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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.

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Then, shortly after, Frank answered.

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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.

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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

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My 5th Healthaversary is Coming: Hot Chocolate 5k with me! December 15, 2013

hot-chocolate-logoEvery January, I reflect back on January 2009, when I first started this blog. I think about how I felt back then. Scared, unhealthy, hopeless. And how far I’ve come. Even with this recent injury, I always knew that I had a core of well being inside that wasn’t going to go away even if I couldn’t do much.

This coming January will be my 5th healthaversary. Five years! And I’m going to celebrate in two ways. One, I’m going to participate in the Hot Chocolate 5k on January 12th in San Francisco. I would LOVE to have as many friends doing it with me. A hot chocolate party! It comes in both 5k and 15k distances. And the “swag bag” is crazy awesome – it’s actually a fleece jacket! What!

2013-HC-this-is-your-goodie-bag_WITH-sizing-chartI’ll also be hosting my traditional walk-to-the-labyrinth and brunch at another time, but I realllly wanted to do something “5-ish” for this special five year commemoration. After the ordeal I went through this fall, I am more grateful than ever for my health. This will be the first 5k since my injury. I am hopeful and optimistic that I will be able to complete the 5k, most likely walking. That pesky hip injury I was dealing with BEFORE my ruptured disc? It’s talking to me again (sigh).

So please please please sign up! 15k or 5k, your choice. You can run like a gazelle or waddle like a wombat (that’ll be me). It’s probably going to be chillyish but we will have some cozy fleece! And hot cocoa! It will be a big, beautiful, Foodie McBody Party. No running necessary! (but it’s certainly allowed and encouraged if you like running)

PRICES ARE GOING UP DECEMBER 30th so please take advantage of the early pricing. If you use the code FOODFOODMUG, you will also get a free hot chocolatey mug on race day. Yay swag!

PRP-Snack-Tray

And…. Ta-da!! As an official Hot Chocolate Blogger, I have been authorized to give away one FREE RACE REGISTRATION!

This has been a really amazing five years. The most challenging, exciting, incredible five years of my life. I’m ready to celebrate.  Join me!

If you want a chance to be the recipient of this free registration, leave me a comment here below and tell me FIVE THINGS that keep you healthy! Also, follow the Hot Chocolate 15/5k on Twitter and Facebook to get all the sweet details.

And the winner of the race registration is… JULES!! Congrats, Jules, I’ll be sending you your registration code. Can’t wait to see you (and everyone else!) out there on January 12th!

HCSANFRANCISCO500X500

 

Grateful. November 29, 2013

a new day

a new day

Yesterday was Thanksgiving day, and I had a lot to be thankful for. Just a few weeks prior, I thought I might have to bail on the holiday altogether, as I had been bailing on many things right and left since September. But thanks to my successful surgery and my gradual recovery, I had a wonderful day that managed to keep the majority of beloved traditions intact.

For the past four years, I have been participating in our local Weight Watchers 5k Turkey “Trot” (mostly a walk, although I did partially jog it a few times). This is something I really did not want to miss; starting the day out with some good company and activity. I had missed my WW members so much and I was hoping to see some of them there.

so excited to see many of my WW members

so excited to see many of my WW members

Hooray! Quite a few of them were there and it was great to walk along the shoreline with them. Pretty soon, though, I was feeling like “whew you guys are walking awfully fast!” and I fell back to the group behind them, and then behind them, and I was walking slower and slower and then I felt my gas tank start to sputter. I knew I had to turn around to the start point. I didn’t  measure the distance but I was guessing it was maybe half – like a mile and a half? The last few blocks back to my car felt like forever. I waited to meet up with them coming back the other way and got to see the fabulous Julie, who has been generously and enthusiastically holding down my meeting for me in my absence. I am forever grateful for HER for giving my members consistency while I’ve been away.

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It was tiring, but I was really really happy to have gone, and to be out there on the shore at sunrise. It felt like the beginning of a new day.

The triple challenge for drive-walk-drive, from 6:30am-9:00am pretty much took the stuffing out of me. I went home, gave instructions for various food preps, and took to my bed for several hours. Whew.

Right before dinner, we had a little holiday card family photo shoot.

intergenerational beauty and silliness

intergenerational beauty and silliness

the guys took care of the bird

the guys took care of the bird

My family has been amazing. A billion more gratitude points for them. They lifted all the heavy pots and pans, reached into high cabinets, chopped and prepped and stirred and did everything that I couldn’t. It all came together into a beautiful meal.

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my plate

my plate

After dinner, I needed another very big lie-down. The one task I had taken on was the Making of the Pan Gravy, and standing over the stove with my neck bent over the pan didn’t prove to be very comfortable in the long run. I was incredibly grateful (AGAIN) to everyone for doing ALL of the cleanup while I took some medication and lay on the couch.

dessert buffet!

dessert buffet!

Round 3 of Thanksgiving tradition: dessert and games! We had good friends come and join us for the grand finale of the evening. We have been playing games after Thanksgiving dinner for as long as I can remember, and it always ends in great hilarity. This time we played the old chaotic game of Pit, and then moved on to Balderdash so that all 14 of us could participate. We were laughing so hard we were wiping tears. Good times.

