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<channel>
	<title>Thought's from Steve's World</title>
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	<description>John Newton's dying words.  "My memory is nearly gone, but I remember two things — that  I remember I am a great sinner, and that Christ is a great Saviour."</description>
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		<title>Thought's from Steve's World</title>
		<link>http://sebrooks.wordpress.com</link>
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		<item>
		<title>Christian Imperialism</title>
		<link>http://sebrooks.wordpress.com/2008/06/16/christian-imperialism/</link>
		<comments>http://sebrooks.wordpress.com/2008/06/16/christian-imperialism/#comments</comments>
		<pubDate>Sun, 15 Jun 2008 22:37:03 +0000</pubDate>
		<dc:creator>sebrooks</dc:creator>
				<category><![CDATA[Church Life]]></category>
		<category><![CDATA[Missions]]></category>

		<guid isPermaLink="false">http://sebrooks.wordpress.com/?p=37</guid>
		<description><![CDATA[Please pray with me for the success of this conference and for the mighty advancement of God&#8217;s Kingdom  <img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=sebrooks.wordpress.com&amp;blog=2454428&amp;post=37&amp;subd=sebrooks&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p>Please pray with me for the success of this conference and for the mighty advancement of God&#8217;s Kingdom</p>
<p> <span style="text-align:center; display: block;"><a href="http://sebrooks.wordpress.com/2008/06/16/christian-imperialism/"><img src="http://img.youtube.com/vi/6V0o3UFjTyI/2.jpg" alt="" /></a></span></p>
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		<item>
		<title>Interviewed for a Organ Transplant Article</title>
		<link>http://sebrooks.wordpress.com/2008/04/15/interviewed-for-a-organ-transplant-article/</link>
		<comments>http://sebrooks.wordpress.com/2008/04/15/interviewed-for-a-organ-transplant-article/#comments</comments>
		<pubDate>Mon, 14 Apr 2008 21:26:55 +0000</pubDate>
		<dc:creator>sebrooks</dc:creator>
				<category><![CDATA[Christian Life]]></category>

		<guid isPermaLink="false">http://sebrooks.wordpress.com/?p=36</guid>
		<description><![CDATA[Dear Friends, I wanted to share this with you, but not until it became official. But last week I was contacted a journalism major from Patrick Henry College in Virginia. She was doing a story on Organ Donation. She found my Xanga site and contacted me through that. We had about a 40 min interview last Friday [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=sebrooks.wordpress.com&amp;blog=2454428&amp;post=36&amp;subd=sebrooks&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p class="itembody snap_preview" style="font-family:Arial,Helvetica,sans-serif;text-align:center;"><span style="font-size:medium;"><em>Dear Friends,</em></span></p>
<p class="itembody snap_preview" style="font-family:Arial,Helvetica,sans-serif;text-align:center;"><span style="font-size:medium;"><em>I wanted to share this with you, but not until it became official. But last week I was contacted a journalism major from Patrick Henry College in Virginia. She was doing a story on Organ Donation. She found my Xanga site and contacted me through that. We had about a 40 min interview last Friday over the phone, about my transplant experience. She contacted me today to let me know that a National online news organization called WorldNetDaily picked this story up and has posted it on their web site.</em></span></p>
<p class="itembody snap_preview" style="font-family:Arial,Helvetica,sans-serif;text-align:center;"><span style="font-size:medium;"><em>Below is the link to the page, my interview does not appear until the end of the article, where you will see a picture of me. Any way I am pretty excited about this, and wanted to share this with you.</em></span></p>
<p class="itembody snap_preview" style="font-family:Arial,Helvetica,sans-serif;text-align:center;"><span style="font-size:medium;"><em>Steve</em></span></p>
<p class="itembody snap_preview" style="font-family:Arial,Helvetica,sans-serif;text-align:center;"><span style="font-size:medium;color:#000000;"><a title="http://www.worldnetdaily.com/index.php?fa=PAGE.view&amp;pageId=60670" href="http://www.worldnetdaily.com/index.php?fa=PAGE.view&amp;pageId=60670" target="_new"><em>http://www.worldnetdaily.com/index.php?fa=PAGE.view&amp;pageId=60670</em></a></span></p>
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		<title>March Madness and is it ever!</title>
		<link>http://sebrooks.wordpress.com/2008/03/19/march-madness-and-is-it-ever/</link>
		<comments>http://sebrooks.wordpress.com/2008/03/19/march-madness-and-is-it-ever/#comments</comments>
		<pubDate>Tue, 18 Mar 2008 21:29:24 +0000</pubDate>
		<dc:creator>sebrooks</dc:creator>
				<category><![CDATA[College Basketball]]></category>
		<category><![CDATA[Humor]]></category>
		<category><![CDATA[marriage]]></category>
		<category><![CDATA[Sports]]></category>

		<guid isPermaLink="false">http://sebrooks.wordpress.com/?p=35</guid>
		<description><![CDATA[March Madness I love this time of the year. This is when all the “experts” come out of the woodwork and start talking about college basketball and predicting who will win the NCAA Championship, and who will be the Cinderella teams, when they are as clueless as the rest of us. So here is my [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=sebrooks.wordpress.com&amp;blog=2454428&amp;post=35&amp;subd=sebrooks&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p><span style="font-family:Georgia;">March Madness</span></p>
