Dr David Hubbard, Neurologist, Complete Talk at Haacke Fundraiser

[bmunkres]

Thank you for sharing this and thank you Dr. Hubbard, and Dr. Haacke - again... ;)

Be well...

[likes2laughnhavefun]

I can't believe the neurologists are standing by and not participating in this procedure. All the while, many of their patients are getting worse and will suffer irreversible damage to their nerves. Perhaps it's time to sue those who refuse to help their patients?

[CONTROVERSYRISING]

Dr Zamboni is putting the shoe on the other foot and Dr Hubbard is lacing it up

[MrLeooreo]

Love you dr. Hubbard.

[walshfarm]

God Bless the whole Hubbard Family!

[07pollee2ndtime]

ok let's try again!! See if this one will post!

I change my view on all neurologists. There are some prepared to think outside the box. I respect and bow to you, dr Hubbard

[gekiryudojo]

Interesting I was Liberated on the 15th Oct I dont have MS any more!

[kkkkkkatherine]

@6:35 "it is Clear that Modern Research SHOULD move away from auto immune theory!

Let's Clean up the SWAMP !!!

Thanks dr hubbard,et.al.

Thanks drbartman for Posting!

[i2bme2]

Dr. Hubbard maybe you could come to Canada and straighten out the neuros here , dont forget you neurology screwdrivers as i think they have a few screws loose or too much wax in their ears so they cant hear properly, good talk .

[ptheglev]

Extremely exciting! Hopefully the arrogance in the neurology-community is about to disintegrate.

[nz9425]

WELL SAID Dr Hubbard, epsecially about the professional bashing that has gone on! As a nurse (never mind the fact that I have MS) I am APPALLED at the assassination of Dr Zamboni and others from so called professionals! This forces me loose complete faith in people who can speak like this about accepted an research paper; it certainly IS NOT a demonstration of their intelligence!

Anne

[MrLeooreo]

DR. HUBBARD - I WILL LIKELY COME TO YOUR CENTER FOR TREATMENT. WE LOVE YOU AND ALL THE DRS. WHO WANT TO HELP US.

[langucha]

I'm So Glad that Dr. Haacke & Dr. Hubbard are Studying this possiblity for Relieving the AWFUL Symptoms that MSers have endured for YEARS!! I'm participating in the Hubbard Study. Even if I only get Minimal Relief for a Limited Time, it pales in comparison to all the Previous meds & therapies I've tried in the 30+ years I've had MS.

[Alexknobsob]

Don't make waves in the stagnant swamp?

[qpmgibbs]

Why aren't the neuros interested? Despite the fact that they have made good careers for themselves based on not treating incurable diseases I can't believe that every single one of them is so self interested that they refuse to even look at the possibility that they may have been wrong all this time. Did they enter the profession to make huge sums of money or to help people to recover from illness. Thank goodness there are people like Haake and Hubbard who are going against the flow. Great video

[msandisue]

Bravo to Dr. Hubbard for his remarks at the end of this presentation about hope and false hope. His outrage at the neurological community who has put obstacles in the path of treating CCSVI is great to see. At least one neurologist has the courage and bravery to speak out against his own on behalf of the patients. Dr. Hubbard is one of the heroes of this story.

[msandisue]

Bluedivingfool1: what you don't seem to understand is that MS patients don't have time to wait for the slow moving research.  A number of studies are being done but our disease progresses every day and we don't have the luxury of a 5 year study. Yes, everyone agrees results are anecdotal but when that's all you have you go with that.

[bluedivingfool1]

I dont agree. A huge trial will ensure that all the side effects etc are vetted out. CCSVI remains anecdotal and does not have enough testing yet. While the traditional medicine has had less than stellar success, I think it is somewhat irresponsible to applaud, endorse and practice CCSVI without sufficient data. Doing this brings medicine back to the dark ages where things may or may not work but no one knows why. Too much black bile!

[irishbear76]

@bluedivingfool1

Thank goodness I found a talented vascular specialist who looked at the "insufficient data" and decided to look into it more,

I had venoplasty of one of my jugulars that was ONLY 60% blocked but caused reflux.

I have not had 1 MS symptom (even the diplopia and fatigue I experienced daily) since my catheter-led venogram with balloon venoplasty..

I have been FREE OF MS for OVER A MONTH NOW.

These guys applaud, endorse, and practice because OUR doctors will not even look@it!

[dely1112]

How wonderful. Thank you Dr. Hubbard - May God bless you mightily!

[swalshable]

Dr Hubbard is another wonderful man fighting for all msers....

[DirtyDirtyFecker]

Dr. Hubbard is awesome!

[MrLeooreo]

neurologists are not listening.. It is OK to be wrong on the autoimmune theory. Get on Board - the truth is here.

[MrLeooreo]

Dr. Hubbard - you are so loved by all the those who have cried out to medical community for help -

[dianagordon]

I am in awe of this man!!

[nanobooo]

The mechanism by where the venous stasis allows RBC and WBC through capillaries and venuoles is due to platelet activation as they release more than 50 immunomodulators and cytokines, most importantly matrixmetalloproteinase 9 (MMP9) and vascular endothelial growth factor (VEGF). Also CCXL-5, monocyte chemotactic factor is critical to monocyte attachment to vessels. Statins were thought to be useful for MS since 2005, but have not been used. Infections are polymicrobial.