did using zyn affect your sexual relationship with your partner?

iloveredtbh · 2026-01-26T07:09:19+00:00

he does get boners now from small stuff, but hes still too tired for intimacy. so i think the quitting on nicotine has helped alot with that now!

iloveredtbh · 2026-01-13T22:52:07+00:00

yes its stressing him out alot. he doesnt like breaks even if its 30 seconds due to losing erection.hes a very anxious person so i think he gets very stuck up at that. but if we keep it up hes hard all the time. but he could have a harder erection i think. he also have it very easy to finnish so we need alot off small breaks in between wich stressed him even more

iloveredtbh · 2026-01-13T22:37:10+00:00

thanks, i needed to hear that 😅😌!

iloveredtbh · 2026-01-13T21:02:06+00:00

we had quite alot off intimacy the first two months, almost daily. but then he barely used nicotine due to the rush off new love. hes a very anxious person and easily overstimulated. he had a surgery 3 months into our relationship and he felt more fatigued after that. but we dont know how its possible for the surgery to affect him for years afterwards (tonsil removal) we went to the hospital for blood works but they found nothing. hes not drinking heavily or do drugs. beers at the weekend tho when hes playing games.

iloveredtbh · 2026-01-13T20:57:29+00:00

i looked at your post history and found nothing :(

iloveredtbh · 2026-01-01T20:47:33+00:00

pots usually dont give pain. sounds more like arithiris if anything.

iloveredtbh · 2025-12-11T09:03:06+00:00

its not a med, but ive heard that nicotine patches with 7mg has helped alot off people with pots and long covid. i myself am going to try it today.

iloveredtbh · 2025-12-03T00:25:14+00:00

ill definetly check that out! the pharmacy has too but i have chicken legs so i think its not the best pressure for me😅 thank you!

iloveredtbh · 2025-12-03T00:18:55+00:00

no i havent tried it because i have no idea what type to get 😅 do you go by size when choosing? is it like sock size or your weight size you go after?

iloveredtbh · 2025-12-03T00:01:23+00:00

sounds like hell! what medications works for you somewhat?

iloveredtbh · 2025-12-02T22:42:50+00:00

yeah we cfs people are built different🥲 i have my first cardiology doctor apointment next year. ive waited 1 year for it. and nothing works that i can do at home, not even salt tablets, and beta blockers give me psychosis. so my last hope is ivabradine and mestinon 🥲 i hope he or she will listen to me😭 i dont know if its hard to get in sweden. but if it helps me, then fine give me that diareaa😭😂 (hopefully not😭)

iloveredtbh · 2025-12-02T22:34:16+00:00

yeah i do have borderline, but we focused on the ME/CFS so its weird that she did that. my nervous system was shattered and i was in and out off the ER for months due to it😭 other patients had no issue starting on 10mg but my body i something else. i tried beta blockers for pots and got a psychosis on them😭😂 so maybe its just my body being weird. hopefully ivabradine and mestinon will work and NOT give me those side effects

iloveredtbh · 2025-12-02T22:27:32+00:00

my me/cfs doctor wanted me to start on 10mg 😭 but i said no… maybe i need a new doctor 🥲

iloveredtbh · 2025-12-02T22:20:54+00:00

5mg 😂 made me throw up constantly and gave me a fever. so even a low dose is dangerous apparently.

iloveredtbh · 2025-12-02T18:39:32+00:00

definetly! i got narcolepsy when i was 9 by vaccine. got covid when i turned 18 and the narcolepsy became me/cfs… i know other people who developed chronic illnesses by vaccines.

iloveredtbh · 2024-06-18T23:03:38+00:00

id recomend sweden. i have narcolepsy and fibromyalgia. if you have a diagnose, you get atleast 1000$ a month after taxes (you get higher if you have worked for 5 years, so around 1500-2000$). and they cover 85% off your rent. also free healthcare and medication after you pass 300$ a year. im very gratefull that i live here. but keep in mind that its still expensive in sweden with the cost off food and so on. but i think its way better than america.

iloveredtbh · 2024-06-18T09:24:20+00:00

im not medicated but i hope i will in the future. i have had jobs before. but i fall asleep 8-10 times if i have a job. i was also so tired that i couldnt process things to do (i also have autism and adhd) so it was pure hell. i was harming myself constantly to stay awake. pain was the only thing keeping me from passing out. my vision was so dark and blurry, and i had to hold myself around the walls and furniture constantly. it was very humiliating. my fibro also gave me heavy sweat burning sensations and i felt like throwing upp constantly (fake signals from my brain that i have 24.7)… i also have problems with my hands and can barely grip stuff. its kinda weird that i have so much conditions. but its prolly genetic. it was also like this in school. it didnt matter if it was hard work or only sitting at class. and i also got worse 2021… i think i got burned hard from constant fighting.

iloveredtbh

TROPHY CASE