Hi, we have had an amazing few days in members group and now have 95 members. We are a very active online support group with some lovely caring members.
This week we have been talking taping, MLD, SLD, how to handle tropical conditions and the use of supplements. Very lively discussions. Please come and join us you find us on the following link;
www.facebook.com/groups/lymphwhatoedema
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.
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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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