Showing posts with label edwards syndrome. Show all posts
Showing posts with label edwards syndrome. Show all posts

Saturday, 21 July 2018

Fliss: Right Where I Am 2018: 6 years 5 months 12 days


2355 days since our lives changed forever. Since I held her in my arms as she took her last breath.  I felt my soul shatter and I couldn’t understand why people could not see right through the hole within me.

A lot has happened since then, another child has come into our lives, our beautiful rainbow who brings us joy every day, along with his brother, who still talks of his sister at times.  I’m not anywhere near where I was, that awful dark place is somewhere I never want to return to but is still there, in the shadows of my mind. Occasionally the memories rear up and the pain is there but on a daily basis I am able to function like an almost normal human being.

I watch my children grow together, play together, laugh and fight together and it doesn’t break my heart as much as it once did.  I’ve worked hard to move away from the place I was, support workers, counselling, online support groups and finally after a lot of resistance (from me) I was prescribed medication.  Not for depression but for PTSD and anxiety that has come from the loss of my child.

One of my biggest achievements I feel is making new friends, one has a daughter who is in the class Ayla would be in and I just know they would have been best friends.  She has 2 brothers and along with my two boys and our other friends 2 sons, she is surrounded by boys.  This does hurt. My heart aches when she mentions that she has no girl to play with.  However, whereas before I would have pushed her and her mum away and actively avoid becoming friends this time I have stepped in, not allowed my pain to stand in the way of what has become a wonderful friendship that I truly value and has led to another equally valued friendship too.  I also have a relationship with her, she’s ace, we have a great time together and she runs to me for hugs and kisses.  These have helped my playground life be a bit easier and not the nerve wracking fear inducing horror that they once were for me.

Ayla has brought some truly beautiful people into my life, some from afar, some much closer, some for a short while, others to stay the distance and show me what having true friends actually means.  All of them I love and appreciate more than they will ever know and because of these people I know that I’m ok, Ayla lives within me, within her Daddy, her brothers and all the many people she has touched the hearts of.  What an amazing girl, it is an honour to be her Mummy, even when it hurts.

~ ~ ~ ~ ~

You can read my previous Right Where I Am post by clicking on the link below:


You can read more my story here:

Friday, 19 October 2012

Fliss: Letter to my Ayla

19th September 2012 

My darling, beautiful Ayla,

A year ago today I was hoping that you would be facing a heart operation when you were only one month old.  What sort of a wish is that? One where you would still be here, you would have had a chance, a good chance, at life.  A year ago today I had no idea, absolutely not a clue, of the horror, the heartbreak and life and soul changing devastation we were about to go through.  From the moment that test showed two lines I felt so different than I did with your big brother.  There wasn’t the excitement I had with him.  Happiness – yes, I was very happy but I couldn’t shake this feeling that something wasn’t right.  I didn’t dread miscarrying, I expected it and was almost surprised that every week you were still there.  I didn’t want to miscarry sweetheart but maybe I knew that I would lose you in some way?

We had an early scan and again I expected to be told that the pregnancy wasn’t viable, there was no heartbeat, something.  The 12 week scan I expected bad news again but there you were waving at us.  But not moving, not like your brother did.  Your Daddy questioned it but the lady said it was fine, our first sign? She couldn’t do the nuchal measurement because you wouldn’t change position, the first sign you would be doing things your way.  I didn’t mind because I knew termination would not have been an option for us.  Even those scans didn’t relieve that worry deep in my heart.  Please sweetheart, don’t think I didn’t want you, I did, I do, so so much.  I knew you would be a girl but I also knew that you were poorly, on some level at least.  I never, not once expected you to be as poorly as you were but I knew something wasn’t right.

We sat outside the room where we were to have your 20 week scan.  The scan that people normally get all excited about, seeing their baby looking more like a baby, finding out girl or boy.  I didn’t I felt sick with fear, I sat there rocking back and forth, looking back now I knew so much more than I realised at the time.  That scan was the start, the real start of your story.  Your miraculous battle to make it into the world.

