Tuesday, April 30, 2013

And Now, News From Our Sponsor…

This isn’t the blog post that I started writing earlier this evening. My intentions led me to write a difficult post that wasn’t at all light-hearted. It was relevant and timely, but altogether not in keeping with the mood that the refreshing, ever so slight breeze wafting through my open window has brought me.

Perhaps it’s just the change in wind direction that has me feeling a bit cheerier tonight, often the wind carries the heavy aroma of garlic from a nearby restaurant. At times enticing, however on days like today when my stomach is feeling especially off from my meds it can be quite unpleasant. Props for the change to breezes from the southwest this evening!

Skipping the heavy post tonight, instead a commercial break brought to you by the season Spring (is it really at long last here? My outside sources are telling me so!)

Images that you see here are ones that I’d photographed in the days when I could walk, run, drive and when deemed necessary crawl on my elbows and belly with my camera to get the shot I wanted. Looking at them doesn’t make me feel the least bit sad or remorseful tonight, I’m taking comfort in the knowledge that I captured these images with intention and appreciation for the beauty I could see through my viewfinder at that time.

Although a good part of my gallery collection featured floral images, I’m far from being an expert botanist. If I’ve accidentally included flowers that display their magic in the summer or fall, please consider them a preview!

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Monday, April 29, 2013

Dressing for the Occasion…

My daughter and I are both night owls. I used to be a solid eight hour per night sleeper, but that pattern has long since disappeared. I blame the almost year long bout with steroids a few years ago for permanently messing up my internal clock.

My daughter on the other hand does get her eight hours, it just so happens that she starts her sleep a whole lot later than I ever did. In the morning when she’s still out for the count, I can quietly catch up on whatever interests me on my iPad. Glancing over at her as she sleeps puts a smile on my face, and makes me feel far less alone.

At this moment she’s online window shopping for dresses, showing me her favourites. Which to me is quite comical given that I would practically have to bribe her to wear a dress when she was young, and now she declares that given the option she’d prefer to wear nothing but.

It’s quite an awakening to realize that I have no idea what the latest trends are. I don’t watch television, don’t get any magazines and not doing any online clothes shopping these days. My wardrobe mission these days is clean clothes that are comfortable to wear in bed. It would be easy to stay in pajamas all day, yet to me that would be a sign that I’ve given up.

We have had a good giggle tonight about how unaware I’ve become of how women are dressing these days. She’s educated me on the finer points of ombre hair, the return of wide leg pants, hair bows and horizontal stripes (flashbacks of my eighties wardrobe!)

As the weather improves, a few friends have expressed offers to take me out for walks. They walk, they push, I sit and enjoy the ride. Sounds like a pretty sweet deal for me.

I suppose it doesn’t really matter whether what I’m wearing is in style if we go out. Seated, I’m undoubtedly going to look a bit rumpled anyway. Experience has taught me that in a wheelchair most people are either looking away, or see just the chair and oxygen tubes. I wonder if anyone would even notice if I wore something completely inappropriate? I have half a mind to slip on a pair of stilettos when I’m out next to let people wonder how I would even get in and out of a wheelchair wearing them.

You might remember from a previous post that I’d given away all my work clothes, along with them went special occasion attire that would have been worn to openings of my photo exhibits, parties and other places that dictated the donning of something a cut about the casual.

When sorting my things out for donation with my best friend a few weeks ago, she gently reminded me that I’ll need to hold back one special occasion outfit. It’s not black (and I hope anyone in attendance on that occasion isn’t wearing black either), and as a final touch – I held back the highest pair of heels I own from the donation pile.

I may be disabled, but when I say goodbye I want to look as if I danced my way out the door. In my head, I will have.

Thursday, April 25, 2013

A New Vocabulary…

My daughter arrived home on Sunday, we’ve had a wonderful time catching up. It’s amazing how quickly we’ve fallen back in pace with each other.

But boy, she sure brought a lot of stuff from school! Finding a place for everything is an exercise in planning, motivation and execution. We could use a touch more of the motivation part, but for now we’re trying to balance enjoying our time together with the chores. Well, her chores. I’m not a lot of help, a backseat unpacker shall we say?

Looking at this as a long term arrangement requires far more than just the desire to spend this time together. We need to be flexible, understanding, compassionate (towards each each other as well as to ourselves) and patient.

In addition to looking after me, my daughter will need to take care of herself and what’s important to her. It will be at my insistence that she gets out (beyond the part-time job she returns to tomorrow) to visit her friends, go on outings, or maybe just sit on a park bench to give herself time alone with her thoughts.

We need to take cues from each other, both verbal and non-verbal.

Did you ever play the game of drawing something on a piece of paper, guided only by the physical description of the item  coming from someone who isn’t allowed to use gestures or say the name of what it is or what it’s used for? We’ve had this sort of comical exchange several times already over the last few days. The most common scenario; she in one room, me in the other  as I try to explain where an item is stored as best as I can remember its location in the apartment.

Although we’re very close and communicate quite well, it’s amazing how four semesters at school for her, and a steep decline in independence for me has brought about the need for some new vocabulary between us.

What thankfully hasn’t changed is what a hand stretched out towards me across the bed means. Mom, I need a hand hug. And my darling, a hand hug is what you shall have as we do our best to get through this together.

Monday, April 22, 2013

There Will Be Days Like This…

It’s often happened that soon after I’ve written a blog post something will happen to hit the point home in some sort of ironic twist.

Yesterday was a case in point. In a “one day I might find this funny, but it could take awhile'” kind of way.

You might remember from previous posts that my daughter was due to arrive home this weekend from university, she’s not returning in September so that she can instead take care of me.

My gratitude towards her is overwhelming. I could go on, but I’ll save that for another post. I’m not missing any opportunities to tell her directly.

My wish was to make her feel as welcome as possible, for her to feel that this is truly her home. Until now she’s been at this apartment for the occasional holiday but hasn’t yet lived here without the expectation of being on her way again.

To make the apartment feel welcoming, my wish was to make space for her clothes and personal items, find a way to give her a small amount of privacy in sharing a one bedroom place, and to have her not feel the true weight of what caring for me entails right off the bat. Part of that was to have a clean apartment waiting, and as of Friday afternoon that was the case thanks to the lovely woman who cleans it for me every ten days.

Within hours the plan started crumbling. Anything that could drop, break, spill, get tipped over, overflow, clog did exactly that. I didn’t have any visitors coming, and for the most part I wasn’t able to rectify much of it myself.

By yesterday midday I had spilled a bag of kitty litter on the carpet (used of course, quite fitting with the way my weekend was proceeding) after the cat had a fight with his litter box (and won, it would seem), the bathtub had clogged,  there was a sticky flood on the bathroom floor with shards of glass mixed in (let’s not even go there with as to how that came about), dishes were piled up on the kitchen counter, and the cat had tipped over his food and it was strewn across the kitchen floor.

There was very little cleaning up that I could do, imagine trying to keep the oxygen tubing out of the way as well as attempting to not use my injured right hand. Not to mention that I can’t get down to floor level on my own, and the pain that is brought on by any moving about.

A phone call went out to my daughter who was packing up her apartment at school, with my sincerest apologies for welcoming her in a few hours with a disaster zone. I was beside myself, this was quite far from how I’d envisioned welcoming her.

The truth is that if she hadn’t been coming home to stay this weekend,  it would now be time to have a serious chat with my support team about how to move forward.

The crushing reality is that I can’t be on my own for extended times anymore, as I have been for sometimes days on end since moving into this apartment. By way of physical weakness and disability I can’t always get myself fed, dressed and stay hydrated. Fetching a glass of water is at times impossible, opening up a sealed bottle of water usually a task beyond my capabilities too.

The forethought that went into each day became exhausting. Had I asked the last person that was here to fetch me enough drinking water (or pre-open bottles for me)? Move wet laundry to the dryer? Fill the humidifier? (a necessity on oxygen therapy) Take out the garbage so that it didn’t start to reek in the passing of a few days with no visitors?

Asking is already hard enough in the first place for me, realizing after they’d left that I’d left out an important request worse.

My daughter has with her return given me gifts that I can never repay. Above all, time with my favourite person. Next, more time in my own home before facing the possible necessity to go elsewhere. Next, fewer physical challenges/more time resting (and accordingly possibly less pain).

I sense that I was being delivered a lesson yesterday, being that despite my objections to my daughter leaving school it has to be this way for now and I need to accept her assistance graciously. In many ways, it’s harder to accept help from her than it is from friends and volunteers. She’s supposed to be off making a life for herself, it should be me looking after her instead of the other way around.

