12 JanMacular Degeneration testimonial

At the end of this post, you’ll hear from Don Biondich, who has ridden his ‘hog’ on six continents and was a certified pilot of nearly every kind of aircraft class… that is before his vision was ravaged by Macular Degeneration.

Don Biondich, one cool hombre


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Age-Related Macular Degeneration (AMD) is a loss of vision because of deterioration in the central portion of the RETINA (the inside surface of the eyeball upon which optical images are focused and then interpreted into sight by rods and cones connected to your brain.)

AMD can be accelerated by genetics and environment, but the root cause, in my opinion, is the same as other age-related diseases such as diabetes, high blood pressure, heart disease, COPD, and cancer….

In my opinion, these conditions are all caused by telomere erosion, as explained in my “Stem Cell Theory of Aging.”

———————->>  If you actually attempt to read my perspicacious yet bemusing blogs, you are probably very smart and should be asking: “Come on Dr. Park, you think everything is caused by telomere erosion!  What is your proof?

Well, in 1999, a very interesting study was performed testing the relationship between retinal cells’ telomere length, senescence and population doubling counts.  And, in just a moment, you should understand it as well as I do!

——————–First, let’s first review a few facts that my blog readers already know:

  1. Cells start with telomeres that measure 10,000 base pairs long but only 4,000 remain in your old age
  2. Cells populations can double only 60 times before replicative senescence (via the Hayflick Limit) dooms their lineage. The study calls the number of times the colony has divided its “Population Doubling Level”  (PDL)

———————- Next, some jargon that you will need to understand this study:

  • Bromodeoxyuridine (BrdU) is a synthetic nucleoside that is an analogue of thymidine (the “T” in the A+T & C+G DNA base pairings.) Antibodies specific for BrdU can be used to detect cells that are still actively dividing (i.e. not yet burned out).
  • β-galactosidase is highly expressed and in senescent cells.

———————- And finally, we can all understand the study!

Invest Ophthalmol Vis Sci. 1999 Jan;40(1):197-202.
Beta-galactosidase histochemistry and telomere loss in senescent retinal pigment epithelial cells.

Matsunaga H, Handa JT, Aotaki-Keen A, Sherwood SW, West MD, Hjelmeland LM.

Department of Ophthalmology, University of California Davis, USA.

Abstract

PURPOSE: To investigate the relation of senescence-related beta-galactosidase activity and telomere shortening to replicative senescence in cultured human retinal pigment epithelial (RPE) cells.

METHODS: A human RPE cell line was serially passaged until 80% of cells were nondividing in a 72-hour 5-bromo-2′-deoxyuridine (BrdU) labeling study. Early- and late-passage cells were double-stained for BrdU and senescence-related beta-galactosidase activity (pH 6). The average chromosomal telomere length at several population doublings was estimated by Southern blot analysis after double digestion of DNA with RsaI and HinfI and using a telomere-specific probe.

RESULTS: BrdU-beta-galactosidase double-staining revealed an inverse correlation between the number of BrdU-labeled nuclei and beta-galactosidase-labeled cells as a function of population doubling level (PDL).

In plain English, that means the more times the colony had divided (PDL), the fewer viable (BrdU+) and more burned-out (Beta galactosidase +) cells there were.

At PDL 58, only 20% of all cells labeled for BrdU, whereas 57% stained for beta-galactosidase. The mean terminal restriction fragment length (TRF) was reduced from 10 kb in early (PDL 12) cultures to 4 kb in late (PDL 57) cultures.

In plain English, that means that after dividing 58 of the theoretical 60 times of the Hayflick Limit, only 20% were still alive, and 57% were burned-out.  The telomere length in cells that had divided only 12 times was 10,000 base pairs.  The telomere length in cells that had divided 57 times was only 4,000 base pairs.


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Last week, the FDA approved an embryonic stem cell trial for treatment of Macular Degeneration, which is very promising since there is currently no adequate treatment for the condition which is known to affect 2% of those over 50, and 30% of people over 75.   And in my opinion, if people could live that long, it would probably affect 99% of people over 130.

Now, as promised, Don’s email from last week:

Dr. Park,

I would like to share with you my results using TA 65.

