Webinar on Coronavirus and people with serious conditions and underlying health issues, with a particular focus on palliative care. Friday 20th March 2020 14:00 UK time

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With the corona virus pandemic evolving, and different countries taking different measures to control the virus, many individuals with palliative care needs and palliative care providers have been asking for guidance and support on the implications for palliative care. ICPCN have provided some links on our website to official WHO guidance along with some key resources, however this webinar will give people the opportunity to explore these issues and hear from individuals with palliative care needs and the WHO, amongst others.

Purpose of the webinar
This webinar has been initiated by people with, or affected by, serious conditions, and is aimed at people living with serious illness and their families, as well as healthcare workers worldwide. The purpose of the webinar is to provide the latest information, guidance and experience on coronavirus and people with serious conditions and underlying health issues with a particular focus on palliative care. 

Date and time of the webinar
The webinar will be held on Friday  2020 at 14:00 UK local time. It is expected to last up to 1.5 hours. 

How to participate?
To participate in the webinar please follow this link:  https://zoom.us/j/194141788

You can submit questions during the webinar and also ahead of time, in this open-access Google document. If the questions are not addressed during the webinar, we will seek to ensure answers are added to the document as they become available.

Phone-in options to join the webinar ID 194 141 788 can be found here

Who is organising the webinar?
The webinar is being organised by the Worldwide Hospice Palliative Care Alliance and Palliative Care Voices. and is being held in partnership with a variety of organisations including ICPCN.

Who will be speaking on the webinar?
One of the objectives of the webinar is to hear the perspective of people with serious illness and those directly affected by palliative care in the face of coronavirus and so Lucy Watts from Palliative Care Voices will be sharing her experiences and the role of communities and what people need. We will also be hearing from the World Health Organisation on their response, along with a range of palliative care organisations.

Who is the webinar aimed at?
The webinar is aimed at those working in palliative care and with people with serious illness globally, along with those living with serious illness and their families.  

 

ICPCN wins award for Excellence in Palliative Care Development

ICPCN recently received an ‘Award for Excellence in Palliative Care Development 2017’ from Global Health & Pharma.

The 2017 Social Care Awards are aimed at giving recognition to individuals, teams and companies responsible for showing excellence in care, compassion and courage in some of the most crucial and challenging industries, including palliative care.

In the 2017 Social Care Awards, Global Health & Pharma (GHP) has rewarded service and innovation in the field of social care. The awards recognise the brave who selflessly and generously give of their time and effort to look after others, without ever asking for recognition or expecting anything in return.
The International Children’s Palliative Care Network (ICPCN) has had the honour of receiving the ‘Award for Excellence in Palliative Care Development 2017’ in the social care awards category.

On hearing of the award Prof Julia Downing, ICPCN's Chief Executive, said that she was thrilled that the charity had been recognised with this award and it reinforced ICPCN's place at the forefront of children's palliative care globally. She added that ICPCN remained committed to being the voice for children needing palliative care around the world. 

 

 

ICPCN trains 30 health care professionals in Lesotho

Under the auspices of the ICPCN and in collaboration with the Lesotho Ministry of Health (MoH) a week-long training of healthcare professionals in the principles of children’s pallaitive care took place in Maseru, the capital of Lesotho, last month. 

The initial training which took place from 16 to 20 January 2017 is being funded by the Open Society Foundations of Southern Africa and is the first training of this kind to take place in the small African mountain kingdom of Lesotho.

The training was led by ICPCN’s Busi Nkosi with assistance from fellow trainers, Joan Marston and Dr Julia Ambler. The 30 healthcare professionals who attended included medical doctors, nurses, pharmacists, Social Workers, priests, a dietician, an Occupational therapist and a Traditional Healer. The aim of this and future training is the development of competence in the deliverance of children’s pallaitive care and the evaluation of its impact at all health centres within the country.

Busi Nkosi reports that  the course was well received and the participants were active and engaged in robust discussions throughout the week.

Lesotho does not have existing children’s palliative care services, despite the need based on the incidence of diseases such as HIV/AIDS and cancer in children. The new collaboration between Lesotho MoH and ICPCN is expected to bring about some positive results.

 

 

An interview with Sabine Kraft: ICPCN’s new Chair of the Board of Trustees

icpcn chair sabine kraft

An in-depth interview with Sabine Kraft, who recently took over the reins as Chair of the International Board of Trustees of the International Children's Palliative Care Network.

Q: What is your present job title and can you describe your role within your organisation?

SK: I am the CEO of the national association of children’s hospices in Germany. My role is defined by the statutes and the mission statement of the charity. Therefore, our priorities are around information, advocacy and advice and support to children's hospice initiatives and children's hospice services. Above all, at the centre of our activities are the families and their children with life-threatening and life limiting diseases. 

We achieve our ‘information to the public’ goals through a strong public presence, through events for the public and the families and through publications; our service mentality and helpline for professionals, families with sick children and people in bereavement who lost a child. Advocacy is a great part of our tasks, we lobby on all levels, in politics and with health insurances to ameliorate the support for child hospice organisations. 

