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Kyla Gardiner - Diagnosed March 2008, Non-germinomous germ cell tumour. Kyla had very little vision when diagnosed with her tumour. She was to do six rounds of chemo and six weeks of radiation. Kyla was a trooper all the way throuh treatment. From the hundreds of needles from bloodwork and I.V.s to be trapped in the P.C.C.U. for her chemo rounds every three weeks. Amazingly, Kyla's vision returned against all doctor's thoughts. Kyla has been cleared for one year but her journey continues as she is due to start hormone injections in December (more needles).


This hat belongs to David Gilchrist.
Guelph & Wellington Brain Tumour Support Group "Two Hats Are Better Than One" Heartfelt thanks to my family, friends and health care professionals. I was diagnosed in July 2000 with a Pilocytic Astrocytoma attached to my brain stem. Surgery, radiation, physiotherapy and a lot of love and support make me the "luckiest mommy in the world." To my loving Mom and beautiful daughter, Kyleigh; you are both truly my source of joy and strength. µ Ruth Russell September 2005. "For those who have succumbed to their illness, may they rest in peace" µ Jodie Brown-Bedford and Jean Brown September 2005.
Katie Guild
Dr. Del Maestro operated 2 weeks after a Valentineħs Day diagnosis. Katie was 7 years old and a fearless tomboy. Today, Katie is a very unique and talented individual who marches to "her own drummer."

In memory of Marion Henderson (Root) April 29, 1929 µ July 29, 1963 "Love you forever!"
Rael Herman I am finished wearing the Du Rag, but it conjures up memories. This was the first head covering I wore post-craniotomy and I hope to never have to wear it again. The experience of buying a Du Rag was enjoyable, despite the circumstances. I have no idea what the future will bring. I am hopeful that I will be one to beat the odds. However, whatever happens, I have had, and will have lots of fantastic experiences along the way. After all, life is about experiences.
Mariana Hope New Glasgow Support Group
Onika Claire Heffler, August 17, 2006 - June 23, 2007
On December 14, 2006, Onika was taken to the emergency room at the IWK for having a very high fever. We knew something was wrong for awhile, she always seemed to be sick, but we were just new parents. After they performer numerous tests in the ER including an MRI, our lives changed forever. The doctors found a large tumour growing on the outside of Onikaħs brain taking up 1/3 of her brain, as well as a small one growing inside her brain. The doctors had never seen a tumour so large in a baby before. It took hours for them to decide what to do and many phone calls. The very next day, Onika underwent brain surgery for 8 ½ hours. The doctors removed about 50% of the tumour safely. She spent two days in ICU; she was a fighter and was recovering quickly. On December 22, 2006, we received the news of the type of tumour she had, which was a glioblastoma, meaning fast growing and cancerous. This was another nightmare; the doctors had never seen this type of tumour in a baby so young before either. In January, it was decided that more surgery was not a safe option, so Onika started chemotherapy. In March she had an MRI and it had showed more bad news. Her tumour continued to grow and the chemo did not work at all. We decided to continue with the next round of chemo because it was drugs she hadnħt received yet, and Onika wanted to fight, so we gave her another fighting chance. She developed along like a little baby, to everyoneħs surprise, a little behind but she was amazing. Onika received another MRI in April and it showed no change in her tumour, this was the best news we ever received, but we knew there was still a long road to travel and the odds of her beating the tumour were not very good, but we never gave up on her, as she wanted to fight. Onika was to receive two more rounds of chemo and she did not respond well right away. She was very sick. Towards the end of May, Onika became very sleepy so the doctors did her MRI early and the results were not good. Her tumour was still growing and all the parts that had died off were filling up with new tumour. We had to make the right decision for Onika and not be selfish on our part. She was already asleep and the chances of her waking up were not very good. We decided to stop all the chemo and give her the best quality of life that she could have with the time she had left. After five days, to everyoneħs surprise, little Miss. Onika woke up. She gave us the best few weeks of smiles and giggles and her little scream for more food that she loved to eat. On June 23, 2006, Onika lost her battle, but her memory will forever live on through all the hearts of the people she touched. She will always be our special angel.


In honour of David Peter Howes
My Dad fought for 11 years! He was a BRAVE Man who inspires me to this day.
From your daughter, Samantha
Sandy (Alexander) Hoyt March 21, 1939 - August 5, 2002 Sandy was known as "… that nice man on the radio…" at radio station CHFI-FM in Toronto. He had a fantastic sense of humour, loved to travel and was an avid cyclist. Sandy was diagnosed with an inoperable anaplastic astrocytoma in March of 2002. His journey with a brain tumour was challenging and brief, yet he humbly surrendered to the dedication, love and care of his closest family and friends, who became known as "Team Sandy." He leaves behind six children: Allison, Tracey, Angela, Gary, Alexander and Jon Ross. We miss our Dear Old Dad. Tracey Hoyt, September 2004.

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À 2003 Brain Tumour Foundation of Canada 1.800.265.5106 Charitable Registration #BN118816339RR0001 |