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@Njc36 here you go

Thanks for this suggestion - it's a great idea and we will definitely reach out to them

We've developed some information that we are hoping to get used to help physios start thinking about PVFS and ME if involved in post COVID rehab https://www.physiosforme.com/covid-19 We are also finding that people are interested in hearing about ME on the back of COVID so we are trying our...

We are a group of physiotherapists in the United Kingdom with a special interest in Myalgic Encephalomyelitis ("ME"). Our aims are: - to educate and inform physiotherapists about ME and appropriate management strategies - to support people with ME to feel confident in seeking physiotherapy...

Absolutely - While we are really interested in the potential results, we must first find out whether it is acceptable to people with all levels of severity of ME to complete the testing procedures and if we can recruit to the study. We are very cautious about causing any detrimental effects to...

You're welcome! We've been working with the Chartered Society of Physiotherapy to try and use the opportunity of COVID to raise awareness It's really nice to get positive feedback so thank you

:);):banghead:

thanks for flagging - another letter to write!

We have written to them as well and it has been removed from there as well

Glad you like it!

Hoping our response should land with them tomorrow

thanks for the tag

We've had some dialogue on twitter with this group - will try and find out bit more and come back

HI there We did actually tweet about this a while ago What should happen and what actually happens are obviously not the same thing!

Yes, it is of interest - I have already skim read it and shared with the other three. More in depth read planned for this weekend! Thank you

You also cannot write to respond to articles published in this journal - we tried!

thank you

for the twitter feed of our response https://www.facebook.com/PhysiosforME/ for the longer version There is a lot more we could say but have tried to get over key messages that would appeal to our physio/OT colleagues who might pick this up

Thanks for highlighting this - we have been in email correspondence with the authors and were quite forceful back to them when they rejected our challenge about the need to highlight the difference for people with ME Will definitely get on this one ASAP

Are you able to point us in their direction? We'd love to make contact with them