Life Extension Magazine®

Hospital waiting room that can make people lifestyle changes

My Recent Life-Altering Event

William Faloon was recently hospitalized and witnessed egregious inefficiency and ineptitude…so much so that he made some major lifestyle changes. This article also discusses simple ways to protect against hospital-acquired infections.

Scientifically reviewed by Dr. Gary Gonzalez, MD, in October 2024. Written by: William Faloon.

William Faloon
William Faloon

I suspect everyone reading this column has experienced harsh real-world events that resulted in their making personal lifestyle changes.

You may have seen a loved one suffer and die from a horrific disease and responded by initiating programs to reduce your risk of encountering the same fate.

In other cases, you are the victim of a preventable illness—and turn your life around afterward to minimize the odds of it recurring.

I had a personal scare recently that put me in the hospital for a brief time. It terrorized me enough, however, to make some major lifestyle changes. I did this not only out of fear of the disease, but also the miseries of being confined to a hospital setting.

Egregious Hospital Ineptitude

In the August 2006 issue of this magazine, we published an in-depth article titled “Death by Medicine.”1 That article reported stunning statistics showing that conventional medicine kills hundreds of thousands of Americans each year, making it a leading cause of death in the United States.2,3

Many of us know of family or friends who encountered serious adverse events in a medical setting. In most cases, however, hospital-inflicted deaths are covered up by doctors who list the cause of death as the disease they were treating, as opposed to the real culprit of incompetently administered hospital procedures.

In several instances, we at Life Extension® have been involved in forcing death certificates to be amended because doctors fraudulently list a cause of death as something other than their own mistakes. We do this to help tear down the wall of deception erected by conventional medicine regarding the numerous errors they commit.

My Ordeal Begins…

For the first time in my life, I developed rather severe chest pains. I did not at first take this seriously, but shortly thereafter visited my local physician for an EKG (electrocardiogram).

What We Are Doing To Reverse Your Biological Age

To my surprise, the EKG results indicated I might be suffering coronary artery blockage and having a heart attack. The doctor suggested that I go to the local emergency room to get a blood test that measures markers such as troponin, which is a type of protein released by the heart when damaged. Troponin and enzymes like creatine kinase are elevated in the blood if there is damage to the heart muscle.

A hospital can perform these blood tests and have the results back in an hour, which is why I had to go to the ER to get them. The hospital did another EKG and the computerized reading indicated probable acute myocardial infarction, which means they thought I may be suffering a heart attack.

So here I was suffering rather intense chest pain with an EKG reading suggesting I was having a heart attack. During that hour waiting for the troponin/creatine kinase blood test results to come back, a lot went through my mind. I thought about the atherogenic diet I consumed in my early years because I did not have affordable access to healthy foods. The enormous amount of thoracic radiation I was needlessly exposed to at an early age also weighed on my mind as a factor that could cause coronary atherosclerosis, even though I have taken good care of my arterial system in later years.

There was a sense of relief when the troponin blood test came back negative, indicating that I had not sustained heart muscle damage. The ER doctor, however, made it clear that troponin levels don’t always elevate right away and that I needed follow-up troponin blood tests eight and sixteen hours later. The only way of having these tests done on an immediate (STAT) basis was to be “admitted” to the hospital.

I recalled some brilliant medical specialist friends of mine in the past who hated hospitals so much that they died rather than capitulate to hospital confinement—despite their intense chest pains. As bad as hospital confinement is, it was better than suffering fatal heart attacks like my friends did.

Like Going Back to the Days of the Soviet Union

Like Going Back to the Days of the Soviet Union

If there is a word to describe why the old Soviet Union collapsed, it might be “inefficiency.” Back in the Soviet days, the central Russian government controlled every aspect of the economy and the result was inefficiencies of unparalleled magnitudes.

I knew about the inherent inefficiencies of modern-day hospitals and was gratified that one of our Life Extension doctors brought me my laptop computer so that I could productively occupy my time while the hospital staff bumbled through the “admissions” process.

It took an outrageous number of hours to be transferred from the ER to a hospital room, but I kept myself busily occupied writing and editing articles for what was the next edition of this magazine, so the wait was not an annoyance.

The ER doctor promised me that the hospital would assign a cardiologist who would monitor me throughout the night in case my condition worsened. I began to question the competence of the so-called cardiologist when certain medications I expected to be prescribed were not. I became even more apprehensive when the so-called cardiologist did not seem to understand why I insisted on particular medications. I found out the next day that the hospital had erroneously called a general practitioner instead of the cardiologist to oversee me.