On the other hand, if I could have only one person by my side as I each day become more vulnerable it is she. I trust her with my life. With the end of my life.

Saturday, April 20, 2013

The Order of Things…

This has been a challenging week, primarily due to my diminishing physical abilities. Something as simple as trying to budge a bar of soap that had adhered itself firmly to the shower shelf when it dried had me upset with myself.

The hand that was free to attempt the soap’s removal caused additional frustrations. I banged it pretty hard on the grab bar (isn’t that irony) a couple of weeks ago in trying to break an impending fall in the bathroom, it would appear that I might have broken a bone or two in the process. Thank goodness for voice dictation software, otherwise nobody would have had emails returned by me this week. My one handed typing technique is coming along nicely too.

A day of mishaps led me to feeling frustrated and a little beaten down tonight. When my best friend called this evening I was ready to answer the phone with a shriek, holding a fistful of hair. But with a hurt hand, I couldn’t even get that right.

We speak every day, but tonight was a longer call of over two hours. The first part of the call, she listened as I whined. I don’t do that often, but there was a long and torturous (for her) whine stuck inside of me that needed to escape. There are a handful of people in this world upon whom I can inflict a rare pity party for myself, she’s always the first volunteer in line and she gently urged to me to get it out of my system this evening.

That complaining being mostly emptied out of me (I still have a good cry deep down inside that needs to get out sometime) we could get on to the cheering up part of the call.

We traded stories of misadventure that had happened when we were small. Bangs, scrapes, cuts, split lips. We were laughing uproariously – the injuries didn’t seem nearly as hilarious at the time!

A couple of incidents that I shared after our exchange of war stories correlate quite well to my frustrations of this week.

My mother has many times told me the story of how when I used to fall into puddles, instead of using my hands to lift myself up I’d cry for someone to come get me. The idea that getting a bit dirtier meant I’d be saving myself sooner was beyond my comprehension.

When I was in kindergarten, I one afternoon came home and broke into tears as soon as I saw my mother. It took a great deal of convincing on her part to share why I didn’t want to go school the next day. For the record, I LOVED school. As far as I’m concerned, I’m still in school and always will be, I never tire of learning.

The look of alarm on my mother’s face suggested that she wondered if something quite sinister might have happened that day. In reality, my teacher had gleefully announced at the end of class that the next day we’d be doing finger painting. The mere thought of dipping my hands into the coloured slime was fodder for nightmares. I’m sure that I was excused from doing it, but remember being pretty ticked off with myself as an adult when my daughter and I finger painted together. How could I have wanted to avoid such a wondrous mess?

This week’s frustrations have mostly been about my inability to keep up with the high standards of tidiness that I set for myself. If there’s a mess, getting it cleaned up these days is usually a task not completed according to my exacting standards due to my mobility and weakness issues or it doesn’t get done at all until somebody arrives to do it for me. More than a handful of friends and family would recognize an unattended mess as being something that could drive me around the bend. And it has this week.

When all else was crashing around me growing up, at least I could control the state of physical space around me. It’s been one of my coping mechanisms since I can remember. When I moved out at a very young age, I was teased mercilessly by my friends about how my wardrobe was sorted by colour. White at one end, black at the other with a carefully coordinated rainbow in between. The spices in the kitchen were sorted alphabetically, every receipt and slip of paper had its place.

I can assure you that as I got older I loosened up a lot, having a child left me no alternative than to be less precise about the order of things so that I could enjoy quality time with her.

Still a neat freak to some degree, disorder will often grind my gears. Not so much because of the mess itself these days, but more so due to my fact that I can’t return things to order on my own any more.

A process of letting go of what I could once do but can no longer, and grasping as firmly as I can onto what is still possible. What a mess.

There was one pleasant connection for me. For all the times I was quite a sissy about getting dirty, I must have been equally adventurous in order to have gotten so many childhood injuries (we’ll ignore the part about about being a complete klutz). Bikes to be ridden with abandon, hills to be tumbled down, horses’ backs to have fallen from, jump ropes to have tripped over, eyes to have been blackened after trying to turn a guest bed into a trampoline.

In life you don’t get dirtied, and you don’t get hurt if you just sit on the sidelines. Although physically I’m not on the field, in spirit I’m still in the game. An albeit messier one.

Friday, April 19, 2013

Forgetting Pain…

Muscle memory. Sometimes I’m glad for it, other times not so much.

Although at no point anymore am I free of physical pain entirely, the intensity of it varies according to a few factors.

Time of day can make a big difference. Pain grows as the day wears on having been on my feet or sitting up. At this time, I’m still able to get to the bathroom on my own so at least a couple of times a day I travel a short distance within the apartment. At night, I’m hoping that my bladder is less demanding. A reminder of needing to get up one last time to go to the bathroom before bed is one I dread.

By the same token, mornings are sometimes a beast. Especially when I’ve done something completely idiotic the night before (as in last night) in trying to retrieve an item that the cat swiped under the fridge. Never, never again will I get down onto the kitchen floor. Doing it while alone was even more asinine. Allow yourself to imagine the visuals, it causes me pain just to think about it much less describe it. I made it even worse by trying to sit on the balcony for a few short minutes last night to enjoy the mild temperatures. Both well intentioned but stupid actions given my current state of disability.

Pain medication alleviates the discomfort to a small degree, for a few short hours at a time. It’s however often not worth the side effects that kick in afterwards.

Distraction can play an important role, not nearly enough of the right kind of it around here. This situation changes in two days when my daughter arrives home from school – there’s nobody I’d rather have helping to keep my mind off of the pain. And such a lovely distraction she is on top of it. I’ve got lots of her adventures to catch up on from the last few months.

At times, like this morning due to last night’s antics, the pain went to epic levels. I had to leave my bed to allow the PSW to change the sheets and for several hours I had not a clue as to how I was going to get myself back to the bedroom from the couch.

At times when the pain is not at epic levels, I quite simply forget how bad it can get. I chide myself for having put my body under of the strain of the pain meds, certain that I could have done without. I truly forget how unbearable it can often be.

As my best friend says, if women were unable to forget the pain of childbirth the world would be full of only children.

I might have mentioned that I’ve been taking on-line courses, of late in the area of neuroscience. I’m fascinated by how the brain works, especially intrigued by the admission of neuroscientists that there is so much not yet known or confirmed about the workings of the human brain.

Quite a blessing to able to forget severe physical pain. One I’m grateful for every time another round hits me, otherwise I suspect that I’d live in deep fear of the next onset. I don’t.

Emotional pain I find to be quite a different story. I don’t live in a world of sadness, but if I choose to think about a painful emotional event the memory can still feel raw and searing. Over time the pain has diminished somewhat, but can be brought back if I allow it.

I happen to think that as much as the emotional pain hurts when I think back to it, it helps me in my drive to better myself as a person. Perhaps we can be more sensitive to others’ emotional pain if we’ve experienced, and remember similar emotions ourselves. I can sharply remember feelings of sadness, humiliation, embarrassment, shame, disappointment among others. They can all come back if I call upon them.

But on the flipside, I can also remember joy with similar clarity when recollecting. It’s happened numerous times over my lifetime that I’ve been doing some lone, mindless task thinking a pleasant thought,  and someone has asked me what was on my mind. I’d had a silly grin on my face and the other person wished to be let in on the secret.

It’s still somewhat easy to do. I’d like to think it’s a wonderful gift I’ve been given, to be able to bring forth a joyful memory when I need it the most. The contrast to unpleasant memories make the joyful ones all that more precious.

Thursday, April 18, 2013

May I Get to Know You?

378 hits and it’s just past 7 p.m.

I’m honoured that so many of you are reading my blog, I’m truly overwhelmed. The numbers of daily visitors over the last few weeks has grown tremendously. My blog stats tell me that about 5-10% are spammers (no, I’m not going to market Rolex watches on my blog for anyone!), but the rest are visitors who came here by choice. Thank you.

This blog was initiated almost four years ago as a way to keep friends up to date on treatments, results (or lack thereof), and general goings-on in our household as they related to my illness. Repeating the same information over and over again in emails and phone calls was taxing for me, and it seemed to be a great solution combining a wish to keep caring friends informed with my love for writing.

It’s grown to be something else. It’s still a vehicle to keep friends up to date, but it’s also become therapeutic for me as my illness progresses – and a way to help relieve the boredom that can set in after spending long hours on my own.

What I miss is the other end of the conversation. Although there are many friends and acquaintances who let me know that they follow my posts, it’s a one sided deal for the most part.

