keep smiling taylor!! i am 31 and have had long battle on my journey with this stupid disease..ups and downs, as anything else in life.. just stay strong.. check out stem cell research, maybe u'll find a way in :) anything goes.. but also keep fighting it in ur mind, never give in, kill it from within, don't let anyone tell u its impossible! you're a true fighter.. well done! :)))
You are a very brave, beautiful and amazing young lady. ^5. Never give up. M.S. may be a disability to some but I feel that it is just another challenge that I must conquer! Hold fast and stay strong Taylor.
@ Vampira305 - I was on Copaxone for almost 11 years and although it kept my relapses to a minimum, it gave me so many keloid scaring that I just couldn't take it any more. There is a new pill on the market now called Gilenya and it works great for me.
I know its easy for me to say stay strong, but U really have to stay strong to fight the fight. Prayer helped us as our Love was put to the test, In the end our Love was what we drew from as it got stronger everyday. I hope the best for u in your battle with M.S....do good...Tim Lia
Im 28 and was diagnosed when I was 23..Fight the good fight sweetie..Im using this illness to fuel my work in film..Actually working on a documentary on how it effects people our age..Teens and 20s..
The picture where you were laying in the hospital bed and your mother was covering up her eyes was so touching. I have so much respect for you and your family, it's unbelievably what you have been trough. I myself have been diagnosed with MS on my 19th and I'm 20 years old now. It was such a struggle for me finding the right medicins and the right doctors and i still haven't found it yet. I'm glad the chemo is working fine with you! You better kick some ass and fight that MS!! :D
Forgot to add - I'm 29 & was diagnosed on 27/02/2008 I have a ten year old daughter and 6 year old boy I work in engineering... I live my life to the full and each day is special! My motto is Live, Love, Laugh x feel free to subscribe to me or add me on Facebook xx
Hey Taylor. I was dx'd at 19 but a MS specialist I see now is positive that my MS started when I was around 8. It's a hellish thing to be diagnosed with a disease they can't cure and worse to be so young. Be grateful for that though because I went through hell growing up knowing something was wrong and docs told me I was making it all up - it was all in my head - which is ironic since I have quite a few lesions in my head!!! Anyway, keep climbing. Contact me if you want to chat! Hang tough
hi taylor, i have MS too! you know something about the CCSVI treatment? i had an angioplasty of my neck veins and my MS is now super weak (gone?)! i'm so happy with it! (sorry for my english, i come from germany). if you want you can write me a personal mail in youtube :) have a great new year!
hola taylor en mi pais se esta implementando un nuevo sistema utilizando celulas madres para ayudar a esta enfermedad...te puedo proporcionar informacion anitapink1915@hotmail.com ya que mi tio padece esta enfermedad.....
Hey Taylor! I'm Tiffany, i also have MS i was diagnose a 19 im 23 now.. I'm currently enrolled in a stem cell transplant in Chicago, starting in January! i dont really check my email much but i would really like to share story's with you! i use Facebook alot so if you would like to talk add me on there =]
Hi,I am herbalist I am show your video that you have MS desease beating you every day if you need my help we able to help you.only you need to do talk to me at Tasomancientherbal@yahoo.com thank you Chea
If you are open to alternatives outside the medical model that are effective against your condition I can forward you information that you can study and understand and have your health restored but it won’t be overnight. If you are not open then I won’t waste my time.
