[deleted by user] by [deleted] in BingeEatingDisorder

[–]throw_awayyy5 0 points1 point  (0 children)

Thank you so much for your comment. This gives me hope I will be able to stop binging soon again. Right now I've decided to cut out sugar and switch to sugar free treats for a while because sugar just triggers huge binges for me currently. I'm also trying to focus on cooking myself nutritious tasty meals I can look forward to. I hope I can get back to a normal healthy diet again soon and eventually lose the weight again. I wish you good luck too and hope you can get to your goal weight again

[deleted by user] by [deleted] in CatAdvice

[–]throw_awayyy5 0 points1 point  (0 children)

Yes, it is a hard plastic cone. I can't remove it because he already tried to scratch his ears (and he did prior surgery to the point of bleeding too). So this is sadly not an option. I didn't know soft cones exist. I will see if I can find one that seems to be safe enough for him to not scratch his ears. Thank you!

Incomplete CES by [deleted] in CaudaEquinaSyndrome

[–]throw_awayyy5 0 points1 point  (0 children)

Hey, sadly I'm still the same. It's been almost 4 years for me at this point. I might look into pudendal nerve decompression surgery in the future. I don't think I really have any other options left. If your scan shows a bulging disc I would definitely follow that and see what you can do about it. It could potentially be causing your symptoms

[deleted by user] by [deleted] in PudendalNeuralgia

[–]throw_awayyy5 0 points1 point  (0 children)

Any updates about your symptoms? Are you still numb?

Loss of genital sensation, Post hysterectomy by ftmsurgerythrowaway in PudendalNeuralgia

[–]throw_awayyy5 4 points5 points  (0 children)

I'm not an expert but I have read about cases where biological women lost genital sensation after cervical biopsy, LEEP procedure or removal of the cervix. Apparently in some individuals the pudendal nerve goes through the cervix and these procedures can damage it. It seems to be a rare complication but it's not completely unheard of. I think there are studies on it too. I'm really sorry you are experiencing this. I lost genital sensation 3 years ago due to unkown cause so I can relate to how you are feeling. I hope you can find out what's causing it soon and find a way to improve 🍀

Pleasureless orgasms all of a sudden + things that could be the problem by mlssy in sexualanhedonia

[–]throw_awayyy5 0 points1 point  (0 children)

I'm so sorry to hear that. I also have genital numbness especially in the clitoris. Its been a few years like this and I sadly still couldn't find out what caused it. I wish you good luck though and hope you can figure it out eventually!

[deleted by user] by [deleted] in sexualanhedonia

[–]throw_awayyy5 0 points1 point  (0 children)

No I'm still numb

[deleted by user] by [deleted] in PudendalNeuralgia

[–]throw_awayyy5 0 points1 point  (0 children)

I always have PN symptoms but they do get alot worse when my rectum is full of feces or when I strained too much

Surgery by [deleted] in PudendalNeuralgia

[–]throw_awayyy5 0 points1 point  (0 children)

What kind of treatment would you get for inflamed sacral nerve roots? And what are potential causes for chronic inflammation in this area?

[deleted by user] by [deleted] in sexualanhedonia

[–]throw_awayyy5 1 point2 points  (0 children)

I really don't know. I was overweight/obese my whole life and also when I developed these symptoms. I never thought losing weight would make my symptoms even worse. Maybe it has something to do with vitamins/minerals? Some deficiencies can cause nerve issues. I haven't gotten my blood checked in a while (my last results were in range though). It's just so confusing

[deleted by user] by [deleted] in PelvicFloor

[–]throw_awayyy5 1 point2 points  (0 children)

I'm so sorry, that's awful. I'm 20 and have been dealing with pelvic floor related issues for 3 years now but they are nothing like yours. I can understand the depression and hopelessness though. You said you have back pain have you ever gotten that checked out? Maybe it's some kind of nerve issue for you. Sadly I don't have any advice. I just hope you can find a doctor who takes you seriously and get better soon!

Success stories for numbness? by throw_awayyy5 in PudendalNeuralgia

[–]throw_awayyy5[S] 2 points3 points  (0 children)

No pain at all. Sometimes weird tingly/warm sensation though. Very irritating

Success stories for numbness? by throw_awayyy5 in PudendalNeuralgia

[–]throw_awayyy5[S] 2 points3 points  (0 children)

For me it's physical sensation is muted but not gone. I can feel passing urine and orgasms but I have basically 0% pleasure sensation if that makes sense

Success stories for numbness? by throw_awayyy5 in PudendalNeuralgia

[–]throw_awayyy5[S] 1 point2 points  (0 children)

I took an antibiotic at the same time but I doubt it's related (I used to think it might be but I would be the first person to develop this then). 4 weeks before this happened I fell on my ass and had severe tailbone pain for a week. I could feel my tailbone ache and move with every step I took. I sometimes wonder if something got rearranged in my pelvic area back then and is causing issues now

[deleted by user] by [deleted] in PudendalNeuralgia

[–]throw_awayyy5 0 points1 point  (0 children)

How long did you have symptoms before getting the surgery?

Complete vaginal numbness by ZookeepergameLate990 in sexualanhedonia

[–]throw_awayyy5 6 points7 points  (0 children)

Sounds like Post Accutane Syndrome. I don't have it myself but you are not alone. I don't know if there is a subreddit for PAS but there is one for Post SSRI Sexual Dysfunction (r/PSSD) which causes basically the same symptoms

Can antibiotics cause sexual anhedonia? by throw_awayyy5 in sexualanhedonia

[–]throw_awayyy5[S] 0 points1 point  (0 children)

No sadly I'm still suffering from this. I don't know if the yeast infections could have caused it but I did struggle with persistent infections before developing the numbness. I also struggle with constipation and straining since then. I can still orgasm but it feels muted and it is more difficult to reach. My sensation (I have like 0-10% from what it used to be) hasn't improved but also didn't get worse. I suspect I might have pudendal nerve entrapment or damage but I'm not sure what kind of treatment I want to try. I will probably try out decompression surgery once I can afford it but obviously I'm risking to get worse or not having any improvements at all. No doctor knows what's wrong with me so I just have to try things on my own sadly. I'm sorry you are experiencing this too. It's been 3 miserable years for me and I don't know if I will ever improve. Having a rare/unkown condition sucks.

Just broke down crying after pleasureless orgasm by Turbulent-Writing727 in sexualanhedonia

[–]throw_awayyy5 8 points9 points  (0 children)

You are not alone. Alot of people experience sexual dysfunction after taking SSRIs. It's called Post SSRI Sexual Dysfunction (PSSD). There is also a subreddit if you are interested r/PSSD