I see my visitor count and I wonder what brings each of you here. What is resonating with you? Are you also facing serious illness? Do we know each other but perhaps haven’t been in contact for awhile (and may I have the privilege of privately catching up with what’s happening in your life?) Is there a subject surrounding serious illness that you’ve been hoping that I’ll raise?

What brought you here today?

Although comments can be posted anonymously here on the blog, I’ve learned that the majority of you prefer to communicate with me in a private email. (sessa1@live.ca) . Either way, I appreciate hearing from you. I really do.

Reminders of life still going on outside of these apartments walls is more welcome and appreciated than I could express in written word.

Thank you to my dear friend D. who offered her encouragement this afternoon to ask “why”. Why not?

Wednesday, April 17, 2013

The Revised Bucket List, Part 3…

The next bucket list item that was to be tackled last week is not so much a wish to be fulfilled, as it is a philosophy to be maintained.

On my bucket list of several years ago was a desire to keep laughing with people I enjoy being with, to maintain the ability to see the humour in situations, and to be able to laugh at myself. I was a “glass half full” woman, and I intended to go out the same way.

Goodness knows that this philosophy has been challenged in the last two years in ways I never thought possible. There were moments that I thought that our situation couldn’t get any worse, and then my daughter and I would get blindsided again.

Although there were many months that I believed I’d never be able to pull off a sincere smile again, they did come back to my face. And along with that, laughter.

One might have thought that it came because others tried to cheer me up, but it surprised me to realize that it came from within. My friends were in shock as they watched what was happening, they grieved along with me and tried to do what they could to help. Laughing wasn’t a priority, getting a roof over our heads was.

I don’t remember when exactly I found myself smiling again, I’d suggest that it accompanied the gratitude I felt as the ground swell of support grew around me. A safety net that allowed me respite from the unthinkable circumstances.

My friend’s last evening of her visit here last week had its sombre moments. We’ve parted now a few times over the last year not knowing if it was the last time we’d be hugging each other goodbye.

Yet without fail, our visits include lots of laughter.

It started out on Friday night innocently enough. My cat was stretched out with all limbs extended, this had reminded me of my friend’s last visit in January when she brought back to mind the name of toy I’d had as a child but couldn’t remember the name of. A cheap rectangle of suede with fur on it, when stroked it would rise up and down like a caterpillar. For years it had bugged me that I couldn’t remember, and in one quick second she delivered to me the answer, “Squirmin’ Herman”.

We then began to look up retro 70’s toy commercials on the iPad, one favourite of mine being for “Super Slider Snow Skates”. I used to love saying those syllables over and over again when the commercial came on, to the point of seriously annoying my mother as I begged for a pair for Christmas.

My friend hadn’t remembered ever seeing that commercial when she was young, and asked me if I got them for Christmas as I had hoped. I answered that I hadn’t. Watching the commercial I see now that my mother had wisdom and insight that at that time I didn’t possess – they would have been a recipe for a cracked limb given my lack of athletic prowess. A klutz like me might have done herself in hurtling down a snowy hillside wearing those contraptions.

More laughter ensued about the 70’s styles, products and fads. Suddenly my friend piped up, “Do you remember the Man They Call Ravine?

What was I not catching on to here? Why call a man a ravine? I looked at her quizzically.

She, in a deep voice starting singing “The Ma-HAN They Call RAVINE!!!!” holding long and strong on the last word.

It was explained to me that Raveen, not ravine, had been a popular performer/illusionist years back who had passed away a few days earlier. I didn’t remember him, or the commercials. But the song in the background of the commercials for his shows that we viewed on YouTube? My friend was not going to head to bed until I could sing the words with the right intonation and tone. A few tries and I received her okay to stop trying. She says I got it right, I say she couldn’t stand one more round of my singing and was tired, it was well past midnight.

She headed off to the bedroom “nook” (if you’ve seen my apartment you know what I’m talking about) and had turned off the light by the time I headed to the bathroom to brush my teeth.

Wouldn’t you know it, I just couldn’t get that tune out of my head. Something about the way the words boomed out, the expression on my friend’s face as she tried to imitate the baritone singer, and my misinterpretation of what was being said in the ad had grabbed my funny bone and wouldn’t let it go. To the point that I was laughing so hard that I thought I would choke on my toothbrush. I has assumed that my friend might already be asleep, so I was trying to do so soundlessly.

I thought I was doing a bang-up job of keeping pretty quiet until I opened the bathroom door. By that time I was laughing so hard I could barely stand, and certainly couldn’t take another step. Trying to stifle it was making it so much worse. I leaned against the wall certain that I was going to fall over or collapse to the ground if I didn’t steady myself.

My friend, turns out, was still awake. And alarmed. She interpreted the muffled giggles as sobbing and called out to ask if I was okay.

All I could get out was…”The Ma-HAN They…” “The Ma-HAN…”  After what seemed liked minutes I was finally able to slow down the chortling and snorting and shuffle off to bed. My shoulders still heaving, a huge smile on my face, I turned off the light and thought about how lucky I am to still laugh like that, and how grateful I was to have had my best friend with me to share the giggle with that night.

My friend called a short while ago from her home in Halifax. A quick glance at the call display assured me that I was safe in answering the phone with “The Ma-HAN they called…” I didn’t make it to the last word this time either.

Tuesday, April 16, 2013

The Revised Bucket List, Part 2

If you’ve been following this blog over the years, you might remember that the item on the top of my bucket list was a trip to New York City, family by my side, camera around my neck.

That didn’t happen, and won’t happen.

Friends, acquaintances and strangers have over the last year participated in “The New York Project”, and have in many ways given me NYC through their own eyes. Photographic diaries, scrapbooks, printed books, souvenirs, postcards, and especially precious to me are the written accounts of their own travels (and some hilarious adventures!)to the city.

There’s a giant canvas on the wall outside the kitchen of the Lower Manhattan skyline that can take me there in spirit anytime I look at it. I marvel that I have enough people in my life who care about me that I can’t narrow it down to the one friend who dropped it off anonymously on the doorstep last summer.

Not that I’m hinting or anything <grin> … but the New York Project remains a going concern.  Stories of favourite places, adventures, amazing meals (food always sneaks in there!) are much appreciated.

I mentioned in the last post that my dear friend from the East Coast wanted to help my realize some bucket list wishes while she was here last week.

New York was out, but perhaps my second favourite city was not. It’s been four months since I was well enough to travel to my Toronto medical team. Not that I don’t adore them and want to see them again, but our goal on this adventure was to hit a favourite spot of mine in the city and it wasn’t the hospital.

We were going to do this right.

A few days prior, a friend who is a make-up artist came by to give me some tips on looking less gruesome (my words, she quickly and kindly disagreed - we’d simply try to make me look like I’d had a good night sleep – something that hasn’t happened in a very long time).

A limo was booked, courtesy of the leftover funds in my small bucket list fund. Perhaps an extravagance, but truly the only way that it seemed that I could be somewhat comfortable for the minimum hour long drive each way. We’d pad the seats with blankets and pillows and I could recline on the way there and back, saving my sitting “allowance” for time in the wheelchair at the destination.

After visiting my favourite spot, the plan was (energy permitting) to stop by three places that offer some favourite food items (if I was looking to satisfy cravings last week, we weren’t going to stop at the steak dinner)  I could rest in the limo while my friend jumped into each location, none of the three were wheelchair accessible anyway.

For days, we watched the weather. It wasn’t looking good, rain and cold winds – but I really didn’t care. After being trapped indoors all winter I’m not sure that I would have even noticed the cold.

The morning of the trip, it became apparent that Mother Nature really wasn’t going to cooperate. Freezing rain was forecast, not a day that anyone should be on the road if avoidable – bucket list or not.

Having gotten myself ready (with help from my friend, blow drying my own hair isn’t something I can do anymore), putting my face on and getting dressed I realized that the trip would have had to have been cancelled regardless of the weather. I’d exhausted myself with the preparations to such a degree that the trip was no longer viable anyway.

For the last months if I had a short trip outside of the apartment planned (I can count all my outings since October on one hand), or had visitors coming I kept myself to strict bed rest the day prior to save up my energy and reduce the strain on my bones and heart.

This formula no longer works. I get what I get when I get it. Without question, moving about at all will exacerbate the pain, but resting beforehand is no longer a guarantee that the pain and exhaustion will be lessened.

As disappointing as it was to give up my revised bucket list trip, it wasn’t devastating.

If I look at it pessimistically, I can say it didn’t hurt that much because I’ve become numb to being let down. By my body, by people who I had thought would stick by me through this ordeal, by the constant barrage of challenges on which I often find myself on the losing end. What was one more letdown?

