When a child is first diagnosed with cancer, families may feel overwhelmed by new information and unsure of the next steps.  When doubts or confusions arise, some families may wish to seek a second opinion.

Parents are the best advocates for their child’s education since they know the unique challenges, strengths, interests, and needs of their child.

The NCCS mentor program was created to help children ages 10-17 adjust to their treatment, increase their self-confidence, reduce anxiety, and offer a connection with someone that understands their journey.

At a time when most children are deciding which sport to play, pediatric cancer patients have their lives disrupted as they are faced with cancer treatments. It has been recognized that the camp experience is very valuable in allowing kids to be kids even as they face the harsh realities of cancer.

Post-traumatic stress disorder (PTSD) is an anxiety disorder that can develop after a life-threatening or terrifying experience – like fighting childhood cancer.

New research is leading to a better understanding of childhood cancer survivorship and the effects of cancer and therapy. Long-term side effects related to cancer and prior treatments are called “late effects” and may be mental, physical, social or even second cancers.

Everyday there is a new diagnosis and a new childhood cancer survivor. To help young adults through their journey, The National Children’s Cancer Society created a publication specifically for survivors of childhood cancer ages 15 or older. The View From Up Here provides detailed information to help with every stage of the survivorship journey and addresses the different struggles that may arise.

Childhood cancer survivors are at risk of developing late effects, which are problems related to cancer treatment that persist after treatment is completed. Recognizing them early gives the best chance of providing effective treatments. In response, many hospitals have established long-term follow-up clinics to monitor survivors beyond treatment.

The transition from a pediatric health care setting to an adult setting can be a difficult process. Cancer survivors treated in the pediatric setting must be able to adapt to a new health care system in a positive manner.

There is a saying that “you cannot pour from an empty cup.” This holds especially true when you are a caregiver to a child diagnosed with cancer. Self-care is the broad term that involves taking the necessary steps to ensure your own health and well-being.

Relationships have normal ups and downs, however, your child’s cancer experience may cause unique emotional challenges that can significantly affect your relationship. The stress from the diagnosis and new responsibilities in caring for your child may cause uncertainty and anxiety.

Did you know The National Children’s Cancer Society (NCCS) has been awarding college scholarships to childhood cancer survivors since 2008? Since that time, the NCCS has awarded over $2 million to 227 survivors to help them fulfill their future dreams.