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<title>News &amp; Press</title>
<link>https://www.acam.org/news/default.asp</link>
<description><![CDATA[  Read about recent events, essential information and the latest community news.  ]]></description>
<lastBuildDate>Fri, 12 Jun 2026 23:03:39 GMT</lastBuildDate>
<pubDate>Fri, 16 Aug 2024 15:55:00 GMT</pubDate>
<copyright>Copyright &#xA9; 2024 American College for Advancement in Medicine (ACAM)</copyright>
<atom:link href="https://www.acam.org/news/news_rss.asp?cat=12427" rel="self" type="application/rss+xml"></atom:link>
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<title>Scientists produce a genetic analysis of Lyme disease bacteria</title>
<link>https://www.acam.org/news/news.asp?id=689413</link>
<guid>https://www.acam.org/news/news.asp?id=689413</guid>
<description><![CDATA[<p>From News Medical website, written by The Graduate Center, CUNY:<br /><span style="text-decoration-line: underline;">Scientists produce a genetic analysis of Lyme disease bacteria</span><br /><a href="https://www.news-medical.net/news/20240816/Scientists-produce-a-genetic-analysis-of-Lyme-disease-bacteria.aspx">https://www.news-medical.net/news/20240816/Scientists-produce-a-genetic-analysis-of-Lyme-disease-bacteria.aspx</a></p><p>A team led by CUNY Graduate Center biologists has produced a genetic analysis of Lyme disease bacteria that may pave the way for improved diagnosis, treatment, and prevention of the tick-borne ailment.<br /><br />Weigang Qiu, a professor of Biology at the CUNY Graduate Center and Hunter College, and an international team including lead author Saymon Akther, a former CUNY Graduate Center Biology Ph.D. student, mapped the complete genetic makeup of 47 strains of Lyme disease-related bacteria from around the world, creating a powerful tool for identifying the bacterial strains that infect patients. Researchers said this could enable more accurate diagnostic tests and treatments tailored to the bacteria causing each patient's illness.<br /><a href="https://www.news-medical.net/news/20240816/Scientists-produce-a-genetic-analysis-of-Lyme-disease-bacteria.aspx">READ MORE</a></p>]]></description>
<pubDate>Fri, 16 Aug 2024 16:55:00 GMT</pubDate>
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<title>Methylene blue–a new/old drug for treating Lyme disease</title>
<link>https://www.acam.org/news/news.asp?id=689419</link>
<guid>https://www.acam.org/news/news.asp?id=689419</guid>
<description><![CDATA[<p>From lymedisease.org, written by Dr. Erica Lehman:<br /><span style="text-decoration-line: underline;">Methylene blue - a new/old drug for treating Lyme disease</span><br /><a href="https://www.lymedisease.org/methylene-blue-lyme-disease/">https://www.lymedisease.org/methylene-blue-lyme-disease/</a></p><p>Methylene blue (MB) is truly a fascinating compound and one of the most revolutionary medications to hit the functional medicine and tick-borne disease spheres.<br /><br />It was first synthesized by a German chemist Heinrich Caro in 1876. Initially, it was known as methylthioninium chloride and later named methylene blue due to its distinctive color.<br /><br />Its early applications include use as a dye and staining agent for biological tissue. It was used in histology and microscopy to enhance the visibility of cell structures because it can stain DNA. I used it early on in my ophthalmic surgery training to mark the sclera (the white part of the eye), for cataract and retinal detachment surgery.<br /><a href="https://www.lymedisease.org/methylene-blue-lyme-disease/">READ MORE</a></p>]]></description>
<pubDate>Wed, 27 Mar 2024 17:02:00 GMT</pubDate>
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<title>Natural Ways to Avoid Ticks and Lyme Disease</title>
<link>https://www.acam.org/news/news.asp?id=689415</link>
<guid>https://www.acam.org/news/news.asp?id=689415</guid>
<description><![CDATA[<p>From The Institute for Natural Medicine website, written by Institute for Natural Medicine Staff:<br /><span style="text-decoration: underline;">Natural Ways to Avoid Ticks and Lyme Disease</span><br /><a href="https://naturemed.org/ticks-lyme-disease/">https://naturemed.org/ticks-lyme-disease/</a></p><p>Discover natural strategies for preventing ticks and Lyme disease, including environmental tips and personal practices to minimize tick encounters and ensure outdoor safety.<br /><br />There are more than 300,000 new cases of Lyme disease diagnosed each year. And while most think of the disease as a summer issue, Lyme disease can occur at any time of the year, which is why being diligent is important year- round, so says the Global Lyme Alliance.<br /><a href="https://naturemed.org/ticks-lyme-disease/">READ MORE</a></p>]]></description>
<pubDate>Fri, 19 Jan 2024 16:59:00 GMT</pubDate>
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<title>The Quiet Epidemic Wrecking Our Children’s Health</title>
<link>https://www.acam.org/news/news.asp?id=689411</link>
<guid>https://www.acam.org/news/news.asp?id=689411</guid>
<description><![CDATA[<p>From The Alliance for Natural Health website, written by the ANH Team:<br /><span style="text-decoration: underline;">The Quiet Epidemic Wrecking Our Children’s Health</span><br /><a href="https://anh-usa.org/the-quiet-epidemic-wrecking-our-childrens-health/">https://anh-usa.org/the-quiet-epidemic-wrecking-our-childrens-health/</a></p><p>Two closely related autoimmune conditions are wreaking havoc with the health of many thousands of American kids, and conventional medicine has little to offer.<br /><br />The conditions are devastating not just for the affected kids, but also for their families. The conditions are called PANS and PANDAS, which stand for Pediatric Acute-onset Neuropsychiatric Syndrome (PANS) and Pediatric Autoimmune Neuropsychiatric Disorder Associated with Streptococcal Infections (PANDAS), respectively. They are estimated to affect one in 200 US children – and this figure may be conservative and be on the increase.<br /><br />Imagine waking up one morning and finding a sudden and deeply disturbing change in the behavior of your 6-year-old child. They could have new and intense concerns about things being disordered or uneven, or find themselves struggling with schoolwork. They could, overnight, develop new compulsions like the need to wash or repeat things a certain number of times, or they’ve developed a tic, hyperactivity, extreme anxiety, or sudden depression.<br /><a href="https://anh-usa.org/the-quiet-epidemic-wrecking-our-childrens-health/">READ MORE</a></p>]]></description>
<pubDate>Tue, 17 Oct 2023 16:48:00 GMT</pubDate>
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<title>PCAC Has Voted YES to Include Compounded Glutathione on the &quot;Able to Compound&quot; List</title>
<link>https://www.acam.org/news/news.asp?id=608039</link>
<guid>https://www.acam.org/news/news.asp?id=608039</guid>
<description><![CDATA[<p>The Pharmacy Compounding Advisory Committee (PCAC) voted <strong>yes </strong>to include Compounded Glutathione on the "able to compound " list, Wednesday, June 8, 2022. As many of us are aware, this is huge news. <br /></p><p><br />The PCAC rarely votes out of line with the FDA's direction,
and ACAM is very pleased with its decision.<br /> Compounded Glutathione has many been prescribed for many potential uses, including helping to reduce oxidative stress, improving insulin resistance in the aging population, reducing cell damage in alcoholic
and nonalcoholic fatty liver disease, reducing symptoms of Parkinson’s disease, increasing mobility for those with peripheral artery disease, and many more that were put in jeopardy by the FDA's ruling.<br /><br />According to the FDA, it has called into question
the safety of compounded drugs out of concern for drug quality problems, such as contamination or too much of one active ingredient, which has resulted in patient injury and death.<br /><br />For those of you that weighed in on your personal experience with these
prescriptions, we thank you for working to help preserve their availability. The future of many more compounded drugs continues to be up for review, and we recommend you stay up to date with these rulings. <br /><br />Compounded Glutathione use cases pulled from:
<a href="https://www.healthline.com/health/glutathione-benefits#glutathione-benefits"><strong><span style="text-decoration: underline;">https://www.healthline.com/health/glutathione-benefits#glutathione-benefits</span></strong></a></p>]]></description>
<pubDate>Thu, 9 Jun 2022 16:08:00 GMT</pubDate>
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<title>Pharmacy Compounding Advisory Committee; Notice of Meeting; Comments Needed by End of Day!</title>
<link>https://www.acam.org/news/news.asp?id=606437</link>
<guid>https://www.acam.org/news/news.asp?id=606437</guid>
<description><![CDATA[<div class="ACT" style="box-sizing: border-box; color: #333333; font-family: 'Helvetica Neue', Helvetica, Arial, sans-serif; background-color: #ffffff;"><h2 style="box-sizing: border-box; font-family: inherit; font-weight: 500; line-height: 1.42858; color: inherit; margin-top: 20px; margin-bottom: 10px; font-size: 18px;">Action</h2></div><p style="box-sizing: border-box; margin: 0px 0px 10px;">Notice; establishment of a public docket; request for comments.</p><div class="SUM" style="box-sizing: border-box; color: #333333; font-family: 'Helvetica Neue', Helvetica, Arial, sans-serif; background-color: #ffffff;"><h2 style="box-sizing: border-box; font-family: inherit; font-weight: 500; line-height: 1.42858; color: inherit; margin-top: 20px; margin-bottom: 10px; font-size: 18px;">Summary</h2></div><p><span style="color: #333333; font-family: 'Helvetica Neue', Helvetica, Arial, sans-serif; background-color: #ffffff;">The Food and Drug Administration (FDA) announces a forthcoming public advisory committee meeting of the Pharmacy Compounding Advisory Committee. The general function of the committee is to provide advice and recommendations to FDA on regulatory issues. The meeting will be open to the public. FDA is establishing a docket for public comment on this document.</span><br /></p><h2 style="box-sizing: border-box; font-family: 'Helvetica Neue', Helvetica, Arial, sans-serif; font-weight: 500; line-height: 1.42858; color: #333333; margin-top: 20px; margin-bottom: 10px; font-size: 18px; background-color: #ffffff;">Dates</h2><p style="box-sizing: border-box; margin: 0px 0px 10px; color: #333333; font-family: 'Helvetica Neue', Helvetica, Arial, sans-serif; background-color: #ffffff;">The meeting will be held on June 8, 2022, from 9:30 a.m. to 5:15 p.m. Eastern Time.<br /><br /><span style="color: #333333; font-family: 'Helvetica Neue', Helvetica, Arial, sans-serif; background-color: #ffffff;"><strong>Comments received on or before May 24, 2022, will be provided to the committee. Comments received after that date will be taken into consideration by FDA. In the event that the meeting is cancelled, FDA will continue to evaluate any relevant applications or information, and consider any comments submitted to the docket, as appropriate.<br /><br /><br /><span style="text-decoration: underline;"><a href="https://www.regulations.gov/document/FDA-2021-N-0357-2586"><span style="font-size: 22px;">LEAVE YOUR COMMENTS HERE</span></a></span></strong></span></p>]]></description>