Delayed Medications

Delayed Medications

I told the ER doctor around 6:00 PM the first day that I needed certain heart medications, and he said they had been ordered from the hospital pharmacy. At 11:00 PM that night the drugs I requested still had not arrived.

When a nurse finally brought them, some were the wrong ones. Each and every time the drugs were mixed up, the supposed cardiologist had to be called to confirm that I could safely take what I was requesting. Fortunately, the general practitioner acquiesced to my requests and I finally got my meds—six hours after I needed them!

At midnight, they did another EKG and the result came back the same, i.e., possible acute myocardial infarction. My chest pains were still severe, but I recalled that the pain had subsided earlier in the day in response to ibuprofen or aspirin. I knew that if I was really suffering coronary artery blockage, that ibuprofen would not alleviate the pain. I again called the so-called cardiologist and asked for a high dose (800 mg) of ibuprofen. It finally arrived and within an hour I was chest pain-free.

A Sleepless Night

Sleeping is so important to maintaining immune function, yet many people find it impossible to sleep in a hospital setting. I am one of those who cannot sleep in a hospital bed.

I spent a long night reflecting on what I could have done to prevent a coronary blockage, if indeed this is what I had.

New Study Uncovers More Hospital Errors Than Previously Thought

I knew from my previous blood test readings and preventive interventions that I was at low risk for coronary artery disease. Yet I dwelled on the fact that my last LDL reading was 101 mg/dL and I knew it should ideally be kept below 80. I also suffer genetically elevated homocysteine levels, typically over 11 µmol/L, even though it should be below 8 µmol/L.

I take a lot of nutrients, drugs, and hormones to keep my cardiac markers at optimal ranges, but I recalled days when only a half dose was taken because of too many distractions. I made a vow that sleepless night to curtail other activities in order to have time to take every single nutrient, drug, and hormone I needed every single day. I told myself, If I am ever diagnosed with vascular disease, I want to know it is because the comprehensive program I follow failed, rather than because I failed to follow the comprehensive program.

I promised myself that even if every other cardiac risk marker was perfect, if there were a slight elevation of even one other marker (such as LDL), that I would double my efforts to suppress it.

The Next Morning

I was greeted early in the morning by the general practitioner, who apologized for the hospital confusing her as a cardiologist. I thanked her for prescribing the medications I requested even though she was not familiar with my rationale for wanting them. She told me the cardiologist I was supposed to have been assigned to would visit me shortly.

Within a half hour, the cardiologist arrived and impressed me with his capability. When I explained my hypothesis that I did not have coronary artery blockage because high-dose ibuprofen completely suppressed the chest pain, he concurred that I was probably suffering from pericarditis, which is an inflammation of the sack surrounding the heart muscle. It sounds serious, but is treatable with anti-inflammatory drugs. It is often caused by a virus or some unknown factor.

The cardiologist explained that my particular EKG readings meant one of two things. Either I was suffering such a severe heart attack that I would not be sitting up talking, or I had pericarditis. Since I suffered no other symptoms, the cardiologist told me that he would order more tests in the hospital and that I should stay another night.

I agreed to more tests but made it clear that I would bolt as soon as the tests were completed. He defined my leaving the hospital that day as “against medical advice” and strongly warned against it. I responded that another night of no sleep was more dangerous than the slight risk of arrhythmia (a heart rhythm disturbance that can be caused by pericarditis in some circumstances).

A Long Day

An echocardiogram was performed early that morning. I rejected the CAT scan the doctor ordered, and he compromised on an MRI instead. I did not get any push back on the CAT scan rejection, as an increasing number of patients seem to be heeding Life Extension’s advice to say NO to unnecessary CAT scans because of the high levels of cancer-causing radiation they emit.

The MRI should have been done mid-afternoon, but another communication error caused it to be delayed till the late evening. The MRI staff wanted my acknowledgment that while the MRI could diagnose pericardititis, it would not rule out pulmonary embolism. I told my nurse that I was not concerned with pulmonary embolism and to proceed immediately with the MRI. The nurse forgot to tell the MRI staff this.

The MRI staff spent most of the day doing nothing but wait around for the nurse to call them back. I spent most of the day asking the nurse when the MRI staff would be ready to perform the diagnostic as I was anxious to escape hospital confinement. I jokingly told people that the hospital was intentionally delaying the MRI test just to force me to stay another night.

It was not until after 8:00 PM that the MRI staff called the nurse to find out if I wanted the MRI. The failure of the afternoon nurse to make one phone call resulted in the MRI staff and me waiting around an extra six hours—typical hospital inefficiency. I finally escaped the miseries of hospital confinement around 10:00 PM that night—which equated to about 31 total hours of jail time from my perspective.

