You are right, dear friend: new year, new hope! We needed this so much and now we can dream for a better future for people with MS! Good luck with everything! I wish you the very best! Hugs, Angela

Thank you, dear Bill, for your support. I understand that it's not easy to change our way of thinking and seeing things and I understand that it will take time for people to be more interested in learning more about this. I am glad that you will ask your doctor about it. It's always good to learn more and we should always be our own best advocate! :) Thanks so much for being such a good friend, hugs Angela

Yes, dear Regina, I agree with you! These news bring hope and I hope that it will bring it to others too! We have to still be realistic and see how things will go in the future but, for now, these are wonderful news! Grazie di essermi amica, ti voglio bene Angela

Good for you, dear Trevor! You are getting closer and closer to finding out if you would be a good candidate for the presidure. You are very active in finding the truth and I like this about you! Keep up the good work and keep us informed of any new findings! Good luck to you! Hugs :) Angela

Dear Anna, thank you for coming to share the good news with me! :) Unfortunately, it seems that the MS society is this country and in mine (in Italy) are not as supportive and excited about Dr. Zamboni's research as the Canadian one is. Then, for now, let's count on the Canadian one to help us study this theory more because we are all very excited and we want to find a way to get better soon! I hope you are doing well, have a great Thanksgiving! Warm hugs, Angela

Dear Daniel, it's good to know that you live in Buffalo and that you are close to the American center that will start this new trial. The hospital's name is: Jacobs Neurological Institute. I just wrote to them to ask more information about the study and I can let you know what they tell me. I hope you are doing well and that you are having a good day, thank you for writing! Angela

@npiltan I believe this too, dear friend! This is the Year that will bring great news to all of us! Good luck with the Liberation procedure! We wish you the very best! Hugs, Angela

I like your strengh and your spirit! and you are absolutely right when you say that we fight every single day because we have MS in our lives and that we will be strong and get what we want and what we believe in because we are used to fighting and to win! :) Have a nice day and thanks so much for writing! (no problems if you have typos!). ciao! Angela

Dear Angela, Your email shows that there is hope. Thank you so much for all you do. I will be sure to ask my doctor about this. I for one am ready for something better than shots and pills. This world needs more people like you. Take care and try to get some sleep. Bill

I will go look at your video right away, dear Astrid! I hope you are doing well and that you are having a good evening! Un bacione, a presto Angela

You are absolutely right about this and I am concerned about the way this discovery will be taken by the medical comunity in this country but the Canadian MS Society is very different and it has already said that it will start giving out grants to the scientists that want to study Dr. Zamboni's research and I feel that this is already a good step! We will have to be push and be strong and ask the society over here to listen to us! I am excited too and we can finally dream a little bit more!

Carissimo Primoz, here you are ready to give me your wonderful support! Please, do ask your doctor about it and ask for the ultra sound to be performed so you can be checked. You know that I want the best for you and for everyone that is dealing with MS and I truly wish that this research can be the beginning of something good that can help us all, un grande abbraccio, a presto Angela

I believe it and i'm going for it very soon. New year with new hopes.

I do think it's a great idea to try to meet somewhere! I do that when I go back to Italy! I make sure to meet with my old friends and with the new ones that I met thanks to KZread and I love doing it! It's really a good idea and I am sure it would be a lot of fun! Ciao! Angela

Great job Angela, I had heard about this someime ago but reading about it was hard to understand. After seeing the news progam it made so much more sense to me. The one thing I am hearing from some friends who are checking in to the studies being done here is the criteria to be included would eliminated a mass majority of MS'ers. Not had the chance to fact check it yet, but that could be a serious problem in getting real advancement with this. Will let you know what I find.

Yes, they let you post the video only one time!

@Zzozze I wish I could stop taking the drug right now but before doing that, I would like to get a little closer to getting the liberation back in my homeland or in this country before I do. Thanks for caring!

