This is a great idea M. I go to a group in my area, have done for years now..it was a life line for me especially in the early days when I didn't know anyone else with fibro, and knew little about it. Yes there is funding available and because fibromyalgia overlaps with other illnesses i.e depression, social isolation etc you can tap into those funds also.

They have groups run through rheumatologist but theh have limited places and are held in the hospital on weekedays. Not good for people who work and lets face it we are all sick of the inside of hospitals.

Hello,
I'm in Maryland, USA. Your idea sounds amazing. Being able to talk to people about what's going with you makes it easier. If I were in Scotland I'd join you.

Have you looked at the charity fibromylgia action uk?

Hi Michael, a few of us get together here in Toronto. It’s lovely
Here there is more access to alternative therapies as it is a large centre
That said I live in a condo lakeside, the streetcar runs by so makes it easier to get to appointments

Actually I’m amazed what is available in this neighbourhood within walking distance
Also the condo Corp has an active social committee which brings in community services, aid, etc.
So it’s going to take some homework and some digging but I’m almost sure a “club” meeting would be proactive. I used to work in a charitable environments and wrote grants to bring in services.
It takes research, but funding and sponsorship is out there
If you wish to brainstorm I’ll help.
Best to you,
Judy