Successful Rehab Blog

September 17, 2009

A Comment on Pregnant Mothers Who Use Drugs and Alcohol

 

Are you or someone you know expecting a baby?

 

Having a baby is a wonderful experience and should be enjoyed to the fullest extent.  Children are the future of Mankind, and have the right to be born healthy and strong, and to grow-up being cared for well by a stable and loving family.

 

Unfortunately, many women drink and use drugs while pregnant, thus endangering the life and health of both themselves and their unborn child. There is no greater heartbreak than to bring a baby into this world with mental or physical damage which could have been prevented by abstaining from the use, or abuse, of alcohol or drugs during pregnancy.

Many babies born to mothers who drink suffer from Fetal Alcohol Syndrome, as well as premature births with low birthweight, and mental retardation. Drinking and using drugs while pregnant can also lead to death for both the mother and her baby.

 

No amount of a drug or alcohol is “safe” for an unborn baby. Due to the fact that a baby’s metabolism is slower than that of an adult, the alcohol or drug remains in the baby’s system longer, potentially causing damage and possible death.

 

 

If you, or someone you know is abusing drugs or alcohol, please call us.  At  SuccessfulRehabServices we have  trained professionals who are here to answer any questions you may have about drugs and alcohol, and to refer you to the best drug rehabilitation services nationwide. You can call us on our toll-free Addiction Helpline at 1-877-873-8532, or visit our website at www.successfulrehabservices.org for more information.

 

There is hope.

 

It is possible to live a drug-free life…

 

 

2009  SuccessfulRehabServices

 

 

 

 

 

 

September 16, 2009

No More ADHD

Filed under: Education — admin @ 10:23 pm

New Video & Blog “No More ADHD”

Dr. Mary Ann Block
Click here to watch video

More than 4 million children in the U.S. alone have been labeled with ADHD and put on drugs documented by the FDA to cause tics, stunted growth, heart attack, stroke and sudden death.  The U.S. Drug Enforcement Administration (DEA) classifies Ritalin, Concerta and other ADHD drugs in the same class of highly addictive drugs as cocaine, morphine and opium.

Psychiatric drugging of kids is big business.  ADHD drugs sales alone generate $3.1 billion a year.  Parents need to be informed that not only is the diagnoses of ADHD completely subjective (a child fidgets, stares out the window, forgets his homework and he can be diagnosed ADHD) but that there are non-drug solutions for solving children’s problems of behavior, attention and learning.  Parents have a right to this information.

Dr. Mary Ann Block, Medical Director & Founder of the Block Center, and author of No More ADHD is our featured blog/video interview this week: click here.

September 8, 2009

Psychiatric Drug Side Effects Search Engine

Filed under: Uncategorized — admin @ 12:12 pm

Psychiatric Drug Side Effects Search Engine

July 1, 2009

The Road Back

Filed under: Uncategorized — admin @ 7:57 am
 
The Road Back  

 
This newsletter comes with a warm smile on my face for people taking a benzodiazepine or anticonvulsant. More relief from side effects is possible!
 
As stated in the book, How to Get Off Psychiatric Drugs Safely, this program is a work in progress, and I do hope it remains that way.
 
Before sharing with all of you the recent breakthrough with benzodiazepines and anticonvulsants, I want to go back to 1999 and work forward to the existing program. If you want to skip all of this and go directly to the break through, move down the page until you see June 30 2009.
 
At the end of the newsletter, I answer the question received a lot, “Do I Need to Take All of the Supplements?”
 
In 1999, it was evident a tapering program needed to be developed for psychoactive medications and NONE were in existence at that time.
 
How This All Started
 
In early 1999, I was talking with my wife and the subject turned to ADHD and Ritalin for some reason. My family and I had never been exposed to psychoactive medication. My wife mentioned in our conversation that in 10 states here in America, if a teacher felt your child had ADHD and wanted your child put on Ritalin, if you refused as a parent to allow this, the state could come into your home and take away your child and charge the parents with child neglect.
 
I looked at her and said “no way, not in America.” I went on the Internet and found the laws that were in place in those states and was shocked. I have children and at the time a child about to enter grade school, so it hit me between the eyes rather hard.
 
I felt I needed to do something about this but did not have a clue where to start. I felt if I did not know this there had to be millions of parents just like me that were in the dark.
 
I decided to learn how to make a web site and just put information on it that I was finding. In the next few months the search engines found my site attractive I guess because the site was now at the top of the first page when anyone did a search on a dug name. Emails began to pour in. Thousands a day at times.
 
Most people were in need of help to get off the drugs and stated, “they wished they knew this information before they went on the drug but how do I get off this stuff.” I sent some e-mails to physicians as well as some telephone calls to a few I had met over the years but I kept researching. This turned into a 14 hour a day project.
 
By the time the physicians responded to my request with what they would do to get a person off a psychoactive medication, I had educated myself at least to the point of knowing what to not do. I found all of the physicians were creating more harm than help with their approach and sent them a reply back that I could not link to their site and detailed why. All of the physicians responded back one more time with,”My God, you are right.”
 
I could not turn my back on what I knew needed to be done for people wanting to get off their medication. Believe me, I would have preferred to play golf or go fishing but for whatever reason I stayed at trying to unravel this jigsaw puzzle. 
 
Sequence of events:
 
1999
A gradual reduction of medications was laid out to allow a 10% reduction of the medication. Reductions were every 14 days.
 
With this approach, around ½ of the people we worked with could get off the medication but they suffered tremendously. The ½ that could not get off the medication suffered each time they tried to lower the dosage and eventually had to go back up to their original dosage.
 
It was very evident something else needed to be tried.
 
2000
We began using a whey protein called Immunocal in an attempt to reduce side effects before a person began lowering their medication. Immunocal was used during the medication reduction as well to help with any withdrawal side effects.
 
Immunocal raises an antioxidant called glutathione. The success rate was better than nothing but limited and very specific to a certain class of drug and to an exact set of side effects.
 
2001
During 2001, we tried a different whey protein that was stronger than Immunocal but the taste let a little to be desired and it was actually too strong for this usage.
 
Omega 3 fish oil was introduced to the program as well in 2001. At that time the fish oil was recommended for help with depression but not brain zaps as it was in a later year.
 
I began researching the ability to predict adverse reactions using a DNA test.
 
2002
This year was spent doing DNA research.
 
2003
I had the opportunity to meet with an attorney and his client a few weeks before they went to trial against Eli Lilly with a Prozac case. The attorney was handed a packet of information regarding human DNA and the ability to predict adverse reactions to psychoactive medication.
When this DNA evidence was introduced in court, the Eli Lilly attorneys instantly asked to meet the judge in his chambers and they settled on the spot. The next day the attorney filed several new lawsuits with DNA and the prediction of adverse reactions as the claim.
 
2004
I wanted more information on DNA drug reaction testing and I wanted to see if there was a use for the test results being of use for tapering off the drugs.
 
I started a DNA testing company called Advanced DNA Testing and began offering a DNA drug reaction test. This test is excellent to do BEFORE taking a medication but it gave zero help with a tapering program.
 
I then moved to doing a different DNA test to see how well the population at large could assimilate nutrients from their food as well as vitamins. This widely opened the door for future changes with the tapering program and with this new information, the success rate of people trying to get off their medication began to finally climb.
 
The use of young green barley juice, along with a powdered carrot juice and an additional barley called Aktivated Barley was introduced to the program. The success rate of the program began to climb even further.
 
The young green barley with the other mixture included would also help the body make glutathione. The Immunocal recommendation was dropped at this time.
 
The current Body Calm liquid was introduced in 2004 as well to assist with daytime anxiety and sleep. Up until our use of the liquid cherry product for anxiety and sleep, no one else had ever used it for this. This cherry was only used by physicians for treating gout.
 
A specific type of Omega 3 fish oil was introduced this year as well. The need for a fish oil that is higher in EPA than DHA was determined and once introduced, the success rate made another nice increase.
 
The year 2004 ended with an acknowledgement of sort from the acting head of the FDA. He gave a press release and stated his recommendation that physicians begin giving a DNA drug reaction test before they prescribe heart medication, cancer medication or psychoactive medication.
 
2005
This was the first year of training physicians and psychiatrists how to get patients off psychoactive medication and how to use DNA testing in their practice.
 
To make it easier for people to use the barley’s and the carrot, reduce the cost and to standardize the formula, Power Barley Formula was created.
 
At the urging of a few people I quickly put a paperback book together and self published. My own feeling is the book left a lot out of the content and should never have been published.
 
During 2005, I also began training other individuals or companies how to use the program.
 
2005 was a rather distracting year altogether and little progress was made with improvement of the program. Some of the people I trained broke a signed non-disclosure agreement and took parts of what I was currently doing and what I had used in the past and created their own tapering program.
 
The problem they have to this date is they only heard the good things I had to say about the whey protein Immunocal. I never told them what they needed to watch out for.
 
So, in your travels on the Internet, if you run into some psychoactive medication tapering program that uses Immunocal, a cherry product for anxiety or sleep, an Omega 3 fish oil, glutathione or a DNA drug reaction test, you found them!
 
