Lympha Press UK

14/01/2026

Lymphoedema after cervical cancer treatment is sadly more common than many realise. Studies show that in the U.K. approx 10% - 40% of people are at risk of developing lower extremity lymphoedema following treatment.

The Lympha Press Compression Therapy Treatment, has been proven, through clinical studies, to help support lymphoedema management, with those who are able to use it regularly, reporting continuous improvement in their mobility and in controlling the swelling, discomfort and pain that is a consequence of the disease.

if you would like to know more about how the Lympha Press can help you or to chat over your options, email: naomi@compressiontherapyuk.com or log on to: www.lymphapress.co.uk





lymphapressuk.com

06/01/2026

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By Your Side is available to UK residents and is free to access. Sign up for six phone calls to chat to one of our trained peer supporters who is here to listen, help and support you wherever you are in your journey with lipoedema.

Fill out the form on our website to get the ball rolling. All we ask is that you commit to the six phone calls to gain the full benefit of the service: https://www.talklipoedema.org/peer-support

LipoedemaCommunity Lipoedema

30/12/2025

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Kick off 2026 at our January Roundtables! 🎉 From research to real-life experience, our clinician and patient Roundtables offer education, support, and meaningful conversation.

Visit linktr.ee/LymphaPress and join us! Registration is free, and recordings are provided after the live event.

17/12/2025

17/12/2025

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Can you spot the key signs and characteristics of lipoedema?

Earlier this year, we showcased these posters at an event where over 4,000 healthcare professionals visited our stand to learn about lipoedema. 🍐

Help us raise more awareness in 2026, donate to Lipoedema UK via our link in bio🩷

04/12/2025

The impressive showing us how to warm up those muscles properly!

As an athlete Didi knows the importance of preparing her body before training and competition. The Lympha Press Optimal pump has a Pre-Therapy programme that opens and clears the lymphatics before switching into the main massage cycle. As with athletes like Didi, preparation is key to getting the best out of your daily Lympha press massage, either through the programming on the Lympha Press Optimal pump or with some easy opening and clearing massage techniques, based on the principals of SLD, before using the Lympha Press Mini Press Pump.

02/12/2025

RePost:

Lymphedema patient Philip W. shared that the results from his were “better than expected.” Not only did it bring meaningful relief from swelling, but it also helped improve long-standing wounds.

His words say it all: “Love it!” 💙

We’re grateful to support patients like Philip with effective, at-home . Discover more at
www.lymphapress.co.uk

25/11/2025

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Special Webinar Announcement! 🎉
Hear about the 2025 Lipedema World Congress 🌏
Thursday 4th December at 6:30pm 🗓️

Join us for an exclusive webinar where our team breaks down the latest insights from this year’s Lipedema World Congress, including key research topics and what they could mean for you.

We’ll also share exciting updates from our new connections with international patient associations and leading experts, and how global partnership is shaping a better future for everyone living with lipoedema.

💗 Want access to the webinar?
Become a member for just £25/year and support our work.

👉 Join via our link in bio 🔗

LipedemaAwareness LipoedemaAwareness PatientSupport LipedemaCommunity LipoedemaCommunity MedicalResearch HealthcareProfessionals WomenHealth PatientEducation

20/11/2025

ONE MORE DAY TO GO!
MEET THE MEMBERS!

For those who suffer with lymphoedema, and live within easy access of Birmingham,
you can still register for ‘Meet the Members’ which is being held at Birmingham and Moseley Rugby Club tomorrow, Friday 21st November, where
Lymphoedema United will be hosting a Face to Face Meet Up for its members.

WHAT TO EXPECT:
There will be an opportunity to engage in a question and answer session with those who specialise in the treatment and care of people with lymphoedema. A perfect opportunity to get answers to those important questions, to help you negotiate your way through the difficulties associated with the disease.

There will also be selection of suppliers exhibiting their compression products, all designed with a focus on making your journey with lymphoedema as comfortable and stress-free as possible, including our MD Naomi Northen-Ellis, who will be available to chat about her own experience of living with lymphoedema, and how her exhaustive searches for an effective treatment, led her to discover the Lympha Press and the benefits of pneumatic compression therapy massage.

You will also get the chance to meet other members of and it’s founder Matt Hazledine, who works tirelessly to not only connect people with lymphoedema to trusted medical experts and key product suppliers, but also to each other, creating a community where members can share their experiences, their highs and their lows with each other. To be a member of , is to be part of a ‘big family group’ where, in Matt’s own words: You Are Never Alone! If you are not already a member it really is worth joining - check the website for more information:
www.lymphoedemaunited.com
It is free to join - and there are many benefits.

If you haven’t already registered to attend tomorrow’s Meet the Members, you need to email Matt direct at:
hello@lymphoedemaunited.com

Hope to see you there!

18/11/2025

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18/11/2025

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The November Lymphedema Patient Roundtable was overflowing with gratitude as panelists and attendees discussed a range of topics, including managing during the holidays, the unique challenges faced by with lymphedema, and the importance of community support.

Guest Brittanee Wright shared her journey toward a diagnosis, highlighting how vital self-advocacy and a good support system can be when living with a chronic condition.

Then, in what’s become an annual tradition during the season of thanks, the Roundtable reflected on — the unexpected positives and personal growth that emerge through life with lymphedema.

Attendee Fenton summed it up beautifully in the chat: “I am grateful for the small victories each day… Lymphedema sucks, but life is grand!”

📺 Catch up on the November Lymphedema Patient Roundtable, now available on the Lympha Press website at lymphapress.com/roundtables

A warm thank-you to our panelists this month:
💙 Karen Ashforth, MS, OTR/L, CLT-LANA (⁠⁠⁠⁠)
💙 Alexa Ercolano, Lymphedema Patient and Lympha Press Marketing and Communications Specialist (⁠⁠⁠⁠⁠)
💙 Angela Jones, Lipolymphedema Patient ()
💙 Brittanee Wright, Lipolymphedema Patient

is proud to offer these monthly Lymphedema Patient Roundtables and support the lymphedema community.

📆 The Roundtables are held on the second Tuesday of each month at 8:00 PM EST. Sign up to attend any of our live webinars via the link in our bio!

11/11/2025

RePosted: i

Top Tip Tuesday #10 = Cellulitis

Do you have ? If so, you may be at risk of getting , a painful and serious infection.

If you’ve had Cellulitis once, you could be prone to further episodes if you have .

It is advisable to carry a Medical Emergency Pack, including a supply of antibiotics (especially when staying away) to use if you show symptoms.

For more information about Cellulitis, visit the website:

https://lymphoedemaunited.com/ information/cellulitis/