A hospital can be a scary place for a child, especially for pediatric cancer patients. Recent studies have proven what Making Headway has known for decades: the hospital’s physical environment affects the patients’ experiences, emotional needs, and health outcomes. Every child at the Hassenfeld Children’s Center is able to benefit from the enhanced playroom and activities supported by Making Headway. Through our programs, Making Headway has transformed the halls and the playroom into a fun, healthy place for children and families. On any given day, children of all ages and backgrounds can be found happily absorbed in arts and crafts activities, games, or munching on healthy, delicious snacks. Professional entertainers and child therapists are also part of the playroom team, helping the whole family feel comfortable, relaxed and welcome.
Making Headway Foundation Awards Research Grants
Chappaqua, NY based foundation funds more than $300,000 in grants for pediatric brain and spinal cord tumor research.
Chappaqua, NY – December 1, 2015: The Board of Directors of Making Headway Foundation recently voted to award more than $300,000 in grants to researchers studying pediatric neuro-oncology.
NYU Langone Medical Center received four grants. The total amount awarded was $251,242. These grants cover neuro psychology screening and assessment for patients; a clinical trials manager; a pediatric neuro-oncology fellowship for Dr. Devorah Segal; and a human brain tissue bio repository for the purpose of obtaining and archiving tissue samples from pediatric brain tumor patients. These samples will be made available to researchers within NYU and to other institutions at no or nominal cost.
Additional grants were made to Columbia University of New York City and The Hospital for Sick Children in Toronto Canada for $30,000 and $25,000, respectively. The Columbia University grant will be to study the long term cognitive & family aspects of recovery from a pediatric brain tumor and will be conducted by Dr. Stephen Sands, Associate Professor of Clinical Psychology.
The Hospital for Sick Children in Toronto, Canada will study the molecular make up of low grade gliomas in children in order to improve clinical decision making. The goal is to enable less toxic therapies for good prognosis patients and improved targeted therapies for children with poor expected outcomes. Drs. Uri Tabori and Cynthia Hawkins will spearhead this project. Making Headway Foundation is partnering with A Kids’ Brain Tumor Cure (PLGA Foundation) on the funding for this study.
“For many years Making Headway has been dedicated to the care of children with brain or spinal cord tumors and their families. Finding better treatments and a cure has always been part of our mission and, with these grants, we take another step forward in that most important aspect of our work,” said Edward Manley, Founder and Board Chair. The Board’s Vice President of Research Sam Schwartz added, “The Board and its Medical Advisors are proud to announce the award of these grants to deserving programs in pediatric neuro-oncology.”
Making Headway Foundation is now in its 20th year. Founded by Edward and Maya Manley of Chappaqua, NY and Clint Greenbaum of Westhampton Beach, NY, its mission is to provide care and comfort for children with brain and spinal cord tumors while funding medical research geared toward better treatments and a cure. The Founders each had a child who survived a pediatric brain tumor.
This story was submitted by one of our patient families. We think you will find it moving and inspiring.
—Making Headway Foundation.
Jack was born with a ticking time bomb in his brain. Some might focus on the negative, the hurt, the pain; but I survive by seeing the small miracles that have kept my son in the fight.
Jack at the age of two was quietly dying. Unable to communicate what was happening to him, and no visible major symptoms we had no idea how sick he really was. Instead of asking WHY my little boy had Cancer and worry about how I almost lost him; I thought about the string of small miracles that led to Doctors diagnosing this seemingly normal healthy little boy with a deadly disease two weeks before it was scheduled to take his life.
On September 17th, Jack was placed in an experimental MRI-Operating Suite. A feature so new at Children’s Hospital Boston that there was only one Neurosurgical team trained to operate in it and they were the team on call that day. I tried to process the words of the lead Neurosurgery as he said, “Jack is a very sick little boy” which I interpreted to mean, please don’t get your hopes up during the 14 hour brain surgery I did not focus on the negative images or morbid scenarios that pounded my sleep deprived brain. I reminded myself that cancer treatment in kids is a marathon, not a sprint. I fought to put hope at the forefront as I waited for the nurse to approach us every thirty minutes during his surgery. Twenty eight “routine” status updates. Like anything about a fourteen hour surgery on your child could possibly be routine! I think they decided on thirty minute status updates because that was the maximum amount of time a parent could be left alone without reassurances.
