2023 COMPREHENSIVE RESEARCH REPORT
The ADNP Kids Research Foundation is committed to keeping the ADNP community informed on the projects that we are funding. To date, since 2018, the foundation has funded over $1.2 million dollars in our program research projects and advocacy. The 2023 Comprehensive Research Report is a breakdown of what programs and projects that the foundation is currently working on. As you will see, we continue to be moving the needle forward full steam ahead, to help our children who suffer with ADNP Syndrome. Science is incredibly complicated, expensive and slow, and without a solid community and support, these projects will not be possible. As we gear up for our biggest fundraiser, we hope this helps motivate and encourage everyone to know that we are funding some incredible therapeutic and curative treatments for our children.
The ADNP Kids Research Foundation is committed to keeping the ADNP community informed on the projects that we are funding. To date, since 2018, the foundation has funded over $1.2 million dollars in our program research projects and advocacy. The 2023 Comprehensive Research Report is a breakdown of what programs and projects that the foundation is currently working on. As you will see, we continue to be moving the needle forward full steam ahead, to help our children who suffer with ADNP Syndrome. Science is incredibly complicated, expensive and slow, and without a solid community and support, these projects will not be possible. As we gear up for our biggest fundraiser, we hope this helps motivate and encourage everyone to know that we are funding some incredible therapeutic and curative treatments for our children.
RESEARCH
The ADNP Kids Research Foundation is funding science to understand the biology of ADNP and identify innovative therapeutic strategies and a cure for all individuals around the world with ADNP syndrome.
The ADNP Kids Research Foundation is funding science to understand the biology of ADNP and identify innovative therapeutic strategies and a cure for all individuals around the world with ADNP syndrome.
- NOTE: We are a 100% volunteer-ran patient organization, we do not pay university overhead fees as part of our grants or sponsorship research projects. If you are interested in discussing a grant opportunity please email [email protected].
Our research is not possible without the support from families like you and the philanthropy from generous donors to fund our projects.
Together we can continue to make strides to increase the quality of life for individuals with ADNP syndrome.
If you would like to support our work on ADNP syndrome, please DONATE here.
Together we can continue to make strides to increase the quality of life for individuals with ADNP syndrome.
If you would like to support our work on ADNP syndrome, please DONATE here.
