Thursday, December 23, 2010

Jingle Bells in the Ped Ward -- A Christmas story


Went to my son’s Christmas concert the other night. Our eleventh at this little school in so many years. Sometimes it’s a full-blown concert; sometimes it’s just an all-school sing-a-long. But hearing all those little voices singing in the darkened but festive gym always tugs at my heartstrings, as it brings to mind the Christmastime I spent with my toddler son in the old, dingy MSA Hospital pediatric ward.

It was December 13, 2004, and for the fourth time in three months, we had presented ourselves at the emergency ward because our 18-month-old toddler was struggling to breathe due to yet another asthma attack. Once again we were rushed to MSA from Chilliwack by ambulance, and brought into the subdued darkened hallways of the creepy night-time pediatric ward.

I was taking an unwelcome crash course in resilience, forced as all mothers are to be there for my child through adverse times. By now, after spending Halloween and our high school reunion weekend in hospital with Miles, Daryl and I were getting somewhat despondent, wondering if these frequent hospitalizations would ever end (they did).

It was well into night-time when we entered the dark ward, and I once again tried to settle my son, who refused the ‘baby jail’ crib with metal bars and insisted on sleeping on top of me on the single narrow cot. I didn’t see the other mothers, but I heard them: each singing a soothing song to her child, and all in the language of their homeland. I can’t recall all their ethnicities any more, just that the universal mother’s lullaby was being sung in several different tongues.

This time Miles was also diagnosed with RSV virus, which meant we were quarantined in a four-bed ward with other sick little ones, unable to stroll the hallways or check out the common room. Miles was once again tethered at the nose to oxygen by a long cord that gave him a bit of mobility, and his striped hospital pajama sleeves were taped shut to prevent him from tearing the cords out.

The next morning, two of the mother-child pairs left, leaving Miles and I alone with our kitty-corner neighbours, a young mother who was a recent immigrant from India, incarcerated in the ped ward with her four-month old son. At first we ignored each other behind the curtains, each focused on the care of her own sick little boy. But boredom and proximity drew us together as the hours and days passed by, and eventually she started to pepper me with questions about baby care, fitness, and Canadian culture.

It was a nice bonding experience as we talked each other through our confinement. The most comical part of this was teaching her Jingle Bells and trying to explain the lyrics to her. She’d heard me singing it to Miles and really wanted to know what it was all about.

And I found myself having to analyze the word to a song that we all sing without a thought at this time of year. “Dashing – it’s kind of like running. A sleigh – you get pulled on it... through the snow… by a horse… well, I’ve never actually been in a one-horse open sleigh, but it sounds fun. Bells on bobtail ring… well, you put these bells on the horse’s tail… I guess you bob the tail first. Bobbing, it’s kind of like a haircut… anyway, the bells ring, that’s why they sing Jingle Bells!”

Through our cross-cultural communion we got each other through the boredom and despair of quarantine at Christmastime.

Later that day Miles was sprung from baby jail again, feeling much better. That night we attended his sister’s school Christmas sing-along at the same school he goes to now. The suddenly robust toddler ran around the perimeter of the darkened gym with his little friend Megan, and I was relieved to be a million miles away from the dark hospital ward as we all enthusiastically belted out Jingle Bells together -- a song I’ve never been able to hear since without being taken back to the pediatric ward at Christmastime.

Tuesday, November 30, 2010

How they see us -- Part 2


Wrestle time!, originally uploaded by Rosedale Annie.

Dad got off a little easier than mum in the profile written by Miles for Father's Day this year:

My dad is ?.:# years old.
(If uncertain, use random typography instead of guessing -- it's more fun)

He lives in Chilliwack.
(Got that right.)

He likes to play New! Super Mario Bros

He also likes to play computer
(Sounds like Miles is profiling himself again)

I like to 'rascli' with my dad.
(A very creative attempt at spelling wrestle.)

My dad likes to eat ribs.

He likes to go to his ofifs.
(And sometimes his office.)

My dad is a very awesome man.
(The highest form of praise.)

I know my Dad loves me because he drives my friends.
(This after impressing them with our 'cool twuck' at his birthday party.)

My dad is special to me because he: bought me a thing that I wanted.
(And the egocentrism creeps in again!)

