This Is MS Multiple Sclerosis Community: Knowledge & Support

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.

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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.

Good luck!
Erika

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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

Godspeed.

Ask him to look for a ‘vagus nerve compression” as well, otherwise best of luck! Arne

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"MS" doesn't exist! - CCSVI dx Nov.2009, 1. angio LVJ & RVJ June 2010, 2. angio RVJ April 2011

Best of Luck! And let us know results.

PN

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Albany 2010. Brooklyn 2011
Hurry up and wait.

Thank you! Muse, can you give me more info on the vagus nerve issue?

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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.

Third times a charm. Best wishes and good luck.

Best of Luck .

all the best!

I hope you find relief right away. Good good tomorrow!

Best wishes.............MarkW

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Mark Walker - Oxfordshire, England. Registered Pharmacist (UK). 10 years of study around MS.
Mark's CCSVI Report 7-Mar-11:
http://www.telegraph.co.uk/health/8359854/MS-experts-in-Britain-have-to-open-their-minds.html

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.

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!

Thanks Everyone. <3

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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.

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.

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"Try - Just A Little Bit Harder" - Janis Joplin
CCSVI procedure Albany Aug 2010
'_MS' is over - if you want it
Patients sans/without patience