Connect
← Return to Does anyone else have MGUS?
Discussion
Blood Cancers & Disorders | Last Active: Sep 19 12:31pm | Replies (818)
Comment receiving replies
@spmreads1
Welcome to Mayo Clinic Connect. Cyroglobulenmia was new to me so I had to check it out. Like many other Members with MGUS, I also have Peripheral neuropathy. None of the accompanying symptoms such as rash. It sounds as though cyroglobulenmia is very rare.
Are you seeing a neurologist next go around or have you been referred to a hematologist/oncologist?
Replies to "@spmreads1 Welcome to Mayo Clinic Connect. Cyroglobulenmia was new to me so I had to check..."
Connect
I have seen a rheumatologist, neurologist, dermatologist, and now a hematologist. There are far too many ‘ologists’ in my life right now. Where is you peripheral neuropathy showing up? Mine is complete numbness of my left foot and partial numbness in my right. I originally went to my GP bc the numbness in my left foot was getting worse and moving up my shin. Then irregularities showed up
in my bloodwork and 4 doctors later, here I am.