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Robyn's 2003
Christmas letter / Message
from Sandy / Robyn's Announcement
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April 24, 2004 -
from Robyn:
"I am here in the hospital,
feeling pretty shitty as a matter of fact. I made the
'mistake' of going to the dentist last week and have ended up with
an absess. This has given mum and Sandy a chance to lay waste
to my house - something she has little chance to do at home.
She says she should come over every couple of weeks and tidy up -
well poop on her! I always intended the cleaning to get taken
care of... but you know what the road to hell is paved with.
I have to admit this isn't t he way I
wanted things to go - not this way. I always suspected
this was the way but it sucks - big time.
I will write more if I feel
better. Until then I love you all and miss you already."
.
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Robyn's
2003 Christmas letter
Happy Holidays 2003
So, how is everybody?
I used to maintain that these annual holiday letters were a cop-out, but certainly, it's an easy way to bring every-one up to date. I've tried to keep in contact via email, and have mostly succeeded, but there are a few people that have fallen by the wayside. To that end, here it is: the ubiquitous end-of-year letter, C'est la vie. I guess the easiest way to let you know what's been going on is to do it this way:
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Most difficult moments of 2003:
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Finding out that the chemo I'd been on for 9 weeks hadn't done any good - in fact, seemed to have exaggerated things a bit. This included having a weekly draining of the pleural cavity about 1 litre of fluid has been syphoned out of the pleural cavity each week, a procedure which is anything but A Good Time.
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Having a blood clot go my right lung. Not fun. Pain beyond belief and because of that...
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Having to go on oxygen for 18 hours a day, whether at home or out. I have an oxygen generator at home, and portable tanks to take with me when I go out. We named our home generator 'R202', But that meant…
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No flying, because of the difficulty of organizing oxygen at the other destination, and because the pressure changes in the plane might make my breathing much more difficult, or could dislodge the clot. And that
meant..
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Having to cancel going to the world science fiction/fantasy convention in Toronto, despite the fact that a very good friend offered to organize whatever oxygen I needed.
Best moments of 2003:
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Believing that the new chemo I'm on is doing the job, because of the side effects I'm noticing, specifically a) Hair thinning: I'm looking at this as a good thing because it means that the mitosis of hair growth has been interrupted, which means the mitosis of tumor cells is being affected in the same way, b) Pleural cavity draining: now, it's happening every two weeks instead of one, and rather than a
litre, we're down to under a litre, c) Bloating: I've had some strange bloating because of what's going on, where I can gain two pant sizes in one day, but on this new chemo, the bloating is much less. I only notice a bit a nausea and tiredness over the three days directly after my treatment. My appetite’s good, and I'm mostly getting a good sleep at night. So, all of these things we believe to be Very Good Signs.
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Spending several weekends up in the mountains, enjoying the fall
colours. So we can’t fly! So what! We'll find a way to celebrate and enjoy everything that's going on, anyway. More on this later.
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Being told that my oxygen levels are up high enough that I only need to we use oxygen towards the end of the two weeks - near when I need to be drained. I certainly don't need my portable tanks anymore, which is great.
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Being given my doctor's blessing to fly! That was the best thing to hear of all. Bruce and I are already planning a trip, maybe in February or March, to Las Vegas, We're hoping my parents can come with us, even if they come only for four days. They need and deserve the break, and we want to show them 'our' Las Vegas.
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I mentioned our trips to the mountains. Bruce and I decided that, while I was feeling good, we'd take off each weekend to enjoy the fall
colours. We'd treat ourselves and stay at a nice hotel in the mountains, and just wander around the forest, eat (way too much) good food and take it nice 'n' easy. I've had people tell me that I'm enjoying myself more while I'm sick than they do while they're well. I have to say, that's not the way to do things, and in fact, it isn't because I'm sick. Bruce and I have always maintained that life is a complete gift, and you *don't* know what's going to happen tomorrow. You could get hit by a bus. You might develop something as innocuous as arthritis - but it could be something that just makes your life more difficult. Why wait until that happens? Why wait until retirement? GO for it - enjoy yourself while you're able, and so what if you spend a bit of money now? Do it - just enjoy yourselves, because you never know.
