The technique is referred to as a bone marrow harvest and is performed under a general anesthesia. The incidence of patients experiencing rejection is rare due to the donor and recipient being the same individual. This remains the only approved method of the SCT therapy. Log on to ccsviclinic. ca for more information.
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.
Dr. Hemangi of Noble continues: “These are early days and certainly all evidence that the combination of liberation and stem cell therapies working together at this point is anecdotal. However I am not aware of other medical facilities in the world that offer the synthesis of both to MS patients on an approved basis and it is indeed a rare opportunity for MS patients to take advantage of a treatment that is quite possibly unique in the world”. Log on to ccsviclinic. ca for more information.
With regard to MS patients, “We are cautious, but nevertheless excited by what patients are telling us. Suffice to say that the few patients who have had the therapy through us are noticing recovery of neuro deficits beyond what the venous angioplasty alone should account for”. Log on to ccsviclinic. ca for more information.
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.
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.
A universal benefit reported by every patient has been the recovery of bladder control. Most MS patients have various bladder control symptoms that include urinary urgency, incontinence, nocturia, or urinary hesitancy as a result of the disruption of electrical impulses from the brain to the nerves and muscles that are involved in emptying the bladder (pudenal nerve, urethral sphincter, detrusor muscle). Log on to ccsviclinic. ca for more information.
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.
“I feel I am completely cured” says Ms. Gianopoulos, “my symptoms have disappeared and I have a recovery of many functions, notably my balance and my muscle strength is all coming (back). Even after six months, I feel like there are good changes happening almost every day. Before, my biggest fear was that the changes wouldn’t (hold). I don’t even worry about having a relapse anymore”. Log on to ccsviclinic. ca for more information.
After 6 months of offering stem cell therapy in combination with the venous angioplasty liberation procedure, patients of CCSVI Clinic have reported excellent health outcomes. Ms. Kasma Gianopoulos of Athens Greece, who was diagnosed with the Relapsing/Remitting form of MS in 1997 called the combination of treatments a “cure”. Log on to ccsviclinic. ca for more information.
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.
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
I just had my anjio MRI scan for this liberation treatment and took the results to my doctor, i had high hopes for this treatment but my doctor told me that i do not have this irregularity on jugular veins, he also said that i was the 12th ms patient with this result. I am so down right now.
@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,
Saw my family doctor whom I deeply respect last week. Told him about my trip to Poland with my sister for her CCSVI treatment. He was very interested and supportive. He won't however be making any radical efforts to change the status quo.
I don't think that my efforts were wasted though. I think that GP physicians have a certain amount of influence over medical policy. They want their patients to have improved quality of life.
@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! :)
@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!
You have such a sweet voice. I wish I lived in the US so that I could meet you and other youtubers with MS. We could have had a meeting in the summer.
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 YouTube and I love doing it!
It's really a good idea and I am sure it would be a lot of fun!
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!
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! :)
Hi thank you so much for sharing angel you are an angel :) well my girlfriend who I love very much have MS and I'm trying to search for a cure so she can be treated anyway I read about Dr. Zamboni cure many times from now but I need to ask you if there's anyway that you can get me his contact number maybe his office number or clinic so I can contact him or his office/assistant it would be a great help and I also want to know if the vains can be blocked again after time if it was unblocked
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 YouTube 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.
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 :)
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!
i'm still searching for an answer, why ms-medicaments helps, when we suppose that mr. zambonis theory is true. do anyone know an answer? (sorry for my english)
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.
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
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.
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!!! :)
@williamjrb no truer words spoken.nothing will come of this in the u.s.a.big pharma and the medical est. want nothing to do with a cure.they're not in the business of putting themselves out of business.just look at all the natural treatments they use on cancer in other parts of the world that have great success and none of these treatments make it to the u.s.a.they suppress these treatments because of the almighty dollar and these bastards know this.the poor people must open their eyes.
@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!
@angelusa73 you know it,s sad to say that things will never really change.there are many diseases that could be wiped out but big pharma and the medical est. won't allow this to happen.I'm assuming you have ms.,sorry to hear that.the evil behind it all is unreal.Like I said,it's a well known fact that big pharma want nothing to do with any of these natural treatments because theirs no money in it for them and they know this.I done some research on suppressed treatments for cancer and it's unreal
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.
