- Joined
- Aug 4, 2019
She needs a KF account.
Megathread SRS and GRS surgeons and associated horrors - the medical community of experimental surgeons, the secret community of home butchers
- Thread starter cuddle striker
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- Joined
- Jul 16, 2023
I am genuinely glad this dude is alive though he will probably suffer for the rest of his life
- Joined
- Dec 15, 2022
He was better off burning that money. That male belly button placement is unmistakable.
He thrills when he drills a bicuspid.
Surely a man with a high probability of psychopathy who specializes in cutting off the breasts of teen girls couldn't be doing it for sexually deviant reasons, right?
>giving an Indian burn to your fake dick
Girahira
kiwifarms.net
- Joined
- Dec 25, 2023
- Joined
- Jul 24, 2017
A woman who is so mentally ill she cant even hear or type the word vagina managed to get a full hysterectomy and her vagina burnt out. She is 6 weeks post OP and, (I know you'll all be shocked to hear this) it's not going well.
Text under spoiler
Who needs to be able to piss anyway?
Text under spoiler
I had a total transvaginal hysterectomy + partial vaginectomy (I am including these terms solely for people using the search function. These terms give me dysphoria to use. This is what I will refer to as my stage 0 of phallo and v-ectomy [as sparingly as possible] for the remainder of this post) on May 16th, 2024 with Dr. Anna Kirby at the University of Washington Medical Center - Northwest. For more background information up to post-op day 8, take a look at my profile for the previous post I made. Potential TW for anatomical/medical/surgical talk. Apologies in advance for the wall of text. Feel free to ask any questions in the comments or through DM. :-)
After making my previous post, things went kind of sideways for me. I was peeing about 50-100mL every 30 minutes, and my bladder was becoming increasingly painful every time I went to the bathroom. I could tell I wasn’t close to fully emptying my bladder, but I was hopeful that my body would just figure it out. I did try peeing with force (even though I knew I wasn’t supposed to) which didn’t really help and made my bladder hurt even more. I tried to catheterize myself which went horribly - the catheter kept slipping into the surgical site and made me bleed, and I was extremely panicky. With all this, I ended up going to my local Kaiser Urgent Care at midnight. I chose to go to Kaiser instead of UWMC because I was afraid of getting a very large emergency room medical bill if I were to go to a hospital out of network. When I eventually got roomed, the doctor contacted urology to insert another foley catheter. The urologist said he could tell my pelvic floor was spasming like crazy even when he was just cleaning the area before inserting the catheter. He said I would likely just need to keep the foley catheter in longer to allow my pelvic floor to heal. They also extended my course of antibiotics (Bactrim) due to my urine culture from earlier that day coming back positive. I was also having intense bladder spasms with the new catheter, so they prescribed oxybutynin which really helped (and made my mouth intensely dry). Despite the nurses and doctors at Kaiser having very little experience with this particular surgery, they were all very respectful and did their best to help me out.
I was not thrilled to have the foley back in, but at least my bladder was no longer in pain and I wasn’t getting up every 30 minutes to go pee. During my last clinic visit, because I was having all the bruising on my butt and I barely passed the void trial, they had set up an appointment for me to actually see Dr. Kirby the day following Memorial Day. She was bummed that I had to go to the emergency room. She was not concerned with the bruising on my butt. She inserted a finger into my rectum to check for an internal hematoma, and said she thought she felt what might be a small hematoma which could be interfering with my ability to pee normally. I asked her what the timeline would look like for my bladder returning to normal and she couldn’t really give me an answer - she said a majority of patients are able to pee fairly normally by this point (post-op day 12), so it was really just a waiting game. When asked what my preference was, I told her I would like to keep the catheter in until my 4-week post-op clinic visit because I really did not want to go through getting another catheter inserted. She said this was reasonable, but if I wanted to try removing it sooner I could just contact the clinic.
