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	<title>Sickle Cell Cure Foundation</title>
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	<link>http://sicklecellcurefoundation.org</link>
	<description>a nonprofit corporation working to cure sickle cell disease</description>
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		<title>Devastation Shall Be Overcome</title>
		<link>http://sicklecellcurefoundation.org/2010/12/devastation-shall-be-overcome/</link>
		<comments>http://sicklecellcurefoundation.org/2010/12/devastation-shall-be-overcome/#comments</comments>
		<pubDate>Fri, 31 Dec 2010 01:43:12 +0000</pubDate>
		<dc:creator>dgs</dc:creator>
				<category><![CDATA[Breaking News]]></category>
		<category><![CDATA[Bill & Melinda Gates Foundation]]></category>
		<category><![CDATA[FDA]]></category>
		<category><![CDATA[gene regulation therapy]]></category>
		<category><![CDATA[Living with SCD]]></category>
		<category><![CDATA[malaria]]></category>
		<category><![CDATA[PHF Research Park]]></category>

		<guid isPermaLink="false">http://sicklecellcurefoundation.org/?p=963</guid>
		<description><![CDATA[The Sickle Cell Cure Foundation, Inc. (SCCF) is a non-profit 501(c)(3) research foundation incorporated in 2006. SCCF chose the PHF Research Park as its world headquarters to conduct translational research using patented treatments aimed at curing two of mankind’s most devastating diseases: malaria and its allied blood disorder, sickle cell disease (SCD). The Bill &#38; [...]]]></description>
			<content:encoded><![CDATA[<p><a href="http://sicklecellcurefoundation.org/wp-content/uploads/2010/12/overcome300x211.jpg"><img class="alignleft size-full wp-image-965" title="overcome300x211" src="http://sicklecellcurefoundation.org/wp-content/uploads/2010/12/overcome300x211.jpg" alt="" width="300" height="211" /></a>The Sickle Cell Cure Foundation, Inc. (SCCF) is a non-profit 501(c)(3) research foundation incorporated in 2006. SCCF chose the PHF Research Park as its world headquarters to conduct translational research using patented treatments aimed at curing two of mankind’s most devastating diseases: malaria and its allied blood disorder, sickle cell disease (SCD). The Bill &amp; Melinda Gates Foundation recently awarded a Grand Challenge Exploration grant to SCCF to conduct its animal safety and efficacy trials. SCCF aims to raise additional funds for human clinical trials required for FDA approval. The therapeutics offered by SCCF are inexpensive, non-invasive, and easy to deliver; and SCCF’s mission fits the Gates’ central philanthropic principle that “all lives have equal value”.</p>
<p>SCD is a disease that co-evolved with malaria among peoples living in equatorial regions where mosquitoes are endemic and serve as vectors for the malaria parasite. In the US, over 70,000 individuals are afflicted with SCD. Globally, an estimated 880,000 die from malaria and 340,000 from SCD annually, with the great majoriy of these deaths being children under the age of five years. SCD afflicts many in western and central African countries, as well as people of Portuguese, Spanish, French Corsican, Sardinian, Sicilian, Italian, Greek, Turkish, Cypriot, Israeli, Arab, and Indian decent. While one copy of the sickle gene confers resistance to the malaria parasite, carrying two copies can result in death. Large public health measures have limited the spread of malaria in developed countries. In contrast, SCD has been neglected. The wide spread occurrence of SCD and recent resurgence of malaria motivated the World Health Organization in May 2006 to list SCD as a neglected disease warranting intensified research. SCCF is mounting a global effort to address this global health problem.</p>
<p>Gene Regulation Therapy (GRT) is the overall research approach employed by SCCF. GRT does not destroy genes, alter them, nor implant them in the patient. Rather, SCCF has discovered how to manipulate “toggle switches” that reactivate the body’s own fetal hemoglobin production. Medical literature has amply documented that the presence of fetal hemoglobin in adult red blood cells at concentrations of 30% or more confers a natural resistance to SCD…and also to malaria. Requiring no refrigeration, the GRT for SCD is natural, non-invasive, and reversible. To maintain its benefits, the patient only requires periodic “recharge” doses to keep the toggle switch “on.” Similar GRT-responsive, “onoff” genetic relationships are the subject of translational research and development. GRT promises effective clinical treatments for many debilitating disorders including diabetes, Parkinson’s, Huntington’s, liver diseases, and certain cancers. SCCF’s business plan for global distribution of Gene Regulation Therapy for SCD estimates a 95% drop in the cost of standard Western treatments. Whereas current treatments only address the symptoms of SCD, SCCF’s approach corrects the primary cause. For the world’s poor majority, SCCF’s business model uses cross-subsidy pricing to deliver the cure to Africa pharmaceutical outlets for as little as US $12.00 per person per year.</p>
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		<slash:comments>15</slash:comments>
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		<item>
		<title>The Sickle Cell Cure Foundation Receives $100,000 Grand Challenges Explorations Grant from the Bill &amp; Melinda Gates Foundation for Innovative Global Health Research</title>
		<link>http://sicklecellcurefoundation.org/2010/05/100000-grand-challenges-explorations-grant/</link>
		<comments>http://sicklecellcurefoundation.org/2010/05/100000-grand-challenges-explorations-grant/#comments</comments>
		<pubDate>Sun, 16 May 2010 00:48:18 +0000</pubDate>
