Implant vs Hormonal coil (IUS)

I gain weight and got chronic fatigue. It was awful.

This i my first time, I discovered skin heat rash at the initial stage, presently loosing weight and loosing hair.

I am so far very happy with the nexplanon implant. I had tried iuds prior, first the copper T, which did not work for me at all, and then mirena, which was good, but I did experience some pelvic pain and discomfort during intimacy. With the nexplanon, my periods stopped for the first year and a half, maybe closer to 2 years. And then was just very light spotting for awhile after that. I am at about 2 years and 6 months, and my period has come back fully, and I am starting to have hormonal acne and mood changes, so I opted to have it replaced, just in case these symptoms are due to the hormones tapering off. I just had it replaced today, so I am not sure whether it will fix the issue, but will keep ypu posted.

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.