Living with Multiple Sclerosis - CCSVI.mpg

[AWDESIGNS8]

hey girl how are you doing today 2011 and have you heard montel williams had ccsvi done what do you think /love ya apil

[laurenvparrott]

@AWDESIGNS8 Hey! I'm doing great! I hope you are too! NO! I haven't heard that!! I'll have to do some research! Have a great weekend :)

[anx1300c]

You're the prettiest girl on youtube. Stay strong!

[laurenvparrott]

@anx1300c Oh my gosh, you are so sweet!! Thank you for saying that!!

[SCUBONZIES]

YOU LOOK SUPER PRETTY

[laurenvparrott]

@SCUBONZIES Oh my gosh, thank you so much!!

[AWDESIGNS8]

HOW LAUREEN ARE YOU THINKING OF HAVING THIS DONE I JUST WANT TO SEE IF I HAVE BLOCKAGE I THINK THAT WOULD BE ONE TEST THEY SHOULD GIVE FOR PEOPLE WHO HAVE MS .LOVE APRIL

[laurenvparrott]

@AWDESIGNS8 Hi April! I'm not having this procedure done any time soon, but it has worked for people! Good luck getting tested!

[AWDESIGNS8]

@laurenvparrott no laureen i'm not getting tested. but i do feel ms people should all get tested and if there is a blockage then people should get it done if it does help. but if you dont have insurance then you cant get it done, that is wrong to give hope and then take it away. what do you think. thats like taking away my avonex if its working then say no more for you its crazy to me.what do you think about it.

[laurenvparrott]

@AWDESIGNS8 Oh I know, I also feel all people with MS should get tested, and it's sad that you need insurance.

[AWDESIGNS8]

@laurenvparrott GEE LAUREN THATS FOR THINKING LIKE I DO I LOOK UP CCSVI ON U-TUBE AND THE PEOPLE WHO GOT IT GOT RID OF THERE SYMPTOMS THATS ALL MS PEOPLE WOULD LOVE . AND I'M HAPPY FOR THEM AND I KNOW GOD WAS WITH THEM TOO. IN ORDER TO DO RESEARCH WE HAVE TO DO IT ON PEOPLE NOT MICE SO I REALLY FEEL DR Z BETTER STEP UP AND TEST PEOPLE WITH MS AND IF THEY HAVE THE BLOCKAGE THEN DO IT FOR THEM. EVEN IF THERE IS NO INSURANCE OR MONEY. MS SOCIETY SHOULD DO THIS TOO.

[laurenvparrott]

@AWDESIGNS8 I agree!

[AWDESIGNS8]

the only thing i can say at least we got back up .

[laurenvparrott]

@AWDESIGNS8 You are so right!

[shockwaveization]

I just finished watching your previous videos and all i can say is Wonderful! how wonderfully amazing it is to see you doing so well. you are an inspiration to more than you know. never give up and always be willing to believe and maintain hope and you will become a well from which many may gain strength. i hope you are doing well and the happiness that you display so strongly here is still yours. god bless.

[laurenvparrott]

@shockwaveization Thank you so much!! My faith is what keeps me going! I really appreciate your comment and I wish you the best! God Bless!

[AWDESIGNS8]

ccsvi is good for people but in my life i'm just taking what i can and do what i can for my ms. put to keep posting it its ok stem cell works to but to much money i'm glad you are putting ccsvi up aand talking about it. but that would be like me talking about avonex because i'm using it , ms is a hard one to figure out every one is different in there ms. love april

[laurenvparrott]

@AWDESIGNS8 I agree with you - I'm going to stay on medication for now until more research had been done.

[AWDESIGNS8]

i'm staying with the avonex untill that doesnt work or there is a cure. nothing eles is can do with ms. every one is different i dont get alot of stuff yet and maybe never will we just got to go with it. i just hope they wil find a cure for this and other illness if this work for you good but it cost money and some people dont have insurance so too keep talking about it doent make sence to me

[AWDESIGNS8]

the only thing i know with the ccsvi its not in the usa and i have no insurance i called for the stem cell and thats 30.000 so thats out i just have to go with avonex and eat better and do things so i'm not stressing which i dont know more. its graet all the opitions we have for ms now i'm not even going to take the pill

[AWDESIGNS8]

laureen where do you live

[AWDESIGNS8]

this is a break through but it cost money and not in the usa just like stem cell . i'm all for hope i will always have hope but when you have no insurance and call to get help its alot of money and then you have to go to another countrys for this stell cell not in the usa 30.000 that is crazy hope that is what we want . i feel in my life time there will be a cure . keep up the good work.

