FLORIDA  EAST  COAST  POST-POLIO  SUPPORT  GROUP - Vol. 7  #6

       12 Eclipse Trail  /  Ormond  Beach,  FL  32174  /  904  676-2435

        E-Mail:-  bgold@iag.net   -  Web Site:-  iag.net/~bgold/polio.htm

                            MAY/JUNE  2000

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WE  WISH  ALL  OUR  FRIENDS

A  FLOWER  FILLED  MOTHER’S  DAY

A  WEATHERPROOF  MEMORIAL  WEEKEND

-and-

A  FANTASTICAL  FATHER’S  DAY

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               MEETING  NOTICE

 

*Saturday, May 20  --  RED  LOBSTER  RESTAURANT

Sunday, June  14  -  Discussion of GINI Conference.

JULY  and  AUGUST -  No Meetings

 

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OUR UPCOMING CONFERENCE

DEC  8  -  10,  2000

 

Well, our conference plans are coming along –  

 

At the end of this newsletter you will find our “Conference Packet” with a list of our speakers and also a Room Reservation Card from the Hilton, and a Conference Registration form.

 

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EASTER  SEAL  SOCIETY

 

I’m sure all of you have gotten name labels in the mail from various groups requesting a donation.  Well, my brother brought in a label sheet he received – imagine my surpris when it turned out to have the following on the reverse side of the label:-

 

Post Polio Syndrome

 

Post polio syndrome is a “second” disability affecting a large number of polio survivors.  If you had polio and are experiencing unexplained symptoms, you may have the late effects of polio, often referred to as post polio syndrome.

 

Post polio symptoms can appear in the muscles that were affected at the time polio was contracted or in previously unaffected areas.  It can appear at any time and is frequently triggered by a trauma such as surgery, death in a family, emotional upheaval, or accident. 

 

Reportedly, there are 1.6 million polio survivors in the United States, many of whom will experience the late effects of polio.

 

Understand that:

·        Post polio syndrome is not a recurrence of the virus.

·        The rate of decline can be very slow if properly treated.

·        Unexplained symptoms do not mean that you are imagining things.

·        It can strike 10 to 50 years after the polio attack.

·        Your participation in the treatment is a must.

·        Information and support are available.

·        Support groups are vital links to educational information.

 

Symptoms:

·        Unaccustomed fatigue – either rapid muscle tiring or feelings of total body exhaustion.

·        New weakness in muscles – both those originally affected and those unaffected.

·        Pain in muscles and/or joints.

·        Breathing difficulties.

·        Swallowing problems.

·        Non-recognition/denial of symptoms by medical  professionals.

·        Function decline.

·        Depression.

·        Muscle spasms/twitching.

·        Sleep problems.

·        Weakness and muscle atrophy.

·        Anxiety.

 

As a first step, a general evaluation should be made to exclude other conditions which may mimic post polio syndrome.  Further diagnosis and treatment by a specialist may then be necessary.  Some of the specialists dealing with post polio syndrome are neurologists, pulmonologists, physiatrists, and orthopedists.  Easter Seals provides therapy services and post polio support groups throughout the United States.  For more information contact your area Easter Seals.

 

Editor’s Note:-  Our local Volusia/ Flagler Easter Seals has been one of our staunchest supporters from the very beginning of our group in May 1993.  On a personal note – it was through an Easter Seal radio blurb that I first learned about post-polio syndrome back in 1986 while still living on Long Island.  I joined that group at its second meeting and was active in it until moving down to Ormond Beach in January 1992.  When it was found that we needed a post-polio support group in Volusia County, Linda Richards (our co-founder) and I went to the local Easter Seals for support and they have been with us ever since.  Thank you Easter Seals for all your help.

 

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UPCOMING   GINI   CONFERENCE

 

The International Polio Network, GINI, will be holding its Eighth International Polio and Independent Living Conference in St. Louis, MO on June 8th to 10th, at the St. Louis Marriott Pavilion Downtown – 800  228-9290 or 314  421-1776 ($119./night).  Be sure to tell them you are with the GINI Post-Polio Meeting.  Registration for the Conference after May 1st is $190. for polio survivor; the meal package is $105.  If you want a registration form or further information you can get it at www.post-polio.org or give GINI a call at 314 534-0475 or Barbara at 904  676-2435.

