Thank you for your efforts in spreading the invaluable word!

Thank you so much, Mark! It was very hard for me to make this video because I don't like talking negativitly about my country but I felt that it was important to let others know how things work over there with these things. I was worried about the reaction I was going to get but everyone seems to be ok with it and I am glad! Thank you for the support. It means a lot to me :) I feel that we are all doing a great job and that things are moving along...Thank you Mark for what you do too! Hugs

Let's hope it will be a matter of time I do belive too that time is the best tool we have while we share, write, be vocal and hope for the best! Thank you so much for being active and for helping! Hugs, Angela

Dear Isabella, once again, you wrote such beautiful words to me and I thank you from the bottom of my heart for being so supportive and so kind to me! I am back from Baltimore where everything went well and where I had the greatest time talking and laughing with the other patients that take Tysabri like me. MS people are wonderful, strong, inspiring and truly special and I am proud of being associated with them! :) You are one of those special people... Merci, je t'embrasse, bises Angela

Thank YOU for coming and for listening to my words. I appreciate it very much! Have a good rest of the day, take care Angela

Angela. Just a wonderful video. A grassroots campaign to get people involved and informed. I could not be more proud of you. CIao Mark

I feel that you did a great job at explaining this to me, dear Daniel! Thank you for doing it because it cleared many things out and you were able to explaing using simple terms that everyone can understand. Thanks! Hugs, Angela

Dear Andrea, I can tell you that there is a lot more freedom of the press in America than there is in Italy given that so many of the media outlets have such close ties to the goverment. Having lived there I have first hand experience and every time I go home, I see it and feel it all over again. Italians are looking to the Usa for information! You are absolutely right when you say that we can do a lot and that we WILL do it because we believe in this with all of our hearts! Thanks! :)

Hi Harmomy It's hard to believe, but I am still awake...it's 2 o'clock in the morning over here and I am still awake! You are funny with the food comment!!!Well, I have many more things to be proud of my country and, if it is going to act properly soon, I will be proud of this too! I am glad that you will meet up with the MS society where you live and that you will talk about this to them. It's good to ask questions and to learn more. Knowledge is power, right? Have a good day! Hugs Angela

Hi Angela, I think everything like this takes time, so don't give up hope. I haven't heard of anthing with the local MS Society down here on this theory, but I am meeting up with them this weekend, so I will be asking lots of questions then. Thank you for sharing it with us, and you should still be very proud of your country :o) (For the food if nothing else!) Harmony

Caro Primoz, it's good to find you here today and to read your comment. I guess you know what I have been talking about really well because you are right there and you see it too every day! We are pushing, writing, calling, sharing...and we are working hard because we want to make sure that we can go on with the studies and find a better treatment for MS! Thank you for the support, caro Primoz. Have a good day and say hi to Slovenia for me! Baci, Angela

Angela I imagine you are overwhelmed. You have to add me on KZread in order to write to you. I had to come back the original video. The support works strangely. I doubt the National MS Society study. There is much corruption there. I am happy that Italy did the right thing in supporting Dr. Zamboni. Thank you for writing and take good care Eileen

Dear Sandy, yes, it is quite frustrating to see how the country that should be extremely proud of having such a hopeful and hard working doctor on his land, is not giving him the support he needs to continue his work. Hopefully, this will change with time and I hope that the medical community will be more willing to support him soon! Thanks for writing and for supporting me :) Warm hugs, Angela

@watzgoodinthe711 Thank you! I hope that every MS patient will be able to get the Liberation some time soon!

Dear Isabella, yes, there is a lot of MS research going on in many countries and I do feel that we are getting much closer to a possible cure each and every day... We just can't give up believing that this is possible and we can't stop dreaming about this! Je t'embrasse, bises Angela

I am happy you made the video. Do not think that in the United States is perfect. Dr. Zamboni is having a hard time too here and in Canada and the United States. The egos are getting in the way. Here is the Pharma Industry which has pressure but I think that economical crisis is going to decide this situation. Thank you.

