Tried again Jo, but don't know where it went. Still says IBM (2) Guess it must be me.
Posting on IBM: Tried again Jo, but don't know... - Myositis UK
Posting on IBM
![bon-bon profile image](https://images.hu-production.be/avatars/58bf5ad10b6fa9e8a44d36bf86b471d7_small@2x_100x100.jpg)
Written by
![bon-bon profile image](https://images.hu-production.be/avatars/58bf5ad10b6fa9e8a44d36bf86b471d7_small@2x_100x100.jpg)
bon-bon
To view profiles and participate in discussions please or .
Not what you're looking for?
You may also like...
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...
IBM diagnosis today
Hi All. I have just been diagnosed with inclusion body Myositis and I am just overwhelmed by this...
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...
Could I have dermatomyositis?
Firstly let me apologise for the length of this. I know it's not a good idea to ask for diagnoses...