Microgynon 30 pill and headaches

Began taking this when i was 14 when i got my first boyfriend and I am now 18 so it is very hard to determine or remember what things i suffered with prior to the pill and what increased while on it. One thing i can say is my skin has never been more oily in my whole life, regular bumps on my forehead which i don’t recall ever having. I can only put this down to hormones/the pill, i’ve tried antibiotics, thousands of pounds worth of skincare, changing shampoos, stopping vaping, bettering my diet, replacing makeup brushes regularly (im talking fortnightly!) and so much more and nothing seems to even touch the sides. cystic acne bumps on my back which seem to worsen in the winter/autumnal months. I have been seen to by uncountable doctors and a dermatologist who have all simply told me to wash my face with a cloth lol (wish i tried that one!!???). I have found my skins got worse through the years but now it’s totally uncontrollable, skincare does not even seem to touch the sides which also convinces me it’s something to do with my contraception. Have found myself very snappy and irritable 24/7 i feel very low… nothing major is happening in my life to be making me feel like that and it’s getting draining. booking another doctors appointment tomorrow to consider changing.

Granted I havent used it for long, i've only noticed positive side effects that I was happy with (Stopped periods, Larger and tender breasts, Better skin) however, I have been having some worse mood swings from time to time, though personally I find that has been managable. So far, I have not been made pregnant after corrcet and consistant use, the pill being my only form of contraception too. Perhaps I just got really lucky with the pill!

I used Microgynon for several years, as advised by my GP from the age of 15. I remember feeling very, very miserable at times and very angry and having a feeling of 'this is not me, this isn't who I am.' After taking the pill for nearly 10 years, I started to experience chronic stomach pain which would result in me being hospitalised every 7-8 months over a 5 year period. The first time I was admitted, I genuinely thought I was going to die. I had never experienced pain like it and was taken to hospital by ambulance. I was under a specialist for gastro problems, had multiple tests multiple times to try and find the cause of my flare ups. I would be put on a morphine drip once admitted and after a few days of tests would be discharged. The cycle repeated itself like this for the next 5 years, each time the pain being worse and eventually on my last hospital admission, blood in my vomit. I had ultra sound scans, blood tests, x-rays, MRI scans, CT scans, biopsies taken from my stomach, a camera that I had to swallow to monitor my digestion, blood and urine samples taken in the dark and sent off to a specialist lab in Cardiff to see if I had an auto immune disease, discussions on could it be cancer? Could it be another rare auto immune disease that was incurable? I had Oramorph prescribed to me at home to take as and when I had a flare up as when I was admitted to A and E each time, this is what I was given. I nearly lost my job working in a primary school due to time off and not really having an explanation in a formal diagnosis as to what was causing this issue, going through a disciplinary each time. Every time I was admitted to A and E, I would be asked if I was on any medication and every time I said 'just the pill'. I asked several health professionals several times, if this could be the cause of my reoccurring pain? I was told each time, no the pill can't do this to you, you would have pain more often. It was the suggested that it could be psychological, basically was it all in my head as tests all came back with nothing. I felt worthless. It was NEVER suggested to me that I should stop taking it to see if it changed anything. One day I decided to stop taking it. This was 5 years ago now and I have not had another episode of chronic stomach pain since. I had follow up appointments with my specialist who said 'it was as rare as hens teeth' for the pill to have caused this but he agreed and truly believed that it had been the cause of my reoccurring, 5 year battle, with chronic and debilitating pain. From being given the pill from such a young age, and a lack of education as to what is in it and what it actually does in order to work, I look back and can't believe what my body went through. Not just with the hospital admissions but with the constant bombardment of hormones that made me feel depressed, angry and at times despondent, all the time being told these feelings are 'normal' side effects. Treat your body with kindness and think about what you are expecting it to tolerate.