Airway Clearance Therapy in Cystic Fibrosis Patients Insights from a Clinician Providing Cystic Fibrosis Care

To Everyone's Surprise, COVID-19 Spared My Lungs

Antibiotic resistance, chronic disease, and covid-19—a triple threat

A Patient and Physician Perspective

A Researcher-Patient's Plea for Broader Inclusion into Cystic Fibrosis Clinical Trials

One number keeps me from taking part in cystic fibrosis trials

My phage therapy experience

Interview: Ella Balasa Chats with CF Researcher about Phage Therapy

The Role of Cystic Fibrosis In My Life

Patient Perspective - My Life since learning of Phage Therapy

What life is like on the new ‘breakthrough’ cystic fibrosis drug

What is Cystic Fibrosis-And What's it Like?

A New Alternative for Pancreatic Enzyme Replacement Therapy (PERT)

Eloxx Pharmaceuticals Nonsense Target Therapy

New Treatment for Lung Transplant Recipients Experiencing Chronic Rejection

Translate Bio Recruiting Class 1 and Nonsense Mutation Patients

A blog dedicated to the introspective thoughts from triumphs and hardship of a life with cystic fibrosis

Sharing about the life hurdles associated with CF and the strength to overcome

Articles pertaining to my life with CF, my advocacy work, and tips for other patients

Could bacteria-eating viruses be drafted to replace antibiotics?

Education and empowerment would provide more equal access to care

Richmond woman warns of global health threat after battling antibiotic-resistant infection

Discuss many aspects of the classic CF journey

Mobilizing pathways to accommodate new transformative treatments - using CF as a case study

Researcher & Patient Collaboration to Humanize Care: Ella Balasa

RareWomen's Health Conversation

How Congress is Addressing a Converging Crisis (3:55)

A Lung Life

Intersection of COVID-19 and AMR

Reducing the Cost of Antimicrobial Resistance

Patient-Centered Principles for a Personalized Medicine Research Agenda Panel

Be the Voice in CF Research

Patient Editorial Board Member

The Value of the Patient Experience Presentation

White Paper: A Patient-Centered Research Agenda Advancing Personalized Medicine

Lend my voice to convey needs of the CF community

Program to improve the knowledge of CF infections

Passionate individuals who use their voice to tell stories, create change, and inspire others living with chronic disease.