<pubDate>Tue, 24 May 2022 16:05:00 GMT</pubDate>
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<title>Compounding: Regulatory Policy Information</title>
<link>https://www.acam.org/news/news.asp?id=510255</link>
<guid>https://www.acam.org/news/news.asp?id=510255</guid>
<description><![CDATA[<span style="font-family: Arial;"><br />
I am pleased to invite a representative of your organization to participate in a virtual listening session with the FDA regarding drug compounding. FDA has regularly held listening sessions with groups of interested stakeholders to discuss FDA’s efforts to implement the compounding provisions of the Drug Quality and Security Act since the Act was signed into law in November, 2013. &nbsp;<br />
&nbsp;<br />
Since our last meetings, we have issued numerous draft and final policy documents on drug compounding and related topics and are continuing our implementation efforts.&nbsp; (See <a href="https://www.fda.gov/drugs/human-drug-compounding/regulatory-policy-information" target="_blank">https://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/PharmacyCompounding/ucm166743.htm</a>.) &nbsp;<br />
&nbsp;<br />
Because we continue to receive positive feedback concerning prior sessions, we have decided to hold a series of similar meetings again this year. We will hold listening sessions with: pharmacy, consumer and industry organizations; hospital organizations; medical and insurer organizations; and outsourcing facilities registered under section 503B.<br />
&nbsp;<br />
Please plan on joining us for the listening session for medical and insurer organizations on June 23, 2020, 10:00AM-12:00PM Eastern Time. Due to the COVID-19 public health emergency we will be holding this year’s sessions virtually. <br />
&nbsp;<br />
Prior to the sessions, we will share recommended discussion topics that are of particular interest to the Agency. They are not intended to limit conversation. We value hearing stakeholder perspectives on all topics related to compounding. <br />
&nbsp;<br />
To allow sufficient time for discussion we will not begin the sessions with formal spoken statements from participants, but we welcome the submission of written statements which you may provide in advance of, or following, the session. <br />
&nbsp;<br />
In addition, if your statement or comments during the listening session address topics that are relevant to open FDA dockets (e.g., for draft guidance’s), we strongly recommend that you submit comments or other information to the relevant docket(s).<br />
&nbsp;<br />
Please respond by close of business on June 4, 2020 to Janis Fleischer, Professional Affairs and Stakeholder Engagement, Janis.Fleischer@fda.hhs.gov, or 240-402-2579 concerning your attendance.&nbsp; Please provide the names and titles of the representatives from your organization who will attend the meeting.&nbsp; To facilitate discussion, please limit participants to no more than three representatives from your organization. <br />
&nbsp;<br />
Information to access the virtual listening and informational sessions will be provided prior to the meeting. <br />
&nbsp;<br />
We hope you will be able to join us.<br />
Janis Fleischer, MBA<br />
Center for Drug Evaluation and Research<br />
Professional Affairs and Stakeholder Engagement<br />
U.S. Food and Drug Administration<br />
<br />
</span><br />
<br />]]></description>
<pubDate>Fri, 29 May 2020 20:56:43 GMT</pubDate>
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<title>Invitation to Virtual FDA Listening Sessions on Drug Compounding</title>
<link>https://www.acam.org/news/news.asp?id=509567</link>
<guid>https://www.acam.org/news/news.asp?id=509567</guid>
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            <p style="color: #323130; margin: 0px;"><span style="font-size: 14px;"><a name="x__Hlk40875327" style="margin: 0px; padding: 0px; border: 0px;"><span style="color: #000000; margin: 0px; padding: 0px; border: 0px;">Good afternoon,</span></a></span></p>
            <p style="color: #323130; margin: 0px;"><span style="color: #000000;"><span style="margin: 0px; padding: 0px; border: 0px; font-size: 14px;"><br />
            I am pleased to invite a representative of your organization to participate in a virtual<br />
            listening session with the FDA regarding drug compounding. FDA has regularly<br />
            held listening sessions with groups of interested stakeholders to discuss FDA’s efforts<br />
            to implement the compounding provisions of the Drug Quality and Security Act since<br />
            the Act was signed into law in November, 2013.&nbsp;</span></span></p>
            <p style="color: #323130; margin: 0px;"><span style="color: #000000;"><span style="margin: 0px; padding: 0px; border: 0px; font-size: 14px;"></span></span></p>
            <p style="color: #323130; margin: 0px;"><span style="font-size: 14px;"><span style="color: inherit; margin: 0px; padding: 0px; border: 0px;"><span style="color: #000000; margin: 0px; padding: 0px; border: 0px;">Since our last meetings, we have issued numerous draft and final policy documents<br />
            on drug compounding and related topics and are continuing our implementation efforts.&nbsp; (See&nbsp;</span></span><a href="https://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/PharmacyCompounding/ucm166743.htm" target="_blank" rel="noopener noreferrer" data-auth="NotApplicable" style="margin: 0px; padding: 0px; border: 0px;"><span style="color: inherit; margin: 0px; padding: 0px; border: 0px;"><span style="color: inherit; margin: 0px; padding: 0px; border: 0px;">https://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/PharmacyCompounding/ucm166743.htm</span></span></a><span style="color: inherit; margin: 0px; padding: 0px; border: 0px;"><span style="color: inherit; margin: 0px; padding: 0px; border: 0px;">.)&nbsp;</span></span></span></p>
            <p style="color: #323130; margin: 0px;"><span style="color: inherit; margin: 0px; padding: 0px; border: 0px; font-size: 14px;"></span></p>
            <p style="color: #323130; margin: 0px;"><span style="color: #000000; margin: 0px; padding: 0px; border: 0px; font-size: 14px;"><br />
            Because we continue to receive positive feedback concerning prior sessions, we have<br />
            decided to hold a series of similar meetings again this year. We will hold listening<br />
            sessions with: pharmacy, consumer and industry organizations; hospital organizations;<br />
            medical and insurer organizations; and outsourcing facilities registered under section 503B.</span></p>
            <p style="color: #323130; margin: 0px;"><span style="color: #000000;"><span style="margin: 0px; padding: 0px; border: 0px; font-size: 14px;"></span></span></p>
            <p style="color: #323130; margin: 0px;"><span style="color: #000000;"><span style="background-color: yellow; margin: 0px; padding: 0px; border: 0px; font-size: 14px;"><br />
            Please plan on joining us for the&nbsp;</span><span style="background-color: yellow; margin: 0px; padding: 0px; border: 0px; font-size: 14px;"><b>listening session for medical and insurer<br />
            organizations on&nbsp;</b></span><span style="background-color: yellow; margin: 0px; padding: 0px; border: 0px; font-size: 14px;"></span><span style="background-color: yellow; margin: 0px; padding: 0px; border: 0px; font-size: 14px;"><b>June 23, 2020,</b></span><span style="margin: 0px; padding: 0px; border: 0px; font-size: 14px;"></span><span style="background-color: yellow; margin: 0px; padding: 0px; border: 0px; font-size: 14px;"><b>10:00AM-12:00PM Eastern Time.&nbsp;</b></span><span style="background-color: yellow; margin: 0px; padding: 0px; border: 0px; font-size: 14px;">Due to the COVID-19<br />
            public health emergency we will be holding this year’s sessions virtually.</span></span></p>
            &nbsp;
            <p style="color: #323130; margin: 0px;"><span style="color: #000000;"><span style="margin: 0px; padding: 0px; border: 0px; font-size: 14px;">Prior to the sessions, we will share recommended discussion topics that are of<br />
            particular interest to the Agency. They are not intended to limit conversation. We value<br />
            hearing stakeholder perspectives on all topics related to compounding.<br />
            </span></span></p>
            <p style="color: #323130; margin: 0px;"><span style="color: #000000;"><span style="margin: 0px; padding: 0px; border: 0px; font-size: 14px;"></span></span></p>
            <p style="color: #323130; margin: 0px;"><span style="color: #000000;"><span style="margin: 0px; padding: 0px; border: 0px; font-size: 14px;">To allow sufficient time for discussion we will not begin the sessions with formal spoken<br />
            statements from participants, but we welcome the submission of written statements which<br />
            you may provide in advance of, or following, the session.</span></span></p>
            &nbsp;
            <p style="color: #323130; margin: 0px;"><span style="color: #000000;"><span style="margin: 0px; padding: 0px; border: 0px; font-size: 14px;">In addition, if your statement or comments during the listening session address topics that<br />