		<dc:creator>dgs</dc:creator>
				<category><![CDATA[Breaking News]]></category>
		<category><![CDATA[funding]]></category>
		<category><![CDATA[malaria]]></category>
		<category><![CDATA[scientific research]]></category>

		<guid isPermaLink="false">http://sicklecellcurefoundation.org/?p=946</guid>
		<description><![CDATA[The Sickle Cell Cure Foundation, Inc. (SCCF), announced today that it has received a US$100,000 Grand Challenges Explorations grant from the Bill &#38; Melinda Gates Foundation. The grant will support an innovative global health research project conducted by Robert H. Broyles, Ph.D., SCCF President, titled “Malaria Stopped by a Human Protein Therapeutic.” Dr. Broyles’ project [...]]]></description>
			<content:encoded><![CDATA[<p><a href="http://sicklecellcurefoundation.org/wp-content/uploads/2010/05/mosquito240x160.jpg"><img class="alignleft size-full wp-image-951" title="mosquito240x160" src="http://sicklecellcurefoundation.org/wp-content/uploads/2010/05/mosquito240x160.jpg" alt="" width="240" height="160" /></a>The Sickle Cell Cure Foundation, Inc. (SCCF), announced today that it has received a US$100,000 Grand Challenges Explorations grant from the Bill &amp; Melinda Gates Foundation.  The grant will support an innovative global health research project conducted by Robert H. Broyles, Ph.D., SCCF President, titled “Malaria Stopped by a Human Protein Therapeutic.”</p>
<p>Dr. Broyles’ project is one of 78 grants announced by the Gates Foundation in the fourth funding round of Grand Challenges Explorations, an initiative to help scientists around the world explore bold and largely unproven ways to improve health in developing countries.  The grants were provided to scientists in 18 countries on six continents.</p>
<p>To receive funding, Dr. Broyles showed in a two-page application how his idea falls outside current scientific paradigms and might lead to significant advances in global health.  The initiative is highly competitive, receiving almost 2,700 proposals in this round.</p>
<p>The research of Dr. Broyles and The Sickle Cell Cure Foundation, Inc., of Oklahoma City. will build on the recent discovery that elevated fetal hemoglobin (HbF), which alleviates sickle cell disease, can also confer malaria resistance. Broyles and his team will test the ability of a stable human protein to reactivate a silent gene that encodes for HbF, making red blood cells inhospitable to malaria parasites. If successful, the idea is to target the therapy in the host to reduce malaria infections.<br />
Dr. Broyles earned the Ph.D. degree in biochemistry from Wake Forest University Medical Center, Winston-Salem, N.C., did postdoctoral research at Florida State University, has held faculty positions at the University of Wisconsin -Milwaukee and the University of Oklahoma Health Sciences Center, and has served as a visiting research scientist at the National Institutes of Health, the Woods Hole Marine Biological Laboratory, and the Oklahoma Medical Research Foundation. In 2006, Dr. Broyles founded The Sickle Cell Cure Foundation, Inc. (SCCF), a 501(c)(3) nonprofit research foundation dedicated to a universal cure for sickle cell and related diseases.<br />
&#8220;We have discovered a way of shutting off the sickle cell gene and reactivating a fetal hemoglobin gene in its place, a switch known to stop all the bad, deadly manifestations of SCD,&#8221; says Broyles. &#8220;The realization that this same manipulation will make people resistant to malaria is even more exciting.&#8221;</p>
<p>“The winners of these grants show the bold thinking we need to tackle some of the world’s greatest health challenges,” said Dr. Tachi Yamada, president of the Gates Foundation’s Global Health Program.  “I’m excited about their ideas and look forward to seeing some of these exploratory projects turn into life-saving breakthroughs.”</p>
<p>About Grand Challenges Explorations</p>
<p>Grand Challenges Explorations is a five-year, $100 million initiative of the Gates Foundation to promote innovation in global health.  The program uses an agile, streamlined grant process – applications are limited to two pages, and preliminary data are not required.  Proposals are reviewed and selected by a committee of foundation staff and external experts, and grant decisions are made within approximately three months of the close of the funding round.</p>
<p>Applications for the current round of Grand Challenges Explorations are being accepted through May 19, 2010.  Grant application instructions, including the list of topics for which proposals are currently being accepted, are available at <a title="http://www.grandchallenges.org/explorations" href="http://www.grandchallenges.org/explorations" target="_blank">http://www.grandchallenges.org/explorations</a>.</p>
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		<slash:comments>14</slash:comments>
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		<item>
		<title>Eradicating a Deadly Disease Through Science, Love and Music.</title>
		<link>http://sicklecellcurefoundation.org/2010/02/eradicating-a-deadly-disease-through-science-love-and-music/</link>
		<comments>http://sicklecellcurefoundation.org/2010/02/eradicating-a-deadly-disease-through-science-love-and-music/#comments</comments>
		<pubDate>Sat, 27 Feb 2010 22:12:13 +0000</pubDate>
		<dc:creator>broylesr</dc:creator>
				<category><![CDATA[Breaking News]]></category>
		<category><![CDATA[funding]]></category>
		<category><![CDATA[Living with SCD]]></category>
		<category><![CDATA[scientific research]]></category>
		<category><![CDATA[Sickle Cell Disease]]></category>
		<category><![CDATA[sickle cell disease cure]]></category>