The optimist in me can revel in the joys of the planning of our adventure, appreciate the fact that despite not getting out the door I still had my best friend with me, and that instead of getting out I had the pleasure of spending time with a few new friends who came by for a visit.

Not to say that I won’t attempt the trip again in the future, but often the thought of something enjoyable has to take the place of actually doing or having what I’d like. And often, that’s enough.

Still more to come on bucket list week…

Sunday, April 14, 2013

The Revised Bucket List, Part 1…

A few years back I wrote about my bucket list, as of earlier this week unfulfilled.

As you might know from my last post, my dearest friend spent the better part of this week with me. Before she arrived, we spent time discussing how she might be able to help see items on my bucket list come to fruition while she was here.

When I was first diagnosed, I would repeatedly tell my family how grateful I was that my appetite wasn’t affected by ECD – this girl loved her food! I had hoped to keep cooking meals, at the very least eat pretty much whatever I had a penchant for.

Little by little, this wish crept away. First it was the inability to drive, I could no longer fetch groceries. In the beginning, my ex would happily fetch whatever ingredients I needed and I kept cooking for my family. Like many family cooks, I prepared what my family wanted and rarely made anything that suited my tastes if it didn’t match theirs.

Then bone pain, fatigue and weakness became more of a hindrance. My ex had never cooked a meal during our marriage so prepared food was the only choice. For a short time, I had more of a selection in what I ate. With individual portions available in the prepared food section of the market I could ask him to get me items that I particularly enjoyed without worry about what didn’t appeal to him.

I had to make major adjustments last year when my ex moved out and I was left on my own. I couldn’t fetch my own groceries, nor could I have cooked for myself anyway. I found myself eating a lot of Babybel cheese that a friend would buy in bulk at Costco for me (calcium for my brittle bones!) The medications were really starting to take a toll on my insides. A combination of intense stress and stomach troubles had led to a weight loss of over twenty five pounds in a few short months. My clothes took over me, even size 00 jeans required a belt to stay up.

As grateful as my daughter and I were to have friends give us a roof over our heads for over three months last summer, I was in no shape to cook despite our friends’ offer to use the kitchen whenever I wished. We were made to feel part of the family and were invited to join in with all meals, but I  just couldn’t eat much despite how wonderful the food always was.

Expectations had to be radically adjusted when I moved into this apartment in September. Lack of appetite, loss of strength to make meals, and a shortfall in financial resources to allow the purchase of prepared food led to a general disinterest in eating at all. Revised expectations, I went from “living to eat” to “eating to live” as a philosophy.

From previous posts, you might already know that a wonderful group of volunteers stepped in a few months ago to deliver delicious hot meals several times a week. And friends often bring treats that they know I enjoy. One can only stand so many of the meal replacement drinks each day before finding them abhorrent, the gifts of food were/are welcomed and appreciated.

This group of friends and volunteers has urged me to let them know if I have any cravings, that they would do their best to fulfill any special requests. But you know how it is, when you crave something – the sooner the better! So I try to not let myself think of cravings, instead enjoy whatever has found its way into my fridge and cupboards.

One craving however has stuck with me for months. It shouted out to me as something I wanted to have just once more, a nod to my bucket list wish to eat foods I really enjoy. It wasn’t something that the volunteers could prepare – and until I sold some jewellery a few weeks back it wasn’t in the budget.

A part of that small windfall was going towards my bucket list, no question. Just a few hundred dollars, but it was going to be spent on something that put a smile on my face. And my friend was going to be my accomplice and partner in crime.

Wednesday night, with help from one of the Food Train volunteers taking care of the transport (each and every one of them has offered to help in some way beyond making meals), I had in front of me the object of my desire.

One damned fine Keg steak (for non-Canadian readers, The Keg is a restaurant chain that has built their reputation as a carnivore’s heaven), with a side of crab legs. Garlic mashed potatoes and melted butter on the side. Although I tried to apply some grace in how I ate that meal on the tray while propped up in bed, anyone watching might have believed that it was the first meal I’d had in days.

I wasn’t being a complete piggy, the small windfall also allowed my friend to enjoy her own steak dinner beside me (and after all her considerable generosity over the last year, it was such a small gesture in return). She however, went about things far more elegantly than I. And there was more than enough to enjoy leftovers the next night.

If that’s the last Keg steak I ever have, I’m okay with that. It was even better than I’d remembered, and I’d shared the experience with my dearest friend – and very importantly, my stomach didn’t rebel against it (a small miracle).

And for my Canadian readers, The Keg doesn’t do take-out. I have my friend’s perseverance to thank for getting that fantastic meal in front of me.

We weren’t yet done for the week…

Saturday, April 13, 2013

It’s Nice to Be Missed…

Still here.

To my faithful blog readers, I didn’t mean to alarm you. I’ve received dozens of notes over the last few days asking if I was okay after having taken a few days break from writing the blog.

What I was doing was racking up more subjects to write about, whether I’ll get to them all is another matter entirely. Quite a bevy of topics to select from!

My dear friend from Halifax, whom I’ve mentioned many times on this blog, flew in again to visit for a few days.

We (and I use the “royal we”, it is she who did all the work) spent time clearing out some closet space for my daughter who arrives home next weekend. In our one bedroom apartment there’s one tiny clothes closet, which was inconveniently divided by the previous occupant into two levels that allow nothing longer than a shirt to be hung. My wardrobe has become very small, yet it easily filled up the available closet space leaving no room for my daughter’s clothes.

Items that used valuable space in the front hall had to go find new homes. In particular, my corporate work wardrobe. Try not to laugh when I tell you that I left the corporate world about eleven years ago and had saved my good suits and shoes. For all these years, I believed that I might have occasion to don them again.

Clothing wise, nothing really has compared to how a well fitting, classically styled suit would make me feel. My work clothes were an investment, and each suit would be nipped and tucked by a seamstress immediately after purchase to fit me like a glove. The suit, a pair of pumps and a fresh haircut – I’d feel like I could take on whatever the day could throw me.

It was time to let them go. Seven months ago when I moved here I couldn’t do it, there was still hope left. As silly as that may sound.

This week, it didn’t hurt at all. Okay, maybe a wee bit. Likely far less because I knew where they were going. At the suggestion of, and with the assistance of a friend those suits (and those beautiful leather pumps!) were delivered to a women’s shelter. They’ll be made available to women who could likely use clothing that helps them feel like they can take on whatever the day could throw at them when they face their abusive partner in court.

To the women who might wear these clothes under challenging circumstances, I send wishes for strength and courage to get through those difficult days. I’m sure from time to time I’ll think back on how wearing those suits made me feel, and I’ll be thinking of the battles these women face. May they believe in themselves and trust what they know to be the best path for themselves and their children. If I may speak from experience, that might well be the most important part of the battle.

Monday, April 8, 2013

Accomplishing Little…

A few days ago I wrote that I had forty eight hours on my own laying ahead of me and I had hopes to accomplish something of merit.

I shouldn’t do this to myself. I continue to set lofty goals, and am then disappointed in myself when I accomplish little to none of what I set out to do. It’s not laziness, lack of willpower or distraction.

It’s trying to do something, and not being able to follow through due to exhaustion, pain, and plain and simple physical inability. Limbs don’t bend and move anymore the way I would like them to, and staring at something heavy won’t lift it off the floor. It stays there until someone comes along to move it for me.

I concern myself too often with trying to accomplish what I believe others expect of me. I’m embarrassed that I can’t be productive, useful and helpful in so many of the ways I used to be.

What do others expect of me? Now there’s a question.

Lately I’ve been reading several blogs, books and listening to audiobooks written by others who face/had been facing death. Most recently the audiobook “Mortality” by Christopher Hitchens.

It’s reassuring to find that I’m not the only one who feels like they are letting others down when serious illness strikes. That willing oneself to accomplish more just isn’t enough. Limitations are what they are, wanting things to be otherwise is of no use and only leads to feelings of failure.

The one thing I did accomplish this weekend was a load of laundry, a load of fine washables that had been piling up in the hamper. Maybe that doesn’t sound like a difficult task to most of you; to me it’s quite an undertaking.

It was after midnight last night when my daughter emailed me to ask if she could come home from university for the afternoon, that she needed to see me. She’s in the middle of studying for final exams, we have just two weeks to go before she comes home for an extended stay. My answer of course was yes, nothing could make me happier.

When she arrived late this morning, she immediately noticed that I was wearing a blouse that she had given me at Christmas time. One that I had washed yesterday before I knew she was coming home today. A broader grin on her face wouldn’t have been possible, and she snuggled up beside me for a hug. It’s a very soft blouse and I like to believe that it gets me extra long cuddles.

