Social network for people with long COVID and ME/CFS

[Psm92]

Hi all - Not sure if it's ok to post here, but after struggling with long COVID/ME/CFS for a few years, I've set up a social network site for others with these illnesses. Feel free to check it out.

https://nuracommunity.mn.co

Will have a look at that later. Thank you and I hope your site is a success!

Thanks I'll take a look.

Thanks so much both! It's relatively new, but there's new members joining every day and we'll be looking to host support spaces, and events with experts, etc.

Would love any feedback :)

Thank you, I'll take a look.