Anyone with pelvic pain after radiation for anal cancer?
Comments
-
I had that same reaction after radiation therapy, it was a dull aching pain and tightness in my pelvis and hip joint area. What works for me is stretching this has improve this alot.
2 -
I am starting my treatments in October, my main concern is my bones, I do not have strong bones, I have2 knee replacement, had my pelvic broken in 3 places, I keep hearing that radiation can affect your bones even crack them, have any of you heard that? I hope you are doing better now.
0 -
Stretching is so important for tightness and pain. As far as bone density is concerned, I've read that there can be issues later. I've had 2 bone density scans one after treatment and 5 years after. There was no change, but I take multivitamins and calcium supplements. Hope that helps.
1 -
Yes, they are called insufficiency fractures. Radiation can demineralize the bones πI just finished treatment and am trying to research what I can do to take the best possible care of my bones moving forward. Best of luck to you!
0 -
Wow guess I really am not looking forward to any of this, if I do not do the chemo radiation I only have 18 month with the chemo radiation I have 5 years or more?my bones are my main concern, I want quality not quantity.thank you for the information.ππ»ππ»ππ»ππ»
0 -
Hi Brenda,
I have both back and pelvic pain. The back is the result of deterioration of my lumber area bones due to treatment. Had a fracture of the sacrum but had glue/cement injected and that relieved the pain immediately. Doctors said that my bones are those of an 80yr old woman - I am 60.
The pelvic pain that I am experiencing is associated with the bladder. I started noticing really agonising pain in my pelvis. I realised that I needed to urinate and it was traumatic pain wise. I had a very full bladder and I didnβt sense the need to go to the toilet. The over extended bladder ached and it took me a few days to recover from the experience. I cannot stand for more than 20 - 30 minutes and if I last this long I end up feeling as if my insides are going to fall out! The only relief if I let it get this bad is to lie down. Oh and of course pain medicine.
I have found Tramadol works best for me. But as the pain worsens I need to increase the dose.
I will be having an MRI that looks at what muscles are being used when I pass bm.
I am learning to live with these changes in my body. Nothing seems as if it is going to get better so I manage the best I can. I have been cancer free since treatment in 2017 π΅π»
We are amazing creatures and we have a remarkable ability to adapt to our life circumstances. Pray π for courage and you will learn how much of our pride steals hope from us; you will also learn about being humble in a way you never knew was possible β€οΈ
1
Discussion Boards
- All Discussion Boards
- 6 CSN Information
- 6 Welcome to CSN
- 121.8K Cancer specific
- 2.8K Anal Cancer
- 446 Bladder Cancer
- 309 Bone Cancers
- 1.6K Brain Cancer
- 28.5K Breast Cancer
- 397 Childhood Cancers
- 27.9K Colorectal Cancer
- 4.6K Esophageal Cancer
- 1.2K Gynecological Cancers (other than ovarian and uterine)
- 13K Head and Neck Cancer
- 6.4K Kidney Cancer
- 671 Leukemia
- 792 Liver Cancer
- 4.1K Lung Cancer
- 5.1K Lymphoma (Hodgkin and Non-Hodgkin)
- 237 Multiple Myeloma
- 7.1K Ovarian Cancer
- 61 Pancreatic Cancer
- 487 Peritoneal Cancer
- 5.5K Prostate Cancer
- 1.2K Rare and Other Cancers
- 539 Sarcoma
- 730 Skin Cancer
- 653 Stomach Cancer
- 191 Testicular Cancer
- 1.5K Thyroid Cancer
- 5.8K Uterine/Endometrial Cancer
- 6.3K Lifestyle Discussion Boards