Attitude of Gratitude

I've recently become fascinated with the UK television show Embarrassing Bodies.  I've been following Dr. Christian Jessen) on Twitter for some time (he's adorable, candid, and always has good info).  I don't plug my TV in/don't have cable, but I don't think anything like this exists in the United States.  People in the UK talk about their medical problems on national TV.  Not only do they talk about them, but they quite often get naked and have exams.
following one of the show's doctors (

But I like their take -- that despite the show's title, our bodies are nothing to be embarrassed about, that we owe it to ourselves to get to know our bodies, and to have honest and frank conversations with our medical providers.

Anyways, I was watching an episode last night and they had a feature on a woman who has had arthritis since she was a child.  She's had both hips replaced and both knees replaced.  She uses a wheelchair to get around most of the time, but she's not confined to it. She said something that stuck out to me -- "Arthritis has added something to my life."

For so many people with chronic illnesses,injuries or pain, the illness/injury/pain is about what it has subtracted from his or her life.  We think about the things we can't do or have missed out on, we think about how we feel like our bodies have betrayed us and sold us short.

But man... what a novel concept that chronic illnesses/injuries/pain can actually add to our lives.  I know that my spine injuries have helped me cultivate more compassion for others as well as for myself, and more gratitude for my good days (and even a few of my bad). It has also helped me chill out a bit.

Her statement also reminded me to stop being so adversarial with my back injury. My refuge and relief will come from honoring the gift my injury has given me -- the ability to listen to my body, honor my pain, and returning to trusting my body.

Refuge, but no Relief

If you've read my "About Me" section, you know that I have a degree in English with a minor in creative writing.  When I was younger, my emotions (ahem...anger, sadness, disappointment, rage) made it impossible to communicate sometimes.  Writing was my refuge, the place where I could put pen to paper (in written journals or letters) or fingers to keyboard (on my personal blog that I started in 1998), and create some objective distance from the surface emotions and really figure out what was going on.

There are still times where I turn to writing as my refuge.  The only difference now is that I'm doing it very publicly. I think that's one reason why people connect with my story, my message, and myself:  I've spent years honing my ability to sound unfiltered, raw, and self-aware.  But I do this for myself as much as I do it for any person that reads my blog.  Sometimes life can be so overwhelming that the only way I know how keep my head above water is to write. And so...

Recap:
From late-2007 to the end of 2013, my lower back behaved pretty well.  Between 2011-2012 I was more focused on fixing my neck.  As of February 2013, my lower back hasn't been faring as well.  Not only have I lost feeling in my leg twice while I was in the shower, but also my rebound time after exercising is much slower than it used to be, and I'm having more bad days than I used to (i.e., times when I can't exercise, times when I'm in pain and it's hard to do just about anything, depression because I'm in such pain).

So at the end of January, I made an appointment with my spine surgeon (who I adore, who is a smartypants).  He was hopeful that he could intervene and alleviate some pain.  He assigned some home work -- a few diagnostic tests (MRI, discogram) -- before he could make any decisions about what he could do exactly or whether he could do nothing at all.

Update:
I had spent most of the long weekend in bed -- partly because it was very cold outside (my back does not like cold), partly because I was still exhausted from the discogram, and partly because I was so on edge about my follow-up.  Oh, and probably a bit of depression too.
I tried my best to take a "come what may" attitude, but that didn't work. What I really wanted was for my doctor to walk in and say "WE CAN REBUILD YOU! I have seen all of the tests, I know your history, I have a plan that will leave you pain free and doing cartwheels down the corridors of the hospital."  (NB:  I don't know how to do cartwheels as is...)  I feared that he would say "We missed our window of opportunity.  You're too damaged."

My follow-up appointment with Dr. O'Brien was at 10:15.  The nurse let me know that I was the first of his patients to brave the elements and make the appointment. At 10:45, I started to wonder why I hadn't seen my doctor yet.  I wondered if he was filling in for the other spinal doctor there.  Maybe he had gone for a long coffee break.  Maybe he was standing in front of a mirror rehearsing what he was going to say to me.

