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April 18th, 2022 | Estimated reading time: < 1 minutes
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.
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March 21st, 2022 | Estimated reading time: < 1 minutes
Raising EDS Awareness with Bob and Brad
I am delighted to have teamed up with the most famous physical therapists on the internet (in their opinion of course) – Bob and Brad. If you know them, the theme tune to their famous YouTube channel is probably running through your head right now.
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February 17th, 2022 | Estimated reading time: < 1 minutes
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.
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January 25th, 2022 | Estimated reading time: 2 minutes
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.
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November 18th, 2021 | Estimated reading time: 2 minutes
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.
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October 13th, 2021 | Estimated reading time: 2 minutes
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.
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July 18th, 2021 | Estimated reading time: < 1 minutes
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.
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May 6th, 2021 | Estimated reading time: 2 minutes
Soft is the new strong in hypermobility
Soft is the new strong. This seems the total wrong thing – when we feel loose and disjointed, surely we should be bracing to hold it all together. I discovered that led to more pain and fatigue. So I went soft.
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April 9th, 2021 | Estimated reading time: 2 minutes
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.
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The 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