 

If you’ve never been to the International Polio Conference, you should make every effort to attend.  Besides having the very best speakers, the meting and networking with other polio survivors from all over the world is well worth the trip.

 

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Reprinted from Post Polio Support Group of Orange County, Fountain Valley, CA – March 2000

 

POLIO  ABOVE  THE  NECK

WITH  DR.  SUSAN  PERLMAN

Reported by Mary Clarke Atwood

Editorial assistance by V. Duboucheron, and

S. Perlman, Neurologist

 

          Dr. Susan Perlman, Director of the UCLA Post-Polio Clinic, spoke at the May 2, 1999 meeting of the Orange County Post-Polio Support Group.  In addition to her responsibilities in the Post-Polio Clinic, Dr. Perlman also serves at the University of California-Los Angeles (UCLA) as Associate Clin8ical Professor of Neurology, and Director of the Neurogenetics Clinic.

 

          Previously much attention has been given to post-polio problems involving the limbs -- a weak leg, fatiguing arms, etc.  These manifestations of Post-Polio Syndrome (PPS) occur in people who had spinal poliomyelitis – the acute infection that affected anterior horn cells in the spinal cord segmentally.

 

          People who had nonparalytic polio, by definition had polioencephalitis.  They had involvement of those brain areas above the spinal cord, and could well have had poliovirus changes in the brainstem (bulbar polio).  So breathing and swallowing problems may be present even in people who ostensibly had nonparalytic polio and also in others who may have no complaints about their legs or arms.

 

          This report focuses on the problems of bulbar polio and other problems that are now manifested in people who have PPS.   The cause of these problems is polio damage that occurred in the upper cervical spine and upward.  Bulbar is defined as polio involvement of the motor nerves in the brainstem.

 

Early Studies:-

          Polio autopsy reports following the epidemics of the 1940s and 1950s showed signs of acute polio infection throughout the body; it was not just restricted to the spinal cord.  There were changes found in upper motor neuron pathways and there were changes found in central brain structures that control alertness, central fatigue, and autonomic functions such as temperature regulation etc.  There were also many changes seen in the brainstem itself.

 

          Probably greater than 90% of a polio survivors motor neurons were somehow affected during the acute stage and had some damage, even if not paralytic.  Autopsy studies have shown that during the acute attack as few as 3 or 4% of the motor neurons remained intact.

 

          There are not many polio survivors seen now who had severe residual effects from the acute bulbar polio infection.  This is probably because when there is a 50% loss of the motor neurons that control breathing or swallowing, a person is going to be in serious trouble.  Many did not survive the acute infection.  Those who survived bulbar polio truly are survivors, said Dr. Perlman.

 

Respiratory Problems:-

          There are some people who had only mild breathing weakness with the original polio, (chest wall weakness or a little diaphragmatic weakness) but their breathing centers in the brainstem were actually intact.  People who had true bulbar polio had involvement that didn’t trigger breathing – they needed to be assisted until those centers came back.  So when looking at post-polio breathing problems, people who had primary muscular manifestations should be included along with those who had bulbar polio.

 

          In other parts of the body such as arms and legs, surviving motor neurons remodeled and adopted the injured or orphaned ones in order to take over function.  However this was not as common in the brain and brainstem.  Since the brainstem has less plasticity and flexibility, it was harder for remodeling to occur to the nerves of the pharyngeal muscles and to those of the upper part of the esophagus.  For years, many survivors have been using compensatory strategies, such as swallowing on the other side of their throat.  Those who had residual problems such as vocal cord paralysis may also have been able to compensate for this.  But when the muscles on the “good” side of their throat begin to weaken, they become aware of a “new” problem in that area.

