Get screened in the US. Call CCSVI Clinic (404)461-9560 to schedule your pre- and post procedure screening today in Fargo, ND or email us at apply@ccsviclinic.ca. Find out more at ccsviclinic.ca
I am on the band wagon and agree that there should be research (? studies have been already done) in our country "Canada " ! Getting people back on there feet ,getting involve with society ,will have more federal revenue than people constanly visiting hospitals with health problems, as far as the pharmaceutical companies TUFF LUCK! You took to long and charge too much for things to help symptoms not the cause. Zamboni should receive the Lasker Award for his work!
Our "MS community" is so strong and I'm very proud of them! For those who are worried about their retirement, 401K....sorry...but I don't really feel "bad" for you...at the age of 28 MINE was technically gone due to MS and somehow I've survived. But now....I'm tired of barely getting by. I won't waste a second of health when my MS is stopped in it's tracks. And thanks to people like you Jaimie....I have no doubt my MS is experiencing it's "last days"! Thank you for your will and your fight!
statement I LOVE IT!!!!!! You are so right that we are very strong. Stay Tuned as I will prove to the world in 11 days I am not standing by and waiting.
This is so important as we all know certain people that matter in Our "plumbing problem" as I like to call it, These people are watching our videos. They may not be making comments but I am sure there are plenty of Doctors that are watching and will make a difference.
To All these Doctors on here that are paying attention to our story, I applaud you!!! Thank You. You will be the heros for standing up.
Thank you for illustrating so well how important time is for us...in fact my GP and neurologist in Belgium do just not understand...
But I have good news from Italy: after Buffalo+Zamboni NA trip it starts to open up over here! I already had a doppler in Poland+ fought for 2nd one in Ferrara, but now suddenly after Buffalo easily got appointment for another one at my local hospital. I was amazed! So I'll have doppler 3 x...and continue my lobby...as intervention still difficult
Forgot to say: it's the specific jugular vein doppler. Before my local hospital would not do it. Why I do it 3 x ? Since I know they find the problem and get excited about it (at least that was my experience of the first two). The more people go for doppler at different places, the more venologists become aware and believe + get motivated for intervention.
The MS Societies around the world are worthless. Fuck them! They do what is best for the drug companies. I quite taking my drug which is Copaxone because it is worthless. I get it for free but I refuse to give the drug company money. Obviously, my disease course isn't bad. I hope the drug companies go bankrupt and all the MS employees end up in the soupline!!!!!!!!
Thank You All For Your Great Comments And Yes It Is For All Of You Why I Do What I Do. It Is Your Support That Keeps Me Going. Yes I have Learned Not Everyone Is on The Same Page Although So Many Of Us Are And That Out Weighs The Attacks Both Personally And Physically.
Ok Maybe Not A Beauty Contest (wrong choice of words there lol..) Should have been Talent Contest. There Are So Many Of Us That Have A Talent Yet To Be Discovered Due To MS. We Will Get There !! Hang On....
Very well put! Fantastic! Love it!! You said it all! Yepp, I'll keep it going! But I DON'T wanna compete in a beauty contest (I have 35 days left till I'm 30). Lol
God bless you Jamie! You are amazing to watch and listen to. You are SO right. We have to take care of our own health care. "Diagnose and adios and here's a needle for your arse, see you next year", IS OVER! Thank you for everything you are!
We are up against the disease, naysayers, misconceptions, prejudice, shallow thinking, the status quo, people with very little love in their hearts for their fellow man, people who get rich shoveling drugs at us, an apathetic support system that is trying to decide how to keep their pharmaceutical funds coming in without alienating their members, people that fear change, and that is the shortes list i can muster.
Personal attacks? I am sorry - it does come with the territory of speaking out I find :o( When you have resolve about what you are doing it helps keep perspective. It is wonderful the coverage you are getting in Canada - we can't seem to get it on the last page of the local paper! Well done Canada! The world is watching. (mind you I do wonder if it helps that there has not been coverage here - it means we can get the procedure through back channels before a holding pattern is implemented).
Hi, dear Jamie! It's so good to see you on video and I love communicating with you! It's good to know that you can understand me while I have been going through so much with my family.
It is good to hear that CCSVI is all over the news in Canada and thank you for applauding the people that are raising funds for CCSVI! :)
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Get screened in the US. Call CCSVI Clinic (404)461-9560 to schedule your pre- and post procedure screening today in Fargo, ND or email us at apply@ccsviclinic.ca. Find out more at ccsviclinic.ca
derekdadey1 1 year ago
oin my group on facebook... ccsvi and the liberation treatment in the USA. help me fight
apsugovs32 1 year ago
Hey just wondering if you had the procedure done yet? Your videos are an help for me and all of us.