            are relevant to open FDA dockets (e.g., for draft guidance’s), we strongly recommend that<br />
            you submit comments or other information to the relevant docket(s).<br />
            &nbsp; &nbsp;<br />
            </span></span></p>
            <p style="color: #323130; margin: 0px;"><span style="color: #000000;"><span style="margin: 0px; padding: 0px; border: 0px; font-size: 14px;"></span></span></p>
            <p style="color: #323130; margin: 0px;"><span style="font-size: 14px;"><span style="color: #000000;"><b><span style="margin: 0px; padding: 0px; border: 0px;">Please respond by close of business on June 4, 2020&nbsp;</span></b></span><span style="color: inherit; margin: 0px; padding: 0px; border: 0px;"><span style="color: #000000;">to Janis Fleischer, Professional<br />
            Affairs and Stakeholder Engagement,</span>&nbsp;<span><a href="mailto:Janis.Fleischer@fda.hhs.gov">Janis.Fleischer@fda.hhs.gov</a></span><span style="color: #000000;">, or 240-402-2579<br />
            concerning your attendance. Please provide the names and titles of the representatives<br />
            from your organization who will attend the meeting.&nbsp; To facilitate discussion, please limit<br />
            participants to no more than three representatives from your organization.</span></span></span></p>
            <p style="color: #323130; margin: 0px;"><span style="color: #000000;"><span style="margin: 0px; padding: 0px; border: 0px; font-size: 14px;"></span></span></p>
            <p style="color: #323130; margin: 0px;"><span style="color: #000000;"><span style="margin: 0px; padding: 0px; border: 0px; font-size: 14px;">Information to access the virtual listening and informational sessions will be provided prior<br />
            to the meeting.</span></span></p>
            <p style="color: #323130; margin: 0px;"><span style="color: #000000;"><span style="margin: 0px; padding: 0px; border: 0px; font-size: 14px;"></span></span></p>
            <p style="color: #323130; margin: 0px;"><span style="color: #000000;"><span style="margin: 0px; padding: 0px; border: 0px; font-size: 14px;"><br />
            We hope you will be able to join us.</span></span></p>
            <p style="color: #323130; margin: 0px;"><span style="color: #000000;"><span style="margin: 0px; padding: 0px; border: 0px; font-size: 14px;"></span></span></p>
            <p style="color: #323130; margin: 0px;"><span style="color: inherit; margin: 0px; padding: 0px; border: 0px; font-size: 14px;"><span style="color: #000000;"><br />
            Sincerely,</span><br />
            </span></p>
            <p style="color: #323130; margin: 0px 0px 7.5pt;"><span style="font-size: 14px;"><b><span style="color: #00539b; margin: 0px; padding: 0px; border: 0px;">Janis Fleischer, MBA</span></b><span style="color: #000000; margin: 0px; padding: 0px; border: 0px;"><br />
            <b>Center for Drug Evaluation and Research<br />
            Professional Affairs and Stakeholder Engagement<br />
            U.S. Food and Drug Administration</b></span></span></p>
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</span></p>]]></description>
<pubDate>Tue, 26 May 2020 21:26:27 GMT</pubDate>
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<title>Potential Probiotic or Trigger of Gut Inflammation – The Janus-Faced Nature of Cannabidiol-Rich Cann</title>
<link>https://www.acam.org/news/news.asp?id=507051</link>
<guid>https://www.acam.org/news/news.asp?id=507051</guid>
<description><![CDATA[<p><span style="font-family: Arial;"><strong><span style="text-decoration: underline;">Potential Probiotic or Trigger of Gut Inflammation – The Janus-Faced Nature of Cannabidiol-Rich Cannabis Extract</span></strong><br />
Charles M. Skinner , BS,Intawat Nookaew , PhD,Laura E. Ewing , MScORCID Icon,Thidathip Wongsurawat , PhD,Piroon Jenjaroenpun , PhD,Charles M. Quick , MD,...</span></p>
<p><span style="font-family: Arial;">&nbsp;</span></p>
<p><span style="font-family: Arial;"><strong>Abstract</strong><br />
Cannabidiol (CBD) is the major non-psychotropic phytocannabinoid present in Cannabis sativa. In 2018, Congress designated certain C. sativa plant material as “hemp,” thus removing it from the DEA’s list of controlled substances. As a result, CBD-containing hemp extracts and other CBD products are now widely available and heavily marketed, yet their FDA regulatory status is still hotly debated. The goal of this study was to investigate the effects of a cannabidiol-rich cannabis extract (CRCE) on the gut microbiome and associated histomorphological and molecular changes in the mouse gut mucosa. Male C57BL6/J mice were gavaged with either 0, 61.5, 184.5, or 615 mg/kg/bw of CRCE in sesame oil for 2 weeks (Mon–Fri). Substantial CRCE-induced increases in the relative abundance of A. muciniphila, a bacterial species currently accepted as probiotic, was observed in fecal samples at all doses. This was paralleled by decreases in the relative abundance of other gut bacterial species. Coincident with the observed changes in gut ecology were multiple pro-inflammatory responses, including increased expression of cytokines and chemokines—Il1ß, Cxcl1, and Cxcl2 in the colon tissue. Furthermore, dramatic increases in the relative abundance of A. muciniphila significantly decreased expression of Muc2—a gene intimately associated with gut integrity. Taken together, these findings raise concerns about the safety of long-term CBD usage and underline the need for additional well-designed studies into its tolerability and efficacy.</span></p>
<p><span style="font-family: Arial;">&nbsp;</span></p>
<p><span style="font-family: Arial;"><strong><a href="https://www.tandfonline.com/eprint/PMWHDQP4YHUGKBEZBWAK/full?target=10.1080%2F19390211.2020.1761506&amp;#.XrvuoAm9QQU.linkedin" target="_blank">Read the Full Article Here</a></strong><br />
</span></p>]]></description>
<pubDate>Wed, 13 May 2020 15:44:20 GMT</pubDate>
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<title>COVID-19 Resource Center</title>
<link>https://www.acam.org/news/news.asp?id=497155</link>
<guid>https://www.acam.org/news/news.asp?id=497155</guid>
<description><![CDATA[<p style="text-align: center;"><img alt="" src="https://www.acam.org/resource/resmgr/coronavirus/covid_site_header_cc_1000w.jpg" style="width: 500px; height: 169px; vertical-align: top;" /></p>
<p style="text-align: center;">Navigating the #COVID-19 pandemic as a medical practitioner is particularly precarious &amp; ACAM wants to help! Our interactive website includes medical discussion, resources and tips to work and communicate virtually. <a href="https://www.acam.org/mpage/CoronavirusDiscussion" target="_blank"><strong><span style="font-size: 16px;"><span style="text-decoration: underline;">Join the conversation.</span></span></strong></a></p>]]></description>
<pubDate>Wed, 25 Mar 2020 17:50:47 GMT</pubDate>
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<title>Compounded Medications are at Risk</title>
<link>https://www.acam.org/news/news.asp?id=474816</link>
<guid>https://www.acam.org/news/news.asp?id=474816</guid>
<description><![CDATA[<div style="text-align: center;">
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                        <p><span>Hello,</span></p>
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<p style="text-align: center;">&nbsp;</p>
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                        <p><span>Thousands of patients are at risk of losing access to life-saving compounded medications, and we need your help.</span></p>
                        <p>&nbsp;</p>
                        <p><span>Despite a long history of safe use and patient need,the <b>FDA is in the process of reviewing and potentially blocking patient accessto more than 300 ingredientsused in compounded medications.</b>The FDA’s current position is that if there is an approved pharmaceutical equivalent that will address the condition, the compounded ingredient is not needed. </span></p>
                        <p>&nbsp;</p>
                        <p><span>By dismissing why patients need personalized medicine, the FDA is discounting functional medicine uses and only taking into consideration whether an ingredient addresses a specific disease.</span></p>
                        <p>&nbsp;</p>
                        <p><span>In September, the FDA published a draft rule that - if finalized as currently written - <b>would make 26 ingredients illegal to compound.</b></span><span style="color: #403f42;"> </span></p>
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<p style="text-align: center;">&nbsp;</p>
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                        <p style="text-align: center;"><b><span style="color: #294b93;">Ingredients Impacted</span></b></p>
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<p style="text-align: center;">&nbsp;</p>
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                        <p><span>7-keto dehydroepiandrosterone (DHEA)</span></p>
                        <p><span>Acetyl-L-Carnitine</span></p>
                        <p><span>Alanyl-L-Glutamine</span></p>
                        <p><span>Aloe Vera 200:1 Freeze Dried</span></p>
                        <p><span>Artemisinin</span></p>
                        <p><span>Astragalus extract 10:1</span></p>
                        <p><span>Boswellia</span></p>
                        <p><span>Cesium Chloride</span></p>
                        <p><span>ChondroitinSulfate</span></p>
                        <p><span>Chrysin</span></p>
                        <p><span>Curcumin</span></p>
                        <p><span>D-Ribose</span></p>
                        <p><span>Deoxy-D-Glucose</span></p>
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                        <p><span>Diindolylmethane</span></p>
                        <p><span>Domperidone</span></p>
                        <p><span>Epigallocatechingallate(EGCG)</span></p>
                        <p><span>Germanium Sesquioxide</span></p>
                        <p><span>Glycyrrhizin</span></p>
                        <p><span>Kojicacid</span></p>
                        <p><span>Nettle</span></p>
