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    <title>cysticfibrosissupport at Yahoo! Groups</title>
    <link>http://health.groups.yahoo.com/group/cysticfibrosissupport/</link>
    <description>Cystic Fibrosis Support - A Cystic Fibrosis support group</description>

    <item>
      <title>Please help with my CF Survey</title>
      <pubDate>Wed, 04 Nov 2009 01:18:58 GMT</pubDate>
      <dc:creator>flutterby_akr</dc:creator>
      <link>http://health.groups.yahoo.com/group/cysticfibrosissupport/message/1698</link>
      <guid isPermaLink="true">http://health.groups.yahoo.com/group/cysticfibrosissupport/message/1698</guid>
      <description>Hi All I still really need people to complete my survey, so if you could help I&#39;d really appreciate it. Thanks Alyssa &quot;Creatively Coping with Cystic Fibrosis&quot; </description>
    </item>
    <item>
      <title>David s law</title>
      <pubDate>Wed, 04 Nov 2009 01:18:08 GMT</pubDate>
      <dc:creator>fightcf</dc:creator>
      <link>http://health.groups.yahoo.com/group/cysticfibrosissupport/message/1697</link>
      <guid isPermaLink="true">http://health.groups.yahoo.com/group/cysticfibrosissupport/message/1697</guid>
      <description>Good morning everyone .. How are you all doing? Hey I have a big favor to ask I need to get more people to sign the petition for Davids law today so that</description>
    </item>
    <item>
      <title>CF Surf camp- check out this video</title>
      <pubDate>Mon, 27 Jul 2009 12:41:15 GMT</pubDate>
      <dc:creator>anana1872</dc:creator>
      <link>http://health.groups.yahoo.com/group/cysticfibrosissupport/message/1696</link>
      <guid isPermaLink="true">http://health.groups.yahoo.com/group/cysticfibrosissupport/message/1696</guid>
      <description>Please check out this video. http://www.vimeo.com/5649691 A CF surf camp is put on by the Mauli Ola Foundation, sponsored by Ambry Genetics. They recognize the</description>
    </item>
    <item>
      <title>Please help with my CF Survey</title>
      <pubDate>Wed, 22 Jul 2009 00:13:13 GMT</pubDate>
      <dc:creator>flutterby_akr</dc:creator>
      <link>http://health.groups.yahoo.com/group/cysticfibrosissupport/message/1695</link>
      <guid isPermaLink="true">http://health.groups.yahoo.com/group/cysticfibrosissupport/message/1695</guid>
      <description>My brother and I have CF. Due to this, I am researching how people cope with CF as part of a Psychology Honours degree, and would like to request people</description>
    </item>
    <item>
      <title>Question about DME Coverage for specialty nebulizers</title>
      <pubDate>Wed, 22 Jul 2009 00:13:13 GMT</pubDate>
      <dc:creator>anana1872</dc:creator>
      <link>http://health.groups.yahoo.com/group/cysticfibrosissupport/message/1694</link>
      <guid isPermaLink="true">http://health.groups.yahoo.com/group/cysticfibrosissupport/message/1694</guid>
      <description>I would like to inquire about DME (durable medical equipment)coverage for specialty nebulizers such as eFlow. Is the eFlow covered automatically when the</description>
    </item>
    <item>
      <title>Please join us for the Summer CF Teen and Adult Retreat!!</title>
      <pubDate>Tue, 30 Jun 2009 05:58:58 GMT</pubDate>
      <dc:creator>anana1872</dc:creator>
      <link>http://health.groups.yahoo.com/group/cysticfibrosissupport/message/1693</link>
      <guid isPermaLink="true">http://health.groups.yahoo.com/group/cysticfibrosissupport/message/1693</guid>
      <description>CYSTIC FIBROSIS TEEN &amp; ADULT DAY RETREAT The Great Outdoors: A Breath of Fresh Air! Need support in dealing with the challenges of CF? Looking for some</description>
    </item>
    <item>
      <title>seeking CF minority families for a research project</title>
      <pubDate>Tue, 30 Jun 2009 05:58:55 GMT</pubDate>
      <dc:creator>anana1872</dc:creator>
      <link>http://health.groups.yahoo.com/group/cysticfibrosissupport/message/1692</link>
      <guid isPermaLink="true">http://health.groups.yahoo.com/group/cysticfibrosissupport/message/1692</guid>
      <description>Dear CF Families and Friends, I am sending this to you in case you or someone you know may be interested. The Department of Disability and Human Development at</description>
    </item>
    <item>
      <title>Re: cf daughter not allowed to cheer</title>
      <pubDate>Fri, 05 Jun 2009 12:40:02 GMT</pubDate>
      <dc:creator>Sue Pettit</dc:creator>