Monday, November 29, 2010

How they see us


So the boy, aged almost 7 at the time, filled out profiles of his mum for Mother's Day and his Dad for Father's Day this year. Been hanging on to these little views of ourselves from our progeny because they're quite revealing! Although Miles certainly isn't paying too close attention to his mum's likes and dislikes. My favourite thing is definitely NOT watching dad watch hockey games.

(The above photo, one of my faves, is from when he was 3 and much less concerned with being cool or funny.)

About my Mum
By Miles

(Spelling corrected because the editor in me can't help it.)

What is something your mum always says to you?
Hurry up.

What makes mum happy?
Dad watching hockey.
Um, only in the sense that I'm glad he's got himself a hobby.

What makes mum sad?
My wart (do we sense a little egocentrism here?)

How does your mum make you laugh?
She do not laugh :-(
(He must have observed me on a bad day.)

What was your mum like as a child?
Normal.
(Whew!)

How old is your mum?
59.
(And looking goooooood!)

How tall is your mum?
I do not know.
(As my friend Sandy would say, how tall do I CONSIDER myself to be. That is the question.)

What is her favourite thing to do?
Yell at Molly.
(Well, I have to do it a lot as she is punctuality-challenged, but favourite?)

What does your mum do when you're not around?
Go on the computer.
(Guilty as charged.)

If your mum becomes famous, what will it be for?
Getting people jobs.
(Well, indirectly, by telling them what a great university we have and convincing them and their children to go here.)

What is your mum really good at?
All her yelling.
(Really? He should go live with the Italian auntie for a while and find out what loud is really like!)

What is your mum not very good at?
Running
(Touche.)

What does your mum do for work?
Get people jobs
(Sort of. It's hard to explain media and communications coordinator in the post-secondary sector to a six-year-old.)

What is your mum's favourite food?
Fries.
(Definitely not. Someone's doing a little transference here.)

What makes you proud of your mum?
Getting people jobs
(I guess I should get busy on that then, hey?)

If your mum were a cartoon character, who would she be?
Aloha (from Sponge Bob, apparently)

What do you and your mum do together?
Go geocaching with other people.
(Thank you, Alyson, for being supermom, buying the equipment, doing the research, and letting us tag along on something he obviously enjoys.)

How are you and your mum different?
She is a girl and I am a boy.
(Glad we've got that sorted out.)

How do you know your mum loves you?
I do not know.
(Aw, C'MON! All those bedtime snuggles, stories, hugs, Wii matches, dog walks, movie nights, count for nothing? Not to mention the multiple multi-day hospital stays during your worst asthma phase, oh, and a little carrying you in my belly for nine months, birthing you, and breastfeeding for several years? I guess he's entered the 'too cool to love your mum' stage, at least in his public persona.)

Where is your mum's favourite place to go?
Teapot Hill.
(Well that's one of them, especially when I go with you!)

Friday, May 28, 2010

A little 'me' time


Somehow negotiated a Sunday 'pass' this spring -- giving up precious family time, especially since spring soccer rules our lives Monday through Thursday evenings -- to take an advanced photography course. Enjoying our field trips and the chance to really concentrate on photography and find out how to really work the controls on that Nikon. This shot is from the Cheam Wetlands on April 25.

Wednesday, May 19, 2010

Please support Team Molly in the Walk for Diabetes




Dear friends,

As many of you know our family had the sad and difficult experience of having to incorporate Type 1 diabetes into our lives last year when our daughter Molly was diagnosed at the age of 14.

Since then we've learned a lot about diabetes care and management. Type 1 diabetes generally strikes young people. It is thought to be an auto-immune disorder in which the body attacks and destroys its own pancreatic cells, and it is not preventable or caused by lifestyle choices. Multiple daily doses of insulin keep Molly and other Type 1 diabetics alive, and multiple daily glucose checks help them monitor their blood sugar and health. That's thousands of needle pricks and finger pokes per year. We have maintenance, but we'd like to see a cure. We're doing our part in the search by fundraising through the Juvenile Diabetes Research Foundation Walk to Cure Diabetes on June 13.

