The Lymphoedema Toolbox

15/12/2025

The aim of this survey is to: Gather information about how lymphoedema affects people's relationship with footwear Get valuable feedback on my concept for a shoe specifically designed for people living with lymphoedema Version en français / French version

15/12/2025

HELP NEEDED

IF YOU ARE LIVING WITH LOWER LIMB LYMPHOEDEMA THIS IS FOR YOU!!

We have been contacted by Thomas who is a first year design engineering student and has been working on an adaptive shoe concept specially designed for people living with lymphoedema.
He has prepared a survey (link below) on how lymphoedema has affected people's relationship with footwear, and feedback about his design.
Thomas has asked if we could share his survey, it would be really beneficial to his project. Thank you in advance to anyone who answers!

The aim of this survey is to: Gather information about how lymphoedema affects people's relationship with footwear Get valuable feedback on my concept for a shoe specifically designed for people living with lymphoedema Version en français / French version

13/09/2025

Zoë O’Sullivan, the creator of ‘Lymphia’, has been named as the National Winner for Ireland at the 2025 James Dyson Award

09/06/2025

Don't forget the ROI Virtual Meet-Up hosted by Matt from Lymphoedema United this Thursday the 12th June at 6pm.

To register your free place email hello@lymphunited.com

20/05/2025

Lymphoedema United are organising virtual meet ups across the UK and Ireland. Check out their website to see the dates for virtual meet ups. Register for the Republic of Ireland virtual meet up on the 12th June next by emailing - hello@lymphunited.com

06/03/2024

What are you doing to celebrate World Lymphoedema Day? Share your stories with us

11/11/2023

https://m.facebook.com/story.php?story_fbid=753619773472011&id=100064719860366

10/10/2023

New Book!!!!
Lymphoedema United – You are NOT alone! is on sale NOW from https://lymphoedemaunited.com/book/
34 guests from 14 countries, tell their inspirational stories, sharing personal experiences, challenges and Top Tips to help you to live better with Lymphoedema.

Living with Lymphoedema can truly be a very lonely place. So I hope you can find tips and knowledge in this book to help you on your journey with Lymphoedema and know that you are not alone.

I am truly honored to be part of this fantastic book and thank two wonderful advocates Matt Hazledine and Amy Rivera for allowing me to be part of this wonderful book. Check out chapter 17 😊😊
Order your copy at www.lymphoedemaunited.com/book/
WordzWorth publishing, Amazon and all good online bookstores

27/08/2023

Reduction in swelling after nights rest wearing Haddenham night garment.

26/08/2023

The joys (NOT) of having Lymphoedema.
You take a trip of a lifetime, mind yourself, wear garments, do all the self care things and still the swelling wins 😭

04/08/2023

Saw this on the Lymphoedema Support Network page. This really sums up our daily struggle with Lymphoedema.
Never give up Lymphoedema Warriors ❤️

This seems to sum up the daily journey with lymphoedema. Hope your weekend brings you some happy.