At 10:51 he walked in and, after friendly greetings, said "Well, I've been looking through your test results and scans and I have bad news. Your discogram results indicate that you're not a good surgical candidate as there was high levels of pain at multiple levels. Any surgery could leave you worse off than you are now."

My heart sank with an audible "thud" when it hit the floor.

Just by looking at my face, eyes welling up with tears, he knew just how much I wanted him to have the same definitive and clear plan that he had for my neck. For all the joy that I had when he said I was a good surgical candidate for my neck, he knew there was an equal and opposite reaction for bad news.

Dr. O'Brien handed me the box of tissues as I squeaked out, "Did we miss our opportunity? Did we wait too long?"

He explained why I wasn't a good surgical candidate based on the discogram, and how insurance most likely wouldn't cover the surgery based on those results.

He and I had discussed the discogram results and how I felt that they didn't give accurate results. My understanding was that the test was trying to recreate the pain that I normally feel. My discogram didn't recreate the pain I feel on a normal basis:  the pain that I felt during the discogram was frighteningly new -- the lightning that I felt go down my right leg and the whole-back spasm were both new.

I was relieved when Dr. O'Brien said that it could be considered a "failed discogram" (i.e., not yielding useful information) and not so relieved when he offered to have another doctor redo the discogram (um, I'm sure the other doctor is nice, but hell no). I was also amused when he said that he used to call them "scream-o-grams" but then a bit perturbed as to why he didn't warn me. I felt like I was the odd woman out for screaming my way through it, but apparently this is a normal reaction to needles being stuck in your discs.

I asked Dr. O what he would do if he set aside the discogram and I had a few million bucks, keeping in mind the long game (i.e, what would he advise for the long-term health and flexibility of my spine?).  He said that the x-rays and MRIs both point to L5-S1 being the main culprit of my pain as that was the site with both disc and vertebral degeneration.  He advised against a disc replacement in L5-S1 (they aren't as stable as cervical replacements, they are very hard to revise--the anecdotes alone were reason enough to be cautious about any back surgery) in favor of an Anterior Lumbar Interbody Fusion ("ALIF") using an artificial spacer (i.e, not my own bone [hip], not cadaver bone [eww]). In other words, the very thing I was trying to avoid (based on failure rates/cases, restricted range of motion, and the anecdotal advice of just about everyone I knew) was now my best surgical option.  He said that the U.S. is a few years away from the multi-level devices that he would want to use in my lower back at L3-4, L4-5 (the sister device to my cervical implant, and the next generation of lumbar artificial discs [there hasn't been a major breakthrough since 2004 and 2006]).  An L5-S1 fusion could buy me some time and stabilization.

Dr. O'Brien said he'd give me some time to think about it (or rather, as he knows me kinda well by now, to research the crap out of it) and that we could circle back.  I asked him "what if we petition insurance now?" And he asked me whether I wanted to go against his advice and ask for L5-S1 artificial disc, or whether I was asking for the ALIF.  That kind of threw me cause, well, I don't have a medical degree or 20 years of orthopedic experience.  I have no business making that kind of decision.  Trusting Dr. O'Brien's opinion, and my limited knowledge of L5-S1 disc replacement issues, I begrudgingly asked him to pursue the ALIF.

The thing is this:  insurance could still say "nope, too risky, can't approve it" and then we're just back at the point where we started -- that to do any surgery would cause more damage than just staying the course with conservative (ahem ineffective) treatment.  Or they can approve the ALIF and I could chicken out, preferring to wait until the day when having surgery is a better outcome than doing nothing (i.e., for when my discs completely rupture versus slowly leaking).

I don't know what to do.
I hate not knowing what to do.
I hate not having a crystal ball.
I feel a lump in my throat every time I try to talk about it.
I remember how sad and frustrated I feel on bad days.
I feel the weight of the depression bearing down on me.
I also remember how happy I was when I wasn't restricted by this pain.

