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		<title>Foust Frenzy</title>
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		<title>Finally&#8230;..a venue and a date.</title>
		<link>http://foustfrenzy.wordpress.com/2011/06/27/finally-a-venue-and-a-date/</link>
		<comments>http://foustfrenzy.wordpress.com/2011/06/27/finally-a-venue-and-a-date/#comments</comments>
		<pubDate>Mon, 27 Jun 2011 20:36:51 +0000</pubDate>
		<dc:creator>foustfrenzy</dc:creator>
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		<guid isPermaLink="false">http://foustfrenzy.wordpress.com/?p=252</guid>
		<description><![CDATA[Since the beginning of our journey with Jax&#8217;s illness, we knew that we were hand picked by God to go through all of this craziness.  Not always the easiest thing to swallow but it&#8217;s just the truth.  For the last 6 months or so we knew that one of the reasons God called our family [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=foustfrenzy.wordpress.com&amp;blog=4246270&amp;post=252&amp;subd=foustfrenzy&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p>Since the beginning of our journey with Jax&#8217;s illness, we knew that we were hand picked by God to go through all of this craziness.  Not always the easiest thing to swallow but it&#8217;s just the truth.  For the last 6 months or so we knew that one of the reasons God called our family to experience all of this is because we are not just a sit there and deal with it kind of family.  We take action.  So I am proud to announce that we have finally got a venue and a date for a fundraiser to raise money for funds to help research histiocytosis.  Because of this being an &#8220;orphan&#8221; disease, there is no government funding for research so it&#8217;s really up to those seeking a cure to raise money.  The fundraiser will be held on Oct. 8, 2011 at Paulding Meadows Park from 1:00-5:00 in the afternoon.  It is going to be a fall festival type of event with bounce houses, face painting, and lots of give-aways.  We will be asking for a donation of $25 a family and you will receive lots of coupons and gift certificates with your donation.  If you are a business owner and would like to donate your services, please let me know.  We would greatly appreciate it!!!!  Foust Landscaping will be giving away free lawn care.  SugarSnapPhotography will be giving gift certificates.  And lots of area restaurants will also be giving out coupons.  I have friends and family that are going to be doing face painting.  I am looking into having a petting zoo.  And LOTS more!!!!  So please, mark your calendars for this event and we hope to see you there!!  We are praying that this will also be Jax&#8217;s end of chemo party.</p>
<div id="attachment_253" class="wp-caption alignleft" style="width: 545px"><a href="http://foustfrenzy.files.wordpress.com/2011/06/dsc_0877.jpg"><img class="size-full wp-image-253" title="DSC_0877" src="http://foustfrenzy.files.wordpress.com/2011/06/dsc_0877.jpg?w=535&#038;h=799" alt="" width="535" height="799" /></a><p class="wp-caption-text">I told you he was gonna be the cutest port-wearing beach bum ever!!!</p></div>
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		<title>In the Foust House</title>
		<link>http://foustfrenzy.wordpress.com/2011/04/28/in-the-foust-house/</link>
		<comments>http://foustfrenzy.wordpress.com/2011/04/28/in-the-foust-house/#comments</comments>
		<pubDate>Thu, 28 Apr 2011 00:35:33 +0000</pubDate>
		<dc:creator>foustfrenzy</dc:creator>
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		<description><![CDATA[Jax had his 42nd week of treatment today&#8230;..sheesh!!  This month he has done really well.  He has eaten better, felt better, and is learning a whole lot.  However, the last two days have been pretty rough.  I can always tell when he starts to feel bad b-c he is super clingy, whiny, doesn&#8217;t eat well, [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=foustfrenzy.wordpress.com&amp;blog=4246270&amp;post=248&amp;subd=foustfrenzy&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p>Jax had his 42nd week of treatment today&#8230;..sheesh!!  This month he has done really well.  He has eaten better, felt better, and is learning a whole lot.  However, the last two days have been pretty rough.  I can always tell when he starts to feel bad b-c he is super clingy, whiny, doesn&#8217;t eat well, and starts to take 4 1/2 hr naps.  Last night was especially tough.  He did not sleep well at all.  He talked and moaned and cried.  I haven&#8217;t had to go in his room in the middle of the night since the beginning of this whole journey and last night brought back A LOT of memories&#8230;.not so good ones.  