Skip to main content

The Liebster Blog Award



Today I had a notification to say I had been given The Liebster Blog Award by another blogger and a fellow brave endosister. I will be 100% honest and say I had no idea of what this award meant. After reading the link I was sent I am so grateful to be thought by Endo Joanna from Living With Endo when she was compiling her five favourite blogs for this award.

Liebster is a German word which means "dearest" or "beloved". It is also used to refer to someone's "favorite" and the idea of the Liebster Blog Award is to bring attention to blogs with less than 200 followers that deserve more recognition and encouragement.

I started this blog to help raise awareness of endometriosis. When I was diagnosed I felt so alone and wanted to speak to other people who were going through the same things as me. Twitter and this blog allowed me to do this. I never actually thought others would care to read my blog or my thoughts, it was initially a place to voice what I was feeling. To know that people read my blog and can find some similarities and comfort that they are not alone means so much to me.

Here are the rules:
1. Thank the giver of the award and link back to their blog!
2. Select 5 of your top bloggers & let them know by leaving a comment on their blog!

3. Paste the award on your blog!

Here are my 5 choices for the Liebster Blog Award. Please take a moment to read their blogs when you get a chance. I believe they all provide such honest information and thoughts on their daily life, struggles and successes. All very brave women. The last blog I have referred to also provides updates on research in endo and further links which I think is an interesting read and would recommend.


1. Endo Journey from Endometriosis: The Journey Of A Woman Warrior
2. Begining To Endo from Explore The Journey: From Beginning To End..Ometriosis
3. Foxy from Foxy In The Waiting Room
4. Me Inside And Out from Me Inside And Out
5. Matthew Rosser from Endometriosis Update 
#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 ♡

Endometriosis And New Beginnings

I know I won't be alone in these thoughts on this subject.. Endometriosis and a new relationship..  What do you tell them? How much do you tell them? When do you bring it up?  A million questions have been overloading my mind lately as I start a new chapter in my life. The last few weeks have been a bit of a whirlwind for me. A good one! But, fast moving, exciting and terrifying all at once. The scariest part of it all is how endometriosis will impact everything. Right now, it is behaving. But we all know how quickly that changes. I don't want my life revolving around Endo. It has taken over way too much of it already! Now, I have started enjoying my life again, I'm terrified it will be snatched away to pain once again. I have shared The Spoon Theory with my new boyfriend, who was extremely understanding about it. Which actually made me feel so much at ease. I have explained a few of the symptoms. He knows I get 'bad days' and that i'll need rest ...

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...