<p><span style="font-family:Georgia;"></span><span style="font-family:Georgia;">I love this time of the year. This is when all the “experts” come out of the woodwork and start talking about college basketball and predicting who will win the NCAA Championship, and who will be the Cinderella teams, when they are as clueless as the rest of us. So here is my story…..</span><span style="font-family:Georgia;"><span> </span>My wife gets home from her trip to NYC on Sunday morning and as we are sitting around the lunch table she and my daughter are talking to my son and I about there trip and what they saw. And asked them if they saw Madison Square Garden, and then the subject of “selection Sunday” came up and my wife asked me if Pastor Andy was going to do his yahoo “pick em” league this year I told her I guess so, she said well if he does I want in. She gave me her ID name and she would give her brackets in a day or two. She has done this before but has been beaten like a government mule. But she seemed a little more determined this year. Well last night I came down stairs and was getting ready to make supper. I noticed my wife and daughter was sitting on the couch a talking, I also noticed that ESPN was on TV and Digger and the boys were on talking about the tournament. Now normally in our household when flipping through the channels for some reason ESPN is the channel that zooms by the quickest. (That’s when my wife has control of the remote) </span><span style="font-family:Wingdings;"><span>J</span></span><span style="font-family:Georgia;">. So I thought ok well she is starting to take an interest in sports with me and that was cool. Now keep in mind I am fixing supper so I am preoccupied with what I am doing. Then all of a sudden I start getting peppered with questions like “what is the mascot of Temple”, “what are the school colors of Georgetown”, and “what is a Tar heel” I thought it was a test of my knowledge of college basketball, and was doing pretty good and was feeling…. well a little special cause I thought in my man’s head my wife is finally taking a interest in sports with me. Was I wrong! My wife and daughter are on the couch making their picks for the tournament, based on what I am answering and what she is hearing on ESPN and in some way assimilating <span> </span>all this information and filling our her brackets. So I guess I was impressed in a new way of what March “Madness” really is. </span><span style="font-family:Georgia;">As much as I love her she is going to be burnt like toast!</span></p>
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		<title>Treadmill Test</title>
		<link>http://sebrooks.wordpress.com/2008/03/07/treadmill-test/</link>
		<comments>http://sebrooks.wordpress.com/2008/03/07/treadmill-test/#comments</comments>
		<pubDate>Fri, 07 Mar 2008 04:33:26 +0000</pubDate>
		<dc:creator>sebrooks</dc:creator>
				<category><![CDATA[Christian Life]]></category>

		<guid isPermaLink="false">http://sebrooks.wordpress.com/2008/03/07/treadmill-test/</guid>
		<description><![CDATA[ Today was an interesting day to say the least. Some of you know that before my heart transplant I was involved in a government sponsored clinical trial to see whether a structured cardiac rehab program would help people with congestive heart failure, and whether Medicare should pay a bigger portion of the cost for this [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=sebrooks.wordpress.com&amp;blog=2454428&amp;post=34&amp;subd=sebrooks&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p><span style="font-family:Georgia;"><span> </span><font size="4">Today was an interesting day to say the least. Some of you know that before my heart transplant I was involved in a government sponsored clinical trial to see whether a structured cardiac rehab program would help people with congestive heart failure, and whether Medicare should pay a bigger portion of the cost for this rehab. In order to qualify as a participant in this program I had to go through a series of test like pulmonary type test and a treadmill test where you have your nose clipped shut and you breathe through a mouthpiece, It is very uncomfortable to say the least. They do this to measure your Co2 exchange and to get baseline numbers on you like a good heart rate to try and achieve during a workout. Well it was about this time last year that when I did this treadmill test I couldn’t go more that 6 minutes, and had to cut it off because I was so out of breath. After my transplant they still managed to keep me in this program even though I do not have congestive heart failure anymore. On March 15 this study ends. So as part of winding things up I needed to do this treadmill test again today, so they could compare results. Let me explain something real quick when you do this test along with your nose being clipped shut and breathing through a tube they start the treadmill at a speed and incline for 2 minutes then every 2 minutes the incline and speed change sometime steeper incline and slower speed or visa versa. <span> </span>All the while taking constant blood pressure and measuring you oxygen level. Well today at the ummmm&#8230;. <b>17 minute point</b> I was at a 3mph pace and a 10% percent incline. Anyone that knows treadmills knows that is some work I was blown away when the nurse shut the treadmill done and said they didn’t have a protocol for anything over 10 minutes and most people only average 9-10 minutes. I was pooped but really thought I could have gone another 3 minutes or so. So the point of all this is to bless the name of the Lord for letting me accomplish this today and to see how much has changed in a year and to continue to thank and glorify Him for the strength and recovery he is granting to me. I am continually being amazed.</font></span></p>
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		<title>Donor Family Letter (A lengthy post)</title>
		<link>http://sebrooks.wordpress.com/2008/02/29/donor-family-letter-a-lengthy-post/</link>
		<comments>http://sebrooks.wordpress.com/2008/02/29/donor-family-letter-a-lengthy-post/#comments</comments>
		<pubDate>Thu, 28 Feb 2008 18:25:15 +0000</pubDate>
		<dc:creator>sebrooks</dc:creator>
				<category><![CDATA[Christian Life]]></category>
		<category><![CDATA[College Basketball]]></category>
		<category><![CDATA[Heart Transplant]]></category>
		<category><![CDATA[Sports]]></category>

		<guid isPermaLink="false">http://sebrooks.wordpress.com/2008/02/29/donor-family-letter-a-lengthy-post/</guid>
