Daily Archives: January 1, 2016

The Trouble With Atheism | Documentary Heaven

Posted: January 1, 2016 at 10:44 pm

The Trouble with Atheism is an hour-long documentary on atheism, presented by Rod Liddle. It aired on Channel 4 in December 2006. The documentary focuses on criticizing atheism, as well as science, for its perceived similarities to religion, as well as arrogance and intolerance. The programme includes interviews with a number of prominent scientists, including atheists Richard Dawkins and Peter Atkins and Anglican priest John Polkinghorne. It also includes an interview with Ellen Johnson, the president of American Atheists.

Liddle begins the documentary by surveying common criticisms of religion, and particularly antireligious arguments based on the prevalence of religious violence. He argues that the very stupid human craving for certainty and justification, not religion, is to blame for this violence, and that atheism is becoming just as dogmatic as religion.

In order to support his thesis, Liddle presents numerous examples of actions and words by atheists which he argues are direct parallels of religious attitudes. He characterizes Atkins and Dawkins as fundamentalist atheists and evangelists.

In response to atheistic appeals to science as a superior method for understanding the world than religion, Liddle argues that science itself is akin to religion: the problem for atheists is that science may not be as far away from religion as you might imagine.

He describes Fermilab, a U.S. Department of Energy National Laboratory focused on particle physics, as a temple to science, and characterizes Charles Darwins The Origin of Species as a sacred text for atheists.

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The Human Life Span Defined – Longevity Advice from About.com

Posted: at 10:42 pm

Updated December 15, 2015.

The human life span is themaximum number of years an individual from the human species can live based on observed examples. Though this definition of life span may seem simple enough, it is often confused for other common concepts in the study of the aging, life, and death of living organisms. In order to better understand the human life span, let's dive a little deeper into the concept and its important distinctions from other commonly used terms.

The term life span is most commonly confused with another important concept: life expectancy. While both terms relate to the number of living years, they actually define very different concepts.While the term life span refers to the maximum number of years an individual can live, life expectancy refers to an estimate or an average number of years a person can expect to live.

Most simply put, life expectancy can be attributed to and impacted by an individual and their personal health history, genetics, and lifestyle, whereas life span holds for all living humans.

For example, my life expectancy is affected by personal factors like my family history, my environment, my diet, and even my age and sex. My life expectancy might be different for your life expectancy and it may even change over time. Our life spans, however, are one in the same. We share it as members of the same species. So what is the human life span?

Given that the human life span is defined by the longest observed human life from birth to death, it is a figure that has changed over the years.

For humans, the current accepted maximum life span is 122 years. This age was achieved by Jeane LouiseCalmentof France. Calment lived from February 21, 1975 to August 4, 1997 until she was exactly 122 years and 164 days old. Remarkably, Calmentremained relatively healthy and mentally intact until her 122 birthday.

Though there have certainly been claims of longer lives, none of the claims were acceptably documented and verified. Calment remains the first verified person to reach any age between 116 and 122 and the only verified person to reach the age of 122.

With the United State's average life expectancy currently hovering at around 78.88 years, the age to which most Americans can expect to live is still forty-four years younger than the human life span. So how do we close that gap and elongate our lives? There will always be factors that are out of our individual control like our inherited genes, but we shouldn't discount the impact of those that we can control. It is generally understood that closing the gap between life expectancy and life span can be done through healthier living, less exposure to toxins, the prevention of chronic illnesses, and a little bit of luck.

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Psoriasis – In-Depth Report – NY Times Health

Posted: at 10:41 pm

In-Depth From A.D.A.M. Background

An estimated 7.5 million Americans (2.2% of the population) have psoriasis. Psoriasis is a chronic skin disorder in which there are periodic flare-ups of sharply defined red patches, covered by a silvery, flaky surface. The main disease activity leading to psoriasis occurs in the epidermis, the top five layers of the skin.

The process starts in the basal (bottom) layer of the epidermis, where keratinocytes are made. Keratinocytes are immature skin cells that produce keratin, a tough protein that helps form hair, nails, and skin. In normal cell growth, keratinocytes grow and move from the bottom layer to the skin's surface and shed unnoticed. This process takes about a month.

In people with psoriasis, the keratinocytes multiply very rapidly and travel from the basal layer to the surface in about 4 days. The skin cannot shed these cells quickly enough, so they build up, leading to thick, dry patches, or plaques. Silvery, flaky areas of dead skin build up on the surface of the plaques before being shed. The skin layer underneath (dermis), which contains the nerves and blood and lymphatic vessels, becomes red and swollen.

