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Aptos, CA psychologist: Laugh and make fun of Fritz M who wants a Dutch politician be-headed. What say you?

An Australian guy named Fritz Muhammad just issued recently a death sentence on a Dutch politician. His web site is kalamullah.com

The reason given by Fritz M. is that the Dutch politician “mocked” and “laughed” at Islam and the Prophet.

Oops! No laughter at “real” religion?

What did the Dutch politician do? He said that Islam religion and political ideology are “retarded”. He and his party do not support more Islamic immigrants to Holland.

According to radical Islamist Australian Fritz M., — an Australian citizen working on a Ph.D. — the Dutch politician should be be-headed.

And thus Fritz M. issued a death sentence on the Dutch politician.

Frankly, I think that Australian Fritz M. should work on be-heading small creatures such as fleas and ants. And then work up to be-heading his personal nails.

I say it is time that moderate Christians, Jews and Islams unite. Is this possible?

Let’s laugh and make fun of people like Fritz M. No, not make fun of Islam. Make fun of Fritz M. who wants to use Islam for his purposes.

So what do you say Fritz M.? If anyone wants to Comment on his web site they MUST leave an e-mail. Not here. Say what you like here. And, no “be-heading” will be recommended.

Fritz M’s web site is: kalamullah.com

written by DrCameronJackson@gmail.com

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Friz Muhammad’s fatwa to behead Dutch politician is only binding on the author.

A fatwa is only binding on its author ….

“Following the Salman Rushdie affair, Western media frequently use the term to mean an Islamic death sentence upon someone who is considered an infidel, apostate or a blasphemer.[2] This is indeed one possibility, but is a rare use for a fatwā, and the equation of fatwā with capital punishment is considered offensive by many Muslims.

The term’s correct definition is broader, since a fatwā may concern any aspect of individual life, social norms, religion, war, peace, Jihad and politics.

Most Islamic opinions—millions of fatwā have been issued over the 1,400 year history of Islam—likely deal with issues faced by Muslims in their daily life, such as the customs of marriage, financial affairs, female circumcision or moral questions.

Fatwa are issued in response to questions by ordinary Muslims, and go unnoticed by those not concerned, while the much smaller number of fatwā issued on controversial subjects such as war, Jihad, Dhmimmis, particularly by extremist preachers, sometimes get wide coverage in the media because of their political content (see examples below).

A fatwā is not automatically part of Islamic teachings. While the person issuing it may intend to represent the teachings of Islam accurately, this does not mean that that person’s interpretation will gain universal acceptance. There are many divergent schools within the religion, and even people within the same current of thought will sometimes rule differently on a difficult issue. This means that there are numerous contradictory fatwā, prescribing or proscribing a certain behavior. This puts the burden of choice on the individual Muslim, who, in case of conflict, will be forced to decide whose opinion is more likely to be correct. On the other hand, some fatwās are considered absolute.
[edit]History

In the early days of Islam, fatwās were pronounced by distinguished scholars to provide guidance to other scholars, judges and citizens on how subtle points of Islamic law should be understood, interpreted or applied. There were strict rules on who is eligible to issue a valid fatwā and who could not, as well as on the conditions the fatwā must satisfy to be valid.

According to the usul al-Fiqh (principles of jurisprudence), the fatwā must meet the following conditions in order to be valid:

The fatwā is in line with relevant legal proofs, deduced from Qur’anic verses and ahadith; provided the hadith was not later abrogated by Muhammad.
It is issued by a person (or a board) having due knowledge and sincerity of heart;
It is free from individual opportunism, and not depending on political servitude;
It is adequate with the needs of the contemporary world.

With the existence of modern independent States, each with its own legislative system, or its own body of Ulemas, each country develops and applies its own rules, based on its own interpretation of religious prescriptions.

Many Muslim countries (such as Egypt and Tunisia) have an official Mufti position; a distinguished expert in the Sharia is appointed to this position by the civil authorities of the country. But his fatwās are binding on no one: neither the State that appoints him, nor any citizen.
[edit]Issuer qualifications

See also: Ijazah and Madrasah
During what is often referred to as the Islamic Golden Age, in order for a scholar to be qualified to issue a fatwā, it was required that he obtained an ijazat attadris wa’l-ifta (“license to teach and issue legal opinions”) from a Madrassah in the medieval Islamic legal education system, which was developed by the 9th century during the formation of the Madh’hab legal schools. Later during the Islamic contributions to Medieval Europe, the ijazat attadris wa’l-ifta evolved into the doctorate, or more specifically the Doctor of Laws qualification, in medieval European universities.[3]
To obtain an ijazat attadris wa’l-ifta in the Madrassah system, a student “had to study in a guild school of law, usually four years for the basic undergraduate course” and ten or more years for a post-graduate course. The “doctorate was obtained after an oral examination to determine the originality of the candidate’s thesis,” and to test the student’s “ability to defend them against all objections, in disputations set up for the purpose”, which were scholarly exercises practiced throughout the student’s “career as a graduate student of law.” After students completed their post-graduate education, they were awarded doctorates giving them the status of mudarris (meaning “teacher”), faqih (meaning “master of law”), mufti (meaning “professor of legal opinions”) and which were later translated into Latin as magister, professor and doctor respectively.[3] Note that these terms are not yet standardized nor has a syllabus been agreed upon. hence there is vast variance in qualification and skills based upon schools and teachers
[edit]National level

In nations where Islamic law is the basis of civil law, but has not been codified, as is the case of some Arab countries in the Middle East, fatwā by the national religious leadership are debated prior to being issued. In theory, such fatwā should rarely be contradictory. If two fatwā are potentially contradictory, the ruling bodies (combined civil and religious law) would attempt to define a compromise interpretation that will eliminate the resulting ambiguity. In these cases, the national theocracies expect fatwā to be settled law.
In the majority of Arab countries, however, Islamic law has been codified in each country according to its own rules, and is interpreted by the judicial system according to the national jurisprudence. Fatwā have no direct place in the system, except to clarify very unusual or subtle points of law for experts (not covered by the provisions of modern civil law), or to give moral authority to a given interpretation of a rule.
In nations where Islamic law is not the basis of law (as is the case in various Asian and African countries), different mujtahids can issue contradictory fatwā. In such cases, Muslims would typically honour the fatwā deriving from the leadership of their religious tradition. For example, Sunni Muslims would favor a Sunni fatwā whereas Shiite would follow a Shi’a one.
There exists no international Islamic authority to settle fiqh issues today, in a legislative sense. The closest such organism is the Islamic Fiqh Academy, (a member of the Organization of the Islamic Conference (OIC)), which has 43 member States. But it can only render fatwā that are not binding on anyone.
[edit]Legal implications