The Next Morning

Having written dozens of articles exposing why healthcare costs are needlessly bankrupting the United States, I realized that I had not done enough to uncover hospital inefficiency that results in prohibitive costs combined with mediocre-to-disastrous results.

New Study Uncovers More Hospital Errors Than Previously Thought

An encyclopedia could be written about the errors that routinely occur in the hospital setting.

A recent study published in the peer-reviewed journal Archives of Surgery uncovered unthinkable mistakes by doctors and surgeons7—such as amputating the wrong leg or removing organs from the wrong patient.

This study revealed how doctors in Colorado over a period of 6.5 years operated on the wrong patient at least 25 times and on the wrong part of the body in another 107 patients. Although these serious errors are rare overall, the numbers seen in the study were “considerably higher” than previous estimates.

According to the lead researcher of this study, the surgical blunders uncovered are probably “the tip of the iceberg” and the actual number of patient and surgical site mix-ups is likely much higher.

This particular study analyzed over 27,000 records from a database of medical errors maintained by a company that provides malpractice insurance to about 6,000 physicians in Colorado. This database relied on the physicians themselves reporting the incidents. The errors were caused by a range of slip-ups, including mixing up patient medical records, X-rays, and biopsy samples. All of the mistakes could be traced back to some form of miscommunication.

Some examples of wrong-site errors included removing the wrong ovary or irradiating the wrong organ. Specifically, mix-up of tissue specimen samples in the pathology laboratory occurred on 6 occasions, which led to the unnecessary prostatectomy (prostate gland removal) in a healthy patient in 3 distinct cases. Doctors mixed up the samples and the patients without cancer had unnecessary radical prostatectomies (painful surgeries often with lifetime complications).

The study showed that one-third of the mistakes led to long-term negative consequences (including death) for patients.

Protecting Against Hospital-Acquired Infections

Hospital confinement exposes one to increased risk of contracting bacterial infections that are sometimes antibiotic-resistant. What few people understand is that the infectious bacterium does not always emanate from the hospital. It is often a bacterium that is in you already, but is kept in check by your healthy immune system.

In many cases, a Staphylococcus (staph) bacterium called S. aureus inhabits your nasal passages, and if the hospital swabs this area with an anti-microbial product called mupirocin upon admitting you, your risks of developing infection arising from nasal colonization with S. aureus are markedly reduced.

After I was admitted to the hospital, I recalled a 2010 report published in the New England Journal of Medicine that referenced three studies (published in 1959, 2001, and 2004) that showed 80% of staph infections acquired in the hospital are endogenous, which means that these infections were caused by the patient’s own bacterial contamination. This study showed that if a patient’s nasal passages were decolonized with mupirocin applied twice daily for 5 days, combined with a chlorhexidine body wash, the risk of staph infection was reduced by nearly 60%.4

I asked my nurse about the antiseptic nasal swabs and the response was “we do that,” but he never came back to do it to me. This was how many of my requests were handled—i.e., Soviet Union-style.

We at Life Extension now strongly believe that the lethal combination of insufficient vitamin D (due to no sunlight exposure and no supplements given), lack of sleep (due to chronic hospital staff disturbance), and nutrition deficit (due to micronutrient-depleted food and stressinducing commotion) conspires to rob hospitalized patients of immune function required to suppress bacteria carried in their own bodies.

It does not matter how many sanitary procedures an institution performs if the patient’s immune function is being compromised by standard hospital practices. Anyone hospitalized for an extended period should take assertive measures to maintain immune function as most hospitals fail to pay attention to it. At a minimum, every hospitalized patient should immediately be given enough vitamin D to achieve optimal blood levels of over 50 ng/mL of 25-hydroxyvitamin D.

A number of studies confirm the potent anti-microbial effects of vitamin D, making it essential for hospital-confined patients.5,6

Striking a Balance

At the same time we report on these horrific surgical errors, it is important to acknowledge that hospitals save millions of lives each year, despite their inherent inefficiency and incompetence.

The hospital I went to is in a mid-size town and provided far better service than what I have observed in big-city behemoths. I would go back to this same hospital if need be as I perceive they made fewer errors than other institutions may have.

In the Archives of Surgery study that uncovered so many hospital errors,7 practical approaches to preventing these kinds of mix-ups were proposed that could slash these risks, so there is hope that these types of catastrophes can be prevented in the future.