I received a Christmas gift from the FDA on Christmas Eve. The FDA announced any company that manufactured a barley product that was high enough in soluble fiber could make it health claim that it would help prevent heart disease. If this product would not have been formulated as it was the fiber would have been too low to qualify. At that time in 2005, I was the only one with a barley product that could make the health claim.
 
I knew the Power Barley Formula would also be good for the heart but I did not know how much benefit.
 
2006
Additional advances needed to be made for people with daytime anxiety and insomnia. The liquid cherry had worked better than expected for this but there was still a lot of room for improvement. I had a powered cherry extract made and sent it to a doctor to use with some of his patients. The doctor called me in a few days with staggering results. The product is called Body Calm.
 
The patients he could never quite get over the hump now had no anxiety and their sleep improved dramatically. Some of the patients responded to 1 capsule, while a few others required 3 capsules for complete relief.
 
Essential Protein Formula came as a big surprise for me with its effect on anxiety and insomnia. The product was originally formulated for weight loss. Many people taking an antidepressant begin to gain weight overnight and I wanted to find a solution for this.
 
People taking the Essential Protein Formula began stating their daytime anxiety improved and their sleep improved as well once they started to use the Essential Protein Formula. People taking a benzodiazepine are so sensitive to things I felt this might really work for them. It proved to be the case and as well for people taking an antidepressant or antipsychotic.
 
During 2006, I began writing How to Get Off Psychiatric Drugs Safely and every time I was nearing completion a new discovery was made and the book would go back to square one again.
 
2007
Body Calm Supreme was introduced in 2007 for additional help with daytime anxiety and insomnia. I found clinical trials where a specific herb, passionflower, was used successfully for benzodiazepine withdrawal as well as for alcohol and other drugs. I formulated a passionflower to closely match the type used in the clinical trials and began trying it with people that were still having a difficult time with side effects.
 
The positive results were over night and shortly thereafter, the Body Calm Supreme became part of the program.
 
A major U.S. university began using the existing book, How to Get Off Psychiatric Drugs Safely, as part of their doctoral program for pharmacists.
 
2008
By the spring of this year, more of a separation took place between the pre-tapers used if a person had anxiety or fatigue as a main issue.
 
Knowing the specific success I had with Immunocal years earlier, I added a product called RenewPro to the program if a person has anxiety or insomnia. RenewPro helps create intracellular glutathione naturally and is a whey concentrate, not a whey isolate. I found the successful clinical trials run with Immunocal were with a whey concentrate but Immunocal is now a whey isolate. Difference of night and day.
 
Calcium has been a continual problem with people with anxiety. I first discovered in 2005, by process of elimination, that calcium was aggravating the anxiety in people, especially if they were taking a benzodiazepine.
 
I finally located which cells in the brain were creating the problem and created a calcium, magnesium and vitamin D3 that would relieve the stored calcium creating the problem. I now have a method of use patent for this and the calcium product made is called CalesiumD. Calcium was not the problem but the type of calcium used as well as the percentage of magnesium and D3 is all that needed to be formulated.
 
Don’t let anyone tell you all calcium creates anxiety and you can’t use it. They just do not understand what is happened within the body.
 
To further assist with calcium absorption, a product called Calsorption was introduced. This product will help with calcium absorption by as much as 28%.
 
With the discovery of Interleukin-2 and Interleukin-6, the tapering program made further advances. Interleukin-2 is a protein found in the immune system and this Interleukin-2, if too low will induce anxiety and insomnia.
 
Interleukin-6 is a marker for inflammation in the body. If Interleukin-6 is too high a person WILL begin to have depression.
 
Figuring out how to lower and or raise these Interleukins with people using psychoactive medication resulted in another method of use patent.
 
Beta 1, 3-D Glucan was introduced to raise Interleukin-2.
 
CLA and a specific blend of a probiotic was introduced to help lower Interleukin-6.
 
To get the full effect from the RenewPro a vitamin C and vitamin E needed to be used. A natural vitamin C was introduced as well as a vitamin E. We had recommended people use a vitamin E for years but it was not until 2008 that we really defined what vitamin E to use. It seems vitamin E is often viewed as just some vitamin and vitamin E is just vitamin E. I was wrong. The brand we only recommend for vitamin E is Unique E.
 
2009
The fourth edition of How to Get Off Psychiatric Drugs Safely has finally been published and has been available on Amazon.com and now on Target.com. An agreement has been signed recently with a major book distributor and all books will be available in major bookstores within the next 60 days. They also will provide the books throughout Europe in various languages.
 
I released a weight loss book titled, Lose the Weight Caused by Antidepressants the middle of June. A bit of my research during the early part of 2009 has been in this area. Much to my surprise, this little 52-page book now outsells The South Beach Diet, Kevin Truedeau’s weight loss book and nearly all other weight loss books on Amazon.com and the Target store. 
 
June 30 2009
I feel this next break though is of the same degree with the introduction of Body Calm Supreme for anxiety and insomnia, if not more.
 
If someone is taking a benzodiazepine or anticonvulsant medication, his or her body will be grossly depleted of a B vitamin called Biotin. A multitude of clinical trials confirms this. Biotin is known as vitamin H and as vitamin B7. Unlike some other B vitamins, biotin does not create anxiety or hyperness. It is rare for a person to be deficient in biotin normally but that is not the case if long-term use of an anticonvulsant or benzodiazepine is the case.
 
Your physician can do a blood test for biotin levels as well as check the level of organic acids excreted to confirm the deficiency.
 
Symptoms of biotin deficiency:
 
Pain or tingling in extremities
Appetite decreased
Hair loss
Absence or loss of pigment in hair
Fatty liver
Kidney problems
Skin rash
Seizures
Depression
Scaly red rash around nose or eyes
Fatigue
Hallucinations
Problem with insulin
 
We have been using biotin now with people for the past few months that are or were taking a benzodiazepine or anticonvulsant and the fast results have been staggering.
 
How Much Biotin to Take
 
There are no know side effects to biotin and if your body receives more than it needs it will just eliminate any excess.
 
We have started everyone at 5,000 mcg in the morning and after 3 days if no major change or only a slight improvement increased the biotin to 5,000 mcg in the morning and 5,000 mcg in the afternoon.
 
Increases by an additional 5,000 mcg have been beneficial to get rid of the last bit of what a person was feeling. We have had people take as much as 20,000 mcg in the morning and 20,000 mcg in the afternoon with no side effects and only positive results.
 
Again, relief from what was going on with the people was very fast. I want to make a statement here to ensure there is no confusion that we are treating or curing a disease. If a person takes biotin and feel better after they do, they were only low in biotin, no disease or illness could have been present.
 
As always we strive to only recommend quality nutritional products. We have had a biotin made at a facility that is approved to manufacture drugs by the FDA if they chose to do so (they do not), the facility is regularly inspected by an independent 3rd party to ensure they maintain Good manufacturing Practices and they have also achieved the high standard of ISO 9000 certification and are approved in Europe. The facility is in the United States and is licensed by the state of California.
 
TRB Health (www.trbhealth.com) carries the biotin recommended. You can click here and go directly to the biotin page on their site.
 
Notice: Using biotin as described, along with an anticonvulsant or benzodiazepine or after discontinuation of an anticonvulsant or benzodiazepine is a patent pending method of use. Physicians or other providers must sign a licensing agreement before using.
 
Do I Need to Take All of the Supplements?
 
No you do not.
 
The full line of supplements in this program were included to handle specific side effects that may take place when tapering off psychoactive medication. As you read through the last 10 years of this program, you will notice not all supplements were used throughout. We are trying to continually increase the success rate and have as a major goal to develop a program that will eliminate and or stop all side effects from ever occurring. The inclusion of biotin as well as the other supplements leads to that goal.
 
If budget is a problem, I recommend:
 
You would take the supplements suggested below exactly as it reads in How to get Off Psychiatric Drugs Safely.
 
Benzodiazepines - Biotin, Body Calm, Beta 1, 3-D Glucan and Body Calm Supreme. Anxiety, insomnia and many of the effects associated with being deficient in biotin will probably be your main concerns. Adding the probiotic Supreme will be a good idea if in your budget.
 
Antidepressants (with anxiety insomnia)- Body Calm, Body Calm Supreme, Beta 1, 3-D Glucan, Probiotic Supreme and Essential Protein Formula. Before you start to lower the antidepressant you will need the Ultimate Omega 3 and Unique E.
 
Antidepressants (with fatigue) - Power Barley Formula, Ultimate Omega 3 and Unique E.
 
Antipsychotics - Body Calm, Body Calm Supreme, Essential Protein Formula. If you have anxiety and or insomnia add the Beta 1, 3-D Glucan.
 
My best to you all,
 
Jim Harper
www.theroadback.org
 
 
This information is not approved by the FDA. It is for informational purposes only and is not intended to treat, cure or prevent any illness or disease. Always check with your physician before starting any supplement or altering medication. PLEASE DO NOT QUIT TAKING A PSYCHOACTIVE MEDICATION ABRUPTLY.

