look what we did!

Remember my secret happy project?


We did it! We yarn-bombed a corner of my neighbourhood. We were 10 knitters, 14 installers and one videographer. It was so much work but so much fun. I dare you to watch this short video without smiling:


   
(video: Mark Blevis)


There are lots more photos up at our web site, Frivolknitty.com. It was so much fun - we're already planning for the next time!


An observer pointed out that three of the knitters/installers involved in this project have lived with breast cancer. I don't think it's coincidence that we all wanted to share in a little frivolity.

on finding my Thing

I had a breakthrough moment a few weeks ago. I've written quite a few posts over the last few years about the loss of identity I experienced as a result of having to leave the full-time work force. Letting go of my identity as a long-hour-working-communications-research-professional-activist-labour-staffer was really hard.

Since going into remission (and no longer feeling that fighting for my life was my main job) I've done an awful lot of navel gazing and spent a lot of hours in therapy trying to figure out who I am, since I no longer define myself by The Job.

Sacha, my perceptive and thoughtful son sent me a link to a wonderful article and inspiring article by Jesse Thorn. His instincts were right- I've been looking for my Thing.

I think I've been putting too much weight on each new idea, though. Every potential project would need to give me a new identity - provide the answer for when someone asks "What do you do?" 

But the truth is that no project can fulfill all of anyone's needs. And I was scaring myself off of trying new stuff because I was afraid that it wouldn't work out and that I'd be searching all over again. 

My "aha!" moment came with what should have been a pretty straightforward realization. I'm not looking to redefine myself. Overall, I'm pretty happy with who I am. What I want is to feel fulfilled, purposeful and happy.

I will never be able to define myself with just one word. I am a mother, wife, friend, writer, lover of dogs and books, social observer, activist in and out of the armchair and, occasionally, an opinionated bitch.

My Thing doesn't have to be my everything. I just need to figure out the things I love to do and allow myself the time to do them. I need to be brave and take risks but if today's Thing doesn't work out in the long run, that's OK too.

I may never have a few short words with which I can define myself at cocktail parties but I hardly every go to those anyway. Life isn't about creating an identity that others can understand and judge. Life is about living in the best way that I possibly can.

filling that prescription

A few years ago, I worked my way through the Artist's Way. I found the process to be extremely helpful in getting me past my writer's block and I followed the program dilligently - except for one component. In all twelve weeks, I did the Artist's Date exactly once.

I know in my head that play time fills the soul. And I know that the repetitive motions of knitting can spark creativity and be enormously soothing. Yet I seldom set aside time just to knit unless I'm watching a movie with my kids,out on a knit date or on a road trip. And I know, too that I chose knitting as my play because I usually have a product at the end that someone can use. This makes the time easier to justify.

But human beings need to play in order to be happy. And the benefits of creative time spill over in to so many other aspects of our lives. Blondie, one of my favourite bloggers wrote in a recent post she wrote after a night of insomnia:

...I got up and went to the couch. Sitting on the footrest was the latest cross stitch project I've been working on. It hadn't been touched since sometime last week. I can't even remember when I started it? I picked it up and worked on a little flower. In no time at all, I felt my body and spirit relaxing. I realized I was holding my entire body slightly UP and in a very unusual and stiff way. I was wound up TIGHT. If you touched me, I probably would have zapped you with a long, blue, electric arc. But after a half hour of stitching, I was much more calm. Even the kittehs seemed more relaxed. Collectively, we were detoxing. And after I made some good stitching progress, I made myself go lie back down and try to sleep. Eventually, I did.

Blondie called her post "Prescription for Art." I think this is perfect. Indulging our creative needs should not be an afterthought but a prescription for mental health and happiness. As Blondie points out in her post, art is good for our bodies and our spirits. We should all make time for it. The product need not be perfect. It's the process that matters.

We can't all make great, or even good art. But perhaps this prescription applies most of all to those of us who would never call ourselves "artists." We can all seek inspiration in the world (and from art of all kinds) to make stuff and make ourselves a little happier.

up to something

I have a project.

It's taking some planning and a fair bit of work. It won't change the world but it will make my world  a more fun, brighter place. At least I think so. It may even inspire a few people.

