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 <title>dylansmom&#039;s blog</title>
 <link>https://www.pffd.org/blog/1528</link>
 <description>If you are new to PFFD - I recommend starting with the PFFD book</description>
 <language>en</language>
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 <title>Dylan&#039;s Journey</title>
 <link>https://www.pffd.org/node/670</link>
 <description>&lt;div class=&quot;field field-name-body field-type-text-with-summary field-label-hidden&quot;&gt;&lt;div class=&quot;field-items&quot;&gt;&lt;div class=&quot;field-item even&quot;&gt;&lt;p&gt;Hello, my name is Amanda, and I am a parent of a little boy with PFFD. Dylan is 2 years old and was diagnosed last September (2009). He is scheduled for a hip osteotomy next summer (2011). I am not really sure what that means, other than that he will be in a cast from his chest to his legs for 4-6 weeks after that. I am afraid what that will mean for him, because he is a VERY active little boy. The reason I joined this website was to connect with other parents about what to expect in the coming months and years; from surgeries - to his entire future.&lt;br /&gt;
Please feel free to connect with me through e-mail or send me a message. I am open to any advice, questions, or just to talk.&lt;br /&gt;
Thanks.&lt;br /&gt;&lt;a href=&quot;mailto:amandarenay@sbcglobal.net&quot;&gt;amandarenay@sbcglobal.net&lt;/a&gt;&lt;/p&gt;
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 <pubDate>Wed, 28 Jul 2010 20:25:05 +0000</pubDate>
 <dc:creator>dylansmom</dc:creator>
 <guid isPermaLink="false">670 at https://www.pffd.org</guid>
 <comments>https://www.pffd.org/node/670#comments</comments>
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