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A friend of mine was able to acquire some tickets to the bare naked ladies coming to the JLC for a raffle. I hear they are great seats. There will be more information soon. On
October 28th at 8 pm You can email me at olivia@cherub.ca if you would like to get tickets Leather
Journals If you are interested, well wishers can visit the London Health Sciences Centre web site and send an e card to Olivia Vander Schelde. She loves getting them and actually smiles. It does mom and dads heart good. Thank you to those who visited the St.Wilibrord Credit Union and made a donation to Olivia, we are so incredibly grateful, we can not put into words how much it means to know that people we have never met care for our baby. As well thank you to the Credit Union for starting the trust fund. |
Waiting Tues, May 23, 2006 The holiday delays a life-saving operation for a toddler with a brain tumour. By RANDY RICHMOND, FREE PRESS REPORTER |
Olivia
Vander Schelde toddles around her home north of London like any 18-month-old
child. From couch to footstool, from one parent's lap to another, she
gets around fine. But it won't last. Olivia is carrying a tumour the size of a cherry on her toddler-sized brain stem. It already makes her constantly throw up and, if left untreated, will affect her ability to move and breath, eventually killing her. London's
renowned pediatric neurosurgeon, Dr. Adrianna Ranger, wants to do the
delicate surgery -- booked for at least 20 hours -- on little Olivia as
soon as possible. But the earliest she can operate is June 12.
"She is our baby, our world," Kimberley Vander Schelde says.Kimberley Vander Schelde knows what the May 2-4 weekend used to mean. "Growing up, May 2-4 always meant camping, having fun with friends, and barbecues and getting together with families." Now it has a different meaning. This year, the holiday Monday means surgery to save the life of her 18-month-old daughter Olivia has to be delayed long past what the pediatric neurosurgeon wants because -- it appears -- operating rooms at Children's of Western Ontario are too expensive to run on holiday Mondays.
So here is just Olivia's side of the story. From the day Olivia was born, Nov. 8, 2004, Kimberley suspected there was something wrong. "I started going to the doctors right away saying something just wasn't right. She was always crying." Everyone told her the same thing -- babies cry. "This is my second child," she told them. "My first one wasn't like this." By her first Christmas, Olivia was in considerable pain. She threw up like clockwork each morning. Kimberley took her to doctors, who changed her formula. It helped for a while, but by Olivia's first birthday last November, she was losing weight. Frustrated, Kimberley went back to the doctors. "Enough is enough," she told them. "She is losing weight. She is throwing up. Something is definitely not right." A battery of tests followed. In February, Olivia was to get bloodwork done, but she began throwing up and couldn't stop. The family took Olivia to the hospital in February for what they hoped would be one night of observation. That one night turned into seven weeks. Olivia was put on a feeding tube as doctors tried to figure out what was wrong with her stomach.
"Thank God for that flu bug," Kimberley says now. The CT scan was done last week and showed there was pressure on the brain. Olivia was tilting her head back to ease that pressure. An MRI was done the next day to determine what exactly was on her brain stem. After the MRI, a medical team called Kimberley into an office. "Oh God," she thought. "This can't be good." She walked into a room of grim faces. The MRI showed a tumour, slightly bigger than a cherry, in her brain stem, pressing on her spinal nerves. "It's ironic," Kimberley says. "The tumour is shaped in a perfect teardrop." The tumour was probably growing even as Olivia lay in her mother's womb. The little girl's body grew around the tumour. That may have saved her life, keeping the tumour in check. But the pediatric neurosurgeon, Dr. Adrianna Ranger, told Kimberley she didn't want to wait any more than two weeks for surgery. "Even though it is growing slowly, you never know when it is going to take that next little growth that is going to . . ." Kimberley says, her voice faltering.
But at her parents' home north of London, the big-eyed girl with a shock of red hair plays with Moe the cat, cuddles big sister Holland, 4, and insists on navigating around the furniture to get at a reporter's shiny tape recorder. When she gets hungry, she walks over to the feeding machine she still uses and tugs on the cord.Kimberley is getting no sleep thinking about the operation.Surgeons are going to take off the back of the skull, and the backs of four upper vertebrae, to get the tumour out -- on a small child any average-sized adult could carry in one arm. "She could come out of this and not breathe on her own any more or ever walk again and that scares us to death."In an interview on a grey Victoria Day weekend, Kimberley maintains her composure, fuelled by frustration. When she stops to look at Olivia, the composure falters.
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| WELL WISHES Well wishes for Olivia Vander Schelde can be sent to: olivia@cherub.ca, or by calling 461-9204. |