I did not let fears consume me. Instead of being paralyzed by the situation, I was in awe that Jack was inverted, feet in the air while Harvard’s Chief of Pediatric Neurosurgery led a team operating in my son’s brain with specially developed techniques and equipment. Procedure learned through research and families that had gone before me. I summoned confidence that we were at the right hospital with the right medical professionals who were racing to cut in to the most expensive real estate in the brain before it killed my son.
I do not let myself get angry about what life my son should have had. I am thankful for the life he has. I gather strength from medical staffs that put a reassuring smile on their face and work long days to take care of these kids and their families. I celebrate each birthday as a milestone checked off as one closer to a cure and wish I could share my appreciation with the researchers that dedicate themselves repeatedly for long hours away from their families trying to save mine.
I am brought to my knees in gratitude for the thousands of people who work to raise money and awareness every day to keep funding that research and the people that take care of Jack. I am truly blessed that specific people and organizations have come into our lives right at the time when we needed them most. Organizations like Making Headway Foundation, that are filled with people that have passion and empathy in the work and make it easy for people that want to help to get involved.
In the developed world, Pediatric Cancers are the #1 Cause of Death of children. Secondly, every major advancement in the treatment of adult cancers has come from research and knowledge learned in the treatment of children.
People say things to me like “How do you do it?” or “I couldn’t do that” but the truth is, you could! For your child, you will do anything to prevent one second of unpleasantness. What if months of pain and suffering are the only path to a life with them? Can you endure that?
Take a moment in a quiet place and close your eyes and imagine your kids when they are little and kissing your child goodnight and having to wonder if that might be the last time. Combine that fear with the helplessness you feel as a parent having to watch your child endure a treatment of 15 surgeries and 270 weeks of toxic chemotherapy and not knowing if all that is even enough for them to survive. You might have to do this for the next ten years.
I do not think about the things lost; or what the future holds. I think about the moments gained. I would not ask you to switch places with us. I do not harbor jealousy that YOUR child is healthy and I pray that no other child will ever feel the pain and suffering mine has.
I will not ask you what you are willing to do today to save my child? Instead, I will ask you today what you are willing to do to save your loved ones. I was just like you, I was not a cancer parent, until that one day when I suddenly was.
Will you please join Jack’s fight to cure Pediatric Cancers by funding the very best research in the world.
Jack is a 4th grade student in Mr. Denisson’s class at CSI.
Reauthorization of the Creating Hope Act Passes in the House
July 11, 2015
Great news. Yesterday, the House of Representatives voted to reauthorize the Creating Hope Act when the House passed the 21st Century Cures Act, H.R. 6.
We want to thank Chairman Upton, Congresswoman DeGette and their colleagues for their leadership on 21st Century Cures. 21st Century Cures Act will also increase funding for medical research and innovation at the NIH and FDA, strengthen compassionate use with the Andrea Sloan Compassionate Use Reform and Enhancement (CURE) Act, support the National Pediatric Research Network Act and further rare disease drug development in the OPEN Act.
We want to extend a very special expression of appreciation to Congressman Butterfield, Congressman McCaul, and their staff, Saul Fernandez and Andy Taylor, respectively for their leadership in the Creating Hope Act reauthorization. This victory is theirs.
The Creating Hope Act has wildly exceeded expectations in providing incentives for companies to develop drugs for kids with cancer and other life threatening illnesses. Sanofi recently purchased a Creating Hope Act priority review voucher for $245 million and three new drugs for seriously ill kids have come to market, including Unituxin by United Therapeutics for a pediatric cancer.
We look forward to working with the Senate on the reauthorization of the Creating Hope Act and on the Kids Innovative Drugs Initiative which is designed to increase access to drugs for pediatric cancer research. In that regard, we also look forward to engaging pediatric oncologists to help them access drugs for their own preclinical and clinical research.
It takes many different approaches to raise the funds necessary to cure pediatric brain cancer. The state of Missouri created a Pediatric Cancer Research Trust Fund under the newly enacted Sahara’s Law. It had an excellent first year.
Read how they did it here. http://www.semissourian.com/story/2164379.html
Maybe New York could be next?
The Making Headway Foundation is a 501c3 non-profit organization that supports families of children diagnosed with brain or spinal cord tumors. Over the past 20 years, we have helped thousands of families through unimaginably difficult times, providing a wide range of holistic programs and services. EIN # 13-3906297.
Making Headway Foundation, Inc.
115 King Street
Chappaqua, NY 10514-3460
Telephone: (914) 238-8384
Fax: (914) 238-1693