L-W-O Community supports primary and secondary lymphoedema by promoting emotional wellness, lymphatic health, self-care, patient empowerment, online and in the community.
We support those
living with lymphoedema. their families and carers
Programs and Services
Welcome to the L-W-O Community Programs and Services page. Here you’ll find clear, accessible information about the support we provide for individuals living with lymphoedema, their carers, and healthcare professionals.
Peer Support
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Online Support Group: A safe, moderated space to share experiences and connect with others.
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Community Group: Accessible discussions on self-care, treatment, and daily living on this website.
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Mentorship: Peer-led guidance for those newly diagnosed.
Resources and Guides
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Self-Care Information: Practical advice on compression, skin care, and nutrition.
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Educational Articles: Easy-to-read explanations of lymphoedema management.
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Visual Aids: Infographics and accessible diagrams to support learning.
Advocacy and Awareness
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Campaigns: Amplifying patient voices in healthcare conversations.
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Collaborations: Working with partners like PhysioPod, BLS, LSN, and lymphoedema organisations.
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Events: Participation in awareness weeks and conferences.
Creative Health Communication
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Poetic Health Messages: Blending creativity with clarity to make complex topics accessible.
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Accessible Content: Alt text, captions, and inclusive design for all resources.
Partnerships and Collaboration
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Healthcare Professionals: Proofreading and content support to elevate clarity and credibility.
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Community Organisations: Joint projects to expand reach and impact.
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Explore our Community Engagement Page to discover our partners and the projects we’ve collaborated on.
Upcoming Initiatives
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World Lymphoedema Day 6th March 2026
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Lymphoedema Awareness Month: 1st March - 31st March 2026
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BLS Conference Chester Racecourse October 2026
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Self-Care Week November 2026: Collaborative advocacy and community engagement.
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New Articles: Exploring eczema and its connection to lymphatic health.
How to Get Involved
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Join Our Community: Sign up for support groups and forums.
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Contact Us: Reach out for guidance or collaboration.
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Donate: Support our not-for-profit mission to empower patients.
Listed below is a list of our social media services.
On our primary support group, a warm welcome is awaiting you. With non-medical guidance and assistance, we assist people who have Primary and Secondary Lymphoedema. Please join us. To join, simply respond to our security questions.
You can gain more access to the expanding lymphoedema community by following us on X formerly Twitter.
The L-W-O Community's public face is where we share postings, articles, and research from the lymphoedema community.
Instagram is where we share our posters and videos and interact with people around the world who have lymphoedema.
Based on questions submitted by our members, our YouTube channel provides instructional films with advice and information for living with lymphoedema.
The L-W-O Community, whose concentration is on the lymphoedema community in the UK and beyond, is interacting with the business sector.
Do you have a question?
If you have a question about lymphoedema, fill out the form and we will see how we can help.
