New Books –
How to Live Better with Lymphoedema
&
You are NOT alone!
Lymphoedema United – You are NOT alone! Lymphoedema stories from around the world
Compiled by Amy Rivera & Matt Hazledine
Lymphoedema affects millions of people around the world, yet it is often a lottery whether the appropriate level of healthcare is received. That can leave a person living with this lifelong disease feeling desperate, neglected, and alone.
You are NOT Alone!
Advocates Amy Rivera and Matt Hazledine are joined by 34 people living with lymphoedema from 14 countries around the world, who share their personal experiences and top tips, to help you to live better with lymphoedema.
We pledge to support lymphoedema charities around the world, by donating a proportion of the annual pre-tax profits from this book, which we hope will continue for many years to come.
Thank you for purchasing our book. We hope you find it helpful. If so, please recommend it to others living with lymphoedema.
How to Purchase
Paperback available to buy from WordzWorth publishing, Amazon and all good online bookstores. Cost £25.00
A proportion of profits will be donated to Lymphoedema charities around the world.
Promotional Video
You can view our promotional video for You are NOT alone! via the QR Code below.
Please remember:
Control your lymphoedema, don’t let your lymphoedema control you.
Stay Positive, Keep Talking, Make a Difference.
You are NOT alone!
Promotional Video
You can view our promotional video for You are NOT alone! via the QR Code below.
Please remember:
Control your lymphoedema, don’t let your lymphoedema control you.
Stay Positive, Keep Talking, Make a Difference.
You are NOT alone!
How to Live Better with Lymphoedema – Meet the Experts
By Matt Hazledine
This book is for anyone who has, or loves someone who has, lymphoedema, a chronic and often debilitating lifelong disease that can have a detrimental effect on both physical and mental wellbeing. I wish I’d had a book like this when I was diagnosed with lymphoedema 10 years ago.
Matt Hazledine, founder of Lymphoedema United, shares his personal experiences and useful tips, plus authoritative information and guidance from over 20 medical professionals and experts, will help you to live better with lymphoedema.
With lymphoedema, knowledge is power and you will learn about:
- Finding the right therapist
- Help and support networks
- Self-management techniques
- Therapies, products & surgery
- Research to find a cure
How to Purchase
Paperback available to buy from Wordzworth publishing, Amazon and all good bookstores. Cost £19.99. Kindle; £9.99 via Amazon
How to Purchase
Paperback available to buy from Wordzworth publishing, Amazon and all good bookstores. Cost £19.99. Kindle; £9.99 via Amazon
Also available at Amazon and all good online book stores.
Whether you read the whole book in one go or turn to certain chapters that focus on specific subjects, this is a must have lymphoedema bible that can be referred to again in the future, when needed. 25% of the profits will be donated to the Lymphoedema Research Fund.
“I have known Matt for almost ten years now and can honestly say, I regard him as a compliant patient with the drive to make a positive contribution by helping others with lymphoedema.”
Professor Peter Mortimer MD, FRCP – Professor of Dermatological Medicine
“The fact that Matt lives with lymphedema (LE) was of particular interest to me. I am always looking for the leaders who will forge the changes needed before LDs and LE become global priorities.”
William Repicci – President & CEO, Lymphatic Education & Research Network (LE&RN)
Medical Advice Disclaimer
DISCLAIMER: THIS WEBSITE DOES NOT PROVIDE MEDICAL ADVICE
All material on this website is for informational purposes only and is not a substitute for professional medical advice, diagnosis or treatment.
Always seek the advice of your physician or other qualified health care provider with any questions you may have regarding a medical condition or treatment and before undertaking a new health care regime and never disregard professional medical advice or delay in seeking it because of something you have read on this website.
Reliance on any information provided on this website, by our employees and others appearing on the website is solely at your own risk.
For the avoidance of any doubt, Matt Hazledine has lymphoedema and is not a medical professional.