When Valerie Goldstein lost her battle to cancer at the age of 9, her parents Ed and Sue vowed to help families in similar situations gain easier access to more customized care.

All About the Fund

The Valerie Fund supports comprehensive health care services focusing on psychosocial programs for children with cancer and blood disorders close to home.

About What We Do
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Your participation, time or financial gift ensures that children get everything they need to receive the most effective treatment.

Ways to Help
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Our Annual Walk Event

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Our unique blend of medical care and emotional counseling gives patients and their families the supportive environment they need during treatment and beyond.

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Supporting children with cancer and blood disorders since 1976


The Valerie Fund Blog

Sue and Ed Goldstein: New Jersey Hall of Fame Unsung Heroes Class of 2016

Posted by The Valerie Fund on

The Valerie Fund is proud to announce that Sue and Ed Goldstein will be inducted into the New Jersey Hall of Fame. The determined efforts of the Goldsteins over the last four decades have resulted in access to compassionate care for thousands of children in New Jersey battling cancer and blood disorders. The induction ceremony will be held on Sunday, May 7th in Asbury Park.

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Topics: education, Pediatric Cancer, Blood Disorders, Charity, cancer, Founders, awareness, community events, new jersey, 40 years, nonprofit

Inside Our Centers: St. Joseph's Children's Hospital

Posted by The Valerie Fund on

For the first time in seventeen years, a new Valerie Fund Children's Center has opened at St. Joseph's Children's Hospital in Paterson, NJ. The Passaic County-based outpatient facility neighbors the northern New Jersey counties of Morris and Essex where several other Valerie Fund Centers are located. 

The Pediatric Hematology/Oncology division at St. Joseph's Children's Hospital was established in 1996, and treats a diverse population of patients. Much like the population treated at The Valerie Fund's Newark Beth Israel Center, English is not the primary language of patients and their families. At St. Joseph's Center, 60% are Spanish speaking and 10% speak Arabic. 

The Valerie Fund immediately enhanced the existing core services at St. Joseph's, their social work and child life programs and hired a psychologist, educational liaison and financial specialist. This team is led by Dr. Jill Menell, Chief of Pediatric Hematology/Oncology, and Bill Copeck, Nurse Manager.  

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Topics: child life, social worker, educational liaison, Pediatric Cancer, Blood Disorders, pediatric, cancer, sickle cell, caregivers, awareness, oncology, centers, new jersey, nonprofit

The Valerie Fund Family Welcomes St. Joseph’s Children’s Hospital

Posted by The Valerie Fund on

The Valerie Fund Board of Directors is proud to announce a new Center will join The Valerie Fund healthcare network serving children in our area with cancer and blood disorders. The St. Joseph's Children's Hospital Paterson-based outpatient facility strengthens The Valerie Fund's ability to offer top-notch services and programs for children and their families in other parts of New Jersey. The official date for the inclusion is July 1, 2016.

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Topics: Pediatric Cancer, Blood Disorders, hematology, oncology, centers, out-patient cancer, out-patient, new jersey

Friend to Friend Campaign: Give, Share, Repeat

Posted by The Valerie Fund on

The Valerie Fund would like to share a letter that we received from Ed and Sue Goldstein, founders of The Valerie Fund in support of our Friend to Friend Campaign: Give, Share, Repeat. We are asking all of our supporters to share your knowledge and connection to The Valerie Fund with your friends, family and business associates just as Ed and Sue Goldstein have below. Join us by making a donation of your choice in support of The Valerie Fund Walk and JAG Physical Therapy 5K Run on June 11th. Then, post a letter on your social media about your relationship to The Valerie Fund and asking your friends to do the same and share with their social media. Our goal is to recruit one million supporters for this year's walk! Thank you and we hope you will consider this campaign! 


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Topics: Pediatric Cancer, Blood Disorders, sickle cell, 5k, awareness, walk, run

Paint New Jersey Red and Gold For Awareness!

Posted by The Valerie Fund on

The popular use of various colored ribbons to promote disease awareness provides the perfect synergy to The Valerie Fund’s kickoff of fundraising activities leading up to the 2016 Walk and JAG Physical Therapy 5K Run to be held in Essex County’s Verona Park on Saturday, June 11, 2016.  Red ribbons for Sickle Cell Awareness and gold ribbons for Childhood Cancer are powerful symbols of the Red & Gold Campaign.  These meaningful colors of awareness will be the theme for the 2016 Valerie Fund Walk. 