Do I just go back to that life and pretend I have no restriction, knowing that further damage makes me a better surgical candidate? Or do I just miss out on the life I want, spending my days trying to avoid the inevitable?

I just don't know the right path or if there is one.
I just don't know.

tl;dr options
(1) do nothing and wait for technology to get better
(a) live life normally
(b) remain an inactive hermit
(2) do nothing, live life normally, suffer herniation, have hand forced
(3) do ill-advised artificial disc at L5-S1
(4) try for (improbable) insurance-covered ALIF
(5) Eat ice cream and hide under the covers for a month or two.

Testing My Limits


This past Friday I had yet another MRI on my lower back.  I'm quite glad that MRI tubes don't trigger my claustrophobia (that has more to do with being restrained or in tight quarters with people). I've had enough of them (6?) to know what to expect and to just see it as noisy relaxation time.

The 5/11/2014 MRI radiology report read, in pertinent part:
L3-L4:  Mild diffuse disc bulge/posterior disc protrusion.  There is no significant spinal canal narrowing.  There is no significant neural foraminal narrowing.
L4-L5:  Mild posterior disc protrusion, with posterior annular tear.  There is no significant spinal canal narrowing.  There is mild bilateral facet arthropathy.  There is mild bilateral neuroforaminal narrowing.
L5-S1:  Mild L5 on S1 retrolisthesis with uncovering of the disc.  There is no significant spinal canal narrowing.  In combination with moderate facet arthropathy this contributes to moderate bilateral neuroforaminal narrowing.  
 IMPRESSION:
 1.  Mild L5 on S1 retrolisthesis with uncovering of the disc.  In combination with moderate facet arthropathy this contributes to moderate bilateral neuroforaminal narrowing.  There is no significant spinal canal narrowing. 
 2. Mild posterior disc protrusion, with posterior annular tear at L4-L5 causing no significant spinal canal narrowing.
 3. Acute on chronic endplate degeneration changes at L5-S1.  
*exhales* Okay, that was exhausting to type. I can't imagine what it's like to read if you've never read that before.  One of the places I linked to, the Virginia Spine Institute, had a really good paragraph that I thought I'd share to help you all understand why all that mumbo jumbo above equates to pain (in addition to my most-read post about my back, "A Mile In Her Shoes"):
Just like other ligaments, the discs can be injured. The annulus can tear or rupture anywhere around the disc. If it tears and no disc material is ruptured, this is called an annular tear.  The outer 1/3 of the disc’s annular ring is highly innervated with pain fibers. Thus, if a tear involves the outer 1/3 it may be extremely painful. This tear will heal with scar tissue over time but is more prone to future tears and injury. Studies also indicate that annular tears may lead to premature degeneration of the disc, endplates, and facet joints.
 In comparison, the 2015 radiology report seems pretty tame to the 2014 report:
IMPRESSION: Relatively mild degenerative disc disease at L4-5 and particularly L5-S 1. No significant encroachment on neural structures is seen, Comparison with an outside study of 5/11/2014 shows no significant change.
I dunno, part of me wants to throttle these radiologists for saying that anything about my back pain is mild... but... moving on.