PIT!

PIT!

By ten o’clock another wave of major droopiness was setting in. But that was fine. All of the major holiday traditions had taken place: turkey trot, family photo shoot, dinner, friends and games. I managed to get through out with several big rest breaks and not a whole lot of pain. Considering where I was just four weeks ago, this was nothing short of a miracle.

super thankful for him

super thankful for him

Today is rest day.

 

 

Back In the World (Sort of.) November 23, 2013

#throwbackthursday: sometimes I have to hold onto stuff.

#throwbackthursday: sometimes I have to hold onto stuff.

Little by little. I’m venturing out. I’m doing small things, both in and out of the house.

Everything feels huge. HUGE. The first time I drove the car last week, I felt like a sixteen year old with a new permit, gripping the wheel with white knuckles, waiting long minutes before pulling into traffic. Testing out my neck, my reflexes, my attention, my ability to focus on more than one thing at a time. (the radio, other cars, my husband’s voice) I drove about 5 miles to drop my mother off at her volunteering gig.

I am humbled and amused that my 90 year old mother has about 100x more stamina and energy than I do. She can spend a day stuffing envelopes, come home and walk the dog, then go out to a Golden State Warriors basketball game, cheering and stomping until 10:00pm. All of which would probably kill me at this point.

People are happy to see me out in the world. They tell me I’m looking great! The teeny tiny bandaid at the the back of my neck doesn’t really represent anything. I say, the incision is small but deep. But it’s not just the incision that cut through the tough white fascia in my spine, the muscles and the drilling into my vertebrae. It’s the six weeks of unfathomable pain, of lying in bed trying to find a position, or walking around in ballet position, of counting the minutes before I surrendered and had to just get horizontal again (15 minutes on a really good day, 2 minutes on an average day).

Meanwhile I was forever experimenting with the pharmacy that was multiplying in my bathroom, trying to test the drugs to see which would bring relief without vomiting or psychosis or some other unpleasant side effect. Meanwhile my muscles, so long the pride of my body, have thinned down into thread. I have to be careful with what I lift. Even some plates are still too heavy. I’m better with saucers, single utensils, the little mugs and glasses, not the big ones. Pots and pans are out of the question. I won’t be hauling the turkey next week.

This week I stopped in at the Weight Watchers center to check in with Julie, the fabulous leader who has been filling for me since September. I told her I didn’t think I’d be back this week. Just sitting in a chair listening to her speak tired me out. I couldn’t imagine summoning the energy to stand up in  front of the meeting room. Not yet.

Last night I went back to the Writers Grotto because my beloved office mate was having a pre-nuptial party and I wanted to celebrate with her and the writers I’ve missed for so many months. I wanted to see my little space that I’d missed.

My succulent plants were long dead.

is this a metaphor for something?

is this a metaphor for something?

After a couple of hours of merriment (during which time I mostly slouched in the corner of a sofa, kind of dazed) I felt like I was melting. Unable to speak or hold up my head. I got home around 7:30 and went directly to bed.

Parties are fun, but they take a lot of energy!

Parties are fun, but they take a lot of energy!

This is how it is now. Better, so much better, but so far from where I was. I’ve taken a few walks this week, no more than a mile at a time. I slow-walk, always with a friend, whose arm I can grab if I start to wobble, half a mile to the “It’s Nice To Be Nice” bench. Then I rest. Then walk a half mile back to the car and again, directly to bed. It wipes me.

Alexandra accompanies me on the one-mile marathon

Alexandra accompanies me on the one-mile marathon

Still, I’m managing to get some things done. I’m checking things off my to-do list. Phone calls and getting stuff done that I never had time to do before. Small things.

I’m reading. And writing. Thinking about new directions for the new year.

I’ve started reading Roxana Robinson’s stunning novel, Sparta, and reading about the Marine returning home from Iraq, and how returning from his experience is so surreal and terrifying, how his loved ones want to welcome him back just as he was before.  I know that two months of a herniated disc is not really comparable to four years of war, but it’s been like a little war in my body. It was a shocking kind of attack like I’d never experienced before. Where everything I believed and knew about myself was called into question.

I’m putting my life back together but it’s so much slower and in smaller increments than I ever could have imagined.

 

 

 

Post. Op. November 17, 2013

Pre-Op with my buddy.

Pre-Op with my buddy.

So, it finally happened: I had a cervical laminotomy, microdiskectomy and foraminectomy on Wednesday afternoon. I had been hoping hoping to avoid surgery, but after eight weeks of really relentless pain, I was glad to try something that promised the hope of relief. I won’t lie, I was nervous. And emotional. But ready.

We got to the hospital a few hours ahead of the 3:30pm surgery time. I put on my stylin’ hospital gown (very nice design, with a big pocket in the front!) and settled in to wait. I was visited by the neurosurgeon, the anesthesiologist and the OR nurse. Finally they wheeled me into the operating room. The last thing I remember was going through the swinging doors that said OPERATING ROOM on them, and then… nothing.

