Copper coil (IUD) vs Hormonal coil (IUS)

I got pregnant because my copper coil moved down towards my cervix. Could still feel the strings as normal. For 4 months prior to that I'd been having symptoms of vaginitis (dry feeling during sex without actually being dry and stinging during urination). The doctors told me it couldn't be the coil causing it but I now believe it was, instead they treated me for uti and yeast infection and dermatitis (none of which I actually had). So yeah I suffered pain for 4 months and then got pregnant. I wouldn't recommend because it's so hard to tell it moved, if you get symptoms of vaginitis or vaginal irritation ask for an ultrasound. Getting pregnant at 20 and then having to terminate the pregnancy is traumatic.

I loved the copper coil however it caused very heavy and long periods and I had to get it out after 5 months due to anaemia. I also have pmdd so I wanted to try something hormonal to ease this

Before having the copper coil, I’d tried all other forms of contraceptives. I got to a point where I felt, even though the copper coil would cause more heavier and painful periods, it was non hormonal so thought it was my old option (hormones really don’t suit me) The insertion was pretty bad I won’t lie but when it’s done it’s done! I never could feel my threads and my periods went from 5 days to 10 days. I went from being someone with light periods to unbelievably heavy; to the point I was wearing period knickers with two overlapped night pads for two of the days. The nurses said after 6 months my body would adjust and the bleeding would settle down. They started me on TXA as my ferretin and iron became low. To cut a long story short the bleeding never settled and I was still having ten day long periods. It was a horrible 12 months as I felt the majority of the time I was on a period and doing daily tasks or working proved very very hard some days. I became anaemic and would spend a lot of money on supplements alongside the prescribed iron. The anaemic led to a lower moon, zero sex drive, ravinous appetite and tiredness. I know they say research shows a small percentage gain weight on it and I was one of them. But they always like to say it’s others things like lifestyle. For me I was certain it was the coil due to the anaemia it causes. I’m 155cm and weigh 8 stone 3. I’ve always been that weight and I go to the gym 3-5 days a week, probably twice a week since the coil. I gained a stone in that year.

Not pleasant to put in but completely stopped by periods after few months. Reassuring that no pregnancy, however absolutely 0 sex drive and this effects relationships.

Initial 3 month settling in period is intense, lots of bleeding and emotional side effects plus insertion pain. After 3 months it settled and I thought I had found the holy grail, emotionally stable and no side effects. At 6 months I developed a large ovarian cyst which put me in agony and A&E, doctors said this was caused by the coil and had to remove it. Unfortunately I cant recommend, the search continues.

No periods but developed acne. I also get cysts now regularly (never had before) that burst and hurt so bad that the first time it happened I went to the ER.

only had mirena coil fitted 3 weeks ago but so far it’s been good, i have had quite a lot of lower back pain but other than that i don’t feel any different

Prior to having the mirena coil I had the most horrific periods literally to the point of passing out. I can say I have had my coil in for nearly 6 years and not had a period since and now I feel like I have my life back! It has been one of the decisions I have ever made and also hardly had any hormonal side effects.

I loved the mirena but over 3 different coils, shortly after insertion I would get kidney infections that didn’t respond to antibiotics. The link was only made on the third despite me asking the gyno about it. Such a shame because I loved it otherwise. Kidney infections mostly skipped the uti stage and went straight to them but bacteria wouldn’t grow in pee. If this sounds like you remove it!

Had it inserted at birth during a c section so no pain for insertion. Periods for lighter every month with significantly less pain than before and have virtually stopped after 8 months - just a small amount of spotting.

occasional cramps and sore boobs but I'll take that for no periods and no babies!

I got the Benilexa IUS to treat painful periods and PMS. However, within under two months, it severely exacerbated my PMS, causing sleep deprivation, frequent panic attacks, bouts of crying, and increased suicidal thoughts. This was also experienced during my period. Most importantly, it has completely disrupted my Psoriatic Arthritis management. Despite being on a biologic (adalimumab), the IUD has triggered a massive flare in my right foot that has now progressed to my left foot and ankle. I went from rarely needing NSAIDs to relying on daily ibuprofen. Regarding my psoriasis, I noticed a slight change in dryness/thickness in scales but not much else. My periods were even more awful than before and I had to call sick into work which l've never had to do. I further experienced fluctuating pelvic and ovary pain, with some days better than others. I expected side effects, but not to this extreme, system-wide level. I understand for some women the IUS is life changing in a positive way and a great treatment for endometriosis, etc. However, for other women, it may not be suitable for our body, especially if you have pre-existing conditions like myself. Whether that's due to the small amount of hormones released into the blood stream or the body reacting to a foreign object to the body. Or even both. Please do your research and consult with professionals if you have specific conditions or autoimmune diseases. Because most of the time, they won’t or care to understand your concerns. I've thankfully had it taken out today and was told by the GP it would take a few weeks to see a positive adjustment, flare reduction, and difference to body/mind, to my joints especially. You know your body best, any triggers and what helps. If you have a terrible experience like mine, don't let anyone tell you to put up with the lUS a few more months just to see if it "settles", etc. Advocate for yourself and try all avenues. I’m lucky my threads today were visible as they were not at the last GP appt. And I’m very grateful I had a caring and understanding GP who listened, affirmed my concerns (such as assessing my joints), and believed me.

Super convenient; few side effects though not negligible.