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MGUS Symptoms: What symptoms did you experience? - Mayo Clinic Connect It’s very comforting to know that other people have MGUS and to hear about their experience, but there is so much variation in the diagnosis and possible symptoms that it’s important for you to stay focused on what your physicians are telling you
MGUS with bone pain? - Mayo Clinic Connect While I don't have bone pain I do have other symptoms (tingling in toes, blacking out after bending over, and itching) I link to my diagnosis of IgG Lambda MGUS with an abnormal low light chain ratio Although my monoclonal protein was only 0 5, I was concerned enough about the low and trending light chain ratio to request a bone marrow biopsy
Always run down with MGUS - Mayo Clinic Connect Seems some drs dismiss alot of our symptoms being related to MGUS In my case, as I shared ,my fighter cells are very low, leaving me very susceptible to infection that the drs did say is from the abnormal cells crowding it out IMO, maybe that's why I get so tired, feeling run down I really don't know
Does anyone else have MGUS? - Mayo Clinic Connect I was diagnosed with MGUS last October and although I've done a lot of research, I feel there's still so much I don't know Does anyone else have MGUS?
MGUS and pain - Mayo Clinic Connect MGUS is considered asymptomatic and with a 1% year risk of progressing to SMM or MM However, there can be symptoms such as neuropathy in some people, especially if the MGUS proteins increase
Anyone with MGUS, do you have joint pain? - Mayo Clinic Connect @cass52, I moved your question related to MGUS and joint pain to the Blood Cancers Disorders group so that you can easily connect with other members with monoclonal gammopathy of undetermined significance (MGUS), like @gingerw @mommatracy5 @pmm @raye @omemee @gina5009 @mnmom1 and many others While we wait to others to join the discussion, you may be interested in these related discussions
Long term MGUS: What changes have you had? Dos and Donts? Hello everyone, You can call me Freespirit! I was diagnosed with Monoclonal Gammopathy of Undetermined Significance (MGUS) in 2021 Has anyone here had it that long? What changes have occurred? What can you tell me to do or not to do? Let's start from here Thank you
Newly diagnosed with MGUS and so anxious - Mayo Clinic Connect For MGUS there are no symptoms Calcium levels will be elevated but that is usually when bone lesions start or CRAB symptoms start which means MM which you do not have Rarely does MGUS evolve into SMM Then rarely does SMM evolve to MM it’s usually a slow process Having abnormal M proteins and or elevated immunoglobulins is the first indication of MGUS A baseline has been documented Now
Does anyone know of bruising as a progressing symptom of mgus to MM? If you have an illness pain symptom and have a name and diagnosis, you can move forward with treatment and a game plan or at least acceptance When you are told that MGUS does not cause symptoms, it becomes a never ending list of other doctor specialist appointments trying to figure out what is causing the symptom