I'm not working alone but I'm not sure how many of us there will be. It's something I've been wanting to do for years but an awesome friend proposed a date and an action plan. We're being a little bit subversive, a little bit creative, a little bit brave and deliberately frivolous.

I think I need more fun in my life. I need to do some things just because they make me happy, not aiming for perfection, not trying to be "productive" and not with any particular purpose in mind. We're just going to put our heads together, set our hands to work, make a leap into action and then sit back and see what happens.

I'm having fun.

updating my words and myself

I've been thinking a fair bit about my last two posts.

First thing:

After writing my post about the lack of privacy in the chemo unit at the cancer centre, I was encouraged by several readers to follow my words with some action. I went to the Ottawa Hospital website and filled in the feedback form with a brief comment and a link to my post.

On Tuesday (the first business day after the long week end), I got a phone call from a "patient advocate" at the hospital. She was calling to let me know that they'd received my message and to ask permission to look into my medical files in order to determine with whom they should follow up (I was so stunned by this phone call that that it didn't occur to me until just now that they didn't need my medical info; they already knew that I was writing about the chemo unit and I could have just told them the date and time of my treatment. The irony in my  readily agreeing to this invasion of privacy, so they could follow up on a post about privacy is not lost on me). 

I was impressed to get the call and I have since been wondering about all the times that far more egregious things have happened at the hospital (as well as some equally wonderful things) and how I could have acted on them quite easily. On the other hand, no promise has been made to actually do anything or even to report back to me. The advocate said that I "may notice an improvement" the next time I go for treatment. And if I don't, she said I should fill out the feedback form again.

Second thing:

My last post was the first one I have ever considered taking down after publishing. I don't actually think that I'm a bad friend, generally speaking. I just have days when I tend to dwell on my regrets. In writing the post, I thought that by naming this shame, I might be able to let go of it a little.

I have a tendency to see the world in terms of right and wrong, good and bad (at the risk of sounding totally flaky, I am a textbook 1 on the enneagram scale). This can make me a little (ahem) judgemental  One of the things I like about myself is that, as I have aged and lived, I have also mellowed and come to understand that, a lot of the time, there are very many shades of grey. However, I still tend to be hardest on myself.

One of the things I'm working on is learning to let things go, forgive and move on, without repeating the same mistakes. Progress is not always linear but without a doubt, I am progressing.

i've been a bad friend

I've been brooding a little bit lately over all the ways I have been a bad friend since my breast cancer diagnosis.

I know I have and can still be a good friend much of the time but I've been thinking of how good people have been to me and I feel like I've fallen short in the reciprocation department.

I'm not being too hard on myself for cocooning during the worst of treatment. But there have been lots of good weeks during remission. I have missed so many important events in friends' lives - the births of children, loss of loved ones and serious illness. And now I don't know how to make up for that.

Friends, acquaintances and co-workers have sent me on trips, bought me presents and food, taken me out and sent me beautiful messages of support. I've been better lately at being the kind of person who does these things for others but I think, for longer than I cared to admit, I was too busy staring into my own navel - at least some of the time.

I'm in a pretty good space these days. Today, however, I am especially aware of regret.

it matters

Last Tuesday was treatment day. After a longer wait than usual (40 minutes -  I don't think I've ever waited that long in more than 6 years of treatment), my name was called and I was asked to go to Pod 3 (this sci-fi evoking nomenclature amuses me greatly, given that the world of cancer care is already pretty bizarre).

Despite my long wait, I noticed that Pods 1 and 2 were completely empty. Pod 3, however, was a different story. All 6 spots were occupied and there appeared to be only two nurses helping us all. 

Have you seen 50-50? I loved that film, and by and large, I found it to be a pretty accurate reflection of my own experience. One thing did raise an eyebrow though - the fact that they seated the patients in the treatment room so close together that their knees could touch. I understand that this likely fiction helped to advance the story but in real life I would never enjoy being so 'up close and personal' with my fellow patients.

For a while, things were almost that bad at the old cancer centre until the construction of the new building began. After that, the din was excruciating but it did block out my neighbours' reports to the nurses on the frequency of their bowel movements.