@Zzozze I agree! I don't donate the funds that I raise to the MS society with my Flowers4MS project but I donate it directly to Buffalo! I don't believe that the MS society cares about us at all, unfortunately. You are right when you say that we need to spread the word about this and that we need to contact cardiologists that we want our veins opened! I cannot believe that they would let us walking with them closed in our necks! Thanks for the suggestions! hugs, Angela

i am so new to this but i am certainly looking into it now after your video, thanks

Ive been to the Doctors this morning He had not heard of CCSVI and Dr. Zamboni yet. but he does now!, he was very intrigued and interested and open to the idea of stenosis in the Carotid arties, he mentioned that there had been something about a similar vascular problem in epilepsy that he had read,The upshot is I am to have a Doppler ultrasound ASAP to check it out and then to be referred to a vascular surgeon /consultant so the ball is now rolling I will keep you in formed Trev

Carissimo Dado, guarda il video in Italiano, cosi`lo scoprirai! :) He is an Italian doctor that works in Ferrara and that has found another way to treat Multiple Sclerosis and that found very interesting things about people that have this disease. While we have to still be realistic, we have great hopes for this and we are looking forward to find more about it. Spero che hai capito qualcosa...ho fatto il video anche in Italiano :) Hugs, Angela

Hi Andrea, I am waiting information from the place in Buffalo that I have already contacted. I am curious to find out what the criteria will be but I do imagine that taking Tysabri is not a good thing in this case :) Anyway, we need to find out more because this is really interesting and exciting work. Have a good night and thanks for watching! Angela

Dear Prissie, check which one of our friends has your video now because only one has it :) I used to do this all the time and I would post more than one response just like you did and then, at the end, I would found out that there was only one response allowed! They tell you that somewhere on the screen when you are posting it as a response. I hope this helps! If you have any more questions, know that I am here! :) Ciao!

@joserafaf Dr. Zamboni is a wonderful Italian doctor that made an amazing discovery and, as you can imagine, he is quite busy working in his country at the moment. So much has happened since I made this video: I will contact you privately tomorrow morning and I will let you know more about this. I hope you are doing well. Take good care, hugs Angela

Thank you so much, dear friend. I have tried many times to write a response to your comment and it was taking so long because KZread was having some problems and I decided to send you a private message with the information that you are looking for. I hope you received. Please, let me know if you didn't. Next to this video, there is the explanation of what is CCSVI and, at the bottom, there are addresses and important information that you can use to get in touch with the center in Italy.

@governslayer I would love for more people to listen to us and to be open to other therapies and not only to drugs! Will our world ever change and will people be able to find out about the natural ways to help our bodies? My biggest dream is to stop taking the medicine that I am taking now so I can be drug free again like I was before having my first MS attack. I am sure that there is a lot to be found out about cancer out there and yes, it is unreal, unfortunately.

I am so sorry but I can't add your video as a response if you already added it to someone else's video. It happened before and while I wanted to add your video to mine, it wasn't possible because it was already somewhere else. Unfortunately, they only let us post a response once! I made the same mistake many times before learning about this! I am going to watch your new video right after this! Take good care, hugs Angela

Dear Mody, there is an alternative therapy called chelation therapy and this seems to be helping lots of people to try to get rid of the metals in their bodies. Unfortunately, MS is not an easy disease to figure out and metals are really bad and toxic for us. I am not aware of drugs that can help. I am just aware of the chelation therapy that is used by many alternative doctors. Thank you for your comment. I learn a lot from people that write to me. Take good care, hugs Angela

This time with out Typos We MS people fight a war every day so if they want one then Come on! It is good that the Canadian MS society has taken the lead it will make it easier for the others to follow suit

I am so happy to see that I am not alone in believing this!!! I believe it too and I am quite concerned about it because I see the power that certain companies have here in the States. I always believed in other things more than in drugs (and that is why I do my cranial sacral therapy too) and I am worried the way this new discovery will be taken by the medican comunity here. If we have to, let's go to my homeland and let's have the presidure done there!!! :) Have a wonderful Thanksgiving Day!

IN YOUR FACE (well mine) just Back from the Ultrasound yes there is something strange, with my left jugular vain! and it warrants further investigation the sonographer said (she had difficulty seeing the left Jugular and there was something going on with it !) the right was great and so were the carotid arteries, more later, QED :)

I really hope that this is the cure!!! Not for me, for my aunt and EVERY SINGLE person with MS!

@governslayer It is crazy, I know, dear friend. It is crazy that people are suffering and others don't care! I wonder if they have a heart and if they care at all about anything else but money! Hopefully, the Canadian goverment will start making the right decisions and it will start helping MS patients! I hope that, someday soon, things will change!

