Looks like oxford vaccine (suggested strongly) that it will be passed 28/29 december ........ prof John Cambell health advisor....
Hurrah: Looks like oxford vaccine (suggested strongly... - NRAS
Hurrah
Yippee!
Well this man has been right the whole way through so fingers crossed. I would even think it should be passed under emergency legislation. .do look at ..........YouTube dr John Campbell excellent vaccine news
Excellent!
All sounding hopeful x
Just been looking on the US Creaky Joints website about vaccines for the immunosuppressed and it says both Pfizer and Oxford Zeneca ones are ok for the immunosuppressed and are not live vaccines.
Agreed! NOT a live vaccine but if worried check with docs!
Yes it's worth checking with your Rheumatology Consultant. The timing of when you have the vaccine within the RA medication cycle may be important. I would want only my Rheumy to tell me when that will be.
I would love to be able to speak to my rheumy nurse and/or rheumy re timing and how long needed to wait after Rtx but won’t be able to get in touch with anyone to ask. My GPs wouldn’t know and would admit that! I feel it’s going to be 6 months after Rtx ideally as that’s when your B cells start to repopulate, but await advice or probably read or hear it here before anyone contacts me from rheumatology. They are very slow at my hospital at the best of times.
I do feel some patients may get an NHS letter for the vaccine before they have received the rheumy advice on this. The rheumys are likely waiting for more advice themselves. Some RA meds of course will be straight forward.
Thank you. Hoping Rtx (B cell depleting) infusion patients can have this .. hoping all RA patients can.
Yeah be great to get advice officially.
If you look on the british rheumatology site there are specific there...but I think you still ask your doc .
Thank goodness 😀
I do think that cancer doctors, rheumy doctors and lupus docs and patients etc will all need advice on the ins and outs of the vaccines. They probably have a few weeks now to look at the data before it gets to the " shielding" folk. I cant see they would want everyone in these groups to talk directly to individually talk to each doc ! so my guess is they will make blanket decisions but will have to be soon !!
So I hope out patient groups like NRAS can pressure on our behalf for the answers to what the regime will be on specific drugs , very soon. ??