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Friday, May 07, 2010

My Letter To Steve Medley re: CCSVI


May 4, 2010

Greetings Steve:

My partner has been diagnosed with multiple sclerosis. She wants to have the CCSVI procedure but she does not have the $10,000. required to travel to a foreign country. In the meantime, she is being discriminated simply because she has been diagnosed with multiple sclerosis.

If she was not saddled with the label of this disease, she could go to a vascular surgeon and have the CCSVI treatment. Our politicians and the "system" are content to have her dependent upon pharmaceutical drugs for the rest of her life at a great expense to taxpayers, rather than permitting her to undergo a simple and inexpensive procedure that would free her of the symptoms of multiple sclerosis. How ridiculous!!

Thank you for your honest and unbiased report this morning about CCSVI. I send my congratulations to you and CFRA radio for permitting your guests to voice their experiences about just how inexpensive and effective this CCSVI procedure is.

My observation is that the pharmaceutical corporations in cahoots with the neurologists (who are commonly stock holders of pharmaceutical companies) are selfishly holding the MS patients hostage for future profits - and as of this date - the politicians are not serving we-the-people, but rather Big Pharma.

In my library, I have a copy of the book "The Medical Mafia" authored by Dr. Guylaine Lanctot in 1995. Guylaine Lanctot was a medical doctor in Montreal, Quebec, at that time, but her medical license was suspended at a later date. This morning after your interview I pulled the book off my library shelf and re-read some chapters.

In the Prologue of her book, Guylaine Lanctot writes:

"The fact is that by having been a participant and having collaborated with the industry for 20 years, I discovered the Medical Mafia and its machinations. The only ones responsible are those who pay the bill. And that is us.

Whether you are 9 or 99, understanding your health and governing it in your own way is not a question of age. Secrecy and complexity are the tools of manipulation and control of some by others. Transparency and simplicity are the tools of personal power.

Contrary to what all of us might like to believe, it is not the authorities, medical or political, that are going to bring about the solutions needed. Indeed, it is they that have created the problem and it is they who seek to maintain it. We alone, as patients, as concerned citizens, can open the gate to the prison and realize our dream of health and prosperity."

For more information about Guylaine Lanctot and this book and go to any search engine and type "The Medical Mafia" or "Dr. Guylaine Lanctot" or Dr. Ghislaine Lanctot" or "Madame Ghis."

It is my humble observation that this current so-called "controversy" about the CCSVI treatment is a wake-up call to all Canadians to learn about "The Medical Mafia" - not just those afflicted with multiple sclerosis. It is time for we-the-people to focus on "health and wellness" rather than permitting the pharmaceutical cartel to keep promoting drugs for "sickness and disease."

Thank you Steve Medley, for helping us to promote health and wellness instead of being satisfied to accept only drugging any sickness and disease. Since our tax dollars are being used to pay "government bills" it is time for we-the-people to make our individual resolutions and expose the agenda behind the story. We the families and friends of people who have been diagnosed with multiple sclerosis are doing our part with the help of the internet and the conventional print and electronic media.

Will CFRA take up the greater challenge of exposing "The Medical Mafia?"

Below is a flyer (front and back) that is being passed around to inform people about the CCSVI procedure. When people learn the truth, they wonder why this CCSVI procedure is being denied to MS patients here in Canada.

Yours Truly.
Tom J. Kennedy

c.c. Steve Winogron
     Rebecca Cooney
    The Court of Public Review

*********************************************************

CCSVI - (Chronic Cerebrospinal Venous Insufficiency) in MS Patients

Over the past six months there has been worldwide interest in the important work of Dr. Paolo Zamboni from Italy, who was motivated to pursue the cause of the condition referred to as CCSVI (Chronic Cerebrospinal Venous Insufficiency) since his wife was diagnosed with multiple sclerosis.

Dr. Paolo Zamboni's team has been testing people diagnosed with multiple sclerosis to find out of they have blocked veins in the neck and chest area. Dr. Zamboni's research indicates that these blocked veins result in the myelin damage in the brain and spinal cord.

It has been revealed that a simple Doppler scan is capable of confirming the presence of CCSVI. As of this current date, the MS Society of Canada has only committed to contributing a mere $100,000. per year for a total of two years towards research about CCSVI. This amount is miniscule when compared with the $62 million the MS Society received in 2009 through fundraising to supposedly find a cure for MS by using pharmaceutical medications. This unfair allocation of funds by the MS Society of Canada is unfair and is not acceptable.

This new and innovative approach to the cause and possible treatment of MS is inexpensive - usually less than $2000 - drug free and relatively simple, whereas the cost of pharmaceutical medication for any MS patient is commonly in the range of $20,000+ annually.