A year ago tomorrow we heard the words ‘Your daughter has Edwards Syndrome’.  We had no idea what that meant, how big it was. I hoped it would mean you would be disabled, need special care, have special needs, I never imagined, never, that it actually meant we didn’t get to keep you.  Babies don’t just die because their genes aren’t right, there must be something that can be done, surely? How little I knew then, how little I understood.  How much I know now.  Its hard to remember ever being that ignorant, that naïve.  Before we had that phone call, whilst waiting for the results I remember standing at the fridge thinking about the possible dilemma we could be facing, let nature take its course – give you a chance, or end your story prematurely.  Live with that the rest of our lives.  I stood there thinking this all through, round and round and you, you flipped inside me and gave me the biggest series of kicks and movements as if you were saying, no, shouting at me ‘GIVE ME A CHANCE, I’M HERE, I’M FIGHTING, GIVE ME A CHANCE!!’ and that’s when I knew without a doubt that there was no way, no matter what the diagnosis, there was no other option for us but to carry on, give you a chance, let nature do what it needed to.

It led to the hardest, loneliest time of my life.  I didn’t want to be pregnant anymore; I just wanted it all to go away.  Go to sleep and wake up when it was all over.  But I loved you, oh I loved you so much by then, I was, am, your mummy and I would do anything for you.  I do not regret giving you that chance, not at all and I never ever will.  My love for you is overwhelming, all consuming and everlasting, just like my love for your brother, because I am your mummy.  I can no longer do anything for you so for those 5 months I am glad I did everything I could for you.  I do things to keep your memory alive, show my love for you to the world but it’s not the same, you are free now, you don’t need me.

The guilt I felt and still do in some ways at not being able to protect you, make you better engulfed me for months.  Why couldn’t I make you better? That’s what mummies do, give magic kisses and cuddles, go to the doctor, whatever it takes to make their children better.  But I couldn’t, no matter how much I wanted, wished, begged, I couldn’t.  There was nothing I could do but give you a chance and hope, every decision I made I did what I felt was best for you and I hope you know that my darling and could feel my love for you every second of every day you were here and every second since you went, since we had to say goodbye and give you no more cuddles and kisses.  When I broke inside, never to be completely fixed again, to always have a hole in my heart, a piece of me missing.  Every happy occasion, smile, laugh tainted with the pain and sadness of you not being here, someone missing from our family forever.

So what do we do now? We miss you every day, we light candles, we send you balloons, we talk about you, to you, we see rainbows, sunflowers, butterflies, stars, blow bubbles and think of you.  We use you to drive us in our new perspective on life, we hold you in our hearts as we try to move forward, sometimes stumbling, sometimes slipping back and sometimes falling flat on our faces, but we get back up and carry you with us in everything we do.  Because we love you, forever and always,

Watch over us baby girl and know you’re always with us, 

All my love, 
Mummy xXx

Wednesday, 1 August 2012

Fliss: Incompatible with Life


Our daughter had Trisomy 18 (Edwards Syndrome) and when told the diagnosis we were also told the words 'incompatible with life', despite medical assumptions we carried on with the pregnancy to give our daughter every chance we could.  It was worth it.  I wrote this shortly after she passed away...

Do not tell me my daughter is incompatible with life.

To be 'incompatible with life' you would not be able to exist - ever. But to make it through conception, growth, the development of a heart, lungs, liver, brain and all the other aspects that create a human being - which the name itself proves the existence of life - being - a human, being.

For 9 months our daughter grew inside me, she moved, she played, she slept, she grew stronger and stronger, she developed a personality, a soul.

The body she was given was destined to fail her and yet she continued to fight and she made it into the world to feel all the love that is here for her, from her mummy, her daddy, her brother and so so many more people, family, friends and others far and wide - to touch so many, make them stop and think, shed a tear for her, smile at how strong she is, be inspired by her - how many can say they have done that?

For 70 amazing hours our beautiful daughter fought on with the body she was given until she felt it was time to go, to leave it and spread her wings. But behind she leaves eternal love and pride from Mummy and Daddy and the impact of her strength and bravery on so many people.

Do not tell me my daughter is incompatible with life.