 

          Muscles that control breathing and swallowing are the same groups of muscles that are involved with speech, to some extent.  These groups of muscles are located in the throat.  So people with PPS who are having problems with swallowing, breathing, or shortness of breath during activities of daily living, might also complain of speech problems.  Although facial, jaw, and throat muscles are controlled in the brain stem, they have rarely been thought of in connection with polio.

 

          Are people who had bulbar polio going to be having increasing bulbar dysfunction?  The following criteria re used to determine increasing bulbar problems:

1.     Severity of residual disability.

2.     Residual bulbar or respiratory   signs.

3.     Later age at onset of acute polio (past age 10).

4.     (Possibly) recent falls or injuries; or surgical procedures in the pharyngeal area; or weight gain, because it puts more pressure on the diaphragm and pharyngeal area.

 

Fortunately our bodies have several safety factors to assure that breathing muscles meet our oxygen and carbon dioxide demands.  The primary muscle for breathing is the diaphragm and the secondary breathing muscles are the external intercostals (the muscles between the ribs).  So if a person has a fatigable diaphragm that tires out by the end of the day, the intercostals will kick in and the person will begin breathing from the chest.  There are also accessory respiratory muscles that help lift the chest from the shoulders.

 

With post-polio breathing problems, part of the problem is going to be muscular.  There may be a diaphragm or secondary assistive muscles not kicking in as well as they should.  There can also be central (brain) changes contributing to this, such as decreased respiratory drive, if those centers were affected originally.  There may be changes in the chemoreceptors: perhaps the sensors are not sensing carbon dioxide (CO2) buildup as sensitively as before.

 

Scoliosis can also cause restriction of breathing.  A person who has a scoliotic spine cannot expand his chest as well so he underbreathes because of it.  If scoliosis is getting worse as a post-polio symptom, it’s going to make that aspect worse and will interfere with breathing.

 

When doctors are looking at respiratory problems of PPS patients, they should look at not only peripheral problems and muscular problems, but also central disregulation of breathing as well.  All these factors are addressed at the UCLA sleep lab, directed by Dr. Frisca Yan-Go.

 

Recent Findings:-

          Dr. Perlman cited a report (“Epidemiology of the Post-Polio Syndrome” by J Ramlow, et al. American Journal of Epidemiology, October 1, 1992) that involved 77 subjects with non-paralytic polio and 474 subjects with paralytic polio.  A change in breathing was observed in 10% of the nonparalytic subjects and in 12% of the paralytic ones.  Swallowing problems were noted in 6% of the nonparalytic subjects in 7% of the paralytic ones.

 

          In the larger ongoing studies at polio centers such as Mayo Clinic, Rancho Los Amigos, and centers in Canada, possibly as many as 40% of the people with PPS are having new respiratory complaints.  (About 80% of PPS patients complain about fatigue.)

 

          Another study of 74 polio survivors who were having shortness of breath found two good measuring devices for patients with increasing respiratory problems:

 

1. Forced expiration (a pulmonary function test) can be a very helpful monitor.  This test shows how hard it is for a person with PPS to breathe out and it requires the use of some of the intercostals muscles and the abdominal muscles.  Dr. Perlman recommends this test every year or so for her patients who have significant breathing complaints.

 

2.  The other helpful thing is to monitor CO2 levels in the blood.  The question is not how much oxygen is a person inhaling, but how much CO2 is a person retaining?  Is a patient not breathing fast enough?  Is the person fatiguing so that he cannot ventilate?  It is the amount of ventilation a person gets that clears the CO2.  So if you are ventilating less efficiently, your CO2 levels are going to go up slowly. 

 

For patients at risk, these researchers felt that anything that was in danger of happening could be detected by measuring maximum expiratory pressure and carbon dioxide levels on a regular basis.

         

Swedish research on cardio-respiratory parameters in PPS patients found a significant incidence of deconditioning.  This goes back to the old thought that everybody should be doing some exercise.  Dr. Perlman says doctors are no longer saying people with PPS should do no exercise:  some exercise, conditioning or aerobic exercise, is important.  Survivors can improve heart function, circulation, and breathing to some extent by doing something that increases the heart rate.  These researchers suggested increasing the heart rate to 70% of maximum by using a pool or other equipment.  They felt these were tolerable levels for their PPS patients.