I Have Finally Started Exercising

I Have Finally Started Exercising

I know many of you enjoy physical activity and even get a nice endorphin release in response to heavy workouts or aerobic exercise. I am one of those who fall into the opposite category. I absolutely detest regular exercise of any kind and get no pleasure from it whatsoever.

The frustrating experiences I underwent in the hospital setting succeeded in doing what reading thousands of positive studies about the benefits of physical activity failed to do. All I have to do when I don’t want to exercise is recall the gross incompetence and inefficiencies exhibited during my brief hospital visit.

One fear is that if I had something seriously wrong that required a coronary bypass or stent procedure, I would be at the mercy of a hospital staff that did not even have the common sense to initially find the right doctor.

The thought of my existence being contingent on the medical establishment was frightening enough to adjust my social schedule to make room for 30 minutes of aerobic bicycling (sitting at an angle to minimize damage to my hips and prostate) several times a week and lots more regular activity.

Our Early Attempt to Establish a Life Extension Hospital
Our Early Attempt to Establish a Life Extension Hospital

In the May 1998 issue of Life Extension Magazine®, we proposed to radically improve the efficacy of medical treatment by establishing a hospital that would treat diseases based upon science rather than politics.

We noted that information is expanding at a faster pace than mainstream medicine can keep up with, and there is a need to apply scientific findings faster in the practice of medicine. We discussed the resistance most doctors have about accepting new ideas and how this intransigence slows the pace at which innovative treatments are used to benefit patients. We also discussed the role of pharmaceutical companies and regulatory agencies such as the Food and Drug Administration in blocking the availability of innovative medical therapies.

The solution we proposed was the creation of a Life Extension Medical Center that would make the latest scientific breakthroughs available directly to patients, without the interference of the government, private industry, and overly conservative physicians. In keeping with the Life Extension Foundation’s long-standing policy, a Life Extension Medical Center would offer treatments based only upon solid research published in established peer-reviewed medical journals.

The initial capital for establishing (and defending) such an innovative medical center was estimated to be $5 million. We asked Life Extension Foundation® members if they would consider investing or contributing to such a Life Extension Medical Center, upon presentation of an acceptable business plan. We had firm pledges of over $2.3 million plus a commitment to raise another $4.5 million from private investors.

After further evaluation of this ambitious proposal, we felt that the power of state licensing boards to revoke physicians’ licenses would result in us not being able to retain the competent staff we needed. We knew if we were successful that conventional hospitals losing patients to us would seek to use licensing boards to take away professional licenses, thus crippling our ability to deliver the high-caliber treatments that were the basis for initiating this monumental project.

We notified members who had made financial pledges that it was not feasible to initiate a Life Extension hospital facility at that time.

All My Blood Markers Now Have To Be Optimal

I have my blood tested throughout the year. As I have written in the past, this has already saved my life several times by identifying serious problems early when they were reversible (such as kidney damage inflicted by overuse of the drug ibuprofen).

As you can see by my latest blood test result reprinted on page 18 of this issue, I have achieved optimized status on most of my cardiac risk factors.

After my scare in the hospital, I am determined to move every cardiac marker into optimal ranges. This is challenging because of certain genetic factors that predispose me to having higher than desirable levels of glucose and homocysteine.

This means I have to take extra time and make some social sacrifices to accomplish this. For me, however, the priority is following through with correcting every vascular risk factor.

Critical Importance of Annual Blood Testing

Critical Importance of Annual Blood Testing

No one has been a stronger proponent of regular blood testing than the Life Extension Foundation®.

In the early 1980s, we recommended that all members have their blood tested for a wide range of cardiovascular risk markers. The problem back then was that conventional doctors did not always order the needed tests, the costs were prohibitively high, and people had to schedule another appointment with the doctor’s office for the blood draw.

In 1996, we rectified these failings by offering comprehensive blood testing to Life Extension members nationwide that was affordable and convenient.

While some conventional physicians today recommend blood tests to check glucose, cholesterol, and triglycerides, they rarely check their patients’ levels of C-reactive protein, homocysteine, DHEA, and other cardiac markers.

As a member of the Life Extension Foundation, you don’t have to be victimized by medical ignorance, high prices, or insurance company indifference.

Take Control Over Your Future Health

When looking at the number of diseases that can be detected early through the proper utilization of blood testing, it becomes strikingly apparent that a significant number of heart attacks, strokes, bone fractures, end-stage kidney/liver failure and other degenerative diseases are preventable.

During my recent hospital ordeal, I would have hated to think that I neglected to have annual blood tests done, and as a result, my heart might be slowly dying from oxygen starvation because I failed to take preventive measures.

