Prenatal through age 21
Supporting children across all developmental stages
Supporting children across all developmental stages
Built on 40+ years of our expertise
By phone or video for all parents, in-person for hospice patients
“To compassionately care for children, families, and communities on their sacred journey of love, triumph, exasperation, and grief.”
Our pediatric hospice and palliative care services are designed for children at any stage of serious illness — not only at end of life. Many families partner with us for extended periods of time as their child’s needs evolve. We’ll help you understand your options and create a care plan centered on your child and your family.
Palliative care is a family-centered model that focuses on expert evaluation and management of pain and other symptoms, while also providing support for caregivers and siblings, guidance through anticipatory grief, and coordinated care planning. Early integration of palliative care enhances physical, psychosocial, and spiritual support for children with serious illness and their communities. As a consultative service, we collaborate with your primary medical team to promote quality of life.
Hospice care is an insurance benefit for patients with a prognosis of six months or less. The Medicaid Concurrent Care for Children Requirement, a provision of the Affordable Care Act, allows children under 21 to receive both curative treatments and hospice care at the same time. This holistic approach ensures that children receive comprehensive care, encompassing both their medical needs and comfort care.
Transitions Kids works alongside your child’s existing medical providers, hospitals, specialty clinics, and private duty nursing teams to help improve communication, coordination, and symptom management.
Transitions Kids offers support beginning with perinatal services for children with a potentially life-threatening diagnosis, continuing through childhood and adolescence up to age 21.
Most children receive care at home, but the team also supports families when a child is hospitalized. For children receiving hospice care, Transitions LifeCare’s Hospice Home may also be an option for end-of-life care.
Transitions Kids families have access to pediatric support 24 hours a day, 7 days a week. Whether you have questions about symptoms, medications, changes in your child’s condition, or what to do next, a nurse is available by phone or video to provide guidance, reassurance, and timely support when your family needs it most.
When a child is facing a serious illness, families may need support with more than medical care alone. Transitions Kids has gathered helpful pediatric family resources, including financial assistance options, community programs, wish-granting organizations, and other support services for children and their loved ones.
We’ve made the path to care as clear and gentle as possible. Our team will listen, answer questions, and help your family understand what support may be right for your child.
Call us today at 919.748.0823. You can ask your child’s physician about a referral or connect with us online to learn more about Transitions Kids.
Our team takes time to understand your child’s diagnosis, symptoms, current care plan, and what matters most to your family.
Transitions Kids works alongside your child’s doctors, specialists, hospital team, and other care providers to support comfort and continuity of care.
Your child and family receive compassionate support from a pediatric care team focused on comfort, communication, and quality of life.
Transitions Kids (TK) offers palliative and hospice care to children and families impacted by illness or loss. A referral to TK doesn’t automatically mean that someone is dying–a common fear for many families. TK offers a wide range of support designed to meet the needs of families throughout their journey with serious illness. The care that we provide can be tailored to meet the unique needs of each patient and family, and our team will work with you to identify which level of care will be most appropriate for your family.
While Transitions Kids began in 2015, our organization, Transitions LifeCare, was originally founded as Hospice of Wake County in 1979.
The frequency of visits typically depends on the level of care the patient requires. Palliative care patients receive visits from an interdisciplinary team member for a minimum of every six months, with more frequent visits for symptom management and care coordination as needed. Hospice patients receive weekly nursing visits, with family support and physician visits ranging from weekly to monthly. Your care team will collaborate with you to determine the visit frequency that best meets your needs.
We offer a variety of direct care and support services for patients perinatal to 21 years of age in Chatham, Durham, Franklin, Granville, Harnett, Johnston, Lee, Nash, Orange, Wake and Wilson counties. While we are unable to do home visits outside of this service area, we may be able to provide palliative care support via telehealth.
Yes! TK is a team of sub-specialists with a focus on quality of life. Our services are designed to enhance, not replace, the care that you are already receiving. One of the benefits of TK is the ability to provide coordination among the multiple specialists many of our families see. As an independent agency, we work collaboratively with the local hospitals and specialty clinics. This often allows for more seamless care, better communication between families and providers, and improved symptom management.
Yes! Our services are designed to complement your existing care. We collaborate with hospitals and specialty clinics to ensure seamless care, better communication, and improved symptom management.
Services provided through hospice are covered by insurance. Palliative care physician visits can also be billed through insurance, like other specialists. Generous donations allow us to continue providing care to patients and families, regardless of their ability to pay.
No! In most cases, both services can be provided at the same time. Many of our patients have private duty nurses, and we work collaboratively with their companies to provide care.
Most patients receive support in their home. When a patient is hospitalized, the Kids Team continues to provide support for the patient and family but is not involved in direct medical care. For families where home or hospital is not the best option, patients receiving hospice care may transfer to our inpatient Hospice Home for respite care or symptom management.
Patients are discharged when their family decides services are no longer needed or if they move out of North Carolina. Bereavement services are provided as long as needed after a child’s death.