 

 
   
 
The Road Back  

 
This newsletter comes with a warm smile on my face for people taking a benzodiazepine or anticonvulsant. More relief from side effects is possible!
 
As stated in the book, How to Get Off Psychiatric Drugs Safely, this program is a work in progress, and I do hope it remains that way.
 
Before sharing with all of you the recent breakthrough with benzodiazepines and anticonvulsants, I want to go back to 1999 and work forward to the existing program. If you want to skip all of this and go directly to the break through, move down the page until you see June 30 2009.
 
At the end of the newsletter, I answer the question received a lot, “Do I Need to Take All of the Supplements?”
 
In 1999, it was evident a tapering program needed to be developed for psychoactive medications and NONE were in existence at that time.
 
How This All Started
 
In early 1999, I was talking with my wife and the subject turned to ADHD and Ritalin for some reason. My family and I had never been exposed to psychoactive medication. My wife mentioned in our conversation that in 10 states here in America, if a teacher felt your child had ADHD and wanted your child put on Ritalin, if you refused as a parent to allow this, the state could come into your home and take away your child and charge the parents with child neglect.
 
I looked at her and said “no way, not in America.” I went on the Internet and found the laws that were in place in those states and was shocked. I have children and at the time a child about to enter grade school, so it hit me between the eyes rather hard.
 
I felt I needed to do something about this but did not have a clue where to start. I felt if I did not know this there had to be millions of parents just like me that were in the dark.
 
I decided to learn how to make a web site and just put information on it that I was finding. In the next few months the search engines found my site attractive I guess because the site was now at the top of the first page when anyone did a search on a dug name. Emails began to pour in. Thousands a day at times.
 
Most people were in need of help to get off the drugs and stated, “they wished they knew this information before they went on the drug but how do I get off this stuff.” I sent some e-mails to physicians as well as some telephone calls to a few I had met over the years but I kept researching. This turned into a 14 hour a day project.
 
By the time the physicians responded to my request with what they would do to get a person off a psychoactive medication, I had educated myself at least to the point of knowing what to not do. I found all of the physicians were creating more harm than help with their approach and sent them a reply back that I could not link to their site and detailed why. All of the physicians responded back one more time with,”My God, you are right.”
 
I could not turn my back on what I knew needed to be done for people wanting to get off their medication. Believe me, I would have preferred to play golf or go fishing but for whatever reason I stayed at trying to unravel this jigsaw puzzle. 
 
Sequence of events:
 
1999
A gradual reduction of medications was laid out to allow a 10% reduction of the medication. Reductions were every 14 days.
 
With this approach, around ½ of the people we worked with could get off the medication but they suffered tremendously. The ½ that could not get off the medication suffered each time they tried to lower the dosage and eventually had to go back up to their original dosage.
 
It was very evident something else needed to be tried.
 
2000
We began using a whey protein called Immunocal in an attempt to reduce side effects before a person began lowering their medication. Immunocal was used during the medication reduction as well to help with any withdrawal side effects.
 
Immunocal raises an antioxidant called glutathione. The success rate was better than nothing but limited and very specific to a certain class of drug and to an exact set of side effects.
 
2001
During 2001, we tried a different whey protein that was stronger than Immunocal but the taste let a little to be desired and it was actually too strong for this usage.
 
Omega 3 fish oil was introduced to the program as well in 2001. At that time the fish oil was recommended for help with depression but not brain zaps as it was in a later year.
 
I began researching the ability to predict adverse reactions using a DNA test.
 
2002
This year was spent doing DNA research.
 
2003
I had the opportunity to meet with an attorney and his client a few weeks before they went to trial against Eli Lilly with a Prozac case. The attorney was handed a packet of information regarding human DNA and the ability to predict adverse reactions to psychoactive medication.
When this DNA evidence was introduced in court, the Eli Lilly attorneys instantly asked to meet the judge in his chambers and they settled on the spot. The next day the attorney filed several new lawsuits with DNA and the prediction of adverse reactions as the claim.
 
2004
I wanted more information on DNA drug reaction testing and I wanted to see if there was a use for the test results being of use for tapering off the drugs.
 
I started a DNA testing company called Advanced DNA Testing and began offering a DNA drug reaction test. This test is excellent to do BEFORE taking a medication but it gave zero help with a tapering program.
 
I then moved to doing a different DNA test to see how well the population at large could assimilate nutrients from their food as well as vitamins. This widely opened the door for future changes with the tapering program and with this new information, the success rate of people trying to get off their medication began to finally climb.
 
The use of young green barley juice, along with a powdered carrot juice and an additional barley called Aktivated Barley was introduced to the program. The success rate of the program began to climb even further.
 
The young green barley with the other mixture included would also help the body make glutathione. The Immunocal recommendation was dropped at this time.
 
The current Body Calm liquid was introduced in 2004 as well to assist with daytime anxiety and sleep. Up until our use of the liquid cherry product for anxiety and sleep, no one else had ever used it for this. This cherry was only used by physicians for treating gout.
 
A specific type of Omega 3 fish oil was introduced this year as well. The need for a fish oil that is higher in EPA than DHA was determined and once introduced, the success rate made another nice increase.
 
The year 2004 ended with an acknowledgement of sort from the acting head of the FDA. He gave a press release and stated his recommendation that physicians begin giving a DNA drug reaction test before they prescribe heart medication, cancer medication or psychoactive medication.
 
2005
This was the first year of training physicians and psychiatrists how to get patients off psychoactive medication and how to use DNA testing in their practice.
 
To make it easier for people to use the barley’s and the carrot, reduce the cost and to standardize the formula, Power Barley Formula was created.
 
At the urging of a few people I quickly put a paperback book together and self published. My own feeling is the book left a lot out of the content and should never have been published.
 
During 2005, I also began training other individuals or companies how to use the program.
 
2005 was a rather distracting year altogether and little progress was made with improvement of the program. Some of the people I trained broke a signed non-disclosure agreement and took parts of what I was currently doing and what I had used in the past and created their own tapering program.
 
The problem they have to this date is they only heard the good things I had to say about the whey protein Immunocal. I never told them what they needed to watch out for.
 
So, in your travels on the Internet, if you run into some psychoactive medication tapering program that uses Immunocal, a cherry product for anxiety or sleep, an Omega 3 fish oil, glutathione or a DNA drug reaction test, you found them!
 
I received a Christmas gift from the FDA on Christmas Eve. The FDA announced any company that manufactured a barley product that was high enough in soluble fiber could make it health claim that it would help prevent heart disease. If this product would not have been formulated as it was the fiber would have been too low to qualify. At that time in 2005, I was the only one with a barley product that could make the health claim.
 
I knew the Power Barley Formula would also be good for the heart but I did not know how much benefit.
 
2006
Additional advances needed to be made for people with daytime anxiety and insomnia. The liquid cherry had worked better than expected for this but there was still a lot of room for improvement. I had a powered cherry extract made and sent it to a doctor to use with some of his patients. The doctor called me in a few days with staggering results. The product is called Body Calm.
 
The patients he could never quite get over the hump now had no anxiety and their sleep improved dramatically. Some of the patients responded to 1 capsule, while a few others required 3 capsules for complete relief.
 
Essential Protein Formula came as a big surprise for me with its effect on anxiety and insomnia. The product was originally formulated for weight loss. Many people taking an antidepressant begin to gain weight overnight and I wanted to find a solution for this.
 
People taking the Essential Protein Formula began stating their daytime anxiety improved and their sleep improved as well once they started to use the Essential Protein Formula. People taking a benzodiazepine are so sensitive to things I felt this might really work for them. It proved to be the case and as well for people taking an antidepressant or antipsychotic.
 
During 2006, I began writing How to Get Off Psychiatric Drugs Safely and every time I was nearing completion a new discovery was made and the book would go back to square one again.
 
2007
Body Calm Supreme was introduced in 2007 for additional help with daytime anxiety and insomnia. I found clinical trials where a specific herb, passionflower, was used successfully for benzodiazepine withdrawal as well as for alcohol and other drugs. I formulated a passionflower to closely match the type used in the clinical trials and began trying it with people that were still having a difficult time with side effects.
 
The positive results were over night and shortly thereafter, the Body Calm Supreme became part of the program.
 
A major U.S. university began using the existing book, How to Get Off Psychiatric Drugs Safely, as part of their doctoral program for pharmacists.
 
2008
By the spring of this year, more of a separation took place between the pre-tapers used if a person had anxiety or fatigue as a main issue.
 
Knowing the specific success I had with Immunocal years earlier, I added a product called RenewPro to the program if a person has anxiety or insomnia. RenewPro helps create intracellular glutathione naturally and is a whey concentrate, not a whey isolate. I found the successful clinical trials run with Immunocal were with a whey concentrate but Immunocal is now a whey isolate. Difference of night and day.
 
Calcium has been a continual problem with people with anxiety. I first discovered in 2005, by process of elimination, that calcium was aggravating the anxiety in people, especially if they were taking a benzodiazepine.
 