Hi Taylor..I wish I had the words of wisdom that would strike a chord with you and truly keep you inspired to fight the MonSter...the only thing I can say is one to never never never give up..one day and, yes, in our lifetime, there will be a cure..I feel this with my whole heart..I see that burning light of desire in your eyes to be rid of "it"...please keep the fire lit at all times...much peace love and light to you <3 Jayne (I'm on FB Jayne Thomas)
Taylor, your video touched me deeply. My prayers to you and your family, and my hope is that you'll have a miraculous remission. You are a beautiful girl, with a beautiful heart.
your a beautiful girl, and your video was touching.. I also have MS and i'ma whole lot older than you! :) Your one brave girl, keep on fighting, making your dreams come true..... I have a facebook page, where there are alot of other ppl with ms and a few girls your age too..... look under LifeCoachMs on facebook... :)
I have a daughter named Taylor. Help Jeff Johnson raise money for research to find a cure for Multiple Sclerosis. Visit his fundraising home page at nationalMSsociety home page and add to the URL /goto/jeffjohnson
Keep up the fight. Im 43 and I have MS. I swim 6 miles, bike 75 miles, and run 15K a week. So you see you can fight at any age. God only knows what is in your future. He has given you a this trial for you to fight. The only thing I can say is dont let the dx of ms be a fence to your dreams. Its not fun but I use the pain to remind me that life needs to be lived allways the best you can.
Thanks for sharing this video. My son Zach is 14 and was just diagnosed with MS a few days ago. I'd like to show him this video once the shock of it all subsides. -Peace-
Thanks for sharing this video. My son Zach is 14 and was just diagnosed with MS a few days ago. I'd like to show him this video once the shock of it all subsides. -Peace-
Hello Everyone. I'm here to report with joy that none of you have MS! :)
All you have to do to change your life is visit a wellness centre and have them do a test for ALL HEAVY METALS in your body. You will be shocked at the test results.
They say EVERY human has metals in their body. You can't avoid them.
Once the mercury, aluminum, and tin are out of you along with all other heavy metals you will feel like a new person and be cured of MS within days.
YOU are amazing, I am 17 years old and have MS I have to take a drug called copaxone. I will so share my story with you!!!! its so hard for me sometimes but my family and friends are awemazing.
Your amazing. I am 37 and going through the diagnosis now. But looking at your video makes me ok with what happens. I do believe it is in gods hands. Thank you Taylor for showing me it is ok.
Wow although I do not have MS you are truly amazing and an inspiration to others. One comment below from MsMarshall61 about great nutrition. She is correct there are products that will feed the body balanced nutrition. Your body is a machine and when fed properly it works in ways we never thought possible. I battle fibro but through great nutrition you would never know today.
3 things are all you need. God, family & Ann Boroch. All have helped me survive my ms. You are so much stronger than I was when I was suffering through my attack at 24yrs old. I thought my life was over & I was willing to end it if I had to wake up everyday feeling like I was 100yrs old. YOU, my darling are an inspiration to all of us who suffer. There is a cure & I know you will find it. It starts w/ faith & knowledge, & Ann Boroch is your first step to knowledge, you just have to have faith :)
There is now a Reformed Multiple Sclerosis Society that is urging for the medical community to check out Dr Paolo Zamboni's discovery that MS is caused by poor blood drainage from the brain. The answer to restore this blood drainage from the brain is angioplasty. Watch the before & afters for this surgery called CCSVI on youtube- simply amazing. In just 24 hours a world of difference. Standing on one foot eyes closed in just 24 hours!
I wish people. Could understand the many phases of multiple scleriosis are different. I've had for 8 yrs . Its so hardbto explain. People don't care to understand. So sad you inspire me keep hope. And do the best you can.
Taylor, at 15 ur stronger than i am, ur an insperation to us all, i'm 38 and had M.S for 20 years. My mind is my power, today i am "cured" tomorro who cares.(thats how i run my life). Loved your video so touching. Ur amazing. I am on Avonex, and never have thought about anything else. "if it aint broke why fix it" hope u find ur miracle treatment. and yes each treatment reacts diffrent to each person. take care & ur a winner, keep strong sweetie ♥
Taylor, I was diagnosed at 35 and found it shocking. You are a remarkable young woman to have gone through so much at such an early age. amazing. I'm sure many many people will have recommendations and suggestions but as we know, its very individual. I found help through nutrition and through a change in my belief system. Now, I focus on creating hahalala - health and happiness and love and laughter all - I wish you a long lifetime of hahalala. please get in touch if you need -Lisa@hahalala.com
Taylor your video will touch thousands, well done. You are already an inspiration. Please contact people like Dr. David Hubbard Neurologist at the Hubbard Foundation whose son has MS and CCSVI and Joan Beale of CCSVI Alliance who brought Dr. Zamboni's theory of CCSVI to the world. You have a great future ahead of you and you need to surround yourself with people who are well respected and have up to date information from around the world about all the possible treatments. Please never give up.
