Children and Families

Families with kids facing a life-threatening medical condition in the United States. 

Children and adolescents in the U.S.

Children with cancer and their families, caregivers, young adults, healthcare professionals and researchers related to childhood cancer

Children and adolescents who are currently fighting cancer

U.S. and International, anyone affected by drug shortages

Patients and families living with Aplastic Anemia, Myelodysplastic Syndromes (MDS), Paroxysmal Nocturnal Hemoglobinuria (PNH), and related bone marrow failure diseases

Young cancer survivors who are parents or guardians of small children

U.S. and international childhood cancer foundations, organizations, and advocates, as well as families in the U.S. impacted by childhood cancer. 
 

Individuals, families, caregivers and the bereaved in the U.S. affected by a cancer diagnosis

Patients, caregivers, and healthcare professionals impacted by cancer in the U.S.

People affected by cancer in the U.S. and Canada

Adolescent and young adult cancer patients and survivors

Pediatric (age 4 and up) and adult cancer patients undergoing chemotherapy in the US

Children with cancer and their families in Canada

Children with cancer and their families, survivors, healthcare professionals

Pediatric cancer survivors, families, healthcare professionals, and advocates

Terminally ill children throughout the United States, diagnosed with cancer and in the late stages of their illness, who qualify as low income or financially needy PRIOR to diagnosis, are 18 years old or younger (however, if child is 21 or younger and was diagnosed with their cancer before turning 18 and is still being treated in a pediatric facility, the patient may still qualify), and the application must be submitted by the referring hospital or hospice are team.

Children and adolescents ages 5-18 impacted by serious illness in the US

Kids and young adult cancer patients/survivors ages 3-26

Families caring for children with serious illness and clinicians who support them. 

Pediatric and adult cancer patients, healthcare professionals

Children with cancer and their families

Children and adolescents ages 3 to 18 in the U.S. affected by cancer, along with the healthcare professionals who serve them.

Patients with life-threatening illness and their caregivers

Rare disease caregivers, military/veterans and their families, and other communities in need

Critically ill children, ages 3 to 18 years living in the US with priority to children in the Northeast

Children and adolescents with serious illness ages 6-18 (US and International)

Children in treatment for cancer in grades Pre-K through 12

Children (between the ages of 1 and 18) with conditions that are progressive, degenerative, or malignant and are within two years of their most recent treatment.

Children and adolescents with cancer and their families in the U.S.

Young families with children 18 or under, facing the loss of a parent to a life-threatening illness or living with loss

Children (ages 3-18+) with serious/chronic illness, siblings, as well as children of adult cancer patients

Children with life-threatening medical conditions that have reached the age of 2½ and are under the age of 18 at the time of referral. Children must be referred within one year of the end of treatment. Children must not have already have had a wish granted by any other wish granting organization.

Child and adolescent cancer patients in active treatment who reside in the U.S.

Caregivers to children with cancer, healthcare professionals

Kids and teens with cancer ages 6-18

Patients and caregivers

Children and adolescents whose parent/guardian has cancer (US, Canada, and International)

Families with kids fighting cancer anywhere in the United States

Children with any type of cancer and their families, supporters, researchers

Families effected by childhood illness or injury.

Children ages 8 to 18 with pediatric cancer or other life-threatening illness and their families, primarily in Colorado; other regions served include Arizona, Illinois, Oklahoma, Virginia, and Indiana

Childhood cancer patients and survivors, and their families; healthcare professionals

Children and teens age 21 or younger, worldwide, battling a life-threatening or life-limiting physical, mental or emotional medical challenge

Children and teens with chronic or life-threatening medical conditions in the U.S., Canada, United Kingdom, Israel, Australia, New Zealand; teens ages 13-20 with medical issues worldwide and their teen siblings

Children with cancer and their siblings age 3 ½ - 16

Children in the US ages 5 to 16 diagnosed with serious and chronic illnesses (including cancer) that has resulted in treatment or extended hospital stays within the past 3 years, who could benefit from a boost to improve their quality of life both socially and psychologically

Teens and young adults with cancer, survivors, caregivers, healthcare professionals

Cancer and transplant patients and families, caregivers, survivors

Children with cancer and their families, caregivers, survivors, health professionals

Families with children and adolescents facing cancer

Cancer survivors, previvors (individuals who are genetically predisposed to cancer), and caregivers

Children and adolescents ages 2 -19 years with cancer in the US

Parents with serious illness, their children, and healthcare professionals who serve them in the US, Canada, and internationally.

Families with children aged 18 or younger with a chronic illness