Hi,
Have you met another person with Lymphoedema? Many of our group members haven't. Several had never talked to anyone with Lymphoedema.
I can't imagine having to deal with this on my own. Luckily in Nuneaton thanks to the Mary Ann Evans Hospice we have a lot of support. Setting up the online support group has least given our members someone to talk to that understand their condition and feelings.
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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