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Projects

Holistic Oncological Palliative Care 4 Europe’s Kids (Hope4Kids)

The Hope4Kids – Holistic Oncologic Palliative Care for Europe’s Kids - Joint Action aims to strengthen and harmonise paediatric palliative care (PPC) across Europe for all children living with life-threatening or life-limiting conditions.   

Across Europe, many children live with severe, complex or rare chronic conditions that significantly affect their quality of life and, in many cases, may shorten life expectancy. PPC is not limited to end-of-life care – it is an active and holistic approach that can be provided from the moment of diagnosis, regardless of disease type or stage, and alongside disease-specific or life-prolonging treatments. The aim of PPC is to prevent and relieve suffering through effective management of pain and other distressing symptoms, as well as to provide psychological, social and spiritual support to children and their families.   

Access to specialised PPC across Europe remains uneven, and care is often integrated late or inadequately into routine paediatric services. As a result, children, their families and informal caregivers frequently experience inconsistent care. Hope4Kids responds to these challenges through a comprehensive and coordinated approach. Key deliverables include mapping of PPC systems across Europe; development of harmonised, evidence-based guidelines in PPC; implementation and evaluation of four pilot interventions across more than 17 study sites; and development of education and training programmes for healthcare professionals, parents and informal caregivers such as teachers. Hope4Kids will also build a European PPC network of professionals and collaborate with other European projects.  

The Hope4Kids project has a duration of 4 years and is coordinated by the Princess Máxima Center for pediatric oncology in the Netherlands. The initiative is built on the cooperation of more than 50 partners and over 70 organisations from 23 European countries. Through this collaboration, Hope4Kids addresses inequalities in access to PPC, quality of care, and integration into health systems. Ultimately, this will ensure that every child and family have timely access to high-quality PPC, regardless of place of residence. 

“Funded by the European Union. Views and opinions expressed are however those of the author(s) only and do not necessarily reflect those of the European Union or the European Health and Digital Executive Agency. Neither the European Union nor the granting authority can be held responsible for them.”

 

Lees hier de Nederlandse beschrijving

De Europese Joint Action Hope4Kids – Holistic Oncologic Palliative Care for Europe’s Kids -heeft als doel de kinderpalliatieve zorg te versterken en te harmoniseren voor alle kinderen in Europa met een levensbedreigende of levensverkortende aandoening. In heel Europa leven veel kinderen met ernstige, complexe of zeldzame chronische aandoeningen die hun levenskwaliteit aanzienlijk beïnvloeden, en in veel gevallen de levensverwachting kunnen verkorten. Kinderpalliatieve zorg beperkt zich niet tot zorg aan het levenseinde – het is een actieve en holistische aanpak die kan worden geboden vanaf het moment van de diagnose, ongeacht het type of stadium van de ziekte, en naast ziektespecifieke of levensverlengende behandelingen. Het doel van kinderpalliatieve zorg is het voorkomen en verlichten van lijden door middel van de effectieve behandeling van pijn en andere verontrustende symptomen, evenals het bieden van psychologische, sociale en spirituele ondersteuning aan kinderen en hun families. De toegang tot gespecialiseerde kinderpalliatieve zorg in Europa is nog steeds ongelijk verdeeld, en deze zorg wordt vaak pas laat of onvoldoende geïntegreerd in de reguliere zorg. Als gevolg hiervan krijgen kinderen, hun families en informele zorgverleners (zoals leerkrachten) vaak te maken met inconsistente zorg. Hope4Kids biedt een antwoord op deze uitdagingen door middel van een alomvattende en gecoördineerde aanpak. Belangrijke doelen zijn onder meer het in kaart brengen van kinderpalliatieve zorgsystemen in heel Europa; de ontwikkeling van geharmoniseerde, evidence-based richtlijnen voor kinderpalliatieve zorg; de implementatie en evaluatie van vier pilots op meer dan 17 onderzoekslocaties; en de ontwikkeling van onderwijs- en trainingsprogramma's voor zorgprofessionals, ouders en informele zorgverleners. Hope4Kids zal ook een Europees netwerk van kinderpalliatieve zorgprofessionals opzetten en samenwerken met andere Europese projecten. Het Hope4Kids-project heeft een looptijd van 4 jaar en wordt gecoördineerd door het Prinses Máxima Centrum voor kinderoncologie. Het initiatief is gebaseerd op de samenwerking van meer dan 50 partners en meer dan 70 organisaties uit 23 Europese landen. Door deze samenwerking pakt Hope4Kids ongelijkheden aan op het gebied van toegang tot kinderpalliatieve zorg, kwaliteit van zorg en integratie in gezondheidszorgstelsels. Uiteindelijk zal dit ervoor zorgen dat elk kind en elke familie tijdige en holistische kinderpalliatieve zorg kan ontvangen, ongeacht waar in Europa zij zich bevinden.

