Adult Survivors of Childhood Cancer

Adult Survivors of Childhood Cancer

Tony Correo, a childhood cancer survivor, talks about the value of sharing his own experiences with others who are battling cancer.

People who survive cancers in their childhood or young adulthood may have medical and psychological concerns that last into their adulthood. While most survivors lead healthy, active lives, some have health problems that persist after treatment ends or that develop years after cancer therapy.

If this is the case for you, we hope that you’ll take advantage of our specialized Adult Long-Term Follow-Up Program, which functions as a part of our Adult Survivorship Program. Through this clinic, we provide long-term care that can help prevent, detect, and treat any delayed complications — known as late effects — that can arise.

Most survivors in our program were diagnosed before age 40 and have transitioned to us from our Long-Term Follow-Up Program for Children, or have been referred to us by an MSK medical team.

We care for survivors of many types of cancer, including:

We also help people who received a bone marrow transplant as a child or young adult.

Adult Survivors of Childhood Cancers Support Group
Join fellow adult survivors of childhood cancers for a discussion of the issues unique to this population such as family relationships, changed perspectives, and late effects of treatment.
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Our Survivorship Services

Family physician Kevin Oeffinger directs our team of survivorship experts, which includes physicians, nurse practitioners, a nurse, a psychologist, and a social worker. We provide the following services:

  • Treatment Summary and Survivorship Care Plan – To start, we develop a cancer treatment summary that includes a description of the cancer therapies you received and potential late effects. We update your care plan during each visit.
  • Initial Consultation – We perform a physical exam and counsel you on your health risks and the need for any screening for long-term effects of cancer therapy, such as fasting blood tests, echocardiograms, and bone density tests.
  • Health Education – One of our major goals is to provide you with information about staying healthy. We want you and your family to know about potential effects of past cancer treatments and ways to prevent future health problems.
  • Psychosocial Care – Some survivors struggle with feelings of isolation, fear of recurrence, and stress over coping with ongoing health needs. Our psychologist and social worker can help with these as well as insurance and job-related concerns.

As a comprehensive cancer center, we also offer a variety of support services, from information and guidance on fertility and parenthood to sexual health, integrative medicine, and tobacco cessation.

We work closely with our MSK colleagues who specialize in the care of cancer survivors, including cardiologists, pulmonologists, dermatologists, rehabilitation doctors, radiologists, and surgeons. If you have a healthcare need and we don’t have a specialist available, such as specialized heart surgery, we can refer you to a network of physicians and hospitals in the New York City area.

Transitioning Care

After your first visit with us, we’ll send your primary care physician a letter summarizing your cancer treatment and outlining a plan for your follow-up care. Your physician can then incorporate this into your overall medical plan.

Typically, we see our patients every six to 12 months, though this varies based on the type of cancer therapy you received and any other individual health risks you may have. After each visit, we send a progress report to your primary care physician.