OPEP therapy for bronchiectasis : 17 months of... - COPD Friends

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OPEP therapy for bronchiectasis

Stormfever profile image
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17 months of sticky mucus and blocked airways have resulted in many courses of different antibiotics, a bronchoscopy, lung wash, scans, x-rays. I've had diagnoses of asthma, bronchiectasis, nasal polyps, though scans show no bronchiectasis. Tests do show the persistent presence of HIB, which my doctor has given up on as 'it's very common'.

I'm on a permanent low dose of azithromycin, with doxycycline prescribed for 'flare ups'. I also use carbocisteine and asthma inhalers.

Physiotherapy (mucus clearing breathing exercises) worked a little bit. I've taken expensive herbal remedies none of which has had any impact.

What has seemed to help me for the last week - suddenly - is a little plastic device you exhale into, that causes a percussive rhythm known as OPEP therapy. I think Americans call them 'flutter devices'. It's very peculiar.

Has anyone else used these little devices, with any continued improvement?

Should I press the NHS for nebulisers to increase this remedial effect?

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Stormfever
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R2B_John profile image
R2B_JohnModerator

I have two PEP devices....an Acapella and the Aerobika. For myself, I prefer the Aerobika.In addition, since you mentioned nebulizing. You can connect the nebulizer tubing to these devices so you can use your device and nebulize simultaneously!

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