I finally located which cells in the brain were creating the problem and created a calcium, magnesium and vitamin D3 that would relieve the stored calcium creating the problem. I now have a method of use patent for this and the calcium product made is called CalesiumD. Calcium was not the problem but the type of calcium used as well as the percentage of magnesium and D3 is all that needed to be formulated.
 
Don’t let anyone tell you all calcium creates anxiety and you can’t use it. They just do not understand what is happened within the body.
 
To further assist with calcium absorption, a product called Calsorption was introduced. This product will help with calcium absorption by as much as 28%.
 
With the discovery of Interleukin-2 and Interleukin-6, the tapering program made further advances. Interleukin-2 is a protein found in the immune system and this Interleukin-2, if too low will induce anxiety and insomnia.
 
Interleukin-6 is a marker for inflammation in the body. If Interleukin-6 is too high a person WILL begin to have depression.
 
Figuring out how to lower and or raise these Interleukins with people using psychoactive medication resulted in another method of use patent.
 
Beta 1, 3-D Glucan was introduced to raise Interleukin-2.
 
CLA and a specific blend of a probiotic was introduced to help lower Interleukin-6.
 
To get the full effect from the RenewPro a vitamin C and vitamin E needed to be used. A natural vitamin C was introduced as well as a vitamin E. We had recommended people use a vitamin E for years but it was not until 2008 that we really defined what vitamin E to use. It seems vitamin E is often viewed as just some vitamin and vitamin E is just vitamin E. I was wrong. The brand we only recommend for vitamin E is Unique E.
 
2009
The fourth edition of How to Get Off Psychiatric Drugs Safely has finally been published and has been available on Amazon.com and now on Target.com. An agreement has been signed recently with a major book distributor and all books will be available in major bookstores within the next 60 days. They also will provide the books throughout Europe in various languages.
 
I released a weight loss book titled, Lose the Weight Caused by Antidepressants the middle of June. A bit of my research during the early part of 2009 has been in this area. Much to my surprise, this little 52-page book now outsells The South Beach Diet, Kevin Truedeau’s weight loss book and nearly all other weight loss books on Amazon.com and the Target store. 
 
June 30 2009
I feel this next break though is of the same degree with the introduction of Body Calm Supreme for anxiety and insomnia, if not more.
 
If someone is taking a benzodiazepine or anticonvulsant medication, his or her body will be grossly depleted of a B vitamin called Biotin. A multitude of clinical trials confirms this. Biotin is known as vitamin H and as vitamin B7. Unlike some other B vitamins, biotin does not create anxiety or hyperness. It is rare for a person to be deficient in biotin normally but that is not the case if long-term use of an anticonvulsant or benzodiazepine is the case.
 
Your physician can do a blood test for biotin levels as well as check the level of organic acids excreted to confirm the deficiency.
 
Symptoms of biotin deficiency:
 
Pain or tingling in extremities
Appetite decreased
Hair loss
Absence or loss of pigment in hair
Fatty liver
Kidney problems
Skin rash
Seizures
Depression
Scaly red rash around nose or eyes
Fatigue
Hallucinations
Problem with insulin
 
We have been using biotin now with people for the past few months that are or were taking a benzodiazepine or anticonvulsant and the fast results have been staggering.
 
How Much Biotin to Take
 
There are no know side effects to biotin and if your body receives more than it needs it will just eliminate any excess.
 
We have started everyone at 5,000 mcg in the morning and after 3 days if no major change or only a slight improvement increased the biotin to 5,000 mcg in the morning and 5,000 mcg in the afternoon.
 
Increases by an additional 5,000 mcg have been beneficial to get rid of the last bit of what a person was feeling. We have had people take as much as 20,000 mcg in the morning and 20,000 mcg in the afternoon with no side effects and only positive results.
 
Again, relief from what was going on with the people was very fast. I want to make a statement here to ensure there is no confusion that we are treating or curing a disease. If a person takes biotin and feel better after they do, they were only low in biotin, no disease or illness could have been present.
 
As always we strive to only recommend quality nutritional products. We have had a biotin made at a facility that is approved to manufacture drugs by the FDA if they chose to do so (they do not), the facility is regularly inspected by an independent 3rd party to ensure they maintain Good manufacturing Practices and they have also achieved the high standard of ISO 9000 certification and are approved in Europe. The facility is in the United States and is licensed by the state of California.
 
TRB Health (www.trbhealth.com) carries the biotin recommended. You can click here and go directly to the biotin page on their site.
 
Notice: Using biotin as described, along with an anticonvulsant or benzodiazepine or after discontinuation of an anticonvulsant or benzodiazepine is a patent pending method of use. Physicians or other providers must sign a licensing agreement before using.
 
Do I Need to Take All of the Supplements?
 
No you do not.
 
The full line of supplements in this program were included to handle specific side effects that may take place when tapering off psychoactive medication. As you read through the last 10 years of this program, you will notice not all supplements were used throughout. We are trying to continually increase the success rate and have as a major goal to develop a program that will eliminate and or stop all side effects from ever occurring. The inclusion of biotin as well as the other supplements leads to that goal.
 
If budget is a problem, I recommend:
 
You would take the supplements suggested below exactly as it reads in How to get Off Psychiatric Drugs Safely.
 
Benzodiazepines - Biotin, Body Calm, Beta 1, 3-D Glucan and Body Calm Supreme. Anxiety, insomnia and many of the effects associated with being deficient in biotin will probably be your main concerns. Adding the probiotic Supreme will be a good idea if in your budget.
 
Antidepressants (with anxiety insomnia)- Body Calm, Body Calm Supreme, Beta 1, 3-D Glucan, Probiotic Supreme and Essential Protein Formula. Before you start to lower the antidepressant you will need the Ultimate Omega 3 and Unique E.
 
Antidepressants (with fatigue) - Power Barley Formula, Ultimate Omega 3 and Unique E.
 
Antipsychotics - Body Calm, Body Calm Supreme, Essential Protein Formula. If you have anxiety and or insomnia add the Beta 1, 3-D Glucan.
 
My best to you all,
 
Jim Harper
www.theroadback.org
 
 
This information is not approved by the FDA. It is for informational purposes only and is not intended to treat, cure or prevent any illness or disease. Always check with your physician before starting any supplement or altering medication. PLEASE DO NOT QUIT TAKING A PSYCHOACTIVE MEDICATION ABRUPTLY.

 

 
   
 
The Road Back  

 
This newsletter comes with a warm smile on my face for people taking a benzodiazepine or anticonvulsant. More relief from side effects is possible!
 
As stated in the book, How to Get Off Psychiatric Drugs Safely, this program is a work in progress, and I do hope it remains that way.
 
Before sharing with all of you the recent breakthrough with benzodiazepines and anticonvulsants, I want to go back to 1999 and work forward to the existing program. If you want to skip all of this and go directly to the break through, move down the page until you see June 30 2009.
 
At the end of the newsletter, I answer the question received a lot, “Do I Need to Take All of the Supplements?”
 
In 1999, it was evident a tapering program needed to be developed for psychoactive medications and NONE were in existence at that time.
 
How This All Started
 
In early 1999, I was talking with my wife and the subject turned to ADHD and Ritalin for some reason. My family and I had never been exposed to psychoactive medication. My wife mentioned in our conversation that in 10 states here in America, if a teacher felt your child had ADHD and wanted your child put on Ritalin, if you refused as a parent to allow this, the state could come into your home and take away your child and charge the parents with child neglect.
 
I looked at her and said “no way, not in America.” I went on the Internet and found the laws that were in place in those states and was shocked. I have children and at the time a child about to enter grade school, so it hit me between the eyes rather hard.
 
I felt I needed to do something about this but did not have a clue where to start. I felt if I did not know this there had to be millions of parents just like me that were in the dark.
 
I decided to learn how to make a web site and just put information on it that I was finding. In the next few months the search engines found my site attractive I guess because the site was now at the top of the first page when anyone did a search on a dug name. Emails began to pour in. Thousands a day at times.
 
Most people were in need of help to get off the drugs and stated, “they wished they knew this information before they went on the drug but how do I get off this stuff.” I sent some e-mails to physicians as well as some telephone calls to a few I had met over the years but I kept researching. This turned into a 14 hour a day project.
 
By the time the physicians responded to my request with what they would do to get a person off a psychoactive medication, I had educated myself at least to the point of knowing what to not do. I found all of the physicians were creating more harm than help with their approach and sent them a reply back that I could not link to their site and detailed why. All of the physicians responded back one more time with,”My God, you are right.”
 
I could not turn my back on what I knew needed to be done for people wanting to get off their medication. Believe me, I would have preferred to play golf or go fishing but for whatever reason I stayed at trying to unravel this jigsaw puzzle. 
 
Sequence of events:
 
1999
A gradual reduction of medications was laid out to allow a 10% reduction of the medication. Reductions were every 14 days.
 
With this approach, around ½ of the people we worked with could get off the medication but they suffered tremendously. The ½ that could not get off the medication suffered each time they tried to lower the dosage and eventually had to go back up to their original dosage.
 
It was very evident something else needed to be tried.
 