An amazing young woman her courage and faith leaves me at ahh and just proves to me that I have nothing to complain about and to continue my fight. God bless you Taylor!!!
Dont go to the quack docs out there whom most are money hungry. Pls take care of urself. if you have any questions or concerns feel free to contact me...
I am truly sorry you need to handle this insidicous disease. Pls if your ever thinking about ccsvi do a lot of research with an adult family member. Pls keep in mind ccsvi is in the "experimental stage." its not covered by insurance and if it does get paid for by a insurance carrier its was billed fraudently. if you are interested make sure to get into a clinical trial.
Dont go to the quack docs out there who most are money hungry. pls take care of urself. if you have any questions or concerns feel free to contact me...
I am truly sorry you need to handle this insidicous disePls if your eve thinking about ccsvi do a lot of research with an adult family member. pls keep in mind ccsvi is in the "experimental stage." its not covered by insurance and if it does get paid for by a insurance carrier its was billed fraudently. if you are interested make sure to get into a clinical trial.
Hi sweetie, I am so sorry you are going through all that you are. I cannot imagine being so young and having to fight this awful disease. You are so very strong. Trust me, attitude is so very important! I see alot of posts telling you to be treated for CCSVI- please, PLEASE do tons of research before even considering this option. I myself would never have it done, especially considering the lack of info on it and it's ramifications in the future. Feel free to contact me if you ever need to talk!
Hi sweetie, I am so sorry you are going through all that you are. I cannot imagine being so young and having to fight this awful disease. You are so very strong. Trust me, attitude is so very important! I see alot of posts telling you to be treated for CCSVI- please, PLEASE do tons of research before even considering this option. I myself would never have it done, especially considering the lack of info on it and it's ramifications in the future. Feel free to contact me if you ever need to talk!
Taylor, the best answer to MS, besides the strength and spirit you're showing, is to fight it. Not with drugs and chemotherapy, but by treating CCSVI. Ask those you love to look into it for you. You need the names of clinics that do interventional radiology to perform angioplasty for the treatment of CCSVI in the U.S. They don't allow it in Canada. You'll need money & you'll be sure to get people to come to fundraisers.
Best of luck to you, and let us know how you're doing in your fight
Taylor, I have MS and i have a young daughter too. She is now 12. Your video touched me deeply! Please look into CCSVI. There is huge evidence to support that it's not auto immune but rather vascular. Best wishes!
Taylor, its Chantele, your such a strong girl and i want you too hold on forever :( i miss you and i really hope i can see you soon.. you were one of my best friends and i hear about this! i truely hope u ge better and healthier, i know its uncurable but you can definitely fight for your life and get through this! just wanted to say i love you, and miss you tons <33333
i remember when you were born, and i remember that cute litlle baby, that toothless little girl with the infectious smile and laugh that could get a whole room going. after all youve been through you have that same sparkle in your eyes and amazing positivity. You are stronger than i ever could hope to be and i admire you for for that .
Your video almost made me cry, It looks like you had the same kind of onset I had- sudden and severe. I've heard rumours that people as young as you get this disease but to actually see it is another story. You're strong and you WILL conquer it. Blessings and thanks for sharing.