The move to the new cancer centre has been a huge improvement. I love the light and the air in the new building but most of all, I love the space. During my last couple of visits, though, it has felt like there is a little less space to go around. 

On Tuesday, I cringed as I heard the woman in the bed beside me being grilled about her emotional, physical and financial situation by a community care nurse. I tried to concentrate on my book while the woman across from me was informed that she would need a transfusion. I was very relieved when my own interactions with the nurse were over and I could plug in my ipod and let The Flying Bulger Klezmer Band drown out the voises around me.

I'm a fairly stoic cancer patient and it didn't really occur to me to complain. The nurses were lovely and patient as usual, and they were definitely doing their best to keep on top of everyone's needs. I didn't want to give them a hard time because I was annoyed and embarassed.

But it occurred to me later that these kinds of conditions are also unsafe and unhealthy. I, for one, am extremely reluctant to talk about the intimate changes to my body that are a side effect of treatment, so I can't ask how to mitigate them. My conditioned response in these circumstances is almost always to say "fine!" when asked how I'm doing. These days, that's pretty much the truth but that hasn't always be the case. There was a time, on a quiet treatment day about a year ago that I confided in a nurse that I'd been feeling low. She told me about the counsellors at the psycho-social oncology centre and asked permission to get someone to call me. A few sessions later, I was feeling much better.

I appreciate that I am getting cutting edge treatment and I know that's why I'm still alive. That's why I was initially reluctant to make a fuss about what seem to be little indignities.

But dignity matters. And how we feel as patients has a direct effect on our health. It's not petty or selfish to believe that there should be enough nurses working the floor so that patients don't have to be clustered together.

Maybe I should write someone a letter. Or maybe just a short note and a link to this blog post.

sesame challenged

My younger son was a diagnosed with a bunch of food allergies when he was very young. He's outgrown some of these (eggs, milk) and some seem to be around for the long haul (peanuts and tree nuts). 

Among the most insidious of these is sesame. It was the first allergy we suspected and has always been the one we find the most frustrating. It's in everything - try reading labels on bread products for a few days and you'll see what I mean.

Last year, we were offered the opportunity to do a blood test that can determine the degree of reaction to some common allergens. Out of a possible 100, Daniel's response to peanuts was as high as could be measured (this allergy is not going anywhere any time soon). His sesame reaction was 0.84. That's barely a reaction at all. When Daniel had no reaction to this year's sesame skin test, the doctor suggested a sesame challenge.

This, as I remember it, was our experience:

Sunday:

2:00pm: Tim goes out to buy Sesame Snaps.

3:00pm: Tim tracks down Sesame Snaps, discovers that they "may contain peanuts."

4:00pm Tim makes own version of snaps, with sesame seeds, sugar, ginger and lemon.

10:00pm-2:00am I have insomnia, partly due to sesame challenge. This may also be due the fact that I discover my free games of Chuzzle were re-newed when we reformatted my computer.

Monday:

9:00am: Daniel and I arrive at the allergists office.

9:10am: The doctor explains to us how the day is going to unfold.

9:12am: The nurse is blown away by our home made sesame snaps. Apparently most folks just bring in seeds.

9:20am: Daniel's arm is scratched with a bit of sesame. There's a bit of redness (which might be from being scratched but nothing more). Daniel says that it's itchy but remarks that "it might be psychosomatic."

9:25am: The doctor gives us the go ahead to continue.

9:45am: Daniel eats a bit of sesame snap.

9:50am He insists that his lips and tongue are itchy and swollen. I suspect anxiety (we have never been helicopter parents but I can only imagine how he must feel after practically a life-time of hearing the message - from many directions - that a food allergy can KILL you). The nurse sees no evidence of a reaction.

9:51-9:59: I attempt to distract Daniel with hang-man, offer him lunch out and cupcakes as a reward if he sticks it out.

10:00am: The doctor examines Daniel and sees no evidence of a reaction. Daniel is still anxious. The doc holds up a mirror so Daniel can tell that he looks fine. He soberly informs my eight year old that he can walk away now "but you will have to continue to abstain from eating sesame."

10:05am: I tell Daniel that he can have the whole day off from school.

10:06am: Tim drops off Daniel's DS.

