You are not an ordinary girl, God does not choose regular people for battles like the one you have, You are so genuine and this is not so common in life right now, and just by that you can be and you already are a wonderful public speaker, Your strength makes anyone watching this video living a new experience, and takes all the courage to fight a disease, a huge problem, etc,
May God Keep your gorgeous smile & your optimism always, MS may cos you to shake but will never dare discourage you.
@DrMuthanna77 Thank you so much for your kind message, and for your support!! That mean so much to me! It absolutely gives me the strength to keep moving forward!! I hope you are well!
Help Jeff Johnson find a cure for Multiple Sclerosis. Visit his fundraising home page at nationalMSsociety home page and add to the URL /goto/jeffjohnson
I wanna give you a big hug right now. You are too frickin' cute. I was diagnosed with MS on August 10 of this year. I've started on Copaxone. I haven't had anything remotely close to a flare-up since I've been on it. I'm going strong. I don't plan on having another MS attack!
I really think about you and pray for you and I hope at the moment of posting this, you are doing well and staying strong, and know that complete strangers in this country and world really care about you. God bless you.
@mayra32074 I was diagnosed just this past March. It can be overwhelming. Do your research and speak to a good doctor about the best medication to be on. I did and settled on Copaxone because it is supposed to be best for the liver. I hope you have a good support system. There are a lot of people and groups out there who can help you along the way and give you the support you need. God bless.
My dad has MS. It's really tough for him to walk around in our little house. he didn't even knew he had it until he had a really bad car crash. I feel Really bad for you and him. One time he fell in our kitchen and he really hurt himself. It just makes me sad seeing people with MS. Good luck :)
You are adorable. God bless you sweetheart, I hope you are doing better. I don't know how old this video is but I have watched many of yours to understand as my eldest son was diagnosed about 3 weeks ago. It's been tough because he doesn't want to open up to us and he seems quite bitter. I guess I look at these videos to feel like I will get some answers. Please take care and keep that beautiful smile you seem to always have. Do what you like as it always helps me with stress too. God Bless.
People try to help but unless they've experienced life with MS they can never know the world we've been cast into here?It is very hard dealing with a body you can't rely on from day to day? We can only try our best and hope we come out of the latest episode with limited damage on our live's. Remember! It's Not your fault, You will adapt and the best thing is your friends and family will always love you.!!! You can conquer the world with that lovely smile anyway! Love from Liverpool,yeh,yeh,yeh
@Richie979 Aww, thank you so much for your comment. I completely agree with you about how people will never know, but we are all going to be fine! My grandmother is my angel, and she is watching out for me! Love from the USA!! xoxoxo
It is hard to see alot of movies that making you emotional. I get that way too! I am sorry about your grandmother having cancer! That is such a hard thing!! I will pray for your grandmother!
@LYNXVAL I'm so sorry that it's taken so long to respond. Thank you for your support with my grandmother...it was very hard. Thank you for your prayers! I hope you are doing well!
Why doctor afraid to think whether this disease is cause by chronic Mercury poisoning?? may be they even don't know what is Mercury.
Mercury is a neural-toxic heavy metal ! and it is the second most toxic thing in the world. ( The most toxic thing in the world is "Uranium" - a heavy toxic silvery-white radioactive metallic element.)
Also, how many people know that too many vaccine contain Thimerosal (A Mercury compound) as a preservative? Avoid any Mercury intake, eliminate Mercury from your body and get well.
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
Lauren, I so appreciate your testimony and your honesty. I too have ms. I am moved by the fact that through all of your experiences, though it is obviously very hard on you physically and emotionally..you still have a strong heart and soul. That is what I cling to. This disease can take a lot from me, but I am determined that it WILL NOT take away my heart and soul. It WILL NOT rob me of my spirit. It is so good that you can still laugh at times. I pray for you and give thanks for you. :)
Hey girl I am recently going through testing for ms cause of some of the symptoms.. Anyways, I am think that you are an amazing, courageous person... I am happy that you are around my age and it makes me feel that if you can get through this I can too... Luv ya.. You Rock!!!
@Amanda93461485 Hey! Oh my gosh you are so sweet! I KNOW you can get through this! Please keep me posted and let me know what happens! I hope you have a wonderful holiday season!! Love ya!
Lauren, you are such a sweet young lady!! I have been watching some of your videos, my heart goes out to you. I too have MS, I appreciate what you are doing here for us all. You are so so sweet, I wish you every happines and health in life. You and Anthony are lucky to have eachother. I too have a boyfriend Anthony. Our Anthony's are very similar in a loving caring way. I will keep good wishes and prayers in my heart for you. Thank you and stay sweet as you are. You are an inspiration.
@zsuzska92160 Thank you so much!! I really appreciate your prayers - that really means the world to me! I hope you and Anthony are doing well, and I hope you have a delightful holiday season!
You are beautiful, you are very strong to have the courage to go public like this. Keep going! This illness is not easy at all, I admire your courage and I hope with all my soul that you will feel better soon.
