Monday, June 22, 2015
Comments to the FDA: Homeopathy and Health Freedom
COMMENTS TO THE FDA RE: HOMEOPATHY
[FDA has decided to "review" the regulation of Homeopathy. That's a bad idea. Here are my comments why, posted on the FDA Docket. RF]
I am President of the Institute for Health Research, a recognized NGO -- www.InHeRe.org, and Vice-President of Natural Solutions Foundation, a recognized NGO -- www.GlobalhealthFreedom.org.
I have been trained in both law (licensed to practice in NJ from 1971 through 2006) and homeopathy (Five Elements Center, Mountainside, NJ and Hololinguistic Institute, Toronto). I have personally experienced, over the past five decades, extraordinary examples of traditional homeopathy supporting homeostasis and a healthy status.
I urge FDA to leave traditional homeopathy alone. The best regulatory decision the Agency could make would be to do nothing to disturb the grandfathered status of homeopathy. Congress has enacted a regulatory regime based on permitting traditional homeopathic remedies to be certified by the HPUS. FDA does not have authority to vary that enactment. To do so would be to restrict important privacy and associational interests of members of the public.
State v Biggs (46 SE Reporter 401, 1903): the North Carolina Supreme Court dealt with a person who was advising people as to diet, and administering massage, baths and physical culture. In the Biggs case, the defendant "advertised himself as a 'nonmedical physician'...[and] held himself out to the public to cure disease by 'a system of drugless healing'..." p.401.
That Court held that there could be no "state system of healing" p.402 and while "Those who wish to be treated by practitioners of medicine and surgery had the guaranty that such practitioners had been duly examined...those who had faith in treatment by methods not included in the 'practice of medicine and surgery' as usually understood, had reserved to them the right to practice their faith and be treated, if they chose, by those who openly and avowedly did not use either surgery or drugs in the treatment of diseases..." p.402.
Further, at p.405: "Medicine is an experimental, not an exact science. All the law can do is to regulate and safeguard the use of powerful and dangerous remedies, like the knife and drugs, but it cannot forbid dispensing with them. When the Master, who was himself called the Good Physician, was told that other than his followers were casting out devils and curing diseases, he said, 'Forbid them not.'"
As recently as 2002 the United States Supreme Court reminded FDA, (Thompson v. Western States Medical Center, 535 U.S. 357) , "If the First Amendment means anything, it means that regulating speech must be a last - not first - resort. *** We have previously rejected the notion that the Government has an interest in preventing the dissemination of truthful commercial information in order to prevent members of the public from making bad decisions with the information. *** Even if the Government did argue that it had an interest in preventing misleading advertisements, this interest could be satisfied by the far less restrictive alternative of requiring each compounded drug to be labeled with a warning that the drug had not undergone FDA testing and that its risks were unknown."
FDA does not have authority from Congress to interfere with traditional homeopathy, nor does Congress have authority to permit such interference. Individuals have the right, under international humanitarian law binding on the United States, of Informed Consent to exercise their Freedom of Choice in health care without government burdening that fundamental right.
Comment No. 1jz-8jk4-ukxz in Docket FDA-2015-N-0540
http://www.regulations.gov/#!documentDetail;D=FDA-2015-N-0540-0001
Friday, December 14, 2007
Comments filed with FDA on AERs
Filed 7:15 PM - Comment Number: 215742
Natural Solutions Foundation
www.healthfreedomusa.org
December 14, 2007
To: Food and Drug Administration
Docket No. 2007D-0388
“Draft Guidance for Industry: Questions
and Answers Regarding Adverse Event
Reporting…”
We recommend that all [dietary supplement] AERs include clear indications of any and all prescription and over the counter drugs being used by the person involved. We believe that often supposed “adverse reactions” to nutrients are actually drug – nutrient interactions or nutrient depletions caused by drugs, wherein normal structure and function are changed to the detriment of the person.
The Foundation joins in Maury Silverman’s comments below, including urging that all drugs be labeled to indicate the nutrient depletions they cause, so that truthful AERs can be filed.
