Lympha Press UK

Lympha Press UK Lympha Press® is clinically proven to treat lymphedema. Compression Therapy UK Ltd is the exclusive distributor of Lympha Press® Products in the UK & Ireland

For the treatment and management of Lymphoedema and Lipoedema. The Lympha Press is clinically proven to treat lymphoedema, vascular and circulatory conditions. It is the leading professional compression therapy in the USA and Europe and is new to the UK and Ireland. key features
➜ Delivers one of the safest decongestive lymphatic drainage massages.

➜ Lympha Press Compression Therapy offers a much needed advancement for medical management of Lymphoedema.

➜ Garment choice, suitable for treating individual limbs; providing bilateral arm, leg, torso, groin, genital and abdominal treatments. It is easy to use and extremely comfortable.

RePosted • Places are filling up fast for the Lymphoedema Conference. Have you booked your place yet?For more details...
04/09/2025

RePosted •

Places are filling up fast for the Lymphoedema Conference. Have you booked your place yet?

For more details or to book your place visit

RePosted • Lymphoedema Virtual Meet-ups – Northern Ireland & Republic of Ireland September 2025Living with is hard bu...
04/09/2025

RePosted •

Lymphoedema Virtual Meet-ups – Northern Ireland & Republic of Ireland September 2025

Living with is hard but you are NOT alone!

Register NOW for our Virtual Meet-up for Northern Ireland at 6pm on Thurs 18th Sept and Republic of Ireland at 6pm on Thurs 25th Sept 2025, via MS Teams.

Share your experiences and tips on how to live better with lymphoedema with locals.

Local friendships have been made for when you need a person that understands what you are going through.

Members only. It’s FREE to join https://lymphoedemaunited.com/free-membership/ with loads of benefits.

To register email hello@lymphunited.com

RePosted • 🌟FREE WEBINAR — Unmasking Lipoedema Hosted by the on their website!🌟📅 Tue 16 Sept 2025 • 2:00–6pm BST💻 Onli...
29/08/2025

RePosted • 🌟FREE WEBINAR — Unmasking Lipoedema Hosted by the on their website!🌟
📅 Tue 16 Sept 2025 • 2:00–6pm BST
💻 Online

✨ What to Expect:
A fantastic line-up of international experts and patient voices, discussing everything from diagnosis to the groundbreaking decision by the German Government to fund liposuction for lipoedema.

Speakers Include:
Professor Kristiana Gordon
Professor Manuel Cornely
Dr Mojtaba Ghods
Dr Gabriele Faerber
Dr Anne Williams
Dr Nicki Mazey
Lesley Steinitz PhD
Emily Kearney

This event is hosted by the Royal Society of Medicine. You don’t need a paid membership — just create a free RSM account and book your ticket in under a minute. Swipe the carousel for a step‑by‑step guide! Any questions... drop us a DM 😇

🔗 Link in bio to book.

Tag a friend or clinician who should be there. Let’s raise awareness, share lived experience, and push for better care for those with lipoedema💜

RePosted It’s almost back-to-school season, and the August Lymphedema Patient Roundtable brought their favorite things ...
19/08/2025

RePosted

It’s almost back-to-school season, and the August Lymphedema Patient Roundtable brought their favorite things for a show-and-tell of their personal must-haves for managing their . From and elevation pillows to moisturizers and massagers, the panel covered it all!

Attendees in the chat asked questions that prompted discussion on the different types of nighttime compression, tips for tolerating daytime compression, and the trial-and-error that comes along with finding what works for you and your swelling. The group also talked about practicing acceptance when living with a chronic and progressive condition, and how to adapt to new or changing symptoms without feeling discouraged.

Last but certainly not least, Catherine Rosenberg updated attendees on her recent progress with her wound. Thanks to a multidisciplinary approach to and Catherine’s own self-advocacy, her twenty-plus-month wound-healing journey has come to a remarkable conclusion.

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

Thank you to tonight’s panel:
💙 Karen Ashforth, MS, OTR/L, CLT-LANA (⁠⁠⁠⁠⁠⁠⁠⁠)
💙 Olivia Eggers, Lymphedema Patient ()
💙 Alexa Ercolano, Lymphedema Patient and Lympha Press Marketing and Communications Specialist (⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠)
💙 Angela Jones, Patient and Health Coach (⁠⁠⁠⁠)
💙 Catherine Rosenberg, Lymphedema 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!

RePosted • Most people call lipedema a “fat disorder.” But is that the full story? Here’s a different way to look at it...
18/08/2025

RePosted •

Most people call lipedema a “fat disorder.” But is that the full story?

Here’s a different way to look at it 👇

Lipedema isn’t just about fat.

Research shows it involves connective tissue, the lymphatic system, and blood vessels.
That means weak connective tissue (our body’s scaffolding) + sluggish lymph flow create the perfect storm for swelling.

When fluid sits too long in tissue, it triggers inflammation.
Fibroblasts lay down collagen → fibrosis develops.

That fibrosis weaves through fat cells, which is why lipedema fat feels nodular, painful, and resistant to weight loss.

Hormones (like estrogen), gut health, and diet all influence fluid retention and inflammation, but the root issue seems to be that missing scaffolding in connective tissue.