@angelusa73 watched on the news last night in canada that it may take years of more research on this treatment for ms. sufferers.UNREAL big pharma want to keep people on their drugs and nothing else.they want nothing to do with curing people from this disease and these animals know this.
@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!
@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!
@angelusa73 We have to make the buzz all around the world and not give a single cent to the MS-societies anymore untill they acknowledge the
validity of the angioplasty treatment.
Till then the patients just have to tell their cardiologist that, MS or not, they want their narrowed veins to be opened to improve their quality of life.
@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!
@angelusa73 It is important NOT to quit the drugs before the liberation treatment (or to pretend not quiting them) untill their uselessness is officially acknowledged.
@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.
@governslayer We will have to start considering joined lawsuits, and to threaten the mainstream media that 10 millions MS-patients and relatives will sue them if they keep on doing with the cover up.
We need to contact hundreds of MS-ill lawyers around the world!
@Zzozze Hi again,maybe that's what the people need to do.One big lawsuit.A lady here in my community had the treatment done for MS and has had some great results from the treatment.can you imagine if this treatment became mainstream,what a wonderful thing that would be.I truly believe that this treatment for MS will slowly dwindle away and nothing ever to be heard of it again.Now isn't that sad.like I said before,big pharma and the medical est. are way to powerful.Sorry for the late reply.
You are amazing, Angela!! :-) MS Society just posted an article in its research section about CCSVI. This might be a breakthrough treatment for ms =)))
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!
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!
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!).
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,
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.
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.
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.
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! :)
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 :)
I have heavy toxic elements in my body like Lead, Mercury, Nickel, and I used some drugs to get red of them . But they came back again I think it's so difficult to get red of them !!!
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.
i am so new to this but i am certainly looking into it now after your video, thanks
bespokeplayareas 5 months ago
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The technique is referred to as a bone marrow harvest and is performed under a general anesthesia. The incidence of patients experiencing rejection is rare due to the donor and recipient being the same individual. This remains the only approved method of the SCT therapy. Log on to ccsviclinic. ca for more information.
robert80taylor 7 months ago
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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.
robert80taylor 7 months ago
This has been flagged as spam show
Dr. Hemangi of Noble continues: “These are early days and certainly all evidence that the combination of liberation and stem cell therapies working together at this point is anecdotal. However I am not aware of other medical facilities in the world that offer the synthesis of both to MS patients on an approved basis and it is indeed a rare opportunity for MS patients to take advantage of a treatment that is quite possibly unique in the world”. Log on to ccsviclinic. ca for more information.
robert80taylor 7 months ago
This has been flagged as spam show
With regard to MS patients, “We are cautious, but nevertheless excited by what patients are telling us. Suffice to say that the few patients who have had the therapy through us are noticing recovery of neuro deficits beyond what the venous angioplasty alone should account for”. Log on to ccsviclinic. ca for more information.
robert80taylor 7 months ago
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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.
robert80taylor 7 months ago
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.
robert80taylor 7 months ago
This has been flagged as spam show
A universal benefit reported by every patient has been the recovery of bladder control. Most MS patients have various bladder control symptoms that include urinary urgency, incontinence, nocturia, or urinary hesitancy as a result of the disruption of electrical impulses from the brain to the nerves and muscles that are involved in emptying the bladder (pudenal nerve, urethral sphincter, detrusor muscle). Log on to ccsviclinic. ca for more information.
robert80taylor 7 months ago
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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.
robert80taylor 7 months ago
This has been flagged as spam show
“I feel I am completely cured” says Ms. Gianopoulos, “my symptoms have disappeared and I have a recovery of many functions, notably my balance and my muscle strength is all coming (back). Even after six months, I feel like there are good changes happening almost every day. Before, my biggest fear was that the changes wouldn’t (hold). I don’t even worry about having a relapse anymore”. Log on to ccsviclinic. ca for more information.
robert80taylor 7 months ago
This has been flagged as spam show
After 6 months of offering stem cell therapy in combination with the venous angioplasty liberation procedure, patients of CCSVI Clinic have reported excellent health outcomes. Ms. Kasma Gianopoulos of Athens Greece, who was diagnosed with the Relapsing/Remitting form of MS in 1997 called the combination of treatments a “cure”. Log on to ccsviclinic. ca for more information.
robert80taylor 7 months ago
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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.
