Skip to main content

So Long Lady Parts

I am very grateful hysterectomies have changed over the last few years. I do not have to undergo the invasive surgical procedures many women before me have endured, including longer recovery times. Now it is faster, safer, and easier to recover.

Since I am always getting poked and prodded, it is comforting to think it will be easier and less painful. At this point, I have decided to get off my cancer medications, because I will have to get on a different kind after the hysterectomy, as I will be post-menopausal. I figure, I might as well get a few good weeks before having to take them again.

What's a Robotic Hysterectomy (& Oophorectomy - ovaries removed)?

During a robotic hysterectomy, your surgeon makes five small incisions in your abdomen to provide access for surgical tools. Through these incisions, your surgeon detaches your uterus, and for me, ovaries and fallopian tubes from surrounding tissues.

Image result for robotic hysteroscopy
Related image Related image

If you ever get a chance to watch one of these, it is pretty wicked and kinda gross. Seriously, it is a combination of sci-fi robotic arms handling the surgery and a bodily contortionist. Your head is literally down towards the ground and you abdomen elevated. You look like you're bent backwards. It is crazy (and kinda cool). Heck, I should be sore just from the way they moved my body.

I have actually put this surgery off for a while. I had considered it multiple times due to my cancer medication, Tamoxifin, side effects, but did not want to endure another surgery. I just had enough of being someone's pin-cushion. Now it was necessary, so it made it easier to go through what I figured would be painful... or just another medical surgery.


My surgery went great, my doctor is amazing. Now, I was going to have to spend the night. Of course, I can't do anything normally. I forgot how to breathe. Seriously, after the procedure, I was just happy to stay asleep... and in the low oxygen sleepy-land. I honestly forgot how to breathe... for real. They kept putting oxygen on me and telling me to take deep breaths.

I did not realize that I was continually slowing down. I remember thinking how calm and restful I felt... I thought I was cooperating, while I was really not cooperating.


Throughout the night and morning, I was slightly better. However, they were not willing to release me until I did those ball breathing things. By the way, I looked it up... it's called an incentive spirometer. I had no idea... I just know it was like exercise to get me breathing correctly. I kept holding that ball at a certain point every so often... which by the way sucked. I was like this is harder than it appears (and I am obviously a weakling). I am still not sure I did it enough or correctly, but eventually I got to go home.

The recovery time at home was really not too bad. It is only days before you can get back to all your regular activities. I was up and walking just days after. Little walks, leading to slightly longer little walks. However, the complete recovery takes from six to eight weeks. Meaning I will spend my summer outside of my pool... which is really stinks. I will get to watch everyone else use the pool, or I will avoid the temptation. I will miss my water exercise, as it is my main source of exercised during the summer and something I love doing.

What I am really dreading is getting re-acclimated to the menopausal symptoms...


Image result for menopause symptoms

Comments

  1. This is very interesting, You are a very professional blogger. I’ve joined your feed and look ahead to seeking more of your excellent post. Additionally, I’ve shared your web site in my social networks.
    hormone pellet replacement therapy

    ReplyDelete

Post a Comment

Popular posts from this blog

my longest hardest day yet

Get ready boys and girls... today is a doozy. And a long post too! But before we begin on one of the toughest days I've ever done, let's recap. Mon: Irritating Onc day where I was not told about suspicious fluid around lung/heart in time to get a biopsy & I got contradicting info from his NP the week before.  Tues: Spending the morning getting Immunotherapy and 2 Chemotherapies before going straight to the airport to fly to Houston and enduring long rental car lines and afternoon heavy traffic. A few more checks off this weeks list... a few more to go: Now back to my Wednesday... the Humpday I would like to forget! So, after 8 hours of cancer treatment, flying, and travel in congested Houston the day before, I didn't have much rest because we had to start Wednesday early. My husband and I decided to walk to the medical center since our hotel was close. However, it was not necessarily the easiest or closest walk - tons of traffic, intersections, and some strange indivi...

happy birthday to me... almost

  Let's rewind a bit and start a few days before my birthday... I had my first cancer treatment day on October 3rd - check it out if you haven't read that blog post yet. Let's just think of it as an early birthday gift since my birthday is October 7th. Great gift, right?!? If I have to hear "Happy Early" or "Late Birthday" from another medical person, I might have to smack someone. Especially, since I have spent most of the weeks leading up to and after my birthday at a medical appointment regarding cancer. Not really loving my birthday this year. Let's just say, on my birthday, I woke up with a special chemo-side-effect-surprise at 2am. That fun surprise I will share later... Rewind a Few Days... Update But first, let's go to October 4th, the day after my grueling 8 hours of immunotherapy and two chemotherapies on the 3rd. I woke up swollen, red faced, and fevering, as well as feeling pretty crummy. I didn't have time to dwell on it since I...

from chemo to pee to future rad things

Another week of doctor's appointments and my 2nd week of chemo is complete. I spent about 5-6 hours getting 2 chemotherapies (check me on picture to right, headed into treatment on a very early Tuesday morning). I am super proud of myself. It was a long day, and I have some issues with nausea so they have to push the chemotherapies a bit slower to help me out. And despite feeling pretty tired, right after chemo, I went to the Urologist... well actually his NP. I am not sure if the appointment was successful or not. Mainly, she just prescribed me medicine.  Why? Who doesn't want to hear about my pee issues?!? Not that I hold back from the insanity that revolves around my life and cancer. Plus, I think it is good to share that cancer causes crazy side effects - so others know they are not alone. For me, this cancer go-round, I happen to have bladder issues. My ability to hold pee is going haywire... mainly at night. Because why not? It's not like I don't already have enou...