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Topics: Pediatric Cancer, Blood Disorders, sickle cell, 5k, awareness, walk, run

Reliable Transportation: An Invaluable Resource

Posted by The Valerie Fund on
Untitled.pngSuppose your only option for transporting your sick child to life-saving medical care was to use public transit. Imagine the physical and emotional strain—not to mention the risk of exposure to infection—of having to ride a bus, for instance, in order to reach the medical center where your child receives chemotherapy or a blood transfusion for sickle cell disease. Or, suppose you did not even have access to public transit and had no affordable way to transport your child to treatment at all.
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Topics: Pediatric Cancer, Blood Disorders, childhood cancer, transportation

Founders' Perspective: An Inside Look

Posted by The Valerie Fund on

Sue and Ed Goldstein created The Valerie Fund in 1976 after losing their younger daughter Valerie to cancer. In Valerie’s memory, they were driven to make things better for other children and families fighting that same battle. In 1989 Sue and Ed’s older daughter Stacy was diagnosed with breast cancer and in 2001, at the age of 37, Stacy, too, lost her battle with cancer.

Sue was always in the forefront of getting the word out about The Valerie Fund and parenting a sick child. She co-wrote and co-produced the early Valerie Fund newsletters, and has just recently started writing for her personal blog.

What follows is an enlightening excerpt from Sue’s as-yet-unpublished memoirs titled “Unexpected Lives”. She describes the book as “...told from a mother’s perspective... the story of how one family confronts cancer in its only two children: Valerie, diagnosed when she was three, and years later, Stacy, diagnosed at twenty five." Sue uncovers her family’s will to live fully and enthusiastically. Hovering over all, however, is a dark cloud of uncertainty as ordinary people are faced with extraordinary illness.

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Topics: Pediatric Cancer, moms, Founders, caregivers

Fulfilling a Dream: The Scholarship Program

Posted by The Valerie Fund on

Unless your child is attending a tuition free college (and there are a few of those schools out there), the average cost of getting a four - year degree is now conservatively priced at $180,000 (private) and $95,000 (in state public). While these figures include virtually all of the costs associated with higher learning---tuition, housing, meals, books and school supplies, fees and transportation--- not many people can avoid the sense of sticker shock and foreboding when thoughts turn to paying for this privilege.

As education costs continue to rise, The Valerie Fund Scholarship Committee has seen a steady increase in applications from both pediatric cancer patients and those living with blood disorders. “These are outstanding kids,” says committee member Debbie Schiller, “they’re hardworking and highly motivated to get the best education they can. Their applications reflect a universal anxiety about how to make up the difference between tuition costs and what their families can afford to pay.”

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Topics: Pediatric Cancer, Blood Disorders, cancer, scholarship, scholarship program

Survive and Thrive: Late Effects of Cancer Treatment

Posted by The Valerie Fund on

As medical science allows us to become more proficient at saving the lives of pediatric cancer patients, their need for survivorship support in adolescence and adulthood has grown. Approximately two out of three children experience at least one long term side effect (late effect) of treatment. These side effects may affect any organ depending on the primary cancer diagnosis and the treatment the child received. These may include damage to the heart, lungs, kidneys, sexual organs, as well as cause psychosocial, emotional effects and learning difficulties. In addition, there may be difficulty in obtaining health and life insurance as well as possible discrimination in adulthood obtaining a job.

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Topics: Pediatric Cancer, cancer, LITE, long term follow up, long term care, childhood cancer, side effects, late effects

Camp Happy Times: Helping Kids Be Kids

Posted by The Valerie Fund on


“Mommy, I want to do normal things, like other kids…” 


When your child has cancer, there are no easy answers to this familiar and heart-wrenching refrain. The Valerie Fund has always known this, and in 1983, the organization took a giant step to give children with cancer at least one experience other kids have – going away to summer camp.


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Topics: Pediatric Cancer, camp happy times, camp

The Power of Giving

Learn more about the ways you can help. 

Join in the fight against childhood cancer and blood disorders: donate, participate in an event, or volunteer your time. Our philosophy is that to truly heal the children whose care we are entrusted, we must treat them emotionally, socially, and developmentally, as well as medically.


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