The Guthrie-Koch Scholarship

 The Guthrie-Koch Scholarship celebrates the inspiring legacies of Dr. Robert Guthrie and Dr. Richard Koch, whose groundbreaking work laid the foundation for newborn screening and improved care for those with inherited metabolic conditions. Their dedication opened doors for a new generation, enabling countless young people to pursue their dreams.

Today, flok builds on this vision, supporting the next generation of students with inherited metabolic conditions as they pursue higher education. In the spirit of Dr. Guthrie and Dr. Koch, we’re committed to empowering these young people to thrive. We invite everyone touched by their work to support the Guthrie-Koch Scholarship and invest in a brighter future fo r this community.

Read the profiles of recent scholars.  

The application portal is open until March 15th.

Applying for the Scholarship

Completed applications and recommendation letters must be submitted by March 15th each year.  

  • Eligibility

    Scholarships are open to any individual with one of the inherited metabolic disorders listed on this page, pursuing post-secondary educational or vocational opportunities. 

    Graduate and professional students, as well as Individuals who have previously been awarded this scholarship are not eligible to apply. 

    Residents of any country are eligible. The application form is translatable to languages other than English through Google Translate. Please translate any upload documents (including transcripts and your essay) into English before submitting. 

    Applicants must be accepted to an accredited college or technical school before the scholarship is awarded but may apply for the scholarship before acceptance is confirmed.   

  • Who will review scholarship applications?

    The Guthrie-Koch Scholarship Committee, which includes staff and board members of flok, alumni of the scholarship, and at least one clinician familiar with inherited metabolic conditions. 

  • Conditions that qualify individuals for the Scholarship:

    • Classical Homocystinuria (HCU)
    • Maple Syrup Urine Disease (MSUD)
    • Organic Acidemias
    • Phenylketonuria (PKU)
    • Tyrosinemia
    • Urea Cycle Disorders (UCDs)
  • How to Apply:

    Click the Start Your Application button and enter your email address to get a link to the application portal. 

    Complete the application, which has the following parts:
    – Application
    – Essay or Presentation
    – Diagnosis Verification Form
    – Transcript & Test Scores (if applicable) 

    – Recommendations from 4 adults not related to you who know you from school, work, or community activities. 

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