Wow, Dr Zamboni just keeps pushing forward with ways to help the MS community. One of the issues with CCSVI detection to the point has been the detection of a blockage by neurologists. So, you have many MS patients being misdiagnosed because of a flawed detection process. Now, Dr Zamboni has figured out a way to take the user error out of the equation. He has come up with a process that records blood flow through a plethysmography machine to see if you have blockage. This method eliminates the operator's special training dependency, and makes detection so much quicker and easier.
Here are the details I have right now. The patient wears a collar that measures the volume of fluids in the neck. At first, the patient sits upright in a chair. When the volume stabilizes, the chair is aggessively tilted and the patient is in the supine position. The volume is continuously measured, and this position increases the volume in the neck. Again, the patient is agressively tilted back into an upright position and whamo, an MS patients blood flow takes a long time to decrease again. A normal subjects blood flow decreases almost instantly.
This is so much simpler and more accurate to see if a patient has CCSVI present or not. After they get a positive that the patient has blockage, then they can use doppler and see what extent the blood flow is impeded. This is going to be so much simpler and more effective in diagnosing since it will remove the user error. This is literally a push button method of testing, which should in turn make the whole diagnostic process easier and more reliable. Thank you Dr Zamboni for continuing to find new and creative ways to help MS sufferers. I am so grateful for men like Dr Zamboni and Dr Swank for not giving up when the medical community pushed back on them and tried to disprove their theories. I will keep my eyes open for a diagnostic center that begins to use this technique, and have my wife and daughter tested.
Showing posts with label Dr Paolo Zamboni. Show all posts
Showing posts with label Dr Paolo Zamboni. Show all posts
Thursday, March 17, 2011
Thursday, January 20, 2011
New Year, New MS Discoveries?
2011 could shape up to be an amazing year. With Dr. Zamboni getting the OK to start his Clinical Trial for CCSVI and MS, many others already having the Liberation treatment done and so much dialogue being done about new ideas about Multiple Sclerosis, this year could be a turning point for so many facing this disease. My wife and I have been following all of this very closely but are not at a point to where we feel ready to jump in yet. There is still a lot of details to be worked out concerning after care and a way to create long term opening of the veins, that we are not ready to move forward with the procedure. But, it has been amazing to read stories about progressive MS patients that have seen miraculous recovery from this surgery. We will be following everything with anticipation to see what new technology or technique or method may fix some of the issues that are currently hindering a full recovery for many of the patients.
I know for my wife, the last year and a half have been very interesting. I can honestly say she has had more daily issues with her MS where we live now than almost any other time since her diagnosis. She hasn't had any major attacks or major issues, just annoying issues that have disrupted the routines of our life and affected our daily living. We have made some commitments in 2011 to begin to shape our lives better so we can control more of the things that we know are affecting her health. She is already beginning to take control of some of her dietary habits again, and we are gearing up for some much needed physical training to strengthen and build up our bodies. We have already began to make some major changes in our lives, and I am excited about what the future holds for treatment of MS.
I know for my wife, the last year and a half have been very interesting. I can honestly say she has had more daily issues with her MS where we live now than almost any other time since her diagnosis. She hasn't had any major attacks or major issues, just annoying issues that have disrupted the routines of our life and affected our daily living. We have made some commitments in 2011 to begin to shape our lives better so we can control more of the things that we know are affecting her health. She is already beginning to take control of some of her dietary habits again, and we are gearing up for some much needed physical training to strengthen and build up our bodies. We have already began to make some major changes in our lives, and I am excited about what the future holds for treatment of MS.
Friday, January 22, 2010
Thoughts on CCSVI and Dr. Paolo Zamboni's Research
I have been reading articles and posts all over the net about Dr. Zamboni's research and Chronic Cerebrospinal Venous Insufficiency. One article by Erika Milvy states, "Dr. Zamboni found that, in over 90 percent of people with Multiple Sclerosis, the veins draining blood from the brain were constricted and this led to a buildup of iron in the brain that, he theorized, causes the neurological symptoms of MS." Dr. Zamboni seems to have been driven to this conclusion by his desire to help his wife Elena Zamboni. Dr. Zamboni performed a surgical procedure on his wife to correct this issue and she was one of his first success stories.
After reading these articles I have tried to stay up on the research being done by different universities across the US and Canada. In February more information is supposed to be released and until then we will wait with anticipation. For the past 14 years I have watched as "miracle" cures have hit the media for Multiple Sclerosis, and I have tried to hold on to what we have learned through our own experiences. One of those "miracle" cures was a drug that my wife was set to take in 1990. Fortunately she chose not to take it because it caused major organ failure in the majority of patients that tried it. We have tried to look at this new finding through the lens of these experiences but feel very excited about the possiblities.
After reading one night I asked my wife how she thought life would change if she didn't have to deal with MS everyday. What would change? We sat and dreamed about no fatigue, no worries about over working her body, no worries about going numb or losing eyesight, no more missing events and activities that we have to miss now, and so many other things that we have made choices about that specifically have to do with her MS. It is the first time in our marriage that I can say that we really wondered what it would be like to have true health together, and actually feel there may be a way for that to happen.
I don't know how successful the trials will be, but I do have hope that it may be the beginning of the end. I know that we have personally tested my wife for iron overload and have been baffled by some of the things that have worked and not worked with the treatments we have chosen. I remember her sitting in a magnetic field chair when she was being treated by our naturopath after going numb from the chest down, and she felt great after the treatment. She tried to use the same treatment a year later and it made her feel ill. We had no idea why it made her feel great one time and made her feel awful the next. We still have no solid answer to why, but iron content was one of the issues we were looking at after the treatment. I will share more thoughts later, but for now I wanted to at least acknowledge that we are watching this play out with anticipation and excitement. Our hope is that this research will truly change the way MS is treated.
After reading these articles I have tried to stay up on the research being done by different universities across the US and Canada. In February more information is supposed to be released and until then we will wait with anticipation. For the past 14 years I have watched as "miracle" cures have hit the media for Multiple Sclerosis, and I have tried to hold on to what we have learned through our own experiences. One of those "miracle" cures was a drug that my wife was set to take in 1990. Fortunately she chose not to take it because it caused major organ failure in the majority of patients that tried it. We have tried to look at this new finding through the lens of these experiences but feel very excited about the possiblities.
After reading one night I asked my wife how she thought life would change if she didn't have to deal with MS everyday. What would change? We sat and dreamed about no fatigue, no worries about over working her body, no worries about going numb or losing eyesight, no more missing events and activities that we have to miss now, and so many other things that we have made choices about that specifically have to do with her MS. It is the first time in our marriage that I can say that we really wondered what it would be like to have true health together, and actually feel there may be a way for that to happen.
I don't know how successful the trials will be, but I do have hope that it may be the beginning of the end. I know that we have personally tested my wife for iron overload and have been baffled by some of the things that have worked and not worked with the treatments we have chosen. I remember her sitting in a magnetic field chair when she was being treated by our naturopath after going numb from the chest down, and she felt great after the treatment. She tried to use the same treatment a year later and it made her feel ill. We had no idea why it made her feel great one time and made her feel awful the next. We still have no solid answer to why, but iron content was one of the issues we were looking at after the treatment. I will share more thoughts later, but for now I wanted to at least acknowledge that we are watching this play out with anticipation and excitement. Our hope is that this research will truly change the way MS is treated.
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