Prostate cancer and polymialgia
Posted , 5 users are following.
I was diagnosed with prostate cancer in April afternoon seeing my gp complaining of pains all over my body. Since then I have been having hormone therapy and will begin radiotherapy soon but my pains are getting worse. I had a Gleason score t3a so not too aggressive and the mri scan showed nothing abnormal so I went back to my gp for further tests and he told me that I may have polymialgia. I find this too coincidental so I researched a bit and I read that there is a link between metastatic cancer and the symptoms of polymialgia so now I'm confused as to why I genuinely am in extreme pain at times? Is it a missed diagnosis or is it just coincidence the two illnesses were diagnosed within weeks?
0 likes, 4 replies
richard98806 len51372
Posted
dennis63948 len51372
Posted
After the PSA test process I had to have an MRI to look for a lump, which may be cancer. Then a Biopsy to test for cancer. It was found and was graded at 7 (or 4+3) which is moderate. Anything less than 7 is normally treated as a watch and wait with regular PSA tests. Mine will need treatment.
If you have nothing abnormal then why are you having radiation treatment? If I was you I would ensure that I actually have a possible cancer first, that needs treating!
I have not seen a connection with Polymialgia but what you have, pain all over the body, sounds like the symptoms that a relative has for it.
Good luck.
len51372 dennis63948
Posted
I can only say that they told me the cancer was breaking through the walls of the prostate and so they could not be confident of removing it all with an operation. My original psa reading was 57 and I had two mri scans, one for the whole body and one for the pelvis.I also had a physical check and a biopsy like you
rich22 len51372
Posted
i try to be philosophical about it. as younger people suffer "growing pains" due to bones and body growing, old people suffer growing pains in reverse. after a night's sleep (waking every hour or two), eventually i get pains in the pelvic area. whether they're from diverticulosis or pelvic bone mets, i not only don't know but don't want to know. enough to deal with the 11 other health issues i deal with. but we all must find our personal comfort zone of how much info we process. good luck and prayers with you.
rich in reno