So today when I had to wake him up to go to the doctor, it broke my heart.  Jax&#8217;s sleep is very important to me because I know his body needs it in order to heal.  The ride to the clinic was a little rough and the visit today was as well.  Jax was just not feeling himself at all.  He was running a low-grade temp and had a runny nose.  In spite of not feeling well, they still gave him his chemo.  We also found out today that one of Jax&#8217;s oncologists, Dr. Momin, is leaving the clinic in order to stay home with her 6 month old baby&#8230;.totally understandable.  She will be truly missed, however.  After treatment we headed home and Jax actually fell asleep in the car.  That NEVER happens.  He was exhausted!!!  Jax is now still running a low-grade temp and if it does not start to go down we will have to head to the ER.  Because of Jax&#8217;s liver disease, he is not allowed to have Tylenol or Motrin so we have to wait it out.  And because he has a port, we have to bring him to the ER anytime he runs a fever of 100.5 or higher.  Sooooo, please pray healing over our little biscuit.  He is just feeling really yucky and it breaks my heart for him.  Also, the rest of our family could really use your prayers as well.  I am EXHAUSTED!!! Emotionally and physically.  I just don&#8217;t seem to have the energy to put into the older kids because Jax requires so much of me.  This REALLY effects Bella.  Her love language is quality time and she has a really hard time when she doesn&#8217;t feel like she&#8217;s getting enough attention.  Poor Maddox just gets lost in the shuffle sometimes.  He is just so content and chill but I NEVER want to get comfortable with the fact that he doesn&#8217;t &#8220;require&#8221; as much of me.  I am trying to learn how to let laundry go, not cook dinner every night, or miss a work-out in order to spend more time with them when possible.  VERY HARD FOR ME!!! Soooo, I will stop having my pity party now but I have had so many people tell me how strong I am and I SOOOOOO appreciate that.  However, I do struggle&#8230;.trust me.  We appreciate all of your sweet comments, cards and phone calls.  Sometimes, it&#8217;s what gets me through the day and I am so thankful for each one of them.  I will keep everyone posted on the fever situation but from the sounds that are coming from the monitor, it&#8217;s gonna be a long night.</p>
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		<title>Update on Jax</title>
		<link>http://foustfrenzy.wordpress.com/2011/03/31/update-on-jax/</link>
		<comments>http://foustfrenzy.wordpress.com/2011/03/31/update-on-jax/#comments</comments>
		<pubDate>Thu, 31 Mar 2011 13:55:26 +0000</pubDate>
		<dc:creator>foustfrenzy</dc:creator>
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		<guid isPermaLink="false">http://foustfrenzy.wordpress.com/?p=245</guid>
		<description><![CDATA[Hello to all my prayer warrior friends.  I believe with all my heart that God is honoring all of our prayers in the name of baby Jax.  We had our 10th month of chemo yesterday and Jax has gotten to be one tough little booger.  Every time he has treatment, he has to go to [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=foustfrenzy.wordpress.com&amp;blog=4246270&amp;post=245&amp;subd=foustfrenzy&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p>Hello to all my prayer warrior friends.  I believe with all my heart that God is honoring all of our prayers in the name of baby Jax.  We had our 10th month of chemo yesterday and Jax has gotten to be one tough little booger.  Every time he has treatment, he has to go to triage first to check his blood pressure, oxygen level, temperature, weight, height, head circumference, and get his finger pricked to check his blood counts.  He does so great with all of it.  Yesterday, he didn&#8217;t budge when Ms. Faith pricked his finger.  And this is not just a little finger stick, she has to push on his little finger to make sure she has enough blood for his CBC.  So little Jax just sat there and watched every move Ms. Faith made.  He watched each blood drop into the tube&#8230;he is like his mommy and would rather see what is happening to him instead of looking away.  Once we were finished, we had to go to the play area to wait for a room to open.  He was a little social butterfly.  He waved at all the nurses walking by and was very interested in what all the other kids were doing.  This tells me that he is growing up.  He used to never really have anything to do with other kids except for his brother and sister.  When we got to our room, Jax was very patient.  He put on Nana&#8217;s lipstick and ate snacks.  