Friday, May 3, 2013

Back on the rollercoaster

Well, after my great progress over the past couple of weeks, last weekend was definitely a low point again - the equivalent of making that slow, anticipatory climb right before the rollercoaster sends you racing back down to earth... twisting, backwards, and upside down.  Hopefully, to soon begin another slow climb...

Last Saturday night I was doing my exercises - as usual - before I went to bed. My sleep patterns are so mixed up right now  and my doctor just says sleep when I can, so I do, with not much other choice - I've even given up on the sleeping tablets at the moment as they are simply not working anymore.  So, I'd had a shower - warmed my muscles up - got ready for bed around midnight and started on the exercises I've been doing for the past couple of weeks.

I worked through my 'easy' ones first, leaving the harder ones until the end - my usual routine; it loosens up my movements and addresses my range-of-motion exercises and then I do my (minimal) strength exercises after that.  During my baby-girly-press-ups I felt a bit of a twinge on the top of my shoulder - not where I usually get pain, so I took a break  (this usually involves me on my knees, pulling my arm in tight to my body, and head on the floor - this is not uncommon) and then decided to give the next exercise a go.  The pain didn't seem to be easing really, but because it wasn't my usual 'hotspots' of pain I tried to work through it a bit.  The next two exercises have me on my hands and knees - gave it one shot and decided that wasn't going to happen either.  It's been a while since I've had to give up on my exercises, and I am always aware of making the decision - trying really hard to decide if it is actually better to push through, or to give up.  And I hate giving up.  It's really not in my nature.  However, my body was beginning to dictate so I grudgingly decided it was the right thing to do.

As the pain was increasing though, the one thought running round my spinning head, as I lay face down on the floor was: I hope I can still move my arm.  I have to check. I have to lift it.  Just to check....  So I thought really hard about it and realised that even my left arm felt like a tonne weight - it is so difficult to describe what pain can do... I would say I've experienced pain in my life - broken ribs, fractured sternum, fractured wrist, fractured thumb (among others - mostly gymnastic-related); but not forgetting the infinite list of Lyme symptoms associated with pain...  But what I have now really should have its own word.  It's like saying you're "tired" when you have Lyme (or anything that causes major medical fatigue... like chronic pain), when what you really mean is "I feel like some vampire-type creature who feeds on energy instead of blood has emptied my body and left me devoid of any iota of energy."  

There's just not really a word for it. "Pain" simply isn't enough.

Still determined to make sure I hadn't done any major damage (aaarrrrgghhhh!!) and could still move my arm I lay on my stomach (where I had pretty much collapsed anyway) and reverted to my previous progression - pushing my arms up with my fingertips - still lifting them; still using the muscles, but with some support.  I struggled, but I managed.  Relieved, I pushed up one more time, just to be sure and then it really HIT me. $%^# !! The pain from the muscles' contractions seared down the lateral (right) side of my scapula and radiated deep into my body between my scapula and my thorax.  The pain was like a stone smashing a pane of glass - it just seemed to splinter instantaneously, and simultaneously, in every direction.  

I lay on the ground, my arm bent and tucked in at my side - my protective position - and waited for the pain to subside.  I'm really not sure how long I lay there; I reckon it was about 20-30 minutes but my pain was not calming down, it was definitely getting worse.  At some point, I realised I needed ice, but given I was lying face down with my eyes closed and the room still spinning; feeling so nauseated I could taste it; and was completely drenched in sweat caused by the pain; I did realise going downstairs was not an option.  I had to wake my parents.

For the first time since the two weeks immediately after my surgery, I woke my parents around 1am.  I half-crawled, half-clutched at the walls, got to their bedroom door and struggled to make my voice loud enough to wake them.

By the time they got to me I was sitting on the wee sofa at the bottom of my bed, holding my arm - it felt like I was holding it so it wouldn't fall off.  By this point, my pain was beyond words.  I was sobbing, sweat was literally dripping down my face and upper body and speaking to explain what had happened was a struggle.

My Dad filled my ice machine and hot water bottle for me and my Mum sat with me trying to get me to control my breathing - seemingly impossible.  She got me the meds that would help, applied the prescription pain cream I've just got and helped me up on to my jelly legs and into  bed.  She sat with me for about an hour, calming me down.  It took a long time to stop sobbing, and to breathe normally.  My arm felt 'odd' - as if it wasn't really connected to my body properly.  She did some reiki on my arm and on my head, and eventually the drugs worked, my breathing became steadier, and I did begin to relax.

