Your donation fuels breakthroughs in PACS2 gene mutation research. 

In under a year, we've launched 8 projects and generated essential reagents, that are driving progress in the understanding of mechnism of action behind PACS2 syndrome. [See our impact here: LINK] 

Our mission is to cure PACS2 syndrome, and with your support, we're racing against time to make significant strides. In 2025, we anticipate to embark on our first clinical trials.

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While we actively pursue grant opportunities, the urgency of our cause demands swift action. Our children can't afford to wait for publications and bureaucratic processes. Development windows are closing, and your donation becomes the vital "bridge" that propels us forward—bridging the gap between groundbreaking research and tangible solutions.