and Instagram name, and nobody called me that anymore.

Foodie McBody was a person who, once upon a time, took her health by the reins and galloped into a transformation. There were years of glory. The first 5k! The Weight Watchers Lifetime key! The 10ks, the half marathons. Four of them. The two triathlons and more 5ks than I could count. I loved my health and loved my active body and I was just proud and glad, even through the struggles. I had little bouts here and there – a sprained ankle, a wrist flareup. But they all resolved within a month or two, and then I was back in the saddle again.

But then 2013 happened. I call it my year of pain. When my hip gave up after the Oakland half marathon, my last, and told me I might need to get it replaced. And then the fateful bounce on the trampoline that ruptured my cervical discs and brought me to a halt. When I could do nothing more than move, agonizingly, from one horizontal position to the next. Surgery, recovery and rehab in small, tentative steps.

2014 was supposed to be my comeback year. But it has not been that. After a brief triumphant walking 5k at the start of the year, I have been plagued by a thyroid condition that stalled my metabolism, and a foot ailment that won’t let up. Plantar fasciitis turned to posterior tibialis tendinitis leading to some sort of Achilles problem. My Achilles heel, indeed. Every morning I hobble out of bed like a 90 year old. Actually, I hobble out of bed more painfully and slowly than my own 92 year old mother, which is humbling, to say the least.

my Achilles heel

my Achilles heel

Do I want some cheese with my whine? Well, why not.

2014 has been the year of humble. But if I’m honest I also have to admit that it’s been a year of fear. Recently our family re-watched Spirited Away, one of those hallucinogenic Miyazaki films. One of the most disgusting images is this creature, the Hungry Ghost, that eats everything in sight – frogs, bicycles, humans, and keeps wanting more. It grows into a mountainous blob of sludge, its arms outstretched, and stinkily consumes everything in sight. When our young heroine refuses to be intimidated by the ghost, and doesn’t run away from it, it starts expelling the contents of its innards. Finally it shrinks to a fraction of its enormous size, and silently boards an underwater train, presumably bound for freedom.

That image has haunted me. And I think that that creature is like my fear. It reminds me of the Before version of Foodie McBody. Before I charged into healthy living in 2009, I was afraid of everything. Afraid to move. Even when it felt good.

For much of the time these days, I am paralyzed by fear. Only recently I’ve been able to venture into small, almost laughable activities. I join a weekly AquaFIt class at our pool, where most of the participants are ten, twenty or even thirty years my senior. For an hour we splash around the pool with foam weights and noodles. It feels like play, but when I climb out of the pool, I have to admit it’s kicked my butt.

I walk silently in the redwood forest near my house. Today I did a silent walk and in the quiet green I thought about my fear. The sky was white, a little blue, like the inside of an ice cube. The air I moved through was chilly and perfect, and the sun blinked uncertainly through the clouds every now and then. What am I afraid of? I am afraid of pain. My left heel sent out little jolts. So what, I said. So what. It’s not killing you. I notice. What do I notice. It’s like electricity. It’s like heat. It’s like a twangy little song reminding me that I’m alive. I liked the feeling of my legs. I still have muscles there. They’re still strong. I pushed up the gentle incline and I didn’t wheeze. I didn’t die from shortness of breath. I was doing it. It was just a walk. Calm down, I told myself. You’re okay. There’s nothing to be afraid of.

IMG_7007

Worse than the pain, though, is the shame. The pain of shame. Of knowing where I was three years ago, that relentless athlete that swam in the icy, salty bay. The one who looked fear in the face and climbed on the bicycle, up hills, up so many hills, near whizzing cars and dogs. I ran and ran and ran. Three or four days a week, tweeting about my six pain free miles, my happy eight miles. These days I would consider it a victory to walk a 5k, to make it around Lake Merritt without sitting down, without limping. This is the greatest pain. To look in my closet and push aside the majority of the clothes, because nothing fits.

