New hope for treating multiple sclerosis

[boxerpup7]

your liars. you only give treatment to maggots. because they are allowed to steal cheat and lie, and poison people without their knowing it and then hurt the credibility to get their own way, polical can anyuone say conflict of interest? can anyone say ny?

[muhammadzahmad]

people have different stage of this disease...there maybe one treatment.. but should avoid different things for their different lifestyles...

[onehundredvoices100]

DR PAOLO ZAMBONI IN FERRARA ITALY TREATED HIS MS PATIENTS, FOR BLOCKED VEINS IN THE NECK & OR CHEST. THE MAJORITY OF THESE MS PATIENTS, SOME WITHIN HOURS, STARTED WALKING AGAIN. AS FOR FOLLOW UP STUDIES TO ZAMBONI'S TREATMENT (STENT TO OPEN VEINS THAT DRAIN THE BRAIN) WHY NOT ASK ZAMBONII'S FORMER MS PATIENTS, IF HIS TREATMENT WORKS. -------- DRINKING SODA POP WITH ARTIFICIAL SWEETENERS, CAN MIMIC, MS SYMPTOMS. LACK OF IODINE AND VITAMIN D, MAY CONTRIBUTE OR CAUSE, OTHER MS SYMPTOMS.

[xzaxx]

people there is cure for ALS. it has been cure for this for the past 11 years. its outside of USA its only offered in costa rica. it is not alowed in USA or other countries.

[bouncethatbouncethat]

In my opinion, I believe that there are different types/variations of all diseases i.e. different- and very specific- causes. Medication is a one-size-fits-all, and it assumes that what you have is the same thing as the next person. If you really want to get something treated, get educated and pin-point the treatments that have helped people who are similar to you i.e. have a similar lifestyle, diet or a similar group/severity of symptoms. You know your body better than anyone.

[HumaraCinema]

The results of Dr. P. Zamboni, the author behind the original study on CCSVI, have been challenged in several studies now, and found to be non-reproducible. All tough this is an interesting different approach at trying to look at the causes for MS, it is not recommended to undergo any treatment involving the usage of CCSVI methodology in the treatment of MS.

Google this for more information:

"Chronic cerebrospinal venous insufficiency and multiple sclerosis: science or science fiction?"

[WiseChoice49783]

Listen! I have tried only "one" treatment that is approved by the FDA, I am here to tell ya, that if there is another way to look at this disease and understand it, I am willing to do that. Unfortunately after only one shot, I went deaf and blind for at least (3) minutes, and I can say that felt a lot longer than (3) minutes. I had every other side effect this drug came with along with that. Deafness and blindness were never before reported. I will try Dr. Z's procedure before any injections.

[jubilee203]

Scientist discovered that All NON-Africans have bet. 1%-4% of Neanderthals DNA while 'pure' Africans(sub-saharan) don't have it. It seems like MS is very rare among 'pure' Africans compared to 60% of African Americans who have caucasian blood. I am just wondering if the Neanderthal DNA might have something to do with it. I guess there is an advantage to being 'pure' humans/homo sapiens/Africans with NO Neanderthal admixture. Question: is MS a Neanderthal disease?

[csny19691]

i agree with "UTELLMEGIRL" most Doctors who are researcing are only looking at numbers for their patients to be on a specific type of treatment so big pharmacy can make their money, no one at this point in time has found the answer for the cure. and yes i will agree stop thinking inside the box...then maybe we can have a solution.

[seekirk]

High Saturated Fat diet -> young age (active thymus) -> exposure to herpesviridea or other neurovirus -> high permeability of BBB caused by poor, brittle structure from high saturated fat diet, low levels of vitamin D -> T cells in CNS -> sensitization of T Cells -> later onset of MS -> recovery -> anything that can cause a proper situation for episodes (stress, Epstein Barr, etc.) -> disability

[jessemac13]

I have MS , smoke weed it helps I should know .

[worktosser]

@jessemac13 For me, weed exacerbates my MS - flattens me. Perhaps your claim that weed helps is more from a psychological one? No matter, it's not 'generically applicable' as a medicine for MS. I used to smoke weed.. I should know. lol.

[ab892681]

As a biology student I've been doing research that would suggest that instead of inhibiting the immune system to treat MS, it is better to support the immune system and feed the body so that it can repair itself. I've heard some convincing testimonies from individuals (including Registered Nurses) who using Shaklee supplements have been able to reverse their MS and live PAIN FREE lives. Ask me for more info if you are interested. My email is ab892681@arbor.edu I hope this is helpful.

