I read with interest this week some findings of a survey conducted by Endometriosis UK on their news page.
The survey found that:
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![bullet](http://www.endometriosis-uk.org/images/bullet.gif)
![bullet](http://www.endometriosis-uk.org/images/bullet.gif)
![bullet](http://www.endometriosis-uk.org/images/bullet.gif)
![bullet](http://www.endometriosis-uk.org/images/bullet.gif)
![bullet](http://www.endometriosis-uk.org/images/bullet.gif)
One third waited TEN YEARS.
I had 8 years from initial pain to diagnosis and that was incredibly hard. Not knowing what causes pain or what could be causing it meant I had no idea that endo could be a potential condition and therefore no power to insist on further investigations.
This is why I am so adamant about spreading awareness of endometriosis and it's symptoms so that women don't have to suffer so long without a diagnosis and a pain management plan.
So, symptoms:
- Painful, heavy, or irregular periods
- Pain during or after sex
- Infertility
- Problems on opening bowels
- Fatigue
These are the main bad boys. I would also add in ovarian pain, white hot shooting and burning pains, exhaustion, and abdomen bloating.
Don't sit for 10 years in silence girls, you know your body and if it feels wrong make sure you get seen.
DD
x
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