Is there anything to help stop or slow progression of MGUS?
I am wondering if there is anything anyone is doing to stop or slow the progression of MGUS. I m recently diagnosed and have a lot to learn. My oncologist said there is nothing that can be done. Also could some of you share how long you have had MGUS. I am like I’m sure like all of you very concerned about my MGUS processing. Thank you.
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@dcuste, I noticed that you wished to post a URL to an article with your post. You will be able to add URLs to your posts in a few days. There is a brief period where new members can't post links. We do this to deter spammers and keep the community safe.
Allow me to post it for you:
- How I manage monoclonal gammopathy of undetermined significance https://ashpublications.org/blood/article/131/2/163/37011/How-I-manage-monoclonal-gammopathy-of-undetermined
And the link to the clinical trial you referenced:
- Curcumin and Piperine in Patients on Surveillance for Monoclonal Gammopathy, Smoldering Myeloma or Prostate Cancer https://clinicaltrials.gov/study/NCT04731844
Excellent points, all of which I think, I covered in my reply today! 🙂
Thank you for your response. I was born and raised in San Diego but moved to Arkansas in 1994. Sure miss the San Diego weather. Do you feel that NIR has had a positive effect on MGUS? How often and how long (minutes) do you use your machine? Do you use NIR and LLLT together? I have been using both. What type of MGUS do you have-IGM, IGA etc. And when were you first diagnosed?
Thank you @circawdm for your very informative post. So happy to hear from someone who has incorporated diet and holistic remedies with such positive results. Going from .8 down to .3 M-Spike is so encouraging to hear. My M-Spike was .14 at diagnosis in 2021 and is now .4 and my light chains and all other labs have been normal. I have IGM Lambda MGUS. Did your doctor recommend full body CT’s and bone biopsy? And if so, would you have done them? I called my hematologist’s office today and told them I want to hold off until after the first of the year to give me more time to think about this. I have had 6 CT scans in 5 years for other issues (all negative) and I am concerned about how that radiation can affect one’s body. Your story is inspiring so I value your opinion.
Hi 1oldsoul,
Great news for you! 🙂 The full body CT or a PET scan are both very expensive, and many insurance companies will not pay for them. My doctor never thought they were necessary with a low-risk patient who gets regular blood tests, has no enlarged spleen or liver, etc. Radiation overuse, as you noted, is not good for people with or without any type of cancer or in MGUS' case, "pre-cancer!"
I did have a bone marrow biopsy early on, which I would encourage, so they can see everything and get all of the genetic testing done, and also check for amyloid issues. I later also had a "fat pad biopsy" on my stomach, where in his office surgery area a surgeon specializing in biopsies made just a half-inch incision (after giving me just a local shot of Lidocaine), and then used forceps to quickly pull out maybe an inch of fat thru the incision, and cut it into 3 pieces to be sent to the lab to stain and see if there were any amyloid cells. Ammylodosis is nasty and hard to treat, so when I got a negative result from the Congo stain they used, I was relieved. It took 15 minutes or so and 3 sutures. It discolored/bruised a little for a week. After 4-5 months there was no scar at all. I would suggest doing that and the bone marrow biopsy (have it done in a CT scan bed so the doctor can see the best place to insert the needle). That took 10 minutes to numb things, an IV with a little fentanyl, and local Lidocaine. I felt a little pressure twice, but otherwise, it was no big deal at all.
The hospital had me stay in a "recovery area" recliner for 2 hours afterward, then home. Someone had to drive me of course. My hip muscle was sore for maybe 3-4 days. Otherwise, it was very straightforward. A few doctors do these in their office, which I would NOT recommend! You want to be somewhere they have the right equipment and other things in case they are needed.
That's all I got. 🙂 Feel free to ask any questions. Continued good luck with the MGUS!
Hi @1oldsoul, I read through a few of your earlier posts just so I could get a better understanding. You were diagnosed with MGUS a couple of years ago and your doctor suggested just to watch and wait. Which is very standard practice. For some patients, they never progress beyond the surveillance stage.
It looks as though followup blood results are showing a small upward trend in some of your numbers. It seems like our doctor is being thorough and recommending a few more tests run to see if there are any changes in your bone marrow and its ability to produce healthy blood cells. This would be helpful if there has been any possible progression to MM and as a baseline for future results for comparison.
What is your hesitation with having the tests run?
A year ago he told me that he didn’t think the MGUS would progress to Waldenstrom’s based off of normal light chains, IGM which didn’t seem very high to him and other normal blood work. He now said he wants a “baseline” but I am more concerned about the 2 full body CT scans more so than the bone biopsy because of the fact that I just had 4 CT scans in the past 2 years (other diagnoses) and I’m concerned about so much radiation when it seems other doctors want to watch and wait. I am going to contact him next month and see if he will agree to just do the bone biopsy first.