		<description><![CDATA[As I mentioned in my last post we found out through my transplant coordinators, last week that the family of my heart donor made contact with us through a written letter. On Monday afternoon we received this letter which was little over 4 pages in length and written by the mother of this young man.. [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=sebrooks.wordpress.com&amp;blog=2454428&amp;post=33&amp;subd=sebrooks&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p><span style="font-size:14pt;font-family:Georgia;"><em></em></span><span style="font-size:14pt;font-family:Georgia;"><em></em></span><span style="font-size:14pt;font-family:Georgia;"><em></em></span><span style="font-size:14pt;font-family:Georgia;"><em></em></span><span style="font-size:14pt;font-family:Georgia;"><em></em></span><span style="font-size:14pt;font-family:Georgia;"><em></p>
<p style="margin:0;" class="MsoNormal"><i><span style="font-size:14pt;font-family:Georgia;"></span></i></p>
<p><i><span style="font-size:14pt;font-family:Georgia;">As I mentioned in my last post we found out through my transplant coordinators, last week that the family of my heart donor made contact with us through a written letter. On Monday afternoon we received this letter which was little over 4 pages in length and written by the mother of this young man.. It is obvious that she was very proud of her son and had every right to be. Here are a few things about this young man that we learned. He was 23 and 6 ft 3 inches. He graduated in December of 2006 from a small university with BS in Biology. He has been the only undergraduate in the history of the school to have ever been published. For over 3 years he had been working on an interactive data based program which would be used by neuroscientist as a teaching tool, to help people that have Alzheimer’s and Autism. He was working and researching to help find a cure for the diseases that affect the brain His work has been published on the web and we were told that is has had over 10,000 hits from different teaching hospitals, neuroscientists and medical research hospital. And in April (a month before his death) his site had been visited by 31 different countries and 40 states. He had been contacted and was ready to begin graduate school in August to get his PhD in neuroscience. He had been chosen 1 of 6 internationally to do this.</span></i><i><span style="font-size:14pt;font-family:Georgia;">There was a International Neuroscience Convention with over 12,000 scientist in attendance, sometime after his death is which his picture was put on a jumbo screen and was talked about concerning his contributions to science and the benefits it would give thousands for years to come. (All of what I have just written about has come directly from this letter from his mother). She mentioned that before his death that 2 of his goals were accomplished and that was he was recognized and a scientist and an author. </span></i><i><span style="font-size:14pt;font-family:Georgia;">There are other things she spoke about, his personality and the type of person he was, but I will leave that alone for a while, just to say he wanted to help humanity in any way he could. His mother spoke of a conversation she and her son had regarding organ donation about 2 years ago. She told him that faced with the death of one of her children she did not think she could make that decision or go through with that. But his response was “Mom how could you not? When given the choice how could anyone not chose to help someone in that way”? I would want you to do that for me” (Direct quote from her letter).</span></i><i><span style="font-size:14pt;font-family:Georgia;">Finally, and this is in no way to speak or think highly of myself. But of all the organs he donated I have been the only one to send them a letter of thanks and gratitude. And she made mention that I was the one they had hope to hear from most of all, and said the words I wrote kind and gentle…all I can say is praise to the Lord for helping me write these things to her.</span></i></p>
<p><i><span style="font-size:14pt;font-family:Georgia;"> </span></i><i><span style="font-size:14pt;font-family:Georgia;">One of the frustrating things about the contact between donor and recipient is how sometimes the contact is so impersonal. They do not know my name or where I live just as I do not know where they live or their name of there son’s name. His name was actually whited out in her letter to me. But there are several organizations and hands these types of letter pass through before either one of us get them. An overture has been made to us that they would be glad to sign a waiver for me to have a copy of a DVD that his younger brother put together for his memorial service that we would receive if we wanted. Just to get a fuller picture of the life this young man. I have not decided what to do. I do plan on writing this family again in a couple months. What I have shared is only a small part of her letter to me, but in writing these things I wanted you to know and get a sense of how this young man wanted to help people whether in research or in organ donation. He wanted to be a benefit to people, through his giving of himself.</span></i></p>
<p><i><span style="font-size:14pt;font-family:Georgia;"></span></i><i><span style="font-size:14pt;font-family:Georgia;">In closing; some thoughts.</span></i><i><span style="font-size:14pt;font-family:Georgia;"><span> </span>This has been a lot for my family and me to take in this week. And have tried to keep a spiritual balance on this. One of the things that impressed me is of this “giving spirit” this young man had, and his desire to help “humanity”. I do not know this young man’s spiritual state, nor was anything mentioned in the letter to me except that “to continue to remember them in prayers as they were praying for us.” With that said this whole experience has shown me to give, to help people. Whether it’s with our money, our time, our talents, or sending a note to someone who is hurting, or whatever the challenge is to give, give give. After all was that not the example of Christ? He gave of himself to help the weary and sick, to dwell among sinners bringing them the message of the cross and the need to be born again. The spirit of giving is what has most convicted me, to go outside our comfort zones to help those around us in need and to set before them the example of Christ and to be more of a witness to them. Yes we can make a difference through the power of the Holy Spirit to this lost and dying world. We need to think outside the “box”, and be creative in the way we give ourselves in love and compassion to this world.