CCSVI Success (A Christmas Miracle, Frankly)

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

Postby hannakat » Sun Dec 12, 2010 7:16 am

Thank you for sharing your journey with us. I could feel the love, strength, and commitment in your words and I hope that the words of others, here at TiMS will help you in this battle.

May continued Blessings pour on you and you wife this Christmas season.
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Postby L » Sun Dec 12, 2010 9:49 am

Fantastic! good decisions! I'm very pleased for the both of you.
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Postby HappyPoet » Sun Dec 12, 2010 10:41 am

Your wife's story, told with eloquence and love, is so uplifting and filled with hope that I'm sure everyone who reads your words will be thankful for the true gift they are.

Wishing you and your wife a joyous holiday season.
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Postby orion98665 » Sun Dec 12, 2010 11:33 pm

Mark, what a wonderful story. I haven't posted here lately but after reading
your story I just had to comment and wish you and your wife only the best.
Reading threads like this is what makes this forum worth while. After reading your story I've come to the realization that your wife's improvements are not do to a placebo effect. http://swo.ctv.ca/provincewide/

I just got through watching a news clip just posted today on this forum
under "media coverage" of a women who's speech was clearly affected
by M.S. prior to CCSVI treatment. After treatment here speech is normal.
"Folks how can this be a placebo affect..?" Anyhow, again I wish you and
your wife a Merry Christmas! :wink:
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Postby CCSVIhusband » Mon Dec 13, 2010 12:31 am

orion98665 wrote:Mark, what a wonderful story. I haven't posted here lately but after reading
your story I just had to comment and wish you and your wife only the best.
Reading threads like this is what makes this forum worth while. After reading your story I've come to the realization that your wife's improvements are not do to a placebo effect. http://swo.ctv.ca/provincewide/

I just got through watching a news clip just posted today on this forum
under "media coverage" of a women who's speech was clearly affected
by M.S. prior to CCSVI treatment. After treatment here speech is normal.
"Folks how can this be a placebo affect..?" Anyhow, again I wish you and
your wife a Merry Christmas! :wink:


It's not placebo ... that's just one of the tactics brought up by whoever is against this procedure for whatever reason.

Mark, this was such a great story ... I just wish everyone could read this ...

Happy Christmas.
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Postby eve » Mon Dec 13, 2010 1:01 am

Wishing you and Marcy the best - hoping this is just the beginning of a truly great miracle. Could you please keep us posted on how she is doing? Have a wonderful Christmas.
dx 2002,RRMS,  suspected begin of MS 1978 (age 10)
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Postby pairOdime » Mon Dec 13, 2010 6:36 am

Wonderful, absolutely wonderful outcome. A real Christmas miracle. Thank you so very much for sharing this huge blessing. This is a major medical breakthrough with so much promise.

Merry Christmas :)
It's a paradigm shift
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Postby coach » Mon Dec 13, 2010 7:30 am

I'm with Blossom. Couldn't help but tear up as I read about your and your wife's experience. How wonderful for you! Truly a Christmas miracle. Thanks for sharing it with us. May you be blessed with more improvements. God bless.
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Postby garyak » Mon Dec 13, 2010 10:22 am

Mark, I am still wiping my tears over this miracle that you helped create. This is the christmas story I will share with my wonderful family. The san diego area has the del mar vein clinic that has done over 150 procedures now so keep that in mind.
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Postby MS_HOPE » Mon Dec 13, 2010 11:01 am

Mark, your eloquent and touching story is truly a gift to all of us. Many, many thanks, and very best wishes for continuing improvement in your beloved wife.
CCSVI:  Making Sense of MS
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Postby EJC » Mon Dec 13, 2010 12:14 pm

What a lovely post. As I was reading it it reminded me of the film "Awakenings" with Robin Williams and Robert DeNiro.

It's all about quality of life, and long may your wife's improve.
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Postby Motiak » Tue Dec 14, 2010 6:12 am

Isn't Dr. Hubbard based in San Diego or am I misremembering? That atleast seems like a good place to get followup care if needed. It is great to read a positive story like this though. I wish you and your wife the best.
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Postby HopingHusband » Fri Dec 17, 2010 7:47 pm

Truly wishing you and your wife all the very best !
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Postby 1eye » Fri Dec 17, 2010 8:15 pm

Isn't this a wonderful year for so many people? And this shows what I have been saying all along: CCSVI kills, and Liberation saves lives. Cheers to all the brave doctors: to some this may be a cash cow, but I think it is the work of the angels. And I don't even believe in angels. But I hope you know what I mean. I am the same age. I hope to live a while longer! I hope she continues to improve.
"Try - Just A Little Bit Harder" - Janis Joplin
CCSVI procedure Albany Aug 2010
'MS' is over - if you want it
Patients sans/without patience
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