Menu
header photo

Lymph-what-oedema

Primary & Secondary Lymphoedema Online & in the Community

Terms and Conditions

Welcome to the L-W-O website.  Please read our terms and conditions as the use of this website will be subject to them.

L-W-O stands for lymph-what-oedema however, will be known as L-W-O

  • L-W-O is an Independent not for profit organisation, accessible to any person who has Primary or Secondary lymphoedema or their carers, family or friends. The L-W-O website is written by Gaynor Leech who lives with secondary lymphoedema and is written entirely from a patients point of view. 
  • The information on this website is intended for use by UK residents.  
  • Our overseas visitors are welcome; however, we strongly advise all our visitors consult their own health-care professionals.
  • Material on this website is used for information only and is not intended to be a substitute for independent advice.
  • L-W-O accepts no liability in relation to typographical error.
  • We accept no liability for third party information.
  • The L-W-O website contains links to other websites.  These are provided as useful sources of information and inclusion of such links to other websites does not imply, endorsement by L-W-O, of any kind as to their content or quality.

Page produced by Gaynor Leech October 2016

Page last updated 11/06/2017

Planned review May 2018

Website is an ongoing project therefore, is being reviewed all the time