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Who We Are

The AGO Alliance Poland is a non-profit organization dedicated to supporting research on the ultrarare genetic disease - AGO syndrome (mutations in genes Ago1 and Ago2), as well as raising awareness about the conditions and supporting kids and families affected by the syndrome.

Support the AGO Alliance Poland

AGO Alliance Poland is dedicated to advancing knowledge through innovative research and collaboration. Our team of experts works on identifying key priorities for research and initiatives that will benefit the community. We encourage creativity and innovation in our community and among our researchers to push the research forward and develop the treatment as soon as possible. Time is of the essence for all kids affected by the mutation in Ago1 and Ago2 genes. Join us in our mission to cure the Argonaute syndrome.

How You Can Help

Make a donation to fund our research and programs.

Partner with us to amplify our mission.

Spread the word about AGO syndrome to raise awareness.

Volunteer your time and skills to support our initiatives.

Working with Financial Documents

Annual Statement

The first annual statement for 2024 will be available soon.

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About Us

We are a family of 5 with the eldest son, Albert, affected by AGO syndrome. We aim to develop a treatment for kids suffering from AGO syndrome that will improve their quality of life and offer a cure.

 

Please get in touch with us (Aldona and Aleks)  if you want to support us in our mission to develop a cure.

If you are a caregiver of a child affected by AGO syndrome, please join our online community in AGO Alliance.

Contact: contact@agoresearch.org

Konkurs: konkurs@agoresearch.org

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Bank Details

AGO Alliance Poland

ul. Swieradowska 51B,

02-665 Warsaw, Poland

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Account number: 

18 1600 1462 1717 3293 5000 0001

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International transfers:

SWIFT: PPABPLPK (BNP PARIBAS)

IBAN:PL18 1600 1462 1717 3293 5000 0001 

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