I am 76 years old and in great health for my age. I do have a problem with my eyesight. I have had dry macular degeneration in my right eye for years, however, my eyesight was still excellent. Within the last year and a half my eyesight started to diminish. It is not due to my macular degeneration but rather a loss of vision acuity. All of the ophthalmologists that I consulted said that although I will not go blind my eyesight is slowly going to get worse, so much so that in a couple years I will not be able to drive a car.

Then I saw your TV interview about TA-65 and other news releases on this product and was intrigued about the positive results with eye problems. I am taking four capsules every night and have been doing so for a little over a month. I have noticed that my overall health has improved to the point that I can now stand up from a sitting position without the aid of a product. Now this could be a placebo effect however, I have definite measured results that are very positive as far as my eyesight is concerned.

A grid like Don's describes

Because of my macular degeneration I have been using a grid chart for years to make sure that the dry degeneration does not turn wet which is serious. Since I have been using TA-65 the area of the grid chart that used to be distorted is now diminishing and I can see more of the chart that is not distorted.

The other positive results are that I can now use my computer with much more ease and less straining of my eyes. I like to play solitaire on my computer and the cards, of course, are much smaller than regular deck. Before the treatment I had some difficulty in distinguishing the number eight or nine card. I now can make this distinction and I think this is quite amazing and is a positive measured result.

Also, my vision for distance is improving. The reason I can judge this positively is that as I was experiencing the diminished sight I would practice looking at objects around me. Now these objects are getting clearer and brighter.

I will continue with the program and keep records of my improvements.

Thank you very much for your help and guidance,

Regards,

Don Biondich

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Disclaimer: The preceding testimony is presented as only one man’s experience.

TA-65 is not a cure nor a treatment for AMD.

28 NovRunning up the down escalator

Patients often wonder if after stopping TA-65, their cells will age even faster.  The answer is no; although unpleasant physical withdrawal symptoms are a common complaint after stopping anabolic hormones such as HGH (Human Growth Hormone) injections and sex hormones (testosterone and estrogens.)

Unlike hormones, Telomerase activation doesn’t supercharge gene expression,  it merely recharges the protective length of telomeres, like rechargeable batteries. That charge will then be shared with neighboring telomeres by rebalancing and prevent chromosomal damage that can lead to many, if not most, human diseases.

The musical, Bye, Bye Birdie asked: “What’s the matter with kids today?”

Well, if they inherited their parents’ telomere erosion, there would be a lot wrong with them! They’d be born older and with the DNA damage that mom and dad had acquired before reproducing.

But when a new life is created in a single cell fertilized egg, the telomere length is magically reset, like a pinball machine, to 15,000 base pairs, and the integrity of the DNA library inheritance is nearly error-free from highly error-protected egg and sperm cells.

A lot of cell division means a lot of telomere loss

In fact, because of the frenzied in utero growth and differentiation, you had already burned through 5,000 base pairs, so that on your birthday, only 10,000 remained.

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Since birth, you have lost and average of 1,000 base pairs per decade but lost them faster during stress, whether infectious, toxic, emotional, or from overuse. So, if you’re 60 years old, they could be as short as 4,000 base pairs in some types of stem cells.

Telomerase moves you back up the escalator

Think of your body’s stem cell telomere maintenance efforts like a an effort to walk or run back up a downward-traveling escalator.  Unlike run-of-the-mill cells, which die off from natural telomere shortening, stem cells use telomerase activation to print more and more telomere length.

Unhealthy living slows your upward movement, and may even make you descend faster towards the basement. In contrast, healthy living, via telomerase activation, allows you to run back up the escalator.  Since stopping TA-65 doesn’t speed up the escalator,  you will simply resume your descent from a higher level.

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Telomere erosion can be slowed or even reversed by telomerase activation, whether by exercise, good nutrition, psychosocial and emotional balance, or sleep.  Now, TA-65 is available to you as the world’s first safe and effective telomerase activator.  Think of it as an hour of cardiovascular exercise, four servings of fruits and vegetables, an hour of prayer or mediation, and eight hours of sleep, all in a tiny capsule!  Taking TA-65 is a way to reap the benefits of a healthy lifestyle for people who don’t have the time, inclination, or discipline to do so but do have the equivalent of a Grande Latte and muffin ($6.60) to spend on themselves daily.

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Postscript: For more inspiration from a real-life ‘windmill tilter,’ check out this story about an 80 year-old gentleman named Peter Hildreth who was banned from running up escalators.

