First Pluvicto Infusion Soon
My husband will be getting his first Pluvicto infusion in October. I am trying to obtain as much information as possible so I am able to help him along this long journey.
I appreciate reading the comments about the radiation exposure. Needless to say my anxiety level is at the top of the scale. My main concern right now, though, is how to carry on with our lives between the fusions, knowing that thebimmunity system will be low because of the treatment. The pandemic forced me into more self isolation than I needed and I want to have us live our life between infusions rather than to take extreme precautions because of the low immunity. So, I am interested in hearing how you handle those weeks. I know everyone’s experience is different, but if he feels well and lab tests are ok, what kind of “normalcy” can we expect? What do you do between infusion appointments “
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I have just finished receiving all 6 Pluvicto treatments. I am the Pluvicto Poster Boy in that I have handled these treatments the best of all patients treated by my oncology center.
I would advise you to purchase a dosimeter (about $100 on Amazon) to monitor the daily changes in radiation levels. I would rather know what's going on and be proactive than just trust and blindly follow the advice of the oncologist. I took daily readings at arms length and on my body. My personal experience and take on it is the official guidelines of staying three feet away for three days, etc. are not enough, at least not enough for me who is very concerned about "collateral damage" to loved ones and caregivers.
Based on my personal radiation readings, done every day, I isolated myself completely for the first week after treatment, then allowed myself to be in the same room with others and brief personal contact (a hug, a handshake) but no pronged contact (no sleeping together). After two weeks the radiation half life did it's thing and was negligible. So for the next four weeks it was "normal life".
I didn't feel too bad during the treatment. The usual lack of strength and stamina. My most serious side effect was constipation.
My husband developed febrile neutropenia after his first round of chemotherapy (which was docetaxel years ago) and after that was given an OnPro device after each chemo infusion to inject white blood cell-building medications and prevent any further neutropenia. He has had NO neutropenia during or after his Pluvicto infusions. The Nuclear Medicine team at Mayo Rochester said that for most men, Pluvicto doesn't tank the red and white blood cells to the extent chemotherapy does.
Thank you so much! I will be following!! 🌸🌸
Thanks to all of the wonderful information I gained since my first post, I feel much more at ease as we begin the Pluvicto journey. I hesitate to post this, however, because it sounds so simple, but, I am in my “overthinking “ mode with this issue. At the risk of embarrassing here it is….. how did you handle the dishes during the 3 and 7 day periods. I know they have to be washed separately. Did you put them in the dishwasher after each use or accumulate them for a day and then wash them separately? I was thinking of buying paper products, but I am trying to eliminate BPA products, etc, which most of those have. Even without the BPA’s, there are other chemicals involved!
Any advice is appreciated.
We took no precautions regarding dishes. None of the nuclear medicine or urology providers at Mayo ever mentioned dishes, nor do any of the instructions or materials we have received mention such precautions.