For the Natural Solutions Foundation
Ralph Fucetola JD, Trustee
http://vitaminlawyerhealthfreedom.blogspot.com
Mr. Silverman’s Comments
http://www.healthfreedomusa.org/index.php/?p=475THANK YOU MAURY!
Thursday, September 27, 2007
Does FDA really want public comments?
"Follow the instructions for submitting comments on the agency Web site.
"Written Submissions: Submit written submissions in the following ways:
"FAX: 301-827-6870.
"Mail/Hand delivery/Courier [For paper, disk, or CD-ROM> submissions]: Division of Dockets Management (HFA-305), Food and Drug Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852.
"To ensure more timely processing of comments, FDA is no longer accepting comments submitted to the agency by e-mail. FDA encourages you to continue to submit electronic comments by using the Federal eRulemaking Portal or the agency Web site...
"Instructions: All submissions received must include the agency name and Docket No(s). and/or RIN for this rulemaking. All comments received may be posted without change to http://www.fda.gov/ohrms/dockets/default.htm> , including any personal information provided...
"For access to the docket to read background documents or comments> received, go to http://www.fda.gov/ohrms/dockets/default.htm and insert the docket number(s), found in brackets in the heading of this document, into the "Search'' box and follow the prompts and/or go to the Division of Dockets Management, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852..."
Does the FDA really want public comments? The easiest way for the public to comment is by email -- this route has now be cut off.
Dr. Laibow commented to me: "When Natural Solutions Foundation was encouraging over 200,000 people to comment to FDA on its anti-CAM guidane, the Supervisor of theReceiver of Dockets Office told me that the FDA does NOT tally written comments so this is yet another abuse of FDA authority to stifle public input..." www.healthfreedomusa.org
Wednesday, August 15, 2007
FDA Comment Page Open Again for Health Claims Guidance
"Your Voice Can Be Heard Again!!!
"Good news! This is Kathy Greene, Dr. Rima's assistant.
"Our Natural Solutions Foundation media director, Tom Cowles, told you last week about the roadblocks that had been set up to prevent you from telling the FDA to leave our supplements alone. I've been handling many emails from people who couldn't get through to the FDA but want their voices heard. The great news is we just got a new link to the draft FDA Health Claims Guidance for your comments. The comment period ends in just a few weeks, so we have to act fast! Tell your friends! Tell your neighbors!
"PLEASE FORWARD THIS EMAIL FAR AND WIDE!!!
"The new FDA guidance will make it much harder for vitamin companies to tell you about the health benefits of nutrients.
"ACTION ITEM! Use link below to voice your concern about regulating our supplements!
Click Here to Submit your Comment to the FDA (Full links at bottom of email)
"Many thanks goes to Health Freedom supporter, Marlina, for discovering where the comment page was moved to! Click here to see her Forum page for some great suggestions!
General Stubblebine and Dr. Laibow will be back in Washington DC in about a week, so we want to give them all the ammunition they need: HUNDREDS OF THOUSANDS OF MESSAGES TO FDA AND CONGRESS! So, as the General says, get your mouse ready! Aim! Fire!
Click Here to Submit your Comment to the FDA (Full links at bottom of email)
"Thank you so much for making the Health Freedom movement the powerful expression of citizen concern it has become. I can remember licking stamps and demonstrating at local FDA offices back in 1993 and 1994 to convince Congress to pass DSHEA, the law that lets us talk freely about nutrients. Now it's much easier: all you need do is click your mouse! And it would really be nice if you "double clicked:" once to send your message and then, a second time, right here to help us with your generous donation. We volunteer our time so your voice can be heard, but we must cover the Foundation's expenses, so your voice will have the power it deserves. Please give generously, and click, click!
"Yours in health and freedom,
Kathy Greene
Assistant to Dr. Rima
"FDA Comment Link:
http://www.accessdata.fda.gov/scripts/oc/dockets/comments/getDocketInfo.cfm?EC_DOCUMENT_ID=1640&SORT=&MAXROWS=15&START=106&CID=&AGENCY=FDA