                        <p><span>Nicotinamideadenine dinucleotide(NAD)</span></p>
                        <p><span>Nicotinamideadenine dinucleotidedisodiumreduced (NADH)</span></p>
                        <p><span>Rubidium Chloride</span></p>
                        <p><span>SodiumDichloroacetate</span></p>
                        <p><span>VanadylSulfate</span></p>
                        <p><span>Vasoactiveintestinal peptide</span></p>
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<p style="text-align: center;">&nbsp;</p>
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                        <p><b><span>Use your voice to submit a comment to the proposed rule.</span></b><span> Please note, we are <i>only looking for comments on the 26 ingredients.</i> Comments that mention other ingredients will be ignored by the FDA. The last day to submit a comment is December 4. </span></p>
                        <p>&nbsp;</p>
                        <p><span>Thank you for fighting to protect patient access to compounded medications.</span></p>
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                                                <p style="text-align: center;"><span style="color: white;"><a href="http://r20.rs6.net/tn.jsp?f=001gJs001vcqaUjtucLwSAIe_VnO1HMt4RnkY7q8oqF6a5JTr2HSn7wYyQNxuu_JrTR6Bgd1qAxN5XvYnv1vYJSjY9Q6To1t6Uia-ajeHNlIi-o_Tsw7-98iw_i5AAin0VBEl-XNJAlSQRSloaNBvsO9XaGWSxSS7IrIdD2cTcCj6k=&amp;c=Dkoyw8d2d5S8vKcrI8LiUiGbBds4Tkd2BNQPtaXqKNMqK9cvpjmHBg==&amp;ch=UY39etn7Y-PGbhc-cU6FezRFZRfHPNIJnRTznmhADKHzwOnqmq1WkQ==" target="_blank"><b><span style="color: white;">TAKE ACTION NOW</span></b></a></span></p>
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<p style="text-align: center;">&nbsp;</p>
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                        <p><span style="color: #403f42;">To learn more, click </span><span style="color: #403f42;"><a href="http://r20.rs6.net/tn.jsp?f=001gJs001vcqaUjtucLwSAIe_VnO1HMt4RnkY7q8oqF6a5JTr2HSn7wYwgV4nbFjNl6G8_2JYjQLltL389FzbXqlcLYqC_UDZ0R1AXLoZbN1i7H8qKCRtalhNuLLst8uFZ0D4j3j0pI1z2EONuTsCcJEdO0IHI15xDsQF5QGgbGqdg=&amp;c=Dkoyw8d2d5S8vKcrI8LiUiGbBds4Tkd2BNQPtaXqKNMqK9cvpjmHBg==&amp;ch=UY39etn7Y-PGbhc-cU6FezRFZRfHPNIJnRTznmhADKHzwOnqmq1WkQ==" target="_blank"><span style="color: #48a199;">here.</span></a></span><span style="color: #403f42;"> </span></p>
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<pubDate>Mon, 21 Oct 2019 16:55:21 GMT</pubDate>
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<title>ACTION ALERT: Protect Patient Use of Compounded Medications</title>
<link>https://www.acam.org/news/news.asp?id=449310</link>
<guid>https://www.acam.org/news/news.asp?id=449310</guid>
<description><![CDATA[<iframe title="vimeo-player" src="https://player.vimeo.com/video/332800387" width="640" height="360" frameborder="0"> </iframe><br />
<span style="color: #333333;">Organizations in the field of integrative and natural medicine have launched a coordinated campaign to protect patient access to compounded medications. Despite a long history of safe use and patient need,&nbsp;</span><span style="color: #333333;">the FDA has blocked patient access&nbsp;</span><span style="color: #333333;">to ingredients used in compounded medications and is in the process of reviewing and potentially blocking access to</span><span style="color: #333333;">&nbsp;more than 300 compounded ingredients needed by hundreds of thousands of patients. The groups are now in phase 2 of their fight against the FDA over-reach, constructing a Citizen's Petition.</span><br />
<br />
<em style="color: #333333;"><span><strong>Why is the FDA trying to remove them?</strong></span></em><br style="color: #333333;" />
<span style="color: #333333;">The 2013 Drug Quality &amp; Security Act (DQSA) was passed in response to a meningitis outbreak from contaminated sterile drugs compounded that tragically resulted in dozens of deaths. The law gives the FDA new authority to regulate some compounding facilities to address these safety concerns.&nbsp;</span><br style="color: #333333;" />
<span style="color: #333333;">In passing the DQSA, Congress made clear statements noting the importance of ensuring that the new compounding regulations should not interfere with the practice of medicine.&nbsp;</span><br style="color: #333333;" />
<span style="color: #333333;">Unfortunately, the FDA’s&nbsp;</span><span style="color: #333333;">CURRENT</span><span style="color: #333333;">&nbsp;default position is that if there is an FDA-approved Pharmaceutical Drug for a specific condition, then a compounded substance is unnecessary - despite the needs of thousands of patients who may not be able to use the FDA pharmaceutical safely. &nbsp;</span><br style="color: #333333;" />
<br style="color: #333333;" />
<span style="color: #333333;">*The actions of the FDA are the exact opposite of what Congress intended.*</span><br style="color: #333333;" />
<br style="color: #333333;" />
<span style="color: #333333;"><em><strong>How are patients directly impacted by the new FDA regulations?</strong></em>&nbsp;</span><br style="color: #333333;" />
<em style="color: #333333;">Removing Drugs From Ability to Compound</em><br style="color: #333333;" />
<span style="color: #333333;">The FDA requested that substances that are currently compounded be nominated for a review process to determine indications for use, history of use, safety, etc. Over 300 ingredients were nominated. The FDA divided these into three categories:</span><br style="color: #333333;" />
<span style="color: #333333;">&nbsp; &nbsp; -Category I - 55 substances that the FDA agreed to review in the Pharmacy Compounding Advisory Committee</span><br style="color: #333333;" />
<span style="color: #333333;">&nbsp; &nbsp; -Category II - 4 substances that were deemed too dangerous to compound and immediately banned.</span><br style="color: #333333;" />
<span style="color: #333333;">&nbsp; &nbsp; -Category III - Over 260 substances that the FDA determined there was not enough evidence to support and will not even review. This list will be banned from compounding use without any review, and includes many herbs and natural substances.<br />
<br />
</span><strong><span style="font-size: 16px;">Learn more about the issue and how you can help <a href="https://www.gofundme.com/aanpcompoundedmedications" target="_blank"><span style="text-decoration: underline;">HERE</span></a>.</span></strong>]]></description>
<pubDate>Tue, 30 Apr 2019 21:49:40 GMT</pubDate>
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<title>Action Alert: Save Compounded Medications</title>
<link>https://www.acam.org/news/news.asp?id=388191</link>
<guid>https://www.acam.org/news/news.asp?id=388191</guid>
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            <iframe width="560" height="315" src="https://www.youtube.com/embed/E4JXiqGXOLM" frameborder="0" allow="autoplay; encrypted-media"></iframe><br />
            <span style="color: #494949;">Compounded medications are at risk of being banned by the FDA and its Pharmacy Compounding Advisory Committee. The Agendy is taking long-used safe ingredients off the market, and restricting the ability of doctors to have the drugs that will remain an an approved list available in their office (so-called “office-use.”)<br />
            <br />
            <span style="color: #494949;">Our Citizen’s Petition is getting closer to filing! Phase II of this effort is recruiting coalition partners and organizational allies to sign onto the petition with us to demonstrate the wide ranging negative impact that the FDA’s restrictions on compounded medications is having&nbsp;on practitioners and patients.<br />
            <br />
            <a href="https://www.youcaring.com/patientswhobenefitfromcompoundedmedications-687276" target="_blank">READ THE FULL STORY AND JOIN THE PETITION</a>!</span></span></td>
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<pubDate>Fri, 23 Feb 2018 16:47:16 GMT</pubDate>
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<title>Action Alert: Ensure Methylcobalamin Continues to be Available</title>
<link>https://www.acam.org/news/news.asp?id=387036</link>
<guid>https://www.acam.org/news/news.asp?id=387036</guid>
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            <p style="text-align: left;"><span><strong>Pharmacy Compounding Advisory Committee’s (PCAC) Review Of Methylcobalamin</strong></span></p>
            <p style="text-align: left;"><span>Recently, McGuff Compound Pharmacy Services informed you that the FDA’s PCAC is requesting information on Methylcobalamin<b> </b>for review and inclusion on the 503A bulk drug substances list. They greatly appreciate the information they received, which aided them in meeting the FDA’s initial response deadline.&nbsp; However, now is not the time to let our guards down!&nbsp; We must make our final effort push to meet the FDA’s second deadline of February 23<sup>rd</sup> and provide, “…any additional information that FDA should consider in its evaluation that may help to clarify the role of the nominated methylcobalamin bulk substance in compound drug products in current clinical practice…”&nbsp; &nbsp;</span></p>
            <p style="text-align: left;"><span>McGuff is again requesting your assistance to ensure compounded Methylcobalamin preparations remain available for your patients.&nbsp; Share with them any of the following:</span></p>
            <p style="margin-left: 0.5in; text-align: left;"><span>·<span>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span></span><span>Personal anecdotal experiences you may have using Methylcobalamin in your practice.</span></p>
            <p style="margin-left: 0.5in; text-align: left;"><span>·<span>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span></span><span>Your patients’ experiences with the use of Methylcobalamin—let you patients know their access to this important compounded drug is in jeopardy!</span></p>
            <p style="margin-left: 0.5in; text-align: left;"><span>·<span>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span></span><span>Scientific literature supporting Methylcobalamin uses.</span></p>