Since having the foley reinserted, recovery was going pretty well. I had more energy, I was staying awake for longer periods of time, I wasn’t in much pain, I was moving around the house more easily. I was feeling so good that on post-op day 15 I decided to take a walk outside for the first time since surgery. It was slightly painful internally, but I went nice and slow, and it felt really nice to get out of the house and to stretch my body out. The next morning, I noticed that every now and then my urine from the catheter was slightly pink-tinged, but I was not concerned since it cleared up when I drank water. Later that day, I went to the mall for a little bit and walked around slowly and gently. I was having some pain, but nothing more than just wanting some Tylenol. However, when I got home, my urine had become a much darker pink/red color. I wasn’t having any other concerning symptoms, so I messaged a doctor online through Kaiser’s website (since it was a Friday evening), and they recommended going to urgent care.
I was on the fence about what to do since I was feeling relatively fine and didn’t really want to waste my evening in the emergency room. Then as I was sitting in the living room, I had the most intense pain of my life in my lower abdomen. This was true 10/10 pain. I’ve never experienced anything like it. I inched my way to the couch to lay down, and had my mom bring me the heating pad and oxycodone. My gut told me that this pain meant it was time to go to the emergency room, and that this time I should just go to UWMC - NW since that is where I had my surgery, even if it meant a big bill (it only ended up costing about $250 thankfully). Once the oxycodone kicked in, the pain subsided a bit, but my urine was very red despite how much water I had drank. When I finally got roomed, the doctor ordered some blood tests to make sure I wasn’t bleeding too much, a urine culture to see if this was being caused by another infection, he looked at my bladder using a high-quality ultrasound machine, and he irrigated my foley to make sure it wasn’t clogged. All of my blood levels were normal, the urine culture was totally clean/negative for an infection, the ultrasound didn’t reveal anything beyond a little bit of swelling of my bladder wall, and the catheter was not clogged. This doctor said the bleeding was likely from the balloon of the foley catheter rubbing against my bladder. He also paged the on-call doctor (Dr. Fialkow) for Dr. Kirby’s specialty, and he messaged me directly through MyChart which was sweet of him. We set up a clinic visit for the upcoming Tuesday. It was nice to determine there wasn’t some bigger problem, but I was still in excruciating bladder pain and was dependent on oxycodone every 4 to 6 hours. The pain was so bad that it woke me up from sleep a handful of times. I stayed as still as possible for those 3 days to avoid triggering any more excruciating bladder pain. The oxycodone made me very depressed/sui***al, but there felt like no other option until the clinic visit.
When I went into the clinic, they posed teaching me how to irrigate the catheter myself, but I knew that wasn’t going to help my pain. The only thing that was going to help was removing the catheter all together. Dr. Fialkow was on board with this plan, so we went through the void trial process, and yet again I was only able to pee out about half of what they put into my bladder. I went home without a foley catheter and it hurt my bladder to pee, but at least I didn’t have a UTI anymore so I didn’t feel the urge to pee quite as often. For the next week, I could tell I wasn’t fully emptying my bladder, but it wasn’t getting to a point where I felt like I would need to go to the emergency room. They taught me how to catheterize myself again, but I was never able to do it successfully. My bladder ached quite a bit every time I peed for about a week, but it slowly faded. I could also tell my bladder was no longer distended, meaning I was peeing out everything that was building up in there, and my bladder was returning to its baseline.
Once the bladder pain mostly resolved, I was quickly back to my regular life. I was walking plenty, getting dinner with friends, sitting at my desk, standing for long periods of time, all with no issues beyond some fatigue. I’m just about 6 weeks post-op and am feeling great. I stopped needing to wear pads a few days after having the catheter removed. I’ve returned to the gym (light weights and only upper body for now) and will be returning to work this week. I had an appointment with my PCP and my hormones are all within normal range/no major changes from previous level checks. It’s been a very bumpy road to get to this point, and it felt very long winded with the nonstop clinic and emergency room visits, but the past 6 weeks have flown by. I’m grateful that Dr. Kirby’s office took my concerns seriously and that they were very responsive as I was having issues for what felt like 2 weeks straight. Although my bladder was not cooperating, I’m also grateful to have had no issues with the actual surgical site. I’m glad that this surgery has pretty much been conquered, and that I have about a year to relax between stage 0 and stage 1 of phallo. Now I can just focus on electrolysis and living life.