At least I knew that I did almost everything I should have to prevent it. In other words, if I needed bypass surgery, I had the peace of mind of knowing it was probably not through the fault of my own negligence.

Low-Cost Convenient Blood Testing

Commercial labs charge high prices for comprehensive blood testing. This precludes most people from having critical tests done that can identify correctable cardiac risks before angina or full-blown heart attack emerges.

Life Extension long ago broke down high cost barriers by offering comprehensive Male and Female Blood Test Panels at the lowest prices anywhere. Once a year, we discount these popular panels down to only $199—about 80% less than what commercial labs charge.

Instead of having to make a doctor’s appointment, we send you a prepared requisition form and list of drawing stations in your area where you can go at your convenience.

The Blood Test Super Sale lasts only two months, so please order your requisition kit soon to take advantage of these extra discounted prices. You can have your blood drawn anytime after receiving your requisition kit. The results of your blood tests are mailed directly to you. If you have any questions when your results come back, you are welcome to call our Health Advisor helpline.

The description on the next page details what’s included in the Male and Female Blood Test Panels and how easy it is to order them.

This year we have added a new test called sex hormone-binding globulin (SHBG) at no extra charge to the Male and Female Panels. By measuring SHBG levels in the blood, we are better able to ascertain how much testosterone and other hormones are biologically available to tissues in the body.

Annual blood testing is the single most effective method of detecting abnormalities that can be corrected before they lead to serious illness or death. A call to 1-800-208-3444 is all you have to do to order these comprehensive tests at extra-discounted prices.

For longer life,

For Longer Life

William Faloon

Male and Female Blood Test Panels

Unlike commercial blood tests that evaluate only a narrow range of risk factors, Life Extension’s Male and Female Blood Test Panels measure a wide range of blood markers that predispose people to common age-related diseases. Just look at the huge numbers of parameters included in the Male and Female Blood Test Panels:

Male Panel

Lipid Profile

Total Cholesterol
LDL (low-density lipoprotein) calculated
HDL (high-density lipoprotein)
Triglycerides

Cardiac Markers

C-Reactive Protein (high sensitivity)
Homocysteine

NEW &
Improved

Now Includes
SHBG!

Hormones

DHEA-S
Free Testosterone
Total Testosterone
Estradiol (an estrogen)
TSH (thyroid function)
Sex Hormone-Binding Globulin (SHBG)

 

Metabolic Profile

Glucose
Kidney function tests: creatinine, BUN, uric acid, BUN/creatinine ratio
Liver function tests: AST, ALT, LDH, GGT, bilirubin, alkaline phosphatase
Blood minerals: calcium, potassium, phosphorus, sodium, chloride, iron
Blood proteins: albumin, globulin, total protein, albumin/globulin ratio

Complete Blood Count (CBC)

Red Blood Cell count including:
hemoglobin, hematocrit, MCV, MCH, MCHC, RDW
White Blood Cell count including: lymphocytes, monocytes, eosinophils, neutrophils, basophils Platelet count

Cancer Marker

PSA (Prostate Specific Antigen)

Female Panel

Lipid Profile

Total Cholesterol
LDL (low-density lipoprotein) calculated
HDL (high-density lipoprotein)
Triglycerides

Cardiac Markers

C-Reactive Protein (high sensitivity)
Homocysteine

NEW &
Improved

Now Includes
SHBG!

Hormones

Progesterone
DHEA-S
Free and Total Testosterone
Estradiol (an estrogen)
TSH (thyroid function)
Sex Hormone-Binding Globulin (SHBG)

Metabolic Profile

Glucose
Kidney function tests: creatinine, BUN, uric acid, BUN/creatinine ratio
Liver function tests: AST, ALT, LDH, GGT, bilirubin, alkaline phosphatase
Blood minerals: calcium, potassium, phosphorus, sodium, chloride, iron
Blood proteins: albumin, globulin, total protein, albumin/globulin ratio

Complete Blood Count (CBC)

Red Blood Cell count including: hemoglobin, hematocrit, MCV, MCH, MCHC, RDW
White Blood Cell count including:
lymphocytes, monocytes, eosinophils, neutrophils, basophils Platelet count

Non-member retail price: $400 • Everyday member price: $269
Blood Test Super Sale member price: $199Enjoy these savings until June 6, 2011

To obtain these comprehensive Male or Female Panels at these low prices,
call 1-800-208-3444 to order your requisition forms.
Then—at your convenience—you can visit one of the blood-drawing facilities provided by LabCorp in your area. (Restrictions apply in NY, NJ, RI, MA)

If you plan to use the result of these blood tests to assist in a medically supervised weight loss program,
consider ordering the Male or Female Weight Loss Panel for the blood test super sale
member price of $224.25 through June 6, 2011.
These panels were designed to offer additional hormones for those desiring assistance with weight loss.

