Pain specialist physio & coach, special interests - ME/CFS, long covid & PoTS. Integrating compassion & yoga. Author-Dancing through Life:A Guide to Living Well
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-f…@thecsp
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-bo…
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 🧵 ...
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
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 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/lacticacids…
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
I’m running another embodied #rest workshop Friday this week 10.30-12, it was full & now there’s once space available (the video says 2 but ones already gone from posting on instagram/facebook earlier today). Would you like to join us? #yoga#yoganidra#nervoussystemregulation
I’m not using this platform much but do pop on now and then. You could follow my Facebook or Instagram pages. I have a YouTube channel which I’m hoping to add more content/resources to this year . Will link these three platforms in the comments in case they are of interest.
I’m running an embodied #rest workshop online on 13th Jan 3-4.30. The workshop includes a gentle #yoga practice, a #yoganidra practice (a form of #meditation that offers deep rest) and a little #reflection. It’s offered on donation a basis. More info linked in comments.
Our book has gone back up the physio book charts. People buying for Xmas maybe. Thank you to all. Let's hope this means an improvement in the care of all #pwme and #longcovid@PhysiosForME
A Physiotherapist's Guide to Understanding and Managing ME/CFS amzn.eu/d/98ivmqs