            <p style="margin-left: 0.5in; text-align: left;"><span>·<span>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span></span><span>Statements or guidelines from professional medical societies regarding Methylcobalamin uses.</span></p>
            <p style="text-align: left;"><span>Be aware that your response or your patient’s may be referenced in their statements to FDA’s PCAC.</span></p>
            <p style="text-align: left;"><span>We must act!&nbsp; Methylcobalamin is too important for our patients!&nbsp; The FDA’s PCAC must be persuaded of its medical therapeutic value.&nbsp; We will not have another chance to fight for this cause.&nbsp; We must do everything possible to ensure Methylcobalamin continues to be available for your patients and your practice!</span></p>
            <p style="text-align: left;"><span>Please forward any information to </span><span><a href="mailto:pharmacyanswers@mcguff.com?subject=Methylcobalamin,%20PCAC%20Review%20Information"><span style="text-decoration: underline;">pharmacyanswers@mcguff.com</span></a></span><span><span style="text-decoration: underline;">&nbsp;</span></span><span> under the subject heading of, “Methylcobalamin, PCAC Review Information.”&nbsp; If preferred, you may also fax the requested information to 877-444-1155.</span></p>
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<pubDate>Thu, 15 Feb 2018 16:51:28 GMT</pubDate>
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<title>ANH-USA Needs Your Help to Protect the Use of Natural Hormones!</title>
<link>https://www.acam.org/news/news.asp?id=379805</link>
<guid>https://www.acam.org/news/news.asp?id=379805</guid>
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                                                                                    <div style="margin: 0px; text-align: center;"><span><a href="https://default.salsalabs.org/Tc6b81c50-7e6b-45e2-9bf8-182960911255/03c0cd7f-f52f-11e6-8776-12e7222c7e03" target="_blank" rel="noopener noreferrer"><span><img alt="" data-imagetype="External" src="https://default.salsalabs.org/9c78f8d8-387b-4e67-a787-e4e3b98c4159/2e68056d-28bd-496e-8820-05a2be8c5075.png" width="528" id="_x0000_i1025" style="border-width: 0px; border-style: solid;" /></span></a></span></div>
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                                                                                                </span><span>Dear Subscriber,</span></div>
                                                                                                <div style="margin: 14pt 0px 7.5pt;"><span><b>We’re doing it!&nbsp;</b></span><span>Alliance for Natural Health-USA is meeting with agency decision makers and your elected officials to tell them about the 2.5 million women who rely on natural hormone replacement therapies in the U.S. With enough public pressure, we CAN block them from banning critical women’s hormones like estriol—just as ANH members did in 2008!</span><span><b>We need your help to turn up the heat!</b></span></div>
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                                                                                                <div style="margin-right: 0px; margin-bottom: 7.5pt; margin-left: 0px;"><span>There is still</span><span><b>so much to do</b></span><span>to stop the FDA from targeting estriol and other critical non-pharmaceutical hormones. We need the press, the public, and our lawmakers to know that women can’t be left with dangerous</span><span><b>pharmaceuticals</b></span><span><b>linked to cancer</b></span><span>as their only option.</span></div>
                                                                                                <div style="margin: 14pt 0px 7.5pt;"><span>Help us meet our overall year-end goal of $40,000 to stop the FDA’s war on women’s health. Your</span><span><b>100% tax-deductible gift</b></span><span>will go directly toward our public education efforts—our</span><span><b>most important political tool</b></span><span>to keep the pressure on Congress and the FDA!</span></div>
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                                                                                                <div style="margin-right: 0px; margin-bottom: 7.5pt; margin-left: 0px;"><span>Subscriber, as a nonprofit dependent on your support, we simply could not have achieved our successes without the strength of our grassroots army. Thank you for fighting for natural health!</span></div>
                                                                                                <div style="margin: 14pt 0px 7.5pt;"><span>Yours in health and wellness,</span></div>
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                                                                                                <div style="background-color: #cccccc; margin: 14pt 0px 7.5pt; text-align: center;"><span>Alliance for Natural Health USA</span><span><br />
                                                                                                3525 Piedmont Rd. NE</span><span><br />
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                                                                                                Atlanta, Georgia 30305</span><span><br />
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<pubDate>Thu, 21 Dec 2017 18:07:25 GMT</pubDate>
</item>
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<title>ACAM ACTION ALERT: Help License NDs in Rhode Island</title>
<link>https://www.acam.org/news/news.asp?id=342663</link>
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                                                <a name="LETTER.BLOCK4"></a><font color="#000000" face="Arial, Helvetica, sans-serif"><span style="font-size: 24px;"><b>JOIN THE EFFORT TO LICENSE NDs IN RHODE ISLAND</b></span></font><br />
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                                                            <div><strong></strong>
                                                            <p style="margin-bottom: 4.5pt;"><span><span style="font-size: 14px;">Submitted by M. Feibelman, ND<br />
                                                            President, Rhode Island Association of Naturopathic Physicians</span><br />
                                                            </span><img alt="" src="https://acam.site-ym.com/resource/resmgr/images/RIANP.jpg" style="left: 864.292px; width: 359px; height: 62px; float: right; margin: 5px;" /><span><span style="font-size: 14px;">
                                                            <br />
                                                            On behalf of the Rhode Island Association of Naturopathic Physicians (RIANP), I would like to invite you to join in our efforts to license naturopathic doctors in Rhode Island. As you may know,&nbsp;we are a small organization (in the smallest state) - and our licensure and legislative efforts here would be so much greater if we can increase our numbers and our collective voice.&nbsp;&nbsp;</span></span></p>
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                                                                        <p><span style="font-size: 14px;">Are you interested in helping RI join the other licensed New England states (MA, CT, VT, NH, and ME)? <br />
                                                                        <br />
                                                                        Would you consider practicing in Rhode Island if the state licensed NDs? <br />
                                                                        <br />
                                                                        We whole-heartedly invite and welcome you to contact the chairs of the Senate and House Health Committees and let your voice be heard. <strong>Taking action is easy and won't take more than a couple of minutes of your time.&nbsp;<br />
                                                                        <span style="font-size: 20px;"><a href="http://r20.rs6.net/tn.jsp?f=001fJfoE5AshTxqYkC0ga3VFgewRQzJK5LzRVao_dHd7uCSNW4yvlcQh0NgyoiTid2jsOMQYEPUiZJtOKvw2y_IMzQLXBaL3VhpFi1E4UC3sQEK6UWKFLuRb4vSIutxLR6nAVEwmxi-BbG5viZyCNttjx2RtVyJ3Yp6UIXUYP6JQpgQ0gVFhk_sJnljkEJS-6P3&amp;c=xG6Uu_b8--t7ygc1Vdq_jiCE9Qe3E6VRhe2ZI4wsMSHQ66fyqkePew==&amp;ch=_ga1U-iP2ruamfhrWloxWhEqh5dfup4QZB8GYfh_tXXrnYh-Wmen4A==" target="_blank" shape="rect" alt="http://www.naturopathic.org/lac#/55">CLICK HERE TO GET STARTED!</a></span></strong></span></p>
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                                                            <p style="margin-bottom: 4.5pt;"><span style="font-size: 14px;"><br />
                                                            Also, if you will be at the DC FLI this weekend (April 28-30) - the RIANP will be there selling "Naturopathic Physicians are Wicked Good Doctors" T-shirts, A-Z children's herb books, home-made herbal teas (one for adrenal/nervous system support, one for immune/warming support), tinctures, and salves - all to benefit the RIANP and our licensure efforts. <br />
                                                            Check out our table then.<br />
                                                            <br />
                                                            Lastly, please&nbsp;Like&nbsp;us on Facebook:&nbsp;</span><span style="font-size: 14px;"><a href="http://r20.rs6.net/tn.jsp?f=001fJfoE5AshTxqYkC0ga3VFgewRQzJK5LzRVao_dHd7uCSNW4yvlcQh0NgyoiTid2jfzq-nLzUx8TSxA8zWu3WFI-s5efM8_m7L8lBaVY47HkNwr5PlS2v7BTxFGd69fRXu9cFHZ3ZGVmg52CzOKb7dUBAQIH-OcdKU80RSrVIW2pjPvGZShiuPmKEaddCNDLmvFyptq5GYojpI9xl_tbSdg==&amp;c=xG6Uu_b8--t7ygc1Vdq_jiCE9Qe3E6VRhe2ZI4wsMSHQ66fyqkePew==&amp;ch=_ga1U-iP2ruamfhrWloxWhEqh5dfup4QZB8GYfh_tXXrnYh-Wmen4A==" target="_blank" shape="rect" alt="https://www.facebook.com/RINaturopathicAssociation/"><span><strong><span style="color: #0083a9;"><span style="text-decoration: underline;">Rhode Island Association of Naturopathic Physicians</span></span></strong></span></a></span><span style="font-size: 14px;">.<br />
                                                            <br />