Beautiful young lady with a true fighting spirit -you could teach me a few things in strength..WOW this video really touched me. I've been struggling with an undiagnosed illness, and I see how much you have had to endure at such a young age. Thanks for sharing your story of strength and inspiration...Gentle hugs go out to you...
keep smiling taylor!! i am 31 and have had long battle on my journey with this stupid disease..ups and downs, as anything else in life.. just stay strong.. check out stem cell research, maybe u'll find a way in :) anything goes.. but also keep fighting it in ur mind, never give in, kill it from within, don't let anyone tell u its impossible! you're a true fighter.. well done! :)))
love
sandyd15 2 days ago
God bless you! :)
CLovesMusic5 6 days ago
You are a very brave, beautiful and amazing young lady. ^5. Never give up. M.S. may be a disability to some but I feel that it is just another challenge that I must conquer! Hold fast and stay strong Taylor.
@ Vampira305 - I was on Copaxone for almost 11 years and although it kept my relapses to a minimum, it gave me so many keloid scaring that I just couldn't take it any more. There is a new pill on the market now called Gilenya and it works great for me.
Ang4Indie 1 week ago
God Bless you :)
Vampira305 2 weeks ago
Im 29 and got my DX on 02/01/2012 I will be taking Copaxone soon and cant wait for it to start working. The brain fog really sucks!
Bigbully0110 2 weeks ago
I know its easy for me to say stay strong, but U really have to stay strong to fight the fight. Prayer helped us as our Love was put to the test, In the end our Love was what we drew from as it got stronger everyday. I hope the best for u in your battle with M.S....do good...Tim Lia
easyalia51 3 weeks ago
Im 28 and was diagnosed when I was 23..Fight the good fight sweetie..Im using this illness to fuel my work in film..Actually working on a documentary on how it effects people our age..Teens and 20s..
BOBBIEWANKENOBI 3 weeks ago
Fight on!!! I'm 30 now and I was DX with MS when I was 18. You're too young for this mess..but you're a true fighter!!! <3
steffi1281 3 weeks ago
Hi
i got ms when i was 12 years old, i am 16 years old now, and i know how it is to have ms.
We should just fight
xxILOVEMUSIC100 3 weeks ago
I find it very inspiring how you managed to smile in some of those pictures...
TheGreatestChuck 1 month ago
The picture where you were laying in the hospital bed and your mother was covering up her eyes was so touching. I have so much respect for you and your family, it's unbelievably what you have been trough. I myself have been diagnosed with MS on my 19th and I'm 20 years old now. It was such a struggle for me finding the right medicins and the right doctors and i still haven't found it yet. I'm glad the chemo is working fine with you! You better kick some ass and fight that MS!! :D
TheEternalScream 1 month ago
I have MS&my daughter who is 13teen will be undergoing test.My prayer tht she does not get it.I pray in the name of Jesus.
2011iam4god 1 month ago
Forgot to add - I'm 29 & was diagnosed on 27/02/2008 I have a ten year old daughter and 6 year old boy I work in engineering... I live my life to the full and each day is special! My motto is Live, Love, Laugh x feel free to subscribe to me or add me on Facebook xx
ms26babe 1 month ago
Hi Taylor - to all of you lovely young people I don't know what to say alls I can say is it's a long hard fight and we will win this battle !
ms26babe 1 month ago
hi taylor i am 14 and was diagnosed when i was 10
if you could add me on facebook it would be fantastic to talk to someone
hilmir98 1 month ago
Hey Taylor. I was dx'd at 19 but a MS specialist I see now is positive that my MS started when I was around 8. It's a hellish thing to be diagnosed with a disease they can't cure and worse to be so young. Be grateful for that though because I went through hell growing up knowing something was wrong and docs told me I was making it all up - it was all in my head - which is ironic since I have quite a few lesions in my head!!! Anyway, keep climbing. Contact me if you want to chat! Hang tough
megster347 1 month ago
hi taylor, i have MS too! you know something about the CCSVI treatment? i had an angioplasty of my neck veins and my MS is now super weak (gone?)! i'm so happy with it! (sorry for my english, i come from germany). if you want you can write me a personal mail in youtube :) have a great new year!