</span></i><i><span style="font-size:14pt;font-family:Georgia;">The last thing that I have been challenged with is that whether we are a scientist, a teacher, a wife, mother, a pastor, a worker in a office, or whatever our calling we do it…. we work <span> </span>to the glory of God. This should be something we desire to do anyway in seeing the gift&#8230;.. the giving of the Son of God for our sins. How can we do any less? Let us strive to live as the question is asked “what is the chief end of man” It is the glorify God and to enjoy him forever. Are we doing that? I know this has been a lengthy post but my desire has been for you to get a sense of this young man, and to pray for his family as they continually daily deal with the loss of their son and that maybe as time goes by that through this relationship that has been formed by God’s Providence that he would have testimony to this family and that good can come out of this tragedy.</span></i><i><span style="font-size:14pt;font-family:Georgia;"><span> </span>Its sometimes hard not to feel guilty about having the transplant, and to see the type of person I received this gift from, but these are emotions that I think are normal. But I must realize that this was the young man’s wishes, and it was God’s Providence for these events to have taken place. And it is my desire that I would continue to bless and praise the Lord and give him glory for his goodness to me and well as my family, in these difficult events that have taken place in the last several months and to also have deeper heart-felt compassion for those who are hurting.</span></i></p>
<p><i><span style="font-size:14pt;font-family:Georgia;"></span></i><i><span style="font-size:14pt;font-family:Georgia;"></span></i><i><span style="font-size:14pt;font-family:Georgia;">Blessings to you</span></i></p>
<p><i><span style="font-size:14pt;font-family:Georgia;"></span></i><i><span style="font-size:14pt;font-family:Georgia;"></span></i><i><span style="font-size:14pt;font-family:Georgia;">Steve</span></i> </p>
<p></em></span></p>
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		<title>The Government, A Treadmill, &amp; Kelvin Sampson</title>
		<link>http://sebrooks.wordpress.com/2008/02/20/the-government-a-treadmill-kelvin-sampson/</link>
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		<pubDate>Tue, 19 Feb 2008 22:37:24 +0000</pubDate>
		<dc:creator>sebrooks</dc:creator>
				<category><![CDATA[Christian Life]]></category>
		<category><![CDATA[Humor]]></category>
		<category><![CDATA[Hymns and Worship]]></category>
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		<category><![CDATA[Organ Donation]]></category>
		<category><![CDATA[Organ Transplants]]></category>

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		<description><![CDATA[I know what a combination. The first part of this will be about the government and a treadmill. You may ask “what’s the connection there”? Well here is the story. Before my heart transplant I was selected to participate in a government clinical trial for people who feel under a certain criteria with congestive heart [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=sebrooks.wordpress.com&amp;blog=2454428&amp;post=32&amp;subd=sebrooks&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p><i><span style="font-family:Georgia;">I know what a combination. The first part of this will be about the government and a treadmill. You may ask “what’s the connection there”? Well here is the story. Before my heart transplant I was selected to participate in a government clinical trial for people who feel under a certain criteria with congestive heart failure and the benefit of cardiac rehab, and whether Medicare should help pay for this or not. For my participation in this clinical trial was, that I would receive a free treadmill. I was to have completed 32 sessions for this to happen. Well I only completed about 6 sessions, and then I had a heart transplant. I remember lying in my hospital bed one day thinking “no more congestive heart failure, means no treadmill”. Now don’t get me wrong I much rather have a new heart than a free treadmill. So I told my exercise nurse that now with a new heart I was out of the program. Well to make a long story short she was able to keep me in the program and the cardiac rehab I have been doing here since my transplant went toward the sessions I needed to get this treadmill. So on Valentine’s Day a big semi rolls up in front of the house with this new treadmill. Yesterday my son and I put it together. Now this is what I love about the government.<span>  </span>They can spend thousands on new toilet seats and nonsense like that. I thought that I was going to get a pretty decent quality treadmill. Was I wrong! I have never heard of this brand, and the quality of the treadmill is really suspect. But I am not complaining just making an observation. It looks like we may get a year or two use out of it and hey it was free.</span></i></p>
<p><i><span style="font-family:Georgia;"></span></i><i><span style="font-family:Georgia;">Ok Kelvin Sampson.</span></i></p>
<p><i><span style="font-family:Georgia;"></span></i><i><span style="font-family:Georgia;">As much as I have enjoyed watching IU this year and see their success for a change, I can’t help be disappointed for guys like DJ White and Eric Gordon. If Sampson is found to have violated these rules then I think Sampson should be fired as well as the athletic director Greenspan. He knew in hiring Sampson he was hiring a coach with a lot of baggage. It was a bad hire from the start. I do not think however that IU should be banned from post season play. Why penalize the players who have worked hard for the actions of their coach? If the players violated NCAA rules then yes they should be banned from post-season play. But again as I said why make them suffer because of their coach. Not that I am a big Bobby Knight fan or that I would like to see him come back to IU which would be very doubtful. I still think the man is a genius as a basketball coach is concerned. He is a purest as to how the game should be played. And say what you want about Knight in 29 years he has not broken any NCAA rules….yes a chair or two but that about it</span></i><i><span style="font-family:Wingdings;"><span>J</span></span></i><i><span style="font-family:Georgia;">. He is had one of the highest graduation rates among his players and has done great things in the community as well. But his behavior on and off the court has diminished those facts. Well that’s my ramble for the day. I hope the header now makes sense.</span></i></p>
