Patients Prostate cancer
Posted on 12/5/19 10:25 PM
just had my Dr. visit a few days ago. My PSA was 0.01!!!!!! That is even lower than last month, and no Lupron shot! My PT hasn’t started yet. He increased my calcium and that helped a bit. I still have really bad days and some not too bad. Today is one of the bad ones. Been in bed most of the day and just ache all over.
I get a bit of relief from the pain meds. It that true for you too? I mean, not just the pain of the cancer but the aches of the therapy side effects.
I did get an Exgeva shot for bone strength, and the effects were like the Lupron. I read up on it and found out it can deplete calcium in the body. I added a supplement and my Dr. said I should have been taking it all along. He ordered some from the pharmacy plus vitamin D. Said it should help. Do you take any supplements that help?
Welcome to the neighborhood. Do you have your medical set up here yet? I wish you all the best.
Posted on 12/5/19 10:34 PM
just wanted to ask how old you are. You mentioned once you were skiing just two years ago. I am 71 and was walking 5 miles a day before Lupron. Seems so long ago....
Posted on 12/5/19 10:58 PM
Rich, I actually am staying with my Dr.s down in OC. My last PSA jumped up a little after a two months off my regular 4 month cycle. Went from 0.23 to 0.78. The meds help me with both the pain from the Lupron and the Mets. I am on 3 different meds now. The hydrocodiene, a generic for Soma and the ms.cotin. Still have bad days and tolerable days. Unfortunately, my Dr sent my scripts to the local CVS and my first experience has been really terrible. So will be trying the rite-aid. Hope that you have a better day tomorrow. Just getting ready to turn 68. My best. Jim
Posted on 12/5/19 11:10 PM
yes, getting pain meds these days is difficult. My first prescription was really a mess I was told they don’t stock anything and try a different pharmacy. I tried ALL pharmacies. In the end I had to wait a month for it to be filled. But once in the system, no problems ( so far).
Posted on 1/22/20 9:28 PM
My oncologists told me that there would be no pain from the Lupron unless the cancer had already metastasized. I agreed to try it and have not experienced any unbearable side effects during the one week since the first injection. The worst side effect is the constant fatigue, which keeps me in bed for 12 hours a day and yet I cannot sleep. I am very unhappy at the chemical castration effect of the drug. I decided to start calcium, tumeric and ginger supplements as well as a protein booster to counter the worst side effects I was told to expect. I am now ready to begin radiation. I was only offered one option, a nine week fives a week treatment.
So many people are given such different information and and offered different options. The copay for the Lupron is more than $550 every three months for each injection.
I have had more counseling on how to pay for the treatments than how to deal with the side effects. I have separate oncologists for the radiation and the hormone therapy. As with urologists there is an assembly line approach and each doctor has to be told of my concerns for my dignity, privacy and safety. Rachel Maddow observed that the doctor does not concern himself with compassion for the patient's pain and discomfort but focuses on destroying the cancer. When I was in labor management programs I partnered with a veterinarian student. When I asked him why he was taking so many labor relations courses he told me he could handle the animals but was concerned with difficulties of dealing with staff. I think this is the same attitude prevalent among many doctors. They focus on the disease and forget that they are dealing with sentient human beings who need information to make informed decisions about their bodies. The patient has to do the research to get information from doctors who only reluctantly provide information the patient desires and needs. I also have noticed a resentment from the doctor when I share information I have learned fro the web.
I would appreciate and help in dealing with this issue and if others are having thee same experiences with Lupron as I have had and what to expect next.
Posted on 2/3/20 7:37 PM
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Posted on 2/5/20 4:48 AM
Is there any treatment for cancer which does not involve slash, burn, poison and hormone therapy to make men into females>?
Posted on 2/18/20 5:46 PM
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Posted on 10/24/20 8:41 PM
Thank all of you who commented. It is important to learn from the experiences of others. You provide a real service in informing about the things the doctors do not concern themselves with and do not consider important. One of my biggest problems is that the time will come when they stop letting estrogens dominate my body and allow some male hormones to let me be a man.