http://csvi-ms.net/en
This may not interest many here. But it holds great importance to me. It involves a treatment for MS. The theroy is, the viens carrying blood to the heart are restricted, thus not allowing blood flow, and damaging the brain. It seems to have been sucessfully done for many people. My Neuro scoffs at it.
My question, if it does work, shouldn't insurance companies be jumping for joy? Instead of paying for thousands of dollars in meds to treat symptoms, they may be off the hook so to speak?
what about those like me already on S.S. ? shouldn't the governments be pleased with these results as well? ( get your arse back to work )
As far as I go, my greatest fear has never been that I will go blind, or be unable to walk...It's that there may be a hereditray link, and MS hits women much more than men,, thus I fear for the well being of my daughters.
This disease seems to prevail in the northern hemispheres, scandanavians, English,Russians, so on....
I have never seen anything on any news channel about it?
Hoax?
Originally posted by Hugh GlassNone of Zamboni's results have been replicated, and diseases that would be comorbid with MS given Zamboni's hypothesis have not been observed. Probably not a hoax, but it could be sloppy research.
http://csvi-ms.net/en
This may not interest many here. But it holds great importance to me. It involves a treatment for MS. The theroy is, the viens carrying blood to the heart are restricted, thus not allowing blood flow, and damaging the brain. It seems to have been sucessfully done for many people. My Neuro scoffs at it.
My question, if it does wor ...[text shortened]... English,Russians, so on....
I have never seen anything on any news channel about it?
Hoax?
Originally posted by bbarrIt's kind of sad, if it doesn't prove out...you would not believe how many people are jumping on the band wagon for this treatment..... it offers hope, some of these people are in wheel chairs, and it just makes me feel so sad...
None of Zamboni's results have been replicated, and diseases that would be comorbid with MS given Zamboni's hypothesis have not been observed. Probably not a hoax, but it could be sloppy research.
I had to quit going to the group meetings, I felt out of place.....
Originally posted by Hugh GlassMy mother, aunt and sister have MS, thankfully fairly mild cases. Believe me, I wish this research was borne out.
It's kind of sad, if it doesn't prove out...you would not believe how many people are jumping on the band wagon for this treatment..... it offers hope, some of these people are in wheel chairs, and it just makes me feel so sad...
I had to quit going to the group meetings, I felt out of place.....
Originally posted by bbarrI'm sorry to hear that. My case is mild as well...... I'm 55 years old, and I can make this a-ok.....
My mother, aunt and sister have MS, thankfully fairly mild cases. Believe me, I wish this research was borne out.
I hope it come through as well....... check out my last post,, it made me cry to hear this woman...
Originally posted by DrKFI understand her excitement,, I injected interferons for over a year,, I could not get over the 2 day flu symptoms it has.... it was worse than the MS at times.
'tis but a small thing, but an ex of mine with MS is quite excited at the prospect of taking beta interferon orally rather than by self-administered injection (to the extent of trying to get on-board for the next wave of mass trials). Regular injections are never a good thing.
I just read my first post, where a lady was tested, and she did not have blockage in her viens.... so I don't know where to go...I don't think I want to spend the 10K for this yet...