[laurenvparrott]

@AWDESIGNS8 I agree with you...everything is SO expensive! I'm also hoping for a cure! I wish you the best!

[AWDESIGNS8]

@laurenvparrott i have a funny feeling there will be a cure in my life time and they have a pill out now for ms so that is a break through you had it now for 8 years has your stop since your on your therpy for ms. when you go get your mri how are you doing. love ya april

[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!

[laurenvparrott]

@rebecawatson57 Thank you so much for this information! I wish you the very best!

[AWDESIGNS8]

@rebecawatson57 i have no insurance can they do this for me if needed

[dashu666]

You are cute :).

[laurenvparrott]

@dashu666 Aww, thank you!

[guitarobsessed85]

@laurenvparrott The best part about you being very attractive is that you thank everyone who tells you which shows you aren't full of yourself. Most people start to ignore those comments because they come to expect them but it seems you truly appreciate being blessed in this aspect. I think you're one of the few attractive people who deserve to be so.

[laurenvparrott]

@guitarobsessed85 Oh my gosh, thank you for saying that! I do truly appreciate any type of compliment, and I try to give them in return! I do feel extremely blessed and try to stay as positive as possible!

[guitarobsessed85]

I have a few questions. First: Could extreme light sensitivity/vision issues (no blurriness or loss of vision and no loss of color) that lasts a few hours but never more be Optic Neuritis? I have been having this issue a few times a year for about two years.

I also have the feeling of warm water running down my legs on occasion. Could this be a sign of MS?

My grandmother and great grandmother both had MS. After they were unable to walk for 5 years they spontaneously lost all MS signs/symptoms

[laurenvparrott]

@guitarobsessed85 Oh gosh, personally I've never had those symptoms, but I would defintiely mention that to your doctor. I wish I could be more helpful, but I'm not a doctor so I don't want to tell you the wrong thing. I wish you the very best!

[guitarobsessed85]

@laurenvparrott I injured the back of my spine doing heavy squats and was rushed to the hospital because I passed out and kept throwing up right before my vision issues started. I had brain scans which were all fine but they never had my spine checked. I would get checked out but I have no health insurance as I am the epitome of starving artist. Could you tell me your first symptoms, even before they were extremely noticeable?

[laurenvparrott]

@guitarobsessed85 My first symptoms were drop foot and fatigue. I wrote you a message - I really hope you can find someone to test you! I wish you the best!

[guitarobsessed85]

@laurenvparrott I am not really looking for you to give me a diagnosis haha. I'm just wondering if these even sound like MS symptoms at all. I am just worried about hot feelings in my legs. They don't get worse with intense exercise or with being in a hot shower or sauna. It happens at random and is very transient. It only lasts a few seconds at a time but I'm worried about it.

[laurenvparrott]

@guitarobsessed85 I would definitely mention that to your doctor!

[catimini34]

I think the same ! I'm no in the hurry to do the liberation procedure to me, especially because I'm lucky to have a MS not so bad still I'm under Copaxone.

I don't believe there is only one solution against the MS ... it's much complicated to fight against this strange disease.

I think some people want to make money ... I'll do the procedure when it'll be available in my country !

Do you still get Tysabri ?

[laurenvparrott]

@catimini34 I agree! And yes, I'm still taking Tysabri and I feel great!

[catimini34]

Hi ! What do you think now about the Zamboni method ?

In France my neurologist is not for it .. he told me it's a joke :(

I wonder if he really looked all the videos on the web about the "liberation" !

Maybe it's difficult for him to accept that other doctors might have found one of the causes of the MS ! because no more need him ! :(

[laurenvparrott]

@catimini34 Hello! I still believe that The Liberation Procedure has a lot of potential in helping patients with MS. I'm the type of person that likes to wait until there is data suggesting that it is 100% effective before I try getting the procedure done. I'm still really excited about it, but I want to wait until more research has been done. I hope you are doing well!!

[worktosser]

Your looking good Lauren. I can see the improvement Ty has made for you. You said it yourself, "Let's just wait and see". I have been following this research myself, not to the extent you have :) but it does offer promise. I hope someday that MS goes the way of polio.. meaning.. no more. So many of my 'brothers and sisters' have it worse than myself but it only takes one bad day to hate it. :) I am a bit of a skeptic but just the thought of a tangible cure.. (fingers crossed)

[laurenvparrott]

@worktosser Thank you so much! I feel the same way about improving other diseases and getting cures!!

