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#MumdayMonday The Heart Warrior Mum

I have been a very busy little bee and have written a guest blog piece for the Too Much Mothering Information series #MumdayMonday.

I am the Heart Warrior Mum.

Please go over and check it out, and while you are there check out the other great posts from this wonderful lady!!!

click here to go to toomuchmotheringinformation.com

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In less than four days’ time, my eldest child will celebrate his fourth birthday.
Birthdays are always emotional especially when looking back, I class his birth as one of the most traumatic times of my life.
I recently wrote about how four years it still haunts me.
I didn’t just become a new mum, I became a NICU (Neo Natal Intensive Care Unit) Mum.
It was a title I didn’t ask for and we were part of a club we didn’t ask to join.
I have now spent nearly 4 years writing about our story on this blog, and for other publications and websites.
I have tried to raise awareness of the issues that affected us, I have tried to bring about change but ultimately and I hope I am right in saying I have helped other NICU Mum and CHD (Congenital Heart Defect) parents.
I have tried to process some of the emotions surrounding our NICU experience and use them to do something positive.
I had so much I wanted to say this #nicuawareness…

New Year... Same Old Me

Well, I can officially say this is my first post of 2019 and also for a little while too, I hope it is the first of many more regular posts again.
The truth is, I lost my blogging mojo and fell into a bit of a social media wormhole constantly comparing myself to others, seeing them announce their plans and features and wondering if I was really good enough.
I have been questioning whether people really are interested in what I have to say as she types from her bed (I have been told that all the best writers do this from a fellow writer!) with her two kids being bribed with Milky Ways and Toy Story 2 for the umpteenth time.
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I don't want your pity, just to retell our story.

When I tell someone about Elijah's heart condition (Tetralogy of Fallot a severe congential heart defect) I tend to guess their reaction.
After four years we tend to be met with the same response.
One that is slightly uncomfortable, one that sees them struggling to find the words after we tell them that we watched as our six month old baby was wheeled away into theatre, not knowing if we would see him alive again.
Perhaps a glimmer of relief that it isn't their child that will face struggles, future surgeries, restrictions and life long appointments.
We tend to be met with sympathy for our situation, which is greatfully recieved.
Some have a relative or a friend they know that CHD has also resided in so have an insight into what our lives are like.
Some ask questions which I jump at the chance of answering.
Asking me questions about Elijah's condition means I am spreading awareness, educating others about CHD.
Something that up until four years ago we didn't even know…