Welcome!

On behalf of the International Lymphoedema Framework and the Scientific Committee Board, thank you for your interest in participating at our 11th International Lymphoedema Framework Conference, which will be held between 13th - 15th June in Nottingham. 

REGISTER NOW (in-person conference) REGISTER NOW (virtual conference)

This year’s conference will be hosted by the International Lymphoedema Framework (ILF) in collaboration with the Welsh Framework, Lymphoedema Wales and the International Lipoedema Association (ILA).

The theme for this year’s conference is ‘Stronger Together’. And together, we aim to achieve a greater awareness of lymphoedema alongside related disorders, to raise awareness and prioritise lymphoedema on the healthcare agenda, worldwide.

We are also pleased to announce that the Patient Day will be returning on Thursday 15th June.

We look forward to welcoming you in Nottingham and to another successful ILF Conference.

Kind regards,
Christine Moffatt CBE (ILF Chair) and Melanie Thomas (Scientific Committee Chair)

Scientific programme

Details on the programme and our speakers.

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Registration and fees

Information on fees and entitlements.

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Conference information

All the details you need regarding the conference.

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Sponsors & exhibitors

Meet our sponsors and find our who will be exhibiting.

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Patient day

We are pleased to announce that the Patient Day will be returning on Thursday 15th June.

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Abstract submissions

All the details you need regarding abstract submissions.

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Scientific and Organising Committee

Scientific Chair

Melanie Thomas, Clinical Director Lymphoedema Wales Clinical Network (ILF)
 

Chair ILF

Christine Moffatt CBE, Professor of Clinical Nursing Research at the University of Nottingham School of Nursing, Midwifery and Physiotherapy, United Kingdom, (ILF)

The ILF would like to thank all of our Scientific and Organising Committee board members for their contributions.

Scientific Committee

Ellie Dring, Representative NTU
Jane Rankin, Lymphoedema Network Northern Ireland
Kate Sinclair, British Lymphology Society
Kay Morris, National Lymphoedema Partnership
Linda Gibson, Professor NTU
Margaret-Anne Garner, Scottish Lymphoedema Practitioners Network
Dr Narahari, ILF Board Member
Carol Ellis, MLD UK
Rebecca Elwell, BLS, CLSIG
Dr Rhian Noble-Jones, LCNW, British Lymphology Society
Sandro Michelini, Italian Framework
Dr Tobias Bertsch, International Lipoedema Association
Tonny Karlsmark, ILF Board Member
Vaughan Keeley, Derby Lymphoedema Service
 
 

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Collaborating Associations

The International Lymphoedema Framework (ILF)
 
The ILF was established as a UK charity in 2009. The framework developed from a project aiming at bringing together the main stakeholders involved in the management of lymphoedema in the United Kingdom in 2002, but the ILF rapidly spread to become an international project with an objective to support individual countries develop a long-term strategy for lymphoedema management.
 
Today the ILF works in partnership with 15 national frameworks around the world, all working to improve the management of lymphoedema and related disorders.
 
The ILF believe:

• That patients should always be at the heart our objectives and achievements
• Improvement of lymphoedema management is a dynamic process that will require ongoing research and implementation into practice
• International collaboration is essential
• We are stronger together

 
The ILF goals:

• To increase awareness by raising the profile of lymphoedema.
• Facilitate and contribute towards better access to treatment for patients worldwide.
• Provide a better understanding of the needs of patients for the health care industry.
• Promote, initiate and support research & education programmes.
• Promote and document best practice.

 
Click here to become an affiliate of the ILF
Click here for more information on the ILF
 

The Lymphoedema Wales Clinical Network
In April 2011, the Welsh Government allocated £1 million recurring to implement the Strategy for Lymphoedema in Wales published two years previously. The Strategy aims to enable all lymphoedema patients access to the appropriate services at the right place, right time and with the right person regardless of whether their lymphoedema is related to cancer or not.
 
The All Wales Lymphoedema Network Board has been established to maintain a strategic oversight of the Strategy for Lymphoedema in Wales. The Chair of the Network Board is Fiona Jenkins, Executive Director of Therapies and Health Sciences for Cardiff & Vale University Health Board.
 
The Network has been coordinated through a virtual network approach, for NHS Wales to:

• Oversee the planning of services for NHS Wales, ensuring recommendations in the Strategy are implemented locally
• Oversee clinical education and training requirements for the network area
• Advise on how Health Boards should respond to strategic developments as they arise
• Provide the source of composite advice of Health Boards to Welsh Government when required
• Advise on allocation of funding as services change or as funding arrangements change

Click here to visit the Lymphoedema Wales Clinical Network Website
 

The International Lipoedema Association (ILA)
 
The International Lipoedema Association (ILA) was founded in 2021 by 60 renowned healthcare professionals from 22 countries.

We aim to create the best possible treatment for our lipoedema patients by collaborating in an international, diverse, inclusive, and multidisciplinary team. Our holistic treatment approach is based on clinical evidence, long-standing experience, and a passion for improved therapy outcomes.

Click here to visit the International Lipoedema Association Website
 

REGISTER NOW

We would also like to thank Nottingham University Hospitals and Nottingham Trent University for supporting the ILF 2023 Conference.