[tocamelaconga]

What is the deal with MS targeting the best looking people. Talk about shallow. lol

[laurenvparrott]

@tocamelaconga Awww, that is so sweet of you to say!!

[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

[laurenvparrott]

@derekdadey1 Thanks for the information!

[ThePennygirl]

Some compassion from doctors when all else fails for other treatment would be nice! ( you sound like a biogen salesman)

OH so do you intend to take Tysabri for for the rest of your life ? You have to many mirrors try seeing others!

[laurenvparrott]

@ThePennygirl I agree with you! I'm going to continue taking Tysabri for now at least! As long as it is working, I'll continue!!

[ThePennygirl]

I know how Tysabri has helped you so much Lauren! But it failed me as all other CRAB drugs! Am please for so many others also! But at what price? It nearly killed me!

Will you ever post more stuff regarding CCSVI ? for folks like me that are no longer cash cows! to big pharma? I need help! and yesterday kicked to the curb! NOT because of lack of Inus. but because I WANT CCSVI I have no other JUNK medicines to wheelchair me along. Please share any ideas.

Glad your well

[laurenvparrott]

@ThePennygirl Oh my gosh I'm so sorry. I really don't know as much about CCSVI as other YouTubers. I would watch videos by irishbear76 and angelusa73. I wish you the best!!

[MrLeooreo]

it comes to CCSVI, the interests of the neurologists and the societies are best served by having CCSVI marginalized, by not funding any CCSVI treatment research, and by lobbying the government to not allow any treatment of impaired venous drainage in persons with MS despite the obvious health hazard such a condition represents. The reasons for such actions are straightforward.

[sigoak71]

I wrote to you a couple of months ago and have since become a father. My major worry was once I became a father was how I would be an embarrassment to my daughter. This procedure, if nothing else, has given me a glimmer of hope. YOU were a ray of hope for me in my darkest days and I pray my daughter is as emotionally strong as you. THANK YOU AND GOD BLESS!!!

[laurenvparrott]

@sigoak71 Congratulations!! I'm sure you will be a wonderful father, and if your daughter is anything like you, she will be proud of you no matter what! I also think CCSVI is very promising and I wish you the very best with everything! God Bless You!

[kkkkkkatherine]

Yes, GOD bless the Italians!!!

Laurenvparrott COULD you be any more joyful?? LOL!!! Liberation treatment IS AN ANSWER to MANY ppl's Prayers!!!!

All glory be to GOD!!!  Thanks for video documenting your genuine response!!

[laurenvparrott]

@kkkkkkatherine Thank you so much for writing! I love your comment! God Bless Italians!! :) I hope you are doing well!

[terepooh22]

Glad your full of happiness. I am too. Will be treated this fall. Oh and this has been covered up for over 100 years. They suspected this a long time ago but did the studies wrong. Yes, neuros have been suckered punched rightly so. They would rather see us die than try something new like LDN or CCSVI treatment. Funny how other countries even third world are less corrupt than the USA by offering treatment. I had 22 doeses of TY prioe to my last 1.5 years on LDN which is far superior for me to TY.

[laurenvparrott]

@terepooh22 I'm glad you're full of happiness! I know, everything is so controversial in the US!

[glykoseme]

Thank you and God Bless you Lauren for posting this exciting news!!....God Bless all with MS....hopefully MS will soon bew a thing of the past.....:)

[laurenvparrott]

@glykoseme Thank you so much for your comment! God Bless you too!

[ajrussell94]

MS is an auto immne disease whch causes ur own body to attck tself Th reason y ppl in Canada spcfclly Saskatchwn hve mor cases is cause its linkd to Vitamin D deficiency U naturaly get vitamin D from th sun CCSVI is found in 56.4% of ppl wth ms but also 22.4% of ppl wthout Ths could just b concdence Th reason y th government dsnt use its cause 4 all they knw it could alleviate symptoms temporarily but jst mke it wrse A cure is accptd by association, cause, benefts outweigh & rsk is it a effectve

[laurenvparrott]

@ajrussell94 Thanks for your comment

[Zzozze]

@laurenvparrott : ajrussell94 is a MS-business troll pasting the same comment on all CCSVI-related vids.

[laurenvparrott]

@Zzozze :)

[Zzozze]

@ajrussell94 The cause has been shown to be a genetic narrowing of jugular veins, the overpressure leading to a blood-brain barrier breakdown...

But...