10:10am-12:00pm: Testing resumes. Ever larger amounts of sesame are consumed without hesitation or reaction.The last couple of times, Daniel barely looks up from his Pokemon game.

12:00pm: We are dismissed, with one fewer food allergy on Daniel's list. The doctor (who remarks that Daniel is "a different kid" now that the test is over) instructs Daniel to eat lots of sesame in the next little while.

12:30pm: We celebrate!

Anyone know a good falafel recipe?

re-emerging

I don't know whether it's the unseasonably warm and sunny weather (It's about time I noticed that I get depressed every winter and recover every spring), a recent change of scenery or just the passage of time but I feel myself re-engaging with the world.

Shortly after writing my last post, I decided to "give up" on forcing myself to write. I was spending tons of time staring at the blank screen or coming up with creative ways to avoid writing - and feeling pretty miserable about it. What I was doing wasn't working and I had to make a change. So I decided to walk away.

But lately my heart beats a little faster when I think about putting pen to paper and fingers to keyboard. The creative synapses are buzzing and I have lots of ideas for new projects and a whole new approach to how I go about doing them.

It feels good.

lost my mojo

Mid-winter blues.

Bored.

No new ideas ("said it all before" syndrome).

Too much loss.

Whatever the reason, I have not felt much like blogging (or doing any writing) lately. 

I couldn't even muster up the energy to blog about the recent Komen debacle (although I took it all in with great interest).

And I can barely bring myself to think about Rachel (a scathingly brilliant and funny anti-pinkwashing activist and kindred spirit) or Susan (an equally brilliant leader, founder of Mothers With Cancer and mother of two young boys) without becoming undone. They deserve the kind of tributes others have written but I can only say who devastated I am that cancer has taken two more wonderful women.

So, I've been taking a break. 

And fallen out of the habit.

I think I might be ready to come back soon. Or to get back to writing down some thoughts.

And spring will come soon too.

Meanwhile, please know that all my latest tests have been gloriously normal. I'm doing OK. I just need to get past this dry spell, so I can return to writing with joy and enthusiasm.

3 truths

No one can understand hot flashes unless they have experienced one.


It is so much easier to appreciate the beauty of one's own community when viewed through a visitor's eyes.


This is the definition of  good friends: You don't think twice about letting your kid go to their place for dinner wearing pajamas. And when you get there you discover that their kid is still in pajamas too!

photo: M. Slavitch

and the winner is...

Nancy from Nancy's Point! I'll be sending her a copy of Not Done Yet early next week.


Thanks so much to everyone who entered.


I'm hoping to have an ebook version of my book out soon. This will make it so much easier to send out (and no more shipping costs!)

not done yet: a giveaway

I'm feeling completely uninspired on the  blogging front, so I've decided to run my first ever contest. 


Would you like to win a copy of my book, Not Done Yet: Living Through Breast Cancer? To enter, just tell me why you'd like to have the book (it can be serious or funny) in the comments section and I'll pick a winner at random, on Friday, January 27th. Contest closes Thursday, January 26th at midnight.


There are only a few unsold copies left, so get one while you can.


In other news, I'm reliably informed that my publisher is planning on re-releasing Not Done Yet as an ebook. No more shipping costs!

Pink Ribbons Inc.

3 tips

I've been asked by BreastCancerAnswers.com to come up with three tips I'd like to share about going through breast cancer treatment. This poses an interesting challenge. I had to ask myself, "Out of all the good advice I've received and doled out, what three things have stayed with me? Living, as I have, in cancer treatment for 6 years, what is most important."


This is what I came up with:


1. Don't be too hard on  yourself and don't compare yourself to anyone else (why yes, this is one tip - the two statements go together, OK?). Just as every cancer is different, treatments vary widely and so do our responses. Just because that you've been told that Jane worked full time and ran 5k every day of treatment doesn't mean that you ought to be doing these things. And conversely, you don't have to become a shut in just because Jane chose to stay in bed for weeks at a time. Who knows? Jane's choices may have been made because of what other people told her she should be doing. Do what's right for you.


2. When in doubt, bring a friend. People like to be asked to do specific things to help friends and family going through treatment. Don't be afraid to ask for company. Some of the meds I take leave me so wobbly I couldn't make it home without assistance. But even if I feel fine, I've been very happy to have a friend with me to provide a distraction during treatment or be a second pair of ears during appointments.