         

Researchers in Toronto looked at 3 areas of muscles (respiratory, diaphragm, chest wall), bulbar symptoms, the control rate, and scoliosis.  They found that the control panel in the brainstem was the least important of the group.  These people were having problems because of the diaphragm, chest wall fatigue, or due to progressing scoliosis.

          A few of Dr. Perlman’s patients have experienced increased breathing problems at higher altitudes.  Adjustments can be made so those patients can travel at higher altitudes and not feel short of breath all the time.

 

Swallowing:-

          The motor neurons that control swallowing are located in the brainstem.  In order to have an effective swallow, groups of muscles are used to insure that the food is chewed, forms into a bolus, and goes down properly.  The swallowing center coordinates other activities related to swallowing:  chewing, licking, gagging, coughing, sneezing, vomiting, belching, and breathing to some extent (when a person is swallowing, he doesn’t breathe).  It is hard to eat or swallow at the same time as breathing, because the two groups of muscles and nerves are competing against each other.

 

          There are at least a dozen places in the body where a post-polio patient who had some pharyngeal problems or brainstem related swallowing problems could begin to have trouble now with swallowing – either in the steps or in the sequence of swallowing.  For example, people who have weakness in the jaw muscle as a complication of PPS will find it hard to chew when fatigued.  Or people who have a weak soft palette will find that food is slipping into their throat before it is fully chewed and food or drink – drink especially – may be coming out of their nose.

 

          Swallowing problems have been identified in recent studies.  However it is rare to see a PPS patient who is having constant choking.  Most people can think about it and use their conscious mind to control what is going on, thereby preventing swallowing problems from occurring.  Any part of the gastro-intestinal tract – from the mouth all the way to the bottom – could be slowed, weakened, or not working properly due to PPS.  But don’t assume that every symptom a polio survivor gets is due to PPS.

 

          Although common pathways are used for breathing and swallowing, not everyone who has swallowing problems has breathing problems and not everyone who has breathing problems has swallowing problems.  Bulbar muscles can slowly dysfunction and there can be silent swallowing problems.  In a 1991 swallowing study by Dalakas he concluded “…in bulbar neurons there is a slowly progressive deterioration similar to that in the muscles of the limbs.”

 

Blood Pressure and/or Variable Heart Rate:-

          Can high or low blood pressure be a result of polio and PPS?  Can variable pulse rate be made worse, not because of heart disease, but because of post-polio symptoms affecting the area?

 

          The average internist may be hard pressed to believe it possible for polio to be related to current blood pressure or pulse rate problems.  However, vaso-motor centers that control blood pressure and pulse rate are located in the medulla (in the lower brainstem) and also in the autonomic area of the brain.  Since polio damage has been seen in the brain and in the brainstem, this is an area that needs further study.

 

          As we understand what was involved in acute polio and the amount of brain that was involved, recovered motor neurons that might have looked quite complete on the surface could actually be functioning on very shaky ground.  “The majority of motor neurons, in whatever region the poliovirus got to, were probably affected in some way or another”, said Dr. Perlman.

 

To contact UCLA Post-Polio Clinic:-

            Dr. Susan Perlman

            300 UCLA Medical Plaza, Suite B200

            Los Angeles, CA  90024-6975

            Phone  310-794-1195

Audio Tape:-

            A recording of this complete talk is available for $5.00 + $2.00 postage and handling.  Contact:

            Ken Baragar

            817 Irving Place

            Anaheim, CA  92805-5025

            Phone  714-535-2710

         

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Editor’s Note:-  The following article, although having basically nothing to do with PPS, is a good article on health in general.  I remember my mother giving me a spoonful of cod liver oil every morning (ugh!!).

 

Reprinted from USA Weekend, March 3-5, 2000

BOOST  YOUR  BRAIN

                                                                                                            By Jean Carper

 

Conventional wisdom:  We are born with a brain of a certain size and potential, and we can do little to improve it.  Our intellectual and emotional destiny is decided at birth.