There is a binding rule that saves the fatwā pronouncements from creating judicial havoc, whether within a Muslim country or at the level of the Islamic world in general: it is unanimously agreed that a fatwā is only binding on its author. This was underlined by Sheikh Abdul Mohsen Al-Obeikan, vice-minister of Justice of Saudi Arabia, in an interview with the Arabic daily “Asharq al awsat”, as recently as on July 9, 2006, in a discussion of the legal value of a fatwā by the Islamic Fiqh Academy (IFA) on the subject of misyar marriage, which had been rendered by IFA on April 12, 2006.[4] He said : “Even the fatawas of the official Ifta authority (official Saudi fatwā institute) is binding on no one, whether individuals or the State.”
Despite this, some times, even leading religious authorities and theologians misleadingly present their fatwā as obligatory,[5] or try to adopt some “in-between” position.
Thus, the Sheikh of al-Azhar in Cairo, Muhammad Sayid Tantawy, who is the leading religious authority in the Sunni Muslim establishment in Egypt, alongside the Mufti of Egypt, said the following about fatwās issued by himself or the entire Dar al-Ifta:
“Fatwā issued by Al-Azhar are not binding, but they are not just whistling in the wind either; individuals are free to accept them, but Islam recognizes that extenuating circumstances may prevent it. For example, it is the right of Muslims in France who object to the law banning the veil to bring it up to the legislative and judicial authorities. If the judiciary decides in favor of the government because the country is secular, they would be considered to be Muslim individuals acting under compelling circumstances.” Otherwise, in his view, they would be expected to adhere to the fatwā.[6]
In Morocco, where king Mohammed VI is also Amir al-Muminin (Commander of the faithful), the authorities have tried to organize the field by creating a scholars’ council (conseil des oulémas) composed of Muslim scholars (ulema), which is the only one allowed to issue fatwā. In this case, a national theocracy could in fact compel intra-national compliance with the fatwā, since a central authority is the source. Even then, however, the issue would not necessarily be religiously binding for the residents of that nation. For, the state may have the power to put a fatwā in effect, but that does not mean that the fatwā is to be religiously accepted by all. For instance, if a state fatwā council made abortion acceptable in the first trimester without any medical reason, that would have direct impact on official procedures in hospitals and courts in that country. Yet, this would not mean that the Muslims in that nation has to agree with that fatwā, or that fatwā is religiously binding for them.
[edit]Sources

Sources of fatwā include:
Al-Azhar University
Mufti Ebrahim Desai
Darul Iftaa
Cairo University Center of Islamic Research and Studies

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The goal of radical Islamists is to rip Western law and liberty in two says Nonie Darwish

Nonie Darwish contends there is a growing movement in this country willing to shed blood in the name of Islam. “While Americans are busy erasing Christianity from all public sites and erasing God from the lives of children, the Muslims are planning a great jihad on America.”

Islamic law allows men to marry babies age one and consummate the marriage at age eight. In the U.S. this is child abuse – pure and simple.

For an Islamic woman to prove rape she has to have 4 witnesses. How likely is that to happen in the Middle East?

Muslim men in the West demand Shariah Law so the women cannot divorce.

The plan to put a mosque a couple blocks from Ground Zero should be a wake up call. For every American town and community. What do mosques spread?

Let’s find out what Islamic religious leaders teach in local mosques. Is it hatred of Western liberty? Is it the subjection of women and children to the whims of men?

Instead of the Golden Rule, Islam has two systems of ethics — one for Muslims and another for non-Muslims. And the goal of Islam is to take and subjugate others. So says Nonie Darwish, an Islamic woman who converted to Christianity.

Go and attend the local mosque in your community. See for yourself what goes on. And if you don’t like what goes on — use the free speech this county has to say what you think.

Where are the local mosques? In Santa Cruz it is called an Islamic Center: Going to the local home page I see mention of a religious leader protecting Jews and Christians. This was back when Jerusalem was invaded. For more information:

Muslim Islamic Center of Santa Cruz
4401 Capitola Rd. #2,
Capitola, CA 95010
Tel: (831) 479 8982

written by Cameron Jackson
DrCameronJackson@gmail.com

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Obama an autocrat in substance?

Freedom of Assembly is guaranteed by Article 31 in the Russian Constitution. For the 9th time rallies in Russia were forbidden and broken up by force. And what is Obama’s response? The Obama Administration expressed its “concern”. Wow.

Per the Wall Street Journal (WSJ) editorial August 4, 2010 authoritarianism is rising in many places to endanger democracy. Which side is Washington on? Per the WSJ, the Obama Administration stance is “confused”.

The U.S. has cut support for democracy programs in Egypt. When Egypt extended its 29 year old state of emergency the State Department said nothing.

The story is the same in Latin America. Strong men now rule Venezuela, Volivia, Nicaragua, Equador and – of course – Cuba. The U.S. has pulled back support for civic society. And Washington’s response? Obama’s Administration has sought to engage the autocrats.

The Wall Street Journal titled its editorial A Democracy ‘Reset’. It ends with the comment, “How about an Obama freedom agenda?” Well, WSJ editorial writers, don’t hold your breath.

The WSJ forgets where Obama learned his values — in the pews of Rev. Wright’s church where Obama heard for 20 years how America is the cause of the world’s problems. Acts that weaken America abroad fit in with Obama’s agenda to return power to the disenfranchised. Democracy gives power to people. It is in Obama’s interest to engage the autocrats and turn a dim ear to the people ruled by autocrats.

So expect more headlines about beating up and arresting pro-democracy demonstrators. Obama is not interested in freedom or democracy. Obama wants to get rid of capitalism and free markets and substitute government control in its place. So who is the real autocrat in America? Autocrat Obama.

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coffee worsens MS symptoms? One man with MS says so …

Can coffee be a culprit in MS symptoms? Can eliminating coffee help MS sufferers?

Read the comments from MS patients which include one who curred his MS by eliminating caffeine — coffee — from his diet and supplementing with other dietary aides. He hypothesizes that muscle spasms due to caffeine usage caused the blockage in his neck veins …. no more coffee and no more MS symptoms for him.

Italian doctor may have found surprisingly simple cure for Multiple Sclerosis
By Loz Blain

A Major Breakthrough in the treatment of MS

“An Italian doctor has been getting dramatic results with a new type of treatment for Multiple Sclerosis, or MS, which affects up to 2.5 million people worldwide. In an initial study, Dr. Paolo Zamboni took 65 patients with relapsing-remitting MS, performed a simple operation to unblock restricted blood flow out of the brain – and two years after the surgery, 73% of the patients had no symptoms. Dr. Zamboni’s thinking could turn the current understanding of MS on its head, and offer many sufferers a complete cure.

Multiple sclerosis, or MS, has long been regarded as a life sentence of debilitating nerve degeneration. More common in females, the disease affects an estimated 2.5 million people around the world, causing physical and mental disabilities that can gradually destroy a patent’s quality of life.

It’s generally accepted that there’s no cure for MS, only treatments that mitigate the symptoms – but a new way of looking at the disease has opened the door to a simple treatment that is causing radical improvements in a small sample of sufferers.

Italian Dr. Paolo Zamboni has put forward the idea that many types of MS are actually caused by a blockage of the pathways that remove excess iron from the brain – and by simply clearing out a couple of major veins to reopen the blood flow, the root cause of the disease can be eliminated.