3. Live in the moment. We all want and hope to put treatment behind us. It really helps me, though, to take a look around and see the things that are good in my life right now. This doesn't come easily to me. I'm someone who lived much of my life looking ahead. I'm working on identifying those things in my life that give me great joy - and then savouring them.


I think that's it. If you've been through cancer treatment, what three tips would you share?

makes me happy

As a way to ease myself out of my winter ennui, my therapist suggested I do some journalling about the things that make me happy. Some of those things are probably evident to anyone who knows me even a little:


Hanging out with my kids.


Laughing with my sweetie.


Watching my dog run in the snow.


Riding my bike.


Reading a good book.


Being in a yarn store with money to burn.




But when I dug a little deeper, I came up with some things that are a little less obvious:


The moments of real connection that can pass between friends and strangers.


Having a good idea.


Eating a healthy, tasty meal I've made myself.


Clicking the "Publish" button on a good blog post.


Getting positive feedback about my writing, especially from other writers.


Looking forward to a trip, whether near or far.


Texting with my BFF.


And, perhaps not surprisingly, it turns out that writing about what makes me happy...makes me happy.

if you can't beat it, sit in it

if it's not on a list, then it doesn't exist

If I have any latent OCD going it, the condition manifests itself in the form of making lists. My name is Laurie and I am a compulsive list maker.

I have to-do lists (of course).

I keep the lists of the books I read (58 in 2011), how many come from the library (40 last year) and how many were by the same author (Michael Connolly was the big winner in 2011. I read 8 of his books).

I also track how much exercise I get (only 130 minutes so far this week. I got off to a slow start) and how many minutes I spend cleaning the house (it's a lot more than you'd think, if you ever saw my place).

I track how many minutes I spend writing and how much time I spend online. I track my weigh and - since January 1st- the number of calories I'm consuming.

It's an addiction. Writing lists and keeping track of things soothes me the in the same way that a piece of fudge can take the edge of a bad day. As with the fudge, I'm not entirely convinced that it's helpful. But I have no intention of stopping. 

In the years since I stopped working at a paid job, I think the lists provide the illusion of the structure that I miss terribly. Sometimes, when my life is feeling out of control, just making a few lists can make me feel calmer. 

As long as the lists don't get too long, or there aren't too many of them, I don't think there a bad thing. The trick is not to let my self-created lists oppress me into paralysis. Or become so time consuming that keeping on top of my lists takes up my whole day.

Maybe I should make a list of all my lists, just to make sure there aren't too many.

Or maybe not.

2012: ditching the Guilt

What Catholic girl (former or otherwise) doesn't learn to feel guilty at a very young age? I was always a bit of an overachiever. I'm good at Guilt.


I feel guilty that I have No Evidence of Disease when other wonderful women have died.


I feel guilty that I'm not working.


I feel guilty that I have insurance.


I feel guilty for being alive.


And, with every clean scan, every month that I continue in treatment that does not include chemotherapy, the guilt just gets worse.


It's not very constructive.


I need to figure out how to free myself from the Guilt. It distorts my perception of myself and others like a greasy hand-print on the lenses of my glasses. I have to figure out who I am and what I want, without having to squint or interpret what's on the other side of the smudges.


It won't be easy. And it may take me more than a year. But that's what I'm working on in 2012.

in other news

My children are still very beautiful.

(photos: Mary Anne Folckomer Register)

not imaginary

It's a running joke in my house, "Mama's talking to her imaginary friends." They're the people I've met online over the last few years, through blogging and various social networks. Of course they are very real people and when bad things happen to them, I do feel it keenly.


S., though, was someone I met in person - at the Conference for Younger Women Affected by Breast Cancer in early 2009 - and with whom I continued to connect online. We first connected because we both had metastatic breast cancer but soon realized that we had much more than the cancer in common - a progressive outlook, quirky gifted children and we both chose to expressive ourselves in creative ways. Unlike me, though, S. was a bona fide artist who used fabric as her medium.