Glysity 1 month ago
hola taylor en mi pais se esta implementando un nuevo sistema utilizando celulas madres para ayudar a esta enfermedad...te puedo proporcionar informacion anitapink1915@hotmail.com ya que mi tio padece esta enfermedad.....
anitamata1915 1 month ago
oops this is my fb name.... lol tiffanyrae542
tiffanyrae542 2 months ago
Hey Taylor! I'm Tiffany, i also have MS i was diagnose a 19 im 23 now.. I'm currently enrolled in a stem cell transplant in Chicago, starting in January! i dont really check my email much but i would really like to share story's with you! i use Facebook alot so if you would like to talk add me on there =]
tiffanyrae542 2 months ago
Hi,I am herbalist I am show your video that you have MS desease beating you every day if you need my help we able to help you.only you need to do talk to me at Tasomancientherbal@yahoo.com thank you Chea
cheasom1 2 months ago
cutie!
missy2131 2 months ago
Comment removed
vancouverislandbass 2 months ago
If you are open to alternatives outside the medical model that are effective against your condition I can forward you information that you can study and understand and have your health restored but it won’t be overnight. If you are not open then I won’t waste my time.
Ray Mikelonis
stemcellrx@comcast.net
517-575-0072
stemcellrx 2 months ago
Hi Taylor..I wish I had the words of wisdom that would strike a chord with you and truly keep you inspired to fight the MonSter...the only thing I can say is one to never never never give up..one day and, yes, in our lifetime, there will be a cure..I feel this with my whole heart..I see that burning light of desire in your eyes to be rid of "it"...please keep the fire lit at all times...much peace love and light to you <3 Jayne (I'm on FB Jayne Thomas)
jayne4ccsvi 2 months ago
Taylor, your video touched me deeply. My prayers to you and your family, and my hope is that you'll have a miraculous remission. You are a beautiful girl, with a beautiful heart.
anniemohon 2 months ago
your a beautiful girl, and your video was touching.. I also have MS and i'ma whole lot older than you! :) Your one brave girl, keep on fighting, making your dreams come true..... I have a facebook page, where there are alot of other ppl with ms and a few girls your age too..... look under LifeCoachMs on facebook... :)
Jenna007able 2 months ago
I have a daughter named Taylor. Help Jeff Johnson raise money for research to 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
Keep up the fight. Im 43 and I have MS. I swim 6 miles, bike 75 miles, and run 15K a week. So you see you can fight at any age. God only knows what is in your future. He has given you a this trial for you to fight. The only thing I can say is dont let the dx of ms be a fence to your dreams. Its not fun but I use the pain to remind me that life needs to be lived allways the best you can.
pcadams1 3 months ago
God bless you xoxo
Velocitygrl34 3 months ago
This has been flagged as spam show
Thanks for sharing this video. My son Zach is 14 and was just diagnosed with MS a few days ago. I'd like to show him this video once the shock of it all subsides. -Peace-
generalbomax 3 months ago
Thanks for sharing this video. My son Zach is 14 and was just diagnosed with MS a few days ago. I'd like to show him this video once the shock of it all subsides. -Peace-
generalbomax 3 months ago
This has been flagged as spam show
Hello Everyone. I'm here to report with joy that none of you have MS! :)
All you have to do to change your life is visit a wellness centre and have them do a test for ALL HEAVY METALS in your body. You will be shocked at the test results.
They say EVERY human has metals in their body. You can't avoid them.
Once the mercury, aluminum, and tin are out of you along with all other heavy metals you will feel like a new person and be cured of MS within days.
I swear this on my own life!
vancouverislandbass 3 months ago
Hey! Talk to me! I cured my OWN MS!
vancouverislandbass 3 months ago
@vancouverislandbass How ??