Have you heard about the MS study examining benefits of apoaequorin for those living with MS? You receive apoaequorin, a supplement that may help symptoms of MS, and fill out a monthly survey tracking improvement.
hola mi nombre es edgar y fue toda una faena para encontrar tu canal que he venido siguiendo des de la pagina de cancer type ,
¿hay algueine que escriba en es pañol? mi ingles no es muy bueno
hello my name is edgar and quisierasaber if someone writes in Spanish so I can communicate and understand well, because I have my girlfriend who is sclerotic and I love anyone Here?
i know this video was made a few years ago, but it means a lot to me that you make these videos. i'm 18 i was diagnosed when i was 17 and it really helps to see someone going through the same things as me.
i want to start making videos about my struggles too, i'm so sorry about your grandmother. people tell me to get the stress out of my life all the time. you said everything i want to say. it's more stressful to try and relax.
@luralisious Thank you so much for your comment! I was diagnosed at 18 so I know exactly where you're coming from. I wish you the very best with everything and I look forward to seeing your videos!
I started the Tysabri and had 2 infusions already. I go for my third infusion next week. How long did it for you to notice Tysabri working for you.? I know we are all different. and suffer from this horrible disease in different ways. I woke up today and had a flare up. I called my MS center and let them know. I'm suppose to let them know if my flare up continues for 24 hours. So far. so good. So that why I ask you, have you had a flare up while taking Tysabri?
@marthab63 Hello! I started noticing improvements after my 3rd infusion of Tysabri. I have not had any relapses since I started taking Tysabri. I wish you the very best with everything!
Poor darling - my heart goes out to you. Thanks for these videos. I'm going to the neurologist again September 1st. I hope to find answers then - or the beginning of the answer.
You're a wonderful girl with an amazing heart. Remember that you're young and there's been medical research advances as well. Don't ever feel sad, there's time and there's alternative treatments towards MS. Try getting foods or taking vitamin supplements that are rich in Omeg 3 Oils. Yoga Excersises help alot as well as cold environments. Don't ever feel sad and always feel free to write.
You're a wonderful girl with an amazing heart. Remember that you're young and there's been medical research advances as well. Don't ever feel sad, there's time and there's alternative treatments towards MS. Try getting foods or taking vitamin supplements that are rich in Omeg 3 Oils. Yoga Excersises help alot as well as cold environments. Don't ever feel sad and always feel free to write.
You're a very wonderful sweet girl with a beautiful heart. Don't worry about MS. I'll be more happy to give you some advice. You're young and there's still time and there's options to improve and there's medical advances now these days. Feel free to write.
Thanks Lauren. I watch your video often to reassure myself. It's really encouraging. I definitely will let you know once I get started. It's hard to be patient. I'm trying. Peace, Love and Happiness! I try to look at the positve in life. I hope it works too! I'm ready !
Thanks Lauren, I have been thru similar things as you have. I can totally relate.. Im going to start on the Tysabri really soon. I was sick when my mom passed away from cancer. I really appreciate your comments. I have to be more patient with myself and my husband and kids. Ya, MS sucks. Ive had since I was 30 and now Im 47. Im hoping Tsabri is gonna help
Oh sweetie! My heart goes out to you, I have MS and my grandma died of cancer and she was my best friend and I never got over it, and this made my MS so much worse ever since please don't stress yourself out, it makes us ache more.
@longleggedmakdaddy Thank you for your support! I'm sorry to hear about your Grandmother :( It's so hard...I still cry about my Grandmother's passing. Yet I know she's in heaven watching over me! God Bless you!
I have not even finished watching one of your video and I am so moved by it.
My wife its about to be diagnosed with MS,they call her today and told her probably yoy have MS we want to talk to you in person she is 39 and we have a 2 yr old and Im so scared because this is so new to me and want to help her as much as I can.I want to thank you for taking your time to this best wishes and Have a Merry Christmas!
Thank you so much for writing! Please know that you and your wife can talk to me anytime!! I promise you, everything is going to be fine and there is a huge network of support here on YouTube! I hope you have a wonderful Christmas!!
Lauren you are very brave, I hope that this whole new liberation thing works out so you can get better. my boyfriend has MS, he is 23 and was diagnosed when he was 16. he has had it pretty good though. I haope you get better hun!!!! I will pray for you : )
you are BRAVE BRAVE BRAVE for sharing so deeply about what you are feeling. my Mom has MS and it is so hard to get her to share sometimes. her approach is that there's nothing she can do about it. so she doesn't want to talk much. that might be changing a little lately but I love hearing what other people are experiencing because it helps me to understand what she's feeling - even when she doesn't feel like sharing THANK YOU THANK YOU THANK YOU
I saw this video just now. Thank you so much for your honesty and sweetness. I don't know how your grandmother did, but I pray for her. I have had MS for 4 yrs and I'm 29 years. Your videos that I've seen so far makes me feel so good and not so alone. Thank oyu so so much.
Your such a sweet girl with a heart of gold I can tell :) Im sorry to hear of the loss of ur grandma too,I found your page when I was watching a friend of mine, page about MS. and I cry everytime you are sad, God loveya sweetie.I wish I could give ya a big hug!
