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Old 09-25-2010, 02:56 PM #21
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according to that link most folks take 2 to 3 months to BEGIN to see improvements. This flys in the face of those posting immediate post operative videos showing them walking out of the hospital. Some are reporting feeling worse after the proceedure.

there is so much conflicting information. it just scares me.
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Old 09-25-2010, 02:59 PM #22
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Yes. I'm left confused.
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Old 09-25-2010, 03:07 PM #23
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Lady - you're getting it done? If so YOU'RE LUCKY!! God I wish "I" could tomorrow make that yesterday!
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Old 09-25-2010, 03:18 PM #24
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I guess like everything with MS it's an individual thing. We all have different sx.......we'll all have different types of "success" with this procedure. I would think alot depends on the severity of your MS when you have CCSVI performed. The worse you are the less pronounced your improvement would be. I'm just guessin'.......
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Old 09-25-2010, 04:23 PM #25
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EXACTLY - DRUGS WORK FOR SOME BUT NOT ALL!

I'm going downhill in a HURRY on Tysabri, Rebif did nothing, Copaxone was amazing 3yrs then down I went! Maybe it's because the majority are women and more likely to not have the b---'s guys do literally but for me, a paraplegic LOSING his hands, come on!

The bunch of you that are stable and happy the way you are that's terrific!
But the bunch of us that are seeing our death bed approach no matter how hard we exercise, ANY possibility's a BEAUTIFUL THING!
Can I get a AMEN?
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Old 09-25-2010, 04:29 PM #26
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Amen, Eddie. I totally understand and I pray that this is the right procedure for you.
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Old 09-25-2010, 05:17 PM #27
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@ Lady. Are you paying for the MRV out of your own pocket?

And the going rate I have seen is $2400 for the MRV.
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Old 09-25-2010, 11:03 PM #28
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Quote:
Originally Posted by Aarcyn View Post
@ Lady. Are you paying for the MRV out of your own pocket?

And the going rate I have seen is $2400 for the MRV.

It depends where you have it done and what type of ins you have. MS is not mentioned, ever. It is Venous Disease for ins, which it is. Medicare or Medicaid pay for most of it. Not for travel expenses, hotel over one night, or meals.

Many private ins companies pay for venous disease procedures all the time. We should not have kinks or blockages in our veins, it's not normal. If it were in our legs they would fix it, right?

Once the veins are fixed (congenital defect, or bone growth or pressure on veins) MS symptoms disappearing are the bonus we get.

Chicken or the egg theory. I will still stay on LDN, others stay on whatever they think is helping them too. Or they may toss their meds. out the window. JMO
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Old 09-26-2010, 02:25 AM #29
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Quote:
Originally Posted by EddieF View Post
EXACTLY - DRUGS WORK FOR SOME BUT NOT ALL!

I'm going downhill in a HURRY on Tysabri, Rebif did nothing, Copaxone was amazing 3yrs then down I went! Maybe it's because the majority are women and more likely to not have the b---'s guys do literally but for me, a paraplegic LOSING his hands, come on!

The bunch of you that are stable and happy the way you are that's terrific!
But the bunch of us that are seeing our death bed approach no matter how hard we exercise, ANY possibility's a BEAUTIFUL THING!
Can I get a AMEN?
Amen Eddie!
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Old 09-26-2010, 11:37 AM #30
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@sw8689 didn't your brother have a procedure in AZ a few month's ago?
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