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Goodness knows, I certainly never expected the word 'cancer' to be so intertwined with my life, but it is, it's there, but I’ll be
damned if Bruce and myself are going to let it stop us doing what ever we're able to. Okay, so maybe the trip to the Taj Mahal is out for the moment, but our attitude is just that: for the moment. If we can't go to the
Taj, we'll go to Vegas and pretend we're at the Taj.
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No, it's not always easy. Yes, there are moments that upset me - but the trick is, keep
'em to 'moments', Like glass blowing- I tried it about 6 months ago, and lasted 20 minutes. My brother was with me, and I was glad he was - I didn't feel 'solid' at all, I hadn't expected to find it so completely fatiguing. Very disappointing, but you know what? That studio will be there when I'm able to blow again. I can't eat the same kinds of spicy foods I used to, but that's okay- there's still a never -ending variety out there that I can eat. It's very frustrating that my concentration is shot - I can't write fiction, and have trouble staying with novels. But again - these words aren't going to evaporate. The books will remain, and when I'm able to write again, I know I will. Meanwhile, I'm not going to beat myself up about anything. Life is what I find when I wake up in the morning, and it's my choice to live it the best way I can. That would be my holiday wish for everyone: live
the very best way you can, and have as much fun as you can. You just never know, and you owe it to yourselves to have a good time. There -- that's enough preaching for one letter.
Bruce and I send you our best and I certainly am humbled by the strength, loyalty and care that my friends have shown me over the last year, Makes It easy to love all of you! |

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Message from Sandy
I never is my wildest dreams thought
I would have to do this, but I am honored to do it. The picture
to the left shows exactly what I think Robyn is doing right
now. Sorry if that's one of your loved ones in the
background...
Many of you don't know the things
that my sister and I did - like sticking gummi bears to our faces to
see how long they would stay, or how we joked that for hallowe'en
all she'd have to do is turn her wig around and she could be cousin
It...but you all knew her in your own
way. Some knew Robyn well, some met her once or in
passing. No matter how or why you knew her, I can honestly say
you were glad that you did.
.
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In these pages you will learn more
about Robyn from Robyn herself - she left a book of instructions for
me (figures), but you will also read what others had to say about
her. You won't be surprised by the fondness that everyone had
for her. There is also a quote someone said reminded them of
Robyn : Life's journey is not to arrive at the grave safely on
a well preserved body, rather to skid sideways, totally worn out,
shouting "...Holy Shit...What a ride!"
There is one favor I have - the next
time some one comes knocking on your door in the middle of dinner,
asking for money to support the cancer fund - think of Robyn.
A handful of change from a thousand people is worth more than $50.00
from one.
Thanks to all of you for being her
friends and for being a part of Robyn and who she was. We miss
her more than words can say.
--
Sandy
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Announcement
- Calgary Herald & Calgary Sun
We regret to inform you that Robyn Herrington finally lost the fight with cancer. She didn’t go willingly, but understood there are just some things you can’t win. Robyn passed away at the Foothills Hospital on Monday, May 3, 2004 at the age of 43 years. Robyn is survived by her loving husband of 23 years Bruce; parents John and Gisela Brown; one brother and one sister. Robyn loved life – her husband, family, in-laws and friends. She knew that she was a much better person for having known them all, and wished only that she had more time. Robyn knew that life was and is a gift; to never take one second for granted. “Challenge yourself; educate yourself; never ‘settle’- always strive for more. Always want more. Always want the best for you and those you love. Never hold grudges or be bitter; love those around you. Love as if there’s no tomorrow, and always have fun.”
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A Memorial Service will be held at FOSTER'S GARDEN CHAPEL, 3220 - 4 Street N.W., (across from Queen's Park Cemetery) on Monday, May 10, 2004 at 3:00 p.m. In lieu of flowers, memorial donations may be made directly to the Alberta Cancer Foundation, c/o The Tom Baker Cancer Centre, 1331 - 29 Street N.W., Calgary Alberta T2N 4N2.
Expressions of Sympathy may be forwarded to the family at www.mem.com
FOSTER'S GARDEN CHAPEL
FUNERAL HOME AND CREMATORIUM
Directors. Telephone: 297-0888.
Honoured Provider of Dignity Memorial
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