This past Monday I had my discogram.  I'm going to annotate what I posted on my Facebook:
my actual discogram
I survived the discogram without fainting or cursing. Though I wanted to do both.
  1. Intramuscular antibiotic in my butt hurt like a mofo.
    [It still does even 2 days later.]
  2. 5 Novocaine needles on my skin
    [This is so I wouldn't feel the introduction of the needles aimed straight at my discs]
  3. 4 needles introduced into my discs (L2-L3, L3-4, L4-5, L5-S1)
    [left quite nice bruises]
  4. Then one by one they introduce contrast dye and pressurized the disc until they reached my absolute pain threshold.
    [I assume that they were measuring how much pressure they could put on my disc before I reached my pain threshold]
  5. So I felt nerve pain radiating down my leg and then my back started spasming uncontrollably.
    [It was like 7 years of pain compressed into 30 minutes.]
  6. At one point it hurt so bad that I told him I didn't want to do it anymore but that I knew I had to
    [The results would help pinpoint which discs were causing the most issues for me -- cause as is the FDA won't let me go 100% Bionic Woman.]
  7. One disc hurt so bad that I cried out in pain and he asked me not to be so loud as to not disturb other patients. I said, "Respectfully, I am the only one getting a discogram. I am not concerned how they feel."
    [I'm really proud that I didn't unleash every single curse that I knew at him.  To be fair, though, I was screaming bloody murder.  He offered to give me a towel to bite down on/yell into.  Really?  Thankfully, his assistant, Tia, just kept alternating between holding my hand and stroking my arm.  She was amazing.]
  8. When all was said and done I was in a ton of pain but could move around.
    [Very slowly, couldn't stand up straight, and sitting was not fun]
  9. Then we got a cab to go to the CT place. My dad told the driver to get me there expediently which was the worst idea ever. Accelerating/decelerating is bad on my back normally... but this was hell.
    [Quicker isn't always better.]
  10. CT was quick.
    [Props to my technician who was sweet and kind]
  11. I am home now. Took drugs. Got a Jack CAT scan.
    [What a good kitteh -- he has rarely left my side these past few days]
  12. Yay! I didn't faint. But that was horrible.
    [I cannot emphasize that enough -- it was HORRIBLE.]

Unfortunately, I can't read the pressure charts that the discogram produced -- except to say that it did its job to cause pain.  Though, I'm not entirely sure if I was able to separate out the pain that I felt going down my leg versus the pain of my entire back having spasms (they stopped once the needles were withdrawn).  I knew going into it that the purpose of the test was to cause pain, but I was not prepared for what happened.  I was in agony from the time he introduced the needles into my discs to the time he pulled them out.  I think I was in too much pain to have my blood pressure drop (vasovagal response).  My self-preservation instinct was to punch this guy in the taco.

I know this isn't the image that they are
interested in, but it's pretty interesting
In stark contrast, the CT was quick, easy, and painless.  I loved that the technician (C/Kathy) even took the time to read how I hurt myself and asked questions about it.  Many doctors haven't cared to ask.   The same radiologist for the 2015 MRI completed the report for my CT exam:
l. Mild degeneration of the L3-4 and L4-S discs with some contrast material present in the anterior epidural spaces at both levels. 
2. Contrast material in the left neural foramen at LS-S 1. This finding should be correlated with the patient's physical examination.
So, my discs are leaking, which they shouldn't.  There was also another term that I need to ask Dr. O'Brien about -- "There appears to be some degeneration of the LS-S1 disc with a heterogeneous opacification of the disc seen particularly on the sagittal images."

My follow-up with my surgeon, Dr. O'Brien, is on Tuesday.  Wish me luck.

Mishmash

I haven't done a bullet-pointed/random thought post in a long time so here goes: 

  • Attended my second Weight Watchers @ Work weigh in.  I'm -1.8lbs.  Why?  A few things: (1) Being sick makes my appetite wonky
    (2) I'm back to food logging and measuring all of my food. That always works for me.
    (3) No Panera/Cosi  and their sodium bomb lunches
    (4) Could just be a normal fluctuation of weight

    I'm glad I asked #WWChat about fruits/veggies being zero points.  I don't eat a lot of meat or processed stuff.  I would always be under my target if I didn't allocate fruits/veggies (especially the ones high on the glycemic index) some value.

    I'm interested in seeing what a meeting looks like outside of work. Luckily for me there's a WW center right down the street!
      
