How many people know that chronic Mercury poisoning cause many disease including Multiple Sclerosis? Do you know Dental Amalgam have 50% Mercury and non-stop leaking Mercury vapor? Do you know Sweden have banned the use of Dental Amalgam in their country already? so please eliminate Mercury from your body is the most important thing to do now.
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
It was so awesome meeting you and feeling your incredible power and sincere love for helping people! I am excited to stay in contact with you and go at this journey together! I am trying to add you on Face Book but cannot find you on there- so call me or email me and we'll will talk and stay in touch! You're nothin but power, and authenticity, and an inspiration to me.
@JoshHewlett Hi Josh!! It's so funny because I totally looked for you on Facebook before I got this comment! I had SOOO much fun talking to you this weekend! I really wanted to make a video tonight but I'm so tired, I think I'll make it tomorrow. We definitely have to keep in touch!! You are so sweet and hilarious! You are an inspiration to me!!
Hi Lauren you look very nice. I'm from Poland now I live in UK, I take Tisabri since January the treatment doesn't help my very much but I have much power, on Friday I take 6th time ,I very enjoy with this treatment. My English is nnot good i hope you help me with this. Thank you Daniel
@danielek1871 Thank you so much! Daniel! So, is the Tysabri slowing the progression of your disease? Do you have any new lesions? I'm so happy that you have much power!
@laurenvparrott hi lauren im dave. my neurologist says i probably have MS. i had 2 MRI done and 2 leisons. i had a relapse 1 year ago and blamed it on my medication. it was balance and not able to walk straight. plus my arms were not right too. in about a week i meet with my neuro for my lumbar results. wish me luck. if i dont have MS i still support you guys and if i do i dont know what to expect. any help is appreciated. i been doing research on MS and found your page. thank you dave
@Drelbaradei Wow! Thank you for writing from Egypt! I think that changing your career is totally fine! You can do whatever is best for your situation!! Good luck and keep in touch!
My name is Craig & i am from Buffalo, NY. I had come across your video by chance when browsng youtube. My grandma has MS and has been steadily on a downward spiral. But over the past little while I have been researching some new and inovative products along with my nutritionist and we have had great success in helping those in wheelchairs/walkers walk again. we use a super potent anti oxidant that mops up free radicals that steal electrons from the myelin causing nerve damage.......
Hi Craig! That is so wonderful that you're helping your grandma. I was extremely close to my grandma and I tried to help her as much as possible as well. Thank you for writing and I wish you all the best!
I love you. You are sooooo amazing. You've inspired me. I don't know if you've yet to respond to my comment on another of your video. The one about your tremors almost being gone. I think you are sooo strong and beautiful and strong.
Lauren, your videos always inspire me. But, I have been having a flare up and need some encouragement. It is frustrating because it is like a nightmare starting all over again. Keep up the good work! Michelle
Hi Michelle! I'm sorry it took so long to get back to you. I'm sorry that you're going through a flare up - hang in there and try to stay positive. I liked to watch funny movies and lay on the couch to relax my muscles. Please keep in touch and remember that this is temporary!!
Hi, I just found your video when trying to find out some more about MS. I think what you are doing taking time out of your day and sharing your experiences with the MS community is just so nice. Also I think you are smokin hot! Keep up the great work = )
Lauren, Your videos really ARE an inspiration. Ive fought MS symptoms for 2 years, having my first exacerbation June 2006. I was diagnosed with RRMS on August 13, 2008 and am starting Copaxone. I am incredibly nervous to start, but after watching all of your videos - I am incredibly motivated to stay on top of therapy! Thank you :) - Nicole (Age 27) Charleston, WV
Thank you so much! I can't tell you how happy I am that these videos have made you feel motivated to stay on top of therapy! Trust me, I was terrified when I took my first shot of Copaxone, but I know that the medication is preventing me from getting any worse. I wish you the best of luck and please keep in touch!!
