Tag Archive for: Levine Children’s Hospital

Levine Children’s Hospital: We’re Doing All We Can to End Childhood Cancer

Content provided by Levine Children’s Hospital

Today, the 5-year survival rate for those with childhood cancers stands at more than 80 percent – up more than 20 points since the 1970s.

That’s encouraging news for families with children with cancer. But there’s still a long way to go, especially when funding for pediatric cancer remains low.

Here at Levine Children’s Hospital, we’re doing all we can to cure the incurable. We sat down with some of the cancer specialists at LCH to hear what excites them about cancer care here in the greater Charlotte area.

Personalized medicine. As part of the Beat Childhood Cancer initiative, LCH researchers are investigating tailored courses of chemotherapy based on a person’s individual genetic makeup. “We give you a personal answer, telling you what drugs may work for a specific tumor. For people who have gone through chemotherapy, that is a very unique thing,” says Javier Oesterheld, MD, medical director for pediatric hematology, oncology, and blood and marrow transplantation.

New technology for rare nerve cancer. LCH is building a dedicated lead-lined room to deliver a special kind of therapy called MIBG to treat neuroblastoma, a form of high-risk nerve cancer. We’ll be one of fewer than 20 centers in the United States to offer this type of therapy, says Dr. Oesterheld.

Dynamic approaches for blood and marrow transplantation. Replacing broken stem cells with healthy cells from a donor is one way to cure many types of cancer. We’re one of 12 institutions in the country studying a new technology that can help kids with cancer who have no other donors. “We have a number of kids who we’re helping save with this  technology, and we’re really privileged to be able to bring this top-level work here to Charlotte,” says Jeffrey Huo, MD, pediatric blood and marrow transplantation specialist.

Immunotherapies. Many new treatments for leukemia involve helping the body itself to fight off the cancerous cells. “We’re now able to trick the body’s own immune system into recognizing the leukemia cells as bad, so it can go and kill those cells,” says Joel Kaplan, MD, a pediatric hematologist-oncologist. “This type of research is one of the most cutting-edge things going on in the nation right now, and we’re contributing to those efforts here at LCH.”

Beyond new therapies, our doctors know that better treatment also includes providing the extra human touch – to be at our best when children are at their worst. “The science of cancer is always changing, which keeps us on our toes,” says Dr. Oesterheld. “But the idea of being able to get a child through probably the worst times of their lives – for us, that’s invaluable.”

Lake Norman Coffee for a Cure Brings in Over $35,000 for Pediatric Cancer Research

2017 Lake Norman Coffee for a Cure. Photo courtesy of Localscroll.com

Our 2nd annual Coffee for a Cure hosted by our ISF Lake Norman chapter was a huge success.  Thank you to the 250 men and women who attended and the sponsors and local businesses who gave time and money to this event.  This event served as a call to action in the fight against pediatric cancer and to educate community members on the importance of bringing pediatric cancer treatments home to Charlotte.  We were able to raise $35,000 and donations have continued to come in.  These funds bring us one step closer to our 2017 $1,000,000 fundraising goal to fund the creation of a MIBG room at Levine Children’s Hospital.

Our Lake Norman chapter could not put on such a wonderful event if it wasn’t for the support of our community businesses who help us through their sponsorship. It is through their passion for charitable giving and making a local impact that we are able to continue Isabella’s fight. Thank you to the following businesses:

2017 Lake Norman Coffee for a Cure. Photos courtesy of Localscroll.com

During the event, we introduced our new major gift society, called The Three Wish Circle, with an annual gift of $5000 or more, donors can take their support of the ISF mission to the next level by funding more research for childhood cancer and help to bring innovative treatment options to our local community.  If you have questions or want to know more about how to take your support to the next level, contact our ISF Development Director, Tia Wackerhagen.

We cannot begin to put words to how grateful that we are for the impact you are helping us make, thank you for your support.. We are so proud of what we have accomplished together and it is because of YOU. We could not do this alone and could not continue our fight without your help. We humbly thank each of you and look forward to a world with no more cancer where we will beat cancer, grow hair and live the dreams of all children fighting the fight.

We appreciate Local Scroll Charlotte for capturing the event, view all photos of the 2017 Lake Norman Coffee for a Cure.