Linkedin

Linkedin: @JA Hope4Kids

Contact

Contact information: wp2@kinderpalliatief.nl

Partners

International Children’s Palliative Care Network (ICPCN)

ICPCN is a global network seeking to improve acces to children’s palliative care. ICPCN’s network includes members in more than 140 countries. Members have access to ICPCN’s newsletter and online resources including educational content in many languages. ICPCN advocates for access and quality of children’s palliative care with the World Health Organization and other global platforms.

ICPCN

European Association for Palliative Care (EAPC)

EAPC is a professional organization “committed to supporting the promotion and development of palliative care throughout Europe and beyond”. Our Center staff frequently attend and present at the EAPC annual conference. In addition they serve in leadership positions and support the administrative work of the EAPC Reference Group for Children and Young People. Our Director, Meggi Schuilling-Otten is currently Chair of the EAPC Reference Group for Children and Young People. This group serves to promote children’s palliative care throughout Europe.

European Association for Palliative Care

Maruzza Foundation

The Maruzza Foundation works to ensure the right to access palliative care for all children who need it. The Maruzza Foundation hosts the Maruzza International Congress in Rome, a major gathering for paediatric palliative care researchers and clinicians.

Maruzza Foundation

Resources

Courageous Parents Network

CPN aims to orient, equip and empower families and others caring for a child with a serious medical condition and provide digital resources and an extensive media library used by families and clinicians.

Center to Advance Palliative Care

The Center to Advance Palliative Care is a US based organization that has supported the growth of palliative care as a specialty clinical service since 1999. Their website offers free resources on pediatric program development, marketing of palliative care, and educational offerings for operations managers and clinicians. Program Development. 

Center to Advance Palliative Care

Childhood Cancer International

CCI is the largest childhood cancer patient support organization, with member organizations in more than 100 countries.

Childhood Cancer International

Together for Short Lives (TFSL)

TFSL is a UK based organization that provides family support (emotional and financial), advocates for children’s palliative care in the UK, and providers resources to clinicians working with children who have life-limiting illnesses. TFSL also hosts an online provider network where clinicians can share expertise with one another.

Research Resources

International News

Guiding Young People with complex needs to adult palliative care

Smooth transitions: Guiding young people to adult palliative care.


Every year, thousands of young people with complex needs face one of the biggest challenges of their lives: leaving paediatric palliative care behind and stepping into the world of adult healthcare. Based on insights from the A10! Program, we* approach this transition in two key phases: first, the preparation of both the patient and their family to face adulthood with confidence and resilience; and second, the transfer of care, which emphasizes collaboration between care teams, building new relationships, ensuring continuity and safety, and creating a supportive experience for everyone involved.

1. Preparation: Building Confidence and Resilience

Personalized Care Plans: Creating Unique Journeys
In the transition to adult palliative care, there is no one-size-fits-all path. That is why transition programs should prioritise individualised care plans. These personalised plans address not only medical requirements but also social and emotional needs, making transitions feel more manageable. By collaborating with primary care providers, pediatric specialists, and adult care teams, we ensure that every voice, especially the family’s, is heard.

Eric, a young patient affected by a rare, complex condition, worried about leaving the comfort of pediatric care. Together, we devised a gradual transition plan that included joint visits with both pediatric and adult care teams, giving the family time to adjust to the new faces and systems at their own pace. In their words, “We couldn’t have done this without the understanding and support each of you provided.” 

"When we started working with young people like Eric, we saw how daunting this process could be. Watching him overcome these challenges with the right support has been one of the most rewarding moments."

