CCSVI, Having MS and US Healthcare

The US healthcare system and not being able to be treated for CCSVI. Basically, our healthcare system is screwed up. See link for Multiple Sclerosis Treatment: World Drug Market 2012-2022
Read more here: http://www.sacbee.com/2011/12/27/4146965/multiple-sclerosis-treatment-world.h...

Category:

Education

Tags:

• Chronic Cerebrospinal

[trosper]

Judy i agree totall with everything you sed. Rick Simpson is a hero for making Run From the Cure. I believe i will making a video soon talking about this issue. i am tired of bein cornholed by my dipshit doctors. Keep up the fight and i shall be by your side

[donotconcede]

@trosper He is indeed. Will send you a message on it. Rick Simpson is a hero and they've made him a criminal for saving lives. I am totally with you on everything you say in your videos and follow every single one. Wish you lived closer as we could definitely hang out for all we agree on. hugs, Jude

[Lynneheal]

Id love to meet ya too one day also Judy youre a loverly lady

[donotconcede]

@Lynneheal :) /huggles

[MrMarkafisher]

MS really sucks big time, keep well Judy.

[donotconcede]

@MrMarkafisher Yes it does. And so do our evil MS societies and governments. Mark how are YOU doing?

[sagaertj]

if they would save 5% of the money spent in election campains and spend it in research or madical treatments, it would make a big difference for a lot of people.

Healtcare here is controlled by goverment,and i hope it stays that way.

I have the standard obligatory insurence, and i only have to pay 10€ /month for my medications

Without the insureance its 1200€ thats over 1500$ /month.

I am happy its anobligatory insurence so its democratic for every one.., its bad if it is going commercial.



[MrMarkafisher]

@donotconcede I'll pm you.

[donotconcede]

@donotconcede because of a fucking insurance company that decides so many people's fates . .that is worried about their fucking profits instead of lives. GRRRR.

:) I could go on but ranting is like screaming into the wind. We need pitch forks and torches. again, love you and hope you are hanging in there. xxxoooxx

[donotconcede]

@MSVlogSupport :) love you Andrea. You also inspired part of this video. These f'n companies have us totally at their mercy. All we can do is hope and pray there is some drug to help ease our suffering. That is all they will offer us and how society has been conditioned.

I think of how I felt after my first procedure. I think of Mike (Damizia) and HOW excellent he was doing. I think of YOU doing that Lotus yoga stance. That your doc is NOT allowed to make you better.

[donotconcede]

@jayne4ccsvi That is SO much the truth. And even doctors themselves. I actually have a neurologist, that claimed to wish to have my Interventional radiologist come down, and the IR is not really following up or making that happen. GRRRR I am SO frustrated.

Jayne, been thinking about you and hoping you are doing well. I'm so glad the internet has allowed us to know one another. Thanks for all your kind words and your wisdom. Warm hugs. :) <3 back. :)

[donotconcede]

@msandisue Its unbelievable that something that could make us so much better is not allowed. I've had 2.5 procedures, & where i went (American access care) will not do the billing so that Medicare will cover the procedure. It used to but they sold AAC & perhaps it is the new large company that owns it now who will not bill it as separate from MS. Plus there's other stuff too with AAC. When my medicare comes through, I'm going to see if Vascular Access centers will bill medicare.