I had needed that moment. An ever so small sense of accomplishment, that the effort to do a load of laundry yesterday meant something to my daughter. She wouldn’t have expected it, and likely would have insisted that the laundry wait until she was here this afternoon if she had known of my plans. It was my luck that the one load of laundry I felt up to tackling included the sweater she’d given me. It felt good that on a rare instance, I could exceed expectation. The feeling of letting others down is simply exhausting and I needed a short break from that.

Sunday, April 7, 2013

How to Make the Bad Stuff Go Away…

A very young lady by the name of Emma just made my day. Years from now it’s unlikely that she’ll remember our conversation, but it’s one that I’ll not soon forget.

A week or so back her Mom brought me a hot meal as part of the Food Train program for which she (being Mom), and about a dozen or so other volunteers donate their time, ingredients and cooking talents to make sure people like me in our area get a chance at regular, hot, nutritious food. Without meals (and yummy snacks!)  being brought to me by these volunteers and my friends, my diet would mainly consist of meal replacement drinks (not a terribly attractive option at the hungriest of times) and Babybel cheese (but even unwrapping those on some days is more than my fingers can handle).

It was her Mom’s first visit to me, and I was looking forward to meeting her. That day was not a good one physically, and I was confined to bed. As luck would allow that Monday afternoon, a friend was visiting who could do take care of door duties. I had let my friend know that if Mom felt comfortable, she could come down the hall to the bedroom so that we could meet.

When my friend opened the door, I could hear additional voices. Voices of little people. Before I knew it, I had Mom at the bedroom door holding her toddler and young Emma (in kindergarten) was standing at my bedside, close enough to put her hands on the covers.

A very engaging young lady, we spoke of school, red ponies and various other topics which she covered off with enthused expression and gesture.

It was one of those moments that filled me with great delight (as a former family photographer, this sort of interaction would have been the absolute highlight of a photo session), but it also made me miss my photography days so deeply.

On Friday I received an envelope in the mail. It’s the day that my mail is usually fetched for me from downstairs, typically it’s bills, flyers and nothing that’s likely to put a smile on my face. This envelope however had Emma’s name in the top left corner. I waited until after my PSW left before opening it. Inside was a letter, a picture Emma had drawn, a sticker and a tattoo.

What she wrote is between she and I, but I will tell you it let forth a torrent of happy tears sliding down my face.

I wanted to thank Emma for her thoughtfulness, but wanted to wait until I had a bit of a voice to speak with – it went AWOL again Friday night and had returned this afternoon. Well, now it’s gone again – but I take my opportunities when they come.

We just a short while ago finished a lovely chat, she on speakerphone so I could hear her parents’ contributions to the conversation as well. We’ve made a plan for her to come back to help me apply the tattoo - of Cinderella, Emma has selected my elbow as the perfect spot. I’ll wear it proudly. And I’ll be careful not to scrub it off in the bath so it lasts as long as possible.

Emma told me about soccer practice this afternoon, and then said that she has something very important to tell me. “I love you”. At that moment I was so grateful that she was on the phone and couldn’t see my face. I tried to keep a steady tone to my voice, but inside I was melting.

It made me realize how much I miss having children in my life. The photo sessions always lifted me to a place of remembering how much I enjoyed the different stages my own daughter went through. When asked if I missed a particular age/stage, my answer was always the same – it only gets better as each day goes along.

And it has. I enjoy my daughter’s company more than ever. The nice thing about memories is that they can be recalled and lived over again, so I’ve never truly lost those moments when she used to crawl up into my lap and snuggle into the crook of my neck, animatedly tell me about her school day, and proudly show me her latest creations. In the late hours of last night when neither of us could sleep, she’d sent me a link to crazy science discoveries that she knew that I’d enjoy as much as she had.

This morning started out with a heaviness in my heart as I was being reminded of just how warm the day is becoming, and that I can’t go out to enjoy it. I was thinking about my short and quite reasonable bucket list, and how not one of the goals came to fruition. (I should qualify it with an acknowledgement of how many generous souls tried to give me the New York City experience – top on my list - in other ways). That in trying to help someone else who was in my life at the time realize the most important item on their bucket list, I had forfeited my own.

Sometimes you need to ask for what you need (as I did in my last blog post with the help of Lisa Bonchek Adams’ writing), and sometimes what you need just gets handed to you. Thank you Emma, I love you too. Blessings appear everywhere when I keep an open heart.

Saturday, April 6, 2013

What a Girl Needs…

Sugar has not won out today. Maybe that’s not entirely true, I did have half a bag of chocolate covered cashews for breakfast but I have every intention of getting something nutritious into me today.That’s what happens when I neglect to restock the meal replacement drinks in my bedroom. I change my statement. Sugar WILL NOT win out today.

Instead of gorging on sweets all weekend I’m going to make a valiant attempt to produce something of merit over the next few days. I’m not entirely sure what that is yet, there are so many items on my to-do list it can be a touch daunting at times. Maybe it’s here on the blog, maybe it’s a personal project – but I have almost forty eight hours ahead of me alone in the apartment and I want them to count.

I ask myself, how do I measure if something I do or create is of merit? Many, many emails over the last few months from readers letting me know that my posts have made them cry. Happy and sad tears. And posts have brought forth bouts of laughter. Regardless of the emotions that my posts induce, hearing that what I write has stirred up feelings in readers tells me that although I may feel completely useless to the outside world in so many ways, I still have something to offer. We all need to feel needed, and thank you for letting me know that many of you look forward to checking in here.

I’m going to contradict myself now. Rather than offer something of my own creation, I’d like to share a blog post written by another woman dealing with serious illness. I shared an article a few weeks back written for the Huffington Post by Lisa Bonchek Adams, a woman living with Stage 4 metastatic breast cancer. She writes a blog that I follow, her Twitter entries also often give me food for thought as a patient with a different disease, but fairly similar trajectory. One that like mine, will take her life.

I’ve asked her permission to share this post, which she most graciously granted. Rather than offer the link, I’m going to offer the full text here. What she writes is relevant to other blog topics that have been swirling in my head, especially after a rather excruciating visit to a Hamilton hospital about ten days ago. I anticipate, and hope, that this will have been my last hospital visit ever. I will share more details when I’m ready, but let it suffice to say for now that Lisa’s writings do tie into my experience at that appointment.

From hereon in in this post, the words are Lisa’s. I thank her for her courage in sharing her thoughts and experiences with everyone who cares to listen.

For those who wanted to hear my interview on Doctor Radio and weren’t able to listen on Wednesday, here is a link to a downloadable audio file of the one hour show. Thanks to my brother, Mark, for doing this. That show leads directly into today’s discussion.

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I always get some heat about posting essays about the stupid things people say to those with cancer.

I know people come here expecting to learn. That’s what I’m trying to do: educate. People inevitably vary in their responses to what people say. After all, responses to books, movies, and comedians are all over the place.

Occasionally people will get defensive and say, “Well, I have said one of those ‘stupid’ things and I meant well.” I am going to take an unpopular stance and say that meaning well isn’t always enough.

Maybe the listener is scared. Maybe they’ve had cancer or a family member with it. Maybe they are just uncomfortable talking about illness and death. It’s important to remember: it’s not about you. It’s about the person with the illness. If you are a friend you will need to get over your discomfort or get out of the way. What you don’t want is for the ill person to have to be consoling the listener or trying to minimize the seriousness of what they’re feeling.

Do not turn it back on you, or when you had cancer, or when your child or mother or 2nd grade teacher did. It’s not necessarily the same. Types of cancer are not the same. Even subtypes of cancer are not the same. Now, I’m not saying you should always avoid interjecting something to let the other person know that you’ve had experience with cancer. But the first thing out of your mouth shouldn’t be to connect it to someone else and what their outcome was, good or bad.

Different diseases cannot be compared. Different cases of the same disease cannot necessarily be compared, either. Chiming in with, “Oh, my second cousin’s boyfriend’s dog walker had breast cancer” doesn’t help a person, especially if it’s followed by “She suffered in pain for a long time and died.” (yes, this gets said more often than you can imagine.) The other end of the spectrum is, “Oh I know someone who had that. They’re fine now.” (Okay, but some people are not fine… should they be jealous? Feel inadequate?) Someone told me in response to learning I had metastatic breast cancer that his wife “had a bit of that last year.”

If you had a coworker who worked the entire time she had treatment, that’s great. We are happy for her, truly. But that bears no relation to how someone else can handle their surgeries, treatments, and side effects. So while you might think it’s supportive (in your mind you’re saying, “See, I’m being supportive and reassuring her that it might not be as bad as she thinks”) what that person may reasonably hear is, “Wow, if you have to take time off work you are weak, or at least not as strong as my coworker was.”