		<guid isPermaLink="false">http://sicklecellcurefoundation.org/?p=904</guid>
		<description><![CDATA[Article by Laura Jenney Of Mindsweep Entertainment &#38; Promotions VPofMindsweep@aol.com Jacksonville, FL 1-20-2010 The arrival of the year 2010 is an exciting time indeed! Not only are we embracing the beginning of a brand new year, but a brand new decade as well. It&#8217;s a time of great possibilities and full of promise. A time [...]]]></description>
			<content:encoded><![CDATA[<p><a href="http://sicklecellcurefoundation.org/wp-content/uploads/2010/02/Jameel.jpg"><img src="http://sicklecellcurefoundation.org/wp-content/uploads/2010/02/Jameel.jpg" alt="" title="Jameel" width="240" height="267" class="alignleft size-full wp-image-906" /></a>Article by Laura Jenney<br />
Of Mindsweep Entertainment &amp; Promotions<br />
VPofMindsweep@aol.com<br />
Jacksonville, FL<br />
1-20-2010</p>
<p>The arrival of the year 2010 is an exciting time indeed! Not only are we embracing the beginning of a brand new year, but a brand new decade as well. It&#8217;s a time of great possibilities and full of promise. A time of new beginnings, as we say goodbye to things of the past while ridding ourselves of the negative effects of old habits, patterns and thinking; and embark upon &#8216;the bold new NOW&#8217;, with great determination to better and/or to reinvent ourselves, to strive to be THE BEST we can be; be THE MOST we can be; progressing forward towards the attainment of our dreams and goals, and striving to arrive at our ultimate state of Zen in 2010. &#8230;In doing so, not only on an individual level, but on a community, national and global level as well, we are in fact, casting the mold of our tomorrows.</p>
<p>We are off to an excellent start, as you can now add to your list of New Year&#8217;s resolutions that while having an absolute blast this year while doing so, YOU can help eradicate a deadly disease off the face of the planet in the process! &#8230;Now I know some of you are probably thinking at this point that &#8220;Ms. Laura has worked with ONE TOO MANY rock stars in 2009,&#8221; but it&#8217;s the truth! (&#8230;About the eradicating a deadly disease thing anyway.) Allow me enlighten you to the details&#8230;</p>
<p>Via the hard work, dedication, and deep compassion of two absolutely brilliant men, Doctor and esteemed Bio Chemist Robert H. Broyles and Musician/Songwriter, Promoter, Talk Show Host, Radio Personality J. R. Perry III, an immense amount of suffering worldwide can be eliminated this year by the eradication of the deadly disease Sickle Cell Anemia for which Dr. Robert H. Broyles HAS THE CURE; and by which J. R. Perry is helping to raise the funding, (and awareness), needed to get this cure to those who need it, (and to hasten the process of doing so), via organizing a series of super dynamic concerts worldwide, featuring renowned and/or legendary acts in every genre imaginable.</p>
<div id="attachment_908" class="wp-caption aligncenter" style="width: 456px"><a href="http://sicklecellcurefoundation.org/wp-content/uploads/2010/02/LoveDrop1.jpg"><img class="size-full wp-image-908" title="LoveDrop" src="http://sicklecellcurefoundation.org/wp-content/uploads/2010/02/LoveDrop1.jpg" alt="" width="446" height="248" /></a><p class="wp-caption-text">(Dr. Robert H. Broyles left, J. R. Perry right.)</p></div>
<p>Dr. Robert H. Broyles, who is the Founder and President of The Sickle Cell Cure Foundation, and has discovered/developed a cure for the disease via primarily the utilization of Gene Regulation Therapy, and has secured and obtained the US patent for this proven way it would work on April, 14, 2009.</p>
<p>(Though Dr. Robert H. Broyles actually discovered a way in which the cure would work as early as 2006; though getting it into the hands of those who need it is an extremely slow moving and arduous task, largely due to the extreme amount of bureaucratic &#8216;red tape&#8217; involved in the process.)</p>
<p>SCCF&#8217;s patents in Australia, and the European Union, (France, Germany, and Greece), are also already secured and maintained through Dr. Broyles&#8217; outstanding work to not only end this deadly disease, but quite possibly Parkinson&#8217;s Disease and other diseases as well, through Gene Regulation Therapy and Iron Management.</p>
<p>Not only is Doctor Robert H. Broyles an incredibly brilliant scientist, (one of the Principal Investigative Scientists in the field of Gene Regulation Therapy for Sickle Cell Disease, with over thirty-five years of research experience to add to his extraordinarily impressive and numerous credits), Dr. Broyles is an extremely kind man of sincere and deep care and compassion for those he has dedicated his life to heal. &#8216;Doctor Bob,&#8217; (as I have nick named him out of my ultimate respect and admiration for him as both a scientist and as a great individual), shares an example of the many e-mails from people all around the world, which greatly moves Dr. Broyles, and serves as his driving force for doing the amazing and outstanding work that he does. Here is one example of the many e-mails in which Dr. Robert Broyles receives regularly: &#8220;Please, I beg you in the name of the most high-grade God. How do I access the cure? This pain is too much. Please don&#8217;t let me die. Please.&#8221; Needless to say, Dr. Robert H. Broyles is not only a man of exceptional mind, but also a man of exceptional heart and soul as well, for the work he has done and continues to do with great determination and dedication; which in my opinion, is worthy of a Nobel Prize. I would also like to add that out of the many renowned stars that I have worked with over the years as a PR, Press and Media Relations Specialist, (mostly in the music industry, though I have also written for/about a number of high profile, US political figures as well), I have to say that Dr. Robert H. Broyles is indeed THE brightest shining true &#8216;superstar&#8217; I have ever had the pleasure of working with thus far!</p>