                                                            If you have any questions, feel free&nbsp;to email us at&nbsp;</span><span style="font-size: 14px;"><a href="mailto:RINaturopaths@gmail.com" target="_blank" shape="rect"><span>RINaturopaths@gmail.com</span></a></span><span style="font-size: 14px;">.<br />
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<pubDate>Thu, 27 Apr 2017 19:16:34 GMT</pubDate>
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<title>ACAM ACTION ALERT: GIVE BIG to ACAM Education Foundation May 4-5</title>
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<pubDate>Tue, 25 Apr 2017 18:06:15 GMT</pubDate>
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<title>ACAM ACTION ALERT: Will FDA get off the sidelines to protect American children?</title>
<link>https://www.acam.org/news/news.asp?id=340152</link>
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                                                            <div><b>Will FDA get off the sidelines to protect American children?</b></div>
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                                                            <div><strong><span style="font-size: 14px;">Submitted by Charles G. Brown:&nbsp;President - World Alliance for Mercury-Free Dentistry<br />
                                                            <br />
                                                            </span></strong>
                                                            <p><span style="font-size: 14px;">In the dental amalgam arena, the U.S. Food and&nbsp;Drug Administration (FDA) prefers to sit and watch from the sidelines: &nbsp;</span></p>
                                                            <ul>
                                                                <li style="margin-left: 0in;"><span style="font-size: 14px;">Scientists on FDA’s own advisory panels told FDA that mercury dental fillings pose a risk to children and other sensitive populations. &nbsp;As one expert explained in no uncertain terms, “definitely not in pregnant women and definitely not in those below 6 years of age.” &nbsp;But FDA just sat and watched.</span></li>
                                                            </ul>
                                                            <ul>
                                                                <li style="margin-left: 0in;"><span style="font-size: 14px;">Amalgam manufacturers in other countries warned against amalgam use in children and pregnant women. &nbsp;They cautioned that amalgam is “not suitable for use in children and during pregnancy” in the United Kingdom, nor is it appropriate for children&nbsp;and women of childbearing age in Germany. &nbsp;But FDA just sat and watched.</span></li>
                                                            </ul>
                                                            <ul>
                                                                <li style="margin-left: 0in;"><span style="font-size: 14px;">Other governments implemented policies that discourage, restrict, or prohibit the use of amalgam in children, pregnant women, and other sensitive populations. &nbsp;Sweden, Denmark, Finland, Germany, Canada, Australia, the United Kingdom, and Norway all took&nbsp;steps to protect their children from dental mercury. &nbsp;But FDA just sat and watched.</span></li>
                                                            </ul>
                                                            <p style="text-align: center;"><span style="font-size: 20px;"><strong style="color: #000000; text-align: center;"><span style="color: #0083a9;"><a href="http://toxicteeth.us1.list-manage.com/track/click?u=27e2f2d4d51d0311acb2ec134&amp;id=b341746b3a&amp;e=4e7e659181" target="_blank"><span style="text-decoration: underline;">Click here to sign our online petition telling FDA to act!*</span></a></span></strong></span></p>
                                                            <p><span style="font-size: 14px;">Now comes an event that FDA cannot just sit and watch: the European Union has voted to ban amalgam for children under 15, pregnant women, and breastfeeding mothers in response to the game-changing Minamata Convention on Mercury. &nbsp;<br />
                                                            <br />
                                                            The European Union is FDA’s chief rival for supremacy as the world’s leading health regulator. &nbsp;As FDA has boasted, “Under the EU system, the public are being used as guinea pigs….We don't use our people as guinea pigs in the U.S.”<br />
                                                            <br />
                                                            Really? &nbsp;<br />
                                                            <br />
                                                            In its amalgam rule, FDA itself concedes that “The developing neurological systems in fetuses and young children may be more sensitive to the neurotoxic effects of mercury vapor.” &nbsp;FDA also admits that there is no scientific proof that amalgam is safe for these populations: “Very limited to no clinical information is available regarding long-term health outcomes in pregnant women and their developing fetuses, and children under the age of six, including infants who are breastfed.”<br />
                                                            <br />
                                                            Yet FDA promotes subjecting&nbsp;children to this risky, unproven mercury product like&nbsp;guinea pigs....while the European Union is withdrawing its children from&nbsp;this toxic experiment.&nbsp;<br />
                                                            <br />
                                                            So Consumers for Dental Choice is challenging FDA to catch up with the European Union – and the many scientists, manufacturers, and other governments that already take steps to keep amalgam out of children’s mouths. &nbsp;We’ve filed a formal citizen petition, but FDA needs to hear from you too! &nbsp;Here’s how you can send a message to FDA:&nbsp;<br />
                                                            &nbsp;</span></p>
                                                            <p style="text-align: center;"><span style="font-size: 20px;"><strong><a href="http://toxicteeth.us1.list-manage.com/track/click?u=27e2f2d4d51d0311acb2ec134&amp;id=b341746b3a&amp;e=4e7e659181" target="_blank"><span style="color: #0083a9;"><span><span style="text-decoration: underline;">Click here to sign our online petition telling FDA to act!*</span></span></span></a></strong></span></p>
                                                            <span style="font-size: 14px;"><strong><br />
                                                            FDA needs to stop sitting in the grandstands with the pro-mercury American Dental Association – it’s time to go to bat for America’s children.</strong></span><br />
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<pubDate>Tue, 11 Apr 2017 22:56:30 GMT</pubDate>
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<title>ACAM ACTION ALERT: The Next Big CAM Battle is Here and It&apos;s Ugly</title>
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                                                            <div><b>The Next Big CAM Battle is Here and It's Ugly</b></div>
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                                                            <div><strong><span style="font-size: 14px;"></span></strong>
                                                            <div id="rootDiv">
                                                            <div id="footerContainer" style="text-align: left;">Submitted by RickJaffe, Esq.<br />
                                                            <span style="color: #000000;"><a href="mailto:rickjaffeesquire@gmail.com"><span style="color: #0083a9;"><span style="text-decoration: underline;">rickjaffeesquire@gmail.com</span></span></a><br />
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                                                            <p><span style="font-size: 14px;">CAM or integrative medicine doctors have had their problems with the state medical boards. And CAM organizations have had their run-ins with governmental agencies. However, the groups have always survived in large part because they have had a steady income from membership dues and from their annual conferences, where their members learn the latest and greatest from their thought leaders. But the CAM organizations’ income stream is now in jeopardy, and thus so is their existence, based on what looks to be well-planned, systematic effort to put CAM groups out of business, and stop the dissemination information about CAM therapies.<br />
                                                            <br />
                                                            <strong>AND THAT MY FRIENDS IS A VERY BIG DEAL.</strong><br />
                                                            <br />
                                                            Here is what’s going on: For months, at least two CAM groups have been under review/ investigation by the primary private CME accrediting company, the ACCME (Accreditation Counsel for Continuing Medical Education). Recently, the ACCME has determined that a significant portion of the groups’ prior year’s CME courses does not meet various ACCME standards. ACCME is demanding that everyone involved in these courses be informed that:&nbsp;<br />
                                                            “they were presented invalid information….” and that the groups: “instruct them [everyone] to avoid making any clinical decisions for testing and/or treatment based on what was presented, and<br />
                                                            direct the registrants to accurate and valid sources of information for the problems or systems presented.”<br />
                                                            <br />
                                                            I should point out that this “incorrect” information came from some of the most accomplished, respected and published thought leaders/teachers in the CAM community. These folks have been giving CME courses without incident for decades.<br />