My husband ... well it's obvious when he's going through a tough time.
You are not only helping people with MS Lauren... you are helping a young wife who's in anguish watching the man of her dreams suffer... you give so much hope!
Thank you so much - my Grandma passed away in December of 2007, a few days after I made this video, but I know she's in heaven watching over me. I hope you and your Grandma are doing well!!
Hi Lauren, I was hoping I could send you a private message. My son is Tommy, who you have helped so much in dealing with his MS. But somethings I would like to keep private. If this is possible please let me know. Thanks for sharing, it helps so many people. Sending you a big hug. Thanks again, Vanessa aka Tommy's Mom.
Hi Lauren, I just wanted to say hi and that I'm in Limboland as the call it, havin glots of ms symptoms and no diagnosis as yet. I'm waitng for my first MRI next week bu tt all the sy mptoms are driving me nuts. I'ma medical typis who , as you can see can't type mcu any moer and used to be a scrapper for the Oz mags until recently and now I can't do that either. Thank you for your videos, they are a help to hsoe of us new to htis and kt makes it easier to see your strength. Keep well, love Lu
Hello! I'm sorry, I know how difficult Limboland is...believe me. Please let me know how your MRI results come back. As soon as you know what the problem is, you'll get help and you'll be able to type again...I'm sure of it! Good luck and I hope to hear from you soon!
Thank you for your words , many thanks for your courage to show us "your fellows in MS" how it really feels. I've been living withit for 5 years now, i hope i can live a beter life.
I was officially diagnosed in October, but I'd had one episode in 2005 (right before I started college at the University of Michigan). It was crazy because the doctors had assured me that I'd be fine since they weren't seeing anything on the regular MRI's I'd had for 3 years. Watching your video was so inspiring because for a long time I felt like no one understood what I was going through. Thanks so much for that and I will keep your Grandmother in my prayers.
Oh my gosh, you are a sweetheart! I'm glad that you've been officially diagnosed - not knowing is the worst. Did you graduate from U of M yet? That's awesome that you went there. I'm so glad you can relate to my videos! If you ever have any questions, please don't hesitate to ask. I wish you the very best!!
I'm glad that you wrote! I'm graduating in May!! I am lucky to have my family around, since I am from Ann Arbor. I'm also participating in the clinical trial for the new drug Campath 1H, so I should receive my first treatment this month!
Hi Aly! Thank you so much for your comment. It's so true - taking stress out of your life is impossible. Thank you for your condolences. I'm so sorry to hear about your father in law. I hope you're having a wonderful 2009 so far, and I hope your kids are doing well!
im really sorry about your grandmother, she is in a better place, try not to think too much about it if you can help it. How re you doing? Relapses will go away, i have the same problems with my hands, even when im typing, took my mri yesturday, stress is the only thing i have to fight. Good luck with you, get better.
Thank you so much for your concern. I'm doing very well and I pray to her all the time! Yes, stress is the only thing that I have to fight so I try hard not to get stressed! Good luck to you as well!
hola lauren no se si puedas leer espanol pero igual te mando el mensaje mi esposo le diagnosticaron ms y siempre trato que tenga el mismo espiritu que tiene tu .cuidate mucho y suerte
Dude at college i got a scare in my last months and every since then i go for check ups and so worried am gonna have a relapse and the doc tells me i have ms , i go in jan for a check up , this week i had a few problems but i think am ok. Dude dont cry i hate seeing girls cry . Man i hope you have a good year.
You are such a sweetheart! I really hope everything goes well for you. If it is MS, you're going to be fine. With all the medications out there, you'll be stablized and I'm positive that you can handle whatever happens. Please keep me posted and write if you have any quetions!!
Keep strong. I feel so bad seeing anyone going through something that makes life hard. I have heart problems and it started when I was 32. Keep strong. I try.
So pleased you play the piano, the last attack finished off this skill because my hand-connections have re-grown around the wheel chair. So keep tinkering! And tell the voices of subvocal thinking, internal and external that we all have, to SHUT UP.
Hello Lauen, I have MS I was DX FEB. 2008. I get tremors and I walk with a limp. How long ago did you start having bad tremors. Since you've been dx for 7 yrs. I mri my nero. says I've probaly had it for about 4 yrs. Keep it up.
Lauren - I found your videos from Maya at scrapbookgraphics. I am a digiscrapper inspired by your story. Not sure if you heard but their is a kit for sale by Songbird Ave where the profits go to MS. I plan on buying it.
You are so brave and your videos will do wonders for anyone going through MS. Thank you.
(One more thing. I am also a fellow spartan and am from the detroit area! :))
i can relate however my comment is bit late i am in hospital myself due to pml from tysabri i cant walk due to spaticity
pmltysabrisucks 11 hours ago
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DOES ANYONE HAVE ANY SUGGESTIONS OF TREATMENTS FOR SPASTICITY???
jewel791 3 days ago
You are not an ordinary girl, God does not choose regular people for battles like the one you have, You are so genuine and this is not so common in life right now, and just by that you can be and you already are a wonderful public speaker, Your strength makes anyone watching this video living a new experience, and takes all the courage to fight a disease, a huge problem, etc,
May God Keep your gorgeous smile & your optimism always, MS may cos you to shake but will never dare discourage you.