Dr. Zamboni’s revelations came as part of a very personal mission – to cure his wife as she began a downward spiral after diagnosis. Reading everything he could on the subject, Dr. Zamboni found a number of century-old sources citing excess iron as a possible cause of MS. It happened to dovetail with some research he had been doing previously on how a buildup of iron can damage blood vessels in the legs – could it be that a buildup of iron was somehow damaging blood vessels in the brain?

He immediately took to the ultrasound machine to see if the idea had any merit – and made a staggering discovery. More than 90% of people with MS have some sort of malformation or blockage in the veins that drain blood from the brain. Including, as it turned out, his wife.

He formed a hypothesis on how this could lead to MS: iron builds up in the brain, blocking and damaging these crucial blood vessels. As the vessels rupture, they allow both the iron itself, and immune cells from the bloodstream, to cross the blood-brain barrier into the cerebro-spinal fluid. Once the immune cells have direct access to the immune system, they begin to attack the myelin sheathing of the cerebral nerves – Multiple Sclerosis develops.

He named the problem Chronic Cerebro-Spinal Venous Insufficiency, or CCSVI.

Zamboni immediately scheduled his wife for a simple operation to unblock the veins – a catheter was threaded up through blood vessels in the groin area, all the way up to the effected area, and then a small balloon was inflated to clear out the blockage. It’s a standard and relatively risk-free operation – and the results were immediate. In the three years since the surgery, Dr. Zamboni’s wife has not had an attack.

Widening out his study, Dr. Zamboni then tried the same operation on a group of 65 MS-sufferers, identifying blood drainage blockages in the brain and unblocking them – and more than 73% of the patients are completely free of the symptoms of MS, two years after the operation.

In some cases, a balloon is not enough to fully open the vein channel, which collapses either as soon as the balloon is removed, or sometime later. In these cases, a metal stent can easily be used, which remains in place holding the vein open permanently.

Dr. Zamboni’s lucky find is yet to be accepted by the medical community, which is traditionally slow to accept revolutionary ideas. Still, most agree that while further study needs to be undertaken before this is looked upon as a cure for MS, the results thus far have been very positive.

Naturally, support groups for MS sufferers are buzzing with the news that a simple operation could free patients from what they have always been told would be a lifelong affliction, and further studies are being undertaken by researchers around the world hoping to confirm the link between CCSVI and MS, and open the door for the treatment to become available for sufferers worldwide.

It’s certainly a very exciting find for MS sufferers, as it represents a possible complete cure, as opposed to an ongoing treatment of symptoms. We wish Dr. Zamboni and the various teams looking further into this issue the best of luck.

Via The Globe and Mail.

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» Brain» Cure» Medical» Multiple Sclerosis» Nerves» Research» Surgery
User Comments (60)

A very positive development, thanks to my Italian brethren!… toot-toot!

Facebook User
– November 26, 2009 @ 04:11 am PST

An amazing new, and an amazing information tool as well. Worth any web surfing time to delight you discovering top research and insights on science and technology.

Best wishes.

Gonzalo

Gonzalo Villouta
– November 26, 2009 @ 05:11 am PST

God willing.

Jennifer Schroeder Zordan
– November 26, 2009 @ 06:11 am PST

I hope this works out, but something is setting off my skeptic alarm.

For one thing, 73% of 65 people is 47.45 people. So lucky Mr. 48 was cured on his right side only?

Anyway, I look forward to more detail.

Frac
– November 26, 2009 @ 07:11 am PST

You’ve got to wonder how many other such simple procedures there are???!!!

David Mahan
– November 26, 2009 @ 08:11 am PST

What is disturbing is the fact that fellow Mser’s are so desperate for a cure that they tend do avoid asking the right questions when it comes to these “miracles”. What if 95% or so people with MS have this condition because it’s a cause/symptom of MS, and not the cause of MS? I do not want to seem pessimistic, but I would reserve judgment for when more data is available.

Ted Nehme
– November 26, 2009 @ 05:11 pm PST

This wouldn’t be the first time excess iron has been implicated in disease. It’s well known that too much iron is a risk factor in atheroschlerosis, which is why male-specific multivitamin supplements no longer contain iron. There’s even some evidence excess iron increases the risk of cancer.

Spirit of 76
– November 26, 2009 @ 09:11 pm PST

65 people plus his wife makes it 66 people.

73% makes it 48.18 people.

I think the reporter probably meant “more than 72%” and then simplified by writing in 73 instead of writing in 72.7272%

Joe’s Cat
– November 26, 2009 @ 11:11 pm PST

…and that’s not the only new from italy; there is a young guy, Matteo Dall’Osso ( http://www.matteodallosso.org/ ), who healed himself from MS against all doctor’s opinion (except Dr. Zamboni, who helped him too), just by depuring (in a special way) his body from metals (he has got a metabolic disease that avoid his body to dispose off metals at a normal rate).

So it seems that MS could be the result of metallic accumulation in the body, due to a cause (vein occlution) or another (metabolic disfunction).

The real risk about these MS treatments is that they are too economical, simple and they were not discovered by a big pharmaceutic multinational; big opposing economic interests are able to prevent the diffusion of such discovers. Help the web spread the good news.

Mario Maio
– November 27, 2009 @ 04:11 am PST

please adjust my previous post with the following link to english version of Matteo Dall’Osso web site

Home

Mario Maio
– November 27, 2009 @ 04:11 am PST

J & J, – does this make sense to you?

Debby Baker
– November 27, 2009 @ 08:11 am PST

As the spouse of someone with MS I can tell you that this news has overwhelmed our Thanksgiving. Of course, it came out when it is impossible to get in touch with our specialist. I am sure that she, and every other neurologist/MS doc in the country (if not the world), is going to come back from the holiday to emails and phone calls from their patients.

I too am concerned about the pharmaceutical industry’s response to this. If you could see the level of coordination around establishing new clients for each drug type you’d be astounded. There really are only four mainstream medications for MS at this point. All involve injections (daily, semi-daily, weekly) although there are pill form versions in the pipeline (kind of like Duke Nukem:Forever for the MS crowd). But none of them really alleviate symptoms…they are all about reducing future attacks and the increase in symptoms.

This procedure points to a reduction of symptoms that most MS patients only see following strong IV steroid, and then only temporarily. While I don’t expect this procedure to cure my spouse immediately I do expect to have our doctor(s) examine it deeply and with great urgency. If they do anything less we will find another doctor who is more willing.

As we’ve both said, if this were any other kind of vascular blockage there wouldn’t even be a discussion. If a doctor said that the veins in your brain were blocked (and said nothing about MS) wouldn’t you ask if that blockage could be cleared? It can, by a relatively simple procedure. We only want the same response. I see many visits to cardiologists in our future. And I am looking forward to it.

Nothing Knew
– November 27, 2009 @ 08:11 am PST

The really really really good thing about this is it finally seems to have PROVEN what I’ve been saying for almost twenty years.

Believe it .. or .. not ..