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		<title>Some post transplant observations</title>
		<link>http://sebrooks.wordpress.com/2008/02/16/some-post-transplant-observations/</link>
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		<pubDate>Sat, 16 Feb 2008 05:12:48 +0000</pubDate>
		<dc:creator>sebrooks</dc:creator>
				<category><![CDATA[Christian Life]]></category>

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		<description><![CDATA[Some post transplant observations  1.     We never know how any given day will end. I have a trust in the Lord that all of our steps are ordered by Him and that whatever circumstance great or small is being done for His glory. Also that in life we need to live each day as it [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=sebrooks.wordpress.com&amp;blog=2454428&amp;post=31&amp;subd=sebrooks&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<h4><i><span style="font-weight:normal;font-size:14pt;color:black;"><font face="Times New Roman">Some post transplant observations</font></span></i></h4>
<p><i><span style="font-size:14pt;color:black;"><font face="Times New Roman"> </font></span></i><font face="Times New Roman"><i><span style="font-size:14pt;color:black;"><span>1.<span style="font:7pt 'Times New Roman';">     </span></span></span></i><i><span style="font-size:14pt;color:black;">We never know how any given day will end. I have a trust in the Lord that all of our steps are ordered by Him and that whatever circumstance great or small is being done for His glory. Also that in life we need to live each day as it where perhaps our last, and give ourselves totally to living for the Lord who has given us so much. </span></i></font><font face="Times New Roman"><i><span style="font-size:14pt;color:black;"><span> </span></span></i></font></p>
<p><font face="Times New Roman"><i><span style="font-size:14pt;color:black;"><span>2.<span style="font:7pt 'Times New Roman';">     </span></span></span></i><i><span style="font-size:14pt;color:black;">As already mentioned just how the Lord ordered all on Friday. Being with Pastor Andy, having the man in our church take care of the food, already heading to Indianapolis, being a holiday week, my wife had an extra day off.</span></i></font></p>
<p><font face="Times New Roman"><i><span style="font-size:14pt;color:black;"> </span></i></font><font face="Times New Roman"><i><span style="font-size:14pt;color:black;"><span>3.<span style="font:7pt 'Times New Roman';">     </span></span></span></i><i><span style="font-size:14pt;color:black;">I was told by one person that I was “the luck of the draw” Well we know that this was not luck this was solely the mighty providential working of our God to the good of His people.</span></i></font><i><span style="font-size:14pt;color:black;"><font face="Times New Roman"><span> </span>I do stand stunned and amazed at this last week’s events. Stunned from the point I never thought in my wildest dreams I would have a transplant this soon. But then it has shown me that God’s timing is not ours. And amazed from the point of how quickly I have been recovering. As another side note this transplant was to take between 6-8 hours but the one performed on me was done in 3 ½ hours. I am ashamed to be amazed because we do serve a great and mighty God that has done more abundantly that I ever thought or deserved. But I do Praise his name, I do glorify his name. I have told people that when you see me face to face that I want us together to magnify, glorify and worship this God in the way He has answered specific prayers and the way he ordered all these providences great and small the day of the transplant, and how as many of you prayed for me, God heard your prayers and I stand before you as answered prayer! Did I choose this for myself of course not, but it is God in His wise plan to bring this into my life, and to make me an example and I desire now to be more of a help and encouragement to those who suffer and are under severe trials. I also desire to be more of a servant and lover of our Lord. I know you have indulged me these last few days in talking about this experience, and I appreciate that. I just felt it was a good thing to share my story for the many of you that have prayed for me, and it has been good for me to express my feelings as well. But please rejoice with me in this wonderful God that watches over us and gives us what brings the most glory to Him!</font></span></i><i><span style="font-size:14pt;color:black;"><font face="Times New Roman"> Tomorrow will be my last post on this, but I have had a great number of inquiries on how that we might best be prayed for.</font></span></i><b><span style="font-family:'MS Reference Sans Serif';"> </span></b><font face="Times New Roman"> </font></p>
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		<title>The rest of the Transplant week</title>
		<link>http://sebrooks.wordpress.com/2008/02/15/the-rest-of-the-transplant-week/</link>
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		<pubDate>Fri, 15 Feb 2008 13:45:16 +0000</pubDate>
		<dc:creator>sebrooks</dc:creator>
				<category><![CDATA[Christian Life]]></category>

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		<description><![CDATA[The rest of the Transplant week.  May 26th, 2007 I don’t remember much after that I was told that Pastor Bob and David O’Neal came to see me but I have no recollection of their visits. At about 8:30 Saturday night the breathing tube was removed and was put on oxygen.  I begin to wake [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=sebrooks.wordpress.com&amp;blog=2454428&amp;post=30&amp;subd=sebrooks&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<h4><i><span style="font-size:14pt;color:black;"><font face="Times New Roman">The rest of the Transplant week.</font></span></i></h4>