S. was about my age. She had been diagnosed at Stage 0 but the cancer seemed to have quickly metastasized (was it just very aggressive or had something been missed? This was one of the things we discussed over dinner on the evening we met). We ended up spending all of our free time together, during that long week end in Atlanta - every coffee break, meal and evening. We even grabbed lunch together before grabbing our shuttle to the airport.


We stayed in touch after we got home, exchanging the occasional email and through the Care Pages that S. set up to share news with family and friends. She wrote to me about her latest art project (which integrated images of cancer cells), her daily life and a wonderful trip that her family took to Costa Rica. She also shared her frustration with the fact that no treatments seemed to slow the progression of her cancer.


Last week, I received a notice that S.'s Care Page had been updated. I logged in and found a message from her husband: saying S. had had moved from treatment to hospice care. Yesterday, he contacted us to say that this remarkable woman had passed away in her sleep.


I've run out of words to describe my sadness and the grief I feel on behalf of her family. Another child has lost her mother. It's all so wrong.


Over the week end, Zoom remarked that having cancer brings a lot of people into your life but takes a lot of them out, too. And, the truth is, I would do nothing differently, even knowing I would face loss and be forced to confront the possibility of my own death. The people who have come into my life - online and off- since my cancer diagnosis have improved my life immeasurably. I wouldn't trade that for anything.


But, right now, my heart is aching.

Judy

I'm sure she did not "go gently into that good night." 


Judy was a fighter, a woman whose Facebook page stated "I love my life." And that was life centered around her family and friends, especially her 10 year old son and her husband.


I first met Judy (and I do feel like I knew her, even though we never met in person) when 20 or so women were brought together by Susan to form the group blog, Mothers With Cancer. It was clear from the outset that Judy  would become a particular friend.


She had a passionate sense of social justice, a dark sense of humour and a straightforward manner that endeared her to me immediately. Like me, she loathed the pinkwashing that takes place every October. We even both had dogs who were considered part of the family.


Judy never stopped being angry about cancer. She railed against the unfairness of a world that afflicts so many of us with this evil disease.


At the same time, she never stopped appreciating the beauty in the world around her - in her environment, at work and in her family and friends. She never stopped finding things about which to laugh.


It's because of Judy that I applied for Little Pink Houses. I know that her family's week with the organization was a glorious experience (and so was mine). We often said how great it would be to meet up in person. Jeanine from Pink Houses did meet both of us and told me she is confident that we would have liked each other as much in person as we did online.


Judy, my friend, I miss you already. My heart goes out to everyone who loves you, especially Nate and Frank. Many, many, many people mourn your loss and celebrate your life.

a message in my library book

Deanna: a tribute

Brilliant.


Funny.


Committed.


Accomplished.


Artistic.


Strong.


Insightful.


Perceptive.


Inclusive.


Accepting.


Activist.


Loving mother, daughter, sister, friend.


I struggle for the words to write you the tribute you deserve. You are loved, admired and missed by so many.


My heart goes out to your family. I will hold you in my heart forever and continue to be inspired by you every day.


http://deeupdates.blogspot.com/

re-charging

love

photo: Mary Anne Register Folckomer

open letter to vendors who participate in group-buy programs

Dear Vendors,

I love group-buy deals (those you offer through Living Social, Dealfind, Groupon, Koopon, etc.) but I don't love them as much as I did a few months ago. I've had a few experiences that have turned me off group-buying and made me dislike some of the vendors who have chosen to participate.

Here's my unsolicited advice for any vendors contemplating participating in a group buy opportunity:

Don't act resentful, frustrated or even surprised when I call to cash in on my voucher. You may be regretting your decision to participate or overwhelmed with the response but that's not my fault. And if the point of selling these things is to introduce me to your business, then making me feel like my call is unwelcome is not the way to start our relationship.

Don't complain about the low price you set for your voucher. It makes me feel like you're accusing me of pulling a fast one or trying to rip you off.

Don't sell more vouchers than you can accommodate in a timely fashion. I bought a voucher for house cleaning in early October - but the earliest they can come is January 17, 2012. I'm pissed off and our relationship has yet to begin!

Don't add on additional fees that are not mentioned in the voucher. It's not cool to make me pay a "sign up fee" or tell me that the group-buy people "forgot to account for taxes."