  • I had a thought the other day about dating: I'm statistically pretty average (except for height, I'm in the 95th percentile at 5'9").  Am I too skinny for the guys who dig larger girls and am I too large for guys who dig skinny girls?  Point to ponder.
  • I also had a thought that I put on my FGvW Facebook -- Are women culturally trained to be peckish/undereaters or to believe that they have to "earn" their food/nutrition? Are we culturally trained to understate any and all of our appetites, lest we appear anything but virginal, saintly, restrained, or proper? 
  • Went to my discogram consultation on Monday morning.
    1.   It's not one of those things where someone shows up at your door playing the Bee Gees and dancing.
    2.   It's not a test to see how well you can do the hustle (darn! those lessons in college still go unused). 
    3.   It *is* (as I already knew) a test where they inject contrast dye into 4 of my lumbar discs to determine how degenerated they are. (Imagine a jelly doughnut. Mine is one that's been left on the counter for a week. They're trying to determine where the jelly is).
    4.   This is *not* going to be fun as I have a weeee little problem with needles and fainting (vasovagal response).
    5.   After all the discs have been injected with dye and he studies where the it seeps, I am getting a CT scan to get more detailed information that they can then turn over to my surgeon and we can make some decisions.
    6.   Papa bear is going to help me the day of my discogram (2/9/14).
    7.   The anesthesiologist/pain specialist who is going to do the discogram seemed either tired, hungover, or super mellow. I'm not sure which. But he seemed interested in re-visiting more epidural steroids (nope, I felt lousy after them and they didn't provide long-term relief). He also wondered why I wasn't taking pain meds (opiates -- hydrocodone or oxycodone) on a more regular basis.  I opt for ice because I don't like walking around in a fog, nor do I want to develop a tolerance for the drugs. After 17 years of back issues, I'm just tired of the stopgap remedies. All of these things make it a little easier to live my ordinary life when I want a spectacular one.
    8.   In related news, I'm getting a new MRI for my lower back on 2/6/14. 
  • I said on Twitter today "You know what would be awesome?  If I could run the #Fitbloggin 5k with a healthy back.  That's something to look forward to."  Oh, by the way, I'm co-leading a discussion group with Janet Oberholtzer (OMG, isn't she amazing?) at FitBloggin 2015 called "Living With Pain:  A Survival Guide." 
  • The Flu -- Okay, we know it's 23% effective this year and that it's widespread.  And yet, so many of my coworkers are coming in sick.  If I had to get a doctor's note to clear me to return after my shingles (that were on my hip, thus not a threat to anyone unless they decided to lick my hip), why aren't people being sent home if they have the flu or flu-like symptoms and then required to have a doctor's note?  I really hate double standards that don't use good science.
    Oh, and on that note, please wash your hands.

The date that wasn't

He was cute. He was a cyclist. His OkCupid profile stated that he was interested in mindfulness.  His emails were thoughtful and had correct punctuation. 

Within 2 emails he suggested that he'd like to meet me.  
I replied that I'm not smooth and would probably giggle a lot (I do that out of nervousness on dates sometimes).  He replied "I'm actually quite funny, so it's very likely you will not be able to stop giggling until the end and good bye kiss. What is your availability?"  Okay, Mr. Flirty McFlirterson.  Game on. 

Turned out that he was going to be 2 blocks away at an event for his cycling group.  He invited me to join the group.  Okay, casual introductions.  I asked if I could meet him outside the bar -- just to have a chance to do introductions without having to scream (at night the bar is a cross between a club and karaoke).

We met a few blocks away, and already I knew that he wasn't interested.  He didn't maintain eye contact when greeting me and all the chattiness in the emails became one or two word answers.  And then he said it -- something to the effect of "this is not a date."  Um. Okay. Sure.  My second clue was when we got to the bar -- he didn't even hold the door for me (granted, it's not necessary, but if a guy is interested he usually pulls out all the stops).

Two of his friends were at the bar.  He introduces me to one, and then pulls out his chair.  If you were looking at us from the back it was (me) (him) (friend) (friend).  He sits down, puts his left elbow on the bar and turns to talk to his friends. He completely turned his back to me.  I get it, we're not on a date, but I found that to be terribly rude.