Research supports this tailored approach, showing that individualised care contributes to smoother transitions and improved outcomes (Fegran et al., 2014).

Training and Education: Preparing for New Responsibilities
Preparing young people for adult care starts early, and the program offers tailored, age-appropriate training beginning around age 13. This guidance helps them learn to manage medications, recognise symptoms, and navigate appointments, so that patients gradually build confidence in managing their own health needs. For many, this journey is transformative, helping them transition to a more independent role.

Many young people express similar feelings about the transition, remarking that while it’s difficult to leave behind the familiar team and hospital they've known for years, they recognise that growing up involves taking on new challenges. They often express gratitude for the support received, the way their concerns were heard, and the encouragement provided at every step of the journey.

Reflections like these are common, and research highlights the importance of early preparation, showing that it leads to lower hospital re-admissions and greater self-management skills (Coyne et al., 2019). With the right guidance, young people facing complex health needs can transition more smoothly and confidently into adult care.

Emotional Support: Recognizing the Impact of Change
Leaving familiar healthcare providers and routines can be emotionally challenging. Many young people and families experience fear, sadness, and even a sense of loss as they face this new phase. A holistic approach that includes advising and psychological support helps families navigate these emotions, fostering resilience and a sense of readiness. By addressing these often-overlooked aspects of transition, we help families and patients approach this new chapter with a sense of hope (Young et al., 2016).

2. Transfer: Coordinating and Connecting Care

Multidisciplinary Collaboration: Supporting Patients Holistically
Transitions require a collaborative team. Programs must bring together pediatric specialists, adult providers, palliative care experts, and mental health professionals, creating condition-specific protocols to address each patient’s comprehensive needs. This approach allows us to support both medical needs and the psychological challenges of this transition. Studies show that this coordinated, holistic care improves symptom management and continuity of care (Friedrichsdorf & Bruera, 2018).

Thoughtful Preparation: Taking Steps Together
Planning the transition well in advance, usually 12 to 24 months before the transfer, allows families and providers to prepare thoroughly. During this period, shared meetings, detailed documentation, and formal handovers ensure that no detail is missed, improving communication and helping young people feel more comfortable with new providers. A collaborative approach ensures smoother transitions and improved outcomes. (Betz et al., 2015).

Looking to the Future: The Heart of the A10 Program
For patients and families, transitioning to adult care can feel like stepping into the unknown, but the A10! Program is here to light the way. With early preparation, personalised care plans, and unwavering emotional support, we aim to turn every transition into a journey of growth and empowerment.

References 

  • Fegran, L., et al. (2014). Adolescents' and Young Adults' Transition Experiences when Transferring from Pediatric to Adult Care: A Qualitative Meta-Synthesis. Journal of Advanced Nursing, 70(10), 2296-2310.
  • Coyne, I., et al. (2019). Self-management in children with long-term conditions: Concept analysis. Journal of Advanced Nursing, 75(11), 2584-2596.
  • Young, B., et al. (2016). Emotional Adjustment in Families of Pediatric Chronic Illness. Journal of Child Psychology and Psychiatry, 57(4), 371-382.
  • Friedrichsdorf, S. J., & Bruera, E. (2018). Delivering Pediatric Palliative Care: From Clinical Aspects to Positive Outcomes. Journal of Pain and Symptom Management,
  • Betz, C. L., et al. (2015). Nursing Care for Adolescents with Chronic Conditions: Transitioning to Adult Care. Journal of Pediatric Nursing, 30(5), 1-10.

*This article is authored by Esther Lasheras, Eduard Pellicer, and Sergi Navarro from Sant Joan de Déu Hospital.

Learn More

Webinar on Transition Processes in Paediatric Palliative Care

On 11 October, The Children and Young People’s Reference Group hosted an insightful webinar, "Bridging the Gap: Transition Processes in Paediatric Palliative Care – from Baby to Young Adulthood." Experts and a parent with lived experience shared their perspectives on managing transitions from perinatal to pediatric care and from pediatric to adult care.

Why does this matter? Transition periods are critical for families of children with life-limiting conditions. Well-managed transitions not only improve care quality but also enhance outcomes for patients and their families.

Missed the webinar? Discover the key takeaways and best practices shared by international experts. Watch the webinar recording.


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