Don't treat voucher clients like second class citizens. Unless you've stated this clearly on the voucher, I shouldn't have to wait outside your class/restaurant/spa to make sure that all those who've paid the full freight have been served first and then get whatever is left over.

The goal of participating in the group-buy process should be to attract new customers - ones who will keep coming back. If the voucher experience isn't a positive one for everyone who buys in, then the vendor has indeed wasted time and money.

I know that the group-buy companies engage in some pretty hard sell strategies (I once sat in a cafe and listened to the owner say 'no' several times, in several ways to a group-buy salesperson) but if you've leapt, you might as well make the best of it.

I've had three group-buy experiences so far that have been delightful. Two were with restaurants (Foolish Chicken and Kinki) and one was with a local yarn store (Wabi Sabi). I was already a fan of the chicken place but this just reinforced my loyalty (and I bring lots of others with me). I'd not been to Kinki for years but the experience was so lovely that I'll go again (and again). And the owner of Wabi Sabi was so incredibly helpful and gracious that they've won me over (and I've been telling everyone else to go, too). Those vendors could give lessons to some of the rest of you.

So, vendors, think before you sign up with the group-buy people. And if you decide to participate, be gracious, organized, responsive, welcoming and fair. Don't make me regret having bought what you're selling.

Very sincerely,

a potential customer

Canada Reads 2012

The top five Canada Reads 2012 books were revealed yesterday, as well as the five Canadians who will advocate on their behalf.

Despite my frustrations with how things went down last year and my initial resistance to an all non-fiction Canada Reads, I'm excited. 

The books look interesting and their defenders seem passionate. And almost as diverse as Canadians can be.

I really enjoyed reading last year's book choices. It was the actual debates that set my teeth on edge. If I had been one of the authors of last year's books, I would have been very disappointed in the quality of discussion (except for Sara Quin defending Essex County - she was wonderful). The conversations were generally at the level of a school yard taunts ("Oh yeah! Well I'm going to vote against your book because you didn't like mine!" "I didn't even finish reading your book but I'm going to tear it down anyway!"). There was so little discussion about the actual content of any of the books. How is it that the Canada Reads debates made me less interested in novels I had already read and enjoyed?

But that was last year.

The best part of Canada Reads in any year is reading the books. It's also the biggest commitment. And I've decided to do it.

Will you join me?

The books chosen for 2012 are:

The Game by Ken Dryden (defended by Allan Thicke)

On a Cold Road by Dave Bidini (defended by Stacey McKenzie)

Prisoner of Tehran by Marina Nemat (defended by Arlene Dickenson)

Something Fierce by Carmen Aguirre (defended by Shad)

The Tiger by John Vaillant (defended by Anne-France Goldwater)

i don't understand

The Canadian Task Force on Preventative Health Care has released new guidelines for breast cancer screening. Among other things they have recommended that women under the age of 50 with an "average risk of breast cancer" not be referred for regular mammograms. Women over 50 would only get mammograms every 2-3 years (as opposed to every year). They also advise against regular breast exams and self-examination.

I don't understand.

On their web site, the Task Force gives no reasons for these guideline changes but I have heard several interviews on the radio and the main arguments seem to be that mammograms generate too many false positives, submitting many women to uneccessary biopsies and other intervention. 

There must be more to this. I have to be missing something. I have witnessed the trauma and fear that false postives inflict on the women and their families who live through it. However, I don't think it's as bad as the trauma of being diagnosed at Stage 4 because breast cancer was not caught at an earlier stage. And breast cancer in younger women, is often more aggressive.

Is there a part of this story that I'm missing? Task Force spokespeople insist that the new guidelines were not influenced by the desire to conserve resources. Really? Colour me skeptical.

The Canadian Breast Cancer Foundation released a statement yesterday in support of regular mammography and critical of the new Task Force guidelines:

“The fact is scientific evidence demonstrates that earlier detection and diagnosis can save lives among women 40-49 by at least 25%,” said Sandra Palmaro, CEO, Canadian Breast Cancer Foundation – Ontario Region.

Palmaro added that screening can help find cancers that are smaller and haven’t spread, which can allow for better treatment options and reduced disability and death from breast cancer. Breast cancer continues to be the most frequently diagnosed cancer among Canadian women.