If you’re dealing with surgical complications right now, I hope you can remind yourself that complications are not forever. A resolution will be found eventually. You’ve got this!
After making my previous post, things went kind of sideways for me. I was peeing about 50-100mL every 30 minutes, and my bladder was becoming increasingly painful every time I went to the bathroom. I could tell I wasn’t close to fully emptying my bladder, but I was hopeful that my body would just figure it out. I did try peeing with force (even though I knew I wasn’t supposed to) which didn’t really help and made my bladder hurt even more. I tried to catheterize myself which went horribly - the catheter kept slipping into the surgical site and made me bleed, and I was extremely panicky. With all this, I ended up going to my local Kaiser Urgent Care at midnight. I chose to go to Kaiser instead of UWMC because I was afraid of getting a very large emergency room medical bill if I were to go to a hospital out of network. When I eventually got roomed, the doctor contacted urology to insert another foley catheter. The urologist said he could tell my pelvic floor was spasming like crazy even when he was just cleaning the area before inserting the catheter. He said I would likely just need to keep the foley catheter in longer to allow my pelvic floor to heal. They also extended my course of antibiotics (Bactrim) due to my urine culture from earlier that day coming back positive. I was also having intense bladder spasms with the new catheter, so they prescribed oxybutynin which really helped (and made my mouth intensely dry). Despite the nurses and doctors at Kaiser having very little experience with this particular surgery, they were all very respectful and did their best to help me out.
I was not thrilled to have the foley back in, but at least my bladder was no longer in pain and I wasn’t getting up every 30 minutes to go pee. During my last clinic visit, because I was having all the bruising on my butt and I barely passed the void trial, they had set up an appointment for me to actually see Dr. Kirby the day following Memorial Day. She was bummed that I had to go to the emergency room. She was not concerned with the bruising on my butt. She inserted a finger into my rectum to check for an internal hematoma, and said she thought she felt what might be a small hematoma which could be interfering with my ability to pee normally. I asked her what the timeline would look like for my bladder returning to normal and she couldn’t really give me an answer - she said a majority of patients are able to pee fairly normally by this point (post-op day 12), so it was really just a waiting game. When asked what my preference was, I told her I would like to keep the catheter in until my 4-week post-op clinic visit because I really did not want to go through getting another catheter inserted. She said this was reasonable, but if I wanted to try removing it sooner I could just contact the clinic.
Since having the foley reinserted, recovery was going pretty well. I had more energy, I was staying awake for longer periods of time, I wasn’t in much pain, I was moving around the house more easily. I was feeling so good that on post-op day 15 I decided to take a walk outside for the first time since surgery. It was slightly painful internally, but I went nice and slow, and it felt really nice to get out of the house and to stretch my body out. The next morning, I noticed that every now and then my urine from the catheter was slightly pink-tinged, but I was not concerned since it cleared up when I drank water. Later that day, I went to the mall for a little bit and walked around slowly and gently. I was having some pain, but nothing more than just wanting some Tylenol. However, when I got home, my urine had become a much darker pink/red color. I wasn’t having any other concerning symptoms, so I messaged a doctor online through Kaiser’s website (since it was a Friday evening), and they recommended going to urgent care.