DrMuthanna77 3 weeks ago
@DrMuthanna77 Thank you so much for your kind message, and for your support!! That mean so much to me! It absolutely gives me the strength to keep moving forward!! I hope you are well!
laurenvparrott 2 weeks ago
when i get stressed i cut myself with a razor blade
tboy221 1 month ago
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Help Jeff Johnson find a cure for Multiple Sclerosis. Visit his fundraising home page at nationalMSsociety home page and add to the URL /goto/jeffjohnson
Ekorn999 2 months ago
I wanna give you a big hug right now. You are too frickin' cute. I was diagnosed with MS on August 10 of this year. I've started on Copaxone. I haven't had anything remotely close to a flare-up since I've been on it. I'm going strong. I don't plan on having another MS attack!
I really think about you and pray for you and I hope at the moment of posting this, you are doing well and staying strong, and know that complete strangers in this country and world really care about you. God bless you.
tributevocalist 2 months ago in playlist tributevocalist's favorites
Awww, stay strong you are so beautiful... please get a metal test. PLEASE PLEASE PLEASE PLEASE.
vancouverislandbass 2 months ago
I just Got diagnose today, dont know what to do with my life, it seems like no one understand God bless you be strong
mayra32074 2 months ago
@mayra32074 Everything will be ok, I promise!! God Bless you!
laurenvparrott 2 months ago
@mayra32074 I was diagnosed just this past March. It can be overwhelming. Do your research and speak to a good doctor about the best medication to be on. I did and settled on Copaxone because it is supposed to be best for the liver. I hope you have a good support system. There are a lot of people and groups out there who can help you along the way and give you the support you need. God bless.
missrizzo1 2 months ago
You Are Sooo Courageous! GOD BLESS YOU! J
JasonEBernard1 3 months ago
My dad has MS. It's really tough for him to walk around in our little house. he didn't even knew he had it until he had a really bad car crash. I feel Really bad for you and him. One time he fell in our kitchen and he really hurt himself. It just makes me sad seeing people with MS. Good luck :)
~LiLi
candy822803 3 months ago
You are adorable. God bless you sweetheart, I hope you are doing better. I don't know how old this video is but I have watched many of yours to understand as my eldest son was diagnosed about 3 weeks ago. It's been tough because he doesn't want to open up to us and he seems quite bitter. I guess I look at these videos to feel like I will get some answers. Please take care and keep that beautiful smile you seem to always have. Do what you like as it always helps me with stress too. God Bless.
rvquilter83 4 months ago
@rvquilter83 Thank you! Don't worry, your son will be ok...it takes time. God bless you!!
laurenvparrott 4 months ago
People try to help but unless they've experienced life with MS they can never know the world we've been cast into here?It is very hard dealing with a body you can't rely on from day to day? We can only try our best and hope we come out of the latest episode with limited damage on our live's. Remember! It's Not your fault, You will adapt and the best thing is your friends and family will always love you.!!! You can conquer the world with that lovely smile anyway! Love from Liverpool,yeh,yeh,yeh
Richie979 8 months ago
@Richie979 Aww, thank you so much for your comment. I completely agree with you about how people will never know, but we are all going to be fine! My grandmother is my angel, and she is watching out for me! Love from the USA!! xoxoxo
laurenvparrott 7 months ago
It is hard to see alot of movies that making you emotional. I get that way too! I am sorry about your grandmother having cancer! That is such a hard thing!! I will pray for your grandmother!
LYNXVAL 8 months ago
@LYNXVAL I'm so sorry that it's taken so long to respond. Thank you for your support with my grandmother...it was very hard. Thank you for your prayers! I hope you are doing well!
laurenvparrott 5 months ago
It is hard to see alot of movies that making you emotional. I get that way too!
LYNXVAL 8 months ago
no more stress!!!
no more stress!!!
keep your mind busy!!!
stay happy!!
ms will replase!!
i know!!
it happen to me!!
i got ms
LuckJustBad 9 months ago
@LuckJustBad I like that - you're right!
laurenvparrott 9 months ago
ahhhh...prayers are with you sweetie.
Bodyquest2 9 months ago
@Bodyquest2 Thank you so much!!
laurenvparrott 9 months ago
Why doctor afraid to think whether this disease is cause by chronic Mercury poisoning?? may be they even don't know what is Mercury.