Both Dr. Momin and Dr. George looked at him yesterday and said he looked great.  His liver is still measuring the same but other than that, he has no lesions anywhere.  His scalp and his underarms have also cleared up.  So then it was time for chemo.  Jax was a CHAMP!!!  He has to lie down and I hold his legs while Nana holds his arms.  He usually freaks out but this time, he just smiled at Ms. Elisha as she made funny noises to keep him distracted&#8230;..it worked.  I am so thankful that he is getting used to this whole ordeal but it is also sad that he even knows what any of this is.  So after treatment, I got him dressed and we were on our way.  Elisha called yesterday afternoon with his blood results and they were AMAZING!!!  They are even lower than last month.  Jax&#8217;s GI specialist says that he  believes that since the liver regenerates itself, the new good cells are taking over the old bad cells.  And the chemo is killing out any of the extra histiocytes that his body is making so the lesions are slowly going away.  This has been our prayer from the beginning.  Dr. George told us yesterday that he wants Jax to do chemo until August instead of July.  He has to be on maintenance chemo for a year and that will be in August.  He is going to do his scans again in July to make sure everything still looks good before we end treatment.  Dr. George did say yesterday that he will not be surprised if Jax&#8217;s LCH flares up a few months after treatment.  Jax was sooooo sick (a lot more than we realized) and so little that he thinks it&#8217;s gonna take more than one round of chemo to get rid of the disease completely.  He did also say however, that if he has to go back on chemo it will only be once a month and not every week like we thought.  So overall, we feel like all of this is good news.  Does it still suck?  YES!  Do we still have to pray that his liver gets better once treatment ends instead of worse? YES! But we are confident that our little boy is going to come out of this okay.  That is not something I could&#8217;ve said at the beginning of this journey.  I had faith but I also had to be honest with myself about how sick Jax was.  His GI specialist said that if they didn&#8217;t figure out what was going on with him, and get it fixed quickly when he was in the hospital, he was on the verge of needing a liver transplant.  He was REALLY sick.  I am so thankful that we figured out what was going on with him when we did because his liver couldn&#8217;t have taken much more.  God&#8217;s timing is PERFECT!!  I write all of this for a lot of reasons but one of them is to let everyone know how he&#8217;s doing and what specifically to pray for.  Right now we are praying that when he ends treatment in August, the disease will stay in remission and his liver will continue to heal.  Thank you so much to all of you who keep up with our story.  There are days when I feel discouraged and just flat out mad and alone.  And it&#8217;s those days that we get a card in the mail (which are all displayed in Jax&#8217;s room) or a special gift for him and it reminds me that we are not alone so thank you.  From the bottom of my heart&#8230;&#8230;thank you!!!</p>
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		<title>The many reasons I love my hubs&#8230;..</title>
		<link>http://foustfrenzy.wordpress.com/2011/03/28/the-many-reasons-i-love-my-hubs/</link>
		<comments>http://foustfrenzy.wordpress.com/2011/03/28/the-many-reasons-i-love-my-hubs/#comments</comments>
		<pubDate>Mon, 28 Mar 2011 01:17:37 +0000</pubDate>
		<dc:creator>foustfrenzy</dc:creator>
				<category><![CDATA[Uncategorized]]></category>

		<guid isPermaLink="false">http://foustfrenzy.wordpress.com/?p=238</guid>
		<description><![CDATA[Chris and I are approaching 10 years of marriage next month&#8230;.WOW!!  After 12 years of being together, it becomes easy  to pick apart the things we do not like about each other but for some reason, we&#8217;re not as quick to say what we love about each other.  Well, at least I&#8217;m not.  I am [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=foustfrenzy.wordpress.com&amp;blog=4246270&amp;post=238&amp;subd=foustfrenzy&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p><a href="http://foustfrenzy.files.wordpress.com/2011/03/img_0226.png"><img class="alignleft size-full wp-image-241" title="IMG_0226" src="http://foustfrenzy.files.wordpress.com/2011/03/img_0226.png?w=320&#038;h=480" alt="" width="320" height="480" /></a>Chris and I are approaching 10 years of marriage next month&#8230;.WOW!!  After 12 years of being together, it becomes easy  to pick apart the things we do not like about each other but for some reason, we&#8217;re not as quick to say what we love about each other.  Well, at least I&#8217;m not.  I am determined to turn this around.  My husband is amazing and I am so blessed to have him so I just thought I would list some things that I love about my stud.</p>