What would be something better to say to a coworker? How about “Please tell me how I can help you during this time. Is there something at work I can do to make it easier for you? I hope you know I would like to help if I can. If you can’t think of anything now, that’s okay. Just let me know if/when you do. I’ll ask again to make sure you’re getting the help you might need.”

Asking “Has this been a good week or bad week for you?” seems like a good bet to ask someone you might not be best friends with. It shows concern and they can be as detailed as they want in their response.

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A few weeks ago someone tweeted to me, “As a cancer survivor myself, I know that half the battle is the mindset. Be determined to defeat cancer and you will!” Then followed that one up with “I meant that if we believe we can win against it, we will.”

Comments about someone’s attitude are definite don’ts. Does that mean those who die every day are responsible for their deaths because they are weak-minded? If it were as easy to defeat cancer as mindset, people would not die of it by the thousands every day.

Similarly, comments about appearance while rampant, can strike the wrong chord. I can’t tell you how many times people find out about my stage 4 diagnosis and say, “But you LOOK just fine!” The two are not always correlated, most especially at the time of diagnosis. This is why many people don’t know they have cancer and are completely taken by surprise. When people tell me “You look great!” I know they mean something nice by it. But the rest of that comment, the dark underbelly, is “You don’t look like you’re dying” or in some ways more insidious, “If you look that good you can’t possibly be that sick/it can’t be that serious.”

Don’t say you know exactly how someone feels if you don’t have evidence to back that up. Being a compassionate person and caring friend does not require personal experience that is identical to what the person is going through. Let me say that again, a different way: in my opinion you don’t need to have had cancer to be a caring friend. It might help you to be a good friend if you have had cancer, but it’s no guarantee. People “do” cancer differently. While the experience does make us members of the club, it doesn’t mean we will necessarily agree on how to deal with it. Part of what I try to do here is level the playing field. I try to bring you information and advice you can use so that you will know more about helping than you did before.

Don’t tell them that their science-based treatments are bunk and what they really need to be doing is just changing their diet, breathing pure oxygen, or relieving their constipation to be cured of cancer. Do not tell someone who is in the middle of treatment that chemotherapy is a waste of time. You may think your suggestions of supplements/vitamins/tea are harmless, however, there are serious interactions that can dull the effectiveness of chemotherapy and other treatments. Not all lotions are good to use during radiation treatment. Not all vitamins are good additions.

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I like what @travisbhartwell tweeted to me: “Mindset changes the days you have, not the number of days you have.”

The worst thing that can happen is that friends disappear. This is happening to me in spades. It may be that they are afraid they’ll say the “wrong” thing and end up being written about. But I think it also has to do with the fact that death and illness make people uncomfortable. I represent their fears. People who should be in touch with me at least every week or two (because that is how often we saw each other before) have just dropped away.

That said, there are so many people in my life who are so wonderful. Who offer to help, who make it easy to accept it. Who send notes or emails of support months after the initial shock. Who keep asking what they can do. Who pointedly give ways they can help and ask if I could use it.

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One thing I think is very important is to always say to someone who is ill or has experienced a death in the family: do not write me a thank you note for this. Do not feel the need to answer this email. Do not call me back.

If you live near the person ask them, “Would it be helpful if I texted you before I run errands so that I can pick something up for you?” Texting and email help because talking on the phone is almost always too much of an ordeal and/or inconvenient. I have friends who email me at the beginning of the week to say, “I’ll be at the grocery store, the drugstore, and the post office this week. Can I do anything there for you?” Some will text on the spur of the moment, “Running to Costco. Need anything?” These are invaluable offers.

If you have no knowledge of what information you are being told, admit it. People with serious illnesses do not expect you to know everything about their new diagnosis. They are probably learning a lot of information in a short period of time and may not even know the details of their diagnosis and treatment. They don’t expect you to have the knowledge but you need a way to connect. I recommend when someone tells you about a diagnosis you don’t know much/anything about you say, “I don’t know anything about what that diagnosis means. Would you mind telling me about it, and what it means for you?”

How is it impacting your day-to-day life and what part of that can I help you with?

I’m so sorry to hear that.

What is the worst part of this for you and how can I help make that a bit easier for you?

If your friend is dying or has a relative who is, and they refer to the death or how difficult treatment/daily life is, don’t brush it off, dismiss it, or say, “Oh, you’re not going to die. You’ll be fine. It will all be okay. Things will work out.” Saying this to someone with stage 4 cancer comes across as dismissive of the seriousness of their diagnosis.

If the listener says, “Oh, that’s depressing, let’s not talk about dying,” it can isolate the person who is ill, making them feel they should not be thinking about what is a very real concern or outcome. As Julie Klam points out in her book Friendkeeping, acknowledging someone’s wishes should be paramount. She tells the story of her mother and her mother’s friend Patty who was dying of cancer. Patty wanted to give Julie’s mom a pendant. Rather than gratefully accepting it, Julie’s mom insisted Patty would wear it again, that she would get better. Instead, she died a few days later. Years later when recounting the story with regret, Julie’s mom said, “She knew she was dying. It probably would’ve been comforting to her for me to acknowledge that… I was just afraid that she had some small glimmer of hope. I just didn’t know.” I would bet that if that same scenario happened again, Julie’s mom would act differently.

Later in the chapter Julie recounts being a friend to someone who had to terminate a pregnancy. She asks Julie a question that continues to haunt me: “Will anything ever be good again?”  It echoes in my mind now: Will anything ever be good again? Will anything ever be good again?

The truth of the matter is that for some it will. For some people, it won’t.

Check in with your friend intermittently. Give her reminders that she is not forgotten even if she is not out in public. I love getting cards or texts or emails that tell me what my friends are up to. As I write this a friend texted me to say she was eating at one of our favorite places. “I miss your company” she said. How can you not love that?

I love written notes. I save my favorites. When I’m having a bad day there is something about pulling out a card, seeing handwriting, reading a message. It’s just more personal than seeing it on a screen. Of course texts and emails are great for frequent check-ins, but for a special message? Real paper can’t be beat.

Other winners to me are notes that remind me of a funny experience a friend and I had, a favorite memory. Many people know I love my garden and flowers. They will send me a pretty card and tell me what they saw at the farmer’s market or in their own garden or what they’re looking forward to about Spring. Sometimes they will tell me about being on vacation and how they thought of me when they saw the water or the tropical plants and they remembered a trip I’d blogged about.

Some send a favorite poem or story or memory. I like those. I don’t like religious quotations or cards that focus on people praying for me or hoping for a miracle. That assumes I am a religious person (I am not and I don’t believe in miracles). I think cards should focus on the person— the connection to that person, your friendship, not what types of religious comfort or explanation the writer endorses.

One Twitter friend, Neil Shurley, wrote me a song titled “We Love You, Lisa,” and then made a video with people holding up signs that say those same words. I still watch it. I always cry. It’s one of my favorite things anyone has ever done for me. This, from what most people would term a stranger. Another friend, Nichole Bernier, took photographs that people sent her, combined them with poems and sayings and turned them into a photo book for me. When I’m down it’s another thing I reach for to feel support.

Does the person who is ill have children? If so, you can do what one room mom did for me this year: For school events Lizzie always asked if I felt well enough to join on any party or field trip. She offered rides to school performances. When I could not attend, she (and other moms) took photos and videos and sent them to me… without being asked. My friend Zerlina put together a playdate calendar and a dozen moms signed up in rotation to have Tristan over three times a week for playdates for the past six months. This was especially helpful. Sometimes I’ve been well enough to say we would host the playdate. But knowing there was fun built in with his friends was a relief to me.

Finally, I always love my mother’s suggestion for one of the best questions you can ask in any situation whether it be posed to a friend, a spouse, a child, a coworker. When someone comes to you with a complaint, a problem, or a rant asking the simple question, “Do you just want me to listen or do you want my advice?” is a wonderful way to be supportive. Sometimes a friend just needs to cry and vent, no advice wanted. By asking you will show sensitivity to the distinction. This is what I mean by not needing to have had the same experience to be a good friend. Listening matters. It’s free, and all you have to do is offer (and follow through).

And if you have a serious illness how do you respond when someone asks you how you are? If you don’t want to answer in detail, one suggestion is to say, “There are good days and bad days. Today is a … day.” This response is also a good one after the death of a loved one. If you are having a good day it allows you to acknowledge they’re not all like that. If you’re having a bad day it expresses that you know they won’t all be like that, either.

