The Cystic Fibrosis (CF) is a genetic disorder that is hereditary in nature and is known to cause your body to produce thick and sticky mucus. This mucus accumulates both in the lungs and the digestive tract, which causes problems with breath and the inability to absorb nutrients readily. CF is a life time disease in which continuous care is needed to combat infections and ensure good productivity.
CF symptoms can vary by age and severity, but often include:
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.
Our team of expert cystic fibrosis specialists at GastroDoxs Katy provides unique care planning- involving high-quality airway treatment, focused inhaled therapies, nutrition instructions, and enzyme supplementation as well as a frequent follow-up with specialists. Our mission is to make you breathe easier, ensure you grow optimally and get better life. Ready to get started? You can contact our office in the city of Katy or schedule an appointment via the Internet and start your own individual CF treatment course today.
We've successfully treated more than 1k patients, helping individuals improve their digestive health and overall well-being through expert, personalized care.
With over 20 years of experience, GastroDoxs has been a trusted provider of gastroenterology care, focusing on delivering the best outcomes for patients
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.
Due to the progress in treatment, an increasing number of CF patients can nowadays move well into their 40s, 50s, or even later. There is variation in life expectancy depending on an individual's health, treatment compliance, and receiving specialized care.
The combination of newborn screening, sweat chloride tests, and genetic tests to detect CFTR gene defects is used to diagnose CF.
Yes. There are others with less severe gene mutations and they can be left undiagnosed until adolescence or adult age when they are affected by recurrent lung infections or digestive problems.
A CF diet consists of a high-calorie, high-protein diet, the replacement of pancreatic enzymes, and vitamins A, D, E, and K which are fat-soluble vitamins to assist in growth and vitamin absorption.
The airway clearance measures and the inhaled therapies like antibiotics and mucolytics via nebulization aid in removing thick mucus as well as minimizing lung infections.
It is suggested to visit every three months to check the condition, test lung function, and readjust treatment, and to make further visits in case of disease progression or complications.
In severe situations, lung transplantation can be suggested. Complications that can be handled through other procedures include nasal polyps and intestinal blockages.
Yes. Anxiety, depression, or the stress of living with a chronic condition might result. We also provide referrals to support and counseling in order to ensure emotional stability.
Absolutely. Exercise aids in clearing the lungs, improving cardiovascular function, and strengthening muscles. The programs are based on an individual's ability and health status.
You can make an appointment with us through our online request form or through our Katy office, GastroDoxs Katy. You will be mentored by our team.