"Biogen Idec derives most of its income from sales of multiple sclerosis treatment Avonex", and 100% for Serono. You see where the problem is :(

It's not won yet :((

[AWDESIGNS8]

@Zzozze im on avonex no side effect yet i'm just gratefull there is somethings out there for us i know people who tryed the shots and just didnt work so now on nothing and doing great 15 to 20 years . they just watch what they eat get exersize and god is in there life. we just have to have hope your mind can do wonders can heal you. ann boroch did heal her self and god she had ms check her out on u-tube. just seeing her gives me hope love april

[Zzozze]

@AWDESIGNS8 Yep, the efficiency of the shots is very random...

Exercizing is good as long one takes care not to increase the blood pressure and not to overheat. The "sitting-sleeping" (keeping the head higher than the body) is reported to help as well.

A good optimistic mood improves everyday's life but sadly doesn't prevent bad relapses. My opinion remains ASAP the operation that work, even if it annoys neurologists and Big-Pharma.

[Zzozze]

@ajrussell94 "MS is an auto immne disease " It isn't.

Just copying and pasting the pharma-propaganda doesn't make it become true!

[Zzozze]

@kodiak1966 I just wonder who the hell did flag your post as spam :((

Ernesto Bertarelli?

Mister Merck?

[watzgoodinthe711]

Low Dose Naltrexone and 4AP is good for Multiple sclerosis

[laurenvparrott]

@watzgoodinthe711 I have heard that, are you taking them?

[watzgoodinthe711]

@laurenvparrott yes after one year i had no more lesions on the mri and no progression.. it helps a little with the symptoms but i'm doing much better.... LDN is very cheap also its costs me $15 a month at a compounding pharmacy and the 4AP is like $40.. those are the two top medications for MS in my opinion

[laurenvparrott]

@watzgoodinthe711 I'm so glad it's working for you!

[mmariissa]

my step dad has MS,

we're desperately trying to get him his surgery because he's relapsing right now.

I hope we can get it done soon, because it's hard to see him struggle.

This breakthrough is a huge huge source of hope and joy, for sure.

[laurenvparrott]

@mmariissa This truly is a huge source of hope and joy! I really wish the very best for your step Dad and your family. Please keep in touch!

[whitejellyfungus]

you're hot.

I was diagnosed 2 years ago and progressively got worse. I was on Copaxone but no longer due to poor insurance coverage. So... I have been taking high potency Vitamin D and drinking lots of filtered water and just about a month ago I started feeling remarkably better, consistently.

Coincidence? Maybe,

[laurenvparrott]

@whitejellyfungus That's wonderful!! I'm so glad you're feeling well!

[laurenvparrott]

@whitejellyfungus That's wonderful!! I'm so glad you're feeling well!

[AWDESIGNS8]

@whitejellyfungus check out ann boroch on u-tube see she healed her self of ms i swear its what we eat. and take vitamins there good for you god is with you and you can out live ms. love april

[drewfuss2121]

I'm pretty sure that all of the lesions on the spinal cord caused by MS cause a million different things to go on in an MSer patient. I wasn't able to bend my right knee for a few months, and my neurologist told me that intravaneous steroids (home-health) and baclofen help the spinal cord inflammation. She said things on the spine (lesions) cause all different kind of problems to be caused. I'm going to see my neuro on 3/24/10 and talk more about what's going on with my disease. Best wishes!

[laurenvparrott]

@drewfuss2121 I wish you the very best!

[AWDESIGNS8]

@drewfuss2121 hi i have a bulging disc my back hurts often i too have ms there was 2 spots in my spine the doctor said ms doesnt cause all and even if you have ms you can still have back pain god is with you love april

[npiltan]

Thank you, i will inform you after the surgery, by the way now i have so much walking difficulty.

[laurenvparrott]

@npiltan I wish you the best!

[npiltan]

this is it. i'm going to do it very soon.

[laurenvparrott]

@npiltan That's great! Good luck and keep me posted!

[M4RYM00]

I got the great news about CCSVI a few days ago! i'm like you; I cant stop smiling! It makes sence.Its only a matter of time now..... Good luck

[laurenvparrott]

That's wonderful! Good luck to you too!

[cityonfire31811]

so you know about it! dats great! shoulda checked ya homepage first! lmao

[williamr5101]

This all making sense.I use to be a boxer and been hit pretty hard. My problems started after boxing

[laurenvparrott]

Wow - you're obviously a strong person. I'm sure you can handle anything. I wish you the best!

[danielek1871]

It's very good. Thank you

[laurenvparrott]

Thanks for writing!

