L-W-O Community
Primary, Secondary & Paediatric
Lymphoedema
Online & in the Community
Promoting Lymphatic Health,
Self-Care
Patient Empowerment &
Community Engagement
Community Engagement
This is the L-W-O Community Engagement page. It's an excellent opportunity to educate guests about the backdrop, context, and history of the volunteer work I've done over the previous ten and a half years. I am aware that organisations in our community have historically been wary of collaborating with patient groups because they are very protective of the work they undertake.
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As the founder of L-W-O Community, I am passionate about community involvement because I feel that by collaborating with other groups, individuals, or organisations, we can do so much more as a team to educate, enlighten, and raise awareness about lymphoedema.
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Mary Fickling PhysioPod UK
One of the most fantastic aspects of my volunteer activities has been meeting new individuals. I have met some amazing people while managing L-W-O Community, whether they are one of our members or one of the many professionals in our community.
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One lovely person I became acquainted with in 2017 via Twitter is Mary Fickling Director of PhysioPod UK. Mary has been a big supporter of ours, sharing our posts, sometimes offering advice, and becoming a valued friend. We met first in 2018 and had fun at the MLD Conference in 2019. Read more about Mary, PhysioPod UK and learn about Deep Oscillation...
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The British Lymphology Society (BLS)
For the past four years, I've enjoyed writing articles for the quarterly BLS News and Views magazine, making movement videos for the EveryBodyCan campaign, and, in 2022, collaborating with Matt Hazledine to co-present at five workshops at the BLS conference with the topic ‘Understanding the Patient Agenda’, under the mentorship of Kate Sinclair, Lorraine Brown and Jane Board.​
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Patient accounts of the lack of assistance they believe they receive in controlling their lymphoedema are profoundly upsetting. However, I learned a lot from participating in these workshops, and it really helped me appreciate lymphoedema specialists' viewpoints, as well as the limits that their jobs impose on them and the emotional toll that this may often take on their mental health.​
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Based on the work we conducted before and during the 2022 conference workshops we then compiled two resource sheets which were launched at the 2023 BLS Conference during two speed sessions, titled ‘Frequently Asked Questions’ and ‘Tips Before You Attend Your First Appointment.’ Kate Sinclair, Yolande Borthwick, Lorraine Brown, Matt Hazledine, and yours truly make up the 2023 project workshop team. Prior to conference Karen Friett joined the team. Both sessions were a great success, with positive outcomes and it has been agreed that we will work together for a further twelve months with aim of presenting further information at the BLS Conference 7th – 9th October 2024 to be held at Chester Race Course, so do come an join us.
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Gaynor talking to BLS members at a speed session in October 2023 at the BLS conference held at Chester Racecourse.
Are you a member of BLS?
Join the UK's most dynamic organisation for Lymphoedema Professionals! BLS now has about 400 members. Nurses and physiotherapists make up the majority of the membership, along with doctors, occupational therapists, and manual lymphatic drainage therapists.
Membership is available to all healthcare professionals and anybody with an interest in lymphoedema and its treatment, so you, too, can join. Corporations and industrial groups also contribute to the growth of lymphoedema and the Society.
Or why not become a Friend of the BLS to receive their free Newsletter.
You will find details on how to become a member of BLS by clicking on this link:
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Jane Wigg Lymphoedema Training Academy
Jane Wigg is widely recognised as a key figure in Lymphoedema treatment and development, research, and teaching, and she is well-known for her desire to 'optimise treatment' for persons living with lymphoedema. Jane is director and lead trainer of the Lymphoedema Training Academy.
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The Lymphoedema Training Academy (LTA) is an International, multi award winning education provider, continually recognised for the vast improvements it has made in the world of lymphology.
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Mary Fickling and I, decided to ask Jane whether she would be happy to answer questions from L-W-O Community members as part of the LAW2021/WLD2021 campaign. However due to time restraints it was decided to reschedule this special strand until 1st August 2021, and I am thrilled this continued throughout 2022. You can watch all the 'Dear Jane' videos below. Either on our YouTube channel or on this our Dear Jane page.
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Matt Hazledine Lymphoedema United
I could never have predicted where my lymphoedema awareness journey would lead. I had no plan, and my social media skills were non-existent. My objective was to understand my lymphoedema, and if I could help one person avoid experiencing the doom I felt when I was diagnosed with this lifelong, incurable condition, that would be a bonus.
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Through my journey, I have met many people, and in 2018, at the LSN Conference (Lymphoedema Support Network), I was introduced to Matt Hazledine. He contacted me three years later to ask if I would contribute a chapter for his book, something I had not expected.
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Our journeys started around the same time I was diagnosed in May 2011 and Matt was diagnosed in June 2011, although our experiences with lymphoedema are quite different. We share the same goal of raising lymphoedema awareness through community engagement and patient empowerment.
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Matt and I have worked on various projects together, and we have both been part of the BLS Patient Project Workshop since 2022. In addition, I wrote a chapter for a second book that he and patient advocate Amy Rivera from Ninjas Fighting Lymphoedema Foundation collaborated on, detailing thirty-four heart-warming stories from all across the world. Matt also interviewed me on my lymphoedema journey which you can see on his YouTube channel.
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How to LIVE BETTER with lYMPHOEDEMA
Meet the Experts
Lymphoedema United
You are NOT alone!
Click Images to
Purchase
Check out Matt's website: Lymphoedema United
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The website provides information and guidance from a panel of medical experts, along with a secure place where people living with lymphoedema can unite directly with others, product providers and organisations.
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Patient Advocates for Lymphedema in Europe
I was originally approached to join the European Patient Advocacy Group as a patient representative in late 2019. This has resulted in collaboration with other patient associations throughout Europe, including the Lymphoedema Support Network from the United Kingdom.
Together, we created our first manifesto in March 2020, which has been repeated annually with a call to action to increase the profile of lymphoedema in the UK and Europe and was released on March 6th, World Lymphoedema Day. The manifesto is translated into the language of the patient association involved, and it has been a huge success and highly appreciated around the world.
Each year, we have expanded our activities. This year, alongside the paper manifesto, we launched a video version of the manifesto, with countries from Europe and the UK taking part. In addition, we issued a press release.
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To see the work I have been involved with the European Patient Advocacy group visit L-W-Os World Lymphoedema page
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You can also follow this group on Facebook
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Out in the Community
Teams and Zoom meetings have become a frequent part of my volunteer work, but I enjoy visiting people in the community and talking to them face-to-face rather than through a screen.
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Over the previous ten and a half years, I've delivered speeches to breast cancer organisations, attended conferences, and taken part in workshops. I have met many people from the UK and Europe.
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I've taken a variety of courses, including radio, public speaking, and working in the voluntary sector. In addition, I have completed numerous healthcare courses in order to improve my knowledge and enable me to write and speak about my enthusiasm for raising lymphoedema awareness. The material on this page is only a snapshot of how much effort has gone into the development of the L-W-O community.