CCSVIROMANIA 9 months ago
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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
I just had my anjio MRI scan for this liberation treatment and took the results to my doctor, i had high hopes for this treatment but my doctor told me that i do not have this irregularity on jugular veins, he also said that i was the 12th ms patient with this result. I am so down right now.
loktar1234 1 year ago
I am looking for clinics or hospitals in Latin America or the Southeast US that implement the CCSVI cure. Any recommendations?
Shelby350fan 1 year ago
@Shelby350fan My son had the Liberation Treatment done Feb 9th- it is amazing
He is 26 yrs old, 6ft 1in and 205lbs, he was a Police Officer until his MS hit him. He was in perfect health and physical condition.
Yesterday he and his wife Jaimie danced in the sand on a beach in California 24hrs after having this done.
460gman 1 year ago
Dr. I want to get in touch wth him tell how can I?? so plese send me a clue and you are so right
joserafaf 1 year ago
@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
angelusa73 1 year ago
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Saw my family doctor whom I deeply respect last week. Told him about my trip to Poland with my sister for her CCSVI treatment. He was very interested and supportive. He won't however be making any radical efforts to change the status quo.
I don't think that my efforts were wasted though. I think that GP physicians have a certain amount of influence over medical policy. They want their patients to have improved quality of life.
fanwuren 1 year ago
I really hope that this is the cure!!! Not for me, for my aunt and EVERY SINGLE person with MS!
lebanese996 1 year ago
@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! :)
angelusa73 1 year ago
da samo tako nastavote
SuperSasab 1 year ago
I believe it and i'm going for it very soon.
New year with new hopes.
npiltan 1 year ago
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
angelusa73 1 year ago
@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
angelusa73 1 year ago
You have such a sweet voice. I wish I lived in the US so that I could meet you and other youtubers with MS. We could have had a meeting in the summer.
Prissie28 2 years ago 2
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 YouTube and I love doing it!
It's really a good idea and I am sure it would be a lot of fun!
Ciao!
Angela
angelusa73 2 years ago
I'm adding a video response about this subject, if that's ok by you. Thank You. I makes sence when you talk about your blood serculation problems.
Prissie28 2 years ago
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
angelusa73 2 years ago
Really? That's strange. Besides from you, I added it as a response video to MDVlogsSupport and IrishBear76.
So you can only add it to ONE video? That's too bad..
Anyway, thanc for your feedback. I really appreciate it.
Prissie28 2 years ago
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!
angelusa73 2 years ago
Yes, they let you post the video only one time!
angelusa73 2 years ago
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
angelusa73 2 years ago
Hi thank you so much for sharing angel you are an angel :) well my girlfriend who I love very much have MS and I'm trying to search for a cure so she can be treated anyway I read about Dr. Zamboni cure many times from now but I need to ask you if there's anyway that you can get me his contact number maybe his office number or clinic so I can contact him or his office/assistant it would be a great help and I also want to know if the vains can be blocked again after time if it was unblocked
VivaLibano 2 years ago
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 YouTube 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.
angelusa73 2 years ago
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 :)
gekiryudojo 2 years ago
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
angelusa73 2 years ago
i'm still searching for an answer, why ms-medicaments helps, when we suppose that mr. zambonis theory is true. do anyone know an answer? (sorry for my english)
Glysity 2 years ago
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!
angelusa73 2 years ago
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
gekiryudojo 2 years ago 2
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.
williamjrb 2 years ago 8
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!
angelusa73 2 years ago
@williamjrb no truer words spoken.nothing will come of this in the u.s.a.big pharma and the medical est. want nothing to do with a cure.they're not in the business of putting themselves out of business.just look at all the natural treatments they use on cancer in other parts of the world that have great success and none of these treatments make it to the u.s.a.they suppress these treatments because of the almighty dollar and these bastards know this.the poor people must open their eyes.