This is also why:

✨ Compression is non-negotiable (it’s our external scaffolding).
✨ Lymphatic exercises (walking, rebounding, vibration, MLD) help move fluid.
✨ Addressing gut health & inflammation makes everything easier.

💛 The takeaway: Lipedema is complex, and we’re still learning. But thinking of it as a connective tissue + fluid disorder that remodels fat over time makes a lot of sense, and it explains why compression is such a game changer for many of us.

RePosted • The Lipedema Roundtable is always full of interesting information and heartfelt sharing. This month ou...
15/08/2025

RePosted •

The Lipedema Roundtable is always full of interesting information and heartfelt sharing. This month our special guests will be Marti Klein from and

Posted • Lipoedema in the legs can affect different people in different ways. Do you see legs similar to yours in thes...
15/08/2025

Posted • Lipoedema in the legs can affect different people in different ways. Do you see legs similar to yours in these photos?

Share our post to raise awareness that not all lipoedema symptoms are the same for everyone!

For those who suffer with Lipoedema, please do take time to watch this webinar video (link below), featuring Dr Karen H...
13/08/2025

For those who suffer with Lipoedema, please do take time to watch this webinar video (link below), featuring Dr Karen Herbst, a Board Certified Endocrinologist and Lipoedema specialist physician, discussing her latest research into the important relationship between compression therapy and lipoedema, with members of Clinical Team.

If you would like more information on how to become a member of Lipoedema UK, please visit their webpage: www.lipoedema.co.uk

Webinar Link:

https://www.youtube.com/watch?v=1LqHYmIMuKg


This lovely comment was sent to us by an 88 year old female patient who has lived with primary lymphoedema throughout he...
04/08/2025

This lovely comment was sent to us by an 88 year old female patient who has lived with primary lymphoedema throughout her life. She has been using the Lympha Press for just over three years now, and, in her own words considers it ‘the best investment she has ever made’. You can tell by her words the difference it has made to both her condition and her life.

We endeavour to have an ongoing relationship with all of our clients, and we are always at the end of the phone should they have any questions, or need advice. The Lympha Press is a way of life, not a five minute quick fix. It truly helps everyone who uses it, and we know how much our clients will see, and feel, the change in their condition, as well as the positive impact it will have on their life, and it is this that makes us happy and drives us on.

The Lympha Press will help men and women who suffer with oedema issues.

For more information on the Lympha Press and how it can help you, or to chat over your options, call Naomi on: 01491 522 907 / email: naomi@compressiontherapyuk.com or log on to:
https://lymphapress.co.uk/contact/


The Lympha Press is a saviour for anyone who is suffering with Lymphoedema or Lipoedema, and we promise, that is not a s...
29/07/2025

The Lympha Press is a saviour for anyone who is suffering with Lymphoedema or Lipoedema, and we promise, that is not a sales pitch, it is a fact.

For those who don’t know, it was Naomi Northen-Ellis, Director of Compression Therapy UK, who discovered the Lympha Press, when searching for an effective solution to treat her own Lymphoedema. After trying it out for a couple of weeks, the results she got from it were so phenomenal that she wanted to make it readily available for fellow sufferers - and so that is exactly what she did. It is therefore so gratifying when we hear back from clients who have bought a Lympha Press and want to let us know just how much it has helped their condition. Here is just one example of the many messages we receive:

This lady is a 45 year old patient, who has been using the Mini Press Pump and ‘Comfy Arm Sleeve’ to treat her lymphoedema and pain after treatment for breast cancer
and chest lymphoedema:

“I am seeing great improvements [in my condition] and I am no longer in pain; it’s really like magic! I would recommend this to anyone who is considering investing in a Lympha Press Compression Pump.”

If you would like more information on Lympha Press and how it can help you, or to chat over your options, call Naomi on: 01491 522 907 / email: naomi@compressiontherapyuk.com or log on to: https://lymphapress.co.uk/contact/




Do you use bandaging in the management of your lymphoedema? Do you want to be able to safely and effectively self-banda...
22/07/2025

Do you use bandaging in the management of your lymphoedema? Do you want to be able to safely and effectively self-bandage?

If the answer is ‘yes’ to both of the questions above, then Fast’n Go is exactly what you need! It is an absolute game changer: a single layer hybrid bandage system that is so comfortable and so easy to use.

Find out how switching to Fast’n Go can improve the efficacy and comfort of bandaging at home by visiting: www.selfbandaging.co.uk

This YouTube video (link below), will show you just how easy self-bandaging can be.

https://m.youtube.com/watch?v=uXM4iEHsoEo

-bandaging

RePosted • By Your Side is our peer support programme where you can be paired up with one of our trained supporters, wh...
16/07/2025

RePosted •

By Your Side is our peer support programme where you can be paired up with one of our trained supporters, who have lived experience of lipoedema. Spend time talking about life with lipoedema, ideas for self-care or finding support in your area.

Our By Your Side programme is perfect for those newly-diagnosed or for those struggling with symptoms of lipoedema. You can find more details on our website, including details of how to sign up: www.talklipoedema.org/peer-support

This support programme is currently available to UK residents only.

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