
Co-Founder & CEO
Nathan Ragheb
Leads social media strategy, content creation, and business development. Grew @htsa_bros to 1,037 followers and 1M+ views.
Student-led. Community-powered.
We're HTSA Bros. We bring people together to raise Heterotaxy awareness, support families, and make a difference in our community.
Our next chapter
150 Comfort and Play Kits.One goal. More moments of joy for children in local hospitals.
Our first chapter · Phase 1 impact
Coming together, again
Entrepreneurship & Innovation Center · Franklin, TN
Run with purpose
Help turn a winter 5K into moments of comfort and play. Together, we're working toward 150 kits filled with toys, games, and creative activities for children in local hospitals.
Runner entry fees and registration details coming soon.
Why we do this
Heterotaxy Syndrome is a rare congenital condition in which internal organs are abnormally arranged in the chest and abdomen.[1]
We're here to make reliable information easier to find and build a community around affected families.
Learn about HeterotaxyEvidence-based education, social media challenges, and local outreach help more people understand Heterotaxy.
School collaborations, community events, and business partnerships turn shared purpose into action.
Our next chapter supports Comfort and Play Kits for children in local hospitals through the Hot Cocoa Run.
Stronger together
Our story & purpose
From Franklin, Tennessee, we're bringing communities together for Heterotaxy education, research, and affected families.
Local roots. Shared purpose.
HTSA Bros began when students at Centennial High School in Franklin, Tennessee, saw how deeply Heterotaxy Syndrome affected families in their community.
With a social media strategy, a partnership with Heterotaxy Connection, and a commitment to their community, the team launched a campaign that reached over 1,000,000 people, raised more than $5,300, and brought Heterotaxy awareness to schools, businesses, and families across Middle Tennessee.
See our workWhy Heterotaxy
Heterotaxy Syndrome is a rare congenital condition in which internal organs are abnormally arranged in the chest and abdomen.[1]
Because Heterotaxy can affect the heart, lungs, liver, spleen, intestines, and other organs, families may need coordinated care across several specialties.[2] Our mission is to make reliable information easier to find while supporting research and affected families.
Heterotaxy is estimated to affect about 1 in 10,000 people worldwide, although it may be underdiagnosed.[1]
A multidisciplinary clinical review reports complex cardiovascular malformations in more than 80% of children with Heterotaxy.[2]
Heterotaxy Syndrome accounts for approximately 3% of congenital heart defects.[1]
What guides us
To close the knowledge gap on Heterotaxy Syndrome by educating communities, raising funds for research, and supporting affected families through partnerships and events.
A world where every child with Heterotaxy receives timely diagnosis, adequate funding for treatment, and a community that understands and supports their journey.
Our work
Running challenges, school collaborations, and local partnerships. See how our first phase turned awareness into action.
Phase 1 impact
March 2025 — January 2026
A look at the work behind the numbers.
Launched @htsa_bros on Instagram with a running challenge — 1 mile per 10 new followers — paired with evidence-based Heterotaxy education content.
1,000,000+ views · 1,037 followers · 80K likes
Created a GoFundMe page linked to Heterotaxy Connection, distributing it across social media and to 10+ local businesses and 5 school organizations.
$705 raised · 130+ donors
Conducted 25+ community interviews with students and followers to assess awareness levels and refine our content strategy. Views spiked from 10,345 to 34,567 biweekly following strategy changes.
25+ interviewed · 3× view increase
Collaborated with DECA, HOSA, JAG, and NHS at Centennial High School to expand volunteer capacity and school-wide awareness.
Schoolwide collaboration · 30+ volunteers
Distributed 260 evidence-based infographic pamphlets across local high schools in collaboration with Heterotaxy Connection and Vanderbilt University Biology professors.
260 flyers · 4 high schools
Secured 5 local business partnerships with Costco, Fleet Feet, Whole Foods, Sprouts, and Honest Coffee Roasters — generating $2,800 in in-kind and cash support.
5 businesses · $2,800 in support
Hosted Centennial's first-ever Heterotaxy 5K with 120+ participants, 30 volunteers, prizes from Fleet Feet, and a pre-race educational presentation on Heterotaxy.
120+ participants · $1,829 raised · 30 volunteers
The next chapter
Our next 5K is the Hot Cocoa Run on January 16, 2027. Help us work toward 150 Comfort and Play Kits for children in local hospitals.
Explore the Hot Cocoa RunMeet HTSA Bros
Meet the people bringing Heterotaxy awareness to our schools, businesses, and community.
Our leadership

Co-Founder & CEO
Leads social media strategy, content creation, and business development. Grew @htsa_bros to 1,037 followers and 1M+ views.

Co-Founder & CFO
Leads community outreach and medical professional partnerships. Connected with Heterotaxy Connection CEO Necia Sabin to direct donations.

Director of Outreach & COO
Pioneers and executes awareness campaigns with local businesses and schools. Coordinated school club partnerships across WCS.
Join the effort
Help at an event, share our work, or bring your business into the conversation. We'd love to connect.
Get involvedGet involved
Volunteer your time, support the Hot Cocoa Run, or help more people learn about Heterotaxy. It starts with you.
Put your business behind our January 16, 2027 5K and our goal of 150 Comfort and Play Kits. Packages begin at $250, with your business logo on the event shirt and a banner displayed at the EIC and our 5K event.
Help at events, distribute flyers, or assist with social media. No experience needed — just a passion for making a difference. Specific Hot Cocoa Run volunteer roles are coming soon.
Interested in supporting HTSA Bros through your business or organization? Let's explore how we can work together to advance Heterotaxy awareness and support families.
Follow our journey
Follow @htsa_bros for weekly Heterotaxy education, behind-the-scenes campaign updates, and our ongoing running challenge.
Follow @htsa_brosJanuary 16, 2027 · 8:00 a.m. · Franklin, TN
A winter run for our community. Moments of comfort and play for children in local hospitals.
Your event-day essentials
Small gifts. Meaningful moments.
Your support helps provide toys, games, and creative activities for children in local hospitals, while supporting the event that makes it possible.
5K business sponsorships
Help fund Comfort and Play Kits and event fees. Support toys, games, and creative activities for hospitalized children, along with the costs that make this event possible.
Ask about this packageHelp cover food and water for our runners. Support refreshments that keep participants hydrated and welcomed throughout the Hot Cocoa Run.
Ask about this packageHelp fund prizes and medals for our winners. Support the awards that celebrate our runners and recognize their achievement at the finish line.
Ask about this packageIncluded with every package
Ready to sponsor? Email htsabros@gmail.com with your business name, contact name, phone/email, preferred package, and business logo. We'll discuss your sponsorship and payment arrangements with you.
Let's make it happen