Jesus Was A Vegetarian!

http://tinyurl.com/2r2nkh

Facebook User
– November 27, 2009 @ 09:11 am PST

Mario Maio says this is an economical treatment. Since when is brain surgery economical?

Things are not usually simple and I am glad we allow “cures” to be looked at critically before jumping on the bandwagon.

Verena
– November 27, 2009 @ 10:11 am PST

What else can we do just to push the simple MRV testing? I just want to get the word out there/

Maria Christodoulou
– November 27, 2009 @ 12:11 pm PST

I’m curious, could vein blockage be associated with weight gain? I gained weight recently and was then recently diagnosed with migraines and then multiple sclerosis. I know that there are plenty of people with multiple sclerosis who are not significantly overweight like I am (I’m ~250 lbs.) but I wonder if perhaps some of us wouldn’t have acquired MS except for such “supplemental influences” as weight gain?

I do struggle with sleep apnea in accordance to my weight gain, too. I wonder if perhaps the same stuff that makes sleep apnea happen (blockage of airflow due to being so fat) can also result in blockage of veins (blockage of bloodflow due to being so fat).

stimpy77
– November 27, 2009 @ 01:11 pm PST

Amazing! Finally someone researches this disease from a new prospective!

Brittny Macphee
– November 27, 2009 @ 01:11 pm PST

Amazing == a potential cure for multiple sclerosis. Two years ago my Tucson doctor discovered that I had high iron levels and recommended giving blood in order to reduce the iron level — no one wants my blood. Fortunately (or not) the health misadventures of 2008 resulted in blood loss and thus reduction in iron levels.

Facebook User
– November 27, 2009 @ 06:11 pm PST

Verena,

This isn’t brain surgery. They don’t have to open up your skull or anything. It’s strictly a balloon angioplasty and it’s even easier because they can enter through the jugular vein close to the brain. A cardiac angioplasty with stents can cost $20-30,000, but in that procedure, they have to go in through the femoral artery in the leg and thread their way up to the heart then around to cardiac blood vessels. Also, MS drugs can cost that much in a single year, so if this actually works, it is definitely more economical.

Spirit of 76
– November 28, 2009 @ 05:11 pm PST

The treatment is now undergoing further investigation – more here from the BBC: http://news.bbc.co.uk/2/hi/health/8374980.stm

Loz
– November 28, 2009 @ 09:11 pm PST

I can’t help but be skeptical because there are MS treatments that do work (they don’t cure but they definitely help the problem) by directly affecting the auto-immune system. I am on Copaxone, for example, and Copaxone’s role is in changing the inflammatory nature of the body’s antibodies. (I’m no medical scientist, I’m a new patient, so forgive me for my inaccuracies in word choice.) It sounds like this new “cure” has nothing to do with the body’s autoimmune system, which makes me wonder how it is that Copaxone makes any difference at all?

stimpy77
– November 29, 2009 @ 05:11 pm PST

It’s not that the medical community is “slow to adopt revolutionary theories”, it’s that we take an oath to “do no harm”, and for new theories scientifically prove to a statistical confidence that a treatment has benefits that outweigh the risks. There *are* risks to angioplasty, including infection and tragically, stroke, so this treatment needs to be proven.

As someone who sees MS patients for optic neuritis, this would indeed be a great breakthrough if the University of Buffalo study confirms with statistical significance and confidence that venous insufficiency is a causal factor for some MS patients, and angioplasty has a benefit worthy of its risk.

Standing by for the science,

Doc Rings

matthew.rings
– November 29, 2009 @ 05:11 pm PST

Also food for skepticism, why does MS statistically show up more in high-altitude regions? Some assumed that certain viruses might be more likely to thrive in high-altitude areas, and my own assumption was that high altitudes, or particularly high latitudes, have less sunlight, hence less vitamin D, hence D deficiency, which leads to autoimmune disorders.

So if indeed MS has a one-to-one relationship to the narrowing of the veins, how can high altitudes & high latitudes have any relationship to that? Theories?

stimpy77
– November 29, 2009 @ 06:11 pm PST

this is a very cool site…amazing technology and scientific inovation

Stephanie Boulianne
– November 29, 2009 @ 07:11 pm PST

Following up on my own ponderings, http://csvi-ms.net/en/content/ccsvi-huge-breakthrough-ms hypothesizes that vitamin D has a direct correlation not only on the autoimmune system but also on the vascular system’s development.

stimpy77
– November 29, 2009 @ 07:11 pm PST

I hope that this treatment from Italy does work out. I mean it obviously has done for some already. What I am pondering over though: Is the whole thing symptom relief or dealing with the cause? If this stricture causes MS, what causes the stricture? And although I am in favour of different (and non-toxic) approaches to solving problems I do believe that MS is an autoimmune disease and people won’t get it (or an array of other autoimmune diseases) if they have a strong immune system. I (with PPMS) take LDN (low dose naltrexone) which is a safe, cheap, out of patent drug which boosts/strengthens/modulates your immune system. People have found relief with LDN (and stopping progression, attacks, tumour growth and more) for a vast number of diseases, including cancers. How come it’s been there for nearly 30 years and hardly anybody knows about it? It’s because there is no money in it, so it’s being kept hidden from the ones who need it most, the suffering patients. Just google LDN and find out about it. I was so lucky to have discovered it and with it the over 100,000 other users. (I agree, I don’t know them all personally, honestly! But many of their stories are all over the internet!) It’s fantastic and what it does is logical, it makes the body heal itself. Silvia

Silvia Lane
– November 30, 2009 @ 04:11 am PST

I am an M.S patient for 18 years. And an M.S researches for 10 years. I am electronic engineer and a university teacher. If you look in Google for Dr. Fernandez Noda and the syndrome Cerebellar Thoracic Outlet Syndrome (CTOS) you will find again a strong relation between blood flow in the brain and M.S symptoms. Fernandez Noda looks for global blood flow from the brain. The veins coming from the brain to the heart enter the atlas vertebra and cross to the C6 and C7 vertebra where the veins go out the vertebrae in their way to the heart. In the outgoing they can be squashed by the sternocleido-mastoideos muscles. Dr. Noda makes a simply operation to liberate that pressure and some M.S patient get better.

I am convinced we can find a solution. I do not have so clear that we can make the solution to go on because the opposition from pharmaceuticals will be uninimaginable.

They are earnig bigs amounts of money whith not-a-solution-at-all. And what they do not want at all is loosing theier clients! We are clients, very goog clients, for them -not patients-. I have a web page http://webs.uvigo.es/xuliofh/entrega2/pagPpalEM.html with some information about M.S. (in spanish 🙁 )

Xulio Fernández Hermida
– November 30, 2009 @ 08:11 am PST

I read many of the comments. two maybe 3 with MS, newly diagnosed, a couple of doctore, then arm chair mathematicians.

As I have had MS for 14 years, take injections every other day, for 14 years at now, at cost of 2400.00/month for one med. Most of you can go ________. I am in luck though, with exercise, diet, family and attitude, I am completely mobile. I can not say it is due to the fact of betaseron, it only slows the progression, I wouldn’t know, I’ve never been off off the stuff. I do know the shots hurt, that’s where the attitude goes bad.