governslayer 1 year ago
@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!
angelusa73 1 year ago
@angelusa73 you know it,s sad to say that things will never really change.there are many diseases that could be wiped out but big pharma and the medical est. won't allow this to happen.I'm assuming you have ms.,sorry to hear that.the evil behind it all is unreal.Like I said,it's a well known fact that big pharma want nothing to do with any of these natural treatments because theirs no money in it for them and they know this.I done some research on suppressed treatments for cancer and it's unreal
governslayer 1 year ago
@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.
angelusa73 1 year ago
@angelusa73 watched on the news last night in canada that it may take years of more research on this treatment for ms. sufferers.UNREAL big pharma want to keep people on their drugs and nothing else.they want nothing to do with curing people from this disease and these animals know this.
governslayer 1 year ago
@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!
angelusa73 1 year ago
@governslayer "Biogen Idec derives most of its income from sales of multiple sclerosis treatment Avonex", same for Serono... :(
Zzozze 1 year ago
@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!
angelusa73 1 year ago
@angelusa73 We have to make the buzz all around the world and not give a single cent to the MS-societies anymore untill they acknowledge the
validity of the angioplasty treatment.
Till then the patients just have to tell their cardiologist that, MS or not, they want their narrowed veins to be opened to improve their quality of life.
It is simply a patient's choice!
Tell your neurologist only AFTER!
Zzozze 1 year ago
@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
angelusa73 1 year ago
@angelusa73 It is important NOT to quit the drugs before the liberation treatment (or to pretend not quiting them) untill their uselessness is officially acknowledged.
Zzozze 1 year ago
@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!
angelusa73 1 year ago
@governslayer We will have to start considering joined lawsuits, and to threaten the mainstream media that 10 millions MS-patients and relatives will sue them if they keep on doing with the cover up.
We need to contact hundreds of MS-ill lawyers around the world!
Zzozze 1 year ago
@Zzozze Hi again,maybe that's what the people need to do.One big lawsuit.A lady here in my community had the treatment done for MS and has had some great results from the treatment.can you imagine if this treatment became mainstream,what a wonderful thing that would be.I truly believe that this treatment for MS will slowly dwindle away and nothing ever to be heard of it again.Now isn't that sad.like I said before,big pharma and the medical est. are way to powerful.Sorry for the late reply.
governslayer 1 year ago
You are amazing, Angela!! :-) MS Society just posted an article in its research section about CCSVI. This might be a breakthrough treatment for ms =)))
Have a WONDERFUL Thanksgiving!! HUGS!!
WithCourage2008 2 years ago
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
angelusa73 2 years ago
the MS society's around the world would be out of a job! no wonder they are not excited but I am :)
gekiryudojo 2 years ago 2
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!
angelusa73 2 years ago
Comment removed
gekiryudojo 2 years ago
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
gekiryudojo 2 years ago
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
angelusa73 2 years ago
Cara Angela !
Like I said you are good girl and thank you for new news about us MSers
As soon I can will ask my Doctor to hear what she will tell me !
Wish you all the best and take good care my dear friend !
Primoz
HubertV2 2 years ago
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
angelusa73 2 years ago
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.
MSVlogSupport 2 years ago
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
angelusa73 2 years ago
I am in buffalo NY and shall inqure as well thank you for sharing the information.
qualisarx 2 years ago
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
angelusa73 2 years ago
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
tazscott14 2 years ago
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
angelusa73 2 years ago
finally! hope it works!
enough drugs that are poisoning us!
picinela 2 years ago
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
angelusa73 2 years ago
Who is the Doctor Zamboni ?!?
telesette 2 years ago
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
angelusa73 2 years ago
I have heavy toxic elements in my body like Lead, Mercury, Nickel, and I used some drugs to get red of them . But they came back again I think it's so difficult to get red of them !!!
Regards
Mody :)
medad1 2 years ago
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
angelusa73 2 years ago