(Lauren....am serious for once.........does the "reply" function work on your comments? If it does, you should use it, otherwise hard to follow......)
And - are you studying 50 languages now? You may need them soon......lol
i think relapses happen progressively, but not necessarily slowly. In my case i got to feel first the leg, then the arm, and finally the face and the voice, the whole process lasting about an hour. This must be normal, because the doctor told me to wait at least 24 hours before seeing him, to wait for the sympthoms to fully develop.
And i had numbness and tingling only on the right side, both the arm and leg, and also the face muscles weak on the same side.
I've only had 1 relapse in 8 years and it was completely due to stress. Every person is different, and every relapse is different. Some people have numbness/weakness only on one side and some don't. It know it's frustrating, but that's how this disease is. I hope this was helpful!
As 1 local lad once said?All you need is Love! Thanx Lauren from across the Pond (England)richie979
Richie979 8 months ago
@Richie979 Aww, you are so sweet! I LOVE that song!! Love from the U.S.!!
laurenvparrott 8 months ago
This has been flagged as spam show
How many people know that chronic Mercury poisoning cause many disease including Multiple Sclerosis? Do you know Dental Amalgam have 50% Mercury and non-stop leaking Mercury vapor? Do you know Sweden have banned the use of Dental Amalgam in their country already? so please eliminate Mercury from your body is the most important thing to do now.
perryhtc 9 months ago
This has been flagged as spam show
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 10 months ago
Hey Lauren-
It was so awesome meeting you and feeling your incredible power and sincere love for helping people! I am excited to stay in contact with you and go at this journey together! I am trying to add you on Face Book but cannot find you on there- so call me or email me and we'll will talk and stay in touch! You're nothin but power, and authenticity, and an inspiration to me.
Your new friend with MS,
Josh Hewlett
JoshHewlett 1 year ago
@JoshHewlett Hi Josh!! It's so funny because I totally looked for you on Facebook before I got this comment! I had SOOO much fun talking to you this weekend! I really wanted to make a video tonight but I'm so tired, I think I'll make it tomorrow. We definitely have to keep in touch!! You are so sweet and hilarious! You are an inspiration to me!!
Take care my new friend with MS!!
Lauren :)
laurenvparrott 1 year ago
Hi Lauren you look very nice. I'm from Poland now I live in UK, I take Tisabri since January the treatment doesn't help my very much but I have much power, on Friday I take 6th time ,I very enjoy with this treatment. My English is nnot good i hope you help me with this. Thank you Daniel
danielek1871 1 year ago
@danielek1871 Thank you so much! Daniel! So, is the Tysabri slowing the progression of your disease? Do you have any new lesions? I'm so happy that you have much power!
laurenvparrott 1 year ago
@laurenvparrott hi lauren im dave. my neurologist says i probably have MS. i had 2 MRI done and 2 leisons. i had a relapse 1 year ago and blamed it on my medication. it was balance and not able to walk straight. plus my arms were not right too. in about a week i meet with my neuro for my lumbar results. wish me luck. if i dont have MS i still support you guys and if i do i dont know what to expect. any help is appreciated. i been doing research on MS and found your page. thank you dave
tboy221 3 months ago
hi
my name is karim 24 years dentist from egypt and have ms
i think i will change my career cuz of ms, but i really saw a hope in life with your video
i was really needing someone to support me specially as i am recently shoked with diagnosis of ms
thanks for this video
Drelbaradei 1 year ago
@Drelbaradei Wow! Thank you for writing from Egypt! I think that changing your career is totally fine! You can do whatever is best for your situation!! Good luck and keep in touch!
laurenvparrott 1 year ago
CANCER CURE = RICK SIMPSON'S HEMP OIL
EssiacHempLaetrile 2 years ago
Comment removed
calritos 2 years ago
and i attended today to that presentation! =) really nice
calritos 2 years ago
That's awesome! Thank you for writing!
