Funding CCSVI and MS Research

[Jessica1963Forester]

Autologous stem cell transplantation is a procedure by which blood-forming stem cells are removed, and later injected back into the patient. All stem cells are taken from the patient themselves and cultured for later injection. In the case of a bone marrow transplant, the HSC are typically removed from the Pelvis through a large needle that can reach into the bone. Log on to ccsviclinic. ca for more information.

[Jessica1963Forester]

Dr.Avneesh Gupte, the Neurosurgeon at Noble Hospital performing the procedure has been encouraged by results in Cerebral Palsy patients as well. “We are fortunate to be able to offer the treatment because not every hospital is able to perform these types of transplants.You must have the specialized medical equipment and specially trained doctors and nurses”. Log on to ccsviclinic.ca for more information.

[Jessica1963Forester]

Other recent MS patients who have had Autologous Stem Cell Transplantation (ASCT), or stem cell therapy have posted videos and comments on YouTube v=jFQr2eqm3Cg. Log on to ccsviclinic. ca for more information.

[Jessica1963Forester]

A group of Canadian patients just back from Noble have reported similar results. “I can actually see what I thought were long-dead muscles forming in my feet” said Larry Vermeersch of Kenora, Ontario. “My balance is back and I’m walking without a cane. I’m a pretty hard guy to convince, but getting these two procedures together has made me a believer. I’m looking forward to the physio ahead because I can feel everything coming back.” Log on to ccsviclinic. ca for more information.

[AWDESIGNS8]

they need to lower the price for this treatment albany its 10.000 i dont have and no insurance medicare does not cover this doctors are saying it does work people who got it done saying it works its just a lot of money for people who dont have it but still have hope. montel Williams say copaxon the shot works for him at least if you have no insurance they work with you to stop the progression of ms .come on dr z wife has it you did it help others

[CCSVIROMANIA]

A new CCSVI clinic it is available in Bucharest, Doctors team from Bucharest are certified by DR.ZAMBONI in Ferrara and by Dr. Simka in Poland to perform the CCSVI treatment/procedures.

The price of the treatment INCLUDING Travel Expenses(flight ticket,accomodation,transfers,­all exams,angioplasty) is 8200 USD for USA/CANADA patients and for europe patients 5100 Euro Incl. Travel expenses.

[AndrewKFletcher]

Thank you for mentioning IBT

Andrew

[kara98222]

I wanted to say another quick thank you to everyone for their comments. They mean a lot to me and I am truly grateful for such a positive response.

[derekdadey1]

Call CCSVI Clinic; (404)461-9560 to schedule your screening today in Fargo, ND or email us at apply@ccsviclinic.ca. Yes, get screened within the US. No waiting….find out more at ccsviclinic.ca

[MsHercules99]

Thank you so much for this video!  AMAZING!! We will get there!

[plasticnitwit]

this is the most heartfelt video ive ever seen,

and now im crying like a baby.. my mother has MS, and had had it for 27 years, and i just picture her, first getting it, still being able to walk and explore like you....

i want her to walk again, i want to walk with her... and i cant.

im so glad theres help for you at this early stage, help that she didnt have when she was diagnosed.

i really hope this new treatment helps, and fast.

ive love to walk with my mother again

[fanwuren]

Nice video Kara. CCSVI liberation works. I've seen it. My sister is completely without symptoms 3 months after the liberation. She was diagnosed less than 2 years ago and was not very far progressed with MS, but she did have many symptoms.

Hang in there.

[vladstef65]

Beautiful. Thank you. I'm doing everything I can, believe me. But thank you for the additional inspiration...

[epompeii6]

OMG Kare you have, and had me in tears as I am writing this to you. This was very touching and great work. I hope that people understand what we go through and help to put an end to all of his. Best of luck.

[lboothalicious]

@kara98222 . This video was TRUELY inspiring. Well done. I am part of a team that is raising awareness of CCSVI (FB CCSVI Australia) and have recently had a win with the MS Society giving us space in a tent at the upcoming MS walk to promote CCSVI. Im curious as to the vid that you refer to in your post, as we need something like that going forward to help raise awareness. There was sooo much impact in that vid. Well done. :)

[AndrewKFletcher]

I can help you Kara. Google inclined bed therapy about tilting beds for ms.

Check out my video abut Inclined bed Therapy

Also visit thisisms and read about experiences of people with ms using IBT.

No surgery required and therapy is free.

[andman1996]

Great Video Kara, it brought tears to my eyes the first time I saw it!

[skaraplis]

Cara, since your vid made me cry when i first watched it i thought i d share here my satisfaction that both my jugs seem to be severely stenosed. I dont know if you have already had a doppler or whatever but if not please give it a chance to any radiologist available. It may be to obvious even for an untrained eye to miss.This goes for everyone else of course.

Good luck to all of us.

[rascal1257]

If each of us with MS, who is able to participate in an MS walk, should wear advertisements about CCSVI to bring awareness to people all over. I'm in a walk in Monticello, NY on 4/17 & I will be handing out flyers with websites that tell all about it. I'm going to look online for buttons I can have made up to advertise CCSVI so my team & I can wear them. We've got to band together on this!

