It’s the other way around for most people but we are not most people.
In the last quarter of 2016, we spent quite a few nights in hospital with Ethan.
It happened quickly and out of the blue, for us.
Not so out of the blue; as doctors and specialists had pointed out to us at the time (over and over) - “Hunter Syndrome is terminal and can progress differently in all children who have it, the only thing that is the same is the fact that it is a terminal condition. We are so sorry”
I can tell you; when doctors and specialist are telling you that they are so ‘sorry’; you still can’t quite believe that your son is terminally ill. Yep, even that far down the rabbit hole you still cling to hope.
Like many parents who face that kind of reality, we decided to disagree with the doctors and fight them at every step. They wanted to sedate Ethan. We refused.
They wanted to take away all medications, as these were obviously not helping, we wanted to try milder medications and sadly, we did agree with the idea of a peg to feed Ethan, as Ethan had lost too much weight and was finding it difficult to eat.
There were no shouting matches with doctors; everything we suggested they tried.
Doctors have to keep you in touch with reality while trying to help you cope too. We are forever grateful to all members of Ethan's team, especially over those long, hard months.
It was only when we would repeat these conversations to family or close friends that we would see their reactions that we began to realise that we were numb to what the doctors were saying or deluded or in denial, whatever word our family, friends and doctors really thought about us, at that time.
We were never fully sure which we were so we decided that we were numb, it sounded better than being in denial.
Eventually our boy came back to us, not completely but mostly.
But the reality of Hunter Syndrome is exactly that; it takes and takes changing our kiddies each and every moment that they are alive.
We are well used to finding a new ‘normal’ with Ethan.
We just never had to find our way through such a rapid, spiraling new ‘normal’ before this.
Ethan has always been declining but much slower and only in a way that you’d notice if you hadn’t seen him in a few years.
This decline took the floorboards from under us, not just the carpet.
That shattered our hearts but we do think it is something our family needs the support of.
In the second quarter of 2017, Ethan began to take medication we felt he would benefit from ...and so our boy came back, little by little, bit by bit.
He went from not eating to only needing his peg for medication.
He went from not communicating to talking, laughing, playing and engaging with us.
He went from violent meltdowns to one meltdown maybe once or twice a week, with zero violence.
The doctors are the reality givers not the hope makers; parents are the hope makers.
We began to give Ethan ‘Charlotte's web oil’ in April 2017. The changes were subtle at first, we were even afraid that we were imagining them.
School saw the difference. Respite too. Doctors and those who called regularly to see Ethan noted the difference too.
He was indeed stabilising and happy once again.
With a condition like Hunter Syndrome, having your child stable is a huge thing.
Our boy started to come back to us, with little bits of speech coming back to him, his love of jigsaws, TV, music and his affection for us returned by December 2017.
It’s now a New Year.
I want Ethan to stay the same, even though I know that’s not realistic, I can still hope after all hope is what got us through last year.
Hunter Syndrome showed us the speed it can amp things up at last year...but it also made us enjoy our Summer, take longer days out with all our boys, it made our Christmas very special, it showed us once again how precious time is…
We hope this year it continues to show our boy some mercy so we can enjoy him for that bit longer.
What’s your in with the old and out with the new for this New Year?
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