Newly diagnosed MGUS

Hi @Shelby and a big welcome to the forum.
I remember coming away from my diagnosis appointment (I have a different blood cancer) and having so many questions. I often think we need a follow appointment to ask these once we start to process the information that’s come as such a shock.
I know there are other forum members on here with the same diagnosis and I’m sure will share their experiences.
There are links below to some recent conversations around Monoclonal gammopathy of unknown significance (MGUS).
MGUS (monoclonal gammopathy of undetermined significance)
6 months after MGUS diagnosis -
I have also included the link to the I formation on the Blood Cancer UK website. Apologies if you have this already - I don’t want to overload you.
What is MGUS | Blood Cancer UK
I was wondering when your next appointment is. I would suggest writing all those questions down. And remember. The support line is there if you need it.
Never apologise for ranting (not that I think you are ranting). This is a space you can say how it really is for you.

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