2025 SPONSORS

HEADLINE SPONSOR:

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Haddenham Healthcare is a company specializing in the treatment of lymphoedema and chronic oedema. Our focus is on providing problem solving solutions to assist therapists in treating their patients - helping them achieve clinical effectiveness and patient compliance. Haddenham have a wide range of innovative and unique products available on Drug Tariff – including the unique and UK patented Easywrap compression wrap and Microfine toecaps.

Click here to find out more about Haddenham

GOLD SPONSOR

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Juzo are a market leading Medical device manufacturer specialising in Oedema Management and Woundcare. We are recognised for innovation in both products and partnerships. We were recognised as an official crown supplier for COVID with our innovative www.juzoassist.co.uk.  This year we have 8 new bras, a whole range of cut and sew garments like ETO and a brand new set of trend colours.

Click here to find about more about Juzo

OTHER SPONSORS:

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H&R Healthcare Ltd is a UK based distributor with over 12 years’ experience supplying innovative and cost-effective medical products to the NHS.

We are proud to represent world-class companies in the areas of Advanced Wound Management, Infection Control, Compression, Lymphoedema and Innovations.

Come and visit us on our stand where you can find out about:

Bio Compression Systems - one of the leading global manufacturers of Gradient Sequential Pneumatic Compression Devices for the treatment of lymphoedema, venous and arterial insufficiency.  

Steve + - a device to aid the application and removal of compression garments for users with poor mobility.  

AndoFlex٠TLC - a two-layer, latex free compression system designed to manage leg ulcers and other related conditions.

Click here to find out more about H&R Healthcare

Patience Choice

Sponsor bio coming soon!

In the meantime, find out more by visiting their website.

Medical compression solutions for you!

Sigvaris compression solutions help you to go easily through your day. To feel strong and secure. They give you the comfort to do everything you want, and they cater to your way of life.

Click here to find out more about Sigvaris Group

THOR is an expert Photobiomodulation (PBM) company. PBM is a light therapy shown to reduce inflammation and pain wherever the beam is applied. Hundreds of RCTs and systematic reviews report that PBM reduces the incidence and severity of Oral Mucositis and is recommended in National Institute for Health and Care Excellence (NICE) guidelines. PBM is also effective on other Cancer Therapy side effects including breast cancer related Lymphoedema, head and neck lymphoedema and dysphagia.

Click here to find out more about THOR

Founded in 1847, Thuasne imagines, develops and manufactures medical devices allowing everyone to become actors in their own health. For 6 generations, the Group offers concrete, adaptive and innovative health solutions including Mobiderm for lymphoedema/lipoedema sufferers.

Mobiderm technology consists of foam cubes within pads, bandages and garments which promote lymphatic circulation and assist in the softening of fibrotic tissue.

Click here to find about more about Thuasne

IN ASSOCIATION WITH:

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The British Lymphology Society (BLS) is the foremost organisation for healthcare professionals involved in managing patients with lymphoedema / chronic oedema and those with an interest in the condition. It is a charity run by and for its members who share its mission:

To actively promote professional standards and the study, understanding and treatment of lymphoedema and its complications.

BLS provides a strong voice for members, offering peer support, resources and guidance to achieve high standards of care and equitable access to treatment across the UK, raise awareness of the condition, promote early detection and intervention with supported self-management. We work with other stakeholders, advise government, NHS and other professional bodies and organisations to effect change and influence practice.

Click here to find out more about The British Lymphology Society

Lipoedema UK are incredibly proud to be the first UK charity for Lipoedema. We are dedicated to raising awareness of Lipoedema, advocating better treatment and our aim is to generate medical interest in the condition leading to new research. Lipoedema UK Board consists of women with Lipoedema and clinicians working in the Lymphoedema clinic at St George’s Hospital in London and throughout the UK. Our work includes educating doctors, health professionals and the public about Lipoedema and its symptoms. It is shocking that a disease first described in the 1940s is still so misunderstood and misdiagnosed. Most women have lived with the condition for decades before realising they have it. Our aim is to put Lipoedema on the medical radar, tackle misdiagnosis and help women get access to the treatment they need, much, much earlier.

We aim to give factual information about the condition, advice on treatments and be a reliable source of information on the options available. We also understand how important emotional support is to cope with the everyday challenges that the condition creates. We have members of all ages from eighteen to 80. Our member’s conferences are a great way of meeting leading experts and making friends who understand your issues. Please support Lipoedema UK. It’s a herculean task ahead of us and requires substantial funding and effort. We would also like to hear your news and stories for our newsletter.

Click here to find out more about Lipoedema UK

The Lymphoedema Support Network is the charity in the UK that works to educate, empower and support those living with or affected by lymphoedema. Our helpline is there to answer questions, direct to further help or just listen. We provide information, written by experts and bearing the PIF Tick quality mark so you know you and your patients can trust it. Videos, website, quarterly magazine, local support groups, self- management book, GP education, we do all we can to ensure those living with lymphoedema live the best life that is possible for them.

Real people, real help, invaluable

Click here to find out more about The Lymphoedema Support Network