2000
We began using a whey protein called Immunocal in an attempt to reduce side effects before a person began lowering their medication. Immunocal was used during the medication reduction as well to help with any withdrawal side effects.
 
Immunocal raises an antioxidant called glutathione. The success rate was better than nothing but limited and very specific to a certain class of drug and to an exact set of side effects.
 
2001
During 2001, we tried a different whey protein that was stronger than Immunocal but the taste let a little to be desired and it was actually too strong for this usage.
 
Omega 3 fish oil was introduced to the program as well in 2001. At that time the fish oil was recommended for help with depression but not brain zaps as it was in a later year.
 
I began researching the ability to predict adverse reactions using a DNA test.
 
2002
This year was spent doing DNA research.
 
2003
I had the opportunity to meet with an attorney and his client a few weeks before they went to trial against Eli Lilly with a Prozac case. The attorney was handed a packet of information regarding human DNA and the ability to predict adverse reactions to psychoactive medication.
When this DNA evidence was introduced in court, the Eli Lilly attorneys instantly asked to meet the judge in his chambers and they settled on the spot. The next day the attorney filed several new lawsuits with DNA and the prediction of adverse reactions as the claim.
 
2004
I wanted more information on DNA drug reaction testing and I wanted to see if there was a use for the test results being of use for tapering off the drugs.
 
I started a DNA testing company called Advanced DNA Testing and began offering a DNA drug reaction test. This test is excellent to do BEFORE taking a medication but it gave zero help with a tapering program.
 
I then moved to doing a different DNA test to see how well the population at large could assimilate nutrients from their food as well as vitamins. This widely opened the door for future changes with the tapering program and with this new information, the success rate of people trying to get off their medication began to finally climb.
 
The use of young green barley juice, along with a powdered carrot juice and an additional barley called Aktivated Barley was introduced to the program. The success rate of the program began to climb even further.
 
The young green barley with the other mixture included would also help the body make glutathione. The Immunocal recommendation was dropped at this time.
 
The current Body Calm liquid was introduced in 2004 as well to assist with daytime anxiety and sleep. Up until our use of the liquid cherry product for anxiety and sleep, no one else had ever used it for this. This cherry was only used by physicians for treating gout.
 
A specific type of Omega 3 fish oil was introduced this year as well. The need for a fish oil that is higher in EPA than DHA was determined and once introduced, the success rate made another nice increase.
 
The year 2004 ended with an acknowledgement of sort from the acting head of the FDA. He gave a press release and stated his recommendation that physicians begin giving a DNA drug reaction test before they prescribe heart medication, cancer medication or psychoactive medication.
 
2005
This was the first year of training physicians and psychiatrists how to get patients off psychoactive medication and how to use DNA testing in their practice.
 
To make it easier for people to use the barley’s and the carrot, reduce the cost and to standardize the formula, Power Barley Formula was created.
 
At the urging of a few people I quickly put a paperback book together and self published. My own feeling is the book left a lot out of the content and should never have been published.
 
During 2005, I also began training other individuals or companies how to use the program.
 
2005 was a rather distracting year altogether and little progress was made with improvement of the program. Some of the people I trained broke a signed non-disclosure agreement and took parts of what I was currently doing and what I had used in the past and created their own tapering program.
 
The problem they have to this date is they only heard the good things I had to say about the whey protein Immunocal. I never told them what they needed to watch out for.
 
So, in your travels on the Internet, if you run into some psychoactive medication tapering program that uses Immunocal, a cherry product for anxiety or sleep, an Omega 3 fish oil, glutathione or a DNA drug reaction test, you found them!
 
I received a Christmas gift from the FDA on Christmas Eve. The FDA announced any company that manufactured a barley product that was high enough in soluble fiber could make it health claim that it would help prevent heart disease. If this product would not have been formulated as it was the fiber would have been too low to qualify. At that time in 2005, I was the only one with a barley product that could make the health claim.
 
I knew the Power Barley Formula would also be good for the heart but I did not know how much benefit.
 
2006
Additional advances needed to be made for people with daytime anxiety and insomnia. The liquid cherry had worked better than expected for this but there was still a lot of room for improvement. I had a powered cherry extract made and sent it to a doctor to use with some of his patients. The doctor called me in a few days with staggering results. The product is called Body Calm.
 
The patients he could never quite get over the hump now had no anxiety and their sleep improved dramatically. Some of the patients responded to 1 capsule, while a few others required 3 capsules for complete relief.
 
Essential Protein Formula came as a big surprise for me with its effect on anxiety and insomnia. The product was originally formulated for weight loss. Many people taking an antidepressant begin to gain weight overnight and I wanted to find a solution for this.
 
People taking the Essential Protein Formula began stating their daytime anxiety improved and their sleep improved as well once they started to use the Essential Protein Formula. People taking a benzodiazepine are so sensitive to things I felt this might really work for them. It proved to be the case and as well for people taking an antidepressant or antipsychotic.
 
During 2006, I began writing How to Get Off Psychiatric Drugs Safely and every time I was nearing completion a new discovery was made and the book would go back to square one again.
 
2007
Body Calm Supreme was introduced in 2007 for additional help with daytime anxiety and insomnia. I found clinical trials where a specific herb, passionflower, was used successfully for benzodiazepine withdrawal as well as for alcohol and other drugs. I formulated a passionflower to closely match the type used in the clinical trials and began trying it with people that were still having a difficult time with side effects.
 
The positive results were over night and shortly thereafter, the Body Calm Supreme became part of the program.
 
A major U.S. university began using the existing book, How to Get Off Psychiatric Drugs Safely, as part of their doctoral program for pharmacists.
 
2008
By the spring of this year, more of a separation took place between the pre-tapers used if a person had anxiety or fatigue as a main issue.
 
Knowing the specific success I had with Immunocal years earlier, I added a product called RenewPro to the program if a person has anxiety or insomnia. RenewPro helps create intracellular glutathione naturally and is a whey concentrate, not a whey isolate. I found the successful clinical trials run with Immunocal were with a whey concentrate but Immunocal is now a whey isolate. Difference of night and day.
 
Calcium has been a continual problem with people with anxiety. I first discovered in 2005, by process of elimination, that calcium was aggravating the anxiety in people, especially if they were taking a benzodiazepine.
 
I finally located which cells in the brain were creating the problem and created a calcium, magnesium and vitamin D3 that would relieve the stored calcium creating the problem. I now have a method of use patent for this and the calcium product made is called CalesiumD. Calcium was not the problem but the type of calcium used as well as the percentage of magnesium and D3 is all that needed to be formulated.
 
Don’t let anyone tell you all calcium creates anxiety and you can’t use it. They just do not understand what is happened within the body.
 
To further assist with calcium absorption, a product called Calsorption was introduced. This product will help with calcium absorption by as much as 28%.
 
With the discovery of Interleukin-2 and Interleukin-6, the tapering program made further advances. Interleukin-2 is a protein found in the immune system and this Interleukin-2, if too low will induce anxiety and insomnia.
 
Interleukin-6 is a marker for inflammation in the body. If Interleukin-6 is too high a person WILL begin to have depression.
 
Figuring out how to lower and or raise these Interleukins with people using psychoactive medication resulted in another method of use patent.
 
Beta 1, 3-D Glucan was introduced to raise Interleukin-2.
 
CLA and a specific blend of a probiotic was introduced to help lower Interleukin-6.
 
To get the full effect from the RenewPro a vitamin C and vitamin E needed to be used. A natural vitamin C was introduced as well as a vitamin E. We had recommended people use a vitamin E for years but it was not until 2008 that we really defined what vitamin E to use. It seems vitamin E is often viewed as just some vitamin and vitamin E is just vitamin E. I was wrong. The brand we only recommend for vitamin E is Unique E.
 
2009
The fourth edition of How to Get Off Psychiatric Drugs Safely has finally been published and has been available on Amazon.com and now on Target.com. An agreement has been signed recently with a major book distributor and all books will be available in major bookstores within the next 60 days. They also will provide the books throughout Europe in various languages.
 
I released a weight loss book titled, Lose the Weight Caused by Antidepressants the middle of June. A bit of my research during the early part of 2009 has been in this area. Much to my surprise, this little 52-page book now outsells The South Beach Diet, Kevin Truedeau’s weight loss book and nearly all other weight loss books on Amazon.com and the Target store. 
 
June 30 2009
I feel this next break though is of the same degree with the introduction of Body Calm Supreme for anxiety and insomnia, if not more.
 
If someone is taking a benzodiazepine or anticonvulsant medication, his or her body will be grossly depleted of a B vitamin called Biotin. A multitude of clinical trials confirms this. Biotin is known as vitamin H and as vitamin B7. Unlike some other B vitamins, biotin does not create anxiety or hyperness. It is rare for a person to be deficient in biotin normally but that is not the case if long-term use of an anticonvulsant or benzodiazepine is the case.
 
Your physician can do a blood test for biotin levels as well as check the level of organic acids excreted to confirm the deficiency.
 
