
Unity Physiotherapy & Wellbeing
@UnityPhysio
Pain specialist physio & coach, special interests - ME/CFS, long covid & PoTS. Integrating compassion & yoga. Author-Dancing through Life:A Guide to Living Well
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My book ‘Dancing through Life: A Guide to Living Well’ has published today 😊 Here’s the link amazon.co.uk/gp/aw/d/B08P29… #livewell #wellbeing #compassion #health #communication #selftalk #exercise #movement #stressmanagement #awareness #mindfulness

Yes 👇🏻
What most autoimmune/inflammatory disorders have in common, including #POTS, #LongCovid, #MECFS, #MCAS and #EDS, is a high prevalence of GI dysfunction, including SIBO, IBS and GERD. No doubt that inflammation, autoimmunity and altered gut microbiome are connected.
Great piece on @BBCBreakfast Physios if you want to know more about working with people with ME visit our @PhysiosForME website Important to recognise that the type of pacing that is needed for people with ME is different to our usual approach physiosforme.com/resources-for-… @thecsp
physiosforme.com
Physios | Physiosforme
Resources for physiotherapists to help them manage people with ME/CFS
You can see the whole clip here: youtu.be/AuqthHADSWw?si… Thank you very much @ABrokenBattery for getting this video up so quickly.
youtube.com
YouTube
BBC Breakfast ME/CFS and Long Covid
First year anniversary of our book. So proud of what we produced.
A year ago today (after much hard work) our book was published. We've heard many accounts of people sharing it with their physios and positive feedback from lots of different professions. You can find out all the info on the book at our blog post physiosforme.com/post/our-book-…
V helpful and informative book. Got me started on my #ME journey.
The ME Association's Clinical & Research Guide (also known as the 'Purple book') If you'd like to purchase the guide (UK- £10), please click the following link: meassociation.org.uk/pbme #pwME #MECFS #MyalgicE #MyalgicEncephalomyelitis #PurpleBook #MEAssociation
So many issues including the big impact on the climate crisis
I still can't get over how bad AI has become. And this is coming from a computer scientist who spent over a decade studying and programming AI. I fucking LOVE AI, but here are 10 reasons I absolutely fucking hate it now, a 🧵 ...
If someone is bedbound with #longcovid & hospitalised, withholding urine bottles will not make them walk to the toilet. They will wet the bed. Withholding feeding will not make them eat. They will starve. Sometimes this job hurts my soul at the lack of human rights.#NHS
A thread of resources for physiotherapists and all Allied Health Professionals for #WorldMEDay You might work with someone with #MyalgicEncephalomyelitis in ANY specialism. 1. For those in specialist services, an in-depth book on understanding and management (with 25% off)
This Sunday is #WorldMEDay To mark the day, our publisher has created a code to get 25% off our book. Use the code "WMED25" at jkp.com Valid until 19th May

#WorldMEDay - we hear you, we see you, we do everything we can to advocate and support you. Wish we could do more. @PhysiosForME
This Sunday is #WorldMEDay To mark the day, our publisher has created a code to get 25% off our book. Use the code "WMED25" at jkp.com Valid until 19th May

This is a great book
This Sunday is #WorldMEDay To mark the day, our publisher has created a code to get 25% off our book. Use the code "WMED25" at jkp.com Valid until 19th May

Please contact me if you would like to get involved in this study. We know that some #pwME have high levels of lactic acid but there are no studies that identify what is normal during every day activity. We want to compare #pwme and healthy comparators. Thanks
🚨Now Recruiting "A pilot study to explore the everyday levels of lactic acid in people with Myalgic Encephalomyelitis and healthy controls" We are looking for 20 #pwme in N Wales, Liverpool, Manchester, Greater Manchester, Cheshire or South Lancashire physiosforme.com/lacticacidstudy
physiosforme.com
Lactic acid study | Physiosforme
Lactic acid study | Physiosforme
ME Research UK and the ME Association have announced funding for a study that aims to create a diagnostic test for ME/CFS using the electrical signature from a simple blood test: bit.ly/doreystudy

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