<p>Another great man of uncommon valor and brilliance in his own fields of expertise who is working hard to bring this cure, (and expedite the process of doing so), to those in need of it is J. R. Perry III; who is in the process of organizing a series of multi-artist concerts worldwide to both, generate funding and awareness concerning this deadly disease.</p>
<p>Because, (to spite misconceptions), Sickle Cell Anemia is a disease that effects people of ALL races, in all countries, and of all social economic status, renowned Promoter and long time Sickle Cell Disease Activist, J. R. Perry&#8217;s exciting concert tour, (&#8220;The Cure Every Cell Tour&#8221;), will feature a dynamic array of outstanding artists from every genre imaginable to strategically generate as much &#8216;broad audience appeal&#8217; as possible to both educate, (on a very large scale), about this deadly and extremely painful disease, dispel the many misconceptions concerning this disease, and to raise the necessary funding to complete the final stages of clinical trials required, (by the medical regulations in the US), before making this cure available to patients within the US. (Though notably, Dr. Broyles&#8217; procedural cure is currently already available outside of the US in a number of other countries.)</p>
<p>J. R. Perry&#8217;s dedicated involvement as both a Sickle Cell Disease Awareness Activist and his hard work and effort at organizing a massive world tour to combat this disease and bring forth the cure is nothing less of a labor of love. J. R. Perry&#8217;s own ten year old son Jameel suffers from Sickle Cell Disease, and has already endured a stroke, (at age 9), and has to receive regular blood transfusions, suffers chronic pain, as well as has a potentially life threatening compromised immune system because of this disease.</p>
<p><div id="attachment_906" class="wp-caption alignleft" style="width: 250px"><a href="http://sicklecellcurefoundation.org/wp-content/uploads/2010/02/Jameel.jpg"><img src="http://sicklecellcurefoundation.org/wp-content/uploads/2010/02/Jameel.jpg" alt="Jameel" title="Jameel" width="240" height="267" class="size-full wp-image-906" /></a><p class="wp-caption-text">Ten year old, Jameel Perry, son of J. R. Perry III.</p></div><br />
Ten year old, Jameel Perry, son of J. R. Perry III.</p>
<p>Though we are at the beginning phases of organizing this historic &#8216;tour for the cure&#8217;, amongst the first outstanding artists to join this effort includes blues, R&amp;B and jazz legend Chick Willis, (www.myspace.com/chickwillis), sizzling Latin/salsa sensations Orquesta Fiesta, (www.myspace.com/clarasalsa), jam&#8217;s absolutely smoking and super fast rising band Bodhi, (www.bodhilive.com), and prolific Vocalist Dan Shafer, (known for his work with a number of renowned bands such as Mercenary, featuring Rusty DAddio of Ronnie James Dio and Richie Blackmore); and well renowned for his work in numerous commercials, and is the Executive Producer of The Rock &amp; Load Show, amongst Dan&#8217;s immense and impressive list of professional credits; (www.myspace.com/danshafer). And most recently, joining in this effort will be world renowned Latin and jazz recording artist Eddie Benitez. (www.myspace.com/eddiebenitez).</p>
<p>More respected artists will be listed in upcoming press releases as they come aboard on this project: as we at Mindsweep Entertainment &amp; Promotions are embarking on a massive PR, press and media, (and cross promotional), campaign to further promote this very important, life saving and history changing tour, (and as a promotions &#8216;perk&#8217; for the artists, sponsors and to everyone associated with this tour, as a token of our sincere and immense amount of appreciation for their involvement and help): and of course, to keep everyone updated on upcoming concert dates, the artists involved, upcoming TV and radio appearances and news concerning this tour. J. R. Perry III incidentally, is also the Owner of Love Drop Radio, where artists involved with this tour will be featured as guests on Love Drop Radio&#8217;s esteemed programming to further promote this noble cause.</p>
<p>Renowned artists that would like to add extra concert dates to their 2010 concert schedule while helping to eradicate this deadly disease in the process by getting involved can do so by contacting me, Laura Jenney at any of the following e-mail addresses: VPofMindsweep@aol.com, Jcongalady@aol.com or laura@tntbooking.com, or by calling 904-378-8357. (The Jcongalady@aol.com e-mail address always gets seen and answered the quickest.)</p>
<p>Concert venues and corporate sponsors that would like to get involved with this phenomenal opportunity and make a huge humanitarian difference via this project and vital cause, please contact J. R. Perry III by e-mail at Lovedropradio@hotmail.com or myself at VPofMindsweep@aol.com. (Sponsorship incentives are absolutely exceptional and unbeatable, I might add!)</p>
<p>For more information about the outstanding work that Dr. Robert H. Broyles and all of those at work at The Sickle Cell Cure Foundation are doing, please visit their web site at http://www.sicklecellcurefoundation.org.</p>
<p>To make a much needed and appreciated donation to help bring forth the cure and to wipe Sickle Cell Disease, (and quite possibly other diseases as well), donations can be made by:</p>
