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Endometriosis
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Endometriosis
I fear it will always come back and I always fear that I will not be taken seriously. I would love to see new, non-invasive treatments and advancements made. I also wish there was funding to help with medical bills related to endo management.
Endometriosis
At its worst, endometriosis pain feels like I’m dying, or I wish I would die – it’s the worst pain I’ve ever experienced. Imagine someone tearing your insides apart and then setting them on fire. Sometimes I can’t believe I can be in that amount of pain and still be conscious.
Endometriosis
It is like fighting for your life every single day. Until the period pain arrives and then you pray to God that you pass out or die.
Endometriosis
I was told I was drug seeking, and attention seeking. All this time my dad thought I was just trying to get out of school, and I was being dramatic. My mum was my only and biggest support. I have lost a lot of faith in the healthcare system.
Endometriosis
People often talk about being gaslit by the medical system. What they don’t talk about is what happens next. It’s when you start gaslighting yourself.
Endometriosis
A lot of people dont understand how bad endo gets and think your a negative person when you complain about pain
Endometriosis
It’s very frustrating and depressing living with this condition because people just see you as normal person and expect you to be able to do what a normal healthy person does
Endometriosis
The beginning was at the very start of my period. Back in 2017, I would have heavy periods where I would nearly blackout.
Endometriosis
I have endometriosis in my womb, ovaries, bladder and bowel plus those organs have fused together due to the endo tissue. The pain I feel every day is no joke.
Endometriosis
Once I was diagnosed I never had follow up
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