Five minutes later more of his friends show up and I just decided to turn on the charm.  I introduced myself to everyone, complimented the ladies on their outfits, their hair, their smiles.  They decided to go upstairs to the dancing/karaoke and I thought it was the perfect time to just slip away because he clearly didn't want me there.  But one of his friends stopped me as I was about to leave and started chatting with me.  He was charming, handsome, and funny.   He knew a bit of ASL.  I taught him some naughty phrases.  I told him my predicament.  He laughed and said "come upstairs anyways."

And it was okay.  His friends were much nicer to me than he was, especially after he disappeared for about an hour.  I had a few great conversations, had a dance party, and even did a karaoke duet with one of them (I killed it, of course).  At some point in the night he ended up standing next to me and I said something to him.  He leaned over to say something to me (including reiterating that it wasn't a date) and put his hand on my butt (which he claims he does to everyone) and I said "Sorry, butt is for dates only."

As the night ended, many of his friends said things to the tune of "I hope to see you out again." Well, considering I'm not an avid cyclist, I doubt that I belong in a cycling meetup group.  But it was just proof that sometimes good things come out of bad situations. I'm a firm believer that you can learn something from even bad dates, can still be gracious and kind even if there's no chemistry, and can even have some fun.
Salty Pirate Face!
I didn't let the dude off the hook.  I don't know about the rest of y'all, but it always feels good to stand up for myself when someone has treated me unkindly.

Huge pet peeve:  apologies that are NOT apologies.  I'm a firm believer that apologies need to recognize that an action caused another person's suffering (taking ownership of one's actions).  "I'm sorry that I turned my back to you and made you feel unwelcome." Don't apologize for how I feel.
And as a friend noted -- this is the guy who wrote "Over the years, I have learned to be quite outgoing and great in social settings."  Padawan, you still have much to learn. 

The Bullet

So... in July 2014, I got an email from an Associate Producer at ZoCo -- Dr. Oz's production company, and an affiliate of Harpo, Oprah's company -- asking me if I wanted to be considered for an "upcoming segment on the show" regarding their "new life change" shows:  "The show would be based around one guest who wants to get on  the right track to changing their life for the better. This will be a great opportunity for someone like yourself who has been on a weight loss journey."  The Associate Producer then listed a bunch of questions IN ALL CAPS (wtf?).  

At the time, I thought about all of my friends who had been published in books, featured in magazines, on local or nation-wide news, or who had achieved international recognition.  I wondered: Was this my time in the sun?

After 30 seconds of due consideration, I penned my response:
[Associate Producer]:
Thanks for reaching out to me -- but I feel that DrOz's promotion of weight loss pills doesn't fit with my mission statement or branding.
Cheers!
-Robby
The more and more I read about Dr. Oz, the more I think that I dodged a bullet.  Earlier in the year the FTC investigated the "doctor" that Dr. Oz backed in regards to the green coffee bean extract diet – Lindsey Duncan – and they've just this week ruled that his claims were deceptive, fining Duncan's companies $9 million.


Does Dr. Oz say some good things? Sure.  But even a broken clock is right twice a day.

More fun links:
Have you ever been courted by a person, site, or product that you have passed on because you don't want your name/reputation tied to it? 

ODI

Let's face it:  I'm a nerd.
I'm a nerd in touch with her emotions and can express them.
But I'm still a nerd.

So when I was up the other night (unable to find a comfortable position in which to sleep + mind preoccupied), I started researching lower back artificial disc replacement studies: the efficacy of multi-level disc replacement; post-op follow-ups in the 2-10 year ranges; comparison of different studies, etc.

A term kept on coming up — ODI — the Oswestry Disability Index.  The short questionnaire is designed to help doctors and researchers gauge where a person is in terms of their pain and how their pain affects their life.  The idea is that a doctor or researcher can ask these questions at various stages in a person's care (prior to surgery and at various post-op intervals) and compare as to whether there was an improvement.

There are 10 sections to the ODI questionnaire, with 6 possible answers in each section. Point values are assigned from 0 to 5 for each question depending on how the patient responds.  The sections are (1) Pain Intensity (2) Personal Care (3) Lifting (4) Walking (5) Sitting (6) Standing (7) Sleeping (8) Sex Life (if applicable) (9) Social Life (10) Traveling.  (Notice "Exercise" is not a category??)


