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Does anyone else have MGUS?

Blood Cancers & Disorders | Last Active: 7 hours ago | Replies (764)

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@laurinea

They say there is no symptoms with MGUS but I totally disagree as it was my symptoms that made them do tests for the diagnosis. I definitely believe my neuropathy is due to the MGUS

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Replies to "They say there is no symptoms with MGUS but I totally disagree as it was my..."

According to the website mymyelomateam.com “A person living with MGUS can be expected to develop peripheral neuropathy .” I have read other articles stating the same and it has been the case with me as well, (diagnosed the MGUS in 2021) although mine is very mild and intermittent.