<?xml version="1.0" encoding="utf-8"?>
<rss version="2.0" xml:base="https://www.pffd.org"  xmlns:dc="http://purl.org/dc/elements/1.1/">
<channel>
 <title>jerdebwalker&#039;s blog</title>
 <link>https://www.pffd.org/blog/1299</link>
 <description>If you are new to PFFD - I recommend starting with the PFFD book</description>
 <language>en</language>
<item>
 <title>Home after Super Hip done Dec. 9, 2009</title>
 <link>https://www.pffd.org/node/624</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;We are home now after our first procedure with Dr. Paley. We went to West Palm Beach Dec. 6 and returned Christmas Eve. Our daughter, now 16 is doing GREAT after this procedure. She required an extra week of rehab stay and we had many frustrations with the communication between Dr. Paley&#039;s office and the hospital, but as far as surgery outcomes we are pleased.&lt;br /&gt;
If you have an older child that is beginning their journey to correct PFFD/CFD and have specific questions you can email me as well as if you have not been to the new facility at St. Mary&#039;s Children&#039;s Hospital:&lt;br /&gt;
jerdebwalker at hotmail dot com (Insert symbols and remove spaces).&lt;br /&gt;
Debbie Walker&lt;/p&gt;
&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;</description>
 <pubDate>Thu, 31 Dec 2009 01:28:14 +0000</pubDate>
 <dc:creator>jerdebwalker</dc:creator>
 <guid isPermaLink="false">624 at https://www.pffd.org</guid>
 <comments>https://www.pffd.org/node/624#comments</comments>
</item>
<item>
 <title>Beginning Our Journey</title>
 <link>https://www.pffd.org/node/543</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;We recently adopted a 15 year old with phocomelia of UE and PFFD. Yesterday was our first appointment with an orthopedic surgeon to discuss the options we have for our daughter at this point.  She hopes to continue with leg lengthening procedures despite her hip most likely needing reconstruction and her knee without ligaments.  Her foot is fully functional even though her left leg  it is 6-8 inches shorter than her right. She also has scoliosis that causes her pelvis to turn. The MD stated he is cautious in his approach and recommended just amputating the foot and getting a well fitting prosthesis.  He also recommended getting a second opinion.  I was looking at maybe going to a Shriner&#039;s hospital but see here many of you have not had success.  Are there any PFFD experts on the west coast?&lt;/p&gt;
&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;</description>
 <pubDate>Tue, 05 May 2009 18:44:00 +0000</pubDate>
 <dc:creator>jerdebwalker</dc:creator>
 <guid isPermaLink="false">543 at https://www.pffd.org</guid>
 <comments>https://www.pffd.org/node/543#comments</comments>
</item>
</channel>
</rss>
