My PCOS Story

I was diagnosed with Polycystic Ovarian/Ovary Syndrome (PCOS) in February 2013.  It only took 10 years...

If you have PCOS, then you know what it does to your body.  For those of you who don't, this video does an awesome job explaining it. 



I was 12, a few months before my 13th birthday, when I got my first AF. After my very first cycle, I battled irregularity and severe cramps.  I went months without an AF.  When my mom realized I wasn't having them, she actually asked me if I was pregnant--at 13!  I was horrified! Thinking that they would regulate naturally, we waited; when they didn't, we went to the GP.  He put me on a short round of BCP to see if it would regulate me.  Needless to say, I was on BCP by the time I was 15.

My grandma found an article about PCOS when I was 15; every symptom it mentioned, I had: few or no AFs, heavy bleeding when I did, oily skin (not really acne) and terrible mood swings.  I took the article to two different GPs, who both told me that it was irrelevant; there was no reason to test me for anything. 

I continued to take BCP until I was 21.  I gained weight like crazy and I blamed the pills, so I stopped taking them.  From that point for the next almost four (!) years, my symptoms got worse: AF stopped, cramps were worse, I developed alopecia and hirsutism.  Eventually my AF went from non-existent, to sporadic, to constant.  I gained even more weight, I was more depressed, I couldn't sleep.

I admit, it took me way too long to see a GYN, but if I couldn't get an answer to what was wrong then, then what would be different now? Plus, no one wants bad news, and I KNEW it was going to be bad news.

When I was diagnosed, I was relieved to have an answer, but I was devastated to hear that I might not be able to have kids.  Yes, I know...there are lots of fertility treatments and drugs to try now, but knowing that your body can't naturally do what it is SUPPOSED to do...that's salty.  

I took a few months to sulk...oh whoa is me.  Why me God?  Why do I have to work harder than everyone else?  One day, out of sheer boredom, I started to research PCOS.  Google was my friend that day!  I searched, and read, and contemplated.  I learned that PCOS is more common than I thought.  I realized that there was a whole community of people who were going through the same thing; they were LIVING with PCOS.  It gave me hope...and that is what this blog is about... to spread awareness, to provide support, and to give encouragement.

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