Mamme e PFAPA

For all parents with children affected by the little-known PFAPA syndrome.

The purpose of this application is helping to know the disease, give advice and tools to manage it, offering help and listening through a network of parents who share their experiences.

INQUIRE

Through the application of mothers and PFAPA in depth what so discover the PFAPA and all its aspects, how to get a diagnosis, what are the greatest risks, what are the most common treatments.

INSTRUMENTS

The application provides some practical tools to improve the quality of life and address some of the problems with which we must live with. There is also a DIARY fevers to mark the dates of the attacks and record the information necessary for monitoring and medical analysis of the disease

SOCIAL NETWORK

All news, events in which you can participate to deepen your knowledge.

You can discover all the channels on which to find and keep in touch, confront and meet other parents like you living with this syndrome and the fight actively. From today you are no longer alone!

Please note:

We are parents, like you, who make available their experience and their time to help and support those who are not yet familiar with the syndrome or feels alone in facing the disease.

We are NOT doctors, we do not provide medical consultations it information on drugs or treatments!

For any health problems, doubts or concerns about the physical condition of your child, contact your pediatrician or family doctor.