Continue to William Faloon’s Complete Blood Results.

References

1. Null G, Dean C, Feldman M, Rasio D, Smith D. Death by medicine. Life Extension Magazine®. 2006 Aug;12(8):66-87.

2. Holland EG, Degruy FV. Drug-induced disorders. Am Fam Physician. 1997 Nov 1;56(7):1781-8, 1791-2.

3. Available at: http://www.whale.to/a/last1.html. Accessed October 29, 2010.

4. Bode LG, Kluytmans JA, Wertheim HF, et al. Preventing surgical-site infections in nasal carriers of Staphylococcus aureus. N Engl J Med. 2010 Jan 7;362(1):9-17.

5. White JH. Vitamin D as an inducer of cathelicidin antimicrobial peptide expression: Past, present and future. J Steroid Biochem Mol Biol. 2010 Jul;121(1-2):234-8.

6. Gombart AF. The vitamin D-antimicrobial peptide pathway and its role in protection against infection. Future Microbiol. 2009 Nov;4:1151-65.

7. Stahel PF, Sabel AL, Victoroff MS, et al. Wrong-site and wrong-patient procedures in the universal protocol era: analysis of a prospective database of physician self-reported occurrences. Arch Surg. 2010 Oct;145(10):978-84.

8. Segala M, ed. Disease Prevention and Treatment. 4th ed. Life Extension Publications, Inc.; 2003:v.

William Faloon’s Blood Test Results as of March 4, 2011

As we age, it becomes increasingly difficult to achieve optimal blood test readings.

For example, aging can cause glucose-insulin levels to spike, along with C-reactive protein (CRP), homocysteine, and lipids (LDL, triglycerides, and total cholesterol).

To protect against deadly atherosclerosis, aggressive individualized interventions are often required.

I am genetically predisposed to develop atherosclerosis at a relatively early age. When I was 35 years old, my LDL was 160 (mg/dL). I took steps at age 35 to reduce it. As you can see on the next page, I got my LDL down to 62 on my last blood draw. I plan to keep it in this low range for the next few years with the objective of reversing atherosclerotic plaque that might have built up in my younger years. I am 56 years old now, by the way.

Despite taking many homocysteine-lowering agents, my homocysteine reading on the last test was 10 (µmol/L). Ideally it should be below 8, but I have never gotten mine below 9. When conventional doctors tell me not to worry about homocysteine, I quickly respond by stating that if I did not aggressively try to lower my homocysteine it would be over 22 right now. I know this based on my father’s high homocysteine levels. (He suffered his first heart attack at age 52.)

I have been keeping my glucose under 90 (mg/dL) recently, but this particular test showed it at 92—a higher than desired level. We know that for optimal protection against vascular disease, glucose should be kept between 70-85. Considering that I take 850 mg of the anti-diabetic drug metformin 2 to 3 times a day, 50 mg of the drug acarbose before carbohydrate-containing meals, and the Calorie Control Weight Management Formula before the two heaviest meals of the day, you would think that I could push glucose down to perfect ranges. A lot of people who follow this program do achieve these low glucose levels, but my body does not respond the same way. I remind conventional critics that if I was not taking these aggressive steps to keep glucose levels in check, I might be diabetic by now.

My HDL of 52 mg/dL is not as high as it usually is, but considering how low my total cholesterol and LDL are, it is satisfactory for now.

One genetic factor favoring me is a virtually nonexistent level of C-reactive protein. It has always been low and seems to be going down as I age (instead of the reverse that happens to most people.).

My estradiol level dropped too low on a previous test, so I stopped taking Arimidex®. As you can see, my estradiol shot up to 43.8 (pg/mL), which I will suppress by taking about 1 mg of Arimidex® each week. DHEA is too high and reflects the 25 mg capsule I took right before my blood was drawn. (Ideally, one should take any hormones approximately 2 hours before the blood test. My DHEA likely did not have time to be converted into its other metabolites and was thus too high.)

My creatinine level moved just over 1.00 mg/dL, which indicates some kidney dysfunction in response to taking a few doses of ibuprofen a few days before my blood was drawn. My creatinine has historically dropped upon cessation of ibuprofen. There should be a warning about kidney toxicity on ibuprofen bottles, but the FDA does not require it.