People never change...only their stem cells do

20 NovWe are not machines

We often think of our bodies as though they were machines.

But machines break down with usage, primarily due to friction.

In contradistinction, your body improves with overuse.  That is to say, more exercise makes your body stronger.  Do you know why?

Exercise activates telomerase

It is because exercise activates telomerase, just like taking TA-65!

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Elizabeth Blackburn, PhD- Nobel Prize winner 2009

Nobel Prize winner, Dr. Elizabeth Blackburn, studied men with prostate cancer and showed that their telomerase activity could be increased by just three months of these healthy behaviors:

1) a diet of low fat, whole foods such as fruits, vegetables, unrefined grains, and legumes, which was also low in refined carbohydrates

2) moderate aerobic exercise (walking 30 minutes/day, 6 days/week)

3) stress management (gentle yoga-based stretching, breathing, meditation, imagery, and progressive relaxation techniques 60 minutes/day, 6 days/week), and a 1-hour group support session, once per week

4) Taking supplements of soy, fish oil, vitamin E, selenium, and vitamin C

Dr. Blackburn’s research suggests that healthy lifestyle choices may be acting via one final common pathway: telomerase activation.  And now, there is a safe way to activate telomerase that over 1,000 people have taken since 2005.

——————— Nature’s experiments ——————–

Not convinced? Consider Nature’s experiment of people completely devoid of telomerase activation, a disease called Dyskeratosis Congenita. Those kids die by age 12 of age-related illnesses such as heart attacks and cancer (N.B. their cancers suggest that chromosomal damage from telomere instability causes cancer, not telomerase activation as the naysayers of TA-65 say, unencumbered by data or a sound theoretical basis.)

Dyskeratosis Congenita suggests that your life expectancy without any telomerase activation is a meager 12 years. The fact is, the more telomerase activity you can muster, the better.

Two other validations of improved longevity being associated with increased telomerase activity come from Ashkenazi Jews who lived to 100 and trees that lived to 5,000 years .

I believe that the other major theories of aging, such as intracellular junk and oxidative damage, are off the mark.  But you might cry foul and tell me:  “Dr. Park, ‘when all you have is a hammer, everything looks like a nail.’ Aging isn’t all attributable to the telomeres and the only reason you think so is because you’re selling TA-65.”

But I would reply that with 92 nails per cell (i.e. telomere caps) and the need to copy and protect them 4.8 trillion times a day, you had better have a lot of hammers at work. The experiments of a Nobel Prize winner AND Mother Nature, as well as the benefits that we, the TA-65 pioneers, have enjoyed, all suggest that telomerase activation is strongly associated with healthier lifestyles and healthier living.

When all you have is nails, you better have a lot of hammers

Taking TA-65 is a safe and natural way to increase your telomerase activity and we believe that is a good thing.   Call me if you would like to join our revolution against aging because “the proof of the pudding is in the eating” and the only way you’ll ever be truly convinced is to what I did: try it yourself.

05 NovFor death begins with life’s first breath…

“For death begins with life’s first breath…and life begins at touch of death.”
- John Oxenham

Your lung function, as measured by FEV1 (forced expiratory volume in 1 second), is highly correlated with of your age and your risk of dying. Mostly because of the inevitable aging of your lung’s stem cells, your measured FEV1 will decrease an average of 1% a year.

lung capacity by age

Lung capacity declines as you age

So starting from an optimal age of 25, a 65 year-old has lost about 40% of his lung volume and that loss will be ongoing and progressive.

Larry was a 65 year-old healthy man who underwent biometric testing before and after taking the supplement TA-65. He changed nothing else in his lifestyle and yet his lung functioning went from a very respectable 3.8 liters to 4.6 liters after only 15 months.


The skeptics among you will say this is just one case, a mere anecdote, and it could represent measuring error, placebo effect, or fraud.

I assure you that these changes are real, but even more compelling is the fact that they did not occur in isolation. In fact, all his objective measurements of aging improved.

His circulation improved dramatically because of softening of his arteries and his vision improved as well, owing to a softening of his lens.

I’ve personally been taking TA-65 for three years and I can tell you that the change is gradual, without any psychotropic or anabolic effects, which is why most people won’t perceive the ongoing improvements. That’s why as a patient of Recharge Biomedical Clinic, we will establish your objective organ reserves so that there can be no doubt about your cellular rejuvenation after taking TA-65.

