A Review Of 2017 From An Empty Armed Mother
Well, here we are again at the end of a year, and so soon too. It doesn’t seem like two minutes...
Read MorePosted by Frankie's Legacy | Dec 31, 2017 | Blog, empty armed mother, Francesco Enrico Ventura, Grief |
Well, here we are again at the end of a year, and so soon too. It doesn’t seem like two minutes...
Read MorePosted by Frankie's Legacy | Nov 5, 2017 | Articles, Awareness Raising, Diagnosis, Family, Good News, Rev'd David Southall, worcestershire royal hospital |
Dear West Midlands Ambulance Service and Worcestershire Acute Hospitals NHS Trust, Many of us have...
Read MorePosted by Frankie's Legacy | May 24, 2017 | Awareness Raising, Bereavement, Blog, Francesco Enrico Ventura |
I know, I know….I have not been as good as updating this blog recently. This is one project where...
Read MorePosted by Frankie's Legacy | Nov 20, 2016 | Blog, Francesco Enrico Ventura, Grief, Keeping Going, Loss, Meeting like-minded people, News, Positivity, Support, Surviving, Things I've Learnt |
“It was the year of fire… the year of destruction… the year we took back what...
Read MorePosted by Frankie's Legacy | Jul 22, 2016 | Blog, Rev'd David Southall, Uncategorized, worcestershire royal hospital |
I was proud and honoured to be asked to help at a charity concert last weekend by my good friend...
Read MoreFrankie was a small pebble dropped into the lake of life…but his ripple will be felt forever…
My blog “Frankie’s Legacy: Love, Loss Grief & Recovery” focuses on raising awareness of early pregnancy loss, stillbirth, neonatal death, cleft lip/palate and rare chromosome disorders.
My much loved and much wanted son Francesco “Frankie” Enrico Ventura was born sleeping on 29/11/2013 and had a severe cleft lip/palate, talipes and an extremely rare chromosome disorder (chromosome 15 duplication syndrome).
This blog focuses on my journey as an empty armed mother, and about how I am surviving stillbirth, celebrating Frankie and creating his lasting legacy as best I can.