Frankie’s Cleft Lip & Palate Story: Cleft Lip & Palate Awareness Week 2015
This week is “Cleft Lip & Palate Awareness Week”, which is run by the Cleft Lip & Palate...
Read MorePosted by Frankie's Legacy | May 9, 2015 | Awareness Raising, Blog, CLAPA, Cleft Lip, Cleft Palate |
This week is “Cleft Lip & Palate Awareness Week”, which is run by the Cleft Lip & Palate...
Read MorePosted by Frankie's Legacy | May 8, 2015 | Awareness Raising, Blog, CLAPA, Cleft Lip, Cleft Palate |
Tomorrow sees the start of Cleft Lip & Palate Awareness Week, which runs from May 9-17 and is...
Read MorePosted by Frankie's Legacy | May 8, 2015 | Awards, Blog |
I don’t ask things like this very often, but would you all consider nominating me for a MAD...
Read MorePosted by Frankie's Legacy | May 5, 2015 | Bereavement, Blog, Francesco Enrico Ventura |
Frankie’s funeral was on Thursday 5th December 2013. On Friday 6th December 2013 the funeral...
Read MorePosted by Frankie's Legacy | May 4, 2015 | Bereavement, Blog, Keeping Going, Meeting like-minded people |
Last night my husband and I decided that we would have my parents round for a roast dinner, and we...
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.