What are my chances that MGUS turns into multiple melanoma?

Posted by dtrgran59 @dtrgran59, Aug 5 3:26pm

What are my chances that MGUS turns into multiple melanoma
What precautions can I do?

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Profile picture for Patty, Volunteer Mentor @pmm

@ladyrose74 and Welcome to the Mayo Clinic Connect! What an exciting development for you! Do let us know what you find out.

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Thank you so much. I send positive energy to everyone

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Profile picture for Patty, Volunteer Mentor @pmm

@ladyrose74 now this is something that I was not aware of… Evidently there’s such a thing as a “transient M protein“ which seems to be associated with low levels of the M paraprotein cases.
https://ashpublications.org/blood/article/140/Supplement%201/2338/491379/Transient-M-Proteins-Epidemiology-Causes-and-the
Have you asked your hem/onc physician about this? What does he or she think?

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My M spike was low and somehow after 18 yrs nothing shows. I have a para protein. I’m sort of confused as I know I am slightly anemic . I had a bone marrow over 18 yrs ago and is what it showed. Now a few months ago my oncologist/ hematologist said on blood tests , no sign of M spike any longer. I have another spot in a few months.

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Profile picture for ladyrose74 @ladyrose74

My M spike was low and somehow after 18 yrs nothing shows. I have a para protein. I’m sort of confused as I know I am slightly anemic . I had a bone marrow over 18 yrs ago and is what it showed. Now a few months ago my oncologist/ hematologist said on blood tests , no sign of M spike any longer. I have another spot in a few months.

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May I ask what a transient M spike is? I’m also diabetic but I stay very thin, basically eat healthy and exercise and laugh a lot. I didn’t know it could disappear. I think maybe they made a mistake on blood tests. Lymphoma and Lukemia were in my family. I pray for me and everyone.

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Hello. I’m newly diagnosed with MGUS. I would like to know more about the disease and its progression and treatment.
Can someone tell me what 1g G Kappa means?

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Just got a red light therapy mat. Has anyone used a red light therapy mat?

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Profile picture for mlreptr @mlreptr

Just got a red light therapy mat. Has anyone used a red light therapy mat?

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@mlreptr
I have a red light therapy device that hangs from the wall (or could be put on a stand) which I originally ordered for painful plantar fasciitis that I had on my left foot for almost a year. I was complete amazed after a week how much better my heel felt and after 2 weeks the fasciitis was virtually gone so I am a big believer in this therapy. I used it directed at the bottom of my feet 4-6” away from the device for 10 minutes a day 5 days a week with 2 off. Consistency is the key and now I use it for my back-degenerative disc disease and hopefully for my MGUS but we are in the process of moving from Arkansas to Texas so I haven’t been consistent lately. My IGG and M spike lab markers were improved on my last blood test so I am hopeful this therapy will help in some small way. The device I use is called the Red Rush 400.

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Profile picture for ladyrose74 @ladyrose74

May I ask what a transient M spike is? I’m also diabetic but I stay very thin, basically eat healthy and exercise and laugh a lot. I didn’t know it could disappear. I think maybe they made a mistake on blood tests. Lymphoma and Lukemia were in my family. I pray for me and everyone.

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@ladyrose74 I found this Mayo Clinic publication where the transient M paraprotein is discussed.
https://www.mayoclinic.org/diseases-conditions/mgus/symptoms-causes/syc-20352362#:~:text=Experts%20don't%20know%20what,By%20Mayo%20Clinic%20Staff
It’s hard to know about lab errors or other anomalies. What does your hematologist/oncologist think?

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Profile picture for googi @googi

Hello. I’m newly diagnosed with MGUS. I would like to know more about the disease and its progression and treatment.
Can someone tell me what 1g G Kappa means?

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Hello @googi, and welcome to the Mayo Clinic connect. i see that you were recently been diagnosed with MGUS. Here is a Mayo Clinic publication that might be helpful to you. There are also many discussions on this message board that address MGUS if you search for them using the magnifying glass at the top of the page.
https://www.mayoclinic.org/diseases-conditions/mgus/symptoms-causes/syc-20352362
So what information did your physician give you about MGUS? Have you been able to speak with him or her since receiving your lab results?
You’ll find that we might be more helpful to you if you give us a little more context of your question. Do you mind doing that?

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