CCSVI - The Solution in Six Minutes - Hubbard Foundation - CCSVI

[MrLeooreo]

what about the spine and azygos veins - does it work same - how do lesions occur there?

[MSVlogSupport]

A very easy to understand way that CCSVI affects all of us with MS. I really don't understand the push back from Neurologist's, isn't their job to help find the best treatmenst for us? Are so many on the pockets of the drug companies? It is so maddening. Thank you Dr. Hubbard for what you are trying to do.

Andrea

[Ausman5]

The man calls it how he sees it. I respect that so thank you Dr Hubbard. It's only a matter of time before this is MS

[QuickQuix]

A huge thank you for this, and all your other video posts. I've watched them all and I can't tell you how much I am encouraged by you and your efforts!

[robertskelowna]

Thank you Dr Hubbard for explaining your thoughts on MS and how CCSVI impacts the disease; a true shame that the rest of your Neurological colleagues don't feel the same way and are closing their minds to this treatment for their patients.

[SHIRLEYRENSHAW]

We have to do something to end all the speculation and show proof. AGREE!

[pastorjeane]

MOST excellent! Clear concise explanation of "MS" - of why my life has changed so drastically, and why I cannot access the treatment that WILL help. Thank you Dr. Hubbard for your commitment to helping us!! PLEASE God - SOON - for us ALL.

[ThePennygirl]

Thank You making this video, I pray it reaches the masses! :)

[pwm1203]

Thank you Dr. Hubbard. Then we only need to convince the neuroes and most of the patients with MS. The whole problem have been misplaced, by letting the neuroes take the responsibility for MS. Patients can only free themselves by throwing away their medication, and start paying money to a fund, treating newly diagnosed MS-patients for CCSVI. Test if they are doing better than the ones, staying on conventional medication.

[BrendaRaven1]

oh yes... big business, big pharma

[kkkkkkatherine]

Thank you Dr. Hubbard: succinct and well spoken!

`

Q. Anyone know a generous millionaire, with sympathies towards 'MS' patients??

A: J.K. Rowling, author of Harry Potter series,et.al.

If only JK Rowling's people could see 'MS' this way...Ms. Rowling's got the Motivation - her Mum died from complications of MS- AND the DEEP POCKETS...

[salchaw]

@kkkkkkatherine hi,

elton john gives a free concert for anyone who donates 1 million to aids research , can we ask him to do the same for m.s

[kkkkkkatherine]

@salchaw -- Mr. Elton John... There's a Great Idea...do ya have his contact info?

[salchaw]

@kkkkkkatherine hi

no i don't , but there's many ways to find out ...

i just don't have time to research it , sorry....

[gingermacqueen]

I had CCSVI and I also found that I had venous insufficiency in my legs! I had no visible varicose veins, thoughbut my legs never got 100% better after CCSVI Since I have vascular issues in my CNS its logical that the rest of my body have vascular issues.I am pleased to say it's been over 1 month since my leg vein ablation & my walking has improved tenfold! Im working out and expect to make a complete recovery! Shame on Doctors who labeled me & others with so called MS & refused to look further

[BevBentley]

Brilliant!! Dr. Hubbard, you give us all so much HOPE. God Bless you and your family. Everyone is so important to you and we feel this. With yourself and Dr. Zamboni and so many other amazing doctors around the world, I have HOPE.

[Northof44]

I look forward to seeing the paper on this from Dr. Hubbard & Dr. Zamboni. Thank-you for this video...Honesty is a wonderful thing!

[PlumRed99]

Oh! The beginning of this vid made me remember of a conversation with my neuro.

Me “I noticed that as the same time my MS suddenly worsened that I developed a massive varicose vein in my leg.”

Neuro “Oh, you should make that a priority to get fixed.”

Me “I’ve also had confirmed by an IR that I have a reflux of blood towards my brain”

Neuro “Your IR is wrong”

End of conversation - quite literally silence.

[boatjohn1]

The fight continues and I'm still fighting. Thanks David.

[53jann]

Nice explanation of what the Hubbard Foundation is doing.