It all sounds so ridiculous, so dramatic and so difficult to understand why I couldn't control it.  I have learned this year that these are all parasympathetic responses to pain - something I'm not in control of, no matter how hard I try to fight it:  it's my brain's reaction to my body's pain.

The next day I was very sore and absolutely exhausted from it all.  Again, it sounds silly to say my body had been through a trauma, but again, that's what's been explained to me.  When they say someone is treated for "shock" at the scene of an accident - it's a genuine physical response to a traumatic event - not something we can control (despite my best efforts this year).  We had friends coming for lunch the next day.  I managed to get dressed - sweatpants and a T-shirt, but it was a step up from my PJs.  I even managed to put a little bronzer and blusher on the grey face staring back at me from the mirror.  Despite that, when our friends arrived, he took one look at me and said, "you don't look too good" - and I looked better than I felt!

It took me a few days to get over that exhausted, physical-trauma feeling and for my pain levels to calm down a little.  I'm still not 'over it' and am hoping it is a blip more than a set back.

My physio thinks that it is likely I broke up some scar tissue with the movement I did.  Why with the same exercises I've been doing?  No idea.  He has been using ultrasound again for a few weeks, and I am taking a supplement (called Lumbrokinase) that is supposed to help with scar tissue; it's possible these things are working and the scar tissue has been weakened and as a result ripped apart.  In the long term, this is a good thing - I need my scar tissue broken up to 'unstick' my frozen scapula, but ultimately it is still tissue ripping apart inside me, and, yes, that hurts much as you'd imagine!  It can cause severe pain - although my reaction was extreme, even for that, apparently.... however, it was pointed out to me that nothing in all of this has been 'normal' - it really doesn't even have a precedent.  It still always raises the question of RSD, or "RSD-type pain" as my therapists prefer (as do I).

In addition, there seem to be some nerve-related issues going on, whether that was also a cause, or is a consequence is unclear.  My right hand burns and has numb patches.  My right arm feels not quite attached to my body - it is a strange sensation, difficult to explain. On Monday at physio, Angelo took measurements as my upper arm was quite swollen. Where it should be atrophied and skinny from lack of use, it still measures 1cm-2cm thicker than my left (good) arm at the same points. I have a compression bandage on my entire right arm now to see if that can help with any fluid or oedema.  It does help ease the burning most of the time.

So right now I am back to the simple ROM movements again, not too much stress on my shoulder and giving my body some time to recover.  Frustrating doesn't even begin to cover  it.

I did try some of the strength exercises under supervision at my physio appointment today, but I couldn't do them all and I didn't feel good.  By the time I'd walked from the clinic to the car, and my Mum had driven (almost) out of the car park, I had to ask her to park again to let my anti-nausea tablet work, as I had jelly legs again and felt like I could be sick from the car moving. (I was able to take enough meds to help things ease off, and we still went for pedicures as planned - something enjoyable and relaxing anyway... and happy pink summery toes now it is flip flop weather!!)





On the positive side, although I seem weaker than before, testing my muscles has shown that I have not done any major damage - my movements are still all there, and my 'new' muscles are still working (except lifting my arm - it is still too painful to have it lifted passively, so no active lifting right now either) and the actual surgical repair is still looking good - a big relief.

The question remains though: why do I still have so much pain on the lateral side?  And why is my pain response still so severe? These have been the main questions for months now - and the answers are still elusive.... and I still feel every week seems to bring more questions.

Which leads me to some wise words from my favourite genius:


“The important thing is not to stop questioning. Curiosity has its own reason for existing.”
  ~ Albert Einstein



Sunday, April 21, 2013

Progress, inspiration, motivation, and smiles

This week has been full of ups and downs.  In amongst those ups and downs, I have made some pretty remarkable steps forward with my shoulder.  I have waited a week to write about it, because, honestly, I've made steps before and within a couple of days they disappear again.  These have stuck for a week, so I'm hoping it is ok to share them now.