Improved lung function creates better health and well-being and that is exactly what Mr. Simpson describes in this CBS news story. Take advantage of this safe and natural telomerase-activating technology to RECHARGE your vitality as well.

Please call or email us with your questions today because we look forward to helping you start your journey back to a more youthful and hopeful you.

“Most persons have died before they expired – died to all earthly longings, so that the last breath is only, as it were, the locking of the door of the already deserted mansion.”
-Oliver Wendell Holmes

29 AugTA-65 in Scientific American

Telomerase Activation Sciences, Inc.
Dear T.A. Sciences Friend,

As a member of our mailing list you have received updates over the past two years about the world of telomerase activation.  We wanted to be sure that you saw this current article below from Scientific American.  It is further validation of the work we do and the exciting promise of telomerase activation.  Feel free to email or call us anytime with your questions about TA-65.

Thanks for your interest in lengthening our Healthspans.
The T.A. Sciences Team!

SCIENTIFIC AMERICAN

News -  August 17, 2009
Anti-Aging Pill Targets Telomeres at the Ends of Chromosomes
Could the secrets to anti-aging be at the tips of our chromosomes?
By Mandy Kendrick

Peter Pan stayed forever young in Neverland. In real life, some scientists are looking at telomeres, or regions of repetitive DNA at the ends of our chromosomes, to try to arrive at something like a real version of this story.

Telomeres consist of up to 3,300 repeats of the DNA sequence TTAGGG. They protect chromosome ends from being mistaken for broken pieces of DNA that would otherwise be fixed by cellular repair machinery. But every time our cells divide, the telomeres shrink. When they get short enough, our cells no longer divide and our body stops making those cells. Over time, this leads to aging and death.

New York-based T.A. Sciences claims to be the only company in the world manufacturing a supplement in a pill form that has been lab tested and shown to stop telomeres from shortening, in hopes of halting the aging process. The product, TA-65, comes from extracts of the Chinese herb astragalus, which has been used for medicinal purposes for more than 1,000 years, says Noel Patton,chief executive officer of the company.

TA-65 is produced at very low levels in the astragalus plant, but the company purifies and concentrates the substance, which is thought to “turn on” the enzyme telomerase (hTERT) that acts to maintain or lengthen telomeres. hTERT is usually “off” in adult cells, except in immune, egg and sperm cells, and in malignant cancer-forming cells.

The TA-65 pill requires no approval from the U.S. Food and Drug Administration because it is marketed as a supplement and not a drug. Therefore, T.A. Sciences cannot make claims about the drug’s efficacy at curing disease. But Patton and Calvin Harley, the chief scientific officer at Geron-the company that discovered TA-65-go on to note that researchers have found a correlation between telomere length and susceptibility to certain aging-related diseases.

T.A. Sciences did five years of testing on TA-65, beginning in 2002.  Results from an anti-aging trial can be found at the company’s Web site. Patton says he has been taking the supplement for two years and that everyone at T.A. Sciences over the age of 40 takes the product.

William Andrews has worked on telomere biology for the past 15 years.  He is the chief executive officer of Sierra Sciences, LLC, a rival company that is screening for chemicals to activate telomerase, but also a T.A. Sciences client for the past two-and-a-half years. He thinks that “taking a telomerase inducer is safer than driving my car to work” but acknowledges that there are some unknown risks with taking the product.
For example, telomerase is the same enzyme that allows cancer cells to stop aging or to become immortal, so there is a chance that TA-65 could keep alive cancer cells that would otherwise die, notes Andrews.

However, telomerase activation should keep all telomeres longer in the first place, and that actually reduces the chances of cells becoming cancerous, Andrews notes. He also says that the enzyme should keep immune cells, which can fight off most cancerous cells, alive longer.

Another problem facing telomere science is that no suitable model organism is available for testing. Animals do not age through telomere shortening in the same way that humans do, Harley notes, adding that “not even mice or monkeys have the same telomere aging system. The best system to ultimately test is going to be the human.”

The potential benefits of the supplement seem to outweigh the risk for patients like Andrews. “People such as myself who elect to take TA-65 and look forward to taking even stronger telomerase inducers in the future must act totally on gut feelings,” Andrews notes.

For those who are less adventurous, other researchers have identified lifestyle changes that can help optimize telomerase activity, without the $14,000-per-year price tag of the TA-65 treatment.