Mercury is a neural-toxic heavy metal ! and it is the second most toxic thing in the world. ( The most toxic thing in the world is "Uranium" - a heavy toxic silvery-white radioactive metallic element.)
perryhtc 9 months ago
@perryhtc Oh gosh, I don't know anything about those things...
laurenvparrott 9 months ago
Also, how many people know that too many vaccine contain Thimerosal (A Mercury compound) as a preservative? Avoid any Mercury intake, eliminate Mercury from your body and get well.
perryhtc 9 months ago
Your My Hero. :D Tear. . ;)
Imelda420 9 months ago
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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
The Gerson Therapy
newmedstudent 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 10 months ago
Aww this is so sad, but you're so brave! I applaud you for even being self-less in such a hard time, trying to encourage others with MS<3
jessface777 10 months ago
@jessface777 Thank you so much!!
laurenvparrott 10 months ago
@jessface777 The Gerson Therapy.....
newmedstudent 9 months ago
Lauren, I so appreciate your testimony and your honesty. I too have ms. I am moved by the fact that through all of your experiences, though it is obviously very hard on you physically and emotionally..you still have a strong heart and soul. That is what I cling to. This disease can take a lot from me, but I am determined that it WILL NOT take away my heart and soul. It WILL NOT rob me of my spirit. It is so good that you can still laugh at times. I pray for you and give thanks for you. :)
MSfriend2U 1 year ago
@MSfriend2U Thank you so much!! Your comment really means a lot! Thanks again and I wish you the very best!!
laurenvparrott 1 year ago
Comment removed
bullsnmudd 1 year ago
hello and happy holidays to you lauren.we're praying for you and sending hugs,prayers,and encouraging good energy smiles.:) :) :) mwaaaah
goldfeatherable 1 year ago
@goldfeatherable Thank you so much!! I wish you very happy holidays, and I'm sending hugs and prayers in return!
laurenvparrott 1 year ago
Hey girl I am recently going through testing for ms cause of some of the symptoms.. Anyways, I am think that you are an amazing, courageous person... I am happy that you are around my age and it makes me feel that if you can get through this I can too... Luv ya.. You Rock!!!
Amanda93461485 1 year ago
@Amanda93461485 Hey! Oh my gosh you are so sweet! I KNOW you can get through this! Please keep me posted and let me know what happens! I hope you have a wonderful holiday season!! Love ya!
laurenvparrott 1 year ago
Lauren, you are such a sweet young lady!! I have been watching some of your videos, my heart goes out to you. I too have MS, I appreciate what you are doing here for us all. You are so so sweet, I wish you every happines and health in life. You and Anthony are lucky to have eachother. I too have a boyfriend Anthony. Our Anthony's are very similar in a loving caring way. I will keep good wishes and prayers in my heart for you. Thank you and stay sweet as you are. You are an inspiration.
zsuzska92160 1 year ago
@zsuzska92160 Thank you so much!! I really appreciate your prayers - that really means the world to me! I hope you and Anthony are doing well, and I hope you have a delightful holiday season!
Lauren :)
laurenvparrott 1 year ago
You are beautiful, you are very strong to have the courage to go public like this. Keep going! This illness is not easy at all, I admire your courage and I hope with all my soul that you will feel better soon.
flore20ani 1 year ago
@flore20ani Thank you so much! You are very kind - I really appreciate it!
laurenvparrott 1 year ago
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Have you heard about the MS study examining benefits of apoaequorin for those living with MS? You receive apoaequorin, a supplement that may help symptoms of MS, and fill out a monthly survey tracking improvement.
MSHopeTrials 1 year ago
por fafor hombres de novias escleroticas help? nesecito urgente mentente tips para entenderla
edgarpia25 1 year ago
@edgarpia25 Non habla español :(
laurenvparrott 1 year ago
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@laurenvparrott Thank you so much for writing......help
edgarpia25 1 year ago
hola mi nombre es edgar y fue toda una faena para encontrar tu canal que he venido siguiendo des de la pagina de cancer type ,
¿hay algueine que escriba en es pañol? mi ingles no es muy bueno
hello my name is edgar and quisierasaber if someone writes in Spanish so I can communicate and understand well, because I have my girlfriend who is sclerotic and I love anyone Here?
edgarpia25 1 year ago
DIANETICS IS THE ANSWER !!
STOP SUFFERING unless you like it.
lmhitar 1 year ago
i know this video was made a few years ago, but it means a lot to me that you make these videos. i'm 18 i was diagnosed when i was 17 and it really helps to see someone going through the same things as me.
i want to start making videos about my struggles too, i'm so sorry about your grandmother. people tell me to get the stress out of my life all the time. you said everything i want to say. it's more stressful to try and relax.
luralisious 1 year ago
@luralisious Thank you so much for your comment! I was diagnosed at 18 so I know exactly where you're coming from. I wish you the very best with everything and I look forward to seeing your videos!
laurenvparrott 1 year ago
Hang in there girl, you seem very sweet and strong! I also have MS but I am much older. I will be 45 this month. Keep the faith and God bless!
jeannelovesjon1 1 year ago
@jeannelovesjon1 Thank you so much! I wish you the best! God Bless!!
laurenvparrott 1 year ago
Comment removed
marthab63 1 year ago
Hi Lauren,
I started the Tysabri and had 2 infusions already. I go for my third infusion next week. How long did it for you to notice Tysabri working for you.? I know we are all different. and suffer from this horrible disease in different ways. I woke up today and had a flare up. I called my MS center and let them know. I'm suppose to let them know if my flare up continues for 24 hours. So far. so good. So that why I ask you, have you had a flare up while taking Tysabri?
marthab63 1 year ago
@marthab63 Hello! I started noticing improvements after my 3rd infusion of Tysabri. I have not had any relapses since I started taking Tysabri. I wish you the very best with everything!
laurenvparrott 1 year ago
Poor darling - my heart goes out to you. Thanks for these videos. I'm going to the neurologist again September 1st. I hope to find answers then - or the beginning of the answer.
