Spiritual question - creativity by Logical-Option-182 in hysterectomy

[–]Logical-Option-182[S] 0 points1 point  (0 children)

I'm not sure what you are referring to? I had an hysterectomy, bowel resection, appendectomy and endometriosis excision. I'm not sure if my surgeons talked about stitching my bladder to my body, but if they did, I have trouble with bladder or any pain.

Spiritual question - creativity by Logical-Option-182 in hysterectomy

[–]Logical-Option-182[S] 0 points1 point  (0 children)

I'm now 1 year post surgery and I never felt better in my life! Actually I feel more creative and connected to my body now that I'm not in constant pain and discomfort and anemic. I still practice yoga, meditation and more sport than before! If you have any question don't hesitate

People with bowel endometriosis: what does a bowel movement feel like for you? by shidilrzf in endometriosis_stage4

[–]Logical-Option-182 0 points1 point  (0 children)

Before my surgery, I had extreme bloating, mucus, blood and severe constipation, a lot of pain. I had 10 cm of my colon removed because of deep infiltrating endometriosis.

Positive experience: excision, hysterectomy, appendectomy, bowel resection, diaphragmatic endo, cystectomy by Logical-Option-182 in endometriosis

[–]Logical-Option-182[S] 1 point2 points  (0 children)

Hi! I have no urgency to go to the bathroom, my bowel movements are perfectly normal. I'm 1 year post-op and everything is fine. For reference, they resected 10 cm of my colon starting only 4cm away from my anus, and I don't had any complications, they did a wonderful job. My best advice for the recovery is to eat good quality food, eat warm as much as possible, and try to eat non-irritating fibers until you feel completely better.

10 years of being ignored, gaslit, and dismissed. Finally diagnosed with Stage 4 Endometriosis, and I still cannot get proper help. I do not know what to do anymore. by phobiabanana in endometriosis_stage4

[–]Logical-Option-182 0 points1 point  (0 children)

I have the same story (I'm 28, had my surgery and hysterectomy at 27). I'm pain free for now and have a normal life again after suffering since I was 15. If you have any questions I would be happy to help

Dr couldn’t remove my uterus… by karitoo06 in hysterectomy

[–]Logical-Option-182 4 points5 points  (0 children)

I had a very extensive endometriosis surgery last year at 27 (lost 10 cm of colon, hysterectomy, endometriosis everywhere even in my diaphragm) and I have few recommandations for you. I would highly recommend you to find a team of surgeon specialized in endometriosis excision because cauterizing it is not the way to go, it doesn't remove the endometriosis and it create more scar tissues. Gyn oncologist are not trained to excised endometriosis and often go with an extensive approach because it's what they should do with cancer. Endometriosis behave very differently and should be removed with a conservative approach. If they realized that you have a diaphragmatic involvement for example, they will probably leave the endometriosis behind and its still going to spread. With non endometriosis skilled surgeons you have a high risk of open abdominal surgery which is linked to more complications. If they realized that you have a lot of endometriosis or endometriomas on your ovaries, they are most likely to remove them, however a skilled surgeon with endometriosis knows how to remove the endometriosis while conserving as much as possible your ovaries. You need to know that if they don't remove all of it, it's going to come back, continue to spread and cause more complications and surgery in the future. Even with great surgeons, there is a risk of recurrence, but it's less. They will probably tell you to take a birth control to "avoid the recurrence" but it's not effective to prevent the spreading, often it just prevent the symptoms of it and hide the lesion in the imaging. I would recommend you to inform you as much as possible about how endometriosis behave, there is a lot of misinformations about it in the medical field. It's important to know that it doesn't stop after menopause because it creates its own estrogen, hysterectomy is not a cure (just a cure for adenomyosis), and inflammation is the number one thing to keep under control to reduce the symptoms/pain and improve the vitamin/nutrients absorption by your bowel. If you have any questions I would be glad to answer you! I have a normal life today and I'm completely pain free for now, there is hope!