 

The new reality:  Our brains are growing, ever-changing organs, and we can dramatically influence their functioning by what we eat, the supplements we take and the physical and mental stimulation we engage in.

 

          Brain researchers have made amazing discoveries over the past few years about  the enormous ability of the brain to reinvent itself constantly.  They have learned, for instance, that by feeding the brain nutrients and other natural substances, we can expand its power, alter mood and reduce susceptibility to brain damage and neurological diseases.  For the first time, scientists are suggesting ways to improve the brain’s biological structure and electrochemical wiring to help us realize our optimal potential for mental achievement, happiness and fulfillment.

 

          How is this possible?  Chemicals in foods and supplements actually can improve the structure of individual braincells and the efficiency of their communication centers so messages are transmitted more clearly and quickly.  Armed with this new knowledge, we can optimize our brain’s wiring to achieve peak mental and emotional well-being at any age  --  whether we are 3 or 93.

 

Just Two Examples of

New Breakthroughs:

 

?  U.S. Department of Agriculture researchers fed a group of young men a diet high in the mineral selenium (220 micrograms daily vs. the 40-60 micro-grams in a typical American diet) for about three months.  Selenium is found in grains, garlic, meat, seafood (oysters, swordfish, tuna) and Brazil nuts, or it can be taken as a supplement.  The new diet sent morale soaring:  The men reported feeling more clearheaded, elated, confident and energetic.  A USDA researcher, psychologist James Penland, says the extra selenium lifted the men’s moods even though they had no signs of selenium deficiency.  In other words, undetected deficiencies may run our moods and we don’t even know it.

 

?  Two types of vitamin E  --   the anti-oxidant powerhouse – can prevent surgery in some patients with severe narrowing of the carotid artery in the neck, one of the biggest causes of stroke.  Cardiologist Marvin Bierenbaum of the Kenneth L. Jordan Heart Research Foundation in Montclair, NJ, gave 50 patients a vitamin E combination of 100 milligrams of alpha tocopherol plus 240 mg of tocotrienols.  This duo acted as a Roto-Rooter through the blockages in 40% of the patients.

 

          So where to begin to boost our brains, based on all this exciting research?

 

1.  Take a multivitamin.  The evidence is utterly compelling that taking modest doses of a variety of vitamins and minerals is excellent brain insurance.  They can preserve and improve intellectual functioning and emotional well-being, most likely at all ages.  For instance, between one third and half of schoolchildren who took a multivitamin-mineral supplement raised their non-verbal IQ scores as much as 25 points, according to several American and British studies.  That’s an astounding 23 million to 35 million U.S. children.  “No known pharmacological drug can cause this type of impact,” says British psychologist David Benton, author of one of the studies.

 

2.  Add antioxidant supplements.  Most brands of multivitamins don’t contain sufficiently high amounts of the powerful brain-protecting antioxidant vitamins E and C, let alone important alpha lipoic acid and coenzyme Q10.  How much should you take?  Dr. Lester Packer at the University of California, Berkeley, recommends 400 to 500 IUs of vitamin E, 500-1,000mg vitamin C, 10-50mg lipoic acid.  (Packer himself takes 100mg divided between the morning and evening, and he says diabetics may need 200-600mg.)  There is no established dose for coQ10, but Packer and other experts recommend 30mg.  You may need 100-200mg if you smoke, have heart disease or are at high risk of degenerative brain disease.  Unfortunately, coQ10 supplements are expensive because Japanese producers have a monopoly.  Should children take anti-oxidants, too?  Yes, says Packer, who recommends half the usual adult dose.