<ul>
<li>Clicking on the gold <strong>Donate button</strong> on the upper right hand side of this webpage, and use a credit card through PayPal; Or&#8230;</li>
<li>Send a check addressed to:<br />
The Sickle Cell Cure Foundation<br />
601 NW 13th Street<br />
Oklahoma City , OK 73103.</li>
</ul>
<p>The Sickle Cell Cure Foundation Inc., or (SCCF), is a nonprofit corporation registered in the State of Oklahoma. It&#8217;s 501(C) (3) status has been approved by the Internal Revenue Service of the United States as of February 12, 2007; and all donations are tax deductible.</p>
<p>And that&#8217;s how YOU TOO can help eradicate the deadly disease Sickle Cell Anemia off the face of the planet while having an absolute blast doing so, simply by attending a concert on the &#8220;The Cure Every Cell Tour&#8221; coming to a concert venue near you very soon! Now isn&#8217;t that an absolutely GREAT resolution to start out a New Year and decade? &#8230;I&#8217;m talking WAAAAY more fun than trying to quit bad habits, dieting and exercise!</p>
<p>The End.</p>
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		<title>Accomplishments for 2009</title>
		<link>http://sicklecellcurefoundation.org/2010/01/accomplishments-for-2009/</link>
		<comments>http://sicklecellcurefoundation.org/2010/01/accomplishments-for-2009/#comments</comments>
		<pubDate>Fri, 08 Jan 2010 03:49:00 +0000</pubDate>
		<dc:creator>dgs</dc:creator>
				<category><![CDATA[News]]></category>

		<guid isPermaLink="false">http://sicklecellcurefoundation.org/?p=842</guid>
		<description><![CDATA[SCCF submits the Continuation in Part (CIP) containing all our experimental results with human pediatric sickle cell patients’ blood to the U.S. Patent Office, March 15, 2009. The U.S. Patent on our sickle cell cure is issued the following month, 4/14/09. SCCF’s patents in the U.S., Canada, Australia, and the European Union (U.K., France, Germany, [...]]]></description>
			<content:encoded><![CDATA[<p><a href="http://sicklecellcurefoundation.org/wp-content/uploads/2010/01/accomplish.jpg"><img class="aligncenter size-full wp-image-889" title="accomplish" src="http://sicklecellcurefoundation.org/wp-content/uploads/2010/01/accomplish.jpg" alt="" width="585" height="222" /></a></p>
<ul>
<li>SCCF submits the Continuation in Part (CIP) containing all our experimental results with human pediatric sickle cell patients’ blood to the U.S. Patent Office, March 15, 2009.</li>
<li><strong>The U.S. Patent on our sickle cell cure is issued the following month, 4/14/09. </strong></li>
<li>SCCF’s patents in the U.S., Canada, Australia, and the European Union (U.K., France, Germany, and Greece) are maintained, and their annuities paid.</li>
<li>The Institutional Review Board (IRB) Protocol for our experiments with human blood from pediatric sickle cell patients is continued for 2009-2010, the 5th consecutive year for this approval rating by the OUHSC IRB for Protection of Human Subjects, acting on behalf of the NIH. These strictly regulated protocols are a critical prerequisite to determine safe and effective dosages before clinical trials in human beings.</li>
<li>SCCF launches our new website in magazine format with comments/blog wherein sickle cell patients from around the world may express their concerns and questions in spring 2009, incorporating the capability for on-line donations: www.sicklecellcurefoundation.org</li>
<li>International RFPP (Request for Proposals to Partner) with SCCF is written by Director of Development, Gary Bricker, and issued (1st round) in summer, 2009.</li>
<li>SCCF submits a grant proposal to the Bill &amp; Melinda Gates Foundation on November 2, 2009, for their Grand Challenges Explorations, Round 4. Our proposal profiles a method the Sickle Cell Disease cure may be used to alleviate and even prevent the tragedy of Malaria. This proposal cleared the hurdle of first level review and is still pending (final decisions, April 2010).</li>
<li>SCCF’s first animal trials in mice approved by the OUHSC Institutional Animal Care and Use Committee (IACUC), November 11, 2009.</li>
<li>New collaboration with Dr. Sunil Joshi, OUHSC, is formed for second phase of animal trials, using transgenic mouse models for human sickle cell disease, December 2009. Stay tuned for developing synergies!</li>
<li>International publicist Laura Jenney joins the &#8220;team&#8221; of SCCF and J.R. Perry III, to promote SCCF and the &#8220;Cure Every Cell&#8221; fundraising music tour, December 2009.</li>
</ul>
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		<title>SCCF Takes On Sickle Cell Disease (SCD)</title>
		<link>http://sicklecellcurefoundation.org/2009/11/sccf-takes-on-sickle-cell-disease-scd/</link>
		<comments>http://sicklecellcurefoundation.org/2009/11/sccf-takes-on-sickle-cell-disease-scd/#comments</comments>
		<pubDate>Wed, 04 Nov 2009 23:39:53 +0000</pubDate>
		<dc:creator>dgs</dc:creator>
				<category><![CDATA[Breaking News]]></category>

		<guid isPermaLink="false">http://sicklecellcurefoundation.org/?p=755</guid>
		<description><![CDATA[Somewhere, every minute, a baby dies of SCD. SCD is the most prevalent genetic disease globally. SCD occurs in many nations and among many races — wherever malaria was once or is still rampant. The Sickle Cell Cure Foundation has a cure for SCD. The SCCF’s cure will give SCD sufferers a normal life. The [...]]]></description>
			<content:encoded><![CDATA[<h3>Somewhere, every minute, a baby dies of SCD.</h3>
<ul>
<li>SCD is the most prevalent genetic disease globally.</li>
<li>SCD occurs in many nations and among many races — wherever malaria was once or is still rampant.
