Lympha Press UK

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

RePost •

18/11/2025

Repost •

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/

11/11/2025

RePosted:

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/

08/11/2025

The LWA worked so hard to stage an excellent conference this year, with experts sharing their latest research and findings around Lipoedema.

At Lympha Press UK we strive to share knowledge and unbiased reccomendations to surgeons and specialists, and it was great to spend time with Dr Corrado Campisi who has worked with a number of our clients.

07/11/2025

Lymphoedema United are hosting a Face to Face Meet-Up at the Birmingham and Mosely Rugby Club on Friday 21st November for their members, where you will also get the opportunity to meet Naomi Northen-Ellis, Director of Lympha Press, and learn more about how pneumatic compression therapy can help in the condition of lymphoedema.

If you are not already a member of Lymphoedema United it really is worth joining – check their website for information www.lymphoedemaunited.com

If you are already a member and want to register to attend on Friday 21st November please email Matt at hello@lymphoedemaunited.com

07/11/2025

We cannot emphasis enough the importance of buying medical grade pumps when investing in the self-management of your lymphoedema and lipoedema. Whilst medical grade products will be a little more expensive, Lympha Press products come with excellent after sales support and advice, a product warranty and of course, years of medical research and clinical studies. It is too easy to waste your hard earned money on a cheap product available on-line to find it really doesn’t work or may in fact worsen your condition because there is no guidance over use.

I had a message from a lady who tried the pump for almost 4 weeks a couple of years ago but never purchased after much messing about. This morning she cheerily told me she had bought a Pulsio pump and 2 leg sleeves that were great.

04/11/2025

We thought you would find this book interesting and informative.

It was written a few years ago by Ann Ehrlich and Dr Elizabeth McMahon. It has excellent reviews on Amazon, and, whilst things have changed a little since the book was first published, it is the voices of patients, therapists, and doctors sharing their personal and inspirational stories, that we thought would be most interesting and enlightening. Solutions to common problems and practical tips on self-care; Activities they enjoy and travel tips; Support groups and outreach to the medical community; Issues in treatment coverage, and more.

You will find ‘Voices of Lymphedema’ on Amazon £10.71. It’s also available as a Kindle book.

01/11/2025

People often ask us what improvement they can expect when using the
Lympha Press. The before and after images shown here, are a perfect example of what can be achieved.

This customer is in her eighties and suffers with lipo-lymphoedema. The ‘before’ image was taken when she began her Lympha Press journey in May 2022. The ‘after’ image shows her legs in May 2025. The improvement is quite stunning.

She likes to use the Lympha Press and full trouser garment daily, for one hour. Not only to continuously improve her Lipo-Lymphoedema, but also because she finds it a very relaxing and enjoyable experience, giving her the opportunity to take time out for herself. She also chooses to have an MLD massage once a week.

NB: Her legs are dimpled due to wearing her Mobiderm bandages whilst using the Lympha Press.

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/

30/10/2025