 

3.  Load up on foods with antioxidants, too.   Think of it this way:  Our whole bodies are exposed to constant assaults by harmful free-radical chemicals that, to be blunt, turn us and our brains rancid, just like a fatty piece of meat that has been left out of the refrigerator too long.  Eventually, free-radical damage can kill brain cells, leading to sharp mental decline.  Alzheimer’s disease and other degenerative brain diseases.  But what if we could don a kind of internal Superman suit that acts as armor to repel or neutralize those perpetual chemical attacks?  Actually, we can.  It’s not difficult to take in high doses of antioxidants in modest amounts of fruits and vegetables.  Just three prunes, one cup of mixed blueberries and strawberries, plus a half cup of cooked spinach would put us over the top for the very highest daily intake of antioxidants recommended by authorities.  Generally brightly colored fruits and berries and dark green leafy vegetables are the ones highest in antioxidants.  Snacking on raisins, berries, apples, grapes, cherries or prunes – instead of or even in addition to the usual chips – could make all the difference in intellectual power and emotional well-being.

 

4.  Sip a cup of tea.  It’s one of the easiest, quickest ways to infuse the body and brain with antioxidants – and with virtually no calories.  Put one tea bag – plain black tea (yes, the stuff you see on supermarket shelves, such as Lipton’s, Twinings or Bigelow) or more exotic Asian green tea – in five ounces of boiling water.  Let it brew for five minutes and drink it.  In an instant you’ve taken in about 1,200 ORAC units of antioxidants      -- about a third to a fourth of the total daily recommended amounts, according to Tufts University researchers.  Iced tea counts, too.  You don’t, however, get significant amounts of antioxidants in herbal teas, commercial bottled teas or powdered tea mixes, according to the Tufts analyses.

 

5.  Get omega-3-type fish oil by eating fish or taking supplements.  The oil actually creates new communication centers in neurons and is absolutely essential for optimal brain functioning and mood.  Without omega-3, your brain cells, stiffen and wither, stifling message transmission.  Stunning new research ties a lack of fish oil in the diet to a whole host of problems, from low intelligence and learning disabilities to depression and degenerative neurological diseases.  Developing brains – in the womb, in infancy and in childhood – especially require omega-3 type fish oil to construct the best neuronal architecture and biochemical wiring.  Children who fail to get enough omega-3 in the early developmental periods may have lower Iqs later in life.  Nor can adult brains achieve top cognitive potential without adequate supplies of omega-3 fatty acids.  In one study, men who ate three quarters of an ounce of fish daily cut their odds of age-related memory decline by 60%, compared with non-fish eaters.  One fraction of fish oil, DHA, has been shown to enhance brain power, speed and efficiency, memory and learning, and may even help prevent and possibly treat Alzheimer’s disease.  Omega-3 fat also tells the brain to feel good, probably by boosting production of the neuro-transmitter serotonin.   New evidence shows that fish oil helps prevent and even relieve major depression.  It also can help block brain damage from alcoholism, and is being tested as a possible treatment for schizophrenia.  How much do we need?  A couple of servings of fish (especially fatty fish such as salmon, mackerel, sardines, herring) or an ounce or two a day is enough to keep brain cells happy.  If you don’t like fish, take about 650mg a day of omega-3s (DHA, or docosahexaenoic acid, and EPA, eicosapentaenoic acid) in capsules.  You can even buy DHA alone (even in vegetarian form), which is specifically recommended for pregnant and lactating women to enhance fetal and infant brain development.

 

6.  Lose the bad fats.  We can take the perfectly good brain w were born with and screw up its communication circuits by feeding it the wrong type of fat – at any age.  Americans typically eat 165 times more potentially brain-destructive oils than brain-building omega-3-type fats.  Because this dynamic organ is made up mostly of the fat we feed it, it becomes the prime target of this dangerous fat imbalance.  Probably the most dangerous to brain cells is saturated animal fat, so pervasive in fast foods such as burgers and shakes.  Also detrimental to cells:  to much polyunsaturated vegetable oil – so-called omega-6s – such as safflower, sunflower and corn oils, that can set up chronic inflammatory responses in brain tissue, thought to eventually lead to subtle brain damage, strokes and Alzheimer’s disease.  Eating trans-fatty acids, in processed foods such as salad dressings, fries, doughnuts and most margarines, also can foster blood-vessel damage that is detrimental to blood circulation in the brain.

