Hi,
I am a 69 year old female. My primary doc casually told me at my checkup this last April that he would run a test to check on my MGUS. This was the first I heard of the diagnosis. I had a SPEP that indicated IgG lambda with 0.2 M Spike. The report referred to a 2008 test which was the same; so I did more digging into old records and retrieved some records from my clinic and the hospital. I found out that this dx was first made (as far as I can determine) in 2004. Hello, doc! It would have been nice to know this info.
I had a BMB done in 2004 to see if there was any detectable reason for my pancytopenia. The conclusion in the letter that I received said the pancytopenia was probably due to my injections of Betaseron for multiple sclerosis. This was when the first SPEP was also done but I wasn't told about it.
It took 12 years to finally get my MS diagnosis in spite of numerous symptoms and it annoys me greatly that I wasn't informed of the MGUS diagnosis. I spent a lot of time researching MS and I could have been researching MGUS at the same time.
One of my sister-in-laws has multiple myeloma and is just finishing radiation for a leg bone tumor. She had been in remission for 8 years. And my granddaughter's new husband has had a SCT for multiple myeloma.
Thanks, Kay
Forums
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Kay - Name: Kay Wilson
- Who do you know with myeloma?: SMM
- When were you/they diagnosed?: 2014
- Age at diagnosis: 72
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