The answers are then converted to a score and the score then determines the percent disability:
0% to 20% (minimal disability): Patients can cope with most activities of daily living. No treatment may be indicated except for suggestions on lifting, posture, physical fitness and diet. Patients with sedentary occupations (ex. secretaries) may experience more problems than others.
21%-40% (moderate disability): Patients may experience more pain and problems with sitting, lifting and standing. Travel and social life are more difficult. Patients may be off work. Personal care, sleeping and sexual activity may not be grossly affected. Conservative treatment may be sufficient. 
41%-60% (severe disability): Pain is a primary problem for these patients, but they may also be experiencing significant problems in travel, personal care, social life, sexual activity and sleep. A detailed evaluation is appropriate. 
61%-80% (crippled): Back pain has an impact on all aspects of daily living and work. Active treatment is required. 
81%-100%: These patients may be bed bound or exaggerating their symptoms. Careful evaluation is recommended.
If I were to take the test today, I would score a 46%.  This makes me sad.  I also realized when doing the test how much I've either had to give up (like playing softball/volleyball or volunteering at the animal shelter) or how much I avoid (dating) cause of my back. It makes me think of all the times I've turned down doing something I want to do (like going to museums) because I know how it'll affect me (walking on marble is the worst).

The questions also made me think of some stories that I've never told.  For instance, the travel section:
  •  I can travel anywhere without pain [0]
  •  I can travel anywhere but it gives me extra pain [1]
  •  Pain is bad but I manage journeys over two hours [2]
  •  Pain restricts me to journeys of less than one hour [3]
  •  Pain restricts me to short necessary journeys under 30 minutes [4]
  •  Pain prevents me from travelling except to receive treatment [5]
Since I have one of those "but you don't look sick/injured" injuries, I don't always get offered a seat on the bus or on the metro (I also feel weird asking for them).  The unexpected acceleration/deceleration of mass transit vehicles as well as their bad suspension often makes me clench my teeth in pain/discomfort.

In 2000, right after going to the ER for the first time for my back (and then being referred to an orthopedist who asked if I had too much rough sex), I went on Spring Break to Hawaii to visit my cousins.  On the leg from LAX to Hawaii, the flight attendant noticed that I kept shifting in my chair and asked me if I was comfortable.  I told her about my lower back pain.  She let me lie down in the bulkhead row.  What an angel. 

I wrote last week that this is "Not the Life I Want To Live" — it took doing this little exercise to actually see the day-to-day impact of my back injury versus feeling hopeless for the future.  This affects me now.   I'm glad I'm going to my doctor tomorrow morning.

Sipping The Kool Aid

"Oh, you're a weight loss blogger?  Have you tried __________________?" 

The minute you tell someone that you're a weight loss/health gain blogger it's like the gates open for the flood of suggestions ("Juice fasting is the BEST! Your body is a toxic wasteland!" "Paleo/Whole30 really gets to the roots of what it means to be human" "Go gluten free! Who cares if you don't have Celiac, an intolerance, or an allergy? Who cares about sugar/fat content? Wheat is EVIL" "YOU MUST GO TO THE CHURCH OF CROSSFIT **froth at the mouth**!!").  Of all the diets people have asked if I've tried I get asked most about Weight Watchers.  

Well... my very first official weigh in was today at lunch:  214.4 lbs (eek!)  
My 5 % goal is 11 lbs. My 10% goal is 21 lbs.  I would personally like to see what 175 lbs (39 lb loss) would look like.

Okay -- so why now?  My office has a pretty robust wellness program -- we have on-site yoga once a week, onsite kettlebells once a week, an in-house gym, various race sponsorship opportunities, etc. This year they offered an incentive:  if we attend more than 50% of the meetings they'll pay for half of the employee's enrollment.  My payroll company also offers up to a $200/year reimbursement for any health/wellness related expense.  Essentially, my 12-week Weight Watchers at Work program is free.  Not bad, right?