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I think we all like to hear that we matter, that we make a difference, that we are loved. In the end, you can never go wrong by telling (or writing) someone what they mean to you, what you like about them, and what you enjoy most about being with them. This is the essence of friendship to me. Some days you need a serious chat. Some days you need a friend to be silly with. Some days you need a friend to go shopping and have a gossip session with and try to put cancer in the back seat for a few hours. There are many ways to be supportive.

My dear friend Cathy texts me every morning to wish me a good day and asks, “How can I help you today?” I most certainly don’t expect that every friend should do this. But boy, it means a lot that she does. I rarely need something these days. But I will someday. And when I do, I know she’ll be there for me.

I have so many people in my world who care. I know how fortunate I am. I hope that some of these suggestions will be helpful and I am sure you will find others as readers comment on the post. You don’t need to have many things to say… a few good options will do.

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I hope you all have a good weekend, we are starting to feel Spring here and boy, does it feel good!

Friday, April 5, 2013

Opening Doors…

At the end of a very long day (although at 10 pm I likely still have at least four hours of wakefulness ahead of me to fill) I’m physically exhausted but feel spiritually fuelled up.

A busy day in my world with a visit from a Personal Support Worker, one of my nurses, three deliveries (if you’re keeping track of my “step allotment” from yesterday’s post, I’m already well past my 100 in just answering the door). And then added bonuses – two visits from friends to round out my day. I love when visits from friends overlap and they have a chance to meet each other, it makes my world feel a bit bigger and warmer when these connections are made.

Even the people delivering somehow find a way into my circle. The Canada Post delivery person knows that I’m not able to leave my apartment and will personally bring up items to me that don’t fit in my mailbox rather than leave them in the lobby as he does for other tenants. I hope that I don’t come across as grumpy when I come to the door, he often rings the buzzer at 8 am – a jolt when I’ve only gotten to sleep a few short hours earlier. At the very least I’m always dishevelled and I wonder if he thinks I spend the whole day in my pajamas.The oxygen tube might suggest that, and it somehow bothers me that anyone might believe that I don’t clean myself up every day. He remembers that I have to pick up the cat before opening the door, a bit of an effort for me but it avoids Scrabble making a mad dash down the hallway. I can’t imagine what excitement he believes lies beyond our front door, the young lad has a pretty good life on this side. What is it with this quest for greener pastures?

The gentleman who several times a month delivers my medications from the pharmacy always has a smile on offer and a few words to say about what’s happening in the outside world. My apartment is far off his route (a favour extended by my wonderful pharmacist) but you’d never hear him complain about it. Another funny (or not so much) twist to being palliative, the insurance company only doles out a thirty day supply of each med at a time. Heaven forbid that they give me more and they go to waste should I pass in between! And I’ve given up on getting them all coordinated to be delivered once a month.

The volunteer who delivered a hot meal to me (tonight, spicy curry with fish and shrimp, so delicious!) is among a group who initially signed up for preparing a meal one or more times a month (a rotating roster that provides shut-ins like me – is there a more appropriate term? -  with fresh meals twice a week). The volunteers have each extended themselves in offering to do more than cook and deliver a meal; all have reached out to allow me to get to know a bit about who they are, introduce me to their children, offer to do things to help on top of cooking a meal for me. People who are essentially strangers offering to come clean my apartment, run errands, do whatever they can to make my life easier.

And so it goes. Day in, day out. Tough battles buffered by so much kindness around me.

My original intent tonight was to write on another subject, one that addresses bridging the extremes. I have two full days ahead of me this weekend without any visitors (I wish I could bank steps and syllables but it doesn’t work like that unfortunately). You might hear more from me over the next few days, or I might have fallen into a sugar coma thanks to the treats that K. and K. brought for me today. It could go either way…

Thursday, April 4, 2013

The Piggy Bank…

I was always good with money. Starting from an early age I had paper routes, babysitting jobs, and even a lemonade stand or two. Bless my neighbours who would fork over a nickel on a hot summer day for a glass of refreshment; my friends and I were unlikely to have had anyone besides those who lived on the street pass by our table with it being a quiet crescent that led to nowhere else.

There was a summer job every year, the one at age sixteen cleaning guest rooms at a downtown Toronto hotel taught me tough lessons about respect and dignity (or lack thereof). I had been hired in another capacity, however when the housekeeping staff went on strike I had to along with everyone else quickly learn what “all hands on deck” meant. I could go into the gruesome details, but I learned how little respect some people have for others with evidence of the messes they leave behind. Sometimes from people you’d least expect. A lesson the universe has tried to teach me over and over again in my adulthood, am I finally learning to steer clear?

Leaving home at a very young age, I had to find gainful employment while still attending high school. One job at Sears in the bedding department (a source of endless amusement for my schoolmates) and also waiting tables at Pizza Hut to get by.

The budget was extremely tight. Like many students I subsisted on a diet of instant soup and ramen noodles. A car was necessary to get back and forth to school and jobs, thank goodness I’d saved and invested my earnings from earlier years to buy that old rust bucket of a gold Hondamatic (I’m showing my age). Even with the tight budget, I understood the value of looking out for my future and opened up my first RRSP (retirement savings plan) at sixteen.

I even managed to go to university on my savings, but my money ran out mid way through second year and I had no choice but to quit and work full-time. This may help you to understand why, although it’s for different reasons, it’s so difficult for me to watch my daughter leave school at this time.

My habit of watching out for the pennies never wavered. Before getting married seven years ago I was so very close to retiring my mortgage on a house in Toronto and had a healthy retirement fund. Some of you know that didn’t turn out so well in the end for me financially. I’m left with deep regret for making decisions during my marriage that I believed were for the overall financial health of our family if looked at it as a long term objective, but ended up being very poor choices indeed when my marriage ended suddenly. Hindsight…

Today, I’m back to that student budget. It is what it is. A reminder yesterday of just how embarrassed I am to be in this situation when a health care worker asked me if I’d moved in to my apartment in the last few weeks. The furnishings are sparse, and as in my student days boxes double as furniture. When friends or my nurses visit in my bedroom, they either jump on the bed or sit on outdoor chairs loaned to me.

Besides living with a very strict financial budget, a budget of another sort needs adhering to. That of my energy. Of the two, this is the one that I find more of a struggle these days.

After another recent downturn in my health, I’ve realized that it wasn’t just a bad patch. It’s just bad. To be simplistic, let’s say that in one twenty four hour period, my reserves will allow for:

100 steps. 5 minutes of standing. 500 spoken syllables. 15 minutes of sitting upright. 10 minutes of reading.

Out of that reserve come trips to the bathroom, maybe about 7 steps each way. A visit to the kitchen for a glass of water might be 35 steps round trip. Answering the apartment door? Probably 15 steps each way.

Standing is the really tough one. Part of that allotment is already shot with walking in the apartment.

Where does the wheelchair fit in? It’s reserved for the rare trips outside of the apartment door. It’s impossible to wheel the chair within the apartment while trying to keep the oxygen hose out of the way, and the carpeting (good Lord, I detest that carpet!) makes it difficult to manoeuvre the chair with my limited arm strength.

As for the syllables, I dearly miss my long conversations with friends. I waste my words in discussions that I’d rather not be having as I try to wade my way through endless red tape.

Where do I fall into debt? Laundry, meal preparation (heating up food is the extent of my cooking repertoire now), opening and closing the window in the apartment for temperature control. Part of that debt is recouped by taking strong pain meds, and I’ve written about the consequences of taking those. It’s a loan that carries an exorbitantly high interest rate.

It’s taken me a long post to get to the point that I started out with in my head. I only have so much energy and I’m pushing the boundaries every day. If I don’t reply to an email or phone call promptly, I truly apologize. If I ask to cut a visit short or cancel altogether, I know you understand – but also know that I’d rather I’d had the energy for a proper catch up.

Being with the ones I love and enjoy spending time with is my top priority. I hate that other chores as basic as taking my daily shower chip away at that small reserve of energy.

As for writing the blog, it’s therapeutic for me and keeps me busy in the hours in which I’m awake but it’s too late to have visitors or chat on the phone (and my dear readers, thank you for coming back. Consistently more than two hundred of you visiting every single day). I have a system worked out now with a bed table to hold my laptop, my phone, remotes, iPad and notebook and pen within easy reach. Meal replacement drinks within steps, and I’ll admit that a supply of chocolate is usually not too far away either.

Adhering to a strict budget of any sort can be challenging. The cutbacks I have to make on my expenditure of energy are by far the ones that hurt the most. They cost what is dearest to me, and put me in a position of feeling more isolated than ever.

