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Cystic Fibrosis

At GastroDoxs, our specialized Cystic Fibrosis clinic in Katy offers state-of-the-art comprehensive respiratory care, ongoing nutritional counseling and advanced personalized treatment plans to support local families, ensuring expert management of this inherited condition while fostering community-focused, compassionate care.

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Texas Medical Board
Harris County Medical Society
American College of Gastroenterology
American Society for Gastrointestinal Endoscopy
Memorial hermann
Houston Methodist leading Medicine
HCA Houston Healthcare
Bharat Pothuri
Symptoms

What is Cystic Fibrosis?

Cystic Fibrosis (CF) is an inherited genetic disorder that causes your body to produce thick, sticky mucus. This mucus builds up in your lungs and digestive tract, leading to breathing problems and difficulty absorbing nutrients. CF is a lifelong condition that requires ongoing care to manage infections and maintain healthy growth.

Common Symptoms

CF symptoms can vary by age and severity, but often include:

  • Persistent coughing or wheezing
  • Frequent lung infections (bronchitis, pneumonia)
  • Poor weight gain or growth despite good appetite
  • Greasy, bulky stools that are hard to flush
  • Sinus congestion or nasal polyps

Causes

Cystic Fibrosis is caused by mutations in the CFTR gene, which controls how salt and water move in and out of cells. These mutations result in thick mucus production and a range of complications.

  • Autosomal recessive inheritance - a child must inherit one defective gene from each parent
  • Faulty CFTR protein disrupts chloride and water transport
  • Build-up of thick mucus in airways and digestive tract
  • Increased risk of lung infections and malnutrition
Treatment

Treatment Options for Cystic Fibrosis in Katy

Treatment includes personalized therapies and supportive care:

  • Airway clearing therapy: Techniques like chest physiotherapy, positive-pressure vests, and percussion help remove thick mucus from the lungs.
  • Inhaled medications: Bronchodilators, mucolytics, and inhaled antibiotics reduce infection risk and keep airways open.
  • Nutrition support: A high-calorie, high-protein diet plus pancreatic enzyme supplements improve digestion, nutrient absorption, and weight gain.
  • Vitamin supplementation: Fat-soluble vitamins (A, D, E, and K) and minerals support overall health and counteract malabsorption.
  • Regular monitoring: Routine checkups include lung function testing (FEV?), sputum cultures, and blood work to track progress and adjust care.
  • Advanced referrals: Access to CFTR modulator therapies, specialized OT/PT for breathing exercises, and lung-transplant evaluation when indicated.

Why Choose GastroDoxs?

At GastroDoxs in Katy, our experienced cystic fibrosis team delivers individualized care plans-combining advanced airway therapies, targeted inhaled medications, nutrition and enzyme support, and regular specialist follow-ups. We're committed to helping you breathe easier, maintain optimal growth, and improve your quality of life. Ready to get started? Call our Katy office today or request an appointment online to begin your personalized CF treatment journey.

1k

Patients Treated

We've successfully treated more than 1k patients, helping individuals improve their digestive health and overall well-being through expert, personalized care.

20Y

Years of Experience

With over 20 years of experience, GastroDoxs has been a trusted provider of gastroenterology care, focusing on delivering the best outcomes for patients

Bharat Pothuri

About the Author

Dr. Bharat Pothuri is a Board-Certified Gastroenterologist and Hepatologist. With extensive experience in digestive health, he specializes in advanced endoscopic procedures, chronic GI disorder management, and preventive care. Dr. Pothuri is dedicated to providing expert, patient-focused insights to help improve gut health and overall well-being.

Frequently Asked Questions

What is the cystic fibrosis age expectancy?

With advances in care, many people with CF now live into their 40s, 50s, or beyond. Life expectancy varies by individual health, treatment adherence, and access to specialized care.

How is CF diagnosed?

CF is diagnosed through a combination of newborn screening, sweat chloride tests, and genetic testing to identify CFTR gene mutations.

Can CF show up in adults?

Yes. Some individuals have milder gene mutations and may not be diagnosed until adolescence or adulthood after experiencing recurrent lung infections or digestive issues.

What's in a CF diet plan?

A CF diet focuses on high-calorie, high-protein foods, pancreatic enzyme replacement, and fat-soluble vitamins (A, D, E, K) to support growth and nutrient absorption.

What cystic fibrosis medical procedure helps the lungs?

Airway clearance techniques and inhaled therapies-such as nebulized antibiotics and mucolytics-help remove thick mucus and reduce lung infections.

How often should I see a CF doctor in Katy?

Routine visits are recommended every three months for assessment, lung function testing, and treatment adjustments, with additional appointments during illness or exacerbations.

Can surgery help CF?

In advanced cases, lung transplantation may be an option. Other procedures can address complications like nasal polyps or intestinal blockages.

Does CF affect mental health?

Yes. Living with a chronic condition can lead to anxiety, depression, or stress. We offer referrals to counseling and support groups to maintain emotional well-being.

Should people with CF exercise?

Absolutely. Regular exercise supports lung clearance, improves cardiovascular health, and builds muscle strength. Programs are tailored to individual ability and health status.

How do I book an appointment?

Call our GastroDoxs Katy office or use our online request form for a fast, convenient appointment setup. Our team will guide you through the process.

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