June: Cancer Survivors Month

Survival is a victory — but care must continue

June is dedicated to people living with and beyond cancer. It is a month of recognition, hope and respect for every person who has faced a cancer diagnosis, completed treatment, continues treatment, or lives with cancer as a long-term condition.

Cancer survival is a major victory. However, for many people, it is not the end of the story. Life after cancer often brings a new reality: follow-up appointments, fear of recurrence, fatigue, emotional distress, changes in body image, work-related challenges, financial pressure, family adjustments and the need to rebuild everyday life with confidence and dignity.

Cancer Survivors Month reminds us that survivorship is not only about living longer. It is also about living better.

A cancer survivor is not only a person who has completed treatment and is disease-free. The term also includes people receiving maintenance treatment, people living with cancer as a chronic condition, and those who continue to experience the physical, emotional, social or economic consequences of the disease and its treatment.

In recent years, advances in early diagnosis, targeted therapies, immunotherapy, surgery, radiotherapy and supportive care have increased the number of people living many years after a cancer diagnosis. This is a major achievement for medicine, research and public health. At the same time, it creates a new responsibility: to ensure that survivorship care is organised, person-centred and accessible to all.

For many survivors, the end of active treatment is a moment of relief and gratitude. Yet it may also bring uncertainty. Some people feel that everyone around them expects them to “go back to normal”, while they are still trying to understand what has changed in their body, their emotions, their relationships and their daily life.

The fear of recurrence, anxiety before follow-up tests, persistent fatigue, pain, cognitive difficulties, changes in sexuality, emotional vulnerability and social isolation are real experiences for many people after cancer. These needs should not be underestimated. Survivors need space to speak, reliable information, access to professional support when needed, and connection with communities and organisations that understand their journey.

Long-term follow-up is also essential. Survivorship care should not focus only on recurrence. It should also include prevention, early recognition of late effects, management of treatment-related complications, support for mental health, healthy lifestyle guidance and personalised monitoring according to each person’s cancer type, treatment history, age and individual risk factors.

The message is not fear. The message is awareness, prevention and continuity of care.

Life after cancer is also about rights. It is about returning to work, accessing social benefits, understanding available services, managing financial toxicity, supporting caregivers, protecting dignity and ensuring equal access to care. Survivorship must be seen as a social, psychological and practical issue — not only a medical one.

At Kapa3, we see every day that cancer does not always end with the last treatment. It continues in the questions people ask about their rights, their next steps, their follow-up, their access to benefits, psychological support, work, family life and social reintegration.

This is why people living with and beyond cancer need holistic support. They need information, guidance, psychosocial care, access to rights and services, empowerment and continuity of care. No one should feel alone after treatment. No one should be left to navigate bureaucracy, uncertainty or lack of information without support.

Cancer Survivors Month invites us to change the way we talk about survival. We should not ask only: “Did the person survive cancer?” We should also ask:

Are they living with quality of life?
Do they have access to the care they need?
Do they know their rights?
Do they receive psychological and social support?
Can they return to work and daily life with dignity?
Is there a follow-up plan?
Is there someone to guide them when they do not know where to turn?

Cancer survival is a victory. But the real challenge is to turn this victory into a life with quality, safety, rights, support and hope.

At Kapa3, we continue to stand beside every person living with and beyond cancer. Through information, guidance, empowerment and human-centred support, we believe that care does not stop at treatment.

It continues in life.

World Palliative Care Day – 11 October 2025

“Leave no one behind: Equity in access to palliative care.”

World Palliative Care Day is a moment to recognize that healthcare is not only about curing disease — it’s also about caring, comforting, and preserving dignity until the very end. Everyone deserves the best possible care, regardless of who they are or where they live.

Globally, more than 50 million people die each year, and it is estimated that around 60% would benefit from hospice and palliative care. Yet access remains deeply unequal: only about 14% of the 73 million adults and children who need palliative care actually receive it. Most of this need is met in high-income countries, while in low- and middle-income regions only 4% of the population in need is served. The COVID-19 pandemic has further exposed these disparities, highlighting the urgent need to integrate palliative care into public health systems worldwide.

Palliative care is about the whole person — their physical comfort, emotional well-being, social environment, and spiritual peace. It aims to ease pain and suffering while supporting families and caregivers through counselling, practical help, and compassion. Studies show that early integration of palliative care in cancer treatment can improve symptom control, quality of life, and even survival rates.

According to the World Health Organization, palliative care development should follow a public health approach that includes policy, education, medicine availability, and community empowerment. In many countries, especially where health resources are limited, training healthcare professionals and raising public awareness can make a real difference. Local communities, volunteers, and patient organizations play a vital role in reaching those who might otherwise be left behind — offering presence, empathy, and human warmth that no medical intervention can replace.

In Greece, the Hellenic Society of Medical Oncology (HeSMO) has emphasized the importance of developing a national palliative care framework. Every year, more than 120,000 people in Greece are estimated to need such care — nearly 37% of them cancer patients — but specialized services remain limited, particularly outside large cities. The HeSMO position paper calls for education, policy support, and the inclusion of palliative care at all levels of the healthcare system.

At Kapa3, we stand with patients and families who face serious illness. Through awareness, advocacy, and human connection, we work toward a healthcare model that values quality of life as much as longevity. Palliative care is not about giving up — it’s about living fully, with dignity, comfort, and compassion, every step of the way.

Read more here