Hello, I thought as ‘MGUS’ is a commonly searched phrase on the forum that it would make sense for there to be a space for those recently diagnosed with MGUS/living with MGUS as while there over 4000 diagnoses every year, people can feel alone living with it and the worry that follows as a small percentage each year will go on to develop a blood cancer such as myeloma or lymphoma.
Do you have MGUS? Are you worried about the possiblity of it becoming a blood cancer? Have you had much support from your GP, friends & family?