There is no ignoring diabetes. It will be with Molly 24/7 for the rest of her life unless a cure is found. At the moment, that means four shots a day, four finger-pricking blood-glucose tests a day, and six carefully timed and balanced meals and snacks, all with the goal of managing her blood sugar levels, as her pancreas can no longer do it for her. It means no going out with friends without remembering her insulin and glucose monitor, and sometimes us driving it to her when she does. It means no more sleeping in as late as she likes or staying up until all hours of the night, or skipping or delaying meals.

It means recognizing, and taking steps to deal with, blood sugar highs and lows to avoid the dangerous effects these can have such as ketoacidosis and coma. It means living as healthy a life as possible now in order to minimize risks of serious side effects in the future. It means far more vigilance and organization than a teenager should have to incorporate into her busy life.

Molly has coped with all these challenges with impressive courage and determination. She continues to balance friends, family, school, homework, three sports, babysitting, and refereeing, all the while maintaining high marks, good fitness, and excellent diabetes management. She even traveled to Europe without her parents!

Families and friends of people with diabetes are an important source of funds for research on cures for Type 1 diabetes. We can truthfully say we never gave much thought to this condition until we were forced to last year. Knowing someone who has Type 1 diabetes really wakes you up to the reality of it.

Please consider sponsoring us. It is the families and friends of diabetics who will help to find the cure by supporting this cause, which is suddenly very personal for us.

Kind regards, and thanks in advance for your support. (For those of you who have supported me in the Run for Mom before, note that this is my new cause and I won't be asking for donations for that one anymore.)

Please click below to support Team Molly, or email me to arrange an in-person donation.

http://jdrfca.donordrive.com/index.cfm?fuseaction=donorDrive.participant&eventID=804&participantID=53386

Anne, Daryl, Molly, Emma, and Miles

Monday, April 12, 2010

Roses in tulips in Rosedale!

Can't resist hopping off to the local tulip field for some photo opps this time of year. This one is taken by Emma.

And it's all for a good cause:
http://www.calla.ca/tulipmania/index.html

Friday, March 19, 2010

Almost all the Russells


Almost all the Russells, originally uploaded by Rosedale Annie.

Saturday, February 20, 2010

Olympic spirit


DSC_0053, originally uploaded by Rosedale Annie.

Thursday, January 21, 2010

After the corn harvest -- image from a mild midwinter


After the corn harvest, originally uploaded by Rosedale Annie.

Now that I work full-time again, opportunities for daylight photography don't much abound. Sometimes I'll find myself rushing by a compelling scene while driving kids from place to place without my camera. But today I found a magic 15 minutes. Had gone to work early so I could leave early to bottle wine. That finished quickly so rushed out to easternmost East Chilliwack to hit Emma's volleyball game, only to discover that it was in town. So found myself going down Chilliwack Central at a leisurely pace and enjoying all the reflection scenes.

See more here, along with some dog-walk along the Fraser shots.

http://www.flickr.com/photos/rosedaleannie/sets/72157623253159748/

Sunday, January 17, 2010

Gomez in the grass


Dog in the trees, originally uploaded by Rosedale Annie.

It's all about the dog now. Sometimes, anyways. Having had a dog in the family for most of my life, I was well aware that they can dominate your free time, requiring walks, outings, and in-your-face attention. And we'd been okay without those demands for the last three years. Sometimes it's nice to go skiing or on a bike ride without worrying about the dog you've left behind. But now that he's here, we've been enjoying rediscovering places to take a dog for an afternoon adventure in Chilliwack.

Tuesday, January 05, 2010

Fraser River reflected


Fraser River reflected, originally uploaded by Rosedale Annie.

The Fraser can be so serene this time of year. Love the blues, beiges, and browns together without the greens to interfere (thanks to my new colleague Carol for this observation). Really enjoyed going off alone with just boy and dog for some one-on-one (and canine friend) time.

Sunday, January 03, 2010

Merry Ukrainian Christmas from the Russell-Roses















Okay, it’s January 3, 2010, and I’m still on holidays so I guess I’m making the Christmas letter deadline just under the wire. I always find the build-up to Christmas so darn busy that it’s hard to find time for the kind of reflection that this kind of project requires. Plus, it took until Dec 24 for us to have all three kids together in one place during daylight hours long enough to snap a nice portrait of them. And, I have to fight them for computer time now that they have memberships to their favourite websites.

