If this is your first visit, check out the community guide. You will have to Join us or Sign in before you can post.
Endometriosis Awareness- My Story

I’m new here. I am a 24 year old female young adult living with this sucky disease. I am certainly happy to share my story. In the middle of two thousand and nineteen I started getting pretty ill. Fast forward many months to last year and I definitely suspected I had it. One of my attacks last April was really bad and left me unable to walk. The pain was that bad on top of things. I have since experienced two more high intensity pain attacks in August and December.
To keep my chronic pain and symptoms at bay I use a combination of pain relief options like a cosy hot water bottle, heating paid, otc pain relief medication, yoga, distraction and deep breathing. My main symptom is foot pain, I have sciatic endometriosis but I know of one other person who has it and she also is at risk of seizures.
To keep my chronic pain and symptoms at bay I use a combination of pain relief options like a cosy hot water bottle, heating paid, otc pain relief medication, yoga, distraction and deep breathing. My main symptom is foot pain, I have sciatic endometriosis but I know of one other person who has it and she also is at risk of seizures.
Replies
Let us know if you want to write a longer post raising awareness of endometriosis, and we can pop it in the Guest Blog categories. There's no pressure at all, but email us on [email protected] if you're interested!
Want to tell us about your experience on the community? Talk to our chatbot here and let us know what you think