                                                            <br />
                                                            Further, in terms of future CME courses at their conferences, ACCME has informed these groups – and this is the key to understand what this is all about – that:<br />
                                                            <br />
                                                            “recommendations involving clinical medicine must be based on evidence that is accepted within the profession of medicine as adequate justification for their indications and contraindications in the care of patients and all patient care recommendations must conform to evidence emanating from guidelines and data that meet generally accepted standards of experimental design, data collection, and analysis.”<br />
                                                            <br />
                                                            In short, ACCME is trying to require these groups to only teach mainstream medicine! This is crazy and a huge deal!<br />
                                                            <br />
                                                            Furthermore, the effect on the members of these organizations who attended the conferences last year and who used these courses to satisfy their state CME requirements is unclear.<br />
                                                            <br />
                                                            I am not familiar with ACCME’s inner workings or guidelines, but it doesn’t seem out of the question that ACCME could contact state boards about these groups’ “noncompliance” and the retroactive withdrawal of CME credits. That could cause the state boards to retroactively hold the doctors non-CME compliant. I’m not saying that this will happen, but only that it’s a possibility. But I am saying that if the idea is to delegitimize CAM and cause problems for its practitioners, notifying the state boards would certainly advance that goal.<br />
                                                            <br />
                                                            A specialty interest group also gets the same treatment<br />
                                                            <br />
                                                            Beyond these two professional groups, a disease based group has recently been informed that its CME status for future conferences has been rescinded by its CME intermediary. The intermediary denies that it received any pressure or orders from ACCME.<br />
                                                            <br />
                                                            Three CAM groups which have previously received ACCME course certification without any undue problems who in the last few months have had their prior CME course approval rescinded and/or their future CME approval withdrawn or placed in serious doubt.<br />
                                                            Is this all a coincidence? Not a chance in hell.<br />
                                                            <br />
                                                            My guess is that more of the same has or is going to happen to other CAM groups.<br />
                                                            <br />
                                                            What to do?<br />
                                                            <br />
                                                            At this stage, these groups need information about what’s behind this campaign to deny CME credit and delegitimize CAM teachings.<br />
                                                            <br />
                                                            We need to get the word out to the CAM community.<br />
                                                            <br />
                                                            Why? Someone out there has to know something or know someone who knows something about how this came about, and who or what group is behind it. (My guess is that ACCME is the vehicle not the originator.) I think there is a smoking gun out there, and if we find it, we can probably reverse ACCME’s decision quickly, so my suggestion is that all the CAM groups and interested parties get the word out to search for the smoking gun.<br />
                                                            <br />
                                                            <strong>But let’s dig in to this and see if there is anything else that can be done. A logical place to start is:<br />
                                                            What exactly is the ACCME and what does it do?</strong><br />
                                                            <br />
                                                            I don’t have any special info on ACCME, but here is what it says about itself:<br />
                                                            <br />
                                                            “CME ACCREDITATION OF, BY, AND FOR THE PROFESSION OF MEDICINE.<br />
                                                            The ACCME was founded in 1981 in order to create a national accreditation system. It is the successor to the Liaison Committee on Continuing Medical Education and the American Medical Association’s Committee on Accreditation of Continuing Medical Education. The ACCME’s purpose is to oversee a voluntary, self-regulatory process for the accreditation of institutions that provide continuing medical education (CME) and develop rigorous standards to ensure that CME activities across the country are independent, free from commercial bias, based on valid content, and effective in meeting physicians’ learning and practice needs. The ACCME accreditation process is of, by, and for the profession of medicine.<br />
                                                            <br />
                                                            The ACCME’s founding and current member organizations are the American Board of Medical Specialties, the American Hospital Association, the American Medical Association, the Association of American Medical Colleges, the Association for Hospital Medical Education, the Council of Medical Specialty Societies, and the Federation of State Medical Boards of the United States.<br />
                                                            <br />
                                                            Throughout its history, the ACCME has been dedicated to maintaining a relevant and responsive accreditation system that supports CME as a strategic asset to US health care quality and safety initiatives.”<br />
                                                            <br />
                                                            Very noble and reassuring, isn’t it?<br />
                                                            <br />
                                                            Basically, it’s a bunch of health care trade associations, organizations in charge of medical education and specialization credentialing. (Ironically, the medical specialty societies are the reason it’s illegal for practitioners to advertise their CAM board certifications.) And last but not least is CAM’s long-time adversary, the Federation of State Medical Boards. So maybe not so reassuring.<br />
                                                            <br />
                                                            Did you know that the ACCME is accountable to the Public? Yea, just ask them and they will tell you so.<br />
                                                            <br />
                                                            Here is what it says about that:<br />
                                                            <br />
                                                            “Accountability to the Public<br />
                                                            The ACCME is accountable to the public for setting and maintaining accreditation requirements that are designed to ensure that CME accredited within the ACCME system is based on valid content, is free from commercial influence or bias, and contributes to the quality and safety of health care. As the US health care system continues to evolve, the ACCME will respond by making changes to its requirements or processes that are necessary to assure that CME serves the best interests of the public.<br />
                                                            <br />
                                                            I’m still not clear exactly how it is accountable to the public, and nothing in its web site gives any further elucidation.I do have a couple ideas of how it might actually be made accountable to the public.<br />
                                                            <br />
                                                            <strong>Some basic facts:</strong><br />
                                                            <br />
                                                            It’s obviously a matter of individual state law what type of courses a state medical board will accept as acceptable CME. The ACCME might be the primary CME credentialer, but it is not the only one. For example, here is the Texas law regarding CME accreditation: It’s Board Rule 166.2 and it requires:<br />
                                                            <br />
                                                            (1) At least 24 credits every 24 months are to be from formal courses that are:<br />
                                                            (A) designated for AMA/PRA Category 1 credit by a CME sponsor accredited by the Accreditation Council for Continuing Medical Education or a state medical society recognized by the Committee for Review and Recognition of the Accreditation Council for Continuing Medical Education;<br />
