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
Screen Shot 2017-09-05 at 11.00.58 AM.png

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

Ways to Help
Screen Shot 2017-09-05 at 11.02.22 AM.png

Our Annual Walk Event

Donate or Join a Team

Visit the Walk

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

Learn More

Supporting children with cancer and blood disorders since 1976


The Valerie Fund Blog

Meet the 2018 Ambassadors: Part 2

Posted by The Valerie Fund on 11/2/18 1:17 PM

In preparation for the Thanksgiving Ball Gala, at The Grove in Cedar Grove, the ambassadors met there a few weeks beforehand for the "Ambassador Orientation." They spent the evening filling out questionnaires, chatting, bonding, eating pizza, and touring the beautiful facility. Many parents of the younger ambassadors also joined the orientation.

An important part of the evening is always the medal ceremony. Each ambassador is awarded a special medal for his/her service to The Valerie Fund to be worn the night of the Gala. The ambassadors also have their picture taken to be featured in the Gala's program along with their handwritten excerpts.

Our blog series continues with personal stories from this year's Thanksgiving Ball Gala ambassadors.

Natasha, age 7

Natasha was diagnosed at age six with Acute Lymphoblastic Leukemia (ALL). She is expected to be in treatment for two years. Natasha enjoys reading and meeting other people, and making new friends through her visits at The Valerie Fund. She said that The Valerie Fund staff, "puts a big smile on the kids' faces." 

Natasha_picture for blog



 Ivan, age 13

Ivan was diagnosed with T-cell Acute Lymphoblastic Leukemia (T-ALL) at age 12. Ivan has been in treatment for the last year and is expected to undergo treatment for three years in total. Ivan keeps busy with his favorite hobbies of playing video games, cards and playing chess with his brother. 

Ivan said, "[The Valerie Fund] helps many families in need who have a child going through tough times. This organization has helped my family by providing us with transportation, food and bill payments. If we can get your help, it will mean a lot to The Valerie Fund." 

Photo - Ivan-379770-edited



Joanna, age 19

Joanna was diagnosed with Non-Hodgkin's Lymphoma at age 18. She underwent treatment for six months and is now attending Rutgers University studying International Business. Joanna is, "loving every minute" of college and said The Valerie Fund helped her by awarding her a scholarship. 

Joanna said, "One of my favorite memories with The Valerie Fund was the day I got the chance to ring the bell in The Valerie Fund Center. I was surrounded by the entire staff I now consider family. We were celebrating the end of my treatment." She continued, "Without The Valerie Fund, my time in the hospital would have been much darker. The Valerie Fund kept me smiling and hopeful throughout the entirety of my treatment."

Joanna_picture for blog



Antwann, age 6

Diagnosed at birth with Sickle Beta Thalassemia, Antwann's treatment will be lifelong. In between his monthly visits to The Valerie Fund Center, Antwann enjoys painting, coloring and playing at the park. His mom said, "The Valerie Fund offers a great environment while my son is receiving treatment. Antwann loves role playing with the doll the child life specialist brings. He finds a great deal of comfort in talking to the doll and "taking blood" from it."

AJ Web



Camila, age 6

Camila was diagnosed with Ependymoma of the brain, a brain tumor, when she was 17-months-old. The duration of her treatment is not known. When Camila is not at The Valerie Fund Center, she loves to dance, sing, play with Play-Doh and make slime. At her summer camp, Camila loved swimming in the pool, eating bagels and playing with other kids.

Camila's family said, "Cancer is a disease that no children should have to go through. The Valerie Fund has helped us emotionally, financially, showing a lot of love that that we are not alone in this. 'God bless.' "


ABOUT THE VALERIE FUND: After their nine-year-old daughter Valerie succumbed to cancer in 1976, Sue and Ed Goldstein were determined that no family should have to travel great distances to receive state-of-the-art medical care. Today, more than 6,000 children with cancer and blood disorders benefit immeasurably by receiving their medical treatment close to home in a child-centered environment. The Valerie Fund ensures they do not have to rely on insurance reimbursements to receive a range of customized therapeutic services that enhance their quality of life. For more information, please visit www.thevaleriefund.org.

 Meet The 2018 Ambassadors: Part 1


GLI Email Banner Final_marketing


Topics: Non-profit, Pediatric Cancer, Blood Disorders, Charity, pediatric, childhood cancer, sickle cell, awareness, hematology, oncology, centers, new jersey, fundraising, nonprofit, ambassadors, advocate, patients

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.


Subscribe to Blog Updates

Recent Posts

Posts by Topic

see all