<ul>
<li>The Sickle Cell Cure Foundation has a cure for SCD.</li>
<li>The SCCF’s cure will give SCD sufferers a normal life.</li>
<li>The SCCF’s cure also provides malaria resistance.</li>
<li> The SCCF has a global plan for cure distribution.</li>
<li>The SCCF needs your help to save lives.</li>
</ul>
<h3>What can you do?</h3>
<ul>
<li>Become a Sickle Cell Cure Foundation member today.</li>
<li>Donate NOW: help stop 500,000 deaths/year.</li>
<li>Pass the word to your friends and acquaintances.</li>
<li>Give generously and regularly.</li>
</ul>
<h3>Why this cure will work worldwide…</h3>
<ul>
<li>The SCCF’s cure is based on the biology of our bodies.</li>
<li>The SCCF’s cure does not alter genes, is not invasive.</li>
<li>The SCCF’s cure does not rely on stem cells.</li>
<li>The SCCF’s cure uses a protein we grow up with.</li>
<li>The SCCF’s discovery gets this protein to the right cells.</li>
<li>The SCCF’s cure is stable, inexpensive, easy to deliver anywhere.</li>
</ul>
<ul>
<li>Other cure attempts are out of reach for most people.</li>
<li>Other cure attempts have severe side effects.</li>
<li>Current treatments are costly and incomplete.</li>
</ul>
<h3>You can make a difference in someone’s life. Please help end the suffering.</h3>
<blockquote><p>Mail checks to:<br />
Sickle Cell Cure Foundation, Inc.,<br />
212 ½ NW 20th St.,<br />
Oklahoma City, OK, 73103;<br />
or donate through PayPal online at http://www.sicklecellcurefoundation.org.</p></blockquote>
</li>
</ul>
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		<slash:comments>36</slash:comments>
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		<item>
		<title>Peer Review &amp; Validations of SCCF&#8217;s Discovery &#8211; Our Credentials</title>
		<link>http://sicklecellcurefoundation.org/2009/11/peer-review-validations-of-sccfs-discovery-our-credentials/</link>
		<comments>http://sicklecellcurefoundation.org/2009/11/peer-review-validations-of-sccfs-discovery-our-credentials/#comments</comments>
		<pubDate>Wed, 04 Nov 2009 23:25:14 +0000</pubDate>
		<dc:creator>dgs</dc:creator>
				<category><![CDATA[Our Research]]></category>

		<guid isPermaLink="false">http://sicklecellcurefoundation.org/?p=757</guid>
		<description><![CDATA[Some people have asked, “Your ‘cure’ works in theory, but does it work in practice?” The answer is, “Yes!!!” The key point is that fetal hemoglobin (HbF) has been shown to be preventive for sickle cell disease in nature, in many labs around the world, in many, many repeated experiments and patient trials over the [...]]]></description>
			<content:encoded><![CDATA[<p><img class="alignleft size-full wp-image-829" title="peer-review-group-300x199" src="http://sicklecellcurefoundation.org/wp-content/uploads/2009/11/peer-review-group-300x199.jpg" alt="peer-review-group-300x199" width="300" height="199" />Some people have asked, “Your ‘cure’ works in theory, but does it work in practice?”  The answer is, “Yes!!!”  The key point is that fetal hemoglobin (HbF) has been shown to be preventive for sickle cell disease in nature, in many labs around the world, in many, many repeated experiments and patient trials over the last thirty years. The problem is that no one has figured out how to stimulate this hemoglobin switch in humans without gene therapy, a bone marrow/stem cell transplant, or use of toxic drugs &#8211; all of which are dangerous, expensive, and not available to 99.99% of the world&#8217;s sufferers. This is what we have now done: found a safe way to induce the HbF switch.  We have found a natural, small, stable human protein that will produce this Hb switch (a) in a test tube, (b) in living primate and human cells, (c) in transgenic mice carrying and expressing the human H-ferritin gene, and (d) in forming red bllod cells obtained from pediatric sickle cell patients. All in all, we have performed almost 200 experiments of 50 different types/designs, each experiment replicated 2-to-10 times by 2, 3, or 5 different investigators &#8211; all  consistently pointing to this same conclusion and its safety.  And we have devised 4 ways to deliver this cure! Now, we need the funds to prove its safety in animals, so that we can then start human trials. We can provide the hope, the science, and the safety; you can help us get the necessary funds.</p>
<p>Our cure has been peer-reviewed via Publications &amp; Patents, Grants Awarded, and invitations for International Presentations.</p>
<p>Publications &amp; Patents: PDF files of a List of 25 Publications; a key paper that established the principle of the cure; and our Patent issued in the U.S., the European Union(10 countries), and Australia, are attached.</p>
<ul>
<li><a href="/wp-content/plugins/downloads-manager/upload/PublicationsList.pdf">Publications List</a></li>