<p><b><i><span style="font-size:14pt;color:black;"><font face="Times New Roman"> May 26th, 2007 </font></span></i></b></p>
<p><b><i><span style="font-size:14pt;color:black;"></span></i></b><b><i><span style="font-size:14pt;color:black;"><font face="Times New Roman">I don’t remember much after that I was told that Pastor Bob and David O’Neal came to see me but I have no recollection of their visits. At about 8:30 Saturday night the breathing tube was removed and was put on oxygen.<span>  </span>I begin to wake up and finally the nurses set me up in bed. I do remember going in and out of sleep. On Sunday they started to remove more of the drainage tubes, and doctors were very pleased with my progress. I do remember Pastor Harold and Sibyl coming to see me and had a good visit with them. On Monday I was able to get in and out of bed several times and all the rest of the chest tubes were removed. On Tuesday I took a 200 ft walk and was so out of breath by the time I got back to my room I thought I was going to pass out. But I was told this was normal. All the nurses and doctors that came to see me said I was about 2-3 days ahead of recovery where most people are at this time. The following day I was moved to a step down ward, where I have a much larger room where I could move around in. I increased my walking each day and feeling much better than I had been. I was there until Saturday when I was released.</font></span></i></b><b><i><span style="font-size:14pt;color:black;"><font face="Times New Roman">Now some other tidbits. I no longer have to take meds for congestive heart failure, but I do have a battery of meds I now take because my immune system is so low and the fear of my body rejecting the new heart. These meds I will take the rest of my life. For the next month I will have a weekly biopsy done to see if there is rejection. My first on was last Thursday and came back at 0% rejection…Praise the Lord! Because of these meds it has got my blood sugar all out of whack, and I have to give myself insulin shots 4 times a day. But the blood sugar should come back in line as some of these meds are adjusted. Anytime I go out in public I have to wear like a surgical mask and refrain from touching and hugging people, this will last for 6 months. As a family we are going through a process in the way we cook our food and prepare meals. Washing of say vegetables and fruits must be washed 3 and 4 times. And we find ourselves washing our hands several times a day. If you would come for a visit Susan would greet you at the door with a little squirt of antibacterial gel. </font></span></i></b><b><i><span style="font-size:14pt;color:black;font-family:Wingdings;"><span>J</span></span></i></b><b><i><span style="font-size:14pt;color:black;"><font face="Times New Roman">. The time that generally a person stays in the hospital is 10-14 days, but I was released little over 7 days. The doctors seemed impressed with my quick recovery, with one telling me that he saw no reason to keep me any longer. Some have asked about the donor like I said in an earlier post they are tight lipped about sharing any detail with the recipient. However he did learn the night of the transplant that the donor was out of state, he was a young man in the age or 24-30. However since that time we learned though a conversation which was started by Pastor Joe. He was concerned and voiced this concern that would this new heart make a difference in my golf game, where I would be able to beat him, the nurse replied that all she could tell him that I would be golfing with a 26 year younger heart than I had before, which would have but this donor man at 24.. I have an option to write this family a letter of gratitude, which I will do. I have to be very discreet in this letter as not to let them know my address or full name and any personal info like that. I can give them my first name but that’s it. And then this letter has to go through several channels before it gets to the donor family. My thoughts were to write them in a few months, just in order that they have time to grieve. I also have been told that this man donated all of his viable organs to others as well. Well that’s about all I can think of right now. I will probably finish these post about this experience, tomorrow as I would just like to make some closing observations about this whole perspective. I wish I had the words to fully express to each person, whether here in Anderson, or Owensboro, and even in Dayton, for your prayers for us; they have meant the world to us. I am grateful to our Lord that He has put this kinship within us to bear one another’s burden and pray for our needs. What<span>  </span>a privilege we have to lift everything to God in prayer. I thank you for indulging me in speaking of this event in my life.</font></span></i></b><font face="Times New Roman"> </font></p>
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		<title>Transplanted Part 2</title>
		<link>http://sebrooks.wordpress.com/2008/02/14/transplanted-part-2/</link>
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		<pubDate>Wed, 13 Feb 2008 18:14:01 +0000</pubDate>
		<dc:creator>sebrooks</dc:creator>
				<category><![CDATA[Christian Life]]></category>

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		<description><![CDATA[Transplanted Part 2 May 25th, 2007 When I get to the hospital I am taken to a room that has been isolated for the 4 hours before my arrival. I then am asked to change into a hospital gown, and get in bed. A doctor Young comes to talk to me and let me know that [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=sebrooks.wordpress.com&amp;blog=2454428&amp;post=29&amp;subd=sebrooks&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<h4><span style="color:black;font-family:'MS Reference Sans Serif';"><em>Transplanted Part 2</em></span></h4>
<p><span style="color:black;font-family:'MS Reference Sans Serif';"><em>May 25<sup>th</sup>, 2007</em></span></p>