561400 2 months ago
This has been flagged as spam show
@561400 Send me an inbox message and I will explain everything.
vancouverislandbass 2 months ago
YOU are amazing, I am 17 years old and have MS I have to take a drug called copaxone. I will so share my story with you!!!! its so hard for me sometimes but my family and friends are awemazing.
tigger93ify 3 months ago
Your amazing. I am 37 and going through the diagnosis now. But looking at your video makes me ok with what happens. I do believe it is in gods hands. Thank you Taylor for showing me it is ok.
sexykymmi 4 months ago
Wow although I do not have MS you are truly amazing and an inspiration to others. One comment below from MsMarshall61 about great nutrition. She is correct there are products that will feed the body balanced nutrition. Your body is a machine and when fed properly it works in ways we never thought possible. I battle fibro but through great nutrition you would never know today.
Nancy
SocialMediaMarketer 4 months ago
3 things are all you need. God, family & Ann Boroch. All have helped me survive my ms. You are so much stronger than I was when I was suffering through my attack at 24yrs old. I thought my life was over & I was willing to end it if I had to wake up everyday feeling like I was 100yrs old. YOU, my darling are an inspiration to all of us who suffer. There is a cure & I know you will find it. It starts w/ faith & knowledge, & Ann Boroch is your first step to knowledge, you just have to have faith :)
nika00chu 6 months ago
This has been flagged as spam show
There is now a Reformed Multiple Sclerosis Society that is urging for the medical community to check out Dr Paolo Zamboni's discovery that MS is caused by poor blood drainage from the brain. The answer to restore this blood drainage from the brain is angioplasty. Watch the before & afters for this surgery called CCSVI on youtube- simply amazing. In just 24 hours a world of difference. Standing on one foot eyes closed in just 24 hours!
2ndSamuel710 6 months ago
Keep up the good work with proper research and treatments!
James
SuperIRONMAN66 6 months ago
I wish people. Could understand the many phases of multiple scleriosis are different. I've had for 8 yrs . Its so hardbto explain. People don't care to understand. So sad you inspire me keep hope. And do the best you can.
22bellas 7 months ago 2
Taylor, at 15 ur stronger than i am, ur an insperation to us all, i'm 38 and had M.S for 20 years. My mind is my power, today i am "cured" tomorro who cares.(thats how i run my life). Loved your video so touching. Ur amazing. I am on Avonex, and never have thought about anything else. "if it aint broke why fix it" hope u find ur miracle treatment. and yes each treatment reacts diffrent to each person. take care & ur a winner, keep strong sweetie ♥
n95johnny 8 months ago 2
Please don't do anything with CCSVI yet.....It is still early days I have been damaged irreversibly from the treatment:( plus I still have MS.
whyworryabout2moro 8 months ago
Taylor, I was diagnosed at 35 and found it shocking. You are a remarkable young woman to have gone through so much at such an early age. amazing. I'm sure many many people will have recommendations and suggestions but as we know, its very individual. I found help through nutrition and through a change in my belief system. Now, I focus on creating hahalala - health and happiness and love and laughter all - I wish you a long lifetime of hahalala. please get in touch if you need -Lisa@hahalala.com
MsMarshall61 8 months ago
Taylor your video will touch thousands, well done. You are already an inspiration. Please contact people like Dr. David Hubbard Neurologist at the Hubbard Foundation whose son has MS and CCSVI and Joan Beale of CCSVI Alliance who brought Dr. Zamboni's theory of CCSVI to the world. You have a great future ahead of you and you need to surround yourself with people who are well respected and have up to date information from around the world about all the possible treatments. Please never give up.
BevBentley 9 months ago
An amazing young woman her courage and faith leaves me at ahh and just proves to me that I have nothing to complain about and to continue my fight. God bless you Taylor!!!
garcialiset 9 months ago
Dont go to the quack docs out there whom most are money hungry. Pls take care of urself. if you have any questions or concerns feel free to contact me...