laurenvparrott 2 years ago
Lauren,
My name is Craig & i am from Buffalo, NY. I had come across your video by chance when browsng youtube. My grandma has MS and has been steadily on a downward spiral. But over the past little while I have been researching some new and inovative products along with my nutritionist and we have had great success in helping those in wheelchairs/walkers walk again. we use a super potent anti oxidant that mops up free radicals that steal electrons from the myelin causing nerve damage.......
gqstyle13 2 years ago
Hi Craig! That is so wonderful that you're helping your grandma. I was extremely close to my grandma and I tried to help her as much as possible as well. Thank you for writing and I wish you all the best!
laurenvparrott 2 years ago
Comment removed
gqstyle13 2 years ago
You are a very kind and lovely person! Keep up the good work. :)
amg4761 3 years ago
Thank you so much!!
laurenvparrott 3 years ago
I love you. You are sooooo amazing. You've inspired me. I don't know if you've yet to respond to my comment on another of your video. The one about your tremors almost being gone. I think you are sooo strong and beautiful and strong.
lolitalov234 3 years ago
You are so sweet - this means so much to me! Thank you very much for writing and I wish you the best!
laurenvparrott 3 years ago
Lauren, your videos always inspire me. But, I have been having a flare up and need some encouragement. It is frustrating because it is like a nightmare starting all over again. Keep up the good work! Michelle
mrsfirecracker 3 years ago
Hi Michelle! I'm sorry it took so long to get back to you. I'm sorry that you're going through a flare up - hang in there and try to stay positive. I liked to watch funny movies and lay on the couch to relax my muscles. Please keep in touch and remember that this is temporary!!
laurenvparrott 3 years ago
Hello Lauren from America,
I watched you're videos and sent you a message.
I am an online marketer, but don't let that scare you.
You are very inspiring and I would love to talk to you about tysabri.
Call me if you have time.
Matt Mortenson,
507-581-5307
ibuzzproautomation 3 years ago
Hi Matt! Thanks for your message! I am in the process of moving into a new house but I will call when I find the time!
laurenvparrott 3 years ago
Hi, I just found your video when trying to find out some more about MS. I think what you are doing taking time out of your day and sharing your experiences with the MS community is just so nice. Also I think you are smokin hot! Keep up the great work = )
secretsage15 3 years ago
Thank you so much! You are really sweet - you made my day!!
laurenvparrott 3 years ago
You are the best advertisement for Tysabri. What a marvelous improvement you've made in your recovery! You give me hope.
teafourtao 3 years ago
Thank you so much! I wish you the best!
laurenvparrott 3 years ago
I love seeing your videos!!! You remind me to always stay positive. Thanks
allicat93 3 years ago
Thank you so much!!
laurenvparrott 3 years ago
Thank you for sharing your thoughts with us.
Best wishes from the Medicine 2.0 Congress.
NCurse3 3 years ago
Thank you very much!!
laurenvparrott 3 years ago
Lauren, you are AMAZING girl! Keep on making those videos we all look forward to seeing. You're such an inspiration!
dmplaura 3 years ago
Thank you so much!! You are so sweet!!!
laurenvparrott 3 years ago
Ciao Ricky!!
Grazie, grazie, grazie!! Sto provando a parlare italiano!!
Lauren :)
laurenvparrott 3 years ago
Bravissima!
wildweaselxp 3 years ago
Grazie!!
laurenvparrott 3 years ago
Ciao!
Continua così che sei sempre la migliore!
Ricky
wildweaselxp 3 years ago
Lauren, you need to keep doing the videos. You're NOT allowed to stop doing them. :D
I just love your videos and it's bringing to me so good motivation. I just love your videos and it's bringing to me so good motivation.
I'm really thankful that I've found you here on YouTube.
Love from Japan! :)
paulohumemoto 3 years ago
Hi Paulo!!
You are so sweet!!! I just love hearing from you!!