Various forms of psoriasis exist. Some can occur alone or at the same time as other types, or one may follow another. The most common type is called plaque psoriasis, also known as psoriasis vulgaris.

Plaque psoriasis leads to skin patches that start off in small areas, about 1/8 of an inch wide. They usually appear in the same areas on opposite sides of the body.

The patches slowly grow larger and develop thick, dry plaque. If the plaque is scratched or scraped, bleeding spots the sizes of pinheads appear underneath. This is known as the Auspitz sign.

Some patches may become ring-shaped (annular), with a clear center and scaly raised borders that may appear wavy and snake-like.

As the disease progresses, eventually separate patches may join together to form larger areas. In some cases, the patches can become very large and cover wide areas of the back or chest. This is known as geographic plaques because the skin lesions resemble maps.

Plaque psoriasis may persist for long periods of time. More often it flares up periodically, triggered by certain factors such as cold weather, infection, or stress.

Patches most often occur on the:

They may also be seen on the:

Psoriasis of the scalp affects about 50% of patients. In some cases, the psoriasis may cover the scalp with thick plaques that extend down from the hairline to the forehead.

Psoriasis patches rarely affect the face in adulthood. In children, psoriasis is most likely to start in the scalp and spread to other parts of the body. Unlike in adults, it also may occur on the face and ears.

Psoriasis Form

Description of Skin Patches

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Guttate Psoriasis

The patches are teardrop-shaped and appear suddenly, usually over the trunk and often on the arms, legs, or scalp. They often disappear without treatment.

Guttate psoriasis can occur as the initial outbreak of psoriasis, often in children and young adults 1 - 3 weeks after a viral or bacterial (usually streptococcal) respiratory or throat infection. A family history of psoriasis and stressful life events are also highly linked with the start of guttate psoriasis.

Guttate psoriasis can also develop in patients who have already had other forms of psoriasis, most often in people treated with widely-applied topical (rub-on) products containing corticosteroids.

Inverse Psoriasis

Patches usually appear as smooth inflamed areas without a scaly surface. They occur in the folds of the skin, such as under the armpits or breast, or in the groin.

Inverse psoriasis may be especially difficult to treat.

Seborrheic Psoriasis

Patches appear as red scaly areas on the scalp, behind the ears, above the shoulder blades, in the armpits or groin, or in the center of the face.

Seborrheic psoriasis may be especially difficult to treat.

Nail Psoriasis

Tiny white pits are scattered in groups across the nail. Toenails and sometimes fingernails may have yellowish spots. Long ridges may also develop across and down the nail.

The nail bed often separates from the skin of the finger and collections of dead skin can build up underneath the nail.

Over half of patients with psoriasis have abnormal changes in their nails, which may appear before other skin symptoms. In some cases, nail psoriasis is the only symptom.

Generalized Erythrodermic Psoriasis (also called psoriatic exfoliative erythroderma)

This is a rare and severe form of psoriasis, in which the skin surface becomes scaly and red. The disease covers all or nearly all of the body.

About 20% of such cases evolve from psoriasis itself. The condition may also be triggered by certain psoriasis treatments, and other medications such as corticosteroids or synthetic antimalarial drugs.

Pustular Psoriasis

Patches become pus-filled and blister-like. The blisters eventually turn brown and form a scaly crust or peel off.

Pustules usually appear on the hands and feet. When they form on the palms and soles, the condition is called palmar-plantar pustulosis.

Pustular psoriasis may erupt as the first occurrence of psoriasis, or it may evolve from plaque psoriasis.

A number of conditions may trigger pustular psoriasis, including infection, pregnancy, certain drugs, and metal allergies.

Pustular psoriasis can also accompany other forms of psoriasis and can be very severe.

Psoriatic arthritis (PsA) is an inflammatory condition that leads to stiff, tender, and inflamed joints. Estimates on its prevalence among people with psoriasis range from 2 - 42%. AIDS patients and those with severe psoriasis are at higher risk for developing PsA.

About 80% of PsA patients have psoriasis in the nails. Arthritic and skin flare-ups tend to occur at the same time. It is not clear whether psoriatic arthritis is a unique disease or a variation of psoriasis, although evidence suggests they are both caused by the same immune system problem.

PsA is often divided into five forms. The forms differ according to the location and severity of the affected joint:

People who start to smoke after developing psoriasis may delay the onset of psoriatic arthritis. However, research has also linked smoking to an increased risk of psoriasis, and because smoking causes serious health problems, it should not be considered as a way to delay this type of psoriasis.