State-of-the-art cancer treatment suite planned for Levine Children’s Hospital

We talk a lot about our $1 MILLION goal this year. Dr. Javier Oesterheld, Levine Children’s Hospital head pediatric oncologist, and Isabella’s mom were on NBC Charlotte this week to discuss the new state-of-the-art MIBG room at Levine’s that will help families with kids facing cancer. Charlotte will be one out of 20 hospitals in the country that will be able to offer this to patients.

WATCH SEGMENT HERE

What is a MIBG, why does it need a room and why is it so expensive? Read More…

The heart of a budding activist

Information and photos provided by Sofia’s mom

Yesterday, current cancer fighting patient Sofia had a fun reason to visit Levine Children’s Hospital.  As Sophia’s mom put it… “Today, we were able to celebrate with our own personal super hero, Dr. Joel Kaplan (Sofia’s head oncologist), as he received a grant from Hyundai Hope on Wheels.  Bonus:  the kids got to put their handprints on his white lab coat and on a brand new car!”

Dr. Kaplan and Levine Children’s Hospital was awarded a $50,000 Impact Grant from Hyundai Hope on Wheels.  This award was presented for his proven track record in providing excellent patient care to families affected by pediatric cancer and to support his continued efforts.  We couldn’t be more thrilled with this news, Dr. Kaplan not only is Sofia’s personal super hero… he was Isabella’s as well.

Sofia was diagnosed with Acute Lymphoblastic Leukemia in January of 2016 at the age of 7.  Before cancer, she was a happy, carefree 2nd grader who played soccer, took all kinds of dance classes, loved arts, crafts, hula-hooping, American Girl dolls and playing with friends and her big brother, Sam. She was blessed with such a sweet and normal childhood.  In the last 1.5 years since our lives were turned upside down, Sofia has continually amazed us with her courage and resilience. Every day we look at her and wonder how such a small girl can possibly withstand all the endless appointments, needles, pokes, tests, chemos, medications and hospital stays without even complaining or feeling sorry for herself.  Our favorite quote that seems to sum Sofia up perfectly is “Though she be but little, she is fierce.”
Sofia is still in treatment and will continue on her chemo regimen until May 2018 for a total of nearly 2.5 years.  We are extremely grateful that she is currently doing well and we are all trying to live as normally as possible between her rounds of chemo at Levine Children’s Hospital.  Sofia has even enjoyed being back in school with her friends after being homebound for one full year.  She still loves all things artsy and creative, especially designing new outfits and accessories for her dolls. She is learning to sew and hopes to be a fashion designer when she grows up. Sofia is excited that she was recently asked to be the Leukemia & Lymphoma Society’s 2018 Charlotte Girl of the Year because she hopes to inspire people to take action in the fight against pediatric cancer.  Behind her shy exterior lies the heart of a budding activist!

$1,000,000 Goal for MIBG Room at Levines

WHY THE $1,000,000 GOAL THIS YEAR? We have gotten this question several times. One simple fact… to bring the leading pediatric cancer treatments to local children in our surrounding communities. We have committed to fund the creation of a MIBG room at Levine Children’s Hospital and anticipate breaking ground in 2018.

WHAT DOES THIS MEAN? In just one year, our local children will not only benefit from the new MIBG room, but also trials involving MIBG therapy. With your 2017 donations, ISF was able to fund the Frontline MIBG Therapy project trial through the Children’s Oncology Group (COG). This trial hopes to reduce the number of children who relapse and reduce the burden of late effects of therapy. It will be ready for children across the country in August 2018 where an MIBG room is available. Guess who will have an MIBG room?

WHAT IS MIBG? A cutting edge, targeted therapy used to treat relapsed or high-risk neuroblastoma with little to no pain and side effects. This treatment requires a highly specialized team to deliver the therapy and a special room to assure that patients, family, and health care providers are safe.

WHY IS BUILDING A ROOM SO EXPENSIVE? The room is specifically designed for this type of therapy and is created with lead shielding due to the radioactive nature of the treatment. These lead walls provide the highest level of protection for patients and families. The MIBG room will have an adjoining suite so the patient will always be close to their family.