People describe their Endometriosis | Living with Endometriosis, diagnosis and symptoms 🌸

Thank you so much to those who got involved and shared their stories with us today 💖 Here are the questions incase you'd like to share your experiences in the comments:

1.was your diagnosis process tricky? I’ve heard it can take a while to have your concerns validated
2.is the pain only when you’re on your period or does it happen other times in the month too?
3. how did you get diagnosed and was it hard/mistaken for something else at first?
4. what has dealing with medical trauma/gaslighting in a doctor patient setting when they ‘are always right’ been like?
5. what does it feel like?
6. I’ve been diagnosed in the last year and would like a description of the pain
7. what are the 3 biggest signs that you might have it?
8. i have endo and sometimes doubt whether its really as bad as it is, do others feel like this?
9. not all sufferers bleed excessively, do you?
10. best way to support someone who has it and what helps the pain?
11.what do you wish more people understood about endo?
12. are the periods longer/heavier?
13. how would you describe your relationship with your reproductive system?
14. what was the hardest thing to accept about this condition?
15. any advice to anyone who thinks they have it but needs to get it through to the doctor as they just aren’t listening?
#endometriosisawareness

Some resources for you:
https://www.endometriosis-uk.org/
mayoclinic.org/diseases-conditions/endometriosis/symptoms-causes/syc-20354656

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