This Is MS Multiple Sclerosis Community: Knowledge & Support

Does tinnitus improve following CCSVI treatment?

i'm not sure ow to answer this.

1st time it totally disapeared
2nd time it was louder and higher pitched

3rd time i hope it all goes away!!!!

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PPMS. Liberated Katowice, Poland
06/05/10 angioplasty RJV-re-stenodsed
26/08/10 stent RJV
28/12/10 follow-up ultrasound intimal hyperplasia

Mine changed - perhaps slightly diminished (PTA 3 times), but I still have it. It did used to be three simultaneous tones ranging between 6 tones, but seems to be down to one tone at once, varying between two different tones.

I am completely deaf in the ringing ear (how weird is that?).

I am investigating BPPV (benign paroxysmal positional vertigo) in relation to my dizziness problems, and the tinnitus.

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My name is not really Johnson. MSed up since 1993

Turbulent blood flow. Narrowing or kinking in a neck artery (carotid artery) or vein in your neck (jugular vein) can cause turbulent blood flow, leading to tinnitus

http://www.mayoclinic.com/health/tinnit ... ION=causes

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Where there is a will, there is a way. "HOPE"

CCSVI Procedure December 2010

It's important to distinguish types of tinnitus. Pulsatile tinnitus, as described above, may be likely to respond to ccsvi treatment.

I don't have pulsatile tinnitus, but I have some neurological tinnitus.

This was discussed very briefly at the patient day yesterday.

Hi, there!! Thanks for sharing tinnitus treatment information here. My grandfather is having tinnitus since six month and we have already visited couple of ENTs for the treatment. Now they also suggested us to follow the CCSVI.