Advocacy
Won the National Rare Artist art competition with a scholarship at Everylife Foundation for rare diseases. This allows me to showcase my art on Capitol Hill in Washington D.C. and create awareness at a national level, fundraise, advocate, and educate congressional staff on rare diseases, and build relationships with members of Congress
TAAF Youth Ambassador
Youth ambassador at TAAF (The Aneurysm and AVM Foundation) (3 years): Plan events and fundraisers. (TAAF walk and the SF Marathon Health and Wellness Exposition)
UNICEF Event Commissioner
plan/find volunteer events, keep track of club members volunteer, hours, manage Google Classroom
Helped host the first Snowflake Ball at Silver Creek High School – managed sponsorship and silent auction aspects of the first Snowflake Ball at Silver Creek High School to raise money for “Doctors without Borders” which helps deliver medical equipment to people in crisis. It’s a humanitarian project present in over 70 countries, with 6 hospitals along the Gaza Strip.
Health Occupations Students of America (HOSA)
Second Place Winner for community awareness for ÅVMs at California’s State Leadership Conference and competitor at Hosa’s International Leadership Conference
Officer For Voiceopedia
Voiceopedia uplifts and empowers Refugee communities locally through facets of activism, social mediums, literacy, and welfare programs all under the umbrella of the umbrella. Activism is essential in spreading awareness of current issues in this modern day. Voiceopedia strives to advocate for disadvantaged communities, creating equity among all individuals.
UNICEF Event Commissioner
The Jumo Health-sponsored 2023 iCAN Summit took place July 10–14, and I had a blast! The Summit was hosted on the University of California San Diego campus in La Jolla, California. I am incredibly grateful for the chance to talk alongside YARR from the EveryLife Foundation for Rare Diseases at Jumo Health’s 2023 iCAN Summit. I had the privilege of giving a presentation titled “Become an Advocacy Superhero!” under the direction of Courtney Felle, the YARR Program Manager at EveryLife Foundation for Rare Diseases, where i shared my experiences advocating for legislation pertaining to rare diseases and public health.
Anthrofusion 