u/aningnik

Has anyone heard of or tried using cinnamon to help with incontinence? I saw it works on a few sources on the web but idk how much it may work. Trying it tonight myself to see and will try it for about a month.

I've went a few years without bedwetting from 2021 - 2024. It was wonderful but it started up again heavily in 2025. I'm having a hard time going back to this after such a lovely time being dry for so long. I've tried diapers, mats, medications, supplements but nothing seems to help. I have even tried seeing a psychiatrist. I can't do alarms either because I'm hard of hearing and won't hear even the loudest of alarms. So idk I'm getting kinda tired of all the washing I have to do. I'm thinking about just going without blankets or sheets or even clothes and just use my plastic waterproof cover and nothing else because I'm tired of washing. I even wet a hotel bed even though I wore a diaper. Idk what to do if there's anything to be done anymore. Sorry just kinda venting.

I've tried depends and adult diapers and even the disposable wet pads and nothing seems to hold it and prevent my sheets from getting wet. I've noticed also that I'm a deep sleeper so waking up to use the bathroom is very rare. Also, even when I do wake up my bladder is overactive whenever I lay down so if I'm sleeping it's not going to notice the little urges and only the one I've been holding for a bit. So the little urges happen very close together and make a big mess but they don't alert my body like if I was holding it for a while. I hope I'm explaining this right please let me know if you understand in the comments. Safe to say I really don't know what to do about those and I'm tired of feeling bad about it.

Started taking Trileptal twice daily morning and night (300mg) and for the past week I'd get just a feeling of numbness and zaps throughout my body. Now it's moved to my neck and face the numbness and zaps and also some heat. I was wondering if this is normal or am I having some sort of allergic reaction?

I hate when I'm expressing my frustration with being limited with most things like meds, food, cosmetics and whatever else I react to and someone who doesn't have this disease comes to me and says they can't do somethings either like eat ice cream or drink milk because they're lactose intolerant... Like I understand that they're trying to make it seem like I'm not the only one suffering but it's not even comparable to this. Idk if I can go anymore and they just have a few things to "avoid" meanwhile my whole life is on standby it feels like because I have other conditions that I can't treat or control because of MCAS! IM SO TIRED OF GOING THROUGH THE FLARES AND REACTIONS AND NOTHING IS HELPING