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hypermobility
![Relationships and Chronic Pain](https://jeanniedibon.com/wp-content/uploads/2023/06/Natasha-Lipman-Post-scaled-1.jpg)
October 11th, 2022
Relationships and Chronic Pain
I recently did a post about pain management. Someone raised the question on the post of ‘how can I communicate my pain to my partner effectively?’
Read more![What really happens when we lock our joints?](https://jeanniedibon.com/wp-content/uploads/2023/06/jdb-hypermobile.jpg)
August 22nd, 2022
What really happens when we lock our joints?
What happens when we lock our Hypermobile Joints? As someone who always stood with locked knees and picked things up with hyperextended elbows, changing this pattern was really important for my joint health.
Read more![Chronic Illness Exercise – Do you mourn your previous regime?](https://jeanniedibon.com/wp-content/uploads/2023/06/box2.jpg)
July 13th, 2022
Chronic Illness Exercise – Do you mourn your previous regime?
What’s your relationship with exercise? Has it changed over the years? Did a chronic illness diagnosis change your approach?
Read more![Has the exercise message been movement at any cost?](https://jeanniedibon.com/wp-content/uploads/2022/06/DSC_3454.jpg)
June 8th, 2022
Has the exercise message been movement at any cost?
Have you ever felt the message was ‘movement at any cost? I was speaking with a client recently who felt this was very much the message she had always perceived. We need to exercise, you must do it every day no matter what, even if it takes an hour or more. Regardless of how you feel or what the body is telling you. And if you don’t do them, you are failing or lazy. This is not the way forward. It is not healthy physically or mentally.
Read more![The Lonely Chronic Illness Life](https://jeanniedibon.com/wp-content/uploads/2022/06/DSC_3599-products.jpg)
May 19th, 2022
The Lonely Chronic Illness Life
Living with a chronic illness can sometimes be lonely. It can be difficult for friends and family to really understand how we are feeling and why we don’t ‘get better’. It drives me crazy when people say ‘you just need a good night sleep’ – like it’s a miracle cure.
Read more![What people don’t see when you live with a chronic illness](https://jeanniedibon.com/wp-content/uploads/2022/06/retreat3.jpg)
April 18th, 2022
What people don’t see when you live with a chronic illness
What’s it like when you go out out – if you do go out out? Is there a lot of preparation and organisation involved? I have friends who don’t have EDS or chronic illness. They fill their weekends with activities from morning till night – doing multiple things in one day. And they don’t seem that tired.
Read more![EDS UK Community Champion Award Winner](https://jeanniedibon.com/wp-content/uploads/2022/06/DSC4418.jpg)
February 17th, 2022
EDS UK Community Champion Award Winner
I’m super proud and delighted to receive the Community Champion Award fromy Ehlers-Danlos Support UK. Thank you to Anne Lavery and Nikki Casey Eds for a lovely day when I was presented with my award.
Read more![Living with Ehlers-Danlos – A Life in Two Halves](https://jeanniedibon.com/wp-content/uploads/2022/06/DSC_3564-about-1.jpg)
January 25th, 2022
Living with Ehlers-Danlos – A Life in Two Halves
Like many of us, I used to see my life in two halves. Pre motherhood, I lived with symptoms on a daily basis like muscular pain, daily migraines, digestive issues (diagnosed as IBS aged 12). I thought everyone had issues every day.
Read more![Hypermobility Flare-Up Management](https://jeanniedibon.com/wp-content/uploads/2022/06/DSC_3697.jpg)
November 18th, 2021
Hypermobility Flare-Up Management
Can we ever really be prepared for a flare-up? And when they arrive, how do we manage them? They can be as unpredictable as the rain. You dress for sun and a sudden downpour arrives. Sometimes we definitely know rain is coming and we can pack an umbrella but sometimes rain, like a flare-up, can appear when the sky seemed so blue. We just weren’t expecting it.
Read more![Feeling Accepted With A Chronic Illness](https://jeanniedibon.com/wp-content/uploads/2022/06/DSC_3564-about-1.jpg)
October 13th, 2021
Feeling Accepted With A Chronic Illness
When I attended my first EDS The Ehlers-Danlos Society conference in Las Vegas in 2017, around 50% of my clients had EDS and hypermobility with pain. I was kindly invited to speak by Lara Bloom CEO of The EDS Society. I had just released the first online hypermobility course, Strengthen Your Hypermobile Core.
Read more![Finding Your Range Hypermobility Podcast : Season 1 Overview](https://jeanniedibon.com/wp-content/uploads/2021/07/blog-photo-podcast-rotated-1.jpg)
July 18th, 2021
Finding Your Range Hypermobility Podcast : Season 1 Overview
Season 1 of this dedicated hypermobility podcast has ended, but we will be back in the Autumn with more amazing and inspiring guests. This was my first attempt at a Podcast, and I have absolutely loved every minute of it. I have had the privilege to interview zebras and experts at the top of their game.
Read more![The Impact of Hypermobile Knees](https://jeanniedibon.com/wp-content/uploads/2021/06/Create-Pilates-1015-colour-web-res-132.jpeg)
April 9th, 2021
The Impact of Hypermobile Knees
Hyperextension of the knees in hypermobility is common. I used the adopt the strangest of standing postures from simple knee locking to crossing one leg over the other or actually wrapping one leg around the other one.
Read moreThe Zebra Club APP
Hypermobility safe, affordable and effective movement, education and community in the comfort of your own home.
The Zebra Club app is a programme based on the Integral Movement Method. In this programme I will carefully guide you through safe exercises to manage your pain.
Learn moreOr download the App on
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