For those affected by MS and wanting new information on CCSVI
I just learned about a private webinar for people with MS that I wanted to make sure you knew about.
Dr. Rudy Cartwright, a brain surgeon and MS specialist, is giving a private webinar where he is going to talk about the CCSVI procedure. But EVEN BETTER...he has invited some people who have recently had the procedure done to share their experience.
I know you won’t want to miss this because not only will you get some great information BUT you'll be able to ask questions during the webinar as well.
The webinar will be next week, Thursday, June 30th at 1:00 pm Eastern (New York time) // 12:00 noon Central // 10:00 am Pacific (Los Angeles
He has some extra spots available and he gave me permission to invite a few of the people who get my newsletter.
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IT DOESN'T COST ANYTHING
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For a full 60 minutes, he’s going to be talking about Dr. Zamboni's CCSVI procedure, including:
1. MS recoverers who have recently had the procedure
2. Information you probably don't know about the procedure
3. Some things to think about if you are considering the procedure
4. Why it might NOT be right for you.
5. What actually happens during the procedure
6. And much, much more!
Dr. Cartwright is great at explaining things in easy to understand terms and concepts so it won’t be like some of the other presentations you’ve listened to. You are going to walk away from this webinar knowing more about CCSVI than you can imagine!
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HERE'S THE BAD NEWS
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The webinar can only hold a set number of people so if you want to be sure to lock your spot in, you need to register immediately by clicking on this link.
If you’ve never been on a webinar before, it’s a piece of cake and actually pretty fun.
You just log-on to your computer, join the webinar by clicking on a special link that Dr. Cartwright will send you, and then you’ll be able to see everything on your computer screen and listen through your computer speakers.
If you won’t be near a computer, you can even call in and just listen to the presentation.
Sounds good don’t you think?
If wanting CCSVI UPDATES, you may not to want to miss this presentation.
Click on this link to register…and I hope to see you on the webinar.
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*** PLEASE TAKE NOTE ***
This WEBINAR IS NOT an "MS Views and News" OR "Stu's Views & MS News" program...
WE ARE MERELY the Messenger for 100's of resources and will continue to provide information to you.
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Regards,
SS
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Disclaimer: 'MS Views and News' (MSVN), does not endorse any products or services found on this blog. It is up to you to seek advice from your healthcare provider. The intent of this blog is to provide information on various medical conditions, medications, treatments, and procedures for your personal knowledge and to keep you informed of current health-related issues. It is not intended to be complete or exhaustive, nor is it a substitute for the advice of your physician. Should you or your family members have any specific medical problem, seek medical care promptly.
5 comments:
Hey Stuart:
Why not have a doctor that actually performs the CCSVI procedure talk about it, instead of a brain surgeon?
Blessings,
Nicki
DEAR ALL-
THIS IS NOT MY PROGRAM... I was only asked to provide the information and as I do for the Pharmaceuticals (and many bash me for this) , I guess I will now get bashed or slammed again for doing what OTHERS do not do....
I am merely a messenger of information.
Regards,
Stuart
I sure have not heard the best things about this procedure. They are praying on a group of people that have been looking for anything that will help with their MS.
re: CCSVI - Like many things in infancy, it has those that streamline for it and other that shy away. There are the believers and there are the skeptics. There are those that will jump-in with two feet to give it a try, maybe their only try for those with severe disability and then there are those that will wait until more is known.
I do not believe that CCSVI is a Hoax for if it were, the MS Societies from around the globe, would not be putting funding towards further CCSVI research.
Research needs to go forward for this and any other aspect that seems odd.
Heck - when Alexander Graham Bell first invented the phone, who knew that that step would eventually revolutionize what we have today... CELL PHONE technology.
MOST of us will sit back and watch the news to see what comes of this procedure. I am included, as are most MS'ers that I know. Yet, there are a few too, whom I know, that have gone for the Doppler and some even with the actual angioplasty. I do not know yet, of anybody who has been 100% successful with regaining what they lost to the disease.
A year ago, their were the CCSVI sympathizers who bashed me for not being gung-ho positive of the procedure. And now, there are those who want me to be gung-ho against the procedure.
I will voice the positives and negatives about this, just as I do for many things in life. And I will Learn by watching and listening what research tells me.
Stay tuned and meanwhile watch and listen...
Regards,
Stuart Schlossman
p.s. - My comments are my own and no organization has swayed me one way or another...
Dr. Cartwright is a brain surgeon and an expert on ms. His daughter-in-law has ms and he developed a program for her and has shared it with others using natural methods and substances. Dr. Cartwright is the first doctor to sponsor this kind of forum that I am aware. Most docs won't talk about it at all. I for one can't wait to hear what these brave ms-ers have to say along w/ Dr. Cartwright.
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