<p><span style="color:black;font-family:'MS Reference Sans Serif';"></span><span style="color:black;font-family:'MS Reference Sans Serif';"><em>When I get to the hospital I am taken to a room that has been isolated for the 4 hours before my arrival. I then am asked to change into a hospital gown, and get in bed. A doctor Young comes to talk to me and let me know that he will be hooking me up to IV’s and starting a reverse affect of a particular medicine I have been taking. As all this was going on Susan was on her way to the high school where my youngest daughter was attending, to get her. By the way the day of all this was Katelyn’s 16<sup>th</sup> birthday. At about 2:30pm they arrived as well as my son and father-in-law. We where told at that time that the transplant may take place between 5-6 that evening. As the day progressed the word of this must have spread because people from church kept filtering in. Well around 5:30 we were told that it might be closer to 9-930 before surgery. In the meantime a nurse found out that it was Katelyn’s birthday and arranged a big chocolate cake to be delivered to my room. So we sang happy birthday to her and everyone ate cake while I just watched…lol. Dr Young kept coming in and just letting me know what they were doing and preparing the family for what I would look like after the surgery. Lora, my transplant coordinator was also in a lot letting us know the status of the situation. Although nothing can be said of the donor or what has happened to him. At about 1015 that night we are told that the plane has taken off and that the donor heart is a really, really, really, good heart. What we were told at that time was that it was from a young man, who was a rather large body size but had been very athletic all his life. So at about 11 I was wheeled to surgery where I said goodbye to my family and started some babble about my last wishes and all that to which Lora told me that I was going to be just fine. So I shut up. I was taken to this holding area where my chest and arms were shaved, and the next thing I remember was being pushed into the surgery room looking up at the surgical lights. That was the last thing I remembered. These next events I will write about is concerning the updates the family received during the course of the night. These were recorded by a dear lady in our church.</em></span><span style="color:black;font-family:'MS Reference Sans Serif';"><em>1:35 am Lora told the family I was on bypass and the heart was here.</em></span><span style="color:black;font-family:'MS Reference Sans Serif';"><em>2:30 am the heart is in and beating and the doctors where putting in drain tubes, and getting ready to take off bypass.</em></span><span style="color:black;font-family:'MS Reference Sans Serif';"><em>3:30 am off bypass and checking for bleeding.</em></span><span style="color:black;font-family:'MS Reference Sans Serif';"><em>4:00 doctors were wiring up sternum. and was being placed on a ventilator </em></span><span style="color:black;font-family:'MS Reference Sans Serif';"><em>4:40 am Lora tells family they were finishing up and sewing everything back in place.</em></span><span style="color:black;font-family:'MS Reference Sans Serif';"><em>4:50 am the transplant surgeon Dr. Salerno tells family I am on the way to recovery and would be weaned off the ventilator later that day and that it was an excellent heart. The surgery was just over 3 1/2 hours.</em></span><span style="color:black;font-family:'MS Reference Sans Serif';"><em>5:15 am family comes in; they said I am puffy and pale, hooked up to a lot of tubes and wires, and of course the ventilator. Lora tells the family that my old heart was the largest of the last 5 transplants, and when they removed it was an angry red color, it literally fit into the 2 hands of the surgeon. But the new one was a very healthy pink color and was the size of his fist. The family is reminded not to get bogged down in details but look at the big picture. They have to make sure brain; lungs, kidneys and heart are all working together.</em></span><span style="color:black;font-family:'MS Reference Sans Serif';"><em>The next thing I do remember was seeing the lovely face of my wife and her telling me that I had a new heart and that it was beating perfectly. And was told that upon that news I flashed a $100.00 smile and gave a thumbs up&#8230;then slipped back into sleep.</em></span><span style="font-size:12pt;color:black;font-family:'MS Reference Sans Serif';"><em>I will stop here for now because I know this has been rather lengthy. But will later this week will finish the rest of the week<strong>.</strong></em></span></p>
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		<title>Transplant Experience Part 1</title>
		<link>http://sebrooks.wordpress.com/2008/02/13/transplant-experience-part-1/</link>
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		<pubDate>Tue, 12 Feb 2008 22:11:59 +0000</pubDate>
		<dc:creator>sebrooks</dc:creator>
				<category><![CDATA[Christian Life]]></category>

		<guid isPermaLink="false">http://sebrooks.wordpress.com/2008/02/13/transplant-experience-part-1/</guid>
		<description><![CDATA[As most of you know and if there are any new readers to this blog,. I was the recipient of a heart transplant on May 26, 2007. I have actually done more writing on this than have spoken about this. I am trying to balance these events and not go around thinking that I am [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=sebrooks.wordpress.com&amp;blog=2454428&amp;post=28&amp;subd=sebrooks&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p><i><span style="font-size:14pt;"><font face="Times New Roman">As most of you know and if there are any new readers to this blog,. I was the recipient of a heart transplant on May 26, 2007. I have actually done more writing on this than have spoken about this. I am trying to balance these events and not go around thinking that I am someone special or important because of this event in my life. I have over the course of the last few months and especially over the last month wanted to bring more awareness to organ donation and the great need there is for as many as would participate with me in becoming donors. But as I have already stated I want to find a balance on this subject as well as balance this against my faith and convictions of the Word of God. I would never want to offend anyone because of my strong belief in this important subject. But I guess when something like this happens to you, then for a while you do find something like this important and develop strong feelings about it. Over the next few days if you will indulge me I am going to make some post that I wrote, a week after my transplant and some observations of that week and the day of and the days preceding the transplant. It is my desire that you will find encouragement and rejoice with me in the Great God we serve.