Not just one disease
This Page is being written
L-W-O Community
For families whose children live with Paediatric and Primary Lymphoedema
About
L-W-O 4 families is part of the L-W-O Community founded by Gaynor Leech in September 2013. All the material on these 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 medial professional: I have lived with lymphoedema since 2011. My great granddaughter has a lymphatic malformation. However, I am passionate as a patient advocate about raising awareness of lymphoedema, supporting families and encouraging families whose children live with paediatric and primary lymphoedema to become their own advocates.
Terms and Conditions
L-W-O is a voluntary non-medical community. Our website does not host advertising. Our 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 child's doctor or professional health care provider. You should never delay seeking medical advice for your child or discontinue medical treatment because of information from this website.
Lymphoedema exists we exist
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