Lots of love from America,
Lauren :)
laurenvparrott 3 years ago
Lauren, Your videos really ARE an inspiration. Ive fought MS symptoms for 2 years, having my first exacerbation June 2006. I was diagnosed with RRMS on August 13, 2008 and am starting Copaxone. I am incredibly nervous to start, but after watching all of your videos - I am incredibly motivated to stay on top of therapy! Thank you :) - Nicole (Age 27) Charleston, WV
mom2kaylantristn 3 years ago
Hi Nicole!
Thank you so much! I can't tell you how happy I am that these videos have made you feel motivated to stay on top of therapy! Trust me, I was terrified when I took my first shot of Copaxone, but I know that the medication is preventing me from getting any worse. I wish you the best of luck and please keep in touch!!
laurenvparrott 3 years ago
good video! I agree about you tube and hope Google is able to keep the ads down!
qualisarx 3 years ago
Thank you!
laurenvparrott 3 years ago
TEST
(Lauren....am serious for once.........does the "reply" function work on your comments? If it does, you should use it, otherwise hard to follow......)
And - are you studying 50 languages now? You may need them soon......lol
:o) ....... Steve
7mumfred7 3 years ago
Steve - I have no idea if the function doesn't work on my computer - I just click respond and hit post comment!!
laurenvparrott 3 years ago
Lauren - OK, am posting this "reply" as a test, to see how it shows up.
Maybe there is an FAQ or "trouble-shoot" page here somewhere for directors.
Anyway, great to get your message that you are working 40 hours per week. Unbelievable, I thought you might be part-time at best !
Ciao.......
:o) :o) :o)
7mumfred7 3 years ago
Hey! I hope this reply shows up too! It not, I will look into FAQ or trouble-shooting.
Yeah, I love my job and I feel blessed!!
Talk to you soon :)
laurenvparrott 3 years ago
wendell3308 hi i hope you are okay :)
lauren constantly mentions TYSABRI and indeed is a spokesperson for a lot of people.
that said she cant mention it in every sentence and breath but having watched all laurens videos you can see the impact.
i hope you can view them all okay, they mean a lot to a lot of people.
hekate180 3 years ago
Thank you so much for your message!
laurenvparrott 3 years ago
this ? is for anyone, did your last attack happen suddenly or was it a slow progression?
and does anybody else have numbness/weakness only on one side?
thank you for your time.......
skullroses 3 years ago
i think relapses happen progressively, but not necessarily slowly. In my case i got to feel first the leg, then the arm, and finally the face and the voice, the whole process lasting about an hour. This must be normal, because the doctor told me to wait at least 24 hours before seeing him, to wait for the sympthoms to fully develop.
And i had numbness and tingling only on the right side, both the arm and leg, and also the face muscles weak on the same side.
I hope to have been useful, greetings
saco88 3 years ago
Thank you for your comment!
laurenvparrott 3 years ago
I've only had 1 relapse in 8 years and it was completely due to stress. Every person is different, and every relapse is different. Some people have numbness/weakness only on one side and some don't. It know it's frustrating, but that's how this disease is. I hope this was helpful!
laurenvparrott 3 years ago
you're suberb my dear! what a fighter!
lizzy890 3 years ago
Thank you so much!
laurenvparrott 3 years ago
...too bad that you didn't mention the name of the drug...
...which has given you & so many other MSers....Hope...
Hope with TYSABRI...right?
Without TYSABRI.....who knows???
wendell3308 3 years ago
I was asked to make a video for a conference in Norway about how the internet has helped me with my disease. I'll explain that in my next video.
Tysabri had been so helpful for me and many others, and I'll say it over and over again!
laurenvparrott 3 years ago
seriously you are amazing!!!!!
all the best :D
peterpan3930 3 years ago 2
You are so sweet! Thank you!
laurenvparrott 3 years ago
You rock Lauren!!!
jcrane722 3 years ago 2
You are so sweet!!
laurenvparrott 3 years ago