Skip to main content

Endometriosis Awareness Month - Week One

The online support this year for endometriosis awareness month has been incredible. We are only one week into the month and I have been overwhelmed with the awareness raised so far. So many women have gone 'yellow for endo'. This is a fantastic campaign that has made my twitter timeline come to life. I love seeing all the yellow profile pics appearing daily!

I have also been taking part in the #endophotochallenge made by EndoHappy. Everyday you post a fact about your endometriosis. This is a wonderful and well thought out campaign that provides a necessary insight to our lives with endo. It's still not too late to join in if you haven't done so yet!

On Facebook, I have been posting awareness posts and pictures. This year I have had an amazing response to my posts. The amount of likes and comments I have had really surprised me. Friends and family have been sharing my status's and people who I rarely talk to on there have contacted me and shown their support. This means so much to me. Spreading the word about endometriosis is vital.

On a more personal level, I am thrilled with the awareness raised by my blog in this first week. I was first contacted by HealthExpress to be awarded with the 'Endometriosis Awareness Blog Award 2015'. The feedback I have had from this has been tremendous. I have been in contact with HealthExpress since and today they confirmed they will continue raising endometriosis awareness to their readers and patients! This is due to the vast response they have had after publishing their article! How amazing is this?! To visit the blog section of their website about women's health click here, http://www.healthexpress.co.uk/blog/womens-health/.

Secondly, I was contacted by a leading online fertility website. They have asked me to write a blog post for their website on endometriosis. I have submitted this article and will hopefully be able to share it with you all very soon!

So much has been achieved already this month. I look forward to seeing what the next three weeks will bring!


#MyEndoDiary

Comments

Popular posts from this blog

Endometriosis: Post op

Ok, so I thought I should update you all after my operation on Tuesday.  I have a lot of mixed emotions after the laparoscopy though and I promise to fill you all in soon. I'm sure many of you have felt the same way I'm feeling now so I will post in the near future about all the details. Sharing information is the best way to know we're not alone in this. But for the moment, I'm just getting my head around things and concentrating on recovery. UPDATED: Endometriosis was found in my ovaries as expected and removed. It was also found on my bowel, but it was left untreated. #MyEndoDiary ♡

A Day In The Life Of An Endo Girl - 16/04/13

Seeing as I've named my Blog 'My Endo Diary' I've decided to start this project, 'A Day In The Life Of An Endo Girl' to portray just a snippet of a day with Endometriosis. Women with Endo are not lazy. Some, such as myself suffer daily pain. Chronic pain. Sometimes mild, sometimes exhausting, sometimes severe. Small things hurt massively. What some people take for granted doing, can take all of my energy. Even down to doing the dishes or making food. Endo is unpredictable. Tomorrow may be a better day. It may be worse. If I look or sound OK one day it doesn't mean I'm better. I'm either hiding the pain from you (I've become quite good at this), having an 'up and down day' (explained below) or on the rare chance having a good day. Every day with Endo for me, is different. However at the moment, they all contain some sort of pain. So here's my first entry. 16/04/13                   5:45am Woken up by Endo pains, stabs in my hips

Endometriosis: When did it all start?

Christmas 2009 is when my life changed. I had always suffered extremely heavy and painful periods. But to me that was normal. I didn't realise then that was a symptom. I was able to manage it. Whether it was wearing two pads, scouring chemists or supermarkets for period pain relief, heat pads, painkillers, holisitc bracelets, taking days off school or spending days in bed. That was my normal. But Christmas 2009 is when more symptoms started coming. Nothing I could put my finger on exactly at the time. I just I knew I didn't feel right. Especially my emotional health. I was so down. With hindsight it must of been changes of my hormone levels as hormones play such a big part in Endometriosis. Looking back, I now know that was the start of the flare. February 2010, I started having stabbing pains in my stomach. I remember the 1st ever time it happened. I was doing normal things. I was actually walking across my landing to get to my bedroom. The pains shot across through my stoma