About us

T

he British Lymphology Society is a dynamic and innovative body providing a strong professional voice and support for those involved in the care and treatment of people with lymphoedema and related lymphatic disorders, including lipoedema.

Through support of its membership, the Society seeks to achieve high standards of care and equitable access to treatment across the UK, raise awareness of the condition, promotes early detection and intervention with supported self management. We work with other stakeholders, advise government, NHS and other professional bodies and organisations.
 
The Society was established in November of 1985, originally as the British Lymphology Interest Group (BLIG). 

 

Our aim of promoting professional standards in lymphoedema care and treatment is supported by our objectives:

 

  • 1) To advance education and knowledge in the field of lymphology and related subjects.
  • 2) To foster interest in and co-ordinate a strategy for improving the management of chronic oedema, particularly lymphoedema.
  • 3) To produce and maintain a register of specialist centres in the United Kingdom and Ireland.
  • 4) To benefit patients by improving the knowledge, expertise and skills of health care professionals  treating them

As a charity we rely on the support of our members and our sponsors to continue to drive improvements in care and service provision. If you are interested in becoming a member of the society please visit our membership area.

Our Working Groups

Our Working Groups

To address specific short-term projects, BLS brings together working groups with agreed Terms of Reference, aims and a work plan. BLS members with a keen interest in contributing to the project may request to join the group.
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Our Scientific Commitee

Our Scientific Commitee

The scientific committee includes doctors, therapists, academics and researchers all with a keen interest in research. It comprises full and honorary members.

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Our Patron

Our Patron

Professor Peter Mortimer is an Honorary Member of the Society. He has been a significant influence in the field of lymphoedema, being one of the founding members of the Society in 1985. He has contributed greatly to our understanding of the condition
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Our Members

Our Members

BLS membership is multi professional, comprising nurses, physiotherapists, doctors, occupational therapists, manual lymphatic drainage therapists, others with an interest in lymphoedema including its treatment and corporate members.

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Our Regional Representatives

Our Regional Representatives

Regional Representatives are members of BLS who undertake to facilitate networking of members in their area. They are key advocates of the Society who make a valuable contribution to enhancement of communication and liaison between local members.
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Support Us

Support Us

As a Charity donations and fundraising are vital to support our work; there are many ways to help us to make a difference for people with lymphoedema.
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Our Trustees

Our Trustees

Our Trustees are BLS members, elected and supported by members to work on their behalf and ensure the legal and governance requirements as a registered charity are met.
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Code of Conduct for Healthcare Support Workers and Adult Social Care Workers in England

As a Healthcare Support Worker or an Adult Social Care Worker, you make a valuable and important contribution to the delivery of high quality healthcare, care and support. Following the guidance set...

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Conference Program 2017

Conference Program

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LYMPHOEDEMA RESEARCH GRANT APPLICATION: PART C

Part C

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LYMPHOEDEMA RESEARCH GRANT APPLICATION: PART B

Part B

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LYMPHOEDEMA RESEARCH GRANT APPLICATION: PART A

Part A

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Proforma For BLSCC Applicants (2013)

Application form for membership of the BLS SC

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BLS Scientific Committee Terms Of Reference 2016

Terms Of Reference For The BLS Scientific Committee 2016

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Chronic Oedema - Lymphoedema

Consensus Statement on the Chronic Oedema – Lymphoedema Interface

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