Symptoms of biotin deficiency:
 
Pain or tingling in extremities
Appetite decreased
Hair loss
Absence or loss of pigment in hair
Fatty liver
Kidney problems
Skin rash
Seizures
Depression
Scaly red rash around nose or eyes
Fatigue
Hallucinations
Problem with insulin
 
We have been using biotin now with people for the past few months that are or were taking a benzodiazepine or anticonvulsant and the fast results have been staggering.
 
How Much Biotin to Take
 
There are no know side effects to biotin and if your body receives more than it needs it will just eliminate any excess.
 
We have started everyone at 5,000 mcg in the morning and after 3 days if no major change or only a slight improvement increased the biotin to 5,000 mcg in the morning and 5,000 mcg in the afternoon.
 
Increases by an additional 5,000 mcg have been beneficial to get rid of the last bit of what a person was feeling. We have had people take as much as 20,000 mcg in the morning and 20,000 mcg in the afternoon with no side effects and only positive results.
 
Again, relief from what was going on with the people was very fast. I want to make a statement here to ensure there is no confusion that we are treating or curing a disease. If a person takes biotin and feel better after they do, they were only low in biotin, no disease or illness could have been present.
 
As always we strive to only recommend quality nutritional products. We have had a biotin made at a facility that is approved to manufacture drugs by the FDA if they chose to do so (they do not), the facility is regularly inspected by an independent 3rd party to ensure they maintain Good manufacturing Practices and they have also achieved the high standard of ISO 9000 certification and are approved in Europe. The facility is in the United States and is licensed by the state of California.
 
TRB Health (www.trbhealth.com) carries the biotin recommended. You can click here and go directly to the biotin page on their site.
 
Notice: Using biotin as described, along with an anticonvulsant or benzodiazepine or after discontinuation of an anticonvulsant or benzodiazepine is a patent pending method of use. Physicians or other providers must sign a licensing agreement before using.
 
Do I Need to Take All of the Supplements?
 
No you do not.
 
The full line of supplements in this program were included to handle specific side effects that may take place when tapering off psychoactive medication. As you read through the last 10 years of this program, you will notice not all supplements were used throughout. We are trying to continually increase the success rate and have as a major goal to develop a program that will eliminate and or stop all side effects from ever occurring. The inclusion of biotin as well as the other supplements leads to that goal.
 
If budget is a problem, I recommend:
 
You would take the supplements suggested below exactly as it reads in How to get Off Psychiatric Drugs Safely.
 
Benzodiazepines - Biotin, Body Calm, Beta 1, 3-D Glucan and Body Calm Supreme. Anxiety, insomnia and many of the effects associated with being deficient in biotin will probably be your main concerns. Adding the probiotic Supreme will be a good idea if in your budget.
 
Antidepressants (with anxiety insomnia)- Body Calm, Body Calm Supreme, Beta 1, 3-D Glucan, Probiotic Supreme and Essential Protein Formula. Before you start to lower the antidepressant you will need the Ultimate Omega 3 and Unique E.
 
Antidepressants (with fatigue) - Power Barley Formula, Ultimate Omega 3 and Unique E.
 
Antipsychotics - Body Calm, Body Calm Supreme, Essential Protein Formula. If you have anxiety and or insomnia add the Beta 1, 3-D Glucan.
 
My best to you all,
 
Jim Harper
www.theroadback.org
 
 
This information is not approved by the FDA. It is for informational purposes only and is not intended to treat, cure or prevent any illness or disease. Always check with your physician before starting any supplement or altering medication. PLEASE DO NOT QUIT TAKING A PSYCHOACTIVE MEDICATION ABRUPTLY.

 

 
   

June 10, 2009

Florida Media Pounding on Child Drugging

Filed under: Uncategorized — admin @ 9:33 am
Florida Media Pounding on Child Drugging

 

Newspapers have been investigating and running lots of articles on Florida child drugging.The articles are being compiled here: http://gabrielmyers.wordpress.com/

The below short excerpts are not news stories - they are editorials  - opinions of the newspapers.   

 


http://www.sun-sentinel.com/news/opinion/sfl-psychotropic-drugs-editorialsbjun08,0,2212606.story

 

Sun Sentinel
Death raises concern about psychotropic drugs.

Editorial Board
June 8, 2009
In 2005, the Legislature approved SB 1090, a bill that tightened state procedures to make sure that psychotropic drugs weren’t prescribed to minors without proper oversight. The law stressed physicians’ need to get consent or a court order before dispensing the drugs…

The investigation continues, and child welfare officials are, again, fending off allegations they use drugs designed for serious mental disorders to subdue behavior. Lawmakers undoubtedly will propose new bills to strengthen laws already on the books.

New legislation is fine. The trick now is to make sure all the rules are being followed.

BOTTOM LINE: Rules must be followed.


 

 

 

http://www.washingtonexaminer.com/opinion/blogs/SharpSticks/UPDATE-Doped-up-foster-child-in-Florida-hangs-himself-He-was-seven-46822507.html

 

Washington Examiner
Doped up foster child in Florida hangs himself. He was seven
.
Local Opinion Editor
June 4, 2009
Sheldon’s subsequent investigation revealed that more than 2,600 foster children in Florida are being doped up - with one in six lacking the legally required consent forms. Children trapped in these state-run “child welfare” programs are being doped up to keep them docile and easy to manage while the adults in charge thumb their noses at the law and cash the checks.

This is beyond disgusting. It’s criminal.

 


http://www.tampabay.com/opinion/editorials/article1007779.ece

 

St. Petersburg Times
Foster care failures

A Times Editorial
June 7, 2009
Two disturbing facts about the Florida foster care system have emerged following the suicide of a 7-year-old boy on psychiatric drugs. First is the extraordinary prescription rate for children under the supervision of the Department of Children and Families. Second is the alarming revelation that a 2005 law aimed at tackling that problem has been repeatedly and systemically ignored…

Such changes will only work if Sheldon succeeds in changing a culture that ignored such safeguards. DCF relies heavily on nonprofit local providers to do its work. Those providers need to fully understand what is at stake, as do their employees. Four years after the Legislature thought it had addressed this problem, a 7-year-old’s suicide is a stark reminder that the system is still terribly flawed. How long will it take to get it right?

 


http://blogs.palmbeachpost.com/opinionzone/2009/06/05/kids-and-drugs-too-much-too-little/

 

Palm Beach Post
Kids and drugs. Too much, too little?

by Opinion Staff
June 6, 2009

Frighteningly, 16 percent of the Florida foster kids given such drugs are taking them without permission from a parent or judge. One such child, 7-year-old Gabriel Myers, who was taking a combination antipsychotic and antidepressant, hanged himself in April in his Broward County foster home….doctors have said that such mind-altering drugs, including many common antidepressants, can lead to thoughts of suicide in children and have put special warnings on the medications.

 


http://www.heraldtribune.com/article/20090607/OPINION/906071021/-1/NEWSSITEMAP#

 

Sarasota Herald Tribune
Drugs carried warnings
 
Opinion 
Sunday, June 7, 2009
Symbyax carries a warning that “antidepressants may increase suicidal thoughts or behaviors in some children… especially within the first few months of treatment or when changing the dose.”

Vyvanse is approved for use in children 6 and over, but the manufacturer notes that the drug should not be taken by those in “agitated states.” Aggression and abnormal behaviors are sometimes associated with its use.

These risks are among the reasons why Florida law requires informed parental consent or judicial order before administering psychiatric medications to foster children. Paperwork in Gabriel’s case indicated consent had been given, but that was erroneous, DCF officials say. A statewide review of psychiatrically medicated foster children found consent documentation lacking in 16 percent of such cases — a potentially serious gap in the safety net.

 


http://www.palmbeachpost.com/opinion/content/opinion/epaper/2009/06/05/a14a_dcf_edit_0606.html

 

Palm Beach Post
Owning up, cleaning up

Editorial
June 05, 2009

The review also found that 16 percent of the children in foster care taking these drugs do not have parental consent or a court order. “That is unacceptable,” said Mr. Sheldon. “Gabriel Myers and all of Florida’s children deserve better.”

Those children who have been prescribed psychotropic drugs must get informed parental consent or a court order before resuming the medication… .This report is an important first step in closely examining not only this case, said Mr. Sheldon, “but in helping to assure that this kind of tragedy never happens again.”

 


http://www.tampabay.com/opinion/editorials/article1000069.ece

 

DCF must do better 
A Times Editorial 
May 12, 2009It has been a common practice for DCF workers and physicians to fail to obtain parental consent when a psychotropic drug is for a nonpsychotherapeutic use, under the mistaken impression that the law didn’t require it… 

 
Sheldon has it right when he says that Gabriel’s death “ought to mean something.” State law needs to be followed when prescribing medication for children in foster care. And particularly when it comes to damaged children, there has to be a recognition that drugs are no substitute for basic human care and attention. 


http://www.miamiherald.com/opinion/editorials/story/1015130.html
 
Miami Herald

Answers needed in case of child’s suicide
April 24, 2009
OUR OPINION: Mistakes apparent in death of seven-year-old Gabriel Myers
 
A good place to begin the examination is with the menu of potent, mind-altering drugs that Gabriel was taking under a doctor’s prescription. The boy was being treated by a Broward psychiatrist who had been red-flagged by a state agency as having ”problematic” prescribing habits, according to a state Medicaid drug-therapy expert. The term applies to doctors with a high volume of prescriptions of mental-health drugs or who prescribe potentially risky drug combinations.
 
