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Old 11-21-2009, 08:54 PM #1
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Default "The Liberation Treatment" Documentary

Did everyone catch this documentary? It had me in tears a few times with the hope it offers for us:

The Liberation Treatment
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Old 11-21-2009, 09:20 PM #2
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I watched it earlier (commented in the other thread about CCSVI) and my email's been sent offering my MRI scans already
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Old 11-21-2009, 10:04 PM #3
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It was very moving and I hope it is the real deal for curing/treating MS patients. Hopefully we are not far away from getting the treatment here.

It seems so simple that it is mindboggling why none of the researchers here have discovered what is going on in the disease. It is of no use to the pharma companies except for those selling balloons, so maybe there will be a fire sale on the old meds.

gmi

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Old 11-21-2009, 10:16 PM #4
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Amazing!!!!!

I wonder if it's too late for some of us. due to progression and damage already done. He did say something to that effect, in the Documentary.
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Old 11-22-2009, 12:16 AM #5
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From what I gathered getting the procedure done would stop any further progression. It appears that it may be too late for getting much better though once a person leaves the RRMS phase.

The criteria for the trials in the US are asking for RRMS, SPMS and PPMS, so there are no concrete delineations yet, or so it appears as to which of us might be helped or not helped. We should know more in another year.

Better yet, no PML!

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Old 11-22-2009, 12:27 AM #6
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I wonder if this could explain the rare, fatal form of MS (marbug?... I can't remember the name). Sudden onset of narrowing (extreme) of the veins, resulting in very limited or no drainage and/or fatal levels of iron in the brain?

Hrm... it's all very interesting to think about, even if it's only 1 piece of the puzzle in the end.
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Old 11-22-2009, 08:25 AM #7
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I have forwarded this to my MS center. Lets see what they say. I have found them to be really open minded about such studies.
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Old 11-22-2009, 11:50 AM #8
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I found this to be very interesting...I haven't read the other thread about ccsvi yet, but I'm going to do some digging, since I see my neuro in a couple of weeks...
thanks for sharing!
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