I woke up and there was a nurse who kept saying, Take another deep breath. Another one. Apparently I had to hang out in recovery for a couple of hours because the breathing thing wasn’t happening to their satisfaction. I had about a minute of “I think I’m going to be sick” but they shot me up with anti-nausea stuff right away and nipped that in the bud, so for the first time I didn’t have terrible vomiting after anesthesia. I was very grateful for this.

Finally they brought me up to my room where Mr. McBody had been waiting for me. I was so happy to see him. And by the time I was awake enough to notice, I realized that the arm/shoulder blade pain that has been torturing me for two months was gone. GONE. AWAY.

I did a lot of sleeping. I managed to get up, with a lot of help from the nurse and Mr. McB, to the bathroom.  The next day (Thursday), the physical therapist came by and stated we were going for a walk around the hall. This sounded very ambitious to me, but lo and behold, holding on to the IV wheel, I did it.

the physical therapist took me on my first walk

the physical therapist took me on my first walk

There was a big board in my room with all of my pertinent information. One thing they do is ask every several hours, What is your goal? (I thought this was kind of amusing). I said my goal was to go home.

Goal: would like to go home.

Goal: would like to go home.

I got home around noon on Thursday. I think I slept most of that day. Friday and Saturday I felt pretty sore in the incision area, which they said was to be expected. Even though my incision was pretty small, it was deep and a lot of stuff had gone on in there. As Mr. McBody is fond of saying, “they really raunched around in there.” He was able to get ahold of my surgery report which I found very interesting.

I had noted that there were these two spots above my ears (on my skull) that were very, very sore and tender. Then I realized that this was because my head was clamped to the table!

The head was secured with the Mayfield head fixation device

Which I suppose was a good and necessary thing. I was taken by how many times the words “careful” and “carefully” were used in the report. Like a dozen. Somehow this made me feel good. I mean, he wouldn’t say “casually” or “messily” but I liked that he made a point of being “careful.”

It became clear that there was a large disk herniation causing marked compression of the ventral nerve root at its exit from the spinal canal… the larger pieces of the herniated disk were mobilized…this resulted in immediate decompression.

Reading this, and talking with the surgeon the next day, made me feel so relieved and also like… so there was a REALLY BIG REASON I have had so much pain. He said that the nerve had basically been strangled and stretched and he was surprised I had been able to go 8 weeks in this condition. I was also so relieved that it was so straightforward – there was a very specific, physical cause for my pain and he fixed it.

So since I’ve been home, I’ve had different pain. The place where the incision happened has been pretty sore, but it mostly bothers me when I’m changing position. (lying down to sitting up is the worst) Once I’m in the new position, it kind of calms down and then I’m good unless I move too much. It’s a completely different sort of pain, and I am noticing that it is improving every day.

Yesterday, Lily came by and took me for a walk up on the trail. We went a whole mile and although it was exhausting, it didn’t make my pain worse. So YAY!

1 mile walk!

1 mile walk!

I feel like I am finally on the road to getting better. I’m still not able to drive (too much head turning) and I don’t have a lot of energy, but that terrible, awful stabbing pain has left the building.

I didn’t get to Minneapolis this week. Which was sad and disappointing. But tonight I am actually going to show up for something on my calendar. I’ll be reading from this new book tonight and I’m going to be out in the world, even for just a few hours.

Yay. Whew. Yay.

 

Ambulatory! November 4, 2013

Filed under: exercise,health,walking — Susan @ 8:26 pm

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News flash: I just walked down the street and back! Super weak and shaky, hanging on my sweetie’s arm, but I did it and it wasn’t so bad. This is improvement!

 

Dehydration is the Devil! October 22, 2013

Filed under: diabetes,health,hospital,injury,lessons learned,pain,struggle — Susan @ 6:30 pm

free-terrible-devil-wallpaper-wallpaper_422_86164That’s a direct quote from Junior. Both of us have had a lot of miserable experience with dehydration. This used to happen with me quite a bit with longer races and it was BRUTAL. Like HERE. But somehow, I did not put all the pieces together this last week and realize that it was the same exact devil. Loss of appetite, nausea, vomiting, sudden weight loss (I was pretty much losing a pound a day and was about 10 lbs down from 2 weeks ago), weakness, just FEELING LIKE DEATH. But since I was already feeling pretty deathish due to the bedrest and neck pain, it was hard to separate it out. It all felt like a version of the same thing. I thought I was feeling bad from various painkillers. I didn’t know which end was up.

But I remember how it used to be after races. I would be literally feeling like death, and then all I needed was fluid, electrolytes, salt. Chicken soup could do wonders and it was like a miracle had occurred. Like putting a dried out old sponge into water, and soak soak soak — voila.

That’s how I feel today. It’s a miracle! I’m ALIVE!

I’m back to my “baseline” which is: fairly OK lying down, more pain when I get up, but overall alert and feeling a lot, lot, lot better. A LOT BETTER! I actually WANTED and ATE a panini sandwich that Junior made for me and it was the most delicious thing ever. I’m on the way back.

It’s amazing what 12 hours of sleep, three liters of IV fluid and some antibiotics (for my urinary tract infection) can do.

 

 
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