CCSVI Clinic Receives Joint IRB Approval for Aftercare Protocol Study.
The joint application between Noble Hospital and CCSVI Clinic has been approved through the IEC Institutional Review Board (IRB) that will allow researchers to use patient data to study their new extended and enhanced aftercare treatment protocol. Please Call 888-419-6855 to know more about participating in the study. Log on to ccsviclinic. ca for more information. Email apply -at- ccsviclinic. ca
You are amazing at what you do. Incredibly moving video.
I don't know much about the treatment for MS, just what I have researched myself. Could you tell me for which types of MS, Copaxone is used for? I have my 2nd appt @ the T.O. MS Clinic coming up @ the beginning of September & I would like to go armed w/ as much of my own info as possible. I don't have an appt like my 1st & have 2 wait another full year for help.
Please continue what you do - information is power.
Thanks Tracy ( for the comments), that really means a lot.
Copaxone is used for relapsing-remitting MS and has really worked wonders for me. What symptoms are you currently experiencing? What changes has MS made to your physical well being? How often are you experiencing these issues/limitations? Let me know, I'll help provide you with any information I can....
a few probs with my leg and feet, but I am holding my head high! I am commanding the feeling to come back to my leg. i'll let you know how it's working. so far, so good, I think. ; )
i also have MS and im 17, its going to be a year in Dec. since i was diagnosed. but ive been on Avonex for about 8 months... wow do i hate needles! hahaha but yeah its cool to see people with MS stay positive! :)
Man this was moving to me because I was diagnosed with MS in 8/08. I also take Copaxone. One positive thing is it got my ass back in the gym. I okay right now just have a little bit of weakness in my left leg sometimes when I lift while walking and of course fatigue. Working out (swimming, weights) helps the fatigue. Sometimes I wonder if I really have MS. I can't come to terms with the fact my own body screwed up on me and is now attacking itself. Please let me know how you're doing. Andy Im34
I would say the last 18 months have been the best years for me in the pass 6, so MS has provided some guidance and new purpose in my life. Once you can completely accept the fact that you have it, your life will change, trust me on that. Are you on facebook or anything? Were all connected and I just meet another young guy (30s) with MS, its cool to talk to people who understand and can relate.
Excuse me, 365 days per year and its still weak protection. Nobody can do that forever, I should know (I have Crohns and I used to be on humira injections). I see the slides about the future too. One question - have you seen the Tysabri MS patients on YouTube ? If not, suggest search for it. It is powerful in stopping MS, and a once-a-month IV. At least you will have education about possibilities.
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CCSVI Clinic Receives Joint IRB Approval for Aftercare Protocol Study.
The joint application between Noble Hospital and CCSVI Clinic has been approved through the IEC Institutional Review Board (IRB) that will allow researchers to use patient data to study their new extended and enhanced aftercare treatment protocol. Please Call 888-419-6855 to know more about participating in the study. Log on to ccsviclinic. ca for more information. Email apply -at- ccsviclinic. ca
Gregmills007 11 months ago
You are an inspiration to me. I would love to get to talk to you.
026jamie 1 year ago
You are amazing at what you do. Incredibly moving video.
I don't know much about the treatment for MS, just what I have researched myself. Could you tell me for which types of MS, Copaxone is used for? I have my 2nd appt @ the T.O. MS Clinic coming up @ the beginning of September & I would like to go armed w/ as much of my own info as possible. I don't have an appt like my 1st & have 2 wait another full year for help.
Please continue what you do - information is power.
TY, Tracy
Traazz 2 years ago
Thanks Tracy ( for the comments), that really means a lot.
Copaxone is used for relapsing-remitting MS and has really worked wonders for me. What symptoms are you currently experiencing? What changes has MS made to your physical well being? How often are you experiencing these issues/limitations? Let me know, I'll help provide you with any information I can....
Aaron
eyesofpassion 2 years ago
Awesome video man. Added as one of my favs.
MSconquer 2 years ago
Thanks!
eyesofpassion 2 years ago
GREAT!!!!
foxy7699jre 2 years ago
Thank you!!
eyesofpassion 2 years ago
Nicely done
xkrazyxboix101 2 years ago
Thank you!
eyesofpassion 2 years ago
Hey Eyes- Great video! Keep up the fight and stay strong!
BTW, I have a theory that what all MS'ers have in common is that we are good looking. You help prove my theory!
Marlo
ps- the pic of you and the needles is incredible!
teslagirlM 2 years ago
Thanks for the comments, how have things been going for you?
eyesofpassion 2 years ago
a few probs with my leg and feet, but I am holding my head high! I am commanding the feeling to come back to my leg. i'll let you know how it's working. so far, so good, I think. ; )
teslagirlM 2 years ago
The power of the mind....keep at it....:)
eyesofpassion 2 years ago
We're in this fight together..keep ur head up..great vid
risquemonmon 3 years ago
Thx!
eyesofpassion 3 years ago
LOVE THE VIDEO
TEERIDER 3 years ago
Thanks!
eyesofpassion 2 years ago
i also have MS and im 17, its going to be a year in Dec. since i was diagnosed. but ive been on Avonex for about 8 months... wow do i hate needles! hahaha but yeah its cool to see people with MS stay positive! :)
I hope u are doing good!
*Roxana
roxy782 3 years ago
I'm hanging in there, how about you?
eyesofpassion 2 years ago
I'm trying to hang in there as well...
Actually, today I went to get an MRI for a check up... Lets see how it comes out...
If you have any questions, please ask, and ill try to answer them! :)
I hope you are doing good!!!
*Roxana
roxy782 2 years ago
Man this was moving to me because I was diagnosed with MS in 8/08. I also take Copaxone. One positive thing is it got my ass back in the gym. I okay right now just have a little bit of weakness in my left leg sometimes when I lift while walking and of course fatigue. Working out (swimming, weights) helps the fatigue. Sometimes I wonder if I really have MS. I can't come to terms with the fact my own body screwed up on me and is now attacking itself. Please let me know how you're doing. Andy Im34
eddysacat 3 years ago
I would say the last 18 months have been the best years for me in the pass 6, so MS has provided some guidance and new purpose in my life. Once you can completely accept the fact that you have it, your life will change, trust me on that. Are you on facebook or anything? Were all connected and I just meet another young guy (30s) with MS, its cool to talk to people who understand and can relate.
eyesofpassion 3 years ago
Excuse me, 365 days per year and its still weak protection. Nobody can do that forever, I should know (I have Crohns and I used to be on humira injections). I see the slides about the future too. One question - have you seen the Tysabri MS patients on YouTube ? If not, suggest search for it. It is powerful in stopping MS, and a once-a-month IV. At least you will have education about possibilities.
GOOD LUCK !
7mumfred7 3 years ago