[skaraplis]

you are most welcome girl.

and seing this video made me feel so related you wouldn't believe. the "if i was a girl with ms i would be her" kind of thing...

Hang in there. There is true hope for us all k?

One more thing: Mykonos should be the first place you visit when you get "liberated" ;)

[skaraplis]

bravo.

[Zzozze]

To much money for MS ends up contraproductive making it a too juicy business for parasites.

What MS-patients now need is political activism.

Don't donate money but be very LOUD and never give up if you don't want to be keept ill a lifetime long!

[margreet0]

Thank you Kara!

[AbraxaMiro]

Amazing video, truly inspiring.

Thank you!

[omexmc80]

The most amazing and touch video I have ever seen.. i can just watch it over and over again..

brings tears to my eyes..

we will fight for the liberation, we will fight for each other and we will fight together as ONE!

I love the MS family... I love you all..

Omar

[bongobarb]

Great video Kara. Obviously, you're a brave and smart woman, a self-thinker as well. CCSVI is a new and marvelous discovery. Hopeful for some and scary for others as all new creations can often be. Your idea of raising funds to support that effort is an awesome way to stand up for what you believe in. I think it will get others motivated in many ways. Keep positive and strong.

Many blessings,

Nicole's Mom

[2953864]

Absolutely Brilliant!

[nicedee81]

Thank you for making this video, Kara. You inspire me... there is hope...we will keep fighting the battle.

All the best,

Nicole

[irishbear76]

Truly a wonderful video.

I was happy to see the links were all places doing continued research on CCSVI.

One day, there will be a society to raise money for.

We are working on that.

I am sure you will be a great help.

God bless.

Mark

[mursmith]

"Being determined to love life with or without this disease" , I like that. What else can one strive for, I shall keep that thought and pass it forward. Thanks. Kam, BC, Canada

[pinoc1001]

Credi iin questa terapia. Noi ci crediamo.

E' più di una speranza: è la causa della sclerosi, dal mio punto di vista, ma non si può ancora dire.

Zamboni e Salvi sono 2 grandi menti.

Nobel now!

[pinoc1001]

Anche io uso LDN .

[Lucretia1419]

Benissimo! Credo che CCSVI e LDN sono bene tutte le due e insieme. Come va con LDN?

[pinoc1001]

bene, ho recuperato la sensibilità sotto i piedi quindi posso stare in piedi senza appoggiarmi al muro per qualche secondo in equilibrio.

[kara98222]

Just wanted to let everyone know that the donation links can be found in the info for the video! And thanks for all the comments:)

[makenziejlee]

I've met this girl once! :)

[dummyRK]

I am from Croatia and I also have MS. You made a great video and I wish you luck.

[davslav]

Hi,, I'm from Zagreb living in New Zealand.Those photos looked like Dalmacija ??No getting away the terror.Yeah bring ters to eyes.Well done,,

davslav

[gingermacqueen]

You did a phenomenal job on this, Kara. My daughter, who is 23, saw you on your video and I could tell it touched a chord with her, to see one of her peers affected by this terrible disease. The fact that you go on and live a quality life despite MS says so much for your character. I am proud to say I know Kara Byrne, she's my FB friend and a sister in the fight for CCSVI.

[Garnetldn]

Low Dose Naltrexone is stopping the progression of MS, and many other auto immune diseases. Because it is out of patent doctors will not promote its use. It is up to the patient to find it and request a prescription. Assistance with finding doctors or otherwise obtaining LDN is available. Google LDN for more information.

Cancer, neurological and auto immune conditions respond to LDN in 80-90% of cases. It is low cost and low toxicity. You have only your health to gain and nothing to lose!!

[jaynecrocker]

I have a partner who suffers from SPMS and I found this video truly inspiring. My partner took beta interferons for 5 years after discovering LDN. He has now found his disease to slow down its progression and please, if anyone is reading this, do look into low dose naltrexone for MS. It isn't a miracle or wonder drug but 100,000 peopl can't be wrong surely? It is safe, harmless, non toxic and works! Thanks.

[cheeseontoast77]

Great video Kara. It looks like you take Copaxone if it`s a daily shot. Please look into LDN (low dose NALTREXONE) which you can take with Copaxone. My husband takes nothing but LDN and has remained stable for 5 years. Just one pill at bedtime and no shots to dread each day. Theres loads of info online - just Google LDN. Stay healthy!

[NoxinHH]

Kara.... Good work, that's really more than cool! Greets from Germany!

[82KiranA]

Someone posted this on Facebook, so I clicked on it. I'm grateful I did. Thank you for creating such a personal message and sharing your private battle. I know far too many who are struggling with MS, and I know they would appreciate a video like this. I hope someone picks this up and uses it for a commercial. Amazing.

[khensel353]

Haha as I said before... this is epic Kara! You are an inspiration to me and everyone around you!!

[chloebelles25]

You are amazing Kara, well done!

[Kelly09191]

I'm proud to be your sister. I cannot believe the response this video is getting, it's amazing! I can't wait to see what this does for research for MS!