If you are not part of the problem, stay away from a possible solution. Show me your creditentials to give your opinions, not just cutting an article to shreds. Go bore people who care.

L Tate

Ltate
– November 30, 2009 @ 10:11 am PST

Interesting

Didier Noel James
– November 30, 2009 @ 10:11 am PST

Actually, I have a hypothesis of MS which suggests simpler treatment that might be less invasive. Human pheromones cause MS. In which case about 150 to 250 mg of healthy adult male facial skin surface lipid p.o. (the face kissing pheromone from your dad), should halt symptom advances. Epigenetic (low-dose chemo) therapy in concert with pheromone treatment while watching sad movies, should fix it for sure. Take 3 5 packs of regular gum, sugarfree, wipe 5 pieces per day on dad’s face, both sides (of his face and of the gum), until you have got 15 to 25 pieces. Now chew the gum. (Of course, make sure Dad’s healthy.)

So how does the Italian surgery work? Do his patients kiss his face a lot? The blood has chemosensitive proteins in it that alter conformation on contact. The angeoplasty might be affecting that somehow. Perhaps this surgery will cure MS like knee replacement cures arthritis? Hope so.

TogetherinParis
– November 30, 2009 @ 09:11 pm PST

Trolling on a post about a potential treatment for a debilitating disease? Especially one that has been peer-reviewed and is currently being tested by independent groups? Wow.

I bet you go to abuse support groups and tell them to “get over it” or drop in at cancer wards and suggest they “think happy thoughts”. You are a beautiful person. See, I can use sarcasm too.

Nothing Knew
– December 1, 2009 @ 07:12 am PST

Zamboni is partially right, some symptoms are, without a doubt, caused by a vascular blockage in the neck region. He just forgets to figure out, what might be the cause to the blockage.

In my case the blockage was caused by spasticity of the neck muscles.

The spasticity in it’s term was caused by porphyrines, released from skeletal muscle cells breaking down.

Cell breakage was caused by chemical imbalance inside the cells.

The chemical imbalance was caused by excess activity of exicatory neurotransmitters, which regulate those pumps.

Excess activity of exicatory neurotransmitters was caused by daily caffeine consumption.

I suffered from ms-symptoms for 20 years. The symptoms were many times so sevbere, that I was unable to get out of bed without help, and with help it took an hour or so, and I was soaking wet of sweat, and crying. In the last phase, I was able to walk short distances very slowly with a walking stick.

I stopped my caffeine habit feb 2008, now I’m totally free from alla symptoms. I am also on alcalic diet and take supplements, E-Epa, carnosine etc..

So, my ms was caused by a chronic poisoning, brought upon me by my drug dependence. I lost more than 20 years of my life in a hell on earth, I’m almost totally recovered now, feel like I was 20, but I’m 55, and the party’s pretty soon over for me.

Facebook User
– December 2, 2009 @ 01:12 am PST

This is exciting news to hear, thank you Aaron for sending me the artical.

Sally Simpson
– December 3, 2009 @ 04:12 am PST

Amazing News. Just an idea but if its caused by blocked veins perhaps nattokinase suplements could help?????

silverneedle
– December 4, 2009 @ 03:12 pm PST

Ok so if this is correct then I have something to throw into the pot. As a teenager I had problems with Iron Deficiency on my blood, so I was fed Iron supplements for many years. What I wonder is, how many people with MS were fed the same Iron supplements. I don’t even want to start thinking there’s a cure at this time, I’m tired of let downs. I’ve read a lot in the past few years about things that can cure MS and at every tunr it falls through.

To the doc above, it may well be that you took an oath to ‘not harm’ anyone. As an MS sufferer I really don’t care, if there is anything out there that has any potential to help me than I want to try it. If it kills me then so be it, after all, it’s just down to how long I want my death sentence to be.

This ‘cure’ has a couple of things that jump to my mind that should really be added to the mix. For me I already said about the iron given to me when I was young, but also I have an additional complaint called Factor 5 Leiden deficiency wich makes the blood clot more than in a normal person. This has given me many vascular problems, including a severe DVT last year for which I am still suffering. I am taking Warfirin for an undetermined length of time to keep my co agulation down.

So to sum up, this ‘cure’ talks about Iron (check) and vascular problems (check). I’m scared to say it but this seems to have a lot of bells ringing for me and what I want to know is, when the hell are the medical profession going to add this up and let people like me try it.

Has a survey been done to see how many MS sufferers have had Iron supplements given as a child? Or would the medical profession who ‘do no harm’ be scared to to that and find out that the very supplement we were given could have contributed to this. I don’t care what caused it, I just want out.

My mum had that balloon thing done through her groin for hardening of the arteries and she’s absolutely fine.

April Prior
– December 7, 2009 @ 05:12 am PST

I have been following this with extreme interest. The article above is good but very brief and there is so much more to it… so if you want more of the story please visit this site and watch the video:

http://www.ctv.ca/servlet/ArticleNews/story/CTVNews/20091120/W5_liberation_091121/20091121?s_name=W5

I also recommend watching all the interview videos to the right of the page for more details. This all becomes more clear and sooooo exciting. It is being taken seriously for sure.

Pam1234
– December 7, 2009 @ 02:12 pm PST

This really does sound promising, and while it is important to err on the side of caution with new treatments, this could be a step in the right direction.

Hal London
– December 8, 2009 @ 08:12 am PST

Sadly enough I’ve passed the stage of Relapsing Remitting….-do you guys think

Secundary Progressive patients have any hope or anything to look forward to??

Facebook User
– December 8, 2009 @ 12:12 pm PST

Hope!

Atticus Finch
– December 26, 2009 @ 01:12 pm PST

For the person who wondered about how the higer altitudes make a difference – the air pressure can effect the blood vessels in the brain and in your whole body – pressure or lack of – can cause blood flow changes – so, that may help explain – especially when going from low to high and back.

Laura Ashley Wheeler
– December 29, 2009 @ 07:12 pm PST

Also food for skepticism, why does MS statistically show up more in high-altitude regions?

THAT is easy.

The altitude causes higher blood cell production and therefore the viscosity of the blood becomes thicker.

The blood doesn’t flow.

Much like the blood flow from the brain when the veins become stricted.

Facebook User
– January 3, 2010 @ 12:01 am PST

This is very interesting, is there any operations done in the U.S. My girlfriend’s Mother has MS. Where can i find more info on this?

Thanks

Kyle Ericson
– January 3, 2010 @ 01:01 pm PST

i have a few questions i need answerd.

for my self i have had thrombosise since i was 17 also low in iron plus i have other medical problems.But we have now learnt that my daughter has m.s we no there is not a lot known about m.s they say it is not passed on my daughter was born with a heart murmer and wene she went on to cows milk as a toddler i would put pentervite into her milk for her supplements she was poorly as a toddler always had a cold and soar ears and throate.could some one please let me no if i did something wrong and this is why she has it.

