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Read Patient Stories: Brain Tumour Hats Tribute
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2010 Info Day Presentations




Online Support Chat

Education Seminar, Vancouver, BC

Southern Ontario BrainWAVE Event

London City Soccer Game, London, ON

Barrie, ON Support Group Town Hall

October is Brain Tumour Awareness Month

Calgary Info Day

Bikers For Brains, London, ON

London Info Day

Halifax Info Day

Fredericton Education Seminar

Ottawa Education Seminar



CABTO and Brain Tumour Foundation of Canada
Hat Tribute

Hats Index (Alphabetical Order by Surname)
A | B | C | D | E - F | G - H | I - L | M | N | O - P | Q - R | S | T - Z 

Christopher Mark Cann October 25, 1985 µ August 8, 2006
Chris was always very positive during his battle with brain cancer. "Thumbs up" was his motto. His big smile and love towards others made him a hero to all who knew him. Chris lost his battle with cancer but won the war, as his home is now in heaven with his heavenly and earthly fathers. Chris left a note that was found by his mom and it said, "I love you all plus Iħm watching over you all. Love by Chris Cann."

 

 

In Loving Memory of  Jennifer Capretta, November 25, 1979 - June 19, 2008

Our beautiful daughter Jennifer, on June 19, 2008, after a long and courageous 6 year battle, passed away from a gliobalstoma multiforme, a deadly malignant type of brain tumour.  She was only 28.  When she was diagnosed at 22, her life was to change forever.  She underwent brain surgery, chemotherapy and aggressive radiation.  But in the end, this horrible disease took away our daughter's personality, her zest for life, her love of seeing and being with family and friends, her appetite and her ability to walk and to take care of herself and many other things.  Jennifer was due to be married on September 29, 2007, but on Labour Day weekend she became extremely ill and ended up back in hospital.  The wedding was canceled. 

No parent should have to wait and watch their child take their last breath.  It is not the natural order of things.  A part of us left this world with Jennifer that night and our family has been changed forever.  Jennifer's younger sister and older brother have also been changed forever.  A cure for this horrible illness must be found.

Jennifer, your courage and strength, beautiful spirit, radiant smile and contagious laugh are treasured in our hearts forever.  You touched so many lives with your fun loving caring ways.  Our precious and beautiful Angel you will always be......unseen, unheard, but always near.  Forever loved, greatly missed and so very dear. 

Love always and forever, your loving family and friends. XOXOXO

Jordan Cranstone

This hat is in memory of our 7 year old son, Jordan.  The oldest of our 3 children, Jordan was an amazing son and brother to his little sisters Paige, and Ella.  He was always happy, smart, and so engaging.  Loved by everyone, his quiet happy manner had a way of instantly making people want to be his friend. 

We brought him to Joseph Brant hospital Feb.6, 2009 after noticing quite suddenly that morning that he was unable to move his eyes to the left.  We were devastated when the CT scan showed a small mass on his brainstem.  We were sent immediately to McMaster Children’s Hospital where he had an MRI which confirmed the findings.  Jordan underwent a biopsy that month, and was diagnosed with a brainstem glioma. 

A favourite patient in the 3C ward, Jordan showed everyone his amazing spirit and courage during his recovery.  He came home eager to get back to school before the March Break and back on his bike when given the all clear by his doctors.  He underwent radiation that spring, and not surprising to anyone, booked his own timeslot for 8:30 in the morning so that he wouldn’t be too late for school. 

During treatment, he showed strength and determination, only missing 2 days of school and facing all his challenges with the same attitude, even after gaining 20 lbs from the steroids, or as he called it, his “crazy medicine”.  We continued to carry on with our family, sharing special experiences and memories throughout the summer, trying to keep our activities as normal as possible.  Jordan’s tumour showed no growth between February and September, and we were so hopeful that Jordan’s case would be a story of success. 

On December 14th, we were given the results of his latest MRI which showed massive tumour growth, giving doctors confirmation that it was a very aggressive tumour and he was given only weeks to months to live. This would prove to be a time where we would learn even more than we already knew just how special our little boy is.  We were able to enjoy an amazing time as a family on our Children’s Wish trip to the Give Kids the World Village in Florida where the kids experienced the magic and wonder of Disney, Universal, Sea World, and the Kennedy Space Centre.

Jordan amazed us with his truly special wisdom in January, as his body continued to lose strength and ability.  With that same amazing determination and spirit, he went back to school.  Week to week, he quickly lost the ability to walk.  Near the end of January, he told us that he knew he was going to die, but that it was okay, as he wiped our tears, telling us that he couldn’t play here anymore. 

Knowing that he was going to a special place in heaven, where there are no more tumours, and no more cancer, he smiled.  We cared for him at home, and the last week of his life, he was able to enjoy afternoon outings with his sisters, a visit to his school to see his classmates, and a special visit from our parish priest.  Watching Jordan listen to Fr. Ray’s words and prayer, we saw that same smile and light in Jordan’s face.  Jordan passed away at home on February, 6, 2010, surrounded by the love of his family, with his sisters holding his hands along with ours. Jordan’s story has had a powerful influence on everyone who knows and loves him

 

Tony Cropo

Tony was diagnosed with an Oligodendroglioma Meningioma tumour. He had a seizure in 1991 when he was 48. He had 30 bouts of radiation. In 2001, the tumour came back and he had 6 bouts of chemo. I'm still here!

 

  

 

  

Would you like to pay tribute to someone's courage? Please consider sending your hat to us!

Brain Tumour Foundation of Canada

620 Colborne Street, Suite 301

London, Ontario  N6B 3R9

 

The hats are a traveling display and a tribute to the amazing individuals who have been affected by this disease. The display is featured at a number of events through-out the year including Spring Sprints, Education Seminars and Information Days as well Brain Tumour Awareness Month events around Canada in October.  Please note if you have sent us a hat, it is already a part of the traveling display.

 

Questions?  Please email Megan Winkler at mwinkler mwinkler@braintumour.ca or call 1-800-265-5106 ext 230.

 

 

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