My PSA of 0.6 ng/mL is desirably low for my age and reflects aggressive measures I have taken for almost a decade to suppress it. (It had been higher in the past.) We know from previous studies that PSA itself can facilitate prostate cancer by breaking down anatomical barriers in the prostate gland that block isolated prostate cancer cells from expanding.

You may notice my iron level is high on the basic test, but I was able to have the lab use the retained blood sample to test for ferritin, which is a much more reliable indicator of one’s body iron stores. Due to the uniqueness in my biochemistry it appears I have higher blood iron, but lower body stores of iron.

My free testosterone level is in the ideal range of 20-25 pg/mL because I use a topical testosterone gel several days a week. At age 43 it was below 8 pg/mL, and I suffered the outward symptoms of testosterone deficiency (such as low energy, abdominal weight gain, and brain fog). I have been on testosterone replacement for the past 12 years and enjoy no longer having symptoms of testosterone deficiency!

My 25-hydroxyvitamin D of 55.8 ng/mL is in the optimal range of 50-80 ng/mL that we suggest at Life Extension. It reflects the 7,000 IU of vitamin D I take each day.

Why Some Doctors Are Confused About Hormones

It should be noted that the hormone reference ranges provided by most labs are age-adjusted ranges, meaning that as we get older, the labs keep lowering the reference range. That is why people who take hormones to restore their levels to what they were when they were young may get back blood results marked high. This can be disconcerting for doctors who are not familiar with the idea of restoring youthful hormone levels. They often end up telling patients to stop taking the hormones without understanding the concept that higher values on blood tests are possible when restoring youthful hormone levels. If you are working with a doctor knowledgeable in hormone restoration, he/she will likely expect to see some higher values above the lab’s age-adjusted reference ranges, depending on the age of the person and the treatment given.

Based on my 30-year medical history of blood testing, I would be very ill or dead now if I had not taken aggressive steps to reverse my individual markers of impending diseases. Blood testing in the past has uncovered elevated PSA and serum calcium; high LDL, triglycerides, glucose, and cholesterol; kidney damage; high homocysteine and estradiol; along with low free testosterone. I took corrective actions, and as you can see by the results below, I have achieved optimal levels of virtually every marker of degenerative disease.

For longer life,

For Longer Life 

William Faloon

Below are William Faloon’s complete blood results.

Patient Name
Faloon, Bill

Sex
M

Age
56

LifeExtension/Natl Diagnostic
1100 W. Commercial Blvd. Ft. Lauderdale, Fl 33309

Control #
09134075014

Draw
03/04/11

Entered
03/04/11

Last Report
03/09/11

ACC: 0913407501482244

PID:

 

General Comments

Tests

Results

 

Units

Reference Interval

Lab

CMP14+LP+4AC+CBC/D/Plt

 

 

 

 

 

Chemistries

 

 

 

 

01

Glucose, Serum

92

 

mg/dL

65-99

01

Uric Acid, Serum

4.9

 

mg/dL

2.4-8.2

01

**Please note reference interval change**

 

 

 

 

 

BUN

20

 

mg/dL

6-24

01

Creatinine, Serum

1.01

 

mg/dL

0.76-1.27

01

eGFR

>59

 

mL/min/1.73

>59

 

eGFR AfricanAmerican

>59

 

mL/min/1.73

>59

 

Note: Persistent reduction for 3 months or more in an eGFR
<60 mL/min/1.73 m2 defines CKD.  Patients with eGFR values >/=60 mL/min/1.73 m2 may also have CKD if evidence of persistent proteinuria is present. Additional information may be found at www.kdoqi.org.

BUN/Creatinine Ratio

20

 

 

9-20

 

Sodium, Serum

139

 

mmol/L

135-145

01

Potassium, Serum

4.2

 

mmol/L

3.5-5.2

01

Chloride, Serum

103

 

mmol/L

97-108

01

Carbon Dioxide, Total

26

 

mmol/L

20-32

01

Calcium, Serum

9.4

 

mg/dL

8.7-10.2

01

Phosphorus, Serum

3.1

 

mg/dL

2.5-4.5

01

Protein, Total, Serum

7.2

 

g/dL

6.0-8.5

01

Albumin, Serum

4.6

 

g/dL

3.5-5.5

01

Globulin, Total

2.6

 

g/dL

1.5-4.5

 

A/G Ratio

1.8

 

 

1.1-2.5

 

Bilirubin, Total

0.6

 

mg/dL

0.0-1.2

01

Alkaline Phosphatase, S

44

 

IU/L

25-150

01

LDH

127

 

IU/L

100-250

01

AST (SGOT)

29

 

IU/L

0-40

01

ALT (SGPT)

28

 

IU/L

0-55

01

Iron, Serum

225

H

ug/dL

40-155

01

Lipids

 

 

 

 

01

Cholesterol, Total

128

 

mg/dL

100-199

01

Triglycerides

69

 

mg/dL

0-149

01

HDL Cholesterol

52

 

mg/dL

>39

01

Comment

 

 

 

 

01

According to ATP-III Guidelines, HDL-C >59 mg/dL is considered a negative risk factor for CHD.