I was on the fence about what to do since I was feeling relatively fine and didn’t really want to waste my evening in the emergency room. Then as I was sitting in the living room, I had the most intense pain of my life in my lower abdomen. This was true 10/10 pain. I’ve never experienced anything like it. I inched my way to the couch to lay down, and had my mom bring me the heating pad and oxycodone. My gut told me that this pain meant it was time to go to the emergency room, and that this time I should just go to UWMC - NW since that is where I had my surgery, even if it meant a big bill (it only ended up costing about $250 thankfully). Once the oxycodone kicked in, the pain subsided a bit, but my urine was very red despite how much water I had drank. When I finally got roomed, the doctor ordered some blood tests to make sure I wasn’t bleeding too much, a urine culture to see if this was being caused by another infection, he looked at my bladder using a high-quality ultrasound machine, and he irrigated my foley to make sure it wasn’t clogged. All of my blood levels were normal, the urine culture was totally clean/negative for an infection, the ultrasound didn’t reveal anything beyond a little bit of swelling of my bladder wall, and the catheter was not clogged. This doctor said the bleeding was likely from the balloon of the foley catheter rubbing against my bladder. He also paged the on-call doctor (Dr. Fialkow) for Dr. Kirby’s specialty, and he messaged me directly through MyChart which was sweet of him. We set up a clinic visit for the upcoming Tuesday. It was nice to determine there wasn’t some bigger problem, but I was still in excruciating bladder pain and was dependent on oxycodone every 4 to 6 hours. The pain was so bad that it woke me up from sleep a handful of times. I stayed as still as possible for those 3 days to avoid triggering any more excruciating bladder pain. The oxycodone made me very depressed/sui***al, but there felt like no other option until the clinic visit.
When I went into the clinic, they posed teaching me how to irrigate the catheter myself, but I knew that wasn’t going to help my pain. The only thing that was going to help was removing the catheter all together. Dr. Fialkow was on board with this plan, so we went through the void trial process, and yet again I was only able to pee out about half of what they put into my bladder. I went home without a foley catheter and it hurt my bladder to pee, but at least I didn’t have a UTI anymore so I didn’t feel the urge to pee quite as often. For the next week, I could tell I wasn’t fully emptying my bladder, but it wasn’t getting to a point where I felt like I would need to go to the emergency room. They taught me how to catheterize myself again, but I was never able to do it successfully. My bladder ached quite a bit every time I peed for about a week, but it slowly faded. I could also tell my bladder was no longer distended, meaning I was peeing out everything that was building up in there, and my bladder was returning to its baseline.
Once the bladder pain mostly resolved, I was quickly back to my regular life. I was walking plenty, getting dinner with friends, sitting at my desk, standing for long periods of time, all with no issues beyond some fatigue. I’m just about 6 weeks post-op and am feeling great. I stopped needing to wear pads a few days after having the catheter removed. I’ve returned to the gym (light weights and only upper body for now) and will be returning to work this week. I had an appointment with my PCP and my hormones are all within normal range/no major changes from previous level checks. It’s been a very bumpy road to get to this point, and it felt very long winded with the nonstop clinic and emergency room visits, but the past 6 weeks have flown by. I’m grateful that Dr. Kirby’s office took my concerns seriously and that they were very responsive as I was having issues for what felt like 2 weeks straight. Although my bladder was not cooperating, I’m also grateful to have had no issues with the actual surgical site. I’m glad that this surgery has pretty much been conquered, and that I have about a year to relax between stage 0 and stage 1 of phallo. Now I can just focus on electrolysis and living life.
If you’re dealing with surgical complications right now, I hope you can remind yourself that complications are not forever. A resolution will be found eventually. You’ve got this!
Who needs to be able to piss anyway?
- Joined
- Mar 17, 2019
She's well on her way of becoming a Gruffin #2.
- Joined
- Jan 31, 2015
If it was that easy your brain would have figured out how to not be a mentally ill tranny Gremlin.
- Joined
- Jan 6, 2019
Life saving!
Is that normal? I mean is it normal to send someone home who isn’t able to void their bladder like that? They do t even let you leave hospital after birth until you’ve had a pee properly. If she’s done in with an inability to void is it ok to send her home unable to? Seems kind of mad to me
- Joined
- Dec 23, 2022
Trannies are just an onion of crazy. She can’t even type out the word vagina, but chooses to have procedures where lots of medical professionals will have to looks at and probably touch her special nono place.
I’m a middle aged woman who has had a couple of kids and she’s probably had way more medical professionals up in her business than the average woman her age. Absolutely insane.
I’m a middle aged woman who has had a couple of kids and she’s probably had way more medical professionals up in her business than the average woman her age. Absolutely insane.
- Joined
- Jun 17, 2024
...and she lives at her mum's. I am neither a mother, nor a parent figure and don't feel like one, but if I had a kid and they trooned out and decided to go all the way, I don't see any other option, than to speak my peace and then kick them out before the srs date, just like many parents, dads in particular, do.
