Pediatric palliative care is specialized support for children living with chronic or life-limiting illnesses. More than just medical care, it’s a comprehensive approach that cares for the child’s body, mind, and spirit — while offering essential support to their families.
The goal is to relieve pain, manage symptoms, and ease the emotional and physical burden of illness. It’s about ensuring respect for each child’s dignity and individuality, providing continuous, personalized care that improves quality of life and helps families stay strong and connected. This includes psychological, social, and spiritual support, resources for siblings, and much-needed respitespaces for primary caregivers.
Learn more about pediatric palliative care and its impact through PEDOPAL .
“You matter for who you are, and you matter to the last moment of your life. We will do all we can not only to help you die peacefully, but also to live until you die.”
families in Spain need pediatric palliative care.
receive comprehensive, appropriate support
fully equipped teams provide 24/7 care and home-based hospitalization
As child mortality decreases, more children and adolescents are living with incurable conditions — creating new needs. These complex realities require specialized care that ensures well-being for both patients and their families, during illness and beyond.
Pediatric palliative care is centered on ensuring comfort, dignity, and quality of life for children facing life-limiting illnesses. It does not aim to extend or shorten life, but to relieve suffering and walk alongside families with empathy and respect.
Pediatric palliative care begins with the diagnosis of an incurable disease, without the need for a short-term prognosis of life to receive it.
They meet the physical, emotional, social and spiritual needs of children and their families. An interdisciplinary team guarantees continuous assistance, prioritizing home care whenever possible.
A commitment to life and well-being. The Madrid 2020 Manifesto promotes Pediatric Palliative Care as an essential right.
In the coming years, we face critical challenges — and meaningful opportunities — to advance pediatric palliative care:
We must foster open, compassionate conversations about serious illness and end-of-life in children, breaking the silence and stigma surrounding death.
It’s urgent to promote legislation that ensures equitable access to pediatric palliative care across the entire country.
Expanding education and training for healthcare professionals is key to providing high-quality, child-centered care tailored to the unique needs of each family.
Families should receive support in the comfort of their own homes, without relying solely on hospital services.
Geographic location should never determine the care a child receives. Equal distribution of resources is vital to ensure that all families, regardless of where they live, have access to palliative care.
Every child and family have the right to receive compassionate, specialized care. Pediatric palliative care must be a guaranteed part of every national healthcare system — not a privilege based on location or available resources. The World Health Organization (WHO) recognizes palliative care as an essential part of universal health coverage. Its full implementation must be a public health priority
Em porque Ao vivo , trabalhamos para melhorar a vida das crianças que não podem ser curadas e a das suas famílias.
Mas não podemos fazê-lo sozinhos. A sua ajuda é fundamental para que mais crianças com: Doenças incuráveis recebem a atenção que merecem. Doe, partilhe ou envolva-se e faça parte da mudança.
Juntos, podemos dar vida à sua vida.