Developing a patient-focused educational resource on early-onset progressive encephalopathy with brain atrophy and thin corpus callosum (PEBAT).
Writing clear, accessible scientific content for patients and families.
Instructor/Facilitator - Spirituality, Faith & GC
University of Washington Genetic Counseling Graduate Program
Seattle, WA
05.2025 - 06.2025
Developed educational content for a class and organized a panel discussion on faith and genetic counseling.
Participant
Tet Festival Health Fair
Seattle, WA
01.2024 - 01.2025
Patient Resource Creator | Jan 2025
Developed a patient-focused educational resource for hematological genetic disorders, simplifying complex genetic information for community members.
Presenter
World DNA Day Conference
Pondicherry, India
04.2024 - 04.2024
Presented virtually on carrier screening in reproductive health.h
Genetic Counseling Intern - Prenatal
University of Washington
Seattle, WA
01.2024 - 03.2024
Drafted clinical documentation including consent forms, inheritance risk assessments, and psychosocial evaluation notes following ACOG and SMFM guidelines.
Provided genetic counseling for chromosomal abnormalities, carrier screening, prenatal screening, invasive testing, and ultrasound markers
Genetic Counseling Intern - Pediatric (Medical Genetics and Hematology)
Seattle Children's Hospital
Seattle, WA
10.2023 - 12.2023
Drafted patient-friendly educational summaries and clinical documentation on genetic conditions.
Collaborated with geneticists, nurses, dietitians, and social workers for patient care
Presenter
Washington State Genetic Counseling Journal Club
Seattle, WA
10.2023 - 10.2023
Created a presentation for the journal article 'Effects of Genetic Counselor Disabilities on Their Professional Experiences.'
Genetic Counseling Intern - Adult and Cancer
University of Washington
Seattle, WA
06.2023 - 08.2023
Developed written summaries on hereditary cancer syndromes and adult-onset conditions for both patients and providers.
Created educational content explaining testing protocols, potential results, risks, benefits, and psychosocial implications in accordance with NCCN guidelines, based on NCCN guidelines.
Family Outreach Navigator - Research/Outreach
ConnectMyVariant
Seattle, WA
04.2023 - 06.2023
Created content for patients with pathogenic variants, translating complex genetic data into accessible language.
Conducted literature reviews using ClinVar and PubMed, synthesizing research into clear, written content for patients and clinicians.
Research & Literature Review (PubMed, ClinVar, GeneReviews)
Team collaboration
Data Analysis & Summaries
Content Development & Educational Design
Tools: Microsoft Office Suite, Google Workspace, Slack, Canva
Community Outreach
Advocacy
Certification
ABGC Certified, 22374
WA State License, GT 61672334
Volunteer Experience
Medical Writer, MedReport Foundation, Virtual, 03/01/25, Present, Contributed to the development of clear, concise, and scientifically accurate medical/genetics content, tailored for a general audience.
Content Creator, LinkedIn (Personal Newsletter - Genes & Chai), Virtual, 02/01/25, Present, Authored reflections on genetic counseling, faith wellness, and professional growth and practice, Created accessible content that encourages reflection and discussion in the genetics community
Advocacy - RARE Compassion Program, Global Genes, Virtual, 03/01/23, 11/30/23, Interviewed families with rare genetic conditions (Galactosemia, OTC, CF, and PKU) and documented patient experiences.
Care Line Counselor, San Francisco Night Ministry, San Francisco, CA, 03/01/21, 06/30/22, Provided high-level customer service and support to individuals in need of emotional support through phone calls (4-hour shifts/week)
Research
Capstone: Designing gene panel for Aplastic Anemia, University of Washington, Seattle, WA, 06/01/23, 03/31/24, Designed an aplastic anemia gene panel, ensuring clinical utility and developing a statement of medical necessity and provider resources
DNA Repair Gene Polymorphisms in Cardiovascular Disease Research Project, Sri Ramachandra Institute of Higher Education and Research, Chennai, India, 01/01/19, 05/31/19, Collected patient data (medical history, lifestyle) and conducted PCR, genotyping, and data analysis on the association between XRCC3 and hOGG1 and Coronary Artery Disease
References
References available upon request.
Timeline
Upcoming Project - Patient Resource Developer
NORD (National Organization for Rare Disorders)
08.2025 - 09.2025
Instructor/Facilitator - Spirituality, Faith & GC
University of Washington Genetic Counseling Graduate Program
05.2025 - 06.2025
Presenter
World DNA Day Conference
04.2024 - 04.2024
Participant
Tet Festival Health Fair
01.2024 - 01.2025
Genetic Counseling Intern - Prenatal
University of Washington
01.2024 - 03.2024
Genetic Counseling Intern - Pediatric (Medical Genetics and Hematology)
Patient Service Representative, Senior at National Organization for Rare DisordersPatient Service Representative, Senior at National Organization for Rare Disorders