VLDL Cholesterol Cal

14

 

mg/dL

5-40

 

LDL Cholesterol Calc

62

 

mg/dL

0-99

 

T. Chol/HDL Ratio

2.5

 

ratio units

0.0-5.0

 

Estimated CHD Risk

< 0.5

 

times avg.

0.0-1.0

 

T. Chol/HDL Ratio

 

 

 

 

 

  Men Women
1/2 Avg.Risk 3.4 3.3
Avg.Risk 5.0 4.4
2X Avg.Risk 9.6 7.1
3X Avg.Risk 23.4 11.0
 
 
       
         
         

The CHD Risk is based on the T. Chol/HDL ratio.  Other factors affect CHD Risk such as hypertension, smoking, diabetes, severe obesity, and family history of premature CHD

 

Tests

Results

 

Units

Reference Interval

Lab

CBC, Platelet Ct, and Diff

 

 

 

 

01

WBC

4.1

 

x10E3/uL

4.0-10.5

01

RBC

4.63

 

x10E6/uL

4.10-5.60

01

Hemoglobin

14.4

 

g/dL

12.5-17.0

01

Hematocrit

43.0

 

%

36.0-50.0

01

MCV

93

 

fL

80-98

01

MCH

31.1

 

pg

27.0-34.0

01

MCHC

33.5

 

g/dL

32.0-36.0

01

RDW

13.3

 

%

11.7-15.0

01

Platelets

166

 

x10E3/uL

140-415

01

Neutrophils

54

 

%

40-74

01

Lymphs

23

 

%

14-46

01

Monocytes

19

H

%

4-13

01

Eos

2

 

%

0-7

01

Basos

2

 

%

0-3

01

Neutrophils (Absolute)

2.3

 

x10E3/uL

1.8-7.8

01

Lymphs (Absolute)

0.9

 

x10E3/uL

0.7-4.5

01

Monocytes(Absolute)

0.8

 

x10E3/uL

0.1-1.0

01

Eos (Absolute)

0.1

 

x10E3/uL

0.0-0.4

01

Baso (Absolute)

0.1

 

x10E3/uL

0.0-0.2

01

Immature Granulocytes

0

 

%

0-1

01

Immature Grans (Abs)

0.0

 

x10E3/uL

0.0-0.1

01

PSA Total+% Free (Serial)

 

 

 

 

 

Prostate Specific Ag, Serum

0.6

 

ng/mL

0.0-4.0

01

Roche ECLIA methodology.

 

 

 

 

 

Testosterone, Free and Total

 

 

 

 

 

Testosterone, Serum

561

 

ng/dL

193-740

01

Free Testosterone (Direct)

20.0

 

pg/mL

7.2-24.0

02

Estradiol

 

 

 

 

 

Estradiol

43.8

H

pg/mL

7.6-42.6

01

Roche ECLIA methodology

 

 

 

 

 

Dehydroepiandrosterone Sulfate

 

 

 

 

 

DHEA-Sulfate

698.9

H

ug/dL

51.7-295.0

01

Vitamin D, 25-Hydroxy

 

 

 

 

 

Vitamin D, 25-Hydroxy

55.8

 

ng/mL

32.0-100.0

01

Recent studies consider the lower limit of 32.0 ng/mL to be a threshold for optimal health. Hollis BW. J Nutr. 2005 Feb;135(2):317-22.

C-Reactive Protein, Cardiac

 

 

 

 

 

C-Reactive Protein, Cardiac

0.22

 

mg/L

0.00-3.00

01

Relative Risk for Future Cardiovascular Event
Low <1.00
Average 1.00 - 3.00
High >3.00

Homocyst(e)ine, Plasma

 

 

 

 

 

Homocyst(e)ine, Plasma

10.0

 

umol/L

0.0-15.0

01

Insulin

6.2

 

uIU/mL

0.0-24.9

01

Sex Horm Binding Glob, Serum

35.8

 

nmol/L

14.5-48.4

01

Ferritin, Serum

26

L

ng/mL

30-400

01