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Six years ago today at 37 weeks pregnant I was in the antenatal clinic for my final scan.
There he was, rolling and kicking, utterly perfect.
I did notice when she went out to ask a colleague to pop in for a moment.
And every instinct started pricking when they smiled kindly and asked us to wait in the reception area for a moment, baby’s growth had slowed and my Obs/gyn would need to review.
Long story short – his growth had stopped two weeks previously, and he needed to be born as soon as possible.
Fast forward to Friday 15th April, 8.02 am when our little man made his grand entrance, and demonstrated that his lungs were none the worse for his early arrival!
If we’d known back in 2011 what we were about to face I’m not sure if we’d have coped. The shock and sheer fear would have been crippling.
The past six years have been a rollercoaster, and we wouldn’t have missed it for the world… this wonderful child has defied his devastating prognosis; at 18 weeks of age we were told he had West Syndrome (infantile spasms).
A kindly doctor gently explained his prognosis - IF he survived to his first birthday we were facing profound disabilities both physically and cognitively, he would be unable to interact or communicate.
As I screamed silently in my own head I was overwhelmed by fear for the future, as I held my tiny beautiful boy and prayed for a miracle.
Miracles come in all shapes and sizes. Sam was not one of the fortunate ones who escape infantile spasms (relatively) unscathed. He has huge challenges and yes, he is classed as profoundly disabled.
But every day, there are miracles… he regained his vision after the seizure activity took it at 1 year of age.
He communicates beautifully with sign language and the wonderful facial expressions he has (and a few choice hand gestures… I did not teach him those!).
Six years of seeing my child grow and develop, six years of love, laughter and wonderful memories.
So happy 6th birthday my little Superstar… thank you for all you are x
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