[dapanyal]

I wish youtube would let me type in URLs because I wanted to say that it looks like it's all true, I wanted to link to the newsletter which pretty much says that the Buffalo study results will be positive..

Search for 'ccsvi facebook' , follow the 1st link and the announcement about the newsletter..

[laurenvparrott]

Thank you for letting me know!

[boorashid12]

Thank you very much lauren i need more information about this doctor and i will travel to him please can you give his contact in other video Again thanks alot

[laurenvparrott]

Hello! I don't actually have any contact information, but if I get some I will make a video and let you know!

[violetmatthers]

Lauren, ME TOO! Thrilled! in the Morning Im seeing my Neurologist here at USC the cutting edge research Hospital here in Ca. This is amazing. And you know, most cures are discovered by accident. and I really want so badly to be excited but I do have a part of me that is skeptical, because I can't believe this! Violet

[laurenvparrott]

Hi Violet!! Please let me know how your appointment goes! Good luck! I'm hoping for the best for all of us!!

[notapplicable66]

When we have MS, our blood brain barrier looks like Swiss cheese, full of holes. Which allows killer T-cells to invade into our brain. T-cells are not suppose to be there. We also have too much iron in our brains. That is because of clogged, thinned, or twisted arteries and veins. T-cells know this iron should not be there. I always believed that our T-cells were not attacking our brain and spinal cords for NO REASON!!!! They were seeing something!!! Namely to much IRON!

[laurenvparrott]

Thank you for this information!

[millie161]

hi lauren is that why my husband is getting so much pain in is head x

[laurenvparrott]

It could be - I would talk to his neurologist :)

[millie161]

hi lauren iv been told that thay as been a cure found for ms is this true x

[laurenvparrott]

Maybe - I would watch Mark's videos (irishbear76) and he explains this theory. It could possibly be a cure!

[haz740]

hey lauren I have seen so many of ur videos thanks alot for posting this video about ccsvi, im due for starting tysabri next week but this new research has made me so happy and got me thinking wether to put my self through tysabri or to go and get neck ultra sound done and this is so big this could be it; I was so scared of tysabri but there can be somthing else without side effects. I havent been able to sleep properly not that I could before anyway , this can change us Msers lifes. Thanks alot

[laurenvparrott]

Thanks for writing! This whole thing is so new and I'm choosing to stay on Tysabri because I feel so great - but we'll see what happens with this!

[mohammedaljobeh]

wow ! that's tremendous !! I always believed it has something to do with my nick ! its all becoming clear now. thank you

[laurenvparrott]

Isn't this exciting!

[Alexknobsob]

This is totally consistent with my personal experience of the disease.

[laurenvparrott]

Doesn't it make sense? It's consistent with my experience too!

[Alexknobsob]

You are at your most beautiful here, radiant in fact.

[laurenvparrott]

My goodness, thank you so much!

[notapplicable66]

Our BBB is thin and full of holes like swiss cheese. The killer T-cells have done this because they are going after all that Iron that is in our brains that shouldn't be there. Get rid of that excess iron by resorting blood flow in clogged arteries or veins and strengthen the BBS so killer T-cells are no longer penetrating it and MS will stop.

[laurenvparrott]

That makes sense to me!

[gekiryudojo]

IN OUR 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 :)

[laurenvparrott]

Wow - amazing! Thank you so much for writing to me! I can't wait to hear more!!!

[gekiryudojo]

I may do another video tonight ! but I do feel very happy even with a dodgy Jugular!

the Ultrasound was so cool as well!

[laurenvparrott]

That's great!

[gekiryudojo]

the sonographer was very good I sent her Doctor zamboni's Protocol last week and even though she had to abide by the Hospital Protocol she had read it and she even had news clippings of Doctor Zamboni and she also did a trail on the ultra-scan so good on her!

This is more evidence as far as Im concerned

[laurenvparrott]

That is awesome!!

[gekiryudojo]

Hi laurenvparrott

sweet Video I understand your excitement!

I will be going for a Doppler ultrasound Scan

tomorrow at 11am (08/12 /2009) I will post the results asap

Trev (gekiryudojo)

[laurenvparrott]

I can't wait to see your results!! Good luck!

[irishbear76]

I COULDN'T HAVE SAID IT BETTER MYSELF!

Great video.

Great smile.

I know what you mean when you talk of these 'tears of joy"

God bless,

Mark

[laurenvparrott]

Thank you so much Mark! That means a lot coming from you! God Bless!

[NikiBoBicki]

oh and sorry I commented before watching the next video :)

[laurenvparrott]

No problem! I'm very optimistic, but I'll wait until I know it works for sure.