So I took the plunge and got myself a fancy schmancy Weight Watchers account (let's be friends!?). I've been allocated 34 daily points along with my 49 flex points.  It's still messing with my mind that certain fruits/veggies are zero points, even if they are high on the glycemic index. But I'm just going to go with it and see what happens.



At the very least it will help me address a few issues that I've pretty much always had, but that are especially important because I can't offset it with exercise as I have done in the past (see back issues): 
  1. meal planning;
  2. portion sizes;
  3. consistency; and
  4. accountability.
So... my new Weight Watchers friends -- have any favorite low-point/power food recipes? 

Not The Life That I Want To Live

Yesterday I awoke to terrible back pain in my mid-back (lower thoracic spine, upper lumbar spine) (yay! new injury?!) that made it hard to turn over in bed, get out of bed, stand up straight, bend down to put on underwear/pants, twist to put on a bra, etc.

In my frustration, I posted a status update to my FGvW Facebook (yes, I have a personal one and a FGvW one, please don't be offended if I don't accept your request to my personal FB):


It's not that I wanted to sulk and have pity for myself;  It's just that it requires so much energy to be optimistic, to keep fighting.  It took all of my energy yesterday to just cover the basics of taking care of myself.  Any leftover energy was put towards consoling myself with snuggles from Jack.

On days like these, sometimes the most compassionate and graceful thing that I can do is to just allow myself to feel the pain, the frustration, the fear, the sadness, the grief.  All of those negative emotions need a safe place to exist and be felt or else they become toxic.  The more I ignore those feelings the more disconnected I feel from my body and the injury.  The disconnection is where suffering lives.

Spending a day staring at the ceiling over your bed is a good time to ponder how to reconnect and end suffering.  I realized that I'm not living the life that I want to live.  I want to be active and be joyful.  Instead, I'm either living in fear of re-injury or I'm recovering from aches and pains that make me feel older than I am (physically, emotionally).  That fear has isolated me and handicapped me in many ways.

I remember a conversation that I had with my former spine doctor where he said that he wouldn't operate on my back until the day I was wheeled into his office.  It's hard trying to live in the shadow of that comment – it's like playing Russian Roulette.  "The Big One" (i.e., the incident that puts me in a wheelchair) could be from doing some crazy activity or from sneezing and anything in-between.  That thought has not liberated me to go balls to the wall; it has paralyzed me to the point that I might as well be in a wheelchair.

With that in mind, I made an appointment next week with my current orthopedic surgeon.  He understands that I want to be proactive when it comes to my spine health.  He understands that I don't want to wait for the day when my bulging discs fail (herniate), and/or that I don't want to push my luck with killing nerves (for instance, did Peyton Manning wait too long to have his surgeries?) Dr. O'Brien performed my cervical disc artificial disc implant at the intersection between the right technology and the right time for me (when I was strong and motivated to recover).

I have a courageous and adventurous heart.  I just want a body that matches.
This is how I end my suffering and begin to live the life I am meant to live.

Suck it up, buttercup.

Confession:  I ate a ginormous everything bagel that I had brought back from Brooklyn and kept in my freezer.  The world tells me that I should hate carbs, but how could I hate anything so perfect?

Can we still be friends if I eat carbs?  Great. Okay, now that I got that out of the way...

I wanted to write a post about how people think that obese/fat people are lazy yet don't realize just how hard many of us work to suck in our guts all day long.  Then I realized I had already written that post four years ago.  (I wonder how many of my followers are fellow gut suckers as well.)

Have I really run out of things to say, or is it just that some things never change?

Sadly, due to a power outage at my office the first Weight Watchers at Work meeting was postponed to later this month.  I think this is good and bad -- I was excited to get started, but I've had the respiratory ick for a while now. I also just finished a round of antibiotics that is knocking my on my ass.  The ZPak is killing every bacteria in my body, good and bad.  I will hit the ground running with Weight Watchers on January 20th.