Follow Up with MO
Hello! I was wondering for those of you that have finished with treatment, how often do you follow up with MO, BS, RO? Being naive, I thought that after I finished up with treatment, I would follow up every six months. I am being asked to follow up with all of my doctors after three months. Is this typical?
Comments
-
Followup
Hi! I finished all treatment in October 2016 and so far I've seen my MO every 3 months. The RO released me in January 2017, and the BS after she removed my port in March 2017. According to my MO I will be seeing her every 3 months for the first 2 years. Not sure if this is typical either.
0 -
Booksandnumbers
Thank you for your response! I live in a different state from my treatment facility so I guess that I didn't realize that I would need to plan for follow up visits out of state every three months, but I will try to look at this as an opportunity for a mini get away every three months...
0 -
Yep
I only have two treatments left and my onocologist has already told me I would be seeing him every 3 mo. for the min. of 2 yrs. When my son was done with his cancer treatments (testecular), he saw his every 3 mo. for 4 yrs. and then it went to every 6 months for a couple of yrs and then one time a year for another 4 yrs.
It is very important to go.
Hugs,
Annie
0 -
Naive
Hi Annie-As I said above, I think that I was a little naive. I thought that after my treatment I would just return to my life as though BC never happened, and just have a mamogram every six months. Is it crazy to want to distance myself as far as possible from all things relating BC treatment??
0 -
3 months
I have been out of treatment now for 11 months. My follow-up appointments followed a 3 month schedule. Over the next 2 weeks I am going "on tour!" as I call it - tests and multiple dr visits. I am expecting that my next set of appointments will go to 6 months if everything checks out ok.
I felt the closeness of the appointments allowed me to bring up SE questions and regulate medication. I had an unusual reaction to AI that surfaced 2 months after I began . . . I was glad for the 3 month appointment so I could get started on sorting out options.
Kathy
0 -
Teach76
Thank you for your response! Again it is probably naive to think that there won't be SE! Everything happened really fast for me, so I think that I am still coming to grips with the fact that my life has been permanently altered.
0 -
oh no it is notmeschellejensen said:Naive
Hi Annie-As I said above, I think that I was a little naive. I thought that after my treatment I would just return to my life as though BC never happened, and just have a mamogram every six months. Is it crazy to want to distance myself as far as possible from all things relating BC treatment??
It is absolutly normal to feel like do. I am not even done yet and I am so over it!
Hugs,
Annie
0 -
Meschmeschellejensen said:Teach76
Thank you for your response! Again it is probably naive to think that there won't be SE! Everything happened really fast for me, so I think that I am still coming to grips with the fact that my life has been permanently altered.
I had another cancer 6 yrs ago, which was treated with chemomand radiation. It is the effects of radiation that are long lasting and the follow ups are important. I always felt relieved to see the doctors every 3 months And when I went to a year apart, I felt a little more uncertain. It took 5 years for me to start feeling back to normal. Now I have breast cancer just when I was getting my life back. I wonder if you could get a local oncologist to do the follow ups? Otherwise, your trips to Phoenix could be viewed as weekend jaunts with your husband and you could have some fun.
0
Discussion Boards
- All Discussion Boards
- 6 CSN Information
- 6 Welcome to CSN
- 121.9K Cancer specific
- 2.8K Anal Cancer
- 446 Bladder Cancer
- 309 Bone Cancers
- 1.6K Brain Cancer
- 28.5K Breast Cancer
- 398 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
- 794 Liver Cancer
- 4.1K Lung Cancer
- 5.1K Lymphoma (Hodgkin and Non-Hodgkin)
- 237 Multiple Myeloma
- 7.1K Ovarian Cancer
- 63 Pancreatic Cancer
- 487 Peritoneal Cancer
- 5.5K Prostate Cancer
- 1.2K Rare and Other Cancers
- 540 Sarcoma
- 734 Skin Cancer
- 653 Stomach Cancer
- 191 Testicular Cancer
- 1.5K Thyroid Cancer
- 5.9K Uterine/Endometrial Cancer
- 6.3K Lifestyle Discussion Boards