We are about to go to our first consultation with a bone marrow transplant specialist. We've been on CyBorD [cyclophosphamide, Velcade [bortezomib], dexamethasone] for the past 5 months, and our oncologist referred us over to Stanford to a BMT specialist.
We are still undecided whether or not we are going to go through with BMT, but I think it is a good idea to at least hear the opinion of a BMT specialist.
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Re: Anyone have a transplant at Stanford?
I have not yet had my transplant, but will be having it this summer at Stanford. I have met with Dr Arai. I am very comfortable with my decision and feel I am in good hands.
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KimT - Name: Kim Tank
- Who do you know with myeloma?: Me
- When were you/they diagnosed?: July 2013
- Age at diagnosis: 53
Re: Anyone have a transplant at Stanford?
Kim, How did the consult go? What types of questions did the doctor ask, did you ask?
Re: Anyone have a transplant at Stanford?
I had my original consult last summer, right after diagnosis, at which time she mainly went over the process. My doctor suggested going ahead with 6-8 months of chemo first. So we did that and did not schedule a transplant.
Well, after a recent BMB, I still have a large number of plasma cells in my bone marrow and my protein in my blood is still low (I have amyloidosis with kidney involvement), so a few weeks ago we talked to her about a stem cell transplant (SCT) and she was in favor.
I saw Dr Arai a couple of weeks ago. I had done my research and am well aware of what it entails. I also had a very good handbook on the procedure that they gave me last summer. This time she went into greater detail of the timeline.
I asked a lot of questions, mainly about how it would work with caregivers, and how long I will be restricted from some activities. I live just outside of the "safe zone", so I will need to stay near Stanford for two weeks after I am released from the hospital. It is inpatient for about 2 weeks, followed by 2 weeks staying close by.
Well, after a recent BMB, I still have a large number of plasma cells in my bone marrow and my protein in my blood is still low (I have amyloidosis with kidney involvement), so a few weeks ago we talked to her about a stem cell transplant (SCT) and she was in favor.
I saw Dr Arai a couple of weeks ago. I had done my research and am well aware of what it entails. I also had a very good handbook on the procedure that they gave me last summer. This time she went into greater detail of the timeline.
I asked a lot of questions, mainly about how it would work with caregivers, and how long I will be restricted from some activities. I live just outside of the "safe zone", so I will need to stay near Stanford for two weeks after I am released from the hospital. It is inpatient for about 2 weeks, followed by 2 weeks staying close by.
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KimT - Name: Kim Tank
- Who do you know with myeloma?: Me
- When were you/they diagnosed?: July 2013
- Age at diagnosis: 53
Re: Anyone have a transplant at Stanford?
Thanks Kim. Very helpful. I was actually expecting a month stay inpatient, 2 weeks doesn't seem to bad or too dangerous.
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