<?xml version="1.0"?>
<rss version="2.0">
   <channel>
      <title>Cystic Fibrosis  by Jaden Pr</title>
      <link>https://padlet.com/lisle202/9j8tlcf88v8q</link>
      <description></description>
      <language>en-us</language>
      <pubDate>2017-05-01 13:21:47 UTC</pubDate>
      <lastBuildDate>2025-08-08 01:41:39 UTC</lastBuildDate>
      <webMaster>hello@padlet.com</webMaster>
      <image>
         <url></url>
      </image>
      <item>
         <title>Prognosis of Cystic Fibrosis</title>
         <author>jp20135</author>
         <link>https://padlet.com/lisle202/9j8tlcf88v8q/wish/169159518</link>
         <description><![CDATA[<div>Cystic Fibrosis is a lung disease which leads to the person who eventually worsens to the point where the person is disabled. The average life span to people who have CF is 37 or younger.</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-05-01 13:23:04 UTC</pubDate>
         <guid>https://padlet.com/lisle202/9j8tlcf88v8q/wish/169159518</guid>
      </item>
      <item>
         <title>Symptoms of Cystic Fibrosis</title>
         <author>jp20135</author>
         <link>https://padlet.com/lisle202/9j8tlcf88v8q/wish/169164231</link>
         <description><![CDATA[<div>Cough<br>Gastrointestinal<br>Respiratory<br>Developmental<br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2017-05-01 13:39:09 UTC</pubDate>
         <guid>https://padlet.com/lisle202/9j8tlcf88v8q/wish/169164231</guid>
      </item>
      <item>
         <title>Treatment of Cystic Fibrosis</title>
         <author>jp20135</author>
         <link>https://padlet.com/lisle202/9j8tlcf88v8q/wish/169404979</link>
         <description><![CDATA[<div>Supportive Care<br>Preventative <br>Medications<br>Self-care<br>Medical Procedures<br>Specialists</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-05-02 13:00:22 UTC</pubDate>
         <guid>https://padlet.com/lisle202/9j8tlcf88v8q/wish/169404979</guid>
      </item>
      <item>
         <title>Genetic Causes of Cystic Fibrosis</title>
         <author>jp20135</author>
         <link>https://padlet.com/lisle202/9j8tlcf88v8q/wish/169406209</link>
         <description><![CDATA[<div>A defect in the CFTR gene causes cystic fibrosis (CF). This gene makes a protein that controls the movement of salt and water in and out of your body's cells. In people who have CF, the gene makes a protein that doesn't work well. This causes thick, sticky mucus and very salty sweat.</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-05-02 13:04:35 UTC</pubDate>
         <guid>https://padlet.com/lisle202/9j8tlcf88v8q/wish/169406209</guid>
      </item>
   </channel>
</rss>
