Hi Lili,
Sorry to be responding to this so late. Myeloma UK have just trained some peer-volunteers to assist on this forum. I am one such person and was treated for myeloma in 2019 with VTD and a stem cell transplant.
I am sorry to hear of your husband’s diagnosis, how is he progressing with treatment.
Regarding the NHS App, I have certainly found that information doesn’t flow as quickly or effectively across different arms of the NHS, so no harm asking around, but I’d recommend talking to your GP as they are (as I understand it) the point of registration for the NHS and everything relating to the Covid vaccination comes through them and not the haematology team.
I’ve been contacted in a timely manner about the first 3 jabs, but not heard anything yet about the 4th jab which is available for more vulnerable people in the UK, including those being treated for myeloma.
Do let us know how you’re getting on, the forum is having a bit of a blood-infusion of its own at present as Myeloma UK aim to make it a more active and useful resource.
Best wishes to you and your husband,
Rich 👍