This communication is to encourage everyone to participate in a letter writing and petition campaign, whether or not someone in your family is affected by MS. Please help us lobby our politicians - both provincial and federal - and the media. Please sign the online petition and/or write your own letters to the Ms. Leona Aglukkaq, Federal Minister of Health, with copies to the media, the MS Society of Canada and friends in cyberspace.

Readers are invited to do their own research by inserting "CCSVI" in any search engine. For those diagnosed with MS, it is a matter of urgency that Dr. Zamboni?s breakthrough be abundantly funded by the MS Society of Canada and Health Canada as it has potential benefit to multiple thousands of people in Canada. It is noteworthy that the government of Kuwait has agreed to fund the procedure for everyone diagnosed with MS in Kuwait.

Thank you...

Online Petition To Support The Liberation Procedure (The Zamboni Procedure):
http://www.gopetition.com/petitions/the-liberation-procedure.html 

**********************************************************************
Relevant Notes:

1. Anyone and everyone is invited to mail a Letter (postage-free) to your MP with a copy to the Federal Minister of Health by addressing it to: House of Commons, Parliament Buildings, Ottawa, Ontario, Canada  K1A 0A6. From Ted.com: "The key to persuading politicians to take up your cause. A hand written letter every month. Find nice paper with a distinctive look and use it every time."

2. There is a walk on Parliament Hill on Wednesday, May 5th, 2010 from 1:00 PM to 3:00 PM - "To make aware to the government the importance and urgency for CCSVI awareness & research" - anyone and everyone is invited to mark your calendars and show up to give your support and help free the multiple thousands MS prisoners from the shackles of misdiagnosis!  More information may be requested from:  Andrew Katz with MS Liberation Group - andrew.katz@sympatico.ca

3. The MS Liberation Group (Ottawa Chapter) has regular meetings at the Jack Purcell Community Centre. To find the details about the next meeting visit their website at:  http://www.msliberation.ca

4. Evan Thornton (from Ottawa) and his brother Duncan Thornton (from Winnipeg) travelled to Poland on March 23, 2010 to experience the "liberation operation" and both brothers are reporting relief from former symptoms of MS. Evan Thornton's blog: http://evanthornton.wordpress.com

5. Duncan Thornton, who had vein-opening treatment at a clinic in Poland, addresses the crowd at Earl Grey Community Centre in Winnipeg, Manitoba recently. Read the article from The Winnipeg Free Press at this website: http://www.winnipegfreepress.com/breakingnews/high-hopes-for-ms-research-91794734.html

6. It is noteworthy that Canada has one of the highest rates of MS in the world, with 240 cases per 100,000 people, while 30 cases per 100,000 people is considered high. Everyday, more people are diagnosed with MS.  The next person could be you, your child, or a friend.... Canada needs this "operation liberation" treatment NOW, so please complete the online petition, write letters, attend events and invite others to multiply and duplicate your efforts.

7. Polysaccarides and polypeptides are commonly referred to as ?nature?s healing miracles.? The Vidacell product, a wholesome cell food made from selected rice grains, contains polysaccarides and polypeptides. In 2003, three multiple sclerosis patients participated in a study reported by Dr. Howard Peiper, whereby they consumed the Vidacell product three times daily. At the conclusion of the study, all of the participants reported a significant reduction in the Multiple Sclerosis related symtpoms. For more information about the Vidacell product please visit this website:
http://www.greatlifeintl.com/?r=314978 and/or send an email to tom@cyberclass.net and insert “Vidacell” in the Subject line.

8. Readers are cordially invited to visit Ann Boroch?s website and learn about her work: http://www.annboroch.com.  Ann is author of the book "Healing Multiple Sclerosis."

5 Comments:

At 11:57 PM, Anonymous Sandra said...

I was diagnosed with Multiple Sclerosis back in 1983. I can hardly walk now and it seems my condition worsens every day. When I first heard about the Liberation procedure and its results from a friend, I thought United States would be the first to conduct the trials. I could never imagine the corruption involved. I ended up applying for this simple procedure in Poland and waiting.. The other options were to get it done in India. After researching the internet extensively, I came across http://www.ccsviclinic.ca/ . They are screening for CCSVI in Fargo, ND and have very affordable packages for the Liberation procedure in India. I called (404)461-9560 and spoke to their nurse administrator Lisa whose priceless support made me realize that we are not alone in the fight against MS. They are screening within the US and Canada, their medical travel package includes flight arrangements and help with the visas, world class accommodation and meals within their hospitals, the liberation procedure, a stent if needed, medications necessary, a site-seeing tour, Pre-and post-procedure supervision, Full medical file including copies of charts, screens, CDs of Venograms, blood work, EKGs, etc. Post Procedure Screenings, follow-up and consultation with surgeons for the next 6 months and so many other provisions Lisa told me about, I can’t recall however you might be able to find out more on their site.. http://ccsviclinic.ca/?page_id=564 . They are providing all of this at just $13000 as compared to the other companies that charge something like $20000 just for the procedure. You may also contact Lisa by emailing her at apply@ccsviclinic.ca or calling her on (404)461-9560. I am getting liberated mid-October and I am so very thankful to everyone at CCSVI Clinic for making this happen!

