Third CCSVI treatment tomorrow

A forum to discuss Chronic Cerebrospinal Venous Insufficiency and its relationship to Multiple Sclerosis.

Third CCSVI treatment tomorrow

Postby magoo » Thu Mar 08, 2012 7:05 am

I am scheduled for my third procedure tomorrow with Dr. McGuckin. I was initially treated by Dr. Dake in 2009 with great results. I had a second procedure with Dr. McGuckin in 2011 because I had a return of symptoms, especially heat intolerance, headaches and fatigue. Again, I had great results. In January of this year I began to experience fatigue, cognitive changes, bladder issues, dizziness and increased headaches. It lasted for two months. I went for an MRI and discovered a new lesion. So, I am heading back to hopefully figure out what's going on with my veins. I will update after my treatment.
Rhonda~
Treated by Dake 10/19/09, McGuckin 4/25/11 and 3/9/12- blockages in both IJVs, azy, L-iliac, L-renal veins. CCSVI changed my life and disease.
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Re: Third CCSVI treatment tomorrow

Postby ErikaSlovakia » Thu Mar 08, 2012 7:15 am

Good luck!
Erika
Aug. 7, 09 Doppler Ultras. in Poland, left Jugul. valve problem, RRMS since 1996, now SPMS,
- Nov.3,09: one stent in the left jug. vein in Katowice, Poland, LDN, never on DMDs
- Jan. 19, 11: control venography in Katowice - negative but I feel worse
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Re: Third CCSVI treatment tomorrow

Postby DougL » Thu Mar 08, 2012 7:17 am

Godspeed.
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Re: Third CCSVI treatment tomorrow

Postby muse » Thu Mar 08, 2012 7:53 am

Ask him to look for a ‘vagus nerve compression” as well, otherwise best of luck! Arne
"MS" doesn't exist! - CCSVI dx Nov.2009, 1. angio LVJ & RVJ June 2010, 2. angio RVJ April 2011, January 2012 2. restenosis, reversed after ~1 year intake of high dosage Magnesium only. ThisIsCCSVIinMS: http://tinyurl.com/nwy5x58
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Re: Third CCSVI treatment tomorrow

Postby PointsNorth » Thu Mar 08, 2012 11:30 am

Best of Luck! And let us know results.

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My Current Regimen http://www.thisisms.com/forum/regimens-f22/topic25634.html
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Re: Third CCSVI treatment tomorrow

Postby magoo » Thu Mar 08, 2012 11:32 am

Thank you! Muse, can you give me more info on the vagus nerve issue?
Rhonda~
Treated by Dake 10/19/09, McGuckin 4/25/11 and 3/9/12- blockages in both IJVs, azy, L-iliac, L-renal veins. CCSVI changed my life and disease.
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Re: Third CCSVI treatment tomorrow

Postby munchkin » Thu Mar 08, 2012 1:15 pm

Third times a charm. Best wishes and good luck.
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Re: Third CCSVI treatment tomorrow

Postby Flashover81 » Thu Mar 08, 2012 2:38 pm

Best of Luck :-D.
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Re: Third CCSVI treatment tomorrow

Postby Cece » Thu Mar 08, 2012 3:41 pm

all the best!
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Re: Third CCSVI treatment tomorrow

Postby bestadmom » Thu Mar 08, 2012 3:47 pm

I hope you find relief right away. Good good tomorrow!
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Re: Third CCSVI treatment tomorrow

Postby MarkW » Thu Mar 08, 2012 4:29 pm

Best wishes.............MarkW
Mark Walker - Oxfordshire, England. Retired Pharmacist. 12 years of study around MS.
Mark's CCSVI Comment:
http://www.telegraph.co.uk/news/health/8359854/MS-experts-in-Britain-have-to-open-their-minds.html
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Re: Third CCSVI treatment tomorrow

Postby dania » Thu Mar 08, 2012 4:38 pm

I hope this works for you but....if it does not I am living proof that here are other ways to get the blood flowing.
All the best.
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Re: Third CCSVI treatment tomorrow

Postby Hooch » Thu Mar 08, 2012 5:06 pm

We wish you all the best. I know that you are a true pioneer and amongest the very first of us to have this done. I am beginning to feel like an "oldie" - Sep. 2010, nearly 18 months on!
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Re: Third CCSVI treatment tomorrow

Postby magoo » Thu Mar 08, 2012 5:17 pm

Thanks Everyone. <3
Rhonda~
Treated by Dake 10/19/09, McGuckin 4/25/11 and 3/9/12- blockages in both IJVs, azy, L-iliac, L-renal veins. CCSVI changed my life and disease.
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Re: Third CCSVI treatment tomorrow

Postby 1eye » Thu Mar 08, 2012 6:47 pm

You know, I don't want to say anything at all about whether you are doing the right thing, and all of that, because I know, it can sometimes not live up to it's reputation, and I have been so adamant about it. I know you don't want to hear, and I don't want to say, anything negative. Myself, I could easily have foolishly left it too long, and now it might be too late to have the thing done again. Don't know. But I just want to say, if it does go south again, and you do end up not wanting to risk it again (and Dania, I am more than respectful of your going for the gusto, too and hope for smooth sailing :-), I think worst case we are all easily better off, even just for having had temporary improvements. I have abundant confidence in yours and a lot of the other interventionalists. Reading Dania's doctor's CV, I think I would let him work on me in a heartbeat, and the same with yours. Regardless of how I feel about it, I hope for the most successful outcomes of all for you. I want you to know I'm on your side, whatever happens. I think that's true of a lot of your friends here. Keep yer thumbs up. It'll be great. Keep yer stick on the ice. Rah, rah, etcetera. Luck and success tomorrow.
The bottom line on MS is,,. They don't know what causes it. So they can't treat it. And this BUGS THEM.

I am not a doctor. Do not take anything I say as medical advice.
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