The precise causes of psoriasis are unknown. It is generally believed to be caused by damage to factors in the immune system, enzymes, and other materials that control skin cell division. This prompts an abnormal immune response, which causes rapid production of immature skin cells and inflammation.

The Normal Immune System Response. The inflammatory process is the result of the body's immune response, which fights infection and heals wounds and injuries:

The Infection Fighters. The primary infection-fighting units are two types of white blood cells: lymphocytes and leukocytes.

Lymphocytes are a type of white blood cell designed to recognize foreign substances (antigens) and launch an offensive or defensive action against them. Lymphocytes include two subtypes known as T cells and B cells:

A type of T cell called a helper T cell stimulates B cells and other white blood cells to attack a foreign substance. In psoriasis, however, the helper T cell appears to direct the B cells to produce autoantibodies ("self" antibodies), which attack skin cells. In psoriatic arthritis, cells in the joints also come under attack.

In psoriasis, helper T cells also release or stimulate the production of powerful immune factors called cytokines. In small amounts, cytokines are very important for healing. However, the high level of these cytokines that occurs in psoriasis can cause serious damage, including inflammation and injury during the psoriasis disease process.

A combination of genes is involved with increasing a person's susceptibility to the conditions leading to psoriasis. However, researchers are still unsure as to exactly how the disease is inherited.

HLA Molecules. The processes leading to all autoimmune diseases involve the human leukocyte antigens (HLA), a group of protein markers found on cells. Most immune disorders are associated with problems in how the body reacts to these different protein markers or antigens. However, other genetic and environmental factors are required to actually trigger the disease.

Four key genes (named PSOR 1 - 4) seem to be involved with psoriasis. Certain variations or changes in these genes may increase the risk of psoriasis. These same variations linked to psoriasis and psoriatic arthritis are also associated with four autoimmune diseases: type 1 diabetes, Grave's disease, celiac disease, and rheumatoid arthritis, suggesting that all of these diseases have the same genetic basis.

The presence of a recently identified variation in a group of genes known as LCE can protect against the development of psoriasis.

Weather, stress, injury, infection, and medications, while not direct causes, are often important in triggering the disease process that initiates and worsens psoriasis.

Weather. Cold, dry weather is a common trigger of psoriasis flare-ups. Hot, damp, sunny weather helps relieve the problem in most patients. However, some people have photosensitive psoriasis, which actually improves in winter and worsens in summer when skin is exposed to sunlight.

Stress and Strong Emotions. Stress, unexpressed anger, and emotional disorders, including depression and anxiety, are strongly associated with psoriasis flare-ups. Research has suggested that stress can trigger specific immune factors associated with psoriasis flares.

Infection. Infections caused by viruses or bacteria can trigger some cases of psoriasis. For example:

Skin Injuries and the Koebner Response. The Koebner response is a delayed response to skin injuries, in which psoriasis develops later at the site of the injury. In some cases, even mild abrasions can cause an eruption, which may be why psoriasis tends to frequently occur on the elbows or knees. However, psoriasis can develop in areas that have not been injured.

Medications. Drugs that can trigger the disease, worsen symptoms, or cause a flare-up include:

Severe flare-ups may occur in people with psoriasis who stop taking their steroid pills by mouth, or who discontinue the use of very strong steroid ointments that cover wide skin areas. The flare-ups may be of various psoriatic forms, including guttate, pustular, and erythrodermic psoriasis. Because these drugs are also used to treat psoriasis, this rebound effect is of particular concern.

Medications that cause rashes (a side effect of many drugs) can trigger psoriasis as part of the Koebner response.

Risk factors for psoriasis include:

A microscopic examination of tissue taken from the affected skin patch is needed to make a definitive diagnosis of psoriasis and to distinguish it from other skin disorders. Usually in psoriasis, the examination will show a large number of dry skin cells, but without many signs of inflammation or infection. Specific changes in the nails are often strong signs of psoriasis.

The severity of psoriasis ranges from one or two flaky inflamed patches to widespread pustular psoriasis that, in rare cases, can be life threatening. To help determine the best treatment for a patient, doctors usually classify the disease as mild to severe. The classification depends on how much of the skin is affected:

The palm of the hand equals 1% of the body.

The severity of the disease is also measured by its effect on a person's quality of life.

The National Psoriasis Foundation has proposed a new classification method. The group suggests a two-tiered system that classifies patients as needing either local or body-wide (systemic) treatment.

