The time is upon us... the meal is prepared and the guests are getting ready to attend. Lets feast!
Thanks to Trish, Scott, KJ, Hope, Terri, Jen, Jacquie, Karen, Laura, Meghan and Brian. I can't tell you how many people have commented on how amazing this team has been.
Thanks also to the ladies at the Cystic Fibrosis Foundation in Vancouver.
Oh crap... who has the serving trays?
40 Women will play one continuous ice hockey game for over 10 days to raise funds for the Canadian Cystic Fibrosis Foundation. This blog is about the experiences of planning a Guinness Record breaking event.
Thursday, August 25, 2011
Puck Drop
The puck drops tomorrow at 8 bells at 8 Rinks in Burnaby. A lot of people have poured endless hours into making this event Epic! My hope is that by the end of the 10 days we have told a story, about what 40 women and a group of hardcore volunteers are willing to do to raise awareness for a disease called Cystic Fibrosis.
Thanks to all those who are taking part in this event. I look forward to the day when we get the news that a Cure has been found! See you at the rink...
Thanks to all those who are taking part in this event. I look forward to the day when we get the news that a Cure has been found! See you at the rink...
Saturday, August 20, 2011
Thursday, August 4, 2011
Wrapping History
So exciting, the Edge is done!
When I asked Eva's dad if he wouldn't mind me plastering her picture on a vehicle. He told me it would be great, Eva loved the attention.
Here it is...
When I asked Eva's dad if he wouldn't mind me plastering her picture on a vehicle. He told me it would be great, Eva loved the attention.
Here it is...
Window of Pain
Window Pain
When you have a chronic, progressive disease
You are guided forward, each step of the way.
You build upon your experiences of pain, disability and vulnerability.
Slowly, layers are added so you are not overwhelmed.
Sometimes you lull yourself to sleep with self pity
(as soothing as a blanket of snow).
The pauses are reprieves: as you adjust and accept.
The memories of what you were once able to do
are as salt to a wound.
So you learn to close the door,
and you're left gaping through a window that once held promise but now is simply a reflection
of what you used to be.
By Lucia Tavano
When you meet someone with Cystic Fibrosis
Your life will change... mine did! My friend Lucia may have saved my life... seems kind of extreme but when a 21 year old is running through life recklessly with little regard for oneself or others anything can happen.
Lucia, my poor sick friend slowed my mind and calmed the waters. I listened to her poetry and she listened to my stories of the outside world as I sat in the chair beside her bed in the hospital.
We would talk about travelling to distant countries, camping on the beaches and making friends. I would bring a flashlight to the hospital, at night we would place a piece of paper over the light, poking holes in it then we'd pretend we were looking at the stars.
After my dear friend died I travelled and saw all those places we spoke about. Because of her I didn't just run through these beautiful places, I sat and breathed in the beauty that surrounded me.
Yep
Lucia, my poor sick friend slowed my mind and calmed the waters. I listened to her poetry and she listened to my stories of the outside world as I sat in the chair beside her bed in the hospital.
We would talk about travelling to distant countries, camping on the beaches and making friends. I would bring a flashlight to the hospital, at night we would place a piece of paper over the light, poking holes in it then we'd pretend we were looking at the stars.
After my dear friend died I travelled and saw all those places we spoke about. Because of her I didn't just run through these beautiful places, I sat and breathed in the beauty that surrounded me.
Yep
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