Willow1120 1 year ago
@Willow1120 I really hope you can find answers from your neurologist!
laurenvparrott 1 year ago
This has been flagged as spam show
Hey Lauren,
You're a wonderful girl with an amazing heart. Remember that you're young and there's been medical research advances as well. Don't ever feel sad, there's time and there's alternative treatments towards MS. Try getting foods or taking vitamin supplements that are rich in Omeg 3 Oils. Yoga Excersises help alot as well as cold environments. Don't ever feel sad and always feel free to write.
czam73 1 year ago
Hey Lauren,
You're a wonderful girl with an amazing heart. Remember that you're young and there's been medical research advances as well. Don't ever feel sad, there's time and there's alternative treatments towards MS. Try getting foods or taking vitamin supplements that are rich in Omeg 3 Oils. Yoga Excersises help alot as well as cold environments. Don't ever feel sad and always feel free to write.
czam73 1 year ago
@czam73 Thank you so much for writing! You are so sweet - I really appreciate your message!!
laurenvparrott 1 year ago
Hey Lauren,
You're a very wonderful sweet girl with a beautiful heart. Don't worry about MS. I'll be more happy to give you some advice. You're young and there's still time and there's options to improve and there's medical advances now these days. Feel free to write.
czam73 1 year ago
i love Your smile. You're fantastic person. dont give up with MS, recover fast, best wishes! :)
enodmeedgraffa 1 year ago
@enodmeedgraffa Thank you so much! That means a lot to me!
laurenvparrott 1 year ago
Thanks Lauren. I watch your video often to reassure myself. It's really encouraging. I definitely will let you know once I get started. It's hard to be patient. I'm trying. Peace, Love and Happiness! I try to look at the positve in life. I hope it works too! I'm ready !
marthab63 1 year ago
@marthab63 That's a great attitude!
laurenvparrott 1 year ago
Thanks Lauren, I have been thru similar things as you have. I can totally relate.. Im going to start on the Tysabri really soon. I was sick when my mom passed away from cancer. I really appreciate your comments. I have to be more patient with myself and my husband and kids. Ya, MS sucks. Ive had since I was 30 and now Im 47. Im hoping Tsabri is gonna help
marthab63 1 year ago
@marthab63 I really hope Tysabri works for you, too! Please keep in touch and let me know. I wish you the best!
laurenvparrott 1 year ago
Oh sweetie! My heart goes out to you, I have MS and my grandma died of cancer and she was my best friend and I never got over it, and this made my MS so much worse ever since please don't stress yourself out, it makes us ache more.
God Bless you dear.
longleggedmakdaddy 1 year ago
@longleggedmakdaddy Thank you for your support! I'm sorry to hear about your Grandmother :( It's so hard...I still cry about my Grandmother's passing. Yet I know she's in heaven watching over me! God Bless you!
laurenvparrott 1 year ago
I have not even finished watching one of your video and I am so moved by it.
My wife its about to be diagnosed with MS,they call her today and told her probably yoy have MS we want to talk to you in person she is 39 and we have a 2 yr old and Im so scared because this is so new to me and want to help her as much as I can.I want to thank you for taking your time to this best wishes and Have a Merry Christmas!
sipapito 2 years ago
Thank you so much for writing! Please know that you and your wife can talk to me anytime!! I promise you, everything is going to be fine and there is a huge network of support here on YouTube! I hope you have a wonderful Christmas!!
laurenvparrott 2 years ago
Lauren you are very brave, I hope that this whole new liberation thing works out so you can get better. my boyfriend has MS, he is 23 and was diagnosed when he was 16. he has had it pretty good though. I haope you get better hun!!!! I will pray for you : )
missmackenzie1 2 years ago
Thank you so much for your message! That was so sweet of you. I wish your boyfriend the very best, and I wish you both luck with everything!
laurenvparrott 2 years ago
you are BRAVE BRAVE BRAVE for sharing so deeply about what you are feeling. my Mom has MS and it is so hard to get her to share sometimes. her approach is that there's nothing she can do about it. so she doesn't want to talk much. that might be changing a little lately but I love hearing what other people are experiencing because it helps me to understand what she's feeling - even when she doesn't feel like sharing THANK YOU THANK YOU THANK YOU
alicepcook 2 years ago
Thank you so much!! You are so kind! I wish you and your mother the very best!
laurenvparrott 2 years ago
I saw this video just now. Thank you so much for your honesty and sweetness. I don't know how your grandmother did, but I pray for her. I have had MS for 4 yrs and I'm 29 years. Your videos that I've seen so far makes me feel so good and not so alone. Thank oyu so so much.