<li><a href="/wp-content/plugins/downloads-manager/upload/PNAS2001.pdf">PNAS 2001</a></li>
<li><a href="/wp-content/plugins/downloads-manager/upload/USPatent7517669FtHgenetransduction.pdf">US Patent #7,517,669 (FtHgenetransduction)</a></li>
</ul>
<p>Grants Awarded: A PDF file of an NIH-form 4-page bio-sketch is attached, with the last two pages listing NIH and other nationally-competitive grants. Dr. Broyles’ curriculum vitae is also attached.</p>
<ul>
<li><a href="/wp-content/plugins/downloads-manager/upload/BROYLES-CV-09.pdf">Dr. Robert Broyles CV</a></li>
<li><a href="/wp-content/plugins/downloads-manager/upload/Grants(pp3&amp;4)&amp;NIHbiosketch.pdf">Grants (pp3&amp;4) &amp; NIH biosketch</a></li>
</ul>
<p>International presentations: PDF files of abstracts of nine invited, international presentations (2003 through 2009) are attached.</p>
<ul>
<li><a href="/wp-content/plugins/downloads-manager/upload/2003 IBIS Bethesda.pdf">2003 IBIS Bethesda.pdf</a></li>
<li><a href="/wp-content/plugins/downloads-manager/upload/2004 ISSCR Boston.pdf">2004 ISSCR Boston.pdf</a></li>
<li><a href="/wp-content/plugins/downloads-manager/upload/2005 IBIS Prague.pdf">2005 IBIS Prague.pdf</a></li>
<li><a href="/wp-content/plugins/downloads-manager/upload/2006 ASH Orlando.pdf">2006 ASH Orlando.pdf</a></li>
<li><a href="/wp-content/plugins/downloads-manager/upload/2006 NSCD Memphis.pdf">2006 NSCD Memphis.pdf</a></li>
<li><a href="/wp-content/plugins/downloads-manager/upload/2007 IBIS Kyoto.pdf">2007 IBIS Kyoto.pdf</a></li>
<li><a href="/wp-content/plugins/downloads-manager/upload/2007 SFRBM Washington, DC.pdf">2007 SFRBM Washington, DC.pdf</a></li>
<li><a href="/wp-content/plugins/downloads-manager/upload/2008 SCDAA NewOrleans.pdf">2008 SCDAA NewOrleans.pdf</a></li>
<li><a href="/wp-content/plugins/downloads-manager/upload/2009 IBIS Porto.pdf">2009 IBIS Porto.pdf</a></li>
</ul>
]]></content:encoded>
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		<slash:comments>10</slash:comments>
		</item>
		<item>
		<title>Plan to cure Sickle Cell Disease (updated 2010/12/30)</title>
		<link>http://sicklecellcurefoundation.org/2009/11/plan-to-cure-sickle-cell-disease/</link>
		<comments>http://sicklecellcurefoundation.org/2009/11/plan-to-cure-sickle-cell-disease/#comments</comments>
		<pubDate>Wed, 04 Nov 2009 18:57:48 +0000</pubDate>
		<dc:creator>dgs</dc:creator>
				<category><![CDATA[Breaking News]]></category>
		<category><![CDATA[Images]]></category>
		<category><![CDATA[Image]]></category>

		<guid isPermaLink="false">http://sicklecellcurefoundation.org/?p=759</guid>
		<description><![CDATA[Plan to Cure or Ameliorate Sickle Cell Disease (SCD), Parkinson’s Disease (PD), and other diseases by Gene Regulation Therapy and Iron Management]]></description>
			<content:encoded><![CDATA[<p>Plan to Cure or Ameliorate Sickle Cell Disease (SCD), Parkinson’s Disease (PD), and other diseases by Gene Regulation Therapy and Iron Management</p>
<p><a href="http://sicklecellcurefoundation.org/wp-content/uploads/2010/12/Plan_to_Cure_or_Ameliorate_Sickle_Cell_Disease1.pdf"><img src="http://sicklecellcurefoundation.org/wp-content/uploads/2010/12/SCCFs-Plan-Progress-A-Summary1.jpg" alt="SCCFs Plan &#038; Progress - A Summary Page 1" width="928px" height="1194px"/></a></p>
]]></content:encoded>
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		<slash:comments>45</slash:comments>
		</item>
		<item>
		<title>National Sickle Cell Month</title>
		<link>http://sicklecellcurefoundation.org/2009/09/national-sickle-cell-month/</link>
		<comments>http://sicklecellcurefoundation.org/2009/09/national-sickle-cell-month/#comments</comments>
		<pubDate>Fri, 04 Sep 2009 23:05:36 +0000</pubDate>
		<dc:creator>broylesr</dc:creator>
				<category><![CDATA[Living with SCD]]></category>
		<category><![CDATA[clinical trials]]></category>
		<category><![CDATA[non-profit]]></category>
		<category><![CDATA[sickle cell cure foundation]]></category>
		<category><![CDATA[Sickle Cell Disease]]></category>
		<category><![CDATA[sickle cell disease cure]]></category>
		<category><![CDATA[united states patent]]></category>

		<guid isPermaLink="false">http://sicklecellcurefoundation.org/?p=743</guid>
		<description><![CDATA[The Sickle Cell Cure Foundation, Inc. (SCCF) has made significant progress in recent months, including a U.S. patent issued 14 April 2009, and further laboratory discoveries showing that less DREPAC is needed than previously believed to reverse sickle cell! To keep this progress going, we need your help! It is our goal to have clinical [...]]]></description>
