I'm about 2 months out from my last surgery, and it was the chillest recovery I've had. I had a bilateral salpingectomy; removing both ovaries and fallopian tubes. It was also laparoscopic, so I have pretty minimal scarring and I had very little pain compared to my other surgeries. My biggest issue was the wait time for the surgery, coming in at about 5 hours. That's mainly an issue because I had to fast at least 8 hours before. I'd ended up fasting 10, just because of the time I fell asleep the night before. So 15 hours of no food or water while stuck in a hospital room is a special kind of torment.
I had a follow up with the surgeon's office a week later, only to be told that it was supposed to be virtual when I showed up at the office. Nowhere in any of my paperwork did it say that it was supposed to be virtual and I wasn't told by any staff at the hospital either. They just told me the date and time. They were able to see me anyway, and everything was going well with recovery. In the end, I was glad they were able to see me in person though, because I got a lot of good information and resources for dealing with Menopause.
Which has lead to me continually being annoyed that no one fucking talks about menopause until it happens. Like, I would have liked to learn about this in a health class at some point. The symptoms are far more vast than "Oh, you get hot flashes sometimes," which is literally all I'd ever heard about it. My hot flashes have actually calmed down a bit, which makes me think that the Zoladex shots were causing them more than anything. What I have been dealing with is more psoriasis flare ups, which can be triggered by menopause, and EXTREME vaginal dryness and atrophy. Like, it hurts to walk around sometimes because of chafing. With those symptoms come decreased libido, painful sex or masturbation, and a plethora of other body and skin issues.
I was considered "lucky" that my cancer diagnoses was caught at an early stage and didn't require chemo or radiation. And I know that if I had to have those treatments, I would have been even more miserable. Still, I don't feel lucky and all of these changes are overwhelming. It's insane to me that every treatment for cancer ends up destroying the rest of the body. Listening to other accounts of breast cancer, I've heard a lot of people say that if they had to do it again, they wouldn't treat it. And like, I get it.
I guess objectively, I'm glad that I'm alive, and that I'll potentially not die in the near future from breast cancer. But I do wonder if it's worth the cost sometimes.