Prissie28 2 years ago
Thank you so much for your message! I really appreciate your comment. Good luck to you and please keep in touch!
laurenvparrott 2 years ago
Your such a sweet girl with a heart of gold I can tell :) Im sorry to hear of the loss of ur grandma too,I found your page when I was watching a friend of mine, page about MS. and I cry everytime you are sad, God loveya sweetie.I wish I could give ya a big hug!
ShroomGirl1975 2 years ago
Thank you so much! It sounds like you have a heart of gold as well - this was a very sweet message!
laurenvparrott 2 years ago
I'm so sorry your grandmother died.
My husband ... well it's obvious when he's going through a tough time.
You are not only helping people with MS Lauren... you are helping a young wife who's in anguish watching the man of her dreams suffer... you give so much hope!
Joey
joeygirlmb 2 years ago
Hi Joey! Thank you so much for your comment! That means so much to me, and I wish you and your husband the very best!
laurenvparrott 2 years ago
Good luck with your grandma i know when my grandma goes through problems i'm going to melt down...try to be strong!
erikahilton 2 years ago
Thank you so much - my Grandma passed away in December of 2007, a few days after I made this video, but I know she's in heaven watching over me. I hope you and your Grandma are doing well!!
laurenvparrott 2 years ago
Hi Lauren, I was hoping I could send you a private message. My son is Tommy, who you have helped so much in dealing with his MS. But somethings I would like to keep private. If this is possible please let me know. Thanks for sharing, it helps so many people. Sending you a big hug. Thanks again, Vanessa aka Tommy's Mom.
vnecker 2 years ago
With all due respect there is no modesty or privacy with MS once you learn that then you have won 90% of the fight.
luceean 2 years ago
Hi Lauren, I just wanted to say hi and that I'm in Limboland as the call it, havin glots of ms symptoms and no diagnosis as yet. I'm waitng for my first MRI next week bu tt all the sy mptoms are driving me nuts. I'ma medical typis who , as you can see can't type mcu any moer and used to be a scrapper for the Oz mags until recently and now I can't do that either. Thank you for your videos, they are a help to hsoe of us new to htis and kt makes it easier to see your strength. Keep well, love Lu
typistinahurry 2 years ago
Hello! I'm sorry, I know how difficult Limboland is...believe me. Please let me know how your MRI results come back. As soon as you know what the problem is, you'll get help and you'll be able to type again...I'm sure of it! Good luck and I hope to hear from you soon!
laurenvparrott 2 years ago
hi!my sister have ms too since 9years and thank god she can live a normal life...
i wish you the best things!!
best wishes from vienna
funkysugarbabe 2 years ago
Thank you so much for writing from Vienna! I wish you and your sister the very best!!
laurenvparrott 2 years ago
Thank you for your words , many thanks for your courage to show us "your fellows in MS" how it really feels. I've been living withit for 5 years now, i hope i can live a beter life.
amigoo45 3 years ago
Thank YOU for your comment! I'm sure you can live a better life...stay positive and keep your chin up!
laurenvparrott 3 years ago
I was officially diagnosed in October, but I'd had one episode in 2005 (right before I started college at the University of Michigan). It was crazy because the doctors had assured me that I'd be fine since they weren't seeing anything on the regular MRI's I'd had for 3 years. Watching your video was so inspiring because for a long time I felt like no one understood what I was going through. Thanks so much for that and I will keep your Grandmother in my prayers.
kyriedearie 3 years ago
Oh my gosh, you are a sweetheart! I'm glad that you've been officially diagnosed - not knowing is the worst. Did you graduate from U of M yet? That's awesome that you went there. I'm so glad you can relate to my videos! If you ever have any questions, please don't hesitate to ask. I wish you the very best!!
laurenvparrott 3 years ago
I'm glad that you wrote! I'm graduating in May!! I am lucky to have my family around, since I am from Ann Arbor. I'm also participating in the clinical trial for the new drug Campath 1H, so I should receive my first treatment this month!
kyriedearie 3 years ago
Oh wow! Only a few more months until you graduate - can you believe it? Good luck with the Campath trial, and please let me know how it goes!
laurenvparrott 3 years ago
bless your heart!!
Ive had ms for 2 years,doing okay.
Ive had 2 relapses.
I know how hard ms can be,and like u said,getting stress out of your life is a buncy of bs!!
I have 2 kids,ones 11,and my baby is 6,yeah,huge stresser!!
ss to hear of your grandma,my father in law just passed away a few months ago of bladder cancer..
aly
macycj 3 years ago
Hi Aly! Thank you so much for your comment. It's so true - taking stress out of your life is impossible. Thank you for your condolences. I'm so sorry to hear about your father in law. I hope you're having a wonderful 2009 so far, and I hope your kids are doing well!
laurenvparrott 3 years ago
I was just diagnosed on 12/10 and your videos have helped me.
serrabeth 3 years ago
I'm glad they have helped you! You are going to be just fine - I hope you enjoy the holidays!! Please write to me anytime!
laurenvparrott 3 years ago
My father has MS... its really nice watching your movies cause it gives me a deeper insight on hows its to live with it, thanks!!
polarlarve 3 years ago
Thank you very much. I wish you and your father the best!
laurenvparrott 3 years ago
im really sorry about your grandmother, she is in a better place, try not to think too much about it if you can help it. How re you doing? Relapses will go away, i have the same problems with my hands, even when im typing, took my mri yesturday, stress is the only thing i have to fight. Good luck with you, get better.