I am responsible for all activities, for the development of standards in the child hospice field, for the introduction of quality measurements, and finally, the biggest challenge, to find supporters and donors, to finance all our activities.

Q: Please would you tell us a little about yourself? 

SK: Work is my passion, family my life! I live together with my partner in a small village in the black forest. We have two grown up children living with us, a daughter of 17 and a son of 19. Both still go to school, but have learnt to adapt to our busy lives. 

We also share the house with the mother of my partner, who had a stroke three years ago. She lost her speech and she cannot move her right arm and leg. Therefore, we experience for ourselves how challenging it is to feel responsible and to organize care for a family member with massive handicaps. My partner is a very loving son for his mother and takes very good care of her. 

My biological and beloved daughter lives close to us in Freiburg. She followed my steps to Northern Ireland and gave birth to a very tiny girl, Matilda, three years ago. The ‘wee’ child is the joy of the whole family. She is healthy, despite only weighing 1200 grams at birth. She is a bit spoilt and – maybe due to the prematurity – also very determined! She was blessed with a brother, Leander, just 2 months ago, healthy and heavy and very relaxed. A wonderful grandson for us. 

And finally, my greatest friend and joy for the last 10 years, my dog Polly, who listened to all the stories about sick children and just everything that moved my mind, had to leave me only a few weeks ago. I miss her so much and yet, my job is so demanding and involves so much travelling that I just must be sensible and wait until I retire to find a new friend.

If somebody would ask me, what I like doing, I would answer – spending time with my family – picnicking in nature, walking and enjoying the peace around me. I always find solutions when I walk; just walk and walk and walk. 

Q: What drew you to work in the field of children’s palliative care, what motivates you to continue and how long have you worked in the field?

SK: As a social worker I experienced working with children in many different fields. I started in a children’s home, then kindergarten, then youth club and finally in a family planning organisation. I met women and families who had to decide on continuing pregnancy with a severely handicapped foetus.

About 15 years ago my nephew died at only 2,5 years of age. Lovis was a lovely and healthy boy and he just died. This trauma motivated me to get involved in palliative care for children. There was no help available in Germany, no specialised group, just nothing but the helplessness of the whole family. When this happened, it turned my life upside down. 

It took me one year to reflect on my attitude towards dying and I finally realised that this was a subject I have been growing up with. At the same time, I started counselling a children's hospice project until the advertisement for the freelance post of CEO for the national association of children’s hospices just caught my heart and soul. There was the light, the passion, the job of my life - and it still is.

Q: Can you describe what it meant to you to be invited to take over as Chair of the ICPCN Board of Trustees?

SK: Somehow or another, I always felt that it could not be true. How can I be chosen for an important role like this? I am only a social worker, not a doctor or a nurse. It was such an honour therefore, and I am struggling to find the right way to contribute. However, I just will give my utmost to do a good job – and as you know – I am used to big challenges – remember the ghost who motivates me!

Q:You have been with ICPCN since its inception in 2005. What role do you believe the organisation has in the development and growth of children’s palliative care globally?   

SK: When I joined the ICPCN, I did so because I am convinced that children in such difficult situations must have a strong lobby. And children are children, anywhere in the world. They have the same rights. And when children are weak, they have even more rights to be supported. It takes global advocacy to develop a sensibility towards the weakest ones of our society. And how else can we make a difference, if not when we act in solidarity all over the world?

ICPCN has raised a great deal of awareness, has helped initiatives to change the world around them. Only a global player like the ICPCN can reach out to the whole world to make it a better world for the estimated 21 million children without adequate palliative care. I do believe that information, education and advocacy must be centralised to enable us to reach out. We are one world, and children are children, no matter where they are born and what they are born into. And we all can do something to make it better – just do one thing for the 21 million children!

Q: What would you like to see ICPCN achieve as an organisation going forward?

SK: ICPCN must become known everywhere in the world. With our online courses on paediatric palliative care we have made a good start, yet, we still have to struggle to finance everything. ICPCN should become the CHANGE ORGANISATION concerning children’s palliative care. In the best case, we become the central competence organisation where people from all over the world can turn to in order to find support. Every government and their health departments in particular, should know about us and ask members of the ICPCN to support them in political health decisions about palliative care. 

And, although this all sounds like a dream, things can only change if we believe in dreams. And while writing this, one could go even further into the ‘dream world’ and wish that an organisation like the ICPCN will make itself ‘redundant’. This would be the greatest fulfilment – no more sick children who must die far too early!

 

Global supermodel named as new ambassador for ICPCN

150128 Micheline Etkin

The International Children’s Palliative Care Network (ICPCN) is thrilled to announce the appointment of the beautiful world-class supermodel, Micheline Etkin, as their new global ambassador. The ICPCN is a worldwide network of individuals and agencies advocating for the rights of children and young people with incurable conditions to receive palliative care.

Micheline, who was born in Lebanon and raised in Sao Paulo, Brazil, now lives with her husband in Arizona and is the mother of three adult children. She is a compassionate philanthropist, well known for her passion for charity work to benefit children.

Click here to view the complete press release