			<content:encoded><![CDATA[<p><strong><img class="alignleft" title="sickle-cells-300x300" src="/wp-content/uploads/2009/09/sickle-cells-300x300.jpg" alt="" width="300" height="300" />The Sickle Cell Cure Foundation, Inc. (SCCF)</strong> has made significant progress in recent months, including a <strong>U.S. patent issued 14 April 2009</strong>, and further laboratory discoveries showing that less <strong>DREPAC</strong> is needed than previously believed to reverse sickle cell! To keep this progress going, we need <strong>your help!</strong> It is our goal to have <strong>clinical trials</strong> underway by this time next year! Please click the <strong>donate button and give generously this month</strong> – National Sickle Cell Month.  SCCF is a 501(c)(3) non-profit research foundation and <strong>all donations</strong> are 100% tax deductible.</p>
]]></content:encoded>
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		<slash:comments>2</slash:comments>
		</item>
		<item>
		<title>About sickle cell disease&#8230;</title>
		<link>http://sicklecellcurefoundation.org/2009/08/about-sickle-cell-disease/</link>
		<comments>http://sicklecellcurefoundation.org/2009/08/about-sickle-cell-disease/#comments</comments>
		<pubDate>Sun, 16 Aug 2009 03:42:52 +0000</pubDate>
		<dc:creator>broylesr</dc:creator>
				<category><![CDATA[Our Research]]></category>
		<category><![CDATA[scientific research]]></category>
		<category><![CDATA[Sickle Cell Disease]]></category>

		<guid isPermaLink="false">http://sicklecellcurefoundation.ecoonamoly.com/?p=442</guid>
		<description><![CDATA[&#8220;Everything we know about genes we learned first about the beta globin gene. Everything we know about molecular disease we first learned about sickle cell disease&#8221; Francis Collins, NIH, former Director of the Human Genome Project]]></description>
			<content:encoded><![CDATA[<p><img class="alignleft" title="Genes" src="/wp-content/uploads/2009/08/genes-75x75.jpg" alt="" width="75" height="75" />&#8220;Everything we know about genes we learned first about the beta globin gene.  Everything we know about molecular disease we first learned about sickle cell disease&#8221;<br />
Francis Collins, NIH, former Director of the Human Genome Project</p>
]]></content:encoded>
			<wfw:commentRss>http://sicklecellcurefoundation.org/2009/08/about-sickle-cell-disease/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>A cure for sickle cell disease from our own bodies&#8230;</title>
		<link>http://sicklecellcurefoundation.org/2009/08/a-cure-for-sickle-cell-disease-from-our-own-bodies/</link>
		<comments>http://sicklecellcurefoundation.org/2009/08/a-cure-for-sickle-cell-disease-from-our-own-bodies/#comments</comments>
		<pubDate>Sun, 09 Aug 2009 05:13:25 +0000</pubDate>
		<dc:creator>broylesr</dc:creator>
				<category><![CDATA[Our Research]]></category>
		<category><![CDATA[sickle cell]]></category>
		<category><![CDATA[Sickle Cell Disease]]></category>
		<category><![CDATA[sickle cell disease cure]]></category>

		<guid isPermaLink="false">http://sicklecellcurefoundation.ecoonamoly.com/?p=241</guid>
		<description><![CDATA[We are very proud to announce major progress in the search for a cure for sickle cell disease (SCD), the first genetic disease to be understood and a major disease that kills an estimated half-million people world-wide each year. As high as one in every four black persons in certain parts of Africa carries the [...]]]></description>
			<content:encoded><![CDATA[<p><img class="alignleft" title="Vitruvian-Man" src="/wp-content/uploads/2009/08/Vitruvian-Man.jpg" alt="" width="300" height="425" />We are very proud to announce major progress in the search for a cure for sickle cell disease (SCD), the first genetic disease to be understood and a major disease that kills an estimated half-million people world-wide each year.  As high as one in every four black persons in certain parts of Africa carries the sickle cell gene.  In the United States the incidence is 1 in 12 for African Americans, and approximately 78,000 have SCD.  Dr. Robert H. Broyles, a medical school professor and researcher in Oklahoma City, has discovered a protein that is grown in our own bodies that will silence the sickle cell gene and activate a normal gene in its place.  Unlike current treatments that are only partially effective or treat the damage caused by SCD, this cure is very specific for the cause, easy to deliver, and beneficial to the whole body.  We are working to get this treatment through safety trials and into the clinics where it will be available to all who have sickle cell disease.  Our vision is a global one: our goal is to get this cure to each of the millions of people world-wide who have SCD and/or Beta-Thalassemia.</p>
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		<slash:comments>150</slash:comments>
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