Our genetics make us unique, our struggles and triumphs unite us.

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Our Mission

Identify, Assist, Treat

Our mission is to help identify and assist individuals with rare genetic disorders, and to work with interested researchers to develop treatment options and cures for those disorders. Our initial focus is on increasing awareness and understanding of patients with DHPS deficiencies and evaluating potential treatments to address those deficiencies.

 

1 IN 10 AMERICANS

ARE AFFECTED BY A RARE DISEASE

 

30 MILLION PEOPLE IN THE US

ARE AFFECTED BY A RARE DISEASE

 

350 MILLION PEOPLE GLOBALLY

ARE AFFECTED BY A RARE DISEASE

 

OVER 7,000

DISTINCT RARE DISEASES EXIST

 

APPROXIMATELY 80%

OF RARE DISEASES ARE CAUSED BY FAULTY GENES

 

50% OF PEOPLE

AFFECTED BY RARE DISEASES ARE CHILDREN, MAKING RARE DISEASES ONE OF THE MOST DEADLY AND DEBILITATING FOR CHILDREN WORLDWIDE, ACCORDING TO THE NATIONAL HEALTH INSTITUTE.

We make it simple for families to get help.

Navigating the conversation no parent wants to have.