But most of all, 2009 just wasn’t the kind of year that we want to spend a lot of time reflecting upon or celebrating, unless we’re celebrating that we survived it and reflecting on the fact that we have the love of family and friends to sustain us. They say that health and wealth are two of the cornerstones of contentment, and we were tested on both fronts this year.

We started the year with a nice snowfall, but a rapid warming trend after that saw flooding in Chilliwack, including in our neighbourhood. While our neighbours experienced actual flooding, our new house is high enough up that we were able to escape with some seepage. Our good friends the Gadsby-Haners rushed over to help us move furniture upstairs in a hurry in case it did flood, and we called upon the generosity of our East Chilliwack friends to collect seven shop vacs within a couple of hours, which we set up at various spots downstairs and kept going all night long, moving from one to another to empty them in a sort of zombie assembly line. Not much sleep for us that night. But now that our house has got through the worst flood the farmer up the year has seen in 50 years with just a little seepage, we’re feeling pretty good about its ability to withstand the elements.

Then there was this little problem called an economic downturn. Like many people in B.C., Daryl’s business depends on a healthy real estate market, and like many, we suffered when the economy took a huge dive in late 2008. We’d regularly see reports of condo developments that were clients of his going under, and the newspaper advertising promoting these developments that is the bulk of his business really dropped off.

Just as we were watching the news on January 10 about the flooding in Chilliwack, the other big story was the financial problems with the Olympic Village, and the City of Vancouver having to bail out the developer. Given that this was one of his biggest clients, that was a pretty depressing newscast. Oh, and during the newscast and ambulance came and took our elderly neighbour away with heart problems as he was so stressed about the flood.

The good news on this front is that things did pick up a bit during the second half of the year, he was eventually paid by most of this clients, and other clients and projects did emerge to help keep us afloat. But we did have to severely curtail our spending after a few years of relative prosperity, and learned new skills such as negotiating with Canada Revenue Service.

But in some ways it was nice to dial it back, stay home, and cocoon. We had each other, our pets, the Wii, books, DVD movies, and the ever-present computer to amuse us.

As always, our family kept very busy with school, work, and sports, so busy that our time together as a whole family was brief, except for the dinner hour, which we try to have together regularly. June is an especially hectic month. With four of us in spring soccer, we had seven soccer games a week going for a while, along with field trips, UFV convocation-related activity, and two kids’ birthdays.

So it took a day spent together in Vancouver on June 14 as a family to really notice that something was not quite right with Molly, who turned 14 in April. We spent Emma’s 11th birthday at the beach, strolling Commercial Drive during a festival, and going for dinner, and noticed that Molly needed to use the washroom with extreme frequency.

I figured it was a simple bladder infection and took her to our doctor. She had Molly do a urine test and then ordered a blood test, as she was concerned about Molly’s high sugar levels. We didn’t hurry to the blood test as it didn’t seem urgent (I guess I was in denial that it could really be something serious).

I took the other kids on a camping trip with several mums and 17 kids to Rathtrevor (lots of fun!), and then stayed on the Island on business for a couple of days, so it was July 3 before we got the blood test done, and July 9 before we visited our doctor for the results: Type 1 Diabetes.

Here’s some advice: If you’re taking your child for what could be calamitous medical news, don’t arrange to meet your husband in Starbucks right after. I was quietly crying into my coffee that morning.

We found out on a Thursday and were told that we’d have to take her to Children’s Hospital for three days, but our local doctor gave us the green light to take our trip to Long Beach on Vancouver Island first, as Molly’s blood sugar levels weren’t dangerously high yet (we caught it early).

So that’s how we found ourselves on a beach, cooking hot dogs on the fire, looking out at whales cavorting in the water, when the endocrinologist called, saying “We need to see Molly right away.”

Once we explained that we were in Tofino, dude, like, watching the whales, you know, he reluctantly let us stay, as long as Molly had a very low carb diet that week, andtook it really easy. He also said to rush her to Port Alberni Hospital if anything went wrong. “Please take good care of Maahhlly,” he urged us in his American accent.

