Apart from updates about Frankie’s Legacy as a charity, and the events that I’ve been working on to raise funds to go towards improving the delivery suite facilities at the Worcestershire Royal Hospital and other hospitals in...
Read MoreOur Family Fun Day organised by Ella Stearn Events is fast approaching and we have some amazing raffle prizes for the event! We would like to thank everyone who has donated vouchers and prizes for the raffle including:...
Read MoreOut of the blue a few weeks ago I received an email from a lady called Angela Phillips, who is part of the Droitwich Lions Ladies, saying that they would like to make a donation to Frankie’s Legacy. I wrote back to her...
Read MoreOn Sunday 20th July 2014 Events Organiser Ella Stearn will be running a family fun day; all money raised will go to Frankie’s Legacy who are raising funds to improve the delivery suite facilities at the Worcestershire Royal...
Read MoreFrankie’s Legacy is supporting the first ever Rare Chromosome Disorder Awareness Week in his memory, as Frankie would have had Chromosome 15 Duplication Syndrome if had lived, which meant he would have been severely...
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Frankie 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.
With much love,
Lisa Ventura MBE FCIIS
Frankie’s Mummy
xxxxx
