Want to talk about Multiple Myeloma: Anyone else?

Posted by Frazer 1 @frazer1, Apr 11, 2012

Asking anyone who is going thru this experience to share any pro's or con's of this disease. As of now I'm in MGUS, will find our next week if it has progress to Smoldering Myeloma.

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Profile picture for Angie P. @ancopau1998

Yes I have MM too. Will be 2 years in Feb 2022.

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Sister diagnosed with MM S3 recently. I am in the forum to learn and be support as she goes through this. Thanks to all of you for sharing

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My sister was recently diagnosed with MM STG 3, aggressive. This has been tough for all. She’s healthy otherwise with no symptoms from the MM. This was found on a routine exam. Doctors says it happened over short period no warning. She is going through chemo, injections, steroids and pills now. Possibly transplant later if chemo doesn’t contain it. 1) Any insights on how MM develops? 2) Are there blood test warning signs? 3) what can we as care supporters or expect as she goes through this journey of treatment? In other words, how can we best help?

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Not much! Gloomy day again. Was a bit depressed to see the upswing though am not sure what the numbers truly mean. At least tests are in should get my next set Revlimid l! Always a worry but hope now on track not to have problems within the tight turnaround time. I guess I am still just too impatient!!!!

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Profile picture for tml @tml

Sadly numbers are up a bit. Had a large drop the first month but the latest tests are back up some. Not sure how problematic this is but a bit depressed. Not sure if there is something else I should do or something else they can give me. I was taken off Darzalex so not sure if that had any impact.

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@tml Look at the trend, not a set of results in particular. That is what your team will be doing, most likely. And remember, this was only one round, right? Your system is getting geared up for the battle.

What are you doing today that will place a smile on your face?
Ginger

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Sadly numbers are up a bit. Had a large drop the first month but the latest tests are back up some. Not sure how problematic this is but a bit depressed. Not sure if there is something else I should do or something else they can give me. I was taken off Darzalex so not sure if that had any impact.

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A friend of my sister’s just had one there. First remission and already home after 17 days since did so well. Fine for her to get one despite having had heart surgery a few years ago.

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Only because Mayo said they would. I had an appointment with another doctor there after my Mayo appointment and their PA spent all the time explaining how hard a transplant was on the heart, etc.

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Profile picture for tml @tml

Lori, so you are back at Mayo!!! I hope all good news!!! I guess this is something done every few years? At least you have good music for that long commute. I guess mine would be a bit longer! I hope I get to that transplant phase. Now they would give me one here but I think not despite the travel issues!!’

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Yes, I am back at Mayo! But just for a day. ☺️ I’m on a 3 month schedule for follow ups to the clinic. For my Acute Myeloid Leukemia I needed stem cells from an unrelated donor, which is called an allogenic transplant. It can get a little complicated with side effects, so I’m checked quarterly at the clinic, sometimes with bone marrow biopsies or follow up tests to make sure the AML isn’t being sneaky. Every couple of weeks I have bloodwork done at my local oncologist. Those results are sent for Mayo evaluation.

I know you have quite a trip to get to Mayo for your transplant. I’m not sure what the followup appointments are like for your autologous transplant (using your cells). That will be an important questions for you to ask when you talk with the transplant doctor at Mayo.

I have to say, this has been the most amazing care I’ve ever had. The transplant team, doctors, nurses, all of them, are so attentive, compassionate and dedicated to ensuring my good health. So I know you’ll experience the same treatment if you choose to come here.

You mentioned that the clinic near you would now give you a transplant? What made them change their minds?

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Yes, have tried CBD. Hmm. Did not realize the impact of the break. I have to ask for the bloodwork numbers as are not automatically posted. Will get them on Thursday. It will be interesting to see them. I should pay more attention to them but often so many are high or low, depressing. Often I guess due to the drugs but still hard to understand if any progress.

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Profile picture for tml @tml

I hope I am on track not to miss any doses but will know in the next few days. I would not be so desperate to get to remission if I did not have the 24/7 issues with my t8. I have mild pain almost every waking hour. It isn’t to the level of taking pain medication but I never can feel totally well. I am not sure what can be done but apparently nothing until I am in remission. It just seems so interminable and now I am having the other issues of swelling and liver in top of that. I know I am lucky not to have had kidney damage. I was beginning to have issues around the time I was diagnosed but that happened before any damage was done. I guess if it is the Enoxaparin it may clear once I no longer am on it but not sure how long that might be. I sure hope that is the case. I was a bit disappointed that my IGG went from 1800 to 1317 but after this second round only to 1150. That is right in the middle of the range but not sure what significance that has. I know I need to be upbeat but hard for me since I was in such a good place last Fall and I blew it by not getting the second opinion then and with my constant reminder that I have damage. I know there is hope that I can get to the transplant so I should focus there. I so hope you can get to remission. It seems like the right strategy with the kidney issues. I guess not much we can do but see how it all plays out. That said, just one of my down days which will likely come every time I get to the Revlimid renewal window!!! At least while I am taking it I feel as if I am making some progress!!!

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@tml Check to see if you can use a warm compress, or massage in the T8 area where you have pain? Also, CBD cream applied topically might work for you.

Please do not beat yourself up for the hiccup in the road last Fall, okay? That is water under the bridge, now.

And as for the slight rash, that is really common. I had a more severe rash on my lower legs area at the beginning, Just used Vitamin E cream to clear it up, and make sure I keep the area moisturized well. My dermatologist wanted to give me a steroid cream, but "nope" from me! Remember, each time you get to the renewal window, your body is at its lowest point for red blood cells and all, so you may feel more tired, more emotional. It comes with the territory.
Ginger

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