In December 2019 we received the exciting news that we were expecting our first child!
In early 2020 we learnt that they had a life limiting condition called Edwards Syndrome (Trisomy 18), and that they were likely to have a life expectancy measured in hours, if they even made it to birth.
From this point on we included her as a member of the family, naming her Henrietta (our Hettie) and including her in family life as much as we could, determined that we would continue fighting for her as long as she did.
She was born by elective C-section in August 2020, and continued to be a fighter. It was at this point we first heard of Acorns Children’s Hospice when we were transferred there from the maternity ward. They were amazing, providing us with care and support as well as caring for Hettie. Hettie was only in the hospice for a few days before she came home with us, but this time allowed us to learn how to feed her and provide her medication via her NG tube.
Our little Hettie was with us for 8 unforgettable weeks, during which time we knew that, alongside the NHS services, Acorns was standing with Hettie. Acorns support for us as a family continues to this day.
They truly are an amazing organization, and I hope to be able to raise not only funds for, but awareness of this charity so that they can continue to be there when children and families are at their most vulnerable.
Worcester News Article