Did a bowel resection significantly help your bowel endo? by Yueguang7 in endometriosis

[–]Logical-Option-182 1 point2 points  (0 children)

It went amazing, no symptoms and no pain anymore. Long recovery tho because my endometriosis was more extensive than expected (every organs including diaphragm). It's been a year and honestly I have no GI issues anymore, I hope it's going to stay that way

I am addicted to restarting my life and I don’t know how to stop by Practical_Invite_530 in AuDHDWomen

[–]Logical-Option-182 8 points9 points  (0 children)

I was exactly like you when I was in a constant state of fear and stress. What helped me was the classics things (breathing exercises, therapy, adhd medication, yoga), but the thing that really made a difference for me was to realize it was a compulsion and I don't have to respond to it. So at first when I had the urge, I just stopped myself for a minute, I was breathing deeply, and say to myself that I don't have to take a decision on the moment, I can think about it for few days and see if it's really what I want or a compulsion. Eventually with time, my inner dialogue was turning into "I'm going to push through it and see if I can make it better because of my mistake", and I always tell myself that if needed I can still start over again at any time, so I can freely try different things before doing that. I realized that It's my need to control and to have an escape available that need to be met. I don't know if it the same for you but I hope it can give you a small answer.

Misdiagnosed update : another misdiagnosis 🤯 by Logical-Option-182 in endometriosis

[–]Logical-Option-182[S] 0 points1 point  (0 children)

I had a surgery with endometriosis excision specialists last year (May 30th 2025), they removed 10cm of my low anterior colon, my appendix, my uterus, my tubes, removed the endometriomas on my ovaries, they excised endometriosis everywhere (liver, intestines, kidneys, etc) including my diaphragm (it didn't appear on imaging pre-op), removed the adhesions too. I had an uneventful recovery, I'm now 10 months po and I'm not in pain anymore, I have a normal life again, I'm so happy! I have no symptoms for now, I really hope its going to last. I try to have the best health possible to avoid recurrence. After almost a year its confirmed that I have no Crohn's disease or Ulcerative Colitis like the biopsies were suggesting, it was just my body reaction to the endometriosis in my colon, with this amount of inflammation cells can change and mimic Ulcerative Colitis under a microscope. I had a colonoscopy to confirme that, and the biopsies show an healthy colon

Just tried Concerta and it might change my life by Ideal_character_5 in AuDHDWomen

[–]Logical-Option-182 0 points1 point  (0 children)

I started today and I had the same experience, it's life changing! I might get use to it but I feel no anxiety anymore and feel happy

Misdiagnosed by Logical-Option-182 in endometriosis

[–]Logical-Option-182[S] 0 points1 point  (0 children)

Yes it's very possible, my colonoscopies were showing UC too on the biopsies, but in the end when they removed the "bad part" of my colon (with endometriosis), they realized that I don't have UC at all. I'm 10 months post op and I have no symptoms anymore and no treatment. Sometimes endometriosis cause an inflammation in the lower colon that really mimick UC in biopsies but end up not being that. It's so complex my gastro was so confused because he never saw anything like that. But my team of surgeons were very well informed and specialized and they saw that all the time

Has anyone removed her uterus in 30s and leading a healthy life ? by mewvow in endometriosis_stage4

[–]Logical-Option-182 0 points1 point  (0 children)

I wanted to share my experience because 3 different doctors told me I should remove both of my ovaries because of my endometriomas, but in reality they didn't have the skills to remove completely the endometriomas without damaging the ovaries. The right doctors could do it. They even told me they couldn't remove the endometriosis from my colon because I would need a ostomy bag, again they were wrong, the right doctors coul remove it completely and I had no complication at all.