 

7.  Take brain-boosting supplements.  Some over-the-counter supplements can help rejuvenate brain-cell activity.  A favorite is ginkgo biloba, and the scientific buzz is so good that countless prestigious scientists take it themselves, hoping to ward off age-related memory loss.  For instance, Jerry Cott, chief of research on pharmacological treatment at the National Institute of Mental Health, takes 240mg of ginkgo a day.  How, exactly, does it slow the gradual decline in mental faculties?  In several studies, Dr. Packer of Berkeley has shown that ginkgo zaps two of the more virulent free radicals that readily savage brain cells.  It also helps increase the circulation of blood and oxygen; many experts think this alone makes ginkgo a formidable brain-booster .  Another potential brain-saving is phosphatidylserine, or PS, reputed to stimulate production of the “memory” neurotransmitter acetylcholine, which may decline as we get older.  Dr. Thomas Crook III gave half of 150 patients, ages 50 to 75 and all with memory problems, 100mg of PS three times a day for 12 weeks.  The other half received a placebo.  All subjects took a battery of neuropsychological tests.  Those taking PS scored about 30% higher on tests of learning and memory, and those with the worst memory deficits benefited the most.  “PS is not a magic bullet,” says Crook.  “It’s not like you’re 75 and take it and become 25.  But it is the first thing we’ve ever seen of many, many compounds that does have a clear measurable effect – and that effect is about 12 years of rolling back the clock .  I really firmly believe PS can roll back virtually all age-related memory impairment.”

 

8.  Watch sugar, including blood sugar.   Eating too much sugar, and certain other carbohydrates, is not a good idea for young or old brains.  Sugar overloads can inspire “insulin resistance,” throwing blood-sugar (glucose) levels out of whack, as well as causing permanent damage to brain cells, leading to malfunction and death.  But because the brain runs on energy derived mostly from carbohydrates, it’s essential to have the right blood sugar available to the brain at every instant to promote memory, learning and other cognitive functions.  Carbohydrates also may influence mood.  But it is a delicate balance.  “Eating white potatoes or white bread is just like eating candy, as far as your body knows,” says Walter Willett, chairman of nutrition at the Harvard School of Public Health.  So, for an optimally functioning brain, restrict these “fast carbs” and instead choose carbohydrates that are digested slowly, including peanuts, dried apricots, dried beans, yogurt, oat bran, All Bran cereal and sourdough bread.  Adding vinegar or lemon juice to foods also suppresses a sharp rise in blood sugar.  So does taking 200 micrograms a day of chromium.

 

Bottom line:-  Our brains grow and change every instant.  The brain thrives on stimulation, exercise, education and the right diet and supplements.  It is never too early or too late to start shaping your brain’s destiny.

 

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TOP  10  ANTIOXIDANT  FOODS

 

In order of greatest concentration:

1.  Prunes                     6.  Cooked kale

2.  Raisins                     7.  Cranberries

3.  Blueberries              8.  Strawberries

4.  Blackberries            9.  Raw Spinach

5.  Garlic                       10.  Raspberries

 

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IMPORTANT  NEWS

YOUR  BRAIN  CAN  USE

 

What we know about how the brain works has exploded in the past decade.  Here are some highlights from groundbreaking research at leading scientific centers, including the National Institutes of Health, Harvard, the University of California, Tufts and other facilities worldwide.

 

" Eating blueberries, one of the foods highest in antioxidants, dramatically reversed memory loss and restored motor coordination and balance in aged animals, according to new Tufts University research.  The animals ate an amount equal to about half a cup a day for humans.

 

"  Middle-aged men with the highest blood level of vitamin B6 scored twice as high on a memory test as those with the lowest B6, found Tufts researchers.  The higher the B6, the higher the memory scores.

 

"  Older people taking vitamin supplements, notably B vitamins, had “higher cognitive performance” than non-supplement takers and “scored as well as or better than younger adults on verbal memory,” according to University of New Mexico researchers.

 

"  High doses of the supplement coenzyme Q10 stimulated dopamine activity in nerve cells, leading the National Institutes of Health to launch new studies of coQ10 as a treatment for Parkinson’s and Huntington’s diseases.