How to find compassion? That is what I want for 2015. The year of compassion. To say, it’s all right. You’re okay, whether you never complete another triathlon again. Whether those 15 pounds stick around like old friends. You’re okay. You’re okay.

These days do not look like 2010 or 2011. These days look like walking in the beautiful trees, like greeting my gray haired companions in the shallow end of the pool. Of meditating every morning, first in silence and then listening to the calm, warm voice of my teacher, leading me through the compassion meditation. Open to the possibility of being kind to yourself, he says. Open to the possibility of appreciating your life.

I’m open.

my walking meditation path

my walking meditation path

 

Plantar Fishy-what?? July 12, 2014

Ah, this blog has become such a litany of woes, I might as well just re-name it “I’m Getting Old, Falling Apart and Whining About It.” Seriously, though. Really?

No sooner had I gotten over the bummershock of having a faulty thyroid, than I began waking up with excruciating, hobble-inducing, holding-onto-walls heel pain. It had started out as a dull ache which I not very brightly ignored. Then while we were on our lovely vacation in San Miguel de Allende, which involved miles of tromping around on picturesque cobblestone streets, lo and behold it worsened every day. I think my foot liked those pretty streets very much.

Plantar fasciitis. OW.

And it pretty much put me off walking except when absolutely necessary, and running, like ever. WAHHH!

More travel happened. A long weekend in Louisiana for an amazing family reunion. Boatloads of crab (no exaggeration at all!). Ten thousand percent humidity. Aching heel. No movement. Pathetic thyroid. All this adding up to… more weight gain, overall bummedeness, etc.

More travel. Back to California, and straight to Pact Camp.  Intense emotions, busy days. NO time to deal with anything. But along the way, I’ve been picking up suggestions and ideas from fellow PF sufferers. Rub your foot with a metal spoon. Icing. Dansko clogs. Splints.

But now I’ve been home a few days, and I’m re-grouping. One great thing that happened while I was zigzagging around the country is that Carla favorite a tweet that said something about The Sock.

shelly jpg

Then, shortly after, Frank answered.

frank

I clicked on the link for the Sock. I watched the video. It was designed by a physical therapist! My people! I sure liked the IDEA of a sock rather than a rigid splint, which I knew would drive me insane within minutes. I read a ton of enthusiastic reviews, and then I ordered.

It arrived yesterday. I put it on before I went to bed. I already had a feeling that keeping my ankle/foot at a 90 degree angle, even if in a flexy sort of way, would be radical. I like to sleep on my stomach or my side, and my feet are pretty much in high-ballerina position all night. Yes, my heel cord was getting SUPER tight.

I didn’t apply it super tightly. I’d read warnings about numb toes and such, if it was too tight. I didn’t want to freak out myself or my toes.

I woke up this morning. The proof is in the STANDING UP, which is normally when I double over from pain and have to grab at the bedpost to stay upright. And then I hop to the bathroom on one foot. It’s not nice.

But this morning — I had the dull ache, but it was equal to what I normally feel after hours of walking around. It was GREATLY improved.

I have been so very discouraged and bummed about this, I didn’t want to write about it until I felt at least a glimmer of hope. Well, it’s glimmering. Here’s to turning a corner and having no new parts fall apart for a while.

I’ve been trying not to feel too sorry for myself when I see friends out and running or walking 5ks, 10ks, half marathons, triathlons every weekend. But I tell myself, I’ll be back. And now I think I might even believe it, a little bit.

image from Clipartbest.com

 

Another Chronic Disease, O Boy June 17, 2014

Five years into being diagnosed with type II diabetes, I finally felt like I had come to some sort of peaceful relationship with it. I felt like I was managing the best I could, and was really pleased late last year when my endocrinologist decided to discontinue my oral medications. I hadn’t even been considering that as a goal, so when she suggested it, I was both surprised and happy.  She said I was doing great. YAY ME!

I was interviewed (and photographed) by Diabetes Health Monitor magazine (a staple in endocrinologist offices everywhere!) and feeling pretty darned good about it all.