In general, severe or widespread psoriasis is harder to treat. However, some forms of psoriasis can be very resistant to treatment, even though they are not categorized as severe. They include:

Many creams, ointments, lotions, and pills are available to treat psoriasis. Some patients require only over-the-counter treatment, or even no treatment.

Many patients with psoriasis, however, do not respond to over-the-counter remedies and lifestyle changes, and require aggressive treatments. In some cases, such treatments need to be lifelong.

In general, there are three treatment options for patients with psoriasis:

Individual needs vary widely, and treatment selection must be carefully discussed with the doctor.

Giving treatment in a stepwise order can help provide quick symptom relief and long-term maintenance. It involves three main steps:

Choices for transitional or maintenance treatments depend on the severity of the condition.

In severe chronic cases, the doctor may recommend rotational therapy. This approach alternates treatments. The goal is to prevent severe side effects or the build-up of resistance from long-term use of a single medicine. An example of a rotational schedule may be the following:

Doctors increasingly use combinations of pills, creams, ointments, and phototherapy instead of single medications. Combinations of oral treatments are particularly useful, because the doses of each drug can be reduced. This lowers the risk of severe side effects. Thousands of combinations are possible, and patients should discuss with their doctors the best treatment for their individual needs.

Topical medications are those applied only to the surface of the body. They come in the following forms:

In general, topical treatments are the first line for mild-to-moderate psoriasis, but they may also be used, alone or in combination, with more powerful treatments for moderate-to-severe cases. Topical medicines rarely clear up symptoms completely, however.

Topical corticosteroids are the mainstay of psoriasis treatment in the United States. These drugs work for most patients because they:

Corticosteroids are available in a wide range of strengths, and are generally given as follows:

Topical steroids are often rated by how strong or potent they are:

In the past, topical steroids were used twice a day. For some patients, certain drugs may work just as well if taken once a day. Both high-potency steroids, and possibly medium-strength steroids, such as triamcinolone (Aureocort, Tri-Adcortyl), may be as beneficial as a once-daily treatment.

However, corticosteroids used alone are not enough for most patients. Combining topical steroids with other topical drugs (see below) is often needed. Many patients also need oral medicines.

Side Effects. The more powerful the corticosteroid, the more effective it is. But more powerful steroid drugs also have a higher risk for severe side effects, which may include:

Loss of Effectiveness. In most cases, patients become tolerant to the effects of the drugs, and the drugs no longer work as well as they should. Some experts recommend using intermittent therapy (also called weekend or pulse therapy). This type of treatment involves applying a high-potency topical medication for 3 full days each week.

A topical form of vitamin D3, calcipotriene (Dovonex) is proving to be both safe and effective. It is now available in a foam preparation, which makes using it even easier. Several other topical vitamin D3-related drugs that are showing promise include maxacalcitol (Oxarol), tacalcitol, and calcitriol (Silkis).

Calcipotriene appears to:

It works just as well as moderate topical corticosteroids, short-term anthralin, and coal tar in improving mild-to-moderate plaque psoriasis. But unlike with steroids, patients do not develop thinning of the skin or tolerance to the drug.

Using the drug in combination with other topical and body-wide treatments may improve its effectiveness. Calcipotriene doesn't work as well as the highest potency corticosteroids, but combining both medications is proving to be more effective than taking either one alone. Taclonex, an ointment containing both calcipotriol and betamethasone, is available for the treatment of adults with psoriasis. Studies show the combination works better than either drug alone.

Combining vitamin D ointments with systemic medicines, notably methotrexate, acitretin, or cyclosporine, increases its effectiveness. Because combining medications allows patients to use lower doses of both medications, it reduces side effects.

Studies also report success in some patients who use vitamin D ointments in combination with phototherapy treatment.

Side Effects. Calcipotriene may cause the following side effects:

Calcipotriene appears to cause greater skin irritation than potent corticosteroids. Diluting the drug with petrolatum or applying topical corticosteroids to sensitive areas may prevent this problem.

Coal tar preparations have been used to treat psoriasis for about 100 years, although their use has declined with the introduction of topical vitamin D3-related medicines. Crude coal tar stops the action of enzymes that contribute to psoriasis, and helps prevent new cell production. Tar is often used in combination with other drugs and with ultraviolet B (UVB) phototherapy.

Side Effects. Preparations have the following drawbacks:

Anthralin (Dritho-Scalp, Drithocreme, Micanol) slows skin cell reproduction and can produce remissions that last for months. It is recommended only for chronic or inactive psoriasis, not for acute or inflamed eruptions. People with kidney problems should use anthralin with caution.