[Daniel7681]

Of course, more drugs. That's where the money is. Why don't we do something useful and cure the disease instead of making the main goal reducing the effects of it. The MS Society is a sham. My family is involved with the societies board (not the very top, but high enough), and the MS Society (at minimum Canada) is fighting the CCSVI treatment all the way, and letting on they are all for it in the media. Behind the closed doors there is something very different going on, know that for fact.

[rebecawatson57]

I was diagnosed with MS back in 1983.Recently I came across ccsviclinic.ca. They are screening in Fargo, ND. Called (404)461-9560 and spoke to Nurse Lisa. Their Liberation Package includes pre-op video consultation with their doctors, flight costs, visas, accommodation within their hospital premises. The treatment includes stent, medications, reports & post-op followup for next 6 mths. Email:apply@ccsviclinic.ca. Getting liberated mid-November. Thankful to CCSVI Clinic for making this happen!

[utellmegirl]

LMAO. all about symptoms and new drugs. new expensive drugs. have to keep big pharma going. well i think not. Dr. Zamboi. CCSVI. 100% of all MS patients showed the same blocked or collapsed arteries in the neck and chest.  Come on Drs stop looking in the box. Really let your mind expand.

[datadatado]

I just started work on this ms problem, looking at work by others who came before me, and all roads lead me to the same place..... get this: smell (olfactory) and taste (gustatory)!!!! now what is that about???? it is all about the immune system--- look into the work of these Doctors and see what I found....

[1allavaleria]

i started with copaxone 10 days ago. have some of you any experiese with that medicine?

[jesser271]

@1allavaleria Get the Autoinject, it works great!

Ive taken it for 2 yrs. I thought I was doing well but I had 2 relapses within 6 months. So I will be starting Betaseron soon.

[omexmc80]

CCSVI !!!!!!!!!!!!!!!!!!!!!!!!!

[largefolder1977]

Had a neighbor who went to an Asian stem cell center... and their condition totally REVERSED! It was AMAZING! They got a stateside evaluation thru SCC International. Website was sccinternational(dot)info

[wonenergy]

@largefolder1977 hey ..i am curiuos about the health of your neighbour now?

[tazscott14]

CCSVI and The Liberation Procedure!

[Vivianne766]

The answer is CCSVI .

I'll be tested next week. Thanks to Dr. Zamboni. It was a plumbing problem doc. !!!

[migo53333]

sorry doc, its ccsvi time

[datadatado]

@migo53333

[imsucree]

How has stem cell research worked for anyone?

[EssiacHempLaetrile]

imsucree ...

You Tube & Google "CCSVI"

Google "pubmed" Enter words "Multiple Sclerosis Cannabinoids"

[karena321]

You're a real cutie, Dr. Segal, however,I am not able, neither do I have the time, nor strength to be anybody's guinea piglet. My latest neuro suggested dif meds, but b4 tried, I was given samples, which had me in a dif state, so NO meds. I am currently chelating, & if you R intersted in my progress, altho the worse hasnt been released, it may B interesting 2U.If this doesn't wk, I'll get a script 4 pot,& smoke my probs away until there is a cure, altho, it will never happen; its a $ thing!

[rsamberg]

Stem Cell Therapy is being done in other countries successfully. Unfortunately, as an American doctor, you can't mention that here.

[sweetjaimelee]

I just got information from a Germany center doing stem cell therapy for MS.. Costs a pretty penny, about $10,000 but man. I'd save up to do that. Stem cell is the answer I think :)

[marlene27]

hey I HAVE A FRIEND THAT HAS MS HE HAD IT FOR ABOUT 6 YEARS AND HE WANTS TO START WALKING AGAIN WHERE IS THE STEM CELL LOCATION AT PLEASE HELP THANKY YOU

[rsamberg]

I am leaving on Jan 3 for Costa Rica to get Stem Cell Therapy at the Institute of Cellular Medicine. I have spoken to approximately 5 people who have had success with it (feel much better) although it is not a cure yet. It does cost of pretty penny. The $10,000 you spoke about is cheap. I'm paying $30,000. I'll let you know how it goes. I'll be there for 1 month.

[kfoulk]

how did it go with the stem cells?

[Entropy56]

Yeah?

[Entropy56]

Are you still alive?

[jordandossett]

This was really good. It is nice to know that research is being done by others than just the pharmaceutical companies. I have MS and I know I often get very frustrated at the lack of information out there. It is really rough having a disease no one can see.

~ jordan

(read my blog on ms and philosophy at 6hundred50thousand (.com) and see my art at jordandossett (.com)).