Contact Details

International Lymphoedema Framework
Tel: +45 7020 0305
Email: info@lympho.org
www.lympho.org

International Lymphoedema Framework

About Us:
The ILF was established as a UK charity by Christine Moffatt CBE and her team in 2009. The Governing Board of Trustees is made up of opinion experts and leaders in their field, from around the world, who volunteer their time and expertise.

Our Purpose and Aims:
The aim of ILF is to improve the management of lymphoedema and related disorders worldwide. This includes also low-resource countries. ILF believes that: Patients should always be at the heart of the Framework Projects; Only a collaborative and multidisciplinary partnership between all stakeholders, recognised as experts, can lead to an improvement in the management of lymphoedema; Improving the management of lymphoedema is a dynamic process requiring ongoing research and implementation into practice; International collaboration is essential.

Benefits to People Living with Lymphoedema:
Patients are in the heart of all activities. Dedicated Patient Days are organised during the conferences. Free resources are available including materials with support of people living with lymphoedema. Read more here

Directories: Therapists/Medical Professionals:
Please find information about ILF’s National Frameworks who can advise on regional health care professionals here National Frameworks – International Lymphoedema Framework

International Lymphoedema Framework

About Us:
The ILF was established as a UK charity by Christine Moffatt CBE and her team in 2009. The Governing Board of Trustees is made up of opinion experts and leaders in their field, from around the world, who volunteer their time and expertise.

Our Purpose and Aims:
The aim of ILF is to improve the management of lymphoedema and related disorders worldwide. This includes also low-resource countries. ILF believes that: Patients should always be at the heart of the Framework Projects; Only a collaborative and multidisciplinary partnership between all stakeholders, recognised as experts, can lead to an improvement in the management of lymphoedema; Improving the management of lymphoedema is a dynamic process requiring ongoing research and implementation into practice; International collaboration is essential.

Benefits to People Living with Lymphoedema:
Patients are in the heart of all activities. Dedicated Patient Days are organised during the conferences. Free resources are available including materials with support of people living with lymphoedema. Read more here

Directories: Therapists/Medical Professionals:
Please find information about ILF’s National Frameworks who can advise on regional health care professionals here National Frameworks – International Lymphoedema Framework

Contact Details

International Lymphoedema Framework
Tel: +45 7020 0305
Email: info@lympho.org
www.lympho.org

How to LIVE BETTER with LYMPHOEDEMA

The new book by Matt Hazledine is available to buy NOW!

25% of pre-tax profits from book sales will be donated to the lymphoedema Research Fund.

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Sign up as a Free Member to receive Exclusive Benefits, including access to Articles and Videos from the Experts, a Unique Discount Code from the Suppliers, Members’ Offers and a Quarterly eNewsletter with the latest news from the lymphoedema community.

How to LIVE BETTER with LYMPHOEDEMA

The new book by Matt Hazledine is available to buy NOW!

25% of pre-tax profits from book sales will be donated to the lymphoedema Research Fund.

Become a member

Sign up as a Free Member to receive Exclusive Benefits, including access to Articles and Videos from the Experts, a Unique Discount Code from the Suppliers, Members’ Offers and a Quarterly eNewsletter with the latest news from the lymphoedema community.

Medical Advice Disclaimer

DISCLAIMER: THIS WEBSITE DOES NOT PROVIDE MEDICAL ADVICE

All material on this website is for informational purposes only and is not a substitute for professional medical advice, diagnosis or treatment.

Always seek the advice of your physician or other qualified health care provider with any questions you may have regarding a medical condition or treatment and before undertaking a new health care regime and never disregard professional medical advice or delay in seeking it because of something you have read on this website.

Reliance on any information provided on this website, by our employees and others appearing on the website is solely at your own risk.

For the avoidance of any doubt, Matt Hazledine has lymphoedema and is not a medical professional.