<?xml version="1.0" encoding="UTF-8"?><rss version="2.0">	<channel>		<title>True CF Awareness Comments</title>		<language>en-us</language>		<link>http://ihavecfsowhat.blogspot.com/2012/04/true-cf-awareness.html</link>		<description>Comments from True CF Awareness</description><item>
<title>Diana</title><link>http://ihavecfsowhat.blogspot.com/2012/04/true-cf-awareness.html#IDComment379388202</link><description>First of all, you&amp;#039;re incredible. Second of all, thank you. My boyfriend has CF, and I&amp;#039;ve always known about it because my uncle had it, and my family has been involved in fundraising and events for as long as I can remember...but it strikes me often, as my boyfriend is going through things, that despite supposedly being  involved, I know very little about the day-to-day of living with CF. It&amp;#039;s always been fundraising, it&amp;#039;s always been general information about the illness and the details--and maybe more importantly, the differences--seem to get skipped. I only know and remember snippets of my uncle&amp;#039;s fight (he was a runner, too, and that was back in the 60&amp;#039;s/70&amp;#039;s--and I remember being 8 and he still was running). There&amp;#039;s all these blanks, and all of these...disconnects with the CFF (as great a foundation as it is!), because I look at these sorts of things and just think--that wasn&amp;#039;t my uncle, that&amp;#039;s not my boyfriend, so who is it and what does it mean? Your blog is filling in some missing pieces for me, and fleshing out some of my wonderings, and I just keep thinking, this is brilliantly done. You have such a great way of writing!  </description><pubDate>Tue, 12 Jun 2012 19:48:29 +0000</pubDate><guid>http://ihavecfsowhat.blogspot.com/2012/04/true-cf-awareness.html#IDComment379388202</guid></item><item>
<title>cindy baldwin</title><link>http://ihavecfsowhat.blogspot.com/2012/04/true-cf-awareness.html#IDComment352791159</link><description>So, I&amp;#039;ve been thinking about this post ever since I read it. I love it, but also feel a little differently on this subject, I think! After thinking about it for days, I finally blogged my thoughts, since they were way too long and complicated for a comment: &lt;a href=&quot;http://www.beingcindy.blogspot.com/2012/05/awareness.html&quot; target=&quot;_blank&quot;&gt;http://www.beingcindy.blogspot.com/2012/05/awaren...&lt;/a&gt; </description><pubDate>Wed, 2 May 2012 17:14:14 +0000</pubDate><guid>http://ihavecfsowhat.blogspot.com/2012/04/true-cf-awareness.html#IDComment352791159</guid></item><item>
<title>Tonya</title><link>http://ihavecfsowhat.blogspot.com/2012/04/true-cf-awareness.html#IDComment348434172</link><description>I agree whole-heartedly, Lauren!  Thank you for writing what I&amp;#039;ve been thinking for a long time!  I remember this analogy being used at CFF events shortly after my son was diagnoed 14 years ago.  I thought it was far-fetched then, and still do. Now it&amp;#039;s being spread around Facebook and reaching many more people than it did before.  It makes me angry!...especially when posted by parents of young children with no lung involvement yet.   </description><pubDate>Thu, 26 Apr 2012 12:52:26 +0000</pubDate><guid>http://ihavecfsowhat.blogspot.com/2012/04/true-cf-awareness.html#IDComment348434172</guid></item><item>
<title>Aubrey Bean</title><link>http://ihavecfsowhat.blogspot.com/2012/04/true-cf-awareness.html#IDComment347307986</link><description>This is awesome..and so true! It&amp;#039;s frustrating when everyone thinks all of us are the same. Thanks for all your blogs they&amp;#039;re awesome and I love reading them!  BTW I found out through your writing that we go to the same hospital, and your doctor actually did a bronch on me last summer! haha keep being awesome girl, we all love reading :) </description><pubDate>Wed, 25 Apr 2012 02:12:04 +0000</pubDate><guid>http://ihavecfsowhat.blogspot.com/2012/04/true-cf-awareness.html#IDComment347307986</guid></item><item>
<title>Michelle Scott </title><link>http://ihavecfsowhat.blogspot.com/2012/04/true-cf-awareness.html#IDComment347263040</link><description>Very well stated!  I would like to share this, as well. </description><pubDate>Wed, 25 Apr 2012 00:53:28 +0000</pubDate><guid>http://ihavecfsowhat.blogspot.com/2012/04/true-cf-awareness.html#IDComment347263040</guid></item><item>
<title>Elicia Otterson</title><link>http://ihavecfsowhat.blogspot.com/2012/04/true-cf-awareness.html#IDComment347240891</link><description>Lauren thank you so very much for this post.  </description><pubDate>Wed, 25 Apr 2012 00:22:13 +0000</pubDate><guid>http://ihavecfsowhat.blogspot.com/2012/04/true-cf-awareness.html#IDComment347240891</guid></item><item>
<title>RunSickboyRun</title><link>http://ihavecfsowhat.blogspot.com/2012/04/true-cf-awareness.html#IDComment346952143</link><description>You took the words right out of my brain and put them into a blog. I saw this post just before I was going to write my own, and I thought so much of it, I shared your post on my blog instead. Thank you so much for your honesty and giving your thoughts on this topic much more delicately than I ever could. </description><pubDate>Tue, 24 Apr 2012 16:29:18 +0000</pubDate><guid>http://ihavecfsowhat.blogspot.com/2012/04/true-cf-awareness.html#IDComment346952143</guid></item>	</channel></rss>