<p>He loves me with a love that I have NEVER known before.  It is so unconditional and has no boundaries.</p>
<p>He is an amazingly engaged father.</p>
<p>He loves not only his kids but everyone else&#8217;s as well&#8230;and they usually love him back.</p>
<p>He is very passionate about his faith.</p>
<p>He loves his family.</p>
<p>He cares about his body and about how he looks without being vain&#8230;..I can&#8217;t stand a frump!</p>
<p>He is a BLAST to be around.  Just this weekend as we were having family night, I was ordering at the Chick-fil-A drive-thru</p>
<p>and he tickled me until I couldn&#8217;t breathe or order my food.  The lady asked me what was so funny and I just had to laugh and     tell her that my husband was a dork.</p>
<p>He is an AMAZING provider and works so very hard for us.</p>
<p>About a month ago, while in Orlando he said God was telling him to give some money to a family that we know.  He never    argued&#8230;.he just obeyed. Not a lot of people see this side of him or even believe it exists <img src='http://s2.wp.com/wp-includes/images/smilies/icon_smile.gif' alt=':)' class='wp-smiley' /> </p>
<p>When he is laying on the couch or cuddling with me in the bed, he rubs his feet together like a cat.</p>
<p>He is good at EVERYTHING he does.  He plays drums, tennis, builds things, loves all sports&#8230;..it&#8217;s not even fair.  I would just      like to have ONE talent and he has like a million.</p>
<p>Sometimes, we like to harmonize to Southern Gospel songs or old hymns.</p>
<p>He makes me feel like the most beautiful woman in the whole world and is constantly complimenting me.</p>
<p>He always asks our kids, &#8220;Don&#8217;t you have the prettiest mommy in the world?&#8221; and they just giggle&#8230;..so sweet.</p>
<p>Even though his frugal ways frustrate me on most days, I find comfort in knowing that he always does what is financially best  for our family.  And if I was in charge, I would spend it all on curtains and throw pillows.</p>
<p>I am very burdened by how many stories I&#8217;ve heard lately of divorce.  It&#8217;s almost become a shock when you hear of people staying married for 10 or 15 years.  I&#8217;m so blessed to be with an amazing man with whom I fall more in love with every day.  I&#8217;m not saying we don&#8217;t have our struggles because that would be crazy.  But at the end of the day, we are more in love than we were when we met and that says a lot.  I love you, Christopher and I love the life that God has allowed us to have together.</p>
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		<title>I wish I had a creative title for this post but I don&#8217;t so here it goes&#8230;..</title>
		<link>http://foustfrenzy.wordpress.com/2011/03/07/i-wish-i-had-a-creative-title-for-this-post-but-i-dont-so-here-it-goes/</link>
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		<pubDate>Mon, 07 Mar 2011 14:33:19 +0000</pubDate>
		<dc:creator>foustfrenzy</dc:creator>
				<category><![CDATA[Uncategorized]]></category>

		<guid isPermaLink="false">http://foustfrenzy.wordpress.com/?p=236</guid>
		<description><![CDATA[I am currently working on a fundraiser to raise money for research on Langerhan&#8217;s Cell Histiocytosis.  (LCH)  As most of you know, LCH is considered a rare disease and therefore the government can not provide the funds needed for research.  The only hope for finding a cure for this rare disease is providing money to [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=foustfrenzy.wordpress.com&amp;blog=4246270&amp;post=236&amp;subd=foustfrenzy&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p>I am currently working on a fundraiser to raise money for research on Langerhan&#8217;s Cell Histiocytosis.  (LCH)  As most of you know, LCH is considered a rare disease and therefore the government can not provide the funds needed for research.  The only hope for finding a cure for this rare disease is providing money to those who are interested in helping find a cure.  Soooooo, I am going to try my darndest to make that happen.  I wanted to see what your opinion was.  I would love to have a fundraiser that families can do or enjoy together&#8230;.kid-friendly.  I know that most people do walks or runs but I was thinking of something more along the lines of a worship concert, or an event where kids can make crafts to give to children going through chemo like hats or bandanas.  What &#8216;cha think???  I would love to know your input going into this process so that I can plan accordingly.  I am working with a social worker from the Aflac Cancer Center and I know she&#8217;s pretty much seen every kind of fundraiser imaginable.  I would love to present something completely different and exciting to her.  I appreciate you taking the time to read this and can&#8217;t wait to hear all of your creative ideas.</p>