[NikiBoBicki]

I have reviewed a lot of the research and spoken to my docs too. Seems like they are optimistic as well! Including my neurologist. So. Not every neuro will shut the idea down. And I know that here in Canada the MS society is gonna be funding research into this area. So. There must be something promising.

Scares me to get my hopes up though. You know? But hey, even if it just turns out to be a really great treatment, that is still good!

[NikiBoBicki]

all that being said...being optimistic is great. I really hope this guy is onto something. Even if it is just a treatment. Lets hope that once his results have be replicated we can know more about what this really means for us.

[NikiBoBicki]

It is exciting for there to be a new development in MS research....but I have a number of friends and family members who are doctors. They are none to impressed.While this Dr. might be on to something, he has not be through a peer review process so I personally think it was irresponsible of him to release the results as a "cure".

All I can say is that I am cautiously optimistic. Be careful, don't give up on your current treatments, and don't do anything until this is PROVEN. God bless!

[laurenvparrott]

That's what I talk about in my next video...I want to remain an Tysabri until results are proven. Thanks for the input :)

[medad1]

Thanks Lauren for these valuable information and I really hope this could be the way to cure of this disease

Mody :)

[laurenvparrott]

Hi Mody! Thank you! I hope so too!

[angelusa73]

Cara Lauren,

I am so glad that you are talking about CCSVI! I know what you mean when you say that you are not able to sleep!

I stay up until 2-4 o'clock in the morning writing to everyone and I love doing it because it gives me hope and it helps me see how things are really moving in many part of the world like Holland, Israel and Canada! (in Italy a little less).

I have been posting the latest news on my page in different languages and I hope it helps.

It's so wonderful to see you happy!

[laurenvparrott]

Ciao Angela! I think it is so great that you are posting the latest news on CCSVI in other languages! That is so awesome!

I'm so happy you're doing well!!

Baci!!

Lauren :)

[angelusa73]

You are so sweet and I am so happy that we are friends!

We will have to continue with the Italian lessons!!!!

Buona Domenica! (have a good Sunday!),

a presto,

ciao

Angela

[laurenvparrott]

Ciao! I love the Italian lessons!! Buona Domenica!

Baci!

Lauren

[laurenvparrott]

Ciao Angela! I think it is so great that you are posting the latest news on CCSVI in other languages! That is so awesome!

I'm so happy you're doing well!!

Baci!!

Lauren :)

[deanaugust]

Hi Lauren.

Great Video.

I am an investor in Elan, and that is how I originally found you on You Tube.

A cardiovascular cure for MS would be detrimental to Tysabri and Elan, I am sure about that.

But a cure would be most important thng.

Everything I read and see on Youtube about CCSVI sounds very interesting.

I just posted info about CCSVI on Yahoo message board, under ELN, so I can read any replies.

Best of Luck to you,

Dean

[dmplaura]

@deanaugust Right. Our crappy neurological disease is, unfortunately, very profitable.

CCSVI is a great finding and hope for us.

Thanks for the vid Lauren! :) xoxo!

[laurenvparrott]

Thanks Laura!!

[laurenvparrott]

Hi Dean - thank you for your message. I will look at your post under the Yahoo Message Board.

[trosper]

they shut him down in italy. hes not aloud to do the procedure anymore. italy kinda sucks a lil

[laurenvparrott]

What a bummer!

[trojantjl]

GET ME OUT OUT OF THIS AWFUL GROUP

[eddysacat]

Hi Lauren,

I first heard about CCSVI two weeks ago and I was so excited that I couldn't even sleep. I found out on a Friday night and had to wait until Monday to call my neurologist. Well, I called him and he tried to make me feel like an idiot. He knew nothing about CCSVI but he said that it was "snake oil". The entire MS establishment is against this. Hopefully, if CCSVI is what it appears to be it will be available within 10 years. Hopefully we all have 10 years to wait....

[laurenvparrott]

I hope so too! I know lots of people are not in agreement with Dr. Zamboni but I'm absolutely hoping for the best!

[MSVlogSupport]

Great Video Lauren! I I agree that we need to be cautiously optimistic. We still have a long ways to ago.

But the news is exciting and it may lead in new ways of thinking about MS and the cause.

Thanks,

Andrea

[laurenvparrott]

Thank you Andrea!!

[vbeachy]

Great video Lauren! YES...it ALL makes sense! Thanks for your great video Lauren!

[laurenvparrott]

Thanks Vern!!