Comment from Taylor, Diane , Drexel University College of Medicine

Document ID: SSA-2006-0149-0052
Document Type: Public Submission
Agency: Social Security Administration
Received Date: April 04 2013, at 12:00 AM Eastern Daylight Time
Date Posted: April 5 2013, at 12:00 AM Eastern Standard Time
Comment Start Date: February 4 2013, at 12:00 AM Eastern Standard Time
Comment Due Date: April 5 2013, at 11:59 PM Eastern Standard Time
Tracking Number: 1jx-84l8-l52v
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As a professional working with adult patients with Cystic Fibrosis, I find these changes to be extremely concerning. The Cystic Fibrosis multi-disciplinary teams work hard to provide care outside of the hospital to accommodate patient needs, improve and maintain quality of life and keep healthcare expenses down. Outpatient treatment of a Cystic Fibrosis exacerbation is intensive and includes but is not limited to, oral, nebulized, intravenous antibiotics and other CF medications and increased airway clearance. Treatments typically take patients 2-3 hours daily to administer. The proposed changes would ultimately cause greater strain on our system. I have seen firsthand what patients fighting this disease must do when they are denied benefits, they are forced to go without medications, treatments and other basic necessities, causing frequent emergency room visits, longer hospitalizations and potentially creating additional health problems.

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