MrsSassy71 11 months ago
I am truly sorry you need to handle this insidicous disease. Pls if your ever thinking about ccsvi do a lot of research with an adult family member. Pls keep in mind ccsvi is in the "experimental stage." its not covered by insurance and if it does get paid for by a insurance carrier its was billed fraudently. if you are interested make sure to get into a clinical trial.
MrsSassy71 11 months ago
Dont go to the quack docs out there who most are money hungry. pls take care of urself. if you have any questions or concerns feel free to contact me...
MrsSassy71 11 months ago
I am truly sorry you need to handle this insidicous disePls if your eve thinking about ccsvi do a lot of research with an adult family member. pls keep in mind ccsvi is in the "experimental stage." its not covered by insurance and if it does get paid for by a insurance carrier its was billed fraudently. if you are interested make sure to get into a clinical trial.
MrsSassy71 11 months ago
I am truly so so sorry youI implore you & a adult family member needs to research ccsvi
MrsSassy71 11 months ago
Hi sweetie, I am so sorry you are going through all that you are. I cannot imagine being so young and having to fight this awful disease. You are so very strong. Trust me, attitude is so very important! I see alot of posts telling you to be treated for CCSVI- please, PLEASE do tons of research before even considering this option. I myself would never have it done, especially considering the lack of info on it and it's ramifications in the future. Feel free to contact me if you ever need to talk!
bettefan1 11 months ago
Hi sweetie, I am so sorry you are going through all that you are. I cannot imagine being so young and having to fight this awful disease. You are so very strong. Trust me, attitude is so very important! I see alot of posts telling you to be treated for CCSVI- please, PLEASE do tons of research before even considering this option. I myself would never have it done, especially considering the lack of info on it and it's ramifications in the future. Feel free to contact me if you ever need to talk!
bettefan1 11 months ago
Taylor, the best answer to MS, besides the strength and spirit you're showing, is to fight it. Not with drugs and chemotherapy, but by treating CCSVI. Ask those you love to look into it for you. You need the names of clinics that do interventional radiology to perform angioplasty for the treatment of CCSVI in the U.S. They don't allow it in Canada. You'll need money & you'll be sure to get people to come to fundraisers.
Best of luck to you, and let us know how you're doing in your fight
curmudgeonine 11 months ago
Taylor, I have MS and i have a young daughter too. She is now 12. Your video touched me deeply! Please look into CCSVI. There is huge evidence to support that it's not auto immune but rather vascular. Best wishes!
ccsvitreat 11 months ago
Taylor, its Chantele, your such a strong girl and i want you too hold on forever :( i miss you and i really hope i can see you soon.. you were one of my best friends and i hear about this! i truely hope u ge better and healthier, i know its uncurable but you can definitely fight for your life and get through this! just wanted to say i love you, and miss you tons <33333
chanchan331 1 year ago
i remember when you were born, and i remember that cute litlle baby, that toothless little girl with the infectious smile and laugh that could get a whole room going. after all youve been through you have that same sparkle in your eyes and amazing positivity. You are stronger than i ever could hope to be and i admire you for for that .
I love you the most pretty girl XOXOXOX
rachellep100 1 year ago
Your video almost made me cry, It looks like you had the same kind of onset I had- sudden and severe. I've heard rumours that people as young as you get this disease but to actually see it is another story. You're strong and you WILL conquer it. Blessings and thanks for sharing.
canadianjuliet 1 year ago
Beautiful young lady with a true fighting spirit -you could teach me a few things in strength..WOW this video really touched me. I've been struggling with an undiagnosed illness, and I see how much you have had to endure at such a young age. Thanks for sharing your story of strength and inspiration...Gentle hugs go out to you...
Jen
tiredofbeingsick 1 year ago
Taylor stay strong you can do this!!
shortyc81 1 year ago
ROCK THE HELL ON!!!..DONT LET IT BEAT YOU!!!...YOU DA WOMAN!!!
topp81101 1 year ago