Founder & Executive Director

Andy Jablonski

Lifelong Short Bowel Syndrome patient, rare-disease advocate, and the driving force behind the Short Bowel Syndrome Foundation since 2010.

📍 Lincoln, Nebraska
🏥 501(c)(3) Public Charity
🌍 Global Patient Community

Andrew (Andy) E. Jablonski is the visionary Founder and Executive Director of the Short Bowel Syndrome Foundation, Inc. (SBSF), a distinguished 501(c)(3) public charity headquartered in Lincoln, Nebraska.

Driven by his own personal journey as a patient, Andy has dedicated over 13 years to a singular, unwavering mission: providing life-changing support, vital resources, and expert advocacy to individuals, caregivers, and medical professionals navigating the daily challenges of Short Bowel Syndrome (SBS). Under his compassionate leadership, SBSF has grown from a local initiative into a global lifeline of hope and resilience.

Leadership Pillars

Four interconnected areas that define Andy’s work and the Foundation’s impact

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Educational Journey

Andy’s professional leadership is grounded in both business strategy and the human experience of chronic illness.

  • Degree in Entrepreneurship — Southeast Community College
  • B.A. in Human Relations (Mental Health & Counseling) — Doane University

This dual foundation equips him to run a national nonprofit while deeply understanding the emotional and psychological realities of intestinal failure.

đź’Š

Rare Disease Industry Expertise

From 2011–2017 Andy served as Patient & Physician Communications Advisor for major pharmaceutical partners:

  • NPS Pharmaceuticals
  • Naia Pharmaceuticals
  • Shire Pharmaceuticals

He played a frontline role advocating for the clinical advancement and patient access of orphan-designated therapies, including GATTEX® (teduglutide).

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Public Speaking & Education

Andy is a sought-after speaker at medical conferences, university hospitals, and rare-disease forums. He shares a dual perspective:

  • Lifelong SBS patient
  • Industry and advocacy expert

His talks humanize clinical data, challenge assumptions, and elevate the patient voice in scientific and clinical settings.

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Digital Peer Support

Recognizing the isolation that accompanies a rare-disease diagnosis, Andy actively manages and moderates multiple online support communities.

  • Pediatric family groups
  • Adult patient networks
  • Global reach across time zones

These spaces allow thousands of families to exchange practical tips, medical experiences, and daily encouragement.

In Depth

A closer look at Andy’s education, industry work, and ongoing advocacy

📚 Educational Foundation

SCC

Degree in Entrepreneurship

Southeast Community College — strategic skills to build and sustain a national nonprofit organization.

DU

B.A. Human Relations

Doane University — specialization in Mental Health & Counseling, providing deep insight into the emotional toll of rare chronic disease.

🔬 Bridging Patients & Pharma

Andy serves as a critical liaison between pharmaceutical innovators developing rare-disease therapies and the specialized gastroenterologists and surgeons who treat SBS.

Patient Advisor
Orphan Drugs
GATTEX® Advocacy
Clinical Access
Physician Education

🌟 A Lifeline of Hope

Andrew Jablonski’s lifelong mission is simple yet profound: to improve the daily quality of life, care equity, and clinical outcomes for everyone affected by Short Bowel Syndrome. His lived experience, combined with professional acumen, continues to give a powerful voice to a community that spent years waiting to be heard.