Wednesday, April 3, 2013

Anticipation…

Many years ago when I was employed in the corporate world it seemed that the weeks leading up to a scheduled vacation would feel longer and more hectic than usual. The closer the vacation date came, the more I felt that I needed the break and would count down the days. The final days at the office could feel endless knowing that a reward was so close. Rarely would the break be anything more than a “staycation” at home, but the idea of spending uninterrupted time with my daughter had tremendous appeal.

Although it’s only two and half weeks until my daughter comes home from university (and it’s only been four days since she was home for Easter) I feel as if I’ve never missed her as much as I do right now. It’s not necessarily a negative feeling, I’m glad that she’s focused on completing her final exams. Despite her delaying her third year of university, she’s still committed to doing her best in finishing off this semester. I’m so proud of her determination to stick to a plan, regardless of how drastically it has been revised due to my illness.

Back in those corporate days I was unfortunately never very good at completely leaving the office behind. Like many of my colleagues, I would keep my pager on, let my supervisors know that I’d be checking my email and voicemail should a work emergency arise. The ties were never severed for more than a couple of days. Where did that get me?

A similar sense of unease comes to me now in anticipation of my daughter’s homecoming. Wouldn’t it be wonderful to be able to leave my health issues (which seem like a fulltime job) completely behind and enjoy our time without reminders? Wouldn’t it be absolutely fantastic to be able to forget that I was sick for at least a few days?

Years ago I had the choice to sever ties with work for a week or two. In hindsight I should have, but didn’t.

This time around we can’t escape.

This wish isn’t for me, it’s for her. Deep down I know that we’ll be able to continue making wonderful memories, but I wish that oxygen tubing wasn’t in the way. She and I (perhaps unfortunately for her!) share a similar sense of warped humour, and I can’t see a wheelchair getting in the way of that. In fact, it’s often the source of a good laugh these days.

We’ll make the most of our time together, we always do. No matter what disagreements have come up between us over the years (and they will continue to, sharing a one bedroom apartment won’t be easy!) never for a moment have I ever never not wanted to see her beautiful face. No matter how angry we might be with each other at the time.

It would however be lovely to kick my illness to the curb for a break now and again. Don’t think we won’t try.

A few weeks ago I posted a video of portraits that I’d shot in 2009. Here is the link to the one I’d posted on YouTube in 2010 (it’s shorter than the last one, mostly due to the fact that I’d had to cut back significantly on working).

Lots of wonderful smiles to be seen in the montage, including a few that belong to people I know to be following this blog. However at the 3:44 minute mark you’ll see two images of the young woman who makes my heart swell most of all (the handsome young man with her is one of my very favourite people too!)

It’s the smile I can’t wait to see in person again. Especially with knowing that she’s making such a huge sacrifice to see one on my face.

2010 Intrepid Lens video

Tuesday, April 2, 2013

Scoring More…and Yaks…

I had no idea that writing about smoking pot in an attempt to relieve pain would be such a popular subject. Hits to the blog were astoundingly high (no pun intended of course) today. I’m able to pull up a few basic stats on what brings readers to my blog – and surprisingly it wasn’t due to searches on keywords such as marijuana, pot or any drug related terms. Thank you for sharing the post with others whom you thought might take an interest. Feedback has been positive, encouraging and had led to more than a few laughs today. Numerous offers to keep me company (and um, to help check on the quality of the supply) should I decide to give pot another try…I'm pretty sure I won’t, but kind offers all the same!

Another bad pain day, another round of Toradol (my stomach is truly going to hate me tomorrow). Others who have taken this medication for severe pain tell me it knocks them out for hours afterwards, in my case it allows me a window to do a few things. Nothing more strenuous than writing a blog post, replying to a few emails, paying bills online and if I’m lucky I have enough juice left in my lungs for a phone call with a friend.

More of my written work is being dictated these days, arm pain and fatigue is making it more difficult to type. My goodness, between the Auto Correct feature and how the voice recognition software has interpreted my dictation, there are some doozies that appear on my screen!

Before correcting manually, today I had my yak taking a trip to the library, my hair was cut with a dandelion, and my cat was doing something inappropriate to be discussing on this blog. Before hitting the send button, I often find myself with a good case of the giggles  - and if it’s the right person, half a mind to let it go through as is so that the recipient can be in on the fun. Or they can wonder if I’ve lost my marbles and am imagining pet yaks. As for Scrabble, no matter what comes up on the screen – he’s probably done the deed - he does have a particular talent for trouble! Yesterday he learned how to zip and unzip my sweatshirt with his teeth. While I was wearing it. At this moment he’s trying to crawl underneath the iPad beside me on the bed, convinced that he’s grown no bigger than the small handful of fluff he was five months ago.

A bit of Toradol induced energy left in me, maybe I’ll do a Google search to see if anyone does take their yak to the library. Or cut their hair with a dandelion. If the searches leads to anywhere besides my own blog, there are some weird things going on out there in the world beyond my bedroom door… or authors aren’t checking what Auto Correct has come up with!

Monday, April 1, 2013

Score!

One very rocky night for pain tonight, I gave in to the lure of the Zofran/Toradol cocktail. The first pill to keep the second one down, the latter following fifteen minutes later in hopes that within an hour I’ll have been given a slight bit of pain relief.

Each time I take this cocktail it’s a game of pro vs. con. Pro?  A bit of pain relief, it even comes with a boost to my appetite for a couple of hours. The con, Toradol is simply wicked on the stomach. Although the Zofran helps with the nausea that hits soon after  ingestion, the day afterwards I have to be prepared for moderate to severe stomach pain.

Every day I weigh the trade-off, and I’m usually on the losing end. In most cases I regret having taken a chance on pain relief and therefore most days go without. Tonight, I went for it – the alternative wasn’t looking so pretty.

Pain management has been a challenge to say the least. I might have mentioned in an earlier post that I have an anaphylactic allergy to opioid medications (pretty much anything that works well on pain), leaving nothing very effective on the table for me to try.

I’ve been blessed with a high tolerance for pain, even after bone surgery I requested nothing stronger than a regular Tylenol. However this is no regular pain that I deal with day in and day out. Tonight the cat snuggled in as the pain got worse, I feared I might drown him with the tears streaming uncontrollably down my face if I didn’t down my cocktail. My friends, we had a solid “8.5” on the pain scale of 1-10.

I’m smiling as I type this (and with this you may gather that tonight the cocktail helped) undoubtedly one or two you might wonder if an alternative pain reliever might be effective. If we’re on the same page, the answer to the question you might ask is yes. I have indeed tried marijuana for pain relief. It’s surprising to me how many people have helpfully (and sometimes in the most humorous of ways) let me know that they could help connect me to a trial dose.

The first try was about eighteen months ago. Imagine the scenario – in my late forties trying weed for the very first time. Not that it wasn’t around me when I was younger, there was ample opportunity to smoke up. I just chose not to, it wasn’t for me. One bout of alcohol intoxication at sixteen taught me that I didn’t care for the feeling of losing control of what I was doing.

My first high was quite the experience. I was at one end of a Skype call with my daughter, she wanted to make sure that I wasn’t on my own and could call for assistance if I had a bad reaction.

I kept my daughter amply amused. I was convinced that the back of my head had turned to mud, and that I’d developed a magical talent for saying words before I’d actually thought them. I think you had to be there, but for my daughter it was raucous entertainment.

The second time didn’t go well. I became so very sad over something I couldn’t even pinpoint. I imagined that perhaps it might be what depression feels like, and it felt simply awful. A feeling I didn’t want to repeat. And neither experiment provided any pain relief anyway.

As the pain increased, I was talked into trying marijuana one more time this past summer – this time legal medical grade supply. I was told that the high might feel different than the last time, it might in turn provide better results for pain relief.

We (I had two accomplices who were taking great delight in bearing witness in hopes that I might break out in goofiness exceeding what I experienced on my first try) snuck outside on a beautiful summer evening. By then I’d already developed difficulty in sitting up for more than a few minutes, and they arranged me on a lounge chair so I could recline. I’m rethinking the “snuck” part of that sentence, it’s been impossible for me to sneak anywhere unnoticed for quite some time. Lumbered outside? How dainty!

I did not disappoint them. I announced I was having “thoughtful thoughts” interrupted by periods of having no thought in my head whatsoever. For anyone who knows me, that’s quite an absurd concept! Ask me anytime what I’m thinking and I will never, ever say “nothing”. Except it would seem when I’m high.

The helpful offers to “score some pain relief” continue to pour in. Thank you, it’s kind that so many would like to be of service in easing my pain. I’m sincerely grateful. And so many offers to share the experience with me! Thank you for such thoughtfulness <grin>