Discussion about this post

User's avatar
FLARE Art & Resources for Endo's avatar

Thank you for sharing your experience🙏💛🎗️

Amy Padilla | Searchlight's avatar

Great article!

I was diagnosed with endometriosis in 2011 after going to the ER three times and seeing three different gynecologists. You would think the other doctors would have been better trained to diagnose the disease! I remember lying on my bed crying because the pain was so bad. I basically had to beg my doctor for the first laparoscopy surgery.

After my diagnosis, I gave up coffee, red meat, dairy, and gluten. My endo flare ups were much less and I was able to manage the disease better than before. What you eat and the supplements you take definitely determines how you are able to live your life with the disease. I also took DIM and CoQ10 supplements, which improved my symptoms dramatically.

I had endometriosis for 14 years. I suffered from horribly heavy periods that were so bad I had to get iron shots because I was losing too much blood each month due to the disease. I ended up getting two laparoscopies, one ablation, and a full hysterectomy and oophorectomy due to my severe endo.

This year is the first year I have had relief after getting a hysterectomy. I recently discovered that endometriosis and trauma are connected. If you’d like to learn more, please check out my article!

https://searchlight.substack.com/p/your-endometriosis-may-have-been

6 more comments...

No posts

Ready for more?