Today, Wednesday April 23, marks the National Day of Cystic Fibrosis, a disease with no cure yet, which is estimated to have an impact on Spain of one in five thousand births.
In the Plaza Juan XXII of Cartagena, Murcia Association has Cystic Fibrosis this morning a c Ampana media outlet that was attended by the Councillor for Health, Ángel Nicolás Bernal, and the Councillor for Women, Clara Hall.
Cystic fibrosis is a serious genetic diseases in the Region of Murcia affects about 143 people, as confirmed by the psychologist of the association, Lali Diaz.
The daily life of this entity is based among other treatments, in a ctivities chest physiotherapy, but also to support families and their needs.
And, in the words of Diaz, the patient environment has the disease, so it is a team effort.
During this National Day Cystic Fibrosis Association has awarded a silver pin to the council of Health, Women and Social Care, presented while his dummy solidarity Pulmonito, with a price of six euros. All revenue from its sale will go to the research of this disease.
Besides the marketplace for solidarity and informative table that have remained all morning in the Plaza Juan XXIII of Cartagena, the work of this association does not stop for the rest of the year, designing a comprehensive program of activities where the will and solidarity are the identity.
Source: Ayuntamiento de Cartagena