Then, a couple of months ago, things started changing. My blood sugars started bumping up. Then they bumped some more. They went higher than I’d ever seen before. I panicked. I called my endocrinologist and begged her to let me resume the medications.  She said okay, and resumed my lowest dose. Sigh.

Then my weight started inching up at a steady rate, despite my doing basically nothing different than I had in the past five years. Now, I’ve been doing Weight Watchers for a long time. And I’ve learned that when I see a surprise gain at the scale, there’s always been a reason. An indulgent weekend. A sedentary retreat. Any of those things. But I’ve always easily been able to right the ship, and come back on course within a very short time.

This time, not so much. I mean, not at all. That in spite of all my best efforts, the ship was not righting. Every few days I’d step on the scale, and every time, it was higher than the time before.

I was starting to freak out. I was starting to dread my WW meetings (which I LOVE) for fear of being called out as fraudulent, bogus, the works.  I was getting frantic that my clothes were getting to be terribly ill-fitting (or non-fitting). My torso was starting to resemble that of a 2nd trimester pregnancy. And I wanted to sleep, like, ALL THE TIME.

What the hell!

For a while, I was in silent paralysis. I couldn’t discuss it or deal with it at all, I was so freaked out. But then I called my doctor(s) who recommended thyroid testing. (and: lo and behold, thyroid problems can cause out of control blood glucose!) An ultrasound revealed an enlarged thyroid. Next step: blood tests. I had the tests last week and this week, while on vacation with my family, I received emails from both doctors. Normal TSH levels are .5-5, and mine is 9. Bingo.

Diagnosis:  hypothyroiditis, or Hashimoto’s disease. Then I nodded. I had about 90% of the symptoms. Weight gain. Puffy face. Fatigue. Brittle hair and nails. Memory issues. Joint pain. Weakness. Vision problems.

Wonderful.

Sigh.

Well, damn.

I’m trying not to be all WHY ME? about this, but damn. Come ON. Okay. So what do I do. I start taking thyroid supplements. I start figuring out how to manage THIS chronic disease.

Part of me is really, really pissed off. But part of me is relieved. That it’s not worse. (it can always be worse, right?) And that this condition has a treatment. For which I am very grateful. I can’t wait for it to start WORKING! (this could take weeks–>months)

As I did when I first started this blog, and basically with every time I’ve every struggled, I know that reaching out with the struggle is better than struggling alone.  I know that finding community and support is better than flailing around alone.

Even thinking about writing this post has made me feel better.

 

Goodbye (sort of), Foodie McBody June 6, 2014

Foodie McBody

Foodie McBody

I just did a little thing that felt like such a BIG thing. I changed my Twitter handle, which has been @foodiemcbody forever. But for the last six months or a year I’ve felt like so much MORE than Foodie McBody. Many people I interact with now, in the writing world and beyond, don’t recognize or know Foodie.

It makes me feel really emotional to make this change. I first took on the name Foodie McBody as an anonymous name when I started this blog. Because I was ashamed of who I was. I was diabetic and overweight and unfit and desperate. I wanted to reach out for community and help, but I was embarrassed to be in the world as ME, Susan Ito. And that’s how Foodie came about.

When I started feeling better about myself, I shed that anonymity. For a long time I was really proud to be Foodie McBody. And I still am. But I’m more than that now. I’m a writer, a memoirist, a physical therapist, a teacher. Sometimes those selves fit with Foodie, and sometimes they don’t.

Last weekend I took a fabulous food-writing class at the San Francisco Writers’ Grotto. We were visited by guest speaker Virginia Miller, who blogs over at The Perfect Spot and also writes for Zagat. (!) I realized in that moment that FoodFoodBodyBody has been and is a food blog. And the writing that I did that day could live here. It was a huge sigh of happiness, the recognition that I could integrate these parts of myself.

For a long time I believed that my fitness stole my writing, and then that my writing could steal my fitness. All of it takes time, after all. Following my injury and surgery in the fall, I’ve definitely been more in the writing world. Trying to find that balance again. But I have deep love for the Foodie McBody part of myself, and deep love for my writing life. @thesusanito is an attempt to bring it all together in one self. I hope those of you who met me as Foodie will continue to be my wonderful healthy community, and those who never knew Foodie will learn about who that part of me is/was.