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		<title>Garlic and Rosemary Roasted Red Potatoes</title>
		<link>http://foustfrenzy.wordpress.com/2011/03/02/garlic-and-rosemary-roasted-red-potatoes/</link>
		<comments>http://foustfrenzy.wordpress.com/2011/03/02/garlic-and-rosemary-roasted-red-potatoes/#comments</comments>
		<pubDate>Wed, 02 Mar 2011 02:18:22 +0000</pubDate>
		<dc:creator>foustfrenzy</dc:creator>
				<category><![CDATA[Uncategorized]]></category>

		<guid isPermaLink="false">http://foustfrenzy.wordpress.com/?p=231</guid>
		<description><![CDATA[This one is pretty self-explanitory but they are oh so yummy!! I usually use about 8 red potatoes for my family (cut into quarters or halves) about 2 tablespoons of dried or fresh rosemary 3 cloves of garlic peeled (I usually give them a &#8220;whop&#8221; or two with a knife to expose the flavor but [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=foustfrenzy.wordpress.com&amp;blog=4246270&amp;post=231&amp;subd=foustfrenzy&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p>This one is pretty self-explanitory but they are oh so yummy!!</p>
<p>I usually use about 8 red potatoes for my family (cut into quarters or halves)</p>
<p>about 2 tablespoons of dried or fresh rosemary</p>
<p>3 cloves of garlic peeled (I usually give them a &#8220;whop&#8221; or two with a knife to expose the flavor but don&#8217;t smoosh it)</p>
<p>about 1/2 cup of Olive Oil</p>
<p>salt and pepper</p>
<p>Mix all these ingredients in a large freezer bag and shake what ya momma gave ya!  When coated, put on a baking sheet and place in a 4oo degree oven for about an hour.  I turn mine about half-way through because they get crispy.  These are yummy and full of flavor.  Serve with your favorite chicken dish or grilled salmon.  So lovely!</p>
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		<title>National Rare Disease Day</title>
		<link>http://foustfrenzy.wordpress.com/2011/02/07/national-rare-disease-day/</link>
		<comments>http://foustfrenzy.wordpress.com/2011/02/07/national-rare-disease-day/#comments</comments>
		<pubDate>Mon, 07 Feb 2011 01:43:04 +0000</pubDate>
		<dc:creator>foustfrenzy</dc:creator>
				<category><![CDATA[Uncategorized]]></category>

		<guid isPermaLink="false">http://foustfrenzy.wordpress.com/?p=224</guid>
		<description><![CDATA[I have recently found out that there is an actual National Rare Disease Day.  Unfortunately, it is only recognized in some states and Georgia is not one of them.  To get our state to recognize this day, we need to email Governor Nathan Deal and request that this day become official in the state of [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=foustfrenzy.wordpress.com&amp;blog=4246270&amp;post=224&amp;subd=foustfrenzy&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p>I have recently found out that there is an actual National Rare Disease Day.  Unfortunately, it is only recognized in some states and Georgia is not one of them.  To get our state to recognize this day, we need to email Governor Nathan Deal and request that this day become official in the state of Georgia.  Go to georgia.gov and find the link on the right side of the page that says Governor Nathan Deal.  Then go to the top of the page and click where it says &#8220;contact us&#8221;.  I am going to post a sample letter and would love it if you guys could help out with this cause.  All you have to do is copy the letter, post it to the email, and add your name at the bottom.  I know that this will take a few minutes of your time but I promise as a mom of a child with a rare disease, your time will be greatly appreciated.  Thanks in advance.</p>
<p>Dear Governor Deal:</p>
<p>We are writing to ask you to declare that the last day in February will be observed on an ongoing basis as <strong>Rare Disease Day </strong>in Georgia each year.  On that day, millions of people around the world observe Rare Disease Day as a way of raising awareness of these diseases, which affect nearly 30 million Americans, and the special challenges encountered by patients and their families.</p>
