My son has had a history of chronic sinusitis, chronic bronchitis, nasal polyps, and asthma. He is being followed by UNC pulmonary.
He had a negative sweat test in April. But, since then, he has been hospitalized once, and has grown both achromobacter and most recently pseudomonas in his lungs. The doctor sent his blood in for genetic testing and one marker came back. I can't remember the name, she was talking so fast! But now they sent his blood off to test against all known mutations of CF and if one of those come back, then we will have the diagnosis.
She has only known of one other person in her practice who has had a negative sweat test but still have CF. Right now, they treat him as a CF patient. If the most recent sputum culture comes back with pseudomonas again, she is going to start him on Tobi. So she seems to think that is what it is.
Is there anyone else out there who has gone through this? He is 7 years old, growing normally, healthy appetite with no other of the more common symptoms of CF, although from my research, the various mutations will account for the difference in symptoms.
Thanks in advance! We won't get the test results back for 2-4 weeks, so the waiting has begun.
He had a negative sweat test in April. But, since then, he has been hospitalized once, and has grown both achromobacter and most recently pseudomonas in his lungs. The doctor sent his blood in for genetic testing and one marker came back. I can't remember the name, she was talking so fast! But now they sent his blood off to test against all known mutations of CF and if one of those come back, then we will have the diagnosis.
She has only known of one other person in her practice who has had a negative sweat test but still have CF. Right now, they treat him as a CF patient. If the most recent sputum culture comes back with pseudomonas again, she is going to start him on Tobi. So she seems to think that is what it is.
Is there anyone else out there who has gone through this? He is 7 years old, growing normally, healthy appetite with no other of the more common symptoms of CF, although from my research, the various mutations will account for the difference in symptoms.
Thanks in advance! We won't get the test results back for 2-4 weeks, so the waiting has begun.