Compared to what I used to do, as a gymnast, and compared to how I used to be at my very sickest (virtually house-bound and hardly able to walk), there are many comparisons to be made.  Focusing on the positive differences is great and motivational; focusing on the distance I still have to go always makes me realise what a huge challenge I have still to continue battling - but I do not believe it is insurmountable.  I believe there will still be rollercoaster days (and weeks) and these will continue to test me; but I am beginning to feel like I can win this fight.... even if it takes more time than I ever imagined.

My HUGE achievements this week have been that I manage to do what can only be described as a 'baby girly press up' - a press up on my knees, bending my elbows about 1cm for my press up.  It is still awkward to get into position (involves bouncing about on my left hand before I can place my right hand into position); my weight is not evenly distributed - but I am putting some weight through my right arm/hand -  a major achievement! I can do two sets of 5 'press ups'... dreaming of the days I could do 20 full press-ups with claps in between in about 20 seconds! Oh well... gotta start somewhere.  I can also hold a 'baby girly plank' position, and then I can also do scapular retractions in this position - two sets of 3! - but my physio is especially excited about this as it means my brain has really figured out how to make my 'new' muscles work.  That's a really big deal.

I have also now progressed from the ability to make my arm shake as I try to lift it to actually raising it about an inch off the floor while lying on my stomach. I do five of these.  My physio tells me it is not one set of five, but five sets of one, since I need to rest in between - so the aim is to get it to two twos and then two threes... baby steps, as it has been all along, but the baby steps are working.  Again, this exercise means my 'new' muscles are 'talking' to my brain again, as it isolates them - they are doing ALL the work here.  Another really big deal.

For months, doctors and physios have also been stressing to me how important it is to strengthen my core, and I simply haven't been able to sustain any core strength exercises because of the pain they cause.  I have literally felt my core muscles turning to mush! This week I've managed to do 20 sit ups (well, crunches really.... on a ball) every day - a whole two sets of 10.   Amazingly, this is actually enough for me to begin to feel my muscles toning up again - in fact, there is actually a visible difference in my tummy which was beginning to develop this little wobbly part for the first time in my life..... disaster averted! (Um, yeah, because THAT was my disaster in all this....)

So that's my daily exercise regime now, along with still some basic range-of-motion movements, just to continue with those and continue to teach my brain how the sequence of movements is supposed to work.  I can't believe how exhausted it makes me, and I do still sweat, but the sparkly lights do not appear (as long as I rest in between exercises) and the impending blackness in response to any effort from those muscles seems to have disappeared..... finally!

The pain is still there, and it is still a major factor but I have decided to see if my body is ready to push through it a little and build some strength, which should then support my muscles more, reducing the pain by increasing the strength.  It's the viscous circle I've been caught in all year, and my physio is very much stressing I have to take it VERY slowly (I am not allowed to try any more headstands....pillows, walls, or anything - no exceptions! Physio's orders. To be honest, it hurt a bit too much anyway, but I did elephant-lift my feet off the floor for a couple of seconds..... I'm viewing it as a positive sign ...) and all my (approved!) exercises are with very low reps, small sets and tiny increments.

I've been taking choline and inositol as a supplement for about 6 weeks now - that is supposed to improve nerve healing (kind of, it's complex - all related to acetylcholine production and pain receptors and generally neurobiology that goes a bit beyond my understanding), but I think it could be helping.

I have also now been having Feldenkrais treatments for a few weeks and I have felt a benefit from these too - I am still unable to really explain them (it's a very slow process, I will try to explain at some point, right now the focus is on visualisation to increase body awareness - I'm really not sure how it's doing anything, but my body reacts pretty strongly to it even though I feel like I lie for 30 minutes and concentrate on moving my eyes in different directions with them closed.  It's really rather weird, but I definitely think it is helping somehow).  Feldenkrais is also supposed to promote nerve healing and the sessions make me sleep - unfortunately during the day; this is not good for my nighttime insomnia, but it's still sleep and they say we heal while we sleep...    

I feel most of my pain is more specific now.  It's still pretty severe at times; my attempts to do anything and go anywhere are still battles to manage mt meds, and fight through the pain, ready to collapse in bed (with my ice machine) as soon as I get home; but even with that, all the crazy parasympathetic pain does feel like it has calmed down a bit more, not entirely, but it's taking a positive step in the right direction.  

In the meantime, I am going to continue to watch this video on Youtube several times a day for pure inspiration, motivation and smiles.  Watch and be amazed!  It's simply mindblowingly amazing!!!