<p>Thousands of Georgia residents join in this annual observance.  Your pronouncement of the day as a recognized event in the state would be greatly appreciated by patients and caregivers, as well as medical professionals, researchers, public health officials, educators, social workers and others serving the rare disease community.</p>
<p>Rare diseases are those that affect fewer than 200,000 Americans, and there are nearly 7,000 such diseases affecting nearly 30 million Americans, according to the National Institutes of Health (NIH).</p>
<p>Rare Disease Day was observed for the first time in the United States in 2009 and was a great success.  The observance was supported by entities such as the National Institutes of Health, Food and Drug Administration, and Social Security Administration, as well as many patient organizations and state and local agencies.</p>
<p>We respectfully ask you to consider designating the last day of February <strong>Rare Disease Day</strong> in Georgia on the basis that:</p>
<ul>
<li>Thousands of residents of Georgia are affected by rare diseases, as patients, friends and family, caregivers, physicians and other medical professionals, providers of social services, and researchers seeking to develop safe, effective treatments</li>
<li>Many rare diseases are serious or even life-threatening</li>
<li>Most rare diseases have no treatment</li>
<li>About half of the people affected by rare diseases in the U.S. are children since many rare diseases are genetic</li>
<li>Research on rare diseases is important because it often adds significantly to the general understanding of more common diseases</li>
</ul>
<p>People with rare diseases experience certain challenges that occur as a result of the fact that their diseases are rare.  These include:</p>
<ul>
<li>Difficulty in obtaining a timely, accurate diagnosis</li>
<li>Limited treatment options</li>
<li>Difficulty in finding physicians or treatment centers with needed expertise</li>
<li>Treatments that are generally more expensive than those for common diseases</li>
<li>Reimbursement issues related to private insurance, Medicare and Medicaid</li>
<li>A sense of isolation and hopelessness</li>
</ul>
<p>Rare disorders affect the entire family of an individual patient. Caregivers endure ongoing stress and isolation managing the medical and financial issues that arise. When there is delay in the diagnosis of a rare genetic disorder, siblings may be born with the same condition. When a rare genetic disorder is diagnosed during adulthood, other family members may need to be informed that they may also be at risk…and this may lead to difficult decisions regarding genetic testing, if such testing is an option.</p>
<p>On the basis of all of the above, we hope you will join other governors around the nation in declaring the last day in the month of February to be observed each year as Rare Disease Day in the state.</p>
<p>With best regards,</p>
<p>Your name</p>
<p>Your organization</p>
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		<title>Comfort food</title>
		<link>http://foustfrenzy.wordpress.com/2011/01/31/comfort-food/</link>
		<comments>http://foustfrenzy.wordpress.com/2011/01/31/comfort-food/#comments</comments>
		<pubDate>Mon, 31 Jan 2011 19:54:04 +0000</pubDate>
		<dc:creator>foustfrenzy</dc:creator>
				<category><![CDATA[Uncategorized]]></category>

		<guid isPermaLink="false">http://foustfrenzy.wordpress.com/?p=214</guid>
		<description><![CDATA[So today&#8217;s recipe is for Beef Stew.  Again, not a complex meal but it has tons of veggies and my kids actually like it.  So here it goes: 1 lb. of Stew meat 1/2 an onion finely chopped 3-4 stalks of celery finely chopped 1 small bag of baby carrotts about 8 red potatoes 1 [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=foustfrenzy.wordpress.com&amp;blog=4246270&amp;post=214&amp;subd=foustfrenzy&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p>So today&#8217;s recipe is for Beef Stew.  Again, not a complex meal but it has tons of veggies and my kids actually like it.  So here it goes:</p>
<p>1 lb. of Stew meat</p>
<p>1/2 an onion finely chopped</p>
<p>3-4 stalks of celery finely chopped</p>
<p>1 small bag of baby carrotts</p>
<p>about 8 red potatoes</p>
<p>1 can of english peas</p>
<p>3/4 butternut squash (cubed)</p>
<p>1 package of Beef Stew seasoning</p>
<p>1 box of Beef Stock</p>
<p>about 2 cups of water</p>
<p>I put my stew in a crockpot but you could also use stockpot or a roasting pot.  I put my crockpot on the stovetop and pour a little olive oil in the bottom of the pot.  Turn stovetop to about medium-high.  While it&#8217;s getting hot, coat stew meat with flour, salt and pepper.  Add meat, celery and onion to the pot and cook until veggies are tender and meat is browned.  Then you add all the other ingredients.  Remove pot from stovetop and turn it on low for 8 hrs. or high for 4 hrs. Depending on your crockpot, times may vary.  Serve with cornbread and we usually eat the leftovers the next night over brown rice.  Super easy and it&#8217;s so yummy on a rainy day.  Let me know if you try it!!</p>