MrRhoover9 1 year ago
I am on the band wagon and agree that there should be research (? studies have been already done) in our country "Canada " ! Getting people back on there feet ,getting involve with society ,will have more federal revenue than people constanly visiting hospitals with health problems, as far as the pharmaceutical companies TUFF LUCK! You took to long and charge too much for things to help symptoms not the cause. Zamboni should receive the Lasker Award for his work!
IGOTAMOVE 1 year ago
Our "MS community" is so strong and I'm very proud of them! For those who are worried about their retirement, 401K....sorry...but I don't really feel "bad" for you...at the age of 28 MINE was technically gone due to MS and somehow I've survived. But now....I'm tired of barely getting by. I won't waste a second of health when my MS is stopped in it's tracks. And thanks to people like you Jaimie....I have no doubt my MS is experiencing it's "last days"! Thank you for your will and your fight!
2muchlivin2do 2 years ago
Won't Waste a second of health is a great
statement I LOVE IT!!!!!! You are so right that we are very strong. Stay Tuned as I will prove to the world in 11 days I am not standing by and waiting.
Take Care everyone
mackierojo 2 years ago
Were not giving up!!
ThePennygirl 2 years ago
This is so important as we all know certain people that matter in Our "plumbing problem" as I like to call it, These people are watching our videos. They may not be making comments but I am sure there are plenty of Doctors that are watching and will make a difference.
To All these Doctors on here that are paying attention to our story, I applaud you!!! Thank You. You will be the heros for standing up.
mackierojo 2 years ago
Dear Jamie,
Thank you for illustrating so well how important time is for us...in fact my GP and neurologist in Belgium do just not understand...
But I have good news from Italy: after Buffalo+Zamboni NA trip it starts to open up over here! I already had a doppler in Poland+ fought for 2nd one in Ferrara, but now suddenly after Buffalo easily got appointment for another one at my local hospital. I was amazed! So I'll have doppler 3 x...and continue my lobby...as intervention still difficult
steffi2italy 2 years ago
Forgot to say: it's the specific jugular vein doppler. Before my local hospital would not do it. Why I do it 3 x ? Since I know they find the problem and get excited about it (at least that was my experience of the first two). The more people go for doppler at different places, the more venologists become aware and believe + get motivated for intervention.
steffi2italy 2 years ago
That is the idea Steffi the more these results keep piling up they will have to do something.
mackierojo 2 years ago
The MS Societies around the world are worthless. Fuck them! They do what is best for the drug companies. I quite taking my drug which is Copaxone because it is worthless. I get it for free but I refuse to give the drug company money. Obviously, my disease course isn't bad. I hope the drug companies go bankrupt and all the MS employees end up in the soupline!!!!!!!!
azshwagg 2 years ago
Thank You All For Your Great Comments And Yes It Is For All Of You Why I Do What I Do. It Is Your Support That Keeps Me Going. Yes I have Learned Not Everyone Is on The Same Page Although So Many Of Us Are And That Out Weighs The Attacks Both Personally And Physically.
Ok Maybe Not A Beauty Contest (wrong choice of words there lol..) Should have been Talent Contest. There Are So Many Of Us That Have A Talent Yet To Be Discovered Due To MS. We Will Get There !! Hang On....
mackierojo 2 years ago
Very well put! Fantastic! Love it!! You said it all! Yepp, I'll keep it going! But I DON'T wanna compete in a beauty contest (I have 35 days left till I'm 30). Lol
Prissie28 2 years ago
God bless you Jamie! You are amazing to watch and listen to. You are SO right. We have to take care of our own health care. "Diagnose and adios and here's a needle for your arse, see you next year", IS OVER! Thank you for everything you are!
Vanda
Keetcha100 2 years ago
We are up against the disease, naysayers, misconceptions, prejudice, shallow thinking, the status quo, people with very little love in their hearts for their fellow man, people who get rich shoveling drugs at us, an apathetic support system that is trying to decide how to keep their pharmaceutical funds coming in without alienating their members, people that fear change, and that is the shortes list i can muster.
YOU are changing the WORLD, dear Jamie.
Feel proud when you see your reflection!!
irishbear76 2 years ago
Stay strong Jaimie!! We love you!!
gingermacqueen 2 years ago
Personal attacks? I am sorry - it does come with the territory of speaking out I find :o( When you have resolve about what you are doing it helps keep perspective. It is wonderful the coverage you are getting in Canada - we can't seem to get it on the last page of the local paper! Well done Canada! The world is watching. (mind you I do wonder if it helps that there has not been coverage here - it means we can get the procedure through back channels before a holding pattern is implemented).
kezzcass 2 years ago
Hi, dear Jamie! It's so good to see you on video and I love communicating with you! It's good to know that you can understand me while I have been going through so much with my family.
It is good to hear that CCSVI is all over the news in Canada and thank you for applauding the people that are raising funds for CCSVI! :)
Have a good day and keep strong!
hugs,
Angela
angelusa73 2 years ago
stay strong, man!! It's happening!!
thepasture 2 years ago