Inspire Others

Speak up and inspire others. Don't be ashamed of your struggles and experiences. We can all help one another. Because we are Endo Warriors. And we are stronger together.


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"How are you feeling?"

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I've been doing pretty good. A month has passed since my last post and recovery has continued in the right direction. Physically I've healed amazingly, mentally I've been doing well too. But today I've wobbled. Next week I return to work. I know!! Where has that 9.5 weeks gone?! I'd be lying if I said I was looking forward to it. I'm actually surprisingly anxious about going back. I was thinking it was just the typical anticipation about what I'm going back to and how I may feel with the tiredness that I still have after my op. But today, I've been feeling quite emotional, and as I sat thinking it through, it dawned on me. I'm not sure it's anything to do with work itself, I think it's because it's "normal". Everything returns to normal when I go back to work. Right now I'm on medical leave, still connected to the hysterectomy, protected in this little bubble. But as of Monday, I'm back to normal life. Except, it's n...
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Womb-less

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Well, here we are 3.5 weeks post "the big op". 3.5 weeks since I lost a part of me. 3.5 weeks since my world changed. But most importantly, 3.5 weeks since my journey to living again started. The day itself came round very quickly. The months notice I had went by in a flash, and before I knew it, I was laying in the hospital. I started my op prep a couple of days before the big day, it was as unpleasant as I had expected. The bowel prep was certainly more aggressive this time, lasting right up until 10 mins before I went down for surgery and it's safe to say I felt utterly rotten. I felt so sick the morning of the op. I was sitting on my bathroom floor next to the toilet thinking oh my goodness, I can't go, I can't leave this bathroom let alone the house. Sheer panic had a hold of me and my anxiety had me sat frozen, pleading with myself to move. It was the toughest battle I've ever had with my own brain before an operation and between you and me, I truly didn...
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Here we go again!

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At the end of last year, I decided I couldn’t wait another 5 months to discuss my latest MRI results in person. I had received a letter saying the adenomyosis was more prominent and for me that was all the confirmation I needed. I wasn’t imagining it, the pain was getting worse and I needed something to be done. I should start by saying I recognise how lucky I am. Not everyone can afford to go private for treatment, especially as a self funding patient. I knew it was going to be pricy but I was at the end of my tether and just needed help. So within a week of enquiring, I was booked in for a consultancy appointment at The Oaks hospital in Colchester knowing I was going to be £180 lighter for a 20 min conversation. Ouch. But hopefully a worthy conversation! Fortunately I was able to see my normal consultant from the NHS privately. However, I was concerned he wouldn’t recognise me or know any of my history, after all he sees hundreds of thousands of women a time, why would he remember me...
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