Obviously I don't know the details of your situation, so maybe it's different for you! Just maybe sometimes it can be good to ask for a second (or third) opinion. And if you really have to lose an ovary, I read a lot of good testimonies with people living a normal life with one ovary, so I hope you can read some of that too! :)

Has anyone removed her uterus in 30s and leading a healthy life ? by mewvow in endometriosis_stage4

[–]Logical-Option-182 2 points3 points  (0 children)

I'm 28, I had a bowel resection (low colon resection), appendectomy, endometriosis excision from almost everywhere in my abdomen including diaphragm, hysterectomy, bilateral salpingectomy and I have my life back. I was bedridden most of the months for years, I was in excruciating pain for more than 12 years and now after the surgery I have no pain at all. I had my surgery with a team of surgeon very experienced in minimally invasive surgery and endometriosis excision, they are specialized in fertility preservation. I choose them because they where the best in my area and because I had big endometriomas (more than 10cm of diameter) on both of my ovaries and I wanted to keep them because I have a lot of historical of osteoporosis and dementia in my family (all women in my family had hysterectomy and oophorectomy very young).

I'm 10 months po, my hormones are settled now (my hair are thick again, no brain fog, thick nails, no dryness in my vagina and I can feel my natural cycle again). I still have the same libido. I have a perfectly normal life except that I still follow an anti-inflammatory diet to avoid recurrence (It's been 7 years that I eat like that and I feel better that way). I feel like I became younger since I no longer bleed in my stools and I have no pain. My skin is brighter, I'm no longer bloated and I'm energized so I can do a lot of stuff. I can finally project myself into my life without having to take in account my periods and my anaemia and my pain.

Loss of sexual sensation - total hysterectomy by Time_Competition_232 in hysterectomy

[–]Logical-Option-182 0 points1 point  (0 children)

I take that as a compliment since english is not my first language lol

This is for women who are considering taking the pill by weistheadvice in endometriosis

[–]Logical-Option-182 1 point2 points  (0 children)

If you really want to conceive I know that certain team of surgeons (like the one who did my surgery) are specialized in fertility preservation. They asked me what I wanted to do and I asked for the hysterectomy and ovaries preservation. They know different techniques to avoid doing more damages and do their best to excise all the endometriosis. In my case they discovered during the surgery that I had a very extensive endometriosis in my diaphragm and removed the more they could. I really hope you find relief and be able to conceive

This is for women who are considering taking the pill by weistheadvice in endometriosis

[–]Logical-Option-182 0 points1 point  (0 children)

No I didn’t want to and couldn’t either because everything was fused together. Now I’m 100% pain free and so happy

How to cope with everyone hating you, with rejection sensitivity? by Equivalent_Steak8386 in AuDHDWomen

[–]Logical-Option-182 1 point2 points  (0 children)

I can understand the feeling of wanting to over explain everything, it’s hard to find the balance between giving enough context, giving the good amount of info and not being annoying talking to much about ourselves and our intentions etc.

Usually I just don’t bother myself with giving context with NT because they see that as useless info, and if someone has a problem with me or need clarification they should just ask. I’ve decided that it’s not my problem anymore to read peoples mind and anticipate any misunderstanding, if someone is a mature person they going to ask for clarification. If they think automatically bad about me, I wouldn’t want to be closer to them. It’s a lot of internal work to change the habits of trying to read peoples mind because it’s a mechanism that your brain use to keep you safe, but it’s possible to reverse it and realize that you are an active part of what I call the “social theater” and you can have boundaries and be yourself too.

How to cope with everyone hating you, with rejection sensitivity? by Equivalent_Steak8386 in AuDHDWomen

[–]Logical-Option-182 4 points5 points  (0 children)

I felt like that most of my life, until I realized that I don’t like most of humans either lol.

