** URGENT CALL TO AID- OLIVIA LUGANI – SURGERY FUND **
Dear Friends, Our daughter Olivia was born with a very rare genetic bone disease. She is now 10 years old, weighs 10kg, is the size of a toddler wearing clothing of a 2yr old, measuring [...]
Dear Friends, Our daughter Olivia was born with a very rare genetic bone disease. She is now 10 years old, weighs 10kg, is the size of a toddler wearing clothing of a 2yr old, measuring [...]
Dear Friends, Olivia is soon turning 10 years old. During these precious, though challenging years of her life, I have compiled a list of world-renowned doctors to support her ongoing medical needs, ie Neurosurgeons, Dentists, [...]
AMAZING SUCCESS TODAY!! After my proposal to the Mayor's office, today I was able to confirm our town will install the 1st ever inclusive play area for children in wheelchairs! I am so proud [...]
Dear Friends, As many of you know, Olivia has a rare genetic condition called Goldblatt Syndrome that affects only 17 other known patients world-wide. She is 8 years old, weighs 10kg and measures 67cm. As [...]
Olivia, the Champion! So proud of my girl! She conquered yet another gruelling 45 minute experience of plastering a thick mould to her upper body in order for the fantastic team at Hospital Poincaré, [...]
Dear Friends, I've been searching for years for an adapted manual wheelchair to assist Olivia with manoeuvring around the apartment. Since moving to France, some doors have certainly opened, but I have to bang [...]
Greetings to all our Friends and Family around the World. May 2020 We wanted to let you know our family is doing well as we #STAYHOME for the 10th week of [...]
FEBRUARY 2020 •As many of you know, Olivia has a rare genetic condition called Goldblatt Syndrome that affects only 17 other known patients world-wide. She is 7 years old, weighs 10kg and [...]
Life in Paris Our move to Paris came as a welcomed surprise in Summer 2019. After extensive research, we made an informed decision to select a french school in [...]