Nick go gators:-)
nsirgado 3 years ago
Thank you so much for your concern. I'm doing very well and I pray to her all the time! Yes, stress is the only thing that I have to fight so I try hard not to get stressed! Good luck to you as well!
laurenvparrott 3 years ago
hola lauren no se si puedas leer espanol pero igual te mando el mensaje mi esposo le diagnosticaron ms y siempre trato que tenga el mismo espiritu que tiene tu .cuidate mucho y suerte
ulisesestaco 3 years ago
Hola! Non habla español pero deseo le y a su marido mucha suerte!
laurenvparrott 3 years ago
Thank You for being.
Domenic (sans)
sans15 3 years ago
You are so sweet Domenic :)
laurenvparrott 3 years ago
keep on going you are doing great!!
angelrain57 3 years ago
Thank you so much!!
laurenvparrott 3 years ago
Dude at college i got a scare in my last months and every since then i go for check ups and so worried am gonna have a relapse and the doc tells me i have ms , i go in jan for a check up , this week i had a few problems but i think am ok. Dude dont cry i hate seeing girls cry . Man i hope you have a good year.
tonymac2008jtv 3 years ago
You are such a sweetheart! I really hope everything goes well for you. If it is MS, you're going to be fine. With all the medications out there, you'll be stablized and I'm positive that you can handle whatever happens. Please keep me posted and write if you have any quetions!!
laurenvparrott 3 years ago
Keep going!
sans15 3 years ago
Thank you! I'm trying!
laurenvparrott 3 years ago
Lauren, you are a beautiful spirit.
Matt
ibuzzproautomation 3 years ago
Aww, thank you so much :)
laurenvparrott 3 years ago
keep it up!!!!!!!! BTW GO BUCKEYESSSSSSSS lol
skullroses 3 years ago
Thank you! Hahah...very funny...GO SPARTANS!
laurenvparrott 3 years ago
Keep strong. I feel so bad seeing anyone going through something that makes life hard. I have heart problems and it started when I was 32. Keep strong. I try.
jenniferashley99 3 years ago
Thank you so much - I wish you well, and hope you are staying strong as well!
laurenvparrott 3 years ago
So pleased you play the piano, the last attack finished off this skill because my hand-connections have re-grown around the wheel chair. So keep tinkering! And tell the voices of subvocal thinking, internal and external that we all have, to SHUT UP.
Alexknobsob 3 years ago
I'm so sorry that your last attack finished off that skill - I wish you the best of luck with everything!
laurenvparrott 3 years ago
YES LET STRESS GO AWAY FROM UR LIFE...in ur mind say ur strong and ignore the MS eat healthy and be strong :)
OMoonliteO77 3 years ago
Thank you! I couldn't agree more!
laurenvparrott 3 years ago
You are awesome girlfriend! You WILL get through this! You're way too strong not to.
meggiemeg86 3 years ago
Thank you so much!
laurenvparrott 3 years ago
Hello Lauen, I have MS I was DX FEB. 2008. I get tremors and I walk with a limp. How long ago did you start having bad tremors. Since you've been dx for 7 yrs. I mri my nero. says I've probaly had it for about 4 yrs. Keep it up.
jgperry73 3 years ago 2
I've had MS for almost 8 years now and the only tremors that I've ever had started in July. They're almost gone now so I'm not too worried about it.
Good luck with everything!
Lauren
laurenvparrott 3 years ago
Lauren - I found your videos from Maya at scrapbookgraphics. I am a digiscrapper inspired by your story. Not sure if you heard but their is a kit for sale by Songbird Ave where the profits go to MS. I plan on buying it.
You are so brave and your videos will do wonders for anyone going through MS. Thank you.
(One more thing. I am also a fellow spartan and am from the detroit area! :))
Hugs!
gingerandjake 3 years ago
Hello! I'm going to look into the kit for sale by Songbird Ave! That's great! Thank you so much for your kind words!
GO GREEN! That's so great that you're a Spartan! And it's nice to hear from someone else in the Detroit area.
I wish you the best!
Lauren :)
laurenvparrott 3 years ago
Don't let MS steal your dreams- you are already an awesome speaker- it is ok to show your emotions too!
Jesus loves you and so do I!
I'll be praying for you sweetie and your GrandMom!
I have MS too- stay strong get your rest and eat well.
Make your GrandMom Proud~ prayers~ Jill
jilljustine 3 years ago
Thank you so much, Jill! I appreciate everything you said! I'm trying my best to make my grandma proud. I hope you're feeling well! God Bless,
Lauren :)
laurenvparrott 3 years ago
Thank you!
laurenvparrott 4 years ago
you're doing great happy for you
jermeal385 4 years ago