@lebanese996 Thank you for the wishes! We are all hoping that this is the cure for MS and it would be amazing if it would be a real cure! We will continue to fight and we will never give up and, someday soon, everyone will be able to get the Liberation procedure! :)

@governslayer Oh, I so know what you mean, dear friend! I am disgusted by the drug companies that make medicine that help us deal with some symptoms while they hurt our bodies in so many other ways and that is why, except for taking Tysabri, I refure to take any other drugs and I use acupuncture, cranial sacral therapy and yoga to deal with my MS. Everything you said is, unfortunately, right but I dream that, someday, we will have the power to change things!

Dr. I want to get in touch wth him tell how can I?? so plese send me a clue and you are so right

I've heard this works with some people who have Dysautonomia too. Have you heard any updated information since you made this video? Many of the journal articles I found are earlier than this year and are asking for more safety studies. Do you know if anybody has taken this further? I just found out through a carotid ultrasound that my arteries on both sides and the vertebral artery have plaque, narrowing and antegrade flow. About 4 years ago I had a primary care doctor who wouldn't even look into this for me because he thought it was all BS. He wouldn't even do the simplest test on vascular stuff. Since then my blood pressure has gone up more and more and it usually is just the diastolic or just the systolic blood pressure, so it is very eratic. Sometimes it's normal but it changes all throughout the day. I had 4+ pitting edema about 2 weeks ago and have been retaining fluid in my legs intermittantly They now want me to take blood pressure medication without treating the cause. When a later doctor ordered this ultrasound done it confirmed what I suspected, then a follow-up one showed that it has gotten worse. Are these doctors in Buffalo actively doing research and is it only on MS patients or are they doing it with other conditions in which this narrowing and blockage occurs too? This treatment sounds promising, but has it become any more accepted than it was in 2009? I sure hope some scientists have continued to work on this and make it more accepted in mainstream medicine. This is where I may be heading next. I just hope I don't run into alot of disbelief and barriers like I did back in 2015. I'd rather have a more permanent solution that pill one pill on top of another.

Hi! I think your English is fine! Unfortunately, I don't have the answer to your quesiton and I so wish that I would, but not even the scientists that have studied this disease for a very long time know much about it. MS drugs don't work for all of us and I had to try so many of them before I found one that seems to be working. Also, some of the drugs might help us but they don't cure us and it's always important to keep on looking for a better treatment that can help us get better. Ciao!

I am looking for clinics or hospitals in Latin America or the Southeast US that implement the CCSVI cure. Any recommendations?

@Zzozze Yap! Unfortunately, that is what these companies do...but don't worry...soon enough, after the Italian doctor will prove that this procedure works and helps MS patients, there will be many people that will STOP taking the drugs and the companies will start losing money!

da samo tako nastavote

Another case of selling hope on the back of quakery

the MS society's around the world would be out of a job! no wonder they are not excited but I am :)

Hi; I think this information is great and I hope this could be study more. But I do not want to sound pesimistic or paranoic; I do not think this will be studied seriously in the states. I say this because this will jeopardize the medicines that are out there for MS and the profits the pharmaceutical companies makes from them. But still I will ask my Dr.

IF YOU HAVE MS,,,CAN WE SEE YOU WALKING..

@angelusa73

9 жыл бұрын

George Kafantaris yes, I am still able to walk and the orogression of the disease comes overtime and it brings more issues with moving over the course of years. I am sorry to tell you: THERE IS NO CURE for MSeven if there are many drugs on the market that help the symptoms of the MS and the doctors and drug companies say that they slow down the progression of the disease but they don't work for everyone and for me they are a good way for pharma to make money because I tried four of them and one called Tysabri and made me worse but we all DIFFERENT and WE ARE STRONG and we can deal with a loy and we WILL. MS FIGHERS are the strongest people I know so please BELIEVE IN YOURSELF and take a day at the time and please be THANKFUL of the smallest things n your life. This what helps me go on. Try it too and good luck. I WISH YOU THE VERY BEST, hugs, Angela :)

@georgekafantaris7807

9 жыл бұрын

dear angela im 52 with ppms..i remember problens from 7 years old.,.and gradually got worse like you say.i dont beleive in the drugs as ive seen people taking them,then i see them in chairs..i take high dose vitamin d and calcium..it does help with numbness but doesnt return the strength,,

@woodywoodlstein9519

7 жыл бұрын

angelusa73 all nonsense A waste of time and money. And a good example of how easily quackery spreads these days

PLEASE CUT THE GARBAGE,,,,THE IS NO CURE,,MORE BOLONY