Even when I never know the whole story and both sides of it, I feel quite sorry for the normal parents, (much less for the TRA handmaiden and munchie-by proxy ones), and it seems to me in some cases, the mother's compassion is gonna stand in the way of her mental well-being. They'd call it transphobia and being unsupportive, but caring for someone who had inflicted upon themselves such horrific things via unnecessary surgery and watch them circling the drain is certainly very challenging in regards to one's own sanity.
Even when I never know the whole story and both sides of it, I feel quite sorry for the normal parents, (much less for the TRA handmaiden and munchie-by proxy ones), and it seems to me in some cases, the mother's compassion is gonna stand in the way of her mental well-being. They'd call it transphobia and being unsupportive, but caring for someone who had inflicted upon themselves such horrific things via unnecessary surgery and watch them circling the drain is certainly very challenging in regards to one's own sanity.
- Joined
- Nov 6, 2023
Ovarit collects instances of men being gross and talking about women’s genitalia like designer commodities, etc
- Joined
- Jun 17, 2024
...of course they compare it to computer parts.
''And then they take the extra length of cable bundle (dick nerves), roll it into a loop and tuck it away somewhere, secure the unused connector (end of the fuckhole) with plastic tie straps (staple? fuck do I know) to the computer frame (pelvic bone) and put back the panels (stitch it up) and now the computer can be switched on with new device installed (troon wakes up from anesthesia).''
''And then they take the extra length of cable bundle (dick nerves), roll it into a loop and tuck it away somewhere, secure the unused connector (end of the fuckhole) with plastic tie straps (staple? fuck do I know) to the computer frame (pelvic bone) and put back the panels (stitch it up) and now the computer can be switched on with new device installed (troon wakes up from anesthesia).''
- Joined
- Oct 23, 2023
This reads like pure nightmare. It's like troons whine about how much their body has betrayed them and how much they want to kill themselves, and the demons that have taken over their lives are like "just wait. lol. lmao"
Except that not only is the body not a computer, but even if it was, these surgeries are like "tears out the monitor. replaces it with a microwave. Uses strips of tape from an old VHS to tie some red licorice where the wires used to be. Shoves play-doh into all the exposed ports."
- Joined
- Aug 24, 2014
Yesterday they say they'd literally die if they don't have their "vagina"; today they wonder if they can wait for a new, advanced model like a graphics card.
I don't hear cancer patients waiting out because the next chemo drug might be just round the corner.
- Joined
- Jan 31, 2015
I love how the troon asks if it's possible to make the old man-hole a new man-hole with a new technique. I hope he gets fooled by some quack.
"Yes sir, new vagina, sir! Advanced new technique, only $2000!"
"Yes sir, new vagina, sir! Advanced new technique, only $2000!"
- Joined
- Jul 25, 2020
...and looking at it, nobody will mistake it as being anything but a computer that somebody tried to convert into a microwave...badly...and smokes and shorts itself out when you try and plug it in.
- Joined
- Apr 6, 2019
Once again, prayers up for Physician's Assistant Abdul, moonlighting at Kaiser to support his elderly mother back in Syria, who walks in having seen "suspected UTI" on the board and finds...all this.
- Joined
- Oct 8, 2020
For those that can't quite fathom where in the pelvic floor the butchers drill the manhole for a penile inversion, I found this. Despite it being a drawing, I now understand why shit-fistulas are so common.
Of course, the outer bits never actually fit that diagram.
Of course, the outer bits never actually fit that diagram.
- Joined
- Mar 17, 2019
The Reddit troon calling himself lesbianonamission whom I featured here last week has made an update post.
Things have not improved:
Things have not improved:
- Joined
- Feb 5, 2021
Agree 1000% with this. Soft, weak parents, almost always the (single) mother, play a huge part in enabling Pooning/Trooning.
The first thing I would do is have my child removed from my insurance. - "Oh, you want to go to quacks who'll encourage you in your folly? Well, you pay for it."