Labelling My Condition – Endometriosis

A personal statement, in regards to my general health

Labelling My Condition – Endometriosis

Pre operation and post operation.

Shortly afterwards I was placed on a drip.

The start of this week has been the roughest I’ve faced in this recent chapter of my life. Aiming to remove a begin lump in my uterus, in theatre consultants discovered extensive Endometriosis tissue, the removal of which left me in a world of pain, unable to stomach food and doped up on a cocktail of morphine and other drugs. 

I have so much respect for the tremendous staff at BMI Droitwich Hospital for their expertise and care. Those who wiped away my tears, sat with me through the night when I was at my worst and made me laugh when I needed it most. Aside from now walking around like an old woman (blame the stiches) I’m equally lucky to have an incredibly supportive family who’ve been nursing me back to health since my hospital discharge.

A final point for all my women in arms; DON’T suffer in silence, DON’T take no for an answer and DON’T ever ignore your body. Endometriosis is notorious for being side-lined by health professionals; don’t be a muppet like me, too scared to rock the boat.

After years of suffering, I finally have a diagnosis. Here’s to a future where I can label my condition, access support groups and, now, better understand myself.

With love xx

Edit: I’ve been overwhelmed with positive well-wishers and messages. Thank you. I’m heavily contemplating writing a separate blog post on how I got to this point. Not necessarily a mini-saga (“it all started when I was 12 years old…”) but a piece covering the last few months. Despite all the pain, there have been a couple of lighter moments that it would be equally nice to share. Stay tuned. x

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