Did you ever feel like your identity was fragmented? What have you done to bring it all together?

 

 

Baby Steps, Baby Sweats, and Goodbye for Now January 5, 2014

Filed under: body image,emotions,exercise,good things,health,injury,Nia — Susan @ 9:59 pm

A couple of weeks ago I sweated for the first time since September. It was a gentle, beautiful, emotional and extraordinary experience. I went to a Nia class, which was one of the very first kinds of movement I ever did, five years ago. Danielle was the instructor, and it was one of her final classes before she leaves for a two-year journey to China. IMG_2220One of the other dancers was Alexis (pictured in my post here 2009). She brought her adorable six-month old baby with her, and danced with her in a front carrier. Her gentle, modified moves were perfect for me, just creakily getting back into movement. She didn’t bend as low or hop in the air or do any sudden moves. Just gentle.

IMG_2221

babydancing

Because it was Winter Solstice weekend, Danielle did a routine called Mandala that involved no spoken instruction. She moved, we followed, and she indicated transitions by clapping her hands. It felt so organic and wonderful. And the music? It made me tear up immediately. She played the music of Kitaro, which brought back really intense memories of a long ago time…

……………………..

Back in one of my first home health physical therapy jobs when I was in my twenties, I had a patient named Oscar. He had a really advanced spinal cord tumor which had left him with paraplegia. I first worked with him in the hospital and then at his home. After some time it became clear that he was not getting better. His final desires were to walk again, however limited, and to go home to his homeland of Argentina. None of his doctors believed in either of these goals as either possible or advisable, but he was a determined guy.

When I visited him at home, he played Kitaro for me for the first time. “Listen,” he said, and he put these huge cushy headphones over my ears. This was at the very beginning of “New Age” music, and I’d never heard anything like it. He believed that it was magical. That it would help him walk. And one day I’ll never forget, he played this music through speakers in his living room, and step by step, he walked about ten steps across the floor. I was holding him by two shaking hands with a gait belt, and pulling his wheelchair by nudging it with my toe, and both of us were sweating bullets. But to the soundtrack of this incredible otherworldly music, he took his last walk.

Next, he asked me to take him to Macy’s in San Francisco so he could buy a traveling outfit – new pants and a jacket, and gifts for his family. It took all that I had to transfer his unwieldy body and his heavy wheelchair into my little Toyota hatchback, but we made it. I wheeled him all through that department store and helped him stand up (in physical therapy terms, using Maximum Assist) so he could see himself in a full length mirror. As we were leaving he said he wanted me to have a gift, and he bought me this beautiful ivory colored poet shirt with huge billowing sleeves. Because you are really a writer, he said. (yeah, he knew) Shortly after, he got onto a plane to Argentina and that was the last I ever heard from him. I assume he made it home for his final wish. But that was one of the most moving and meaningful experiences I ever had as a therapist.

I was young. Super young. And in retrospect I broke all kinds of rules I probably or maybe wouldn’t do now: I took a patient somewhere in my own car (liability no-no!). I accepted a gift from a patient, and lunch too. All these things are super frowned upon now (and probably then as well!). But that experience changed me.

……………………..

Hearing Kitaro again in this return-to-movement class was terribly emotional for me. Danielle was leaving. Oscar had been leaving. I was returning to something I wasn’t sure I’d ever be able to do again. All of this without words, but in stretching and turning and circling around the room. I had a hard time keeping the tears in. (so I didn’t)

Danielle has been an amazing teacher for me  – graceful and strong and fun. I will miss her Michael Jackson Nia classes, her Halloween class, all of them. She sent out so much healing energy to me when I was hurt and I really felt her caring. I will miss her. I’m glad I got to experience her Nia one last time before she goes. Godspeed Danielle, and thank you. oxoxo

IMG_2225