And yes, I'm super jealous.... and probably going to become slightly addicted to this superstar, Damien Walter's YouTube page:





Maybe one day.....

“Dwell in possibility."
  ~ Emily Dickinson




Friday, April 19, 2013

That battle called life

This week has brought extremely sad news from several people in my life; especially two of my very dearest friends. 

It has been accompanied by a reminder that there is evil in people, who seek to terrorise the innocent; destroying lives beyond recognition .

It has been a week that has reminded me that everyone has their own battles and challenges; that we should take a moment - longer - to appreciate what we have, to focus on the positive things in our lives; to truly appreciate the present moment; because life is futile, and precious.  

And everything can change in the blink of an eye.




Among heartbreak and sorrow, amid terror and bombing, it is always uplifting to see that sometimes the worst things bring out the best in humanity: kindness, love, compassion and empathy.  These positives are the things that keep us all going through times of darkness - a glimmer of light to focus on; support from which to draw strength.



Be kind, for everyone you meet is fighting a harder battle
   ~ Plato

Monday, April 15, 2013

The funny side


Today we went out for a few hours. I felt a bit like I'd slept yet another week away (in between my adventures with hair dye... a story for another day!  It's ok, it has a happy ending!)  We had booked dinner at my favourite restaurant, Seasons 52, which has booths and always accommodates my request for a booth so there is space for my pillow!  (I also signed up for a restaurant points system a while ago; booked today because they had 1000 point tables.  2000 points gets you a $20 dining voucher  - if you don't already know about OpenTable - check it out.  Does anyone know if they have a UK version?)

We wandered around the mall for an hour or so before, and after, dinner, just browsing. Really just a change of scenery, little day out.

  On the way home in the car, my TENS machine wires seemed to have moved, and something was painfully pressing into my shoulder blade.  I didn't have the machine on, but I think the electrode connection bit, which is metal had got trapped between a particularly sensitive part of my scapula and the elastic of my (strapless) bra (no shoulder straps = way more comfortable for a sore shoulder… usually).  

Usually, I put the electrodes on before I get dressed, so trying to get them off my back, in the car, with a seatbelt on and a bra, tank top and sweater on top of them was not easy.  I was beginning to sweat with the pain and get that sparkly-dizzy- almost-panicky feeling that comes with the pain increase - I just needed to get rid of the metal bump and I couldn't find it. 

I asked mum to pull over when there was a space off the road.  It seemed like a much longer road than usual…. By the time she had reached a little car park, my seatbelt was off, I had managed to shimmy the strapless bra down to my ankles, and to remove two electrode pads and stick them to the window… having nowhere else to put them.  After she parked I managed to get the other electrodes off, unplug all the wires from the electrode pads and remove the bra from around my ankles.  All without exposing any skin or getting arrested, so all things considered, I suppose that was a success!   

Just another day... might as well see the funny side!


Sunday, April 14, 2013

Look out world...

I think several years ago I would have interpreted this entirely differently - and so would we all; we are all shaped by our own experiences.





But now: I have no idea who I "ought to be" - and I'm ok with that, I think it's back to life being a journey kind-of-thinking.  At one point, in what seems like another lifetime, I would have thought that by the time I was in my thirties there were many things I "ought to be" but now I have learned that different things are the important things.

I'm not "what I want to be" ... or maybe I'm actually ok with this too, honestly, I have no idea what I want to be... Why do I have to be anything?  Why can't I simply be?  Cogito ergo sum? Right?

But I certainly have come a long way from "who I used to be".  I genuinely believe how people handle their problems defines them.  Our problems do not define us unless we let them; we choose how we handle them - and that is what defines us.

And, most importantly, I'm definitely not giving up on "becoming what I know I can be"... Just give me a little bit more time and then look out world, I'll be back!

I feel this fits with this today too:






Saturday, April 13, 2013

I am stronger than this challenge

Applies to every single thing life throws at us:



And perfect for an old favourite, which (in my opinion) can never be over-used....

"That which does not kill us makes us stronger"
~ Friedrich Nietzsche


Friday, April 12, 2013

Serious chocoholic

This week I am suffering from a serious chocolate addiction.  This week I discovered The Christmas Tree Shop is selling Lindt chocolate Santas for 49 cents.  It's dangerous.




However, I do keep telling my Doctor as long as the chocolate makes me feel happier than the painkillers it's all ok.... right?!