The AVA A Vagus Adventure private facebook page (a great resource) has just announced funding for a feasability study on VNS for ME/CFS.
"We are HUGELY excited to announce that after several attempts at obtaining funding we have now been successful at receiving £109,520 from the Chartered Society of Physiotherapy to conduct a feasibility study investigating tVNS for people with ME/CFS!!
Absolutely BRILLIANT news!
PI – Dr Nicola Clague-Baker. Research team includes Dawn Wiley, Andrea Parker, Prof Helen Dawes, Prof Sarah Tyson, Karen Leslie, Dr Michelle Bull and Natalie Hilliard. Thank you to all.
We have a survey running at the moment for anyone with ME/CFS or Long Covid who has tried, or who is currently trying, taVNS. (tVNS via the ear) This data will guide our feasibility study so is very important.
https://www.physiosforme.com/tvnssurvey2
So please PLEASE do fill it out if you can
We have the chance to be part of something bigger here."
Well worth a look if you are interested in VNS for ME/CFS, fibromyalgia etc.
"We are HUGELY excited to announce that after several attempts at obtaining funding we have now been successful at receiving £109,520 from the Chartered Society of Physiotherapy to conduct a feasibility study investigating tVNS for people with ME/CFS!!
PI – Dr Nicola Clague-Baker. Research team includes Dawn Wiley, Andrea Parker, Prof Helen Dawes, Prof Sarah Tyson, Karen Leslie, Dr Michelle Bull and Natalie Hilliard. Thank you to all.
We have a survey running at the moment for anyone with ME/CFS or Long Covid who has tried, or who is currently trying, taVNS. (tVNS via the ear) This data will guide our feasibility study so is very important.
https://www.physiosforme.com/tvnssurvey2
So please PLEASE do fill it out if you can
Well worth a look if you are interested in VNS for ME/CFS, fibromyalgia etc.
![ME/CFS lecture | Dr Nancy Klimas | 2011 [Chronic Fatigue Syndrome / SEID / New Zealand] - YouTube](data:image/gif;base64,R0lGODlhAQABAIAAAAAAAP///yH5BAEAAAAALAAAAAABAAEAAAIBRAA7)