DCF has of history of relying too heavily on psychotropic drugs to manage children in its care. After a series of Miami Herald stories describing the problems, the Florida Legislature passed a law that attempted to control and limit the use of psychotropic drugs on children. The legislation cited a DCF study in 2004 showing that 13 percent of all children in state custody were receiving and least one psychotropic drug. The study also showed that 25 percent of the children living in foster care were being treated with psychotropic drugs, a rate five times higher than in the general population of Medicaid-eligible children.
 


 
 

 

 

June 6, 2009

Psychiatric drugs linked to child’s death…

Filed under: Uncategorized — admin @ 12:46 am
Comments can be made here: http://www.miamiherald.com/news/miami-dade/story/1082376.html 
 

 

Bookmark this page http://gabrielmyers.wordpress.com/ for the latest developments on the investigation of child drugging in Florida.
 
Miami Herald
Lawsuit links psychiatric drugs to Tamarac child’s death
The doctor who prescribed psychiatric drugs for a child who committed suicide was sued Thursday by a mother who claims that he overmedicated her son.

June 5, 2009
By Carol Marbin Miller

A Tamarac mother sued Fort Lauderdale Hospital and a psychiatrist who worked there, saying they overmedicated her teenage son with a cocktail of mental health drugs — some of which have not been approved for the treatment of children.

The boy, Emilio Villamar, died of a sudden heart attack. He was 16.

Emilio, a swimmer and water polo player, was diagnosed with bipolar disorder by Dr. Sohail Punjwani in March 2002. Within the next year, the teen was given 16 different psychiatric drugs, six of which were still being administered when he died, said Michael S. Freedland, who is representing Emilio’s mother, Norma L. Tringali.

Punjwani had also been treating 7-year-old Gabriel Myers, a foster child who had been prescribed several psychiatric drugs before he hanged himself in April. In the wake of Gabriel’s death, the Department of Children & Families has launched a wide-ranging investigation into the agency’s dispensing of mental health drugs.

Norma Tringali, 56, said she asked Punjwani and other medical professionals why her son was being given so many powerful drugs — including six separate anti-psychotic drugs, typically used to treat schizophrenia, and one drug, called Cogentin, that is used primarily to curb the side effects of other drugs.

”[Punjwani] said he needed them,” Tringali said.

”He was over-medicated,” Tringali said of her son. “He was like a zombie, walking with heavy paces, always tired.”

Attorneys for both Punjwani and Fort Lauderdale Hospital did not return messages Thursday afternoon seeking comment.

NEW DETAILS

On Thursday, DCF administrators released new details on the investigation, saying 3,068 children in the agency’s care were taking mind-altering drugs — 118 of them infants, toddlers or youngsters under age 6. That comprises 13 percent of all the kids in DCF’s care.

Teenagers, those aged 13-17, make up 31 percent of the dependent children prescribed mental health drugs. That amounts to 1,695 children taking at least one psychiatric drug, according to the numbers released Thursday.

Thursday’s count includes almost 400 children who were not recorded when DCF released a census of children on medication a week ago. At the time, DCF Secretary George Sheldon acknowledged the census was a bit of a moving target, and agency leaders expected the numbers to rise.

”I have no confidence in the data that was released in 2007 and 2008,” Sheldon told The Miami Herald Thursday, referring to reports DCF submitted those years to the state Senate in response to a 2005 law that required better oversight of dependent children being administered psychiatric drugs.

`WORK IN PROGRESS’

”This is a work in progress,” Sheldon added. “We’ve got to get it better.”

Among the new findings: Of the 50 children in state care younger than age 6 whose files were reviewed by DCF, in not one case had parents or a judge provided informed consent for the use of mind-altering drugs, Sheldon said. “That’s disturbing.”

The 2005 law required the consent of a parent or judge before foster kids can be administered mental health drugs.

”A parent of a child who has been removed will, for all practical purposes, sign anything,” Sheldon said, noting that gaining meaningful permission from a parent overwhelmed by the removal of a child is next to impossible.

Tringali’s lawsuit alleges that Punjwani provided healthcare to Emilio that ”deviated and departed from the prevailing professional standard of care exercised” by most doctors by failing to monitor the effects of anti-psychotic drugs on Emilio’s heart, failing to do regular cardiac testing, and failing to consult with a cardiologist or other doctor with more experience with the heart-related side effects of anti-psychotic drugs.

”These are incredibly powerful drugs, and they require a tremendous amount of monitoring,” said Freedland.

FOUND AT HOSPITAL

Emilio was found slumped over in his room at Fort Lauderdale Hospital — where he was being treated for his mental illness — with blood dripping from his mouth or nose, Tringali said. He was taken by ambulance to Broward General Hospital, where he slipped into a coma.

The teen died March 29, 2003.

”Of course, I was in shock,” Tringali said. “Can you imagine: 16 years old? He was doing sports. He was a good swimmer. He played water polo. He was a very good student.

”It has been very bad for the family, very bad,” she said. “I don’t live one day, not one day, without thinking about Emilio.”



 
 

May 27, 2009

The “Business” of Drugs: Former Army Doctor Nailed for Drug Company Research Fraud

Filed under: Uncategorized — admin @ 1:11 am

winhs_logo2a with URL.gif

 Dear Members,

 The New York Times reports yet another “paid expert” caught forging drug company research reports. This time the hammer falls on a former surgeon from Walter Reed Army Hospital, Dr. Timothy Kuklo, an associate professor of orthopedic surgery and the guilty party in this report.

 Dr. Kuklo forged names and appended them to a published journal article which falsified research data conducted on U.S. soldiers to support exaggerated claims about the effectiveness of Infuse, a bone-growth product made by Medtronic which is already under investigation for false claims and off-label marketing. Not surprising, Medtronic was a company with whom Dr. Kuklo had significant undisclosed financial ties, and this time a separate investigation by the Walter Reed Army Medical Center confirmed the charges.

The Walter Reed report, issued in late 2008 was sent to Medtronic’s chief executive and to the dean of the Washington University School of Medicine, where Dr. Kuklo was employed. However, despite the report, as late as May 13, 2009, a university official declined to say whether it was investigating Dr. Kuklo but confirmed that he remained on the faculty.

The peer review British publication, the Journal of Bone and Joint Surgery, that published the fraudulent article later retracted it, but neither the University nor Medtronic had taken any disciplinary action against Dr. Kuklo.

In response to an inquiry from U.S. Senator Grassley (Sept. 2008) Medtronic provided him with a partial list of outside doctors who were listed as paid consultants for the Infuse drug. Dr. Kuklo, who has personally conducted about 15 paid presentations for Medtronic about the product, was interestingly NOT on that list.

In response to an inquiry by the NY Times, a written statement by a Medtronic spokeswoman indicated that Dr. Kuklo was not included because “some consultants, like Dr. Kuklo, have general agreements that are not specific
to a single therapy or subject matter.”

In other words, such doctors are on unspecified retainer with the company, promoting any number of Medtronic products!

Not easily satisfied with Medtronic’s dubious reply Sen. Grassley is now demanding much more detailed information from Medtronic – including all undisclosed financial arrangements between the company and academic faculty.

 The company since has announced its “disengagement from Dr. Kuklo,” a graduate of West Point, the University of Connecticut medical school and Georgetown Law Center.

Given the serious and potentially criminal charges against Dr. Kuklo – including fraud, forgery, and conducting an unapproved experiment on soldiers – the University of Washington’s failure to take action until a series of articles in The New York Times and more aggressive investigation headed by Sen. Charles Grassley brought pressure to bear, speaks volumes about a pervasive culture of arrogance in the drug company “sponsored” academia.

The University of Washington did not see fit to take action until Friday, May 22, when a spokesperson there indicated that Dr. Kuklo would take a leave of absence from the University.

For the full New York Times article see: http://www.nytimes.com/2009/05/19/business/19surgeon.html

How many of these incidents of falsifying study results, drug company payola and massive criminal and class action settlements need to be revealed before the FDA is jarred out of its complacent support and lack of real oversight of the pharmaceutical industry?

 I say, we already passed that number!

 What do you say?

 

All the best,

Rudi C. Loehwing

Managing Director

World Institute of Natural Health Sciences

www.winhs.org

Americans’ Legal Drug Abuse

Filed under: Uncategorized — admin @ 12:43 am
Please be patient:   It may take a moment for your comment to post here:    http://www.palmbeachpost.com/opinion/content/opinion/epaper/2009/05/21/a12a_swancol_0522.html#comments

Palm Beach Post
COLUMN: Americans’ legal drug abuse

By Rhonda Swan
Palm Beach Post Editorial Writer
May 21, 2009 
 


Maxine is not the woman she used to be.She looks the same, except for the white Afro that used to be black.