                                                            (B) approved for prescribed credit by the American Academy of Family Physicians;<br />
                                                            (C) designated for AOA Category 1-A credit required for osteopathic physicians by an accredited CME sponsor approved by the American Osteopathic Association;<br />
                                                            (D) approved by the Texas Medical Association based on standards established by the AMA for its Physician’s Recognition Award; or<br />
                                                            (E) approved by the board for medical ethics and/or professional responsibility courses only.”<br />
                                                            <br />
                                                            Other states have similar types of CME rules. The bottom line is that ACCME is a very important source of state approved CME accreditation, especially for everyone other than the major national and state medical trade groups. But there’s another way of looking at it. Without a state accepting its accreditation, ACCME doesn’t have much of a purpose or job.<br />
                                                            <br />
                                                            <strong>What About CAM laws?</strong><br />
                                                            <br />
                                                            Texas, California and some other states recognize the rights of patients to receive CAM therapies. Texas, for example, provides that:<br />
                                                            <br />
                                                            “The purpose of this chapter [Texas Board Rule Chapter 200] is to recognize that physicians should be allowed a reasonable and responsible degree of latitude in the kinds of therapies they offer their patients. The Board also recognizes that patients have a right to seek complementary and alternative therapies.” (Board Rule 200.1)<br />
                                                            <br />
                                                            <strong>What are CAM therapies in Texas?</strong><br />
                                                            <br />
                                                            “(1) Complementary and Alternative Medicine–Those health care methods of diagnosis, treatment, or interventions that are not acknowledged to be conventional but that may be offered by some licensed physicians in addition to, or as an alternative to, conventional medicine, and that provide a reasonable potential for therapeutic gain in a patient’s medical condition and that are not reasonably outweighed by the risk of such methods.”<br />
                                                            <br />
                                                            Convention medicine is defined as “Those health care methods of diagnosis, treatment, or interventions that are offered by most licensed physicians as generally accepted methods of routine practice, based upon medical training, experience and review of the peer reviewed scientific literature.”<br />
                                                            (California has a similar definition of CAM at B&amp;C code 2234.1)<br />
                                                            <br />
                                                            So, Texas gives practitioners the right to provide non-conventional, not generally accepted therapies to patients, and patients have the right to receive these CAM or non-conventional therapies.<br />
                                                            <br />
                                                            But even though Texas docs can provide CAM or non-standard therapies to Texas patients, ACCME now takes the position that Texas physicians can’t obtain CME credit for learning about these Texas sanctioned treatments. How can the ACCME be acting consistent with Texas law by its insistence that CAM medical groups can only teach:<br />
                                                            <br />
                                                            “recommendations involving clinical medicine must be based on evidence that is accepted within the profession of medicine as adequate justification for their indications and contraindications in the care of patients and all patient care recommendations must conform to evidence emanating from guidelines and data that meet generally accepted standards of experimental design, data collection, and analysis.”<br />
                                                            <br />
                                                            My view is that ACCME’s position is inconsistent, if not in violation of the Texas CAM Rule (and the California CAM statute) and probably every other state that has a CAM law.<br />
                                                            <br />
                                                            <strong>So, what to do?</strong><br />
                                                            <br />
                                                            Complain to ACCME? Won’t hurt, but it won’t help. It’s doing what it’s doing intentionally, and some external pressure has to be brought forth.<br />
                                                            <br />
                                                            Complain to the boards? Maybe, but it would take a lot of complaints.<br />
                                                            <br />
                                                            In all the big CAM states like Texas and California, I know there are legislators who are pro CAM. My suggestion would be to identify who they are (not hard in Texas). I think the boards in a few of these states need to hear from some legislators about how ACCME is undercutting board rules (in Texas) or the CAM statutes (like in California).<br />
                                                            <br />
                                                            These legislators should copy ACCME on their concerns expressed to the boards. If one of them is on a legislative health committee, even better. Better still would be for a couple states to start an investigation on ACCME’s motives. Maybe even an invitation to appear at a specially called hearing. Legislators can hold hearings for all kinds of reasons. So can federal legislators. I think with all the politically connected CAM docs out there, mulitipled by their politically connected patients, well I think there’s a heap of trouble that could be stirred up for ACCME.<br />
                                                            <br />
                                                            It doesn’t have to happen in every state, or even many states, just a couple of the big ones. The story is going to get out, and questions are going to be raised. The widespread dissemination of ACCME’s action might even turn-up that smoking gun I mentioned earlier. And once the nefarious motive and scope of the conspiracy publicly surfaces, I think ACCME will be forced to rescind its actions. So, we need to shine some light on these jokers.<br />
                                                            <br />
                                                            This could all happen pretty quickly if there’s a big enough outreach to the CAM community.<br />
                                                            Something to think about anyway.<br />
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<pubDate>Wed, 15 Mar 2017 16:15:08 GMT</pubDate>
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<title>ACAM Action Alert: Chelation &amp; TACT 2 Featured on ABC</title>
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                                                            <div><b>CHELATION &amp; TACT 2 FEATURED ON ABC NEWS SEGEMENT</b></div>
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                                                            <div><strong>Tune in tonight, Friday, February 3rd,</strong> to Channel 6 Action News at 11pm &nbsp;(ABC network Philadelphia) and watch Dr. Allan Magaziner of the Magaziner Center for Wellness discuss an important clinical trial to assess the effectiveness of chelation therapy to reduce the risk of future heart attack, stroke or sudden death in diabetics who are over 50 and have had a prior heart attack. Dr. Magaziner is actively recruiting patients for TACT 2, a federally funded, nationwide trial.&nbsp;<br />
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                                                            When analyzing the results of the first Trial to Assess Chelation Therapy (TACT), researchers found that a subgroup of patients with diabetes who received EDTA chelation had fewer cardiovascular events than patients who did not receive EDTA chelation. This was not what researchers were expecting to find.&nbsp;<br />
                                                            <br />
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                                                            <div><span style="color:#36495f;font-family:Arial, sans-serif;">Remarkably, there was a 43% reduction in mortality and a 51% reduction in overall cardiac events which included heart attack, stroke or sudden death in the diabetics who were treated with chelation therapy. This is quite a dramatic turnaround!</span></div>
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                                                            <div>For more information on TACT 2: <a style="color:blue;text-decoration:underline;" track="on" shape="rect" href="http://r20.rs6.net/tn.jsp?t=i5vzswzab.0.0.rpefi4sab.0&amp;id=preview&amp;r=3&amp;p=http%3A%2F%2Ftact2.org%2F" linktype="1" alt="http://tact2.org/" target="_blank">CLICK HERE</a></div>
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<pubDate>Fri, 3 Feb 2017 20:45:41 GMT</pubDate>
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