Thank you so much for your comment and your support! If these doctors would have an open mind, who knows what they would find if they would look right in front of their eyes? Maybe, something as simple as opening a blood vessel or tilting a bed, could help so many people if they would just be willing to listen and to try something outside the norm! Thank you so much for telling me this and for sharing your views on things. I agree with you a lot! Have a good evening, ciao! Angela

Hi there! Thanks so much for your videos. I'm excited about the possibilities for CCSVI. Since there is no MS Society where I live, I am thinking about what my role might be here. I know they do stem cell treatment here in China because there is less regulation. Maybe more can be done with Zamboni's research here.

Hi Isabella I know exactly what you mean Thank you for this Video Trevor

I would so love it if they could study his research there too! I dream about this sooooo much because I hope that we can be helped without having to live a whole life taking drugs... If there is any way that you can let others about this in China too, it would be great! Thank you so much for wanting to help! :) Warm hugs, Angela

Hi Angela, I think these things work the same way all over the world. You did a good thing by promoting Dr. Zamboni. Us MS'ers are a strong community and we will not let this die out. Just look at all the new videos about it and yes I posted mine and some others on my facebook page. We have to network with each other and use any medium we can. I have sent the info to my local news channels as well the paper. It will take time, but we will see some movement I am sure! Andrea

Dear friend, well, finally someone will believe me now!! I have said this because I know my country and I would have never explained how things are in Italy if I wouldn't have known the true so, unfortunately, this is what happens. It is not the first time and it won't be the last one... I am glad that you called the segretary and you got to hear my words on someone else's mouth. Hopefully, with our help, things will get moving. I have about 150 messages to send today. Thank you for helping!

@ecurra19 Hi! So many things happened since I made this video and I am so proud of my country for finally giving support to one of our great minds! Dr. Zamboni didn't have to go anywhere and many Italian regions are giving him full support and they are going to be a part of the national CCSVI study! The regions of Piemonte, Veneto, Emilia Romagna are with him!! I am very happy to say that Italy did the right thing: it's supporting Dr. Zamboni! Thank you for writing and take good care Angela

@giac135 You are ABSOLUTELY RIGHT, dear friend. Why giving us a cure when there is money to be made trough the sale of drugs??? Well, this is going to change SOON because we are aware of Dr. Zamboni's discovery and nothing can be done to hide it now! We have the power to make things change and the patients are going to be the speakers of this new, incredible discovery! If the media will not cover this, we will! Thanks for the comment and let's dream and hope together! :) Hugs, Angela

Dear Daniel, the center is in Buffalo close to you and I had already filled out the application for the clinical but I haven't received an answer yet. I will have to wait a while I guess before I can find out if they will accept me for it. I am willing to come all the way there (it's a 7 hour drive) to be checked and accepted for this.

Thanks Trevor. You know how it is because you live in Europe, right? And because you heard about Italy and the way things work there! Thanks for the comment and for keeping in touch. Are you ready to get another hug??!! :) Angela PS: My name is Angela :)

Caro nuovo amico, purtroppo, non sappiamo ancora se questo nuovo metodo di trattare la sclerosi potra`aiutare tutti noi, anche quelli con la malattia progressiva. Purtroppo abbiamo ancora bisogno di fare studi per scoprirne di piu`ed e`per questo motivo che e`di vitale importanza parlare della scoperta del Dr. Zamboni e fare in modo che la comunita`medica si muova ad accettare la cosa Speriamo che un giorno non troppo lontano si potranno aiutare anche coloro che hanno la SM progressiva. Ciao

@ecurra19 Dear Eileen, I am sorry!!! I accepted the friendship invite as soon as I saw your message so now we can write to each other and share information! I doubt the MS society study too and most patients feel the same as we do! The studies are all trying to prove the same point and they are not treating or helping anyone!!! Thank you so much for being patient with me! :) Now we are all set to send each other messages! Have a nice day and take care, Hugs, Angela

sorry Angela!! please forgive me :) and Thanks for the Hug X yes we are a suspicious lot in Europe take care now Trevor