Watch this video to learn how disability advocacy organizations can customize their medical outreach program for the unique demographics they serve: rural and small areas, medium-sized areas and suburbs, big cities, and state-based organizations.

Rural and small areas:

  • Connect with closest genetic counseling program and SMFM to provide your information and resources. Become best friends with the SMFM or genetic counselor/geneticist that serves your area. 
  • Connect with social worker at nearest birthing hospitals to provide your information and resources.
  • May be able to cover all obstetric medical offices in your area given the number. 
  • Identify the closest hospitals with Level 3 and 4 NICUs: https://www.texaschildrens.org/blog/2014/05/what-do-nicu-levels-mean
  • Providers and hospitals may be in a different state.
  • Consider building relationships with online providers: Genetic Support Foundation. (I serve on the board.)
  • Rural grants.
  • Reflect diversity in resources and use appropriate translations.
  • State resources: connection to newborn screening advisory; congenital cardiac screening (DS)
  • Nurse managers on the weekend (Be aware nuances hospitals)
  • Provide directed training

Medium-sized areas and suburbs of big cities:

  • Identify universities with obstetric and genetic counseling training programs. Build relationships with program directors. More likely to have a UCEDD/LEND program. Utilize students.
  • You may need to coordinate with big city group and other suburbs to differentiate organizations/programs with medical providers. Consider creating a collaborative brochure with a map.
  • May have Down syndrome clinics. Connect for referrals from program coordinator. Partnership.
  • More likely to have Grand Round opportunities.
  • Goal: Identify and cover all MFMs and GCs—added pediatric clinics
  • Military bases?
  • Reflect diversity in resources and use appropriate translations.
  • Need systems for tracking data and updates to medical contact information.
  • Connect with parents who have connections.

Big Cities:

  • Identify universities with obstetric and genetic counseling training programs. Build relationships with program directors. May be multiple. Utilize students. More likely to find researcher allies.
  • Set realistic goals and don’t get overwhelmed. Most likely to stagnate.
  • Data tracking is critical for everyone, but big cities really need a capture rate.
  • More likely to have Down syndrome clinics.
  • Most likely to have a UCEDD/LEND program.
  • Likely to benefit from a volunteer/staff base assigned to different hospitals.
  • More likely to have Grand Round opportunities.
  • VITAL: Reflect diversity in resources and use appropriate translations.
  • VITAL: Need systems for tracking data and updates to medical contact information.
  • Partner with other disability orgs.

State-based organizations:

  • Consider having satellite representatives to serve all regions.
  • Connect with corresponding state and regional medical organizations: https://nccrcg.org
  • State-based grants or appropriations
  • Public health partnerships
  • Connect to UCEDD.
  • VITAL: Reflect diversity in resources and use appropriate translations.
  • VITAL: Need systems for tracking data and updates to medical contact information.
  • Partner with other disability orgs.
  • State Developmental Disabilities Council: grants and budgets under $10,000
  • Dissemination grants to individuals with Ds and families and providers
  • Large Amish population or other hard to reach populations: 
  • Interagency coordinating council
  • Visit them and ask members from those populations: https://ectacenter.org/topics/intercoord/intercoord.asp
Categories: Training