 One of CBCF’s most significant concerns about the Task Force report is that it relied heavily on old data from “randomized controlled trials” (RCT’s) related to breast cancer screening and mammography, some of which are 25 – 40 years old and were based on equipment that is now outdated. There has been an enormous change in breast imaging since that time, including significant improvements to analog technology, and the continued adoption of digital mammography across Canada. Digital mammography has been shown to increase accuracy in younger women pre and perimenopausal women, and women with dense breasts, the group the Task Force recommends be excluded.

This sounds pretty convincing to me. Your thoughts?

Photo: Mary Anne Register Folckomer

metaphor

it is what it is (and what it is is ok)

Herceptin makes me feel lousy. Or maybe it's the Demerol they give me from flopping around like a fish with a fever. Either way, after every treatment I feel achy and hungover for a couple of days.

It's a not nearly as bad as when I also have chemo (and I bounce back more quickly) but I'm still really dragging my butt around, when I bother to get up at all. I'll go for a walk later but it will take every ounce of the meager willpower I possess to get myself dressed and out the door.

I saw the cardio-oncologist again on Monday and that appointment went as well as could possibly be imagined. My heart was slightly damaged by the Adriamycin but has remained just below normal, since being on the Herceptin. The verdict: I can continue with Herceptin. I don't need to have heart scans every three months, as I have been. I don't even need to be followed by a cardio-oncologist unless my ejection fraction dips below 45 (it's currently around 49) or I experience symptoms of heart failure (um, yeah).

It appears that this whole heart scare was a tempest in a teapot - a reminder that when it comes to treatment of women living with metastasis, doctors are just making stuff up as they go along. They really don't know the long term effects of the drugs that keep us alive because our being alive and in remission is still so unusual. It's a bit unnerving but, given the alternative, I'm happy to serve as a human guinea pig.

Cross-posted to Mothers With Cancer. 

what i did on my november vacation

We just got back last night from our post Little Pink Houses of Hope road trip and I'm just too tired to put together very many coherent sentences. I'll write more later this week but I wanted to tell you all that my family had unbelievably fabulous time in Myrtle Beach.

Here are just some of the things I did:

Had my first Krispy Kreme donut.

Discovered real fried chicken and North and South Carolina barbecue and banana pudding.

Gained four pounds.

Spent time in the sun on the beach, walking, playing and just sitting around.

Enjoyed the glorious weather.

Learned how to hula dance and watched a man swallow fire.

Read 575 pages of a book and still have 1000 to go.

Went fishing without touching a pole and had a glorious time.

Blew off NaBloPoMo. I was having to good a time to waste it hunting down wifi.

Went to a concert with celebrity look-alikes who weren't dressed in drag.

Had my first manicure.

Dressed up to have my photo taken.

Played mini-golf.

Learned that southern hospitality is a wonderful thing.

Met many wonderful people.

Enjoyed my beautiful family.

Went for walks by myself.

Relaxed, unwound and chilled out.

Felt supported, cared for, spoiled and restored.

"Lived stronger. Loved harder. Laughed deeper."

I am so grateful to Jeanine, Melissa and all the wonderful volunteers, donors and families who make Little Pink Houses of Hope such a wonderful experience.

taking stock

(from Myrtle Beach, South Carolina)

16 hours of driving

31 hours on the road

countless new people

4 bedrooms, 3 baths

2 happy kids

1 bad sunburn

immeasurable kindness.

roadtrip connection

She made him in about 25 seconds.

I was getting breakfast at a hotel in Woodbrige, Virginia with Daniel at my side when an older woman came up to me and said, “You've got a busy guy there.”

I glanced over at my son, who was making pyramids out of the mini-cereal boxes and smiled. “I definitely do.”

“My grandson was just like that,” the other woman assured me. “And now he's on the national speedskating team. He kicked butt at his last competion.”

“That's great!” I said and meant it. I love these kinds of stories.

“So you, see,” the woman added. “It all works out in the end. His name is John-Henry,” she said proudly.

I promised to look him up, and I did. She wasn't kidding. He is kicking speedskating butt and things really have worked out that formerly “busy boy.”