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Pediatric Cancer Research

About TeamConnor

Connor CruseOn May 15, 2005, after complaining of a mild tummy ache, Joy took four-year-old Connor to the hospital just as any mother would do. After a day of tests, Joy and Tait were stunned to learn just how sick little Connor was.

It was a day that the entire family would remember forever, the day they heard from the doctor, “Your son has cancer.”Connor was diagnosed with Neuroblastoma which is one of the most common solid tumors of early childhood usually found in babies or young children. Most patients, including Connor, have a widespread disease at diagnosis, with a dismal prognosis of 30% survival.

Connor underwent two autonomous stem cell transplants, numerous surgeries, and almost constant chemotherapy beginning immediately following that one dreadful day. He received treatment in Dallas, Boston, New York, Houston, and Guatemala. Joy and Tait spend four years of frantic searching for any treatment that would arrest this disease. There were no special experts guiding them. They were faced with making numerous crucial decisions concerning Connor’s medical care. They did their own research and phoned other parents who had children with Neuroblastoma in order to find trials and experimental treatments that might save little Connors life.

Despite the heroic efforts of his parents and Connor’s fighting spirit, Connor lost his battle with Neuroblastoma on July 10, 2009.

For our most vulnerable, blameless cancer victims, this is unacceptable. That is why the Team Connor Cancer Foundation was formed.

Most pediatric cancer treatments have NOT improved much in the past 20 years. How can progress be made with the dismal amount of attention and funding that pediatric cancer research receives?

Today, there are many children like Connor. Children and families that have exhausted their standard treatment protocol and were not cured of cancer. More dollars means more research and more treatments available for children with cancer, ultimately finding the cure.

With your help, we can help to make the greatest impact possible on a child, saving their life! Please help us to find the cures to all childhood cancers!

All donations are tax-deductible.

 

Did you know?

Cancer is the number one disease killer of children and kills more children per year than cystic fibrosis, muscular dystrophy, asthma and AIDS combined, yet the budget of the National Cancer Institute allocates only 3% of its funds to pediatric cancer research.

There are 15 cases of pediatric cancer diagnosed for every single case of pediatric AIDS and yet the U.S. spends $595,000 for research per victim of pediatric AIDS, yet only $20,000 per victim of pediatric cancer.

The largest children’s oncology group in North America, which supports the clinical and biological research at over 200 participating institutions and treats 90% of children with cancer, received less than half of its requested budget from the federal government this year.

   

2010 Board of Directors
Carolyn Alvey, Joy Cruse,  Matt Russo,  Christie Warrick

2010 Activity Chairs

Carolyn Alvey, Richard Asel, Alex Beilin, Kirsten Black, Eddie Caldwell, Joy Cruse, Tait Cruse, Loren Hsiao, Patrick Matthews, Hugh McFadden, Reed Schnittker, Emily Smith, Janet Smith, Scott Lane, Scott Sweet, Mark Vehslage, Chris Vogeli, Christie Warrick, Chris Wied

Executive Director

Jennifer Bolton

 

 

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Upcoming events

Mission
Through effective and efficient use of resources, TeamConnor will raise awareness, support families, fund treatments, and help find a cure for childhood cancer.

Raised thus far:
07-08: $171,000
2009: $349,700

Organization Status
501(c)

TeamConnor Cancer Foundation
12221 Merit Drive, #1500
Dallas, TX 75251

Telephone:
972 663 7327

E-Mail:
Jennifer Bolton

Links and Resources
Children's Neuroblastoma Cancer Foundation
Lunch for Life
CureSearch
 
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Share It Tees

A website where you can buy a t-shirt with Connor’s “word” (Heroic) on it.

Child Cancer Research Support Treatment