<p>&nbsp;</p>
<p>Sorry, I took the pics with my computer so they&#8217;re backwards.  :)</p>
<p><a href="http://foustfrenzy.files.wordpress.com/2011/01/photo-on-2011-01-29-at-06-49.jpg"><img class="alignleft size-full wp-image-215" title="Photo on 2011-01-29 at 06.49" src="http://foustfrenzy.files.wordpress.com/2011/01/photo-on-2011-01-29-at-06-49.jpg?w=535&#038;h=401" alt="" width="535" height="401" /></a></p>
<p><a href="http://foustfrenzy.files.wordpress.com/2011/01/photo-on-2011-01-29-at-06-51-2.jpg"><img class="alignleft size-full wp-image-216" title="Photo on 2011-01-29 at 06.51 #2" src="http://foustfrenzy.files.wordpress.com/2011/01/photo-on-2011-01-29-at-06-51-2.jpg?w=535&#038;h=401" alt="" width="535" height="401" /></a></p>
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		<title>A little help from my friends&#8230;</title>
		<link>http://foustfrenzy.wordpress.com/2011/01/28/a-little-help-from-my-friends/</link>
		<comments>http://foustfrenzy.wordpress.com/2011/01/28/a-little-help-from-my-friends/#comments</comments>
		<pubDate>Fri, 28 Jan 2011 00:20:57 +0000</pubDate>
		<dc:creator>foustfrenzy</dc:creator>
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		<guid isPermaLink="false">http://foustfrenzy.wordpress.com/?p=211</guid>
		<description><![CDATA[So lately I&#8217;ve been asked by a few people to help them with their meal plans and grocery lists.  This seems to be really stressful for some personalities and I feel like it&#8217;s one of my strong points.  I&#8217;m not sure why but I LOVE making out my menu and grocery list.  So I thought [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=foustfrenzy.wordpress.com&amp;blog=4246270&amp;post=211&amp;subd=foustfrenzy&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p>So lately I&#8217;ve been asked by a few people to help them with their meal plans and grocery lists.  This seems to be really stressful for some personalities and I feel like it&#8217;s one of my strong points.  I&#8217;m not sure why but I LOVE making out my menu and grocery list.  So I thought I would try to post (when able to) a few recipes that my family loves.  I am always on the look out for new kid-friendly meals so when I find a new one why not share it.  I am not a professional chef and I do not make everything from scratch but I try my hardest to make healthy and happy meals for my family.  So here&#8217;s the first one:</p>
<p>BTW-I use mostly organic ingredients but that&#8217;s just my preference.</p>
<p>Homemade Pizza</p>
<p>&nbsp;</p>
<p>Whole wheat pizza dough (I get mine at Harry&#8217;s but I think I&#8217;ve seen them at Target)</p>
<p>Organic pizza sauce</p>
<p>Mozzarella cheese</p>
<p>Applegate Farms sausage and bacon</p>
<p>Zucchini</p>
<p>Bell Pepper</p>
<p>Feta Cheese</p>
<p>It&#8217;s pretty much self-explanitory.  Brush the dough with olive oil then bake for about 10 minutes.  Take out and add sauce and mozzarella cheese.  Half of the pizza is mine and Chris&#8217;s and half is the kiddos.  On the grown-up half I slice zucchini and bell pepper then add crispy bacon and feta cheese&#8230;..YUMMM.  And the the kiddos&#8217; I usually do just sausage or sometimes pineapple and ham.  Then place back in the oven for about 20 minutes and VOILA!  It&#8217;s dinner.  This meal is wonderful for the weekends or nights when I forget to defrost something.  The kids love helping roll out the dough and adding all the toppings.  So there you have it.  It&#8217;s nothing complex but it&#8217;s a crowd pleaser and it&#8217;s a healthy twist on a family fav.  ENJOY!!</p>
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		<title>Our God is Healer, Awesome in Power</title>
		<link>http://foustfrenzy.wordpress.com/2011/01/27/our-god-is-healer-awesome-in-power/</link>
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		<pubDate>Thu, 27 Jan 2011 23:58:18 +0000</pubDate>
		<dc:creator>foustfrenzy</dc:creator>
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		<guid isPermaLink="false">http://foustfrenzy.wordpress.com/?p=209</guid>
