"Crescere un figlio con una MALATTIA RARA"
Little Giacomo needs our help! Giacomo has Angelman syndrome, a rare disease for which there is (yet) no cure. There are two things we can do to help him and all the "angel people": ➡️ Make a donation, even a small one, to Fast Italia - cureangelman.it, which is THE great hope for Giacomo's future and beyond (find the link in the first comment); ➡️ Share this message with as many people as possible, so that anyone who can can contribute! #robadadonne #angelmansyndrome #araradisease ------------------------------------------------------------------------------------------------------------ To stay up to date with our videos, subscribe to our YouTube channel: / @robadadonneit and visit us on our website: https://www.robadadonne.it/ Join our Facebook community: / robadadonne And become our follower on Instagram: / robadadonne
Interview with Luca Trapanese: "Alba must know the truth."
Maddalena, il sorriso di una ragazza “Angelman” 15.12.2020
Autismo: una giornata con Alessio
Klaas schickt 3-Jährigen ALLEINE zum Bäcker | Experte für Alles
Sindrome di Angelman
Golden Retriever Meets Completely Broken Rescue for the First Time
Marco, il bambino con una malattia unica al mondo
IL NOSTRO RAPPORTO CON LA SINDROME DI DOWN
Liebe mit Handicap: Zusammenleben als Paar mit Down-Syndrom | DokThema | Doku | BR
Every Life - Mila's Story (Full)
Sissiland: "I'm not just a person with a DISABILITY, I'm so much more."
SenzaVoce _ Sindrome di Rubinstein-Taybi
Child marriage in Nepal: From bride at 14 to young mother | Kids on the Silk Road (5/10)
Ritardo di crescita e malattie rare: Sindrome di Silver-Russell
“A daughter, her Down syndrome, my choice of love”
MARCHE TARGET - CHILD WITH RARE GENETIC DISEASE
DOMANDE SCOMODE A MAMMA ! / tina e pippo review
Conjoined Sisters Celebrate 10 Years Apart
Telethon 2011 - La storia di Claudia (sindrome di Angelmann)
