NUMA supports the Children's Association with the CCAM , created to help families who have discovered that they are expecting a child with a congenital lung malformation. Emanuela Alberio , mother of two children, found herself facing this situation with the arrival of her second daughter. The first difficulty in managing the pathology consists in making a correct diagnosis, which is essential to avoid the development of serious complications, since often, both in the fetal and neonatal period, symptoms do not appear. NUMA supports children suffering from congenital lung malformation and the costs of families staying in cities where it is possible to find competent hospital medical support.
CLICK THE FOLLOWING LINK AND READ VITTORIA'S STORY
Here you will find information of a medical nature and you can read children's stories with the CCAM , told by their parents.
The stories of our children testify that lung malformations, in most cases, it can be healed.
In this association you will find extraordinary people who put themselves at the service of others, mothers and fathers who are available to be contacted by telephone or in person to listen to your questions, the fears that arise in these cases or simply to give you comfort.
Those who have already been through it are very sensitive and understand your state of mind.
The association helps not only on a moral level, but also through economic contributions to families who find themselves in difficulty in meeting the expenses related to travel and accommodation, to reach the reference hospitals.
Don't feel alone, call us and we will face this journey together.
For any information you can write an email to: info@bambiniconlaccam.it
Or call our friendly number: +39 329 1864 884
If you want to help us you can contribute with a donation:
Banca Popolare di Milano Agency n. 0220 Voghera office (PV)
IBAN: IT48 G 0503 45640 10000 000 28730 made out to Children with the CCAM
- Emanuela Alberio