</font></span></i><i><span style="font-size:14pt;"><font face="Times New Roman">Keep in mind these where my thoughts the week after I got home, and started to keep a journal of the events of this event. After these post I will move on to some other subjects and try and leave this transplant alone for a while.</font></span></i></p>
<p><i><span style="font-size:14pt;"></span></i><i><span style="font-weight:normal;font-size:14pt;color:black;"><font face="Times New Roman"> Transplanted and at Home!</font></span></i></p>
<p><i><span style="font-size:14pt;color:black;"><font face="Times New Roman">May 25<sup>th</sup>, 2007</font></span></i><i><span style="font-size:14pt;color:black;"><font face="Times New Roman"><span> </span></font></span></i></p>
<p><i><span style="font-size:14pt;color:black;"><font face="Times New Roman"><span></span>I received a cell phone call. at 11:13 am. I cannot identify the voice of the caller only by the caller ID I see it’s a transplant coordinator. She says “Steve?” “Have you taken your meds for today”, “are you alone or with someone?” “Have you eaten today?” I just thought she was calling me because I had voiced mailed her earlier about a test result I had done the day before. When I asked her what was going on she says “well there maybe something in the works today for a heart transplant” My stomach went immediately to my throat and thought this couldn’t be I have only been on the list since April 10.</font></span></i><i><span style="font-size:14pt;color:black;"><font face="Times New Roman">Cell phone call 2 came to me at 12:22pm. “Steve this is Lora, it looks like you need to come to the hospital and get checked in don’t rush but get her as soon as you can….I was stunned. No this couldn’t be, or could it really?</font></span></i><i><span style="font-size:14pt;color:black;"><font face="Times New Roman"> </font></span></i><i><span style="font-size:14pt;color:black;"><font face="Times New Roman">Now let me fill in the blanks between phone calls. At about 10:45 that morning I had met with Pastor Andy to go to Sams Club to purchase some meat we were going to use for a cookout on Sunday. We stopped by a local elementary school so Andy could take a video of a presentation of a gift to a teacher. It was after that when on our way to Sam’s that I received the first call. We get to Sams and begin to shop while there we run into a man from our church that was there with his father-in-law. We get all that we needed for the cookout and try some sample’s they were having. We checkout and begin to load the car when the second phone call came. In the providence of our God the man I mentioned from our church had just also checked out. Andy asked him if he could take the meat and store it till Sunday. After being told to come to the hospital I started to get a hold of Susan my wife, my Son, Pastor Joe from Owensboro just to let them know what was going on. Pastor Andy had called his dad and was able to speak to Pastor Tom for a few minutes. On the way to the hospital I broke down several times, wondering what the rest of the day would hold. Would this be a real thing? or a false alarm. I had only began to prepare myself that if the transplant were to happen it may be in September, or Oct, because where I was placed on the list was serious but I knew there were others in worst shape ahead of me. But I also knew that I had a universal blood type that put me at maybe a better advantage. Andy was such a comfort, reminding me that I was a child of God, That God was watching over me, in every detail and to lean myself upon Him. He also was quoting scripture to me as we walked into the hospital. I get to the hospital check in and am wheeled into my room. I will stop here because the next few post will be a continuous unfolding of the days events.</font></span></i><i><span style="font-size:14pt;color:black;"><font face="Times New Roman">But there are some striking providences I would make mention of.</font></span></i></p>
<p><i><span style="font-size:14pt;color:black;"></span></i><i><span style="font-size:14pt;color:black;"><font face="Times New Roman">#1 God is his wise creativity of me, created in me this universal blood type.</font></span></i></p>
<p><i><span style="font-size:14pt;color:black;"></span></i><i><span style="font-size:14pt;color:black;"><font face="Times New Roman">#2 I was not alone but with Pastor Andy.</font></span></i></p>
<p><i><span style="font-size:14pt;color:black;"></span></i><i><span style="font-size:14pt;color:black;"><font face="Times New Roman">#3 The man we met from our church being there at Sam’s</font></span></i></p>
<p><i><span style="font-size:14pt;color:black;"></span></i><i><span style="font-size:14pt;color:black;"><font face="Times New Roman">#4 As Andy and I were discussing whether to go back to Anderson or hang around in Indy at that precise moment the second call came.</font></span></i><i><span style="font-size:14pt;color:black;"><font face="Times New Roman">I am overwhelmed beyond words at times to fully be able to express in words all the feelings and emotions that happened that day as well as the days to follow. I can barely sit and think of the goodness of God, and the loss of this family member whose heart is now beating in me without breaking down in tears of praise to God, and for the spirit of gratitude He has placed within me</font></span></i></p>
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