		<description><![CDATA[As most of you know, Jax had another CT scan on Monday.  His oncologist requested this be done since it has been 6 months since Jax&#8217;s diagnosis.  Jax has had some problems with his liver enzymes being elevated and that was another reason for the scan.  The scan itself takes all of about 5 minutes [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=foustfrenzy.wordpress.com&amp;blog=4246270&amp;post=209&amp;subd=foustfrenzy&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p>As most of you know, Jax had another CT scan on Monday.  His oncologist requested this be done since it has been 6 months since Jax&#8217;s diagnosis.  Jax has had some problems with his liver enzymes being elevated and that was another reason for the scan.  The scan itself takes all of about 5 minutes but the whole process takes an entire day.  Jax&#8217;s scan was scheduled for 12:30 at Scottish Rite Hospital and we had to be there at 11:30 which meant we needed to leave @ 10:15.  The prep for the test is also a booger.  Jax has to be without food from midnight the night before the test and no milk after 7:30 but he can have clear liquids and popsicles up until he has his test.  Once we got to the hospital, we signed in and got sent back pretty quickly.  We were put in a room and started the whole process.  Jax has to drink contrast in order for them to see his organs better.  They mix it with Gatorade and he has an hour to drink about 5 oz.  Then an hour later he has to drink another 5 oz.  Jax did really well with all of this until they had to access his port. That reminds him of when he gets chemo and he was not happy after that.  Around 1:40, they took us back for his test.  The let Chris and I go back with him and I am so glad for that.  They hook him up to blood pressure monitor, heart monitor, and oxygen sensor.  After he&#8217;s all hooked up, the doctor comes in and starts his contrast through his port and then gives him his &#8220;night-night&#8221; drugs.  Jax goes from screaming to crying, to wimpering, and then he&#8217;s out.  The first time he was put to sleep was when we were in the hospital.  They warned us that it&#8217;s really scary to see your baby go limp and fall asleep that fast.  They were right!!  The first time I saw his little body fall asleep that fast and lay there on the table with oxygen on his little face, it was almost too much for me to handle.  I almost hit the floor and one of the nurses and Chris had to help me up and get to a chair.  Every time he&#8217;s been put to sleep since then it has gotten easier but it is still not something you want your child to go through.  So after he was asleep, the machine started and he was through with the scan in about five minutes.  Then the nurses check his vitals and move him to another stretcher and take him back to the room.  This time Jax slept for about 15 minutes before he started to wake-up.  He&#8217;s a little wobbly when he first wakes up so he has to be held like a newborn.  I don&#8217;t mind that part.  :)  After he is good and awake and detached from all the monitors, we are free to go.  By this time it is about 3 o&#8217;clock and Jax is one hungry dude.  I packed him a PB&amp;J, goldfish, and yogurt for the ride home and he pretty much ate most of it.  So after his test, we have to wait for a few days to hear from the doctor and yesterday I finally got the call.  Jax&#8217;s nurse, whom I adore, called with some somewhat good news.  She said that overall Jax&#8217;s scan looked good.  She said that it definitely shows that his liver has some permanent damage (which we kind of knew) but it is still functioning okay so there is no talk of transplant right now. And he has no lesions anywhere else.   None in his chest, abdomen, or pelvis.  Of course we can only assume that the bone marrow is clear as well.  So for now we continue doing chemo once a month and the chemo pill at home every day.  That is the plan until this summer.  Then in July, he will gradually be taken off of his meds and we will have to &#8220;watch and wait&#8221;.  There are a million different scenarios that could happen but for now&#8230;.we are thankful.  Jax is still tolerating all of the meds quite well and still is a million times healthier and happier then he was before his diagnosis.  Again, I can&#8217;t tell you how much it means to us to know that all of you are praying for our family.  I see conversations on facebook about my little baby between people I don&#8217;t even know.  Jax&#8217;s story has touched so many people and that has been our prayer from the beginning of this whole journey.  I feel so honored to be a vessel that God is using to bring glory to himself.  Yes there are days when honestly, I wish he would&#8217;ve chosen someone other than my baby but I try to find comfort in his sovereignty. So there&#8217;s the latest on our little nugget.  Again, thank you!!</p>
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