CISTO PILONIDAL GRUPO E SUPORTE
Starting to change society does not need big steps.
In fact, there are countless examples of social projects with the various ailments, whether proctological or not, that are transforming a person's life in a minute and that are capable of doing the thing that still exists.
We believe that knowledge is crucial, the goal is to share information as a priority of support and assistance
Officially founded on September 14, 2015 by Debbie, today with more than 5K members, the CPGS has as a challenge to bring to society a Pilonidal Disease or Pilonidal Cyst, in its area of knowledge, with its values, principles and powers.
With the growth of CPGS, we have become the largest group of patients on the disease in South America.
If we are brave enough to think we can change the world, we certainly can!
CPGS is a support and support group for
PILONIDAL DISEASE - PILONIDAL CYST.
The group was created on September 14, 2015 by Debbie Signé who suffered for several years in search of answers to her multiple surgeries.
Today we are more than 2800 members in all digital platforms, the Youtube channel has more than 50 thousand views and the numbers continue to grow.
Promote information, research development and support.
Our mission is to alleviate the suffering of our caregivers and their families, seeking resources for medical, psychological, ambulatory, guidance and institutional lectures.
To be among the efficient and recognized philanthropic organizations within the specialty of coloproctology, to make Brazilian index for research development, to establish strategic partnerships ...
Comprehensive, safe and individualized assistance.
Commitment to the institutional culture.
✔WHO CAN BE ATTENDED:
Members of the CPGS with suspected or proven diagnosis and their relatives.