Caroline Sare
– January 3, 2010 @ 03:01 pm PST

Here is the info for US:

“Letter from Dr Michael Dake

Thank you for your inquiry regarding our work on blockages of the veins of the head and neck associated with multiple sclerosis. I wish I could talk personally with each person to explain our ongoing work, but in order to provide a prompt reply to all, I must respond by email. Currently, we are planning a clinical study to rigorously assess the risks and benefits of balloon angioplasty with or without venous stenting in the setting of multiple sclerosis. This controlled format for study will allow all patients to receive endovascular therapy if desired, but will provide a better evaluation of the risks, benefits and indications for different approaches to treating the vein blockages associated with multiple sclerosis.

Please be assured that we will keep your contact information on file and provide periodic updates of our progress until such time as the trial commences . At that point, we hope to be able to speak with you regarding your interest to participate in this clinical study. We anticipate embarking on the study early in 2010. I wish to extend my appreciation to you for your understanding and forbearance as we proceed with deliberate speed in our attempts to develop a multi-disciplinary, collaborative controlled study that will truly advance our understanding of the science underlying the association between venous disease and multiple sclerosis.

I hope to have the opportunity to speak with you in the future.

Sincerely,

MICHAEL D. DAKE, M.D.

Professor, Department of Cardiothoracic Surgery

Stanford University School of Medicine

Falk Cardiovascular Research Center

300 Pasteur Drive

Stanford, CA 94305-5407″

One of my patients is considering that option. When and if he does, I will be able to ascertain the efficacy of the method myself.

Dr. Dimitri Rimsky

Neu-Wellness Institute

Dr. Rimsky
– January 4, 2010 @ 04:01 pm PST

I was just diagnosed and find this fascinating. When I had a physical 8 years ago, my doc told me to stop taking a multi-vitamin with iron because my levels were at the highest end of safe. Interesting.

Laurie Erdman
– January 5, 2010 @ 09:01 am PST

Hmmm… I wonder if there is any corelation of patients with MS and those with Haemochromatosis (an excess of iron in the blood) (or if this hypothesis holds water, If not, why not ?)

Bryn Parrott
– January 8, 2010 @ 11:01 pm PST

Does this new theory hold water if the ms sufferer had actually spent there life being iron deficient, and not taking iron supplements. I have been iron deficient my whole life but, apart from a two month period during a pregnancy where I had iron injections, I have not take iron supplements. Could a blockage in the veins still lead to a damaging build up of iron in the brain, in these circumstances?

Tara Slater
– February 12, 2010 @ 02:02 am PST

hi, i am a patient from dubai (u.a.e) with advanced level of M.S, right now am taking 3 injections of rebif 44 every week for almost 7 years. Hereby i request you to please provide me your full address to enable me to contact you for your medical invitation to come to you for the treatment

your earliest reply is highly appreciated

best regards

hussain mustafa. my contact number as below

mobile no-00971506467089

office no-0097142255422 fax no-0097142254515

hussain
– February 12, 2010 @ 12:02 pm PST

In http://ajdem.mforos.com/1138091/8283791-la-dieta-del-dr-swank-en-el-tratamiento-de-la-esclerosis-multiple/ it can be read “Otra de las novedades en el tratamiento de la Esclerosis Múltiple es el uso de los campos electromagnéticos. Aquí es muy importante aclarar que los campos electromagnéticos que se utilizan, en este caso, son a una intensidad de picotesla, con frecuencias extremadamente bajas y detenidamente controladas. Estas aplicaciones son extracraneales y se dan durante 20 minutos, una vez a la semana.

Hasta hoy, todos los pacientes con Esclerosis Múltiple que han sido tratados con esta clase particular de campos electromagnéticos, han mejorado en forma inmediata y dramática. Su mejoría no sólo fue subjetiva, sino totalmente objetiva.”

It talks abaut treating M.E. patients with electromagnetig fields applied in the head and the good resoults obtained with it. And I think that this resoult can be related with the one of Dr. Paolo Zamboni in this paper. The electromagnetic fields what sure do is shaking the iron particles in the blood making this way more easy for them to move along the veins (like removing dirty water in order all the particles go out with the water).

I am electronic engineer and I consider it will be interesting that Dr. Zamboni consider this point!

Thank you very much

Thank you

xuliofh
– February 16, 2010 @ 01:02 am PST

Skepticism is definitely in order! There are way too few details in this article to know whether this is a promising treatment. It could in fact be harmful.

The study doesn’t seem to include any comparison groups, and without a comparison standard, it’s impossible to draw conclusions from any study.

Specifically, they didn’t screen for venous blockage in a group without MS to see if the blockage is unusually common in MS patients or just common across the board (from other studies, we know that venous blockage is a common condition, so you really need a comparison group to see if it’s MORE common in MS patients).

AND in assessing the treatment, they didn’t have an untreated control group to see how the treated patients’ experience compares with the natural history of MS. Having hope and a sense that something is being done can have a powerful impact on the course of disease and could explain the 2-year remissions experienced by many of the patients. You need a control group to see if that’s what’s happening. I teach public health students how to be careful readers of the medical literature, and my students would tear this article to bits.

I’ve had MS for decades, and I’d love to think that this is a real breakthrough in MS treatment, but with the amount of info provided here, I’m deeply skeptical. I’m afraid that this is more wishful thinking than real progress — and could be dangerous if people adopt this unproven approach and abandon treatments that have been proven to be effective.

Mary Applegate
– February 18, 2010 @ 11:02 pm PST

“CCSVI” is junk science.

The Zamboni Myth: Why “CCSVI” is Surreal

Colin Rose
– February 20, 2010 @ 03:02 pm PST

I am 36 yrs old and was diagnosed with MS two years ago. I have also been diagnosed with two of the genes that cause Haemochromatosis. Co- incidence? Either way its very interesting.

Facebook User
– February 21, 2010 @ 01:02 am PST

An intresting article, I am 26 and was diagonised with MS 3 years before. I am thinking of getting a councelling with yoga gurus to automatically unblock these vessels thru yoga excercise, If I get any improvement, I will definetly inform you guys.

Facebook User
– February 27, 2010 @ 07:02 am PST

Ridiculous these posts about pharmaceutical companies blocking this. Just when have they ever blocked a proven treatment and how would they do that? You listen to too many demagogues and snake oil salesmen. You’re probably hysterical about Toyotas, too, because you cannot do the math.

Ronald Warrick
– March 11, 2010 @ 02:03 pm PST

Wow that actually makes sense dude.

Lou

www.whos-watching.es.tc

Facebook User
– April 11, 2010 @ 11:04 am PDT

“Also food for skepticism, why does MS statistically show up more in high-altitude regions? Some assumed that certain viruses might be more likely to thrive in high-altitude areas, and my own assumption was that high altitudes, or particularly high latitudes, have less sunlight, hence less vitamin D, hence D deficiency, which leads to autoimmune disorders.

So if indeed MS has a one-to-one relationship to the narrowing of the veins, how can high altitudes & high latitudes have any relationship to that? Theories?”

