About us
The Association Sabina Islands by Argininosuccinic Acidemia and Rare Diseases
it is a non-profit agency with national scope. We are a mexican family
affected by the argininosuccinic acidemia that, in the absence of information and timely diagnosis, he decided to
to create this space to support other families and to contribute to improving the quality of life of patients
Our Mission
We Connect, Support
and we Promote the Research
Our initiative arises from the need to create a meeting space, support, and guidance for people affected by Argininosuccinic Acidemia type 1 and 2, their families and the medical community. We seek to raise the awareness of the society and to promote research to improve the quality of life of those suffering from these rare diseases.
Empathy and Respect 🫂
We value the realities and times of each family, offering support.
Perseverance 💪
We remain steadfast in our mission, overcoming each challenge.
Transparency and Collaboration 🤝
We build trust and unite efforts in each initiative.
Commitment To Science 🧬
We promote the research and development of effective treatments.
Team founder
People Committed to the Cause
Our team is comprised of people who have lived close to the impact
of Argininosuccinic Acidemia, and they have dedicated their effort to create a positive change
in the lives of patients and their families
Valentina Gonzalez ArterPresident
Armando Islands SanchezVice president
Rafael Mendoza AguilarFinance and Administration
Join Our Cause
Together we Can Make a Difference
Our organization operates non-profit and relies on the support of people
committed to the cause. You can help through donations,
volunteer, or spreading our mission.
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