In February we will have a face to face session in a pub in Parrs Woods. This will be a joint session with Greater Manchester Long Covid Support as we have been asked by them if we can run some face to face sessions together for a few months. Date TBC
On 2nd Friday of the month ( 13th) we will have Cathy Gordon specialist physiotherapist talking about vestibular issues amongst other things. This will be followed at c. 12.05 with a short Special General Meeting to look at changing our name to “Stockport ME/CFS and Long Covid Group”.
We have just secured Jeanie De Bon to do a session for us on Tuesday 17th at 5pm on Zoom on hypermobility. She has a lot of experience as a physiotherapist looking at hypermobility as well as back pain. She is a renowned authority on hypermobility and EDS and is a recommended source by The Ehlers Danlos Association. She her website for more information.
We will also have ME/CFS and Long Covid adapted yoga each Monday at 2.30pm with Felicity Leigh. Please see the information in the January Activities post to see how to join in.
We will be reviewing whether there is sufficient interest in addition to our other meetings to host a Zoom social and if there is we will include details here. Usually this is a Tuesday or Wednesday evening at 8pm.
We have secured funding from Forever Manchester to run some events in 2026 and there might be additional events happening this month. As they are arranged we will update this post.