      <link>http://health.groups.yahoo.com/group/cysticfibrosissupport/message/1691</link>
      <guid isPermaLink="true">http://health.groups.yahoo.com/group/cysticfibrosissupport/message/1691</guid>
      <description>Hey Everyone!!! As most of you know, Valerie has played on the junior varsity &amp; later the varsity fast and slow pitch softball teams since 7th grade, she</description>
    </item>
    <item>
      <title>Re: cf daughter not allowed to cheer</title>
      <pubDate>Thu, 04 Jun 2009 02:48:53 GMT</pubDate>
      <dc:creator>Reva Lane</dc:creator>
      <link>http://health.groups.yahoo.com/group/cysticfibrosissupport/message/1690</link>
      <guid isPermaLink="true">http://health.groups.yahoo.com/group/cysticfibrosissupport/message/1690</guid>
      <description>My daughter, too, has had problems with some of her teachers.  And I&#39;m a teacher myself!  I finally had to get my daughter an Individualized Health Plan. </description>
    </item>
    <item>
      <title>Re: cf daughter not allowed to cheer</title>
      <pubDate>Wed, 03 Jun 2009 18:39:01 GMT</pubDate>
      <dc:creator>missgoobergirl</dc:creator>
      <link>http://health.groups.yahoo.com/group/cysticfibrosissupport/message/1689</link>
      <guid isPermaLink="true">http://health.groups.yahoo.com/group/cysticfibrosissupport/message/1689</guid>
      <description>... Hi I have some horror stories. It it is so unfair but remember those days well. Sometimes I have to honestly say it was the teachers who were the wrost</description>
    </item>
    <item>
      <title>65_redroses, a CF documentary.</title>
      <pubDate>Tue, 02 Jun 2009 00:09:28 GMT</pubDate>
      <dc:creator>megmucus</dc:creator>
      <link>http://health.groups.yahoo.com/group/cysticfibrosissupport/message/1688</link>
      <guid isPermaLink="true">http://health.groups.yahoo.com/group/cysticfibrosissupport/message/1688</guid>
      <description>&quot; 65_RedRoses is a Canadian documentary that takes an unflinching look into the life of Eva Markvoort as she battles a fatal genetic disease called Cystic</description>
    </item>
    <item>
      <title>cf daughter not allowed to cheer</title>
      <pubDate>Tue, 02 Jun 2009 00:09:08 GMT</pubDate>
      <dc:creator>revalane</dc:creator>
      <link>http://health.groups.yahoo.com/group/cysticfibrosissupport/message/1687</link>
      <guid isPermaLink="true">http://health.groups.yahoo.com/group/cysticfibrosissupport/message/1687</guid>
      <description>My 16 year old daughter has cheered on her school&#39;s varsity cheer team for 2 years.  She absolutely loves cheerleading and is her motivation to get up for</description>
    </item>
    <item>
      <title>New Webcast on Caring for Children with CF</title>
      <pubDate>Tue, 02 Jun 2009 00:08:31 GMT</pubDate>
      <dc:creator>drmccolley</dc:creator>
      <link>http://health.groups.yahoo.com/group/cysticfibrosissupport/message/1686</link>
      <guid isPermaLink="true">http://health.groups.yahoo.com/group/cysticfibrosissupport/message/1686</guid>
      <description>Are you interested in finding out more about best practices for CF care in children? My name is Dr. Susanna McColley, and I&#39;m Head of Pulmonary Medicine and</description>
    </item>
    <item>
      <title>Retreat</title>
      <pubDate>Tue, 31 Mar 2009 13:11:09 GMT</pubDate>
      <dc:creator>missgoobergirl</dc:creator>
      <link>http://health.groups.yahoo.com/group/cysticfibrosissupport/message/1685</link>
      <guid isPermaLink="true">http://health.groups.yahoo.com/group/cysticfibrosissupport/message/1685</guid>
      <description>Hey Everyone..PLEASE READ ! ! ! Growing up I never knew there CF Camps. I wish I did. Everyone talks about how  much fun it was. My husband and I, he also has</description>
    </item>
    <item>
      <title>Results of research blog on CF now available</title>
      <pubDate>Mon, 30 Mar 2009 13:18:28 GMT</pubDate>
      <dc:creator>Belinda Shale</dc:creator>
      <link>http://health.groups.yahoo.com/group/cysticfibrosissupport/message/1684</link>
      <guid isPermaLink="true">http://health.groups.yahoo.com/group/cysticfibrosissupport/message/1684</guid>
      <description>Dear All Please find the results of our CF Research Blog http://www.thepatientsvoice.org/Cystic_Fibrosis/ Feel very free to add any comments you may think will</description>
    </item>

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