Perhaps it is due to changes (evolutionary or short-term) that would occur in either groups of people or individuals when they inhabit higher altitudes. High altitudes tend to be mountainous and cold, so I can see there being some benefit to the people there developing smaller blood vessels to better retain heat. If this were true, you would expect a correlation between MS and people who live in, AND who have ancestry in high altitude places.

Also, do you know if our blood vessels constrict to keep in heat when it’s cold? If so, that could also work as a functional explanation that would explain the increased rate of MS in both people who currently reside in high-altitude areas, as well as those who have a heritage of living there.

Angus James
– April 11, 2010 @ 01:04 pm PDT

Very interesting news. Hope is so important.

Some comments.

Most medicine is “junk science”. Look no further than the Cholesterol hysteria.

MS is not more frequent at high altitudes. It’s more frequent at high latitudes. Northern coun tries like Canada have many more MS patients than southern ones like mexico.

The vitamin d hypothesis is a good one. Taking 3-4 000 iu of Vit D a day can’t hurt. Getting as musch sun as you can get may be helpful too.

Richard Albert
– April 12, 2010 @ 11:04 am PDT

I have recently come across your article about MS saying that it may not be auto-immune after all. I think that is wonderful news, as I have been diagnosed with MS myself about 3 yrs. ago. Currently, I am not taking any meds for it; everyone in my family thinks I should be…..I keep telling them I am going to take this MS and kick it into outer space somewhere, where it can NO LONGER hurt anyone. I would GREATLY APPRECIATE hearing back from you.

e-mail me back and we could exchange phone numbers…I live in the USA, and would love having the procedure performed… however I do not know what you charge for such.

Tabitha Pollock Hershberger
– April 19, 2010 @ 06:04 pm PDT

I really hope that this may lead to something,i’m going to talk about it with my neurologist, i’m wondering what he will say.

Inge Vanhoorne
– April 28, 2010 @ 10:04 am PDT

This is a whole new approach for treating the patients with Multiple Sclerosis. In recent days it has become a new hope for millions of Multiple Sclerosis patients across the world. Dr. Paolo Zamboni, a former vascular surgeon and professor at the University of Ferrara in northern Italy developed this procedure while he was trying to understand the underlying causes for the condition which his wife was into, a Multiple Sclerosis patient.

Doctors and hospitals across the world are developing necessary infrastructure and the expertise required to perform this procedure with good outcomes.

In India few of the doctors at Internationally Accredited Hospitals have already started performing this procedure with excellent outcomes as per international standards. These doctors have developed a multidisciplinary approach involving Neurologists, Neuro-Surgeons, Cardiologists, Cardio-Thoracic Surgeons and Interventional Radiologists. The doctors are abreast of latest developments in this field and continuously in touch with the inventors of this procedure. They are continuously monitoring the procedure outcomes of their patients over a period of time.

Why should you choose India?

In India this procedure is done with excellent outcomes by expert team of doctors at Internationally Accredited Hospital at a cost which is much lower than it would cost you in USA, UK or Europe. Indian Hospitals provide you high quality service and compassionate care and has a world class infrastructure. India is well connected with the world by International flights.

How can you get started?

The first step is to determine whether a patient is a good candidate for this medical procedure or not?

All you need to do is to send the following information to us.

1) MRI of the Cervical (neck region )

2) Doppler Ultrasound of the neck

3) A general medical status and history

We will show these information to our expert doctors and get a opinion from them to you, totally free of cost.

Do not worry if you do not have the above mentioned medical information readily available with you. We have specially designed evaluation package for this procedure. The evaluation can be done here in India on outpatient basis at much lower cost. Based on the findings of the evaluation further line of action can be taken.

Just write to us at help@safemedtrip.com for more information and help.

The Procedure

It all started with the Dr. Paolo Zamboni’s search to find out the root cause of debilitating condition of his wife who was suffering with Multiple Sclerosis. After studying many patients suffering from the same condition, he found that that almost all of them had a narrowing, twisting or outright blockage of the veins that are supposed to flush blood from the brain.

Further Dr. Paolo Zamboni found that whichever patient had this condition, had a high level of deposition of Iron in the veins. Lack of free flow of the blood to the brain possibly explaining the symptoms of MS. Now the idea was to open up such blocks and allow the free flow of blood through veins to brain. This is the reason why this procedure is called as Liberation Procedure. This is done in the similar way as it is done in Coronary Balloon procedure. The patient may have single blockage or multiple blockages. Accordingly the treatment is decided.

safemedtrip.com
– May 6, 2010 @ 12:05 am PDT

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CCSVI chronic cerbrospinal veinous insufficiency treated by angioplasty on hold?

Do you know someone with MS? Do they know about the use of angioplasty to clear blogged veins in the neck? Use of this technique has been put on hold at Stanford Hospital in Palo Alto, CA. Who else is doing it on the west coast? Here is some info:

Of 500 patients with multiple sclerosis (MS) 62% had chronic cerebrospinal veinous insufficiency (CCSVI). MS is not alone in having chronic cerebrospinal veinous insufficiency. In other diseases about 45% also have CCSVI.

Dr. Zamboni, an Italian doctor, treated his own wife with angioplasty — a balloon to clean out the vein that was clogged. Three years later she has had no MS attacks.

Stanford Hospital put on hold its program for treating MS patients with CCSVI after one patient died and another had to have emergency heart surgery.

“Stay on current drug therapy” says Dr. Zivadinov, associate professor of neurology at the University of Buffalo in New York.

Well, that is conservative advise that sounds good. But for patients that experience numerous side effects from the drug therapy that advise may sound hollow.

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dog toys for german shepards that only chew??

As I put into the cruncher the mangled by dog Ultimate Boomerang, I wondered if there is a toy that our 8 month old male German Shepard cannot destroy? Until told otherwise by our vet, we had given him pieces of hard wood with iron on one side. Our dog is dedicated to chewing! Our Shepard at 8 months is 92 pounds of muscle with large jaws that love to chew constantly. Any suggestions?

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Is multiple sclerosis due to CCSVI – a plumbing problem – fixable with surgery?

What causes multiple sclerosis? Think of it in brief like a plumbing problem. Whe things don’t go down properly unfortunately things back up — and the backup causes a mess. How fix it? Clean out the plumbing so that blood moves properly around the body.

So is MS akin to a plumbing problem that can be fixed with surgery?

One hypothesis put forward by Dr. Zamboni of Italy is that there is insufficient drainage of blood from the brain and spinal cord. When veins get blocked they make substitute paths and that blood reverses flow (reflux) back to the brain. That reverse flow may set off the inflammation and immune-mediated damage that has been well described in MS. When the flow of blood becomes natural then the damage to the mylon will stop. Mylon can repair itself over time.

Dr. Zamboni’s hypothesis that CCSVI (chronic cerebrospinal venous insufficiency) contributes to nervous system damage in multiple sclerosis. In 35 individuals treated by Dr. Zamboni with vascular surgery using balloon dilation (J Vasc Surg 2009; 50:1348-1358) 47% of internal jugular veins went back to having restricted blood flow. That means that 53% — more than half — no longer had any venous obstruction.

