Authors: Gaynor Leech, Founder of L-W-O and Sarah Bowring L-W-O Member
In August 2019 Sarah private message me after I asked her how she was coping knowing that she had been poorly with cellulitis.
Breast Cancer
Although Sarah and I have never met, we have often corresponded via our support g…
Author: Gaynor Leech, Founder of L-W-O
After a lovely long break, I will start to ease back into managing our community Monday 20th 2020 the break I needed for my own Wellbeing. In this first blog of the New Year I will set out our future.
There are three of our members stories I wanted to tackl…
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.
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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.
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