But gone is her zany sense of humor, sharp tongue and sassy wit.

 

 

She stares into space with vacant eyes. Walks like a zombie. She speaks primarily when spoken to, her conversation devoid of her familiar quips. She complies rather than commands.I’ve known Maxine my entire life - she taught me how to play pinochle and how to bake a cake - yet she seems more like a stranger I’ve just met.That’s because she’s among the millions of U.S. seniors taking psychotropic drugs, antidepressants, antipsychotics and Alzheimer’s medicines. The traits that used to make people take notice of Maxine, who suffers with post-traumatic stress disorder from an abusive marriage decades ago, are swallowed daily with her anti-psychotic Zyprexa pill.And now, she’s hardly noticeable.

The number of people older than 65 taking these drugs doubled between 1996 and 2006, according to a study released this month. Doctors prescribed 73 percent more drugs for adults with mental-health issues and 50 percent more for children during that period.

Children such as 7-year-old Gabriel Myers, who was taking Symbyax - a combination of Zyprexa and the anti-depressant Prozac, known to cause youngsters to have suicidal thoughts - when he hanged himself at his Broward County foster home last month.

An author of the study, which appeared in the journal Health Affairs, attributed this astounding increase in the use of these powerful drugs to improved access to mental-health care, which has become more mainstream, and more insurers willing to cover the drugs. But it’s also because more doctors prescribe psychotropic drugs as the first and often only treatment, even when they’re not warranted.

Years ago, when I told my primary-care doctor that I was suffering stress-related anxiety and insomnia, he handed me a prescription for Prozac. I trashed it, opting instead to exercise and change my diet.

In February, when my mother was in West Palm Beach’s Columbia Hospital recovering from surgery, I requested a psychiatric consultation because she wasn’t eating. I thought she might benefit from a session with an objective professional.

The hospital psychiatrist visited with her for less than 10 minutes, diagnosed her as depressed based on her answers to five questions, and then prescribed the antidepressant Zoloft and went on his merry way. Counseling wasn’t even considered as an option.

What happened to psychotherapy, once the hallmark of psychiatric treatment? Because of managed care, it’s going the way of the lobotomy. Why engage the human mind and heart to ease mental suffering when popping a pill is so much cheaper? According to a 2008 National Ambulatory Medical Care Survey, only 29 percent of visits to psychiatrists in 2004 and 2005 included psychotherapy, compared with 44 percent in 1996-97. Insurers reimburse more, says the report, for three 15-minute medication management visits than for one 45-to-50-minute outpatient psychotherapy session. Not surprisingly, the patients more likely to receive therapy are those who can pay out of pocket.

Granted, not everyone with a mental-health diagnosis would benefit from therapy alone. Many need these mind-altering, chemical-balancing drugs. But many others could achieve optimal mental health without the assistance of pharmaceuticals.

While we’ve been busy losing the multibillion-dollar war on illegal drugs, a government-sanctioned, multibillion-dollar legal drug industry has blossomed, churning out robots void of personality like Maxine and suicidal children like Gabriel.

When life is lost - mentally, spiritually or physically - does it really matter whether the drug dealer had a medical degree?

 

 

 


28,57 Signatures Against TeenScreen. Petition: http://www.petitiononline.com/TScreen/petition.html  

Video:  http://www.youtube.com/watch?v=RfU9puZQKBY

May 21, 2009

Psychiatric Drugs

Filed under: Uncategorized — admin @ 12:08 am
Full story can be found here: http://www.miamiherald.com/news/5min/story/1056520.html  Letters to the editor here: HeraldEd@MiamiHerald.com
 

Miami Herald
PSYCHIATRIC DRUGS
Lawsuit says too many psychiatric drugs killed boy

A disabled boy was lethally overmedicated, a lawsuit contends, as outrage continues over a child’s suicide while on several drugs last month.
BY CAROL MARBIN MILLERAmid a wide-ranging debate over the proper use of mental health drugs on troubled children, the mother of a disabled boy who died in 2007 is claiming in a lawsuit the boy was overdosed by a cocktail of psychiatric drugs, including two powerful anti-psychotics.

Martha Quesada, the mother of 12-year-old Denis Maltez, filed a wrongful death and medical malpractice lawsuit Monday in Miami-Dade circuit court, claiming Denis’ psychiatrist, Dr. Steven L. Kaplan, and the now-shuttered Rainbow Ranch group home overmedicated Denis and failed to properly monitor his condition … 

Quesada’s lawsuit was filed amid a high-profile investigation by the Department of Children & Families into the death last month of Gabriel Myers, a 7-year-old foster child who had been taking a cocktail of mental health drugs. DCF Secretary George Sheldon appointed a task force to study Gabriel’s case, and the use of psychiatric drugs on foster kids.

‘TOUGH’ TO HANDLE

Kaplan did not return calls for comment. In a June 2007 article in The Miami Herald, Kaplan said ”it’s possible” Denis would have been sleepy at school if he had not been given his medications at the right times. But, Kaplan added, “I never saw him dopey or sleepy.”… 

According to the 28-page lawsuit, Glatt stopped taking Denis to doctors at Jackson Memorial Hospital after he arrived at the group home in May 2006, and substituted Kaplan ”without the consent of [Denis's] mother.” Kaplan was treating several group home clients, the suit claims.

Kaplan prescribed and refilled four mental health drugs: Seroquel and Zyprexa, both anti-psychotic medications; Depakote, an anti-seizure drug sometimes used to stabilize moods; and Clonazepam, a tranquilizer. The lawsuit says the drugs were used “as chemical restraints to control Denis’s behavior.”

Though some of the medications are not approved by the Food and Drug Administration for use on children and carry strong warnings about possible side-effects, Kaplan ”took no steps to ensure that Denis was not suffering any adverse effects from these medications,” the suit claims.

In fact, the suit claims, Kaplan examined the boy only once between between May 26, 2006 and May 23, 2007, the day Denis died. 

There were warning signs that the drugs may have been harming the boy, according to the suit, filed by by Fort Lauderdale attorneys Maria Elena Abate and Howard Talenfeld. In June 2006, teachers at Denis’s school, Ruth Owens Kruse Educational Center, reported the boy was sleeping through class. …
 
DCF would not discuss the investigation with a reporter Tuesday.

 


28,574 Signatures Against TeenScreen. Petition: http://www.petitiononline.com/TScreen/petition.html  

Video:  http://www.youtube.com/watch?v=RfU9puZQKBY  

May 17, 2009

Scandalous Conflicts of Interest…

Filed under: Uncategorized — admin @ 12:29 pm

 The following is from the Consumer Reports Blog on Psychiatric Conflict of Interest:

Scandalous conflicts of interest revealed in psychiatry guidelines

Quick, answer this question: Who writes the guidelines for physicians on how to treat mental illnesses, such as schizophrenia, bipolar disorder or major depression

A) Psychiatrists interested in the welfare of patients with these terrible and debilitating diseases?
B) Academic researchers who are willing to lend their expert opinion to help fellow doctors?
C) People financed by drug companies who can be counted on to write the guidelines in a way that serves the company’s interests?
D.) All of the above.

If you answered D, you’re on the money.

In fact, being “on the money” is the operative phrase here, because a recent report on the conflicts of interest in psychiatric guidelines committees reveal some shocking facts about the financial entanglements of the people putting those guidelines together. 

The study published last month found that 90% of the authors of three American Psychiatric Association (APA) clinical practice guidelines in psychiatry had financial ties to drug companies mentioned in those guidelines. Worse yet, the authors had financial associations including owning equity in the companies that made the recommended medications, being a consultant or corporate board member, or receiving honoraria. And these conflicts were not disclosed in the guideline.

The picture becomes even darker when you narrow in on the conflicts of interest of the authors of the guidelines for just bipolar disorder and schizophrenia: Here, 100% of the authors had such conflicts.

Most people would consider this a worrying state of affairs, including Tufts professor Sheldon Krimsky, one of the co-authors of this report.  In an interview from his office in Boston, he told me that we should be worried about conflicts of interest because they can lead to a “distortion of the scientific record” and that drug companies who fund such activities may lead to an “interpretation of the science in a direction that may not be defensible.”

Authors who disclose their conflicts of interest are only an intermediate step, says Krimsky, and more effort should be made to separate the researchers and the clinicians from the drug manufacturers’ influence.

No doubt, guideline committees such as ones sponsored by the APA need to come clean on their financial conflicts. But they must avoid or minimize them in the first place.

John Santa, director of the Consumer Reports Heath Ratings Center, underscores the point by noting, “It is especially concerning that organizations like the American Psychiatric Association have financial relationships with drug companies and have been slow to appreciate the influence these relationships have created. We rely on professional and consumer organizations to protect patients and doctors from industry, not facilitate their influence.”

Here’s a simple skill-testing question I think the APA’s guidelines gurus could use for prospective committee members:  “Do you have financial ties to drug companies which make psychiatric medications?”  

It doesn’t take a brainiac to figure out where to go from there…

–Alan Cassels

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