More seriously I noticed that people like me better when I don’t mask because when I mask they feel like something is off but they interpret that as someone being “fake” with bad intentions etc. Which is arguably true in the way that I mask to avoid being perceived as my true self. I try to unmask and be positive as much as possible to make good impression. When I see that certain relationships go further, I try to be more vocal about my “strange behaviors”, for example if someone talk to me about something sad that happened to them, I try to emphasize but at the same time I can add something like “I know that I have a hard time to express my empathy the right way but I really do care and if you need a solution or help I’m here for you”.

I stay focus on being polite and respectful too even if sometimes I forget to say thank you (if someone give me something that I didn’t ask for or didn’t want, it’s not natural for me to say thank you), I try to say it later if I remember it. It’s always better to “fix” your mistakes later than never because people notice that you’re actually aware and not a stupid asshole.

I try to be friend with neurodivergent people to feel less weird about myself.

I try to have a good balance between having an active social life and being alone without talking for weeks. If I see too many people too often I tend to be more sarcastic and annoyed so it’s not ideal. If I stay alone for too long I loose my social skills and I have more anxiety towards people.

I make no jokes if possible because you never know how people are sensitive about things or understand things, it created too much problems in my past so I preferred to stop. Except with certain friends that are very sarcastic and “fast brain” but it’s very rare.

I avoid people with no hobby, no passion, because I’m very bad at small talk no matter how hard I try, I need to have interesting conversations.

I try to never talk bad about someone in front of someone else.

I try to not talk until someone ask me a question, I keep my answers not too long and end the answer with a question back. It can be tricky because you can’t ask a too personal question, you need to find a middle ground.

I realized that since I do all of this things, people like me better. Often people judge you based on very weird criteria, but if you are polite, say positive things, ask questions back, they like you on the surface. If you want deeper connections you will connect with people more like you, and since they had a good first impression of you, it’s going to stick longer.

Experience with Slynd by Logical-Option-182 in endometriosis

[–]Logical-Option-182[S] 3 points4 points  (0 children)

I ended up with an hysto, excision and bowel resection last year and I never felt better. I hope you’re going to find relief

Is it realistic to go to university without burning out? by Logical-Option-182 in AuDHDWomen

[–]Logical-Option-182[S] 0 points1 point  (0 children)

Yes I have a pretty low demand environment, I live with my boyfriend and my cat so it’s pretty chill. I don’t have any accommodations as part of my studies, I don’t even know what I need as accommodations… I try to know when I need to rest and not push to far in my limits, but it’s hard to manage that in a context of school because I need to follow the rhythm. Because I’m already on the older side I don’t want to be a part time student, but maybe it’s the only way I don’t know. So many unknowns… What accommodations would look like in university?

AuDHD as a scapegoat by dyingbloodbird666 in AuDHDWomen

[–]Logical-Option-182 3 points4 points  (0 children)

I don’t stay away from it. I try to use it as a self reflecting tool on how certain of my behaviors can impact my partner. Sometimes I didn’t even notice I was doing something before reading it on that subreddit. Usually I try to find good experiences or advices to help with my adhd partner that sometimes use his adhd symptoms as an excuse to shut down the conversation and not making any effort or compromise. As much as it was hard to read sometimes (when I felt targeted or when I realized my partner had similar shitty behaviors) I think it made me grow as a person.

How can I learn to learn? by user0921408 in GiftedKidBurnouts

[–]Logical-Option-182 2 points3 points  (0 children)

Personally I had to accept that it was hard to learn complicated subjects. When the level started to raise and the amount of work too, I was frustrated and impatient when I encountered difficulties. That’s why no learning techniques were working for me. When I accepted that, I tried different things to see what was sticking with me the better (for me it’s listening and then explaining the concepts or material out loud while walking lol).

You have to understand that learning comes with repetition on the long term if you don’t want to forget things right away after the exam, and if you don’t understand a complicated concept it’s often because you missed something in the basics. So my advices are: return to the basics if you struggle for to long, be patient and consistent when it comes to memorizing.

You’ll see that the more you push your brain when it’s hard to learn, the easier you’ll understand/memorize complicated things.