Highlights from the Myositis UK 2019 conference - Myositis UK

Myositis UK

1,264 members515 posts

Highlights from the Myositis UK 2019 conference

Jo-Goode profile image
Jo-GoodeAdministrator
2 Replies

Highlights from the Summer 2019 conference 😬 A fuller version will be in the next Myositis UK newsletter that goes out soon 😁

myositis.org.uk/2019/09/23/...

Written by
Jo-Goode profile image
Jo-Goode
Administrator
To view profiles and participate in discussions please or .
2 Replies
bon-bon profile image
bon-bon

Thanks Jo-Goode. I hope I will have the opportunity to read what the doctors have said about the clinical trials and updates for IBM. I get all my information from your site and the US site. Nothing is being done in Canada. I like your new forum and I get the updates in my inbox so I can follow along. I have a few friends in the UK. One I have met and the others are online.

Jo-Goode profile image
Jo-GoodeAdministrator

Worth keeping an eye on the Canadian Myositis organisation bon bon myositis.ca/

Not what you're looking for?

You may also like...

mistaken diagnosis

Hi I’m just wondering if myositis can be mistaken for PMR ? I am asking because 2 GPS say i have...

Anyone have Drug-induced Myositis?

Hi, I've had a diagnosis of MCAS (Mast Cell Activation Syndrome), but I had an argument with my...

Anyone get calcinosis?

I'm still VERY far from getting a diagnosis (thank you, NHS) and I'd have given up long since if it...

Steroids

Just started 60mg prednisolone this morning and will be taking a reduced dose over the next seven...

IBM people, please post

I have just found my way to the new site. I hope all those with IBM will as well. I miss your...