Welcome to CASA HUNTER.

We are all rare.

Founded on November 26th, 2013, CASA HUNTER is a non-profit organization with no political or religious affiliation. Its aim is to ensure public solutions and sensibility from the private sector and society as a whole towards those with rare diseases, through the joint efforts families, friends, professional medical experts and anyone interested in the cause.

CASA HUNTER is comprised of the parents of children with rare diseases, doctors specialized in genetics, researchers, pharmacists, entrepreneurs concerned with the welfare of society, as well as idealists and human rights activists who felt the need to share their experiences and work towards a better quality of life for these children and their families.

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Our mission

Having a child with a rare disease and not wasting time on regrets. Feeling welcome by creating a welcoming environment for other families facing a similar situation. Being strong enough and building a safe place where to escape, exchange ideas, go across the world in search of doctors, the pharmaceutical industry, clinical studies; in short, whatever it takes to offer comfort and quality of life for all those affected by the disease.

Latest testimonials

When I realized how severe the disease was, I sought treatment to understand the syndrome and to have a closer follow-up. When the diagnosis was confirmed, I did not panic, but I am young; I want to have normal and healthy life, with treatment. Meeting with the CASA HUNTER was precisely due to a mismatch. I went to an appointment with the geneticist, and there I saw professionals with the CASA HUNTER jacket. My cousins also knew about it and we decided to go there. On the first day, I remember...

Felipe Ferreira

Come and volunteer!

Volunteering is the set of actions of social and community interest carried out by people free of personal interest, within projects, programs and other forms of intervention, at the service of individuals, families and the community, developed not-for-profit by public or private entities.

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Make your donation

Bring hope to genetic syndrome patients. Donate through this checking account:
Banco Bradesco N° 237
Branch: 1511-3 | Checking Account: 2830-4