Families

Life After Childhood Cancer: Luke’s Latest Off-Treatment Scans

by Monica Fochtman
April 22, 2013
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When he was 3 years old, Luke, one of five St. Baldrick’s Ambassadors in 2013, was diagnosed with embryonal rhabdomyosarcoma, a type of childhood cancer in the connective tissues. Luke, now 7, has been off treatment and cancer free for over 2 years.

Luke’s mom, Monica, shares the story of Luke’s most recent scans.

As part of Luke’s off-treatment protocol for pediatric cancer, he undergoes regular MRIs of his abdomen and pelvis. Weeks before the procedure, we talk with him about it and give him the option of “sleepy medicine” or no “sleepy medicine.” The procedure takes about 90 minutes from start to finish. Although our facility is equipped with technology to distract him from the noise of the MRI, he opts to take the medicine. This involves going under anesthesia for the procedure. As we talk about what this means, Luke says to us, “I wish I just never had cancer in the first place.” He doesn’t say anything after that. Just matter-of-factly puts it out there.

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Research

Immunogenomics to Create New Therapies for High-Risk Childhood Cancers

by St. Baldrick's Foundation
April 7, 2013

Formerly known as the St. Baldrick’s – Stand Up to Cancer Pediatric Cancer Dream Team, this team is now the St. Baldrick’s EPICC Team (Empowering Pediatric Immunotherapies for Childhood Cancer).

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The Dream Team, funded by Stand Up 2 Cancer and the St. Baldrick’s Foundation, aims to establish genomics-based immunotherapy as the second revolution in childhood cancer. The following is adapted from the Dream Team’s own summary of its proposal.

Curative chemotherapy for cancer was first realized in children. Survival rates for many of the common cancers in children improved dramatically through the last part of the 20th century. However, those cure rates have plateaued since the 1990s, and for some childhood cancers, we have seen little to no improvements.

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Research

Announcing the Stand Up To Cancer – St. Baldrick’s Pediatric Cancer Dream Team [VIDEO]

by Kathleen Ruddy, CEO, St. Baldrick's Foundation
April 7, 2013

Formerly known as the St. Baldrick’s – Stand Up to Cancer Pediatric Cancer Dream Team, this team is now the St. Baldrick’s EPICC Team (Empowering Pediatric Immunotherapies for Childhood Cancer).

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I wish you could have been with us in the room when the first pediatric cancer Dream Team was announced, to be funded by the partnership of the St. Baldrick’s Foundation and Stand Up To Cancer (SU2C).

From a long list of innovative “big ideas,” the scientific reviewers representing both funding organizations had chosen the top four to submit detailed proposals. The experts agreed that any of these would be great investments, but for a grant of $14.5 million over four years, only one could be chosen.

The suspense ended with an enthusiastic round of applause when the winning Dream Team was announced at a reception tonight at the annual meeting of the American Association of Cancer Research (AACR). The evening’s emcee was actor Kyle MacLachlan, and speakers included Nobel Laureate Dr. Philip Sharp, St. Baldrick’s CEO Kathleen Ruddy, and 10-year-old cancer survivor Emma W. and her parents.

And the award goes to:

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Head-Shaving

Dr. Brad Doubles Donations on His Head for Kids With Cancer

by Dr. Brad Clodfelter
March 19, 2013
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Dr. Brad compares haircuts with patient and fellow shavee, Gerry; Dr. Brad’s office sign

“If you shave your head, it will be the most EXPENSIVE haircut you get because you’ll be paying for a divorce! I dare you!”

That was my wife’s response after she found out I was going to go bald at the St. Christina Cardinals event organized by my patient, Rita Kennedy.

Well, not one to back down from a dare, I became a shavee for the first time in 2011.

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Head-Shaving

$7 Million Raised for Childhood Cancer Research

by St. Baldrick's Foundation
March 1, 2013
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Ambassador Luke celebrates $7 Million raised for childhood cancer research

When we asked 2013 St. Baldrick’s Ambassador Luke Fochtman what he wanted to say to all the amazing volunteers out there helping to raise money to help kids just like him live long and healthy lives, he replied with, “Thanks for giving me the chance to build more Legos!”

Thank you, Luke, we couldn’t have said it better!

At just 3 years old, Luke was diagnosed with stage IV embryonal rhabdomyosarcoma, a rare type of childhood cancer that affects the muscles. He endured nearly 70 weeks of aggressive treatments — including multiple rounds of chemotherapy, daily radiation — and suffered through many central line infections. Through it all, Luke remained positive and strong.

Luke’s mom, Monica, says:

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Advocacy

Federal Budget Cuts Threaten Childhood Cancer Research Funding

by Monica Fochtman
February 11, 2013

Monica Fochtman, mom to Luke, a St. Baldrick’s Foundation 2013 Ambassador, shares how the congressional budget sequester affects kids with cancer and how you can help.

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I would like to introduce you to my son, Luke. He is 7 years old. He loves Star Wars, Legos, and art. He is thriving in first grade. He is an older brother, a son, a grandson, a nephew, a cousin, and a loving friend. He is also a childhood cancer survivor.

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Kids with Cancer

Meet Luke

by St. Baldrick's Foundation
January 8, 2013

Diagnosed with stage 4 embryonal rhabdomyosarcoma, cancer of the connective tissues, just five days after his third birthday, Luke endured 70 weeks of treatment – multiple rounds of chemotherapy, six weeks of daily radiation and many central line infections. “The amazing part is that Luke never said no to us. Not once, not ever,” his mom, Monica, recalls. He just fought the cancer. Now, two years off-treatment, he remains cancer free.

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Kids with Cancer

Meet Jordan

by St. Baldrick's Foundation
January 7, 2013

When he was 16, Jordan was diagnosed with a very aggressive soft-tissue sarcoma. The doctor said, “We have your diagnosis. It’s alveolar rhabdomyosarcoma, and you will most likely not survive.” Jordan responded with strength and a sense of calm. He was the very definition of grace, courage and strength. After 23 months of treatment, Jordan passed away five days before his 18th birthday.

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Kids with Cancer

Meet Emily

by St. Baldrick's Foundation
January 6, 2013

In December 2011, Emily was diagnosed with a cancer of the bone, chondroblastic osteosarcoma, in her right tibia. Her “whatever needs to be done” attitude has helped her through the 18 rounds of chemotherapy and a lengthy surgery to remove the tumor along with seven inches of her right tibia. Emily will be in a wheelchair until at least March 2013, but she’s building stamina each day.

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Teens & Young Adults

Sofia: Fighting Childhood Cancer With a Bright Attitude, and a Smile

by St. Baldrick's Foundation
October 16, 2012

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On April 27, 2012, I was diagnosed with Ewing sarcoma — a rare childhood bone cancer that only 200 to 1,000 children get a year. My life has never been the same.

I was the average teenager and had been a cheerleader since I was in third grade. I always enjoyed going out with friends and having fun but when I was diagnosed, I was lucky if my counts were high enough to go to the movies. My summer plans crumbled under the word “cancer.”

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