 
At 3:42 PM, Anonymous jessica forester said...

The CCSVI Liberation Treatment could be the cure but fact remains that the rate of re-occlusion is stuck at 50% and MS patients being treated in the European and Asian countries end up suffering as they did, 3 months ago. While Big Pharmaceutical Corporations and governments in the US and Canada are coming up with new ideas to stop any advancements to the CCSVI theory (Like the superbugs, etc.), millions continue to travel to countries like India and Poland to get this simple procedure and no valuable data is recorded to support the CCSVI theory. Unless we get our position strong enough to support the CCSVI Theory, we will never be able to beat the Pharma Corporations or start the treatment here and many will keep suffering and dying even after having the procedure done. I lost my elder brother last month because of a blood clot in his stent. He got liberated 5 months ago in Poland. We need to prove to the government that this works. Non-profit organizations like the CCSVI Clinic http://www.ccsviclinic.ca/ are tirelessly working to develop safer protocols with teams of world renowned surgeons even though they are feeling the negative pressure from you know who. This Atlanta based Organization has started Clinical Trials for CCSVI and we need to support these groups because they are our only hope to fight for the truth. Without the valuable data that they are collecting offshore, the procedures will not be allowed here, in our own countries.

 
At 12:26 PM, Anonymous CCSVI Clinic said...

It is estimated that the failure rate of the “liberation therapy” may be 50% or higher, even through the most experienced surgeons in Poland & Albany. As more people receive the therapy there is growing concern amongst patients that http://www.ccsviclinic.ca/?p=765 the procedure needs to include a post-procedure protocol that is more effective than simply releasing the patient from the hospital within a day.

 
At 12:27 PM, Anonymous CCSVI Clinic said...

It should be mentioned that our research is under much scrutiny & attack from elements that are trying to control the industry & the dialogue.We would ask you to have the independence of thought to see through their campaign of deceit. http://www.ccsviclinic.ca/?p=783Regular research updates will be published on the Clinic website. Questions about participation may be directed toward the Clinic administration at 888-419-6855.

 
At 10:57 AM, Anonymous jessica forester said...

After 6 months of offering stem cell therapy in combination with the venous angioplasty liberation procedure, patients of CCSVI Clinic have reported excellent health outcomes. Ms. Kasma Gianopoulos of Athens Greece, who was diagnosed with the Relapsing/Remitting form of MS in 1997 called the combination of treatments a “cure”. “I feel I am completely cured” says Ms. Gianopoulos, “my symptoms have disappeared and I have a recovery of many functions, notably my balance and my muscle strength is all coming (back). Even after six months, I feel like there are good changes happening almost every day. Before, my biggest fear was that the changes wouldn’t (hold). I don’t even worry about having a relapse anymore. I’m looking forward to a normal life with my family. I think I would call that a miracle.”

Other recent MS patients who have had Autologous Stem Cell Transplantation (ASCT), or stem cell therapy have posted videos and comments on YouTube. www.youtube.com/watch?v=jFQr2eqm3Cg.

Dr. Avneesh Gupte, the Neurosurgeon at Noble Hospital performing the procedure has been encouraged by results in Cerebral Palsy patients as well. “We are fortunate to be able to offer the treatment because not every hospital is able to perform these types of transplants. You must have the specialized medical equipment and specially trained doctors and nurses”. With regard to MS patients, “We are cautious, but nevertheless excited by what patients are telling us. Suffice to say that the few patients who have had the therapy through us are noticing recovery of neuro deficits beyond what the venous angioplasty only should account for”.

Dr. Unmesh of Noble continues: “These are early days and certainly all evidence that the combination of liberation and stem cell therapies working together at this point is anecdotal. However I am not aware of other medical facilities in the world that offer the synthesis of both to MS patients on an approved basis and it is indeed a rare opportunity for MS patients to take advantage of a treatment that is quite possibly unique in the world”.

Autologous stem cell transplantation is a procedure by which blood-forming stem cells are removed, and later injected back into the patient. All stem cells are taken from the patient themselves and cultured for later injection. In the case of a bone marrow transplant, the HSC are typically removed from the Pelvis through a large needle that can reach into the bone. The technique is referred to as a bone marrow harvest and is performed under a general anesthesia. The incidence of patients experiencing rejection is rare due to the donor and recipient being the same individual.This remains the only approved method of the SCT therapy. For more information visit http://ccsviclinic.ca/?p=838

 

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