Michael D. Drake of Stanford Hospital was doing some of the procedures operations such as Dr. Zimboni did but recently halted. In December 2009 the hospital shut down his 40 patient program. One patient died going home on a plane and another patient had a stent move to the heart requiring emergency surgery. Next possible date for more procedures done at Stanford is tentatively set for June, 2010.

People with MS can look into getting a MRV (V for venous) exam to determine whether their veins are clogged. There are various research programs that MS patients can enroll in.

And there are promising therapies that can assist: low dose naltrexone therapy for one. So far as I can see reading The Promise of Low Dose Naltrexone Therapy by Elaine A. Moore and Samantha Wilkinson and other sources the only BIG no-no is no use of any narcotic while taking LDN. LDN may be helpful for a wide variety of disorders including cancer, Parkinson’s and autism.

Do you know someone who lives with multiple sclerosis? Pass this on to them. On the main page for the national organization for multiple sclerosis you can watch Dr. Zamboni and others discuss the most current findings. Over 140,000 people from all over the world signed up to watch it on the Internet April 14, 2010.That web case is available to watch on the national home page for multiple sclerosis.

If this is a plumbing problem treatable with surgery think of how this will effect the pharmaceutical companies that make beta-interferon and Tysabri. Beta-interferon carries flu-like side effects and Tysabri has lead ot fatal brain disease in rare instances. The pharmaceutical companies make large donations to neurologists who write prescriptions for MS patients.

Anyone who lives with a chronic health condition and who is deteriorating can become quite dependent on their doctors — the neurologists — who have been prescribing medications to them for numerous years. Switch and get angioplasty for a plumbing problem? Get off medications? Take vitamin K and other vitamins and supplements? Use low dose naltrexone to heal the body? Wow! That is a huge step in a different direction.

Yes — the “experts” are having “turf” wars. And the patients and their families may feel like pawns in a chess game. That’s why the Internet is so powerful. Easy to connect with others and for pawns to become Queens and Kings. And for persons with MS to take charge of their own health and destiny.

Some ways for MS patients and their families to take charge:
Connect with other families. Who are other local families dealing with MS? Use the internet to send group e-mail back and forth. Stay in touch. Share stories.

Use technology so you can SEE the persons you are connecting to. All it takes is a laptop, SKYPE and a web camera if not already built into your laptop. This way the person with MS “gets out” and loved ones and others can “get in”. And this way the person with MS can meet new people and start other relationships. That is the wonderful thing about interactive technology. A person with MS may first only want to see their daughter or son. Later, they will want to see and interact with new people they meet over the Internet.

MS tends to be a women’s disease. Male spouses and significant others need to be involved in creating a supportive framework for healing: MS diet, regular contacts with people they love, getting out into the community, assisting the person with MS to do activities that bring pleasure.

Very importantly: help the person on a daily basis to do new things and learn new skills and grow spiritually and emotionally as well as physically. People sense when their skills and abilities are growing or shrinking. So help ensure that skills grow.

Keep track of growth with a notebook. Look where you were and see where you are now.

Encourage independence. Assist MS patients to take initiative, make choices and make decisions. Start with the little decisions — what to wear and eat — and move on to larger decisions. . Such as, is this procedure one that you really want? What is the downside to doing this procedure?

Talk to your doctors. Why not do this form of angioplasty — once proven appropriate based on well done research — right here in Santa Cruz County? Dominican Hospital is excellent and we have first class surgeons who can do angioplasy procedures. For example, Dr. Benjamin Potkin is one local doctor who has the experience and necessary abilities.

Get the best supplements possible. Louden Pharmacy on 41st Avenue is one such pharmacy. The pharmacist, Ray, can provide Low Dose Nalrexone per prescription from your doctor. And he can refer you to professional people who can hone in on other ways to improve your general health.

Get out into the community and see people and do activities. For example, Christ Lutheran Church of Aptos just started a garden so people in the community can grow their own. Part of the garden is for persons with disabilities. In that area the beds are raised and it is wheel chair accessible. Seeing plants grow that the MS patient selected and planted is one way to get out and meet new people. Yesterday, I heard about the garden on the radio and got a plot right next to the gate. That way clients who cannot get out of the car that day can still see their strawberries and tomatoes grow!

And be sure to take care of yourself. It is stressful for family members dealing with MS. What MS patients need, family members who take care of persons with MS also need.

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AT&T BackFlip or some other android? A One Nexus from Google?

Why to GET a Montorola BackFlip. And why to MOVE on to some other cellphone:

Reasons to get a Motorola BackFlip:
1) After my German Shepard pup chomped a hole in my Blackberry — and I needed a quick replacement — I got a Back Flip through AT&T. Since AT&T already is my carrier going from a Blackberry to the BackFlip was a snap. Pull out the SIM card and get the new phone working. Ah, little did I know what was in store for me…

2) The BackFlip has a large, easy to use key board. It “flips” out — hence it can be larger than a slide out key board such as Verizon’s android. Though I never figured out how to capitalize words I did find the keyboard easy to use. (On the Blackberry to capitalize all you have to do is hold the letter and it immediately becomes a capital. )

3) The BackFlip is an AT&T product. Yes that is a reason NOT to get it. Tying to contact New York? Forget AT&T as a carrier. I have a relative that spends considerable time in New York City. Well, AT&T readily “drops” phone calls. I lost 3 phone calls to New York in less than 10 minutes.

Reasons not to get a BackFlip through AT&T:

1) AT&T ptovides NO training to sales concerning the BackFlip. I was told that “next month” they would get some training. So — sales cannot help you concerning your questions. Not with any efficiency anyway.

2) AT&T put Yahoo not Google on the BackFlip as the default brouser. And all the fun things you can do through Google you cannot do with the BackFlip. For example, you can get to Google search — but not easily. It always defaults back to Yahoo. For what every reason — sheer stupidity! — At&T tried to cut Google out of the BackFlip market. I hope it boomerangs on AT&T.

3) I have a blog called Monterey Bay Forum. When I looked at how it was displayed on the BackFlip I decided either I need to change my blog or change my cell phone. I actually tried changing my blog — but I think it is far easier to change my cell phone than my blog. Which I will do.

3) It is not easy to change default settings. Because of visual difficulties I need, for example, larger fonts than provided on the BackFlip. So I went to the android market store to get a free application. But it does not “launch” on the BackFlip. I asked AT&T for help. As I said above, the sales people have no training on the BackFlip. They tried to help but with no success.

Enough said why to get and move on from the BackFlip. Move on to what? I’m going to try the One Nexus by Google. I like a fixed, metal key board which the One Nexus does not have. I know I like Google so on that score the phone should be a success.

Just guessing what I will do … I bet I use the One Nexus for less than a month and then I return it. Why? because I do want a keyboard such as the BackFlip provides. Maybe Balckberry will put out an android with a “flip out” metal keyboard. That would be my ideal. Is that possible? Can Blackberry move into the android market?

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