So we had an uneasy yet relaxing few days on the beach, cooking lots of bacon and eggs and other high protein foods for Molly, watching whales from the beach (in more abundance than we’d ever seen them there) and trying to enjoy our usual beach hikes, campfires, and ocean swims (well, I was the only one crazy enough to actually swim much in the cold water).

Then on Monday morning, the other kids farmed out, we reported to Children’s Hospital where the extremely kind and competent doctors, nurses, and dieticians (and a life-sized cut-out of fellow diabetic Nick Jonas of the Jonas Brothers) helped Molly start her new life, which includes 14 tasks a day for a 14-year-old to deal with and us to bug her about: six carefully planned and timed meals or snacks, four finger-pricking blood sugar tests, and four shots of insulin. It also includes serious things to consider such as avoiding blood sugar ‘lows’, which can be harmful now, and ‘highs’, which can lead to long-term severe health consequences, and deciding appropriate levels of insulin to take. Way more serious stuff than a teenager should have to be worried about. Not as bad as some other things that can happen to you, but not good either.

To say this has added stress to our lives would be an extreme understatement, but we are all coping. Despite the fact that sometimes we have to nag her, and that we all hate the fact that she now has this lifelong condition for which there is treatment but no cure, Molly has showed extreme maturity in dealing with this blow. Her life isn’t as carefree as it should be any more, but she still gets to do all of her former activities.

And unlike Type 2 Diabetes, she can’t prevent or cure it through diet and exercise alone. She will need insulin for the rest of her life unless a cure is found. Essentially, her pancreas has ceased to function properly on its own due to an autoimmune disorder.

Daryl and I often catch ourselves feeling that we’ve done this before, having endured the pain and hardship and fear of having a child with a serious medical condition when Miles went through his multiple emergency hospitalizations for asthma as a toddler. It’s like: hey, we passed that test, endured that trial, why do we have to go through it again, and this time for a condition that’s not going to get better, and will trouble us all (especially Molly) for the rest of our lives? But something that you learn as you get older is that life is just not fair. We led a charmed one for a long time, but that doesn’t mean we had a free pass to trouble-free times forever.

And as much as I can say this has been hard on her parents and siblings, Molly often wisely and correctly reminds us that it’s even harder on her.

And as the months have gone by she has proved herself generally very competent at handling her condition, so much so that we are, with some trepidation, allowing her to travel to Europe on a 10-day school field trip without us this March.

Oh, and did I mention the emergency quadruple bypass my dad had in May? That was intense and scary. It was difficult to visit him so frail and dependent on medical technology and expertise in the hospital after he was the doctor for so long , but he has come out of hit very well and we are delighted to still be enjoying his company. He’s back to walking the dog two times a day, mowing the lawn, and enjoying some travel with Mum.

Within this bummer of a year where the bad news seemed to just keep coming, there was also routine, and fun, and regular accomplishments.

I kept working at UFV, in fact returned to fulltime employment (had been 80 percent) thanks to the benevolence of my employer. That helped on the financial front, but made juggling all those kids’ activities even more difficult. I’m often tearing home just in time to turn around and drive them to something, but we find that sports are very good for them, and just because a boy is the third child and you’re tired of carting them to swimming lessons, that doesn’t mean that a boy doesn’t need to learn how to swim! (And once I get in the pool and do my lengths while he’s in lessons, it feels pretty good to me too!) I continue to enjoy my work and have especially liked working on the history of UFV project, interviewing veteran and retired faculty and staff. I also played women’s soccer again in the spring, with a bunch of mostly over-40 ladies who love leaving our troubles behind and hitting the turf for some kicks. That, combined with badminton, cycling, the gym and now Wii fit, keeps me active (not to mention dog walks -- that’s a bit of foreshadowing).

Daryl kept plugging away at his work, going to the gym, and enjoying his newfound enthusiasm for watching hockey. This fall, his midlife crisis took the form of playing ball hockey in a league. So twice a week, he goes out and chases younger men around the gym, stick in hand. He also bought hiking gear with hopes of doing some overnight trips, but only managed a few day trips as our summer turned out to be so busy. He also seeded and planted a very nice front yard for us. No more meadow. And he’s working on a “dry river” concept for the area leading to the front steps.