As with tar, anthralin's use has also declined since the introduction of the topical vitamin D-related medicines, but newer formulations, such as Micanol, have made its use more tolerable. Micanol (Psoriatec) is an anthralin formulated in microcapsules, which dissolve and allow the drug to be delivered directly to the target skin areas. It is particularly useful for scalp psoriasis, and it is less likely than other formulations to stain.

Side Effects. Anthralin may cause the following side effects:

Patients should not use anthralin on the face. Fair-skinned people should generally avoid it. Triethanolamine (CuraStain) is a chemical that can neutralize anthralin and help reduce irritation from short-contact anthralin treatment. It should be applied 1 or 2 minutes before washing off the anthralin. It is then reapplied after drying the skin.

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The Multiverse: Is There Evidence For It? – Futurism

Posted: at 10:40 pm

Image collected whilst scouring the CMBR (Source)

Some of you may recall a popular article we posted several months ago, dealing with voids and super-void. These celestial regions (which are devoid of stars, galaxies, planets, clusters, and other forms of matter) were initially discovered while physicists were busy mapping the cosmic microwave background radiation (CMB). This radiation is a relic from the big bang; it originated during the opening chapter of our universe, when the cosmos was a mere 380, 000 years in age. This background radiation should be evenly dispersed throughout the universe. Instead, physicists noted a huge cold spot stretching across an expanse of space almost one billion light-years in diameter. This cold spot is located in the constellation of Eridanus, and the discovery baffled astronomers.

Credit: Scientific American (Source)

Since then, many theories have surfaced in an attempt to explain the discrepancy; some of these theories argue that this area might be occupied by auniverse-in-mass black hole or perhaps, it is a leftover souvenirfrom a change in the texture of spacetime. There is also the super-void hypothesis, and some have even suggested that the void is evidence of a parallel (or a sister) universe -meaning that both our universe and our sister-verse belong to a larger multiverse.

The last controversial idea one than many physicists want to believe in was cooked up by Laura Mersini-Houghton, who subsequently made five predictions about the nature of this cold spot in hopes of vindicating the existence of a multiverse. The idea proposed was essentially a landscape multiverse idea. This is something that is believed to be inherently tied to the multiple dimensions of string theory, which gives us an idea of the principles that must be met in order for life to develop in any given universe. In this scenario, our universe is but one in a massively huge number of universes perhaps its just one in an INFINITE number of infinitely large universeshurts your head, doesnt it? (it does mine too)

Out of the five predictions made in Mersini-Houghtons paper, entitled Cosmological Avatars of the Landscape I: Bracketing the SUSY Breaking Scale, 4 have been verified, or at least they havent been ruled out. Here they are as follows:

Lets say our universe is a part of a larger number of multiple universes, our universe most likely formed through a bubble in another universe, created through quantum fluctuations within the vacuum energy (maybe an infinite number of them formed this way too), spawning a universe equipped with its own laws of physics, energy levels, matter concentrations, arrow of time, and entropy level. Some of these said bubbles could collapse in on themselves before undergoing something similar to inflation, with only a certain number of them progressing beyond that point, depending on the characteristics the baby bubble developed early on.

After the bubble stabilizes, it would effectively be cut off from the universe it was born into, losing all of the information from it. However; it could hypothetically interact gravitationally with other universe, which is exactly what Houghton thinks happened in the cold spot in the CMBR an area of space seemingly containing an imprint of another universe apart from our own. Its even possible that in theory, another bubble is developing in our universe.

Though I remain highly skeptical (and so should you. Extraordinary claims require extraordinary evidence, after all) This could very well help explain why our universe appears to be fine-tuned for life from our perspective. After all, if an infinite number of universes exist, an infinite number of them would have each and every characteristic our universe has, with an infinite number of them that are radically different than ours. Can you imagine living in a universe where the arrow of time runs backward, with gravity acting as a repellent force? (basically, a universe where dark energy is the the norm)

Whilst living in a multiverse, its conceivable that such a universe can and does exist. In fact, its quantum mechanics in action. When internal inflation, string theory, Copenhagen interpretation, and the Heisenberg uncertainty principle are thrown into the mix, we get a universe (our universe) created at the whim of a wave function, collapsing with the properties our universe has.

Again with just about everything skepticism is key.Mersini-Houghton, the main proponent of the landscape multiverse idea, is also a fan of string theory. Many of you may know of it as a discombobulated mess that belongs with the crackpot models of the universe instead of acting as if its even plausible to explain the properties of the universe. Were still in the beginning stages of uncovering many universal mysteries so more data is needed.

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The Multiverse: Is There Evidence For It? - Futurism

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