I would like to thank all the people who have viewed this site to reach a 1000 views was beyond my expectations. Please if you have Lymphoedema join me on my Facebook page, Lymphwhatoedema. You will be able to talk to other people with the same condition. Help us spread the word about Lymphoedema.
L-W-O Community
For those living with Primary, Secondary & Paediatric Lymphoedema Online & in the Community
About
L-W-O (lymph-what-oedema) was founded by Gaynor Leech in September 2013. All the material on these web pages is set out in good faith. Thoughts and interpretations are mine. Every effort has been made to acknowledge sources throughout this website. I am not an expert or medical professional; I have lived with lymphoedema since 2011. However, I am passionate about raising awareness of lymphoedema and encouraging you to become your own advocate.
Terms and Conditions
L-W-O is a voluntary non-medical community. Our website does not host advertising. Our working partnerships do not influence our editorial policies. We receive no official funding and rely on donations to operate. Please help us keep this website running, you can make a donation at Go Fund Me Neither our founder nor any volunteer receives a wage. By using this website, you are agreeing to our terms and conditions.
Medical Disclaimer
Information on this website must not be relied upon as an alternative to medical advice from your doctor or professional health care provider. You should never delay seeking medical advice or discontinue medical treatment because of information from this website.
Lymphoedema exists we exist
© 2013 - 2022
