Purchasing A Treasury of Cranberry Recipes

Posted on Jun 11, 2012

NEWS RELEASE

MAY IS CYSTIC FIBROSIS AWARENESS MONTH

CYSTIC FIBROSIS CANADA, CAMPBELL RIVER CHAPTER KICKS OFF CF MONTH WITH LAUNCH OF “A TREASURY OF CRANBERRY RECIPES” COOKBOOK.

The book was compiled by Barb Shook who has worked diligently to bring the book to completion.  Barb was inspired by Beth Hamilton, a long time volunteer for the Campbell River Chapter who passed away 2 years ago.  The Hamilton family have owned and managed Iron River Farms, a local cranberry farm.  When their son Michael was diagnosed with CF, Beth recognized the need to find a cure for this devastating disease.  She worked tirelessly for the CF cause, even when her own health was failing.  Barb could think of no better way to honour Beth’s memory than by producing this excellent recipe book with all proceeds going to help in the fight against cystic fibrosis.  Jo-Ann Wallis, president of the Campbell River Chapter has already bought the book as a Mother’s Day gift and hopes other people will do the same. Wallis said “ the book is full of quick, easy and nutritious recipes – we are so grateful to Barb Shook for all her hard work in putting the book together.”  The $15 book published by Ptarmigan Press can be purchased at Coho Books, Appleseed Cottage, Stonehouse Teas, Kask Graphics or by calling Barb at 250 923 7828 or email .(JavaScript must be enabled to view this email address).

Every Canadian Called on to Fight for People Struggling with CF

Monday, April 30, 2012 (Toronto, ON) — Tomorrow marks the first day of May, Cystic Fibrosis (CF) Awareness Month. Throughout the month, Cystic Fibrosis Canada shines the spotlight on 4,000 Canadians living with this fatal genetic disease, by raising awareness and funds for life-saving CF research and care.

“Every week, two children are diagnosed and one person dies from this devastating disease in Canada,” said Maureen Adamson, CEO of Cystic Fibrosis Canada. “Too many young lives are cut short by cystic fibrosis; almost half of the sufferers who die do not live to see their 25th birthday. We continue to courageously invest in innovative CF research and care, but we can only do this with the generous support of Canadians. May is Cystic Fibrosis Awareness Month and I invite everyone to champion and support our great cause.”

Ryan Morrissette, a dedicated CF Champion, is a 17-year-old dancer and member of the B.C. hip-hop dance crew Freshh. Despite being diagnosed with cystic fibrosis at the age of two, Ryan is embarking on a successful dance career thanks to improvements in CF treatments and care. When diagnosed, his family was told he would not live past his eighth birthday.

“People with CF like me, never get a day off from hours of therapy and dozens of medications that keep us breathing,” said Ryan. “I hope every Canadian will join us by walking and sponsoring the Great Strides walk™ on Sunday, May 27 th in almost 70 places across Canada. And if you’re in B.C., come on out to Great Strides in New Westminster and watch me and Freshh ramp-up the walk with the moves that got us into the Canada’s Got Talent finals coming up on May 13 th!”

Cystic Fibrosis

Cystic fibrosis is the most common fatal genetic disease affecting Canadian children and young adults. It is a multi-system disease that affects mainly the lungs and the digestive system. In the lungs, where the effects are most devastating, a build-up of thick mucus causes severe respiratory problems. Mucus and protein also build up in the digestive tract, making it difficult to digest and absorb nutrients from food. As improved therapies have helped to address the malnutrition issues, ultimately most deaths related to cystic fibrosis are due to lung disease. Currently, there is no cure.

May is Cystic Fibrosis Awareness Month

There are many ways to join the fight against cystic fibrosis during May, Cystic Fibrosis Awareness Month. Canadians can participate or sponsor a walker on Sunday, May 27th, in the Great Strides™ walk in one of 67 locations in Canada; donate to support life-saving CF research and care; help raise awareness about the disease using social media; and participate and fundraise in hundreds of other outstanding events organized by 51 local Cystic Fibrosis Canada chapters across the country. In Campbell River the Great Strides walk will take place at Penfield School.  For more information on the walk or how you can participate go to http://www.crcf.ca or phone 250 850 0875.

Cystic Fibrosis Canada

Cystic Fibrosis Canada is one of the world’s top three charitable organizations committed to finding a cure for cystic fibrosis and is an internationally-recognized leader in funding CF research, innovation, and clinical care. We invest more funding in life-saving CF research and care than any other non-governmental agency in Canada. Since 1960, Cystic Fibrosis Canada has invested more than $140 million in leading research and care, resulting in one of the world’s highest survival rates for Canadians living with cystic fibrosis.

NOTE TO MEDIA: An Electronic Media Kit is available online at http://www.vvcnetwork.ca/cf/20120501/ with May is Cystic Fibrosis Awareness Month interview footage, B-Roll footage, and photographs available for media use in television. Includes Maureen Adamson, CEO, Cystic Fibrosis Canada, Ryan Morrissette, CF Champion, diagnosed at age two, Canadians Fighting Cystic Fibrosis.
For more information, please visit:

The Great Strides™ walk at http://www.cysticfibrosis.ca/greatstrides
Cystic Fibrosis Canada’s website http://www.cysticfibrosis.ca
Cystic Fibrosis Canada on Facebook at http://www.facebook.com/CysticFibrosisCanada
Cystic Fibrosis Canada on Twitter at http://www.twitter.com/CFCanada

For more information contact Chris Black 250 923 4992 or email .(JavaScript must be enabled to view this email address).