Emma got to play school sports for the first time this year, so she added volleyball and basketball to her repertoire as well as soccer. (She also got a bonus unexpected trip to summer camp when Molly had to go to the hospital.) She is growing up, on the cusp of early teenager, and wishes she could fit the clothes at American Eagle, but is still stuck buying her jeans in girl sizes for awhile longer. She keeps busy with sports, playing with friends, and being a fashion maven on the Stardoll website. She’s also serving as an apprentice babysitter, helping Molly on some of her assignments, and she enjoys that very much. She gives us very little trouble, as always, and her weak spot is allowing herself to be bothered by her very bothersome (to her) brother Miles. She’s doing very well in grade six, and will be off to middle school (and uniforms) at Rosedale Middle next year.

Miles is now 6 and in grade one, and the world is one big collection of words waiting to be deciphered. He’s reading menus, signs, packages, newspaper headlines, and of course, books with us in the evenings. He’s also quite good with numbers. He enjoyed playing soccer again this fall on a team with a lot of his buddies from school, and is finally getting the knack of swimming, after several sets of lessons. But most of all he loves his screens – computer (he’s gone from Club Penguin to Moshi Monsters website), Wii (loves his Super Mario), and now his Nintendo DS handheld gameplayer. We have to force, cajole, or bargain him off screen time regularly, and he and Emma are both rationed on the computer with the oven timer. (“20 minutes and then go do something that doesn’t involve a screen.”)

Molly, although her tendency to dawdle can drive us crazy -- especially when getting ready for the bus in the mornings, continues to impress us with her excellent grades in every subject and her ability to juggle school, sports, friends, and Facebook. Her favourite sport is soccer, and her team won the Coastal Cup this spring (best in the Lower Mainland at the silver level). She also plays basketball and volleyball. She is a much-beloved babysitter and is very good with young kids. The fact that she continues to do so well despite the huge extra burden she’s been handed is impressive beyond words.

The four cats continue to eat, sleep, doze, play, and purr. George is 15 and when we brought home a dog bed for the floor (more foreshadowing!) he thought that was great, flopped himself on it, and rarely leaves it for the heights of the couch or the bed anymore.

So that leaves the newest family member: Gomez! I’ll agree that it’s totally illogical for a busy family without a fenced yard should get a dog, but this wasn’t a logical decision. He came to us at a time when we were feeling great sadness as a family, and we (I) decided that we needed something joyous and positive in our lives to counterbalance the heavy blow that Molly’s diagnosis dealt us. In other words, we needed something happy to happen. So a puppy it was! (Paid for through a combo of my bottle-return savings and the kids' allowances.) He’s three-quarters golden retriever, one-quarter muensterlander (German hunting dog), and although he comes with considerable hassles, he has indeed brought joy into our lives. He accompanies us to many soccer games,gets walks from me on the weekends, and even his reluctant master Daryl has come around and is sneaking him out for some forest excursions on weekday mornings.

My friend noted that we’re 10 years into the new millennium in her year-end letter, and I think that’s a noteworthy fact. Ten years ago we had two little girls, four cats, and one dog in a tiny house clinging to the edge of a river in a big yard. Now we have – hey, what do you know – three kids: two big girls and a little boy. The house has now morphed into a modern big structure able to house us all comfortably, now higher up and in the middle of the big yard. Still have four cats and a dog, but the dog and two of the cats are different.

We have just enjoyed a lengthy Christmas break with family and friends. My favourite part of Christmas is the days after the preparations and festivities are over when I can enjoy time with very little on the agenda (although, ever the striver, I aim to read the papers and clean the house and go on a walk and play with the kids and watch a movie and do a puzzle and do Wii fit and read my book, and never accomplish it all).

So although overall we’ve dealt with some tough stuff this year, there has still been joy, and love, and laughter, and friendship, and for that we are grateful. Here’s to 2010!

To see family and pet photos from 2009 go here:
http://www.flickr.com/photos/rosedaleannie/sets/72157623104875864/

For my favourite scenic shots from 2009 go here:
http://www.flickr.com/photos/rosedaleannie/sets/72157622986074399/


All the best to everyone, everywhere.

Anne, Daryl, Molly, Emma, Miles
(and George, Sophie, Moby, Neko, and of course Gomez).