Madde, I was diagnosed when I was just 11 years old, I'm 19 now. At the time I was too young to realize what it could mean for my future and it only really hit me this last year. I have had the same thoughts, that theres nothing I can do and its very frustrating. Its ok to be upset about it for a little while but eventually we have to keep living our lives. I most often use it as a motivator for my physical fitness. Gotta use it while I gotta it. I'll be doing a 5 mile mud run for MS this week!
Beautiful people. They are happier than us with our stupid problems, they appreciate more the things they have left. The cute, Spanish girl brought me to tears- what a beautiful soul, an angel.
I'm 26, and my whole right leg went numb 6 months ago. Then I woke up speaking like I was drunk, handwriting deteriorated, and my balance was off, so I was taken to the hospital for a possible stroke. My speech and writing have come back, but I now get strange brain attacks(which I can now feel coming) where if I'm speaking I suddenly sound like someone has slowed my speech down to 20% speed or very slow motion Those typically last about 5-15 seconds. I'm so scared. Now, in the past 4 days, all 10 toes feel numb, and my right thumb becomes numb randomly through the day. I have 2 MRI'S of the brain wednesday, and 2 more on Thursday. This is so hard to live with, and I haven't even been diagnosed yet(I just know it in my heart), but I know we can all get through this, one day at a time. 🙏✌💕
saraev1119 today i was suppose to get my diagnosis and he said i dont have enough lesions to diagnos me with MS yet ive been found positive for Lhermitte's sign and my upper neck hurts wayyyyy to much... alot of the symthoms that i hear on youtube match my symthoms im having... still i have to go through MRI and perscribed me a pain killer so i wont feel the pain in the nerves and shaking of the thumb.. i get numbness more often than usual.. I praying to my Lord Jesus Christ that he will cure me from this disease what ever it is... Im raising my 4 children alone and its terrifying dealing with all this and feeling fatigued while your at it.. Im Hopeful God will do a miracle and I will be a living testimony that He cured me from this and any other disease
2012 my diagnosis came after a visit to a pre booked ophthalmologist sent me to neuro because I had gone blind in one eye 4 times, after MRI I was later told I had rrMS. 6 months later I had relapse that almost wiped me out. I was 42, I got better, I worked like crazy to fix myself, I still have some pretty bad symptoms but with copaxone (dmt) and some other meds it's okay and I'm still living a normal life. Huge thanks to all who have treated my MS.. It makes it possible to be okay.
ok now really the 7 people that disliked this video plz tell me why these people are opening there hearts to us and trying to sit there and tell us how they got it and what they are going through!
Maybe they were very very, very annoyed by the horribly pathetic piano soundtrack. Just imagine that you were diagnosed x MS, and, already losing hope in having a happy future, you stumble upon this pathetic realitytv drama... Imagine 2 sec. Sheep.
I love this video. After 25 years of MS, watching this video is inspiring and heart breaking. I relate with each of them, but MS has been easier and harder for me.
All we can do is make the best of life. Pain is inevitable, but suffering is optional. I try my best to live in other people's world if I'm not digging mine at the moment.
My neurologist has moved away now. The new doctor has not returned my calls for nearly 2 weeks. I know I am a stubborn guy in his 60s, but this is hard. My wheelchair is broken and I do have a new one on order but the supplier hasn't called me. Living alone is the hardest thing for me really. Forgive me my whining please and be strong.
i am 41 and i now i ive got ms this last 8 months. i have the same feeling, and know with the help of my family i continue my life how i can . i know its not that easy but keep it up god help you
I also have Multiple sclerosis and its been yr.I'm not at all enjoying this.Being subjusted to wheelchair,blind or paralysis are the this I fear the most.
my cousin-in-law carolene was diagnosed when she was still a student in manchester. 30 years on and she needs full time carers, which my cousin is lucky enough to afford. it's the slow progress of the disease that fools people into not really believing it, in a way; some of them lack empathy and if they can't see physical symptoms then they fool themselves into thinking that it can't exist especially since it doesn't affect them!
i have MS since 2012 and undergone treatment last 2015..my 2nd Nuero Doctor said that I should maintain corticosteroid Prednisone so I did,. i became fat and pimples spread all over my face.I was feeling okay so I took the drug for 5months and then here comes a month were i didn't have a period so i thought that I am pregnant.I consulted an OB and find out that steriod is not good for the baby..She said I should ask my neuro.my 1st nuero saw me and ask what happened to my face i said my 2nd nuero told me to maintain steroid.He said Steroid is not for maintenance so He change and give me a multivitamin with Iron..Its been a month since I stopped steroid and take multivitamins with iron and I felt just the same when i was taking steroid but felt relieved knowing that multivitamins was good for me.(after i consulted an OB my peroid came...false alarm) BE STRONG AND HAVE FAITH WE HAVE GOD TO BE WITH US ALWAYS!!
Yes thank you :-). With me it's my right leg that is paralysed. I really do appreciate your kind words. There are still so many people in ignorance about the disease. If you can't see it on the outside than you must be fine on the inside. Thanks for your concern.
I hope it continues for you. I too was diagnosed and refused to accept it because I didn't have symptoms and felt totally healthy as you do. Well after about three years it did hit me HARD and it has been downhill since. I should have been on injections when I was diagnosed and maybe it might have been different.
I was diagnosed with primary progressive ms in 2012 1st symptom 2003 used cannabis oil in 2017 and after 3 doses neuropathic pain stopped as did spasms in both legs and arm havnt had them since
My mom is suffering from dis.. N my biggest fear is dt i might lose my mom soon evn b4 i cud fulfill hr every wish.. Evn though new technology r still producng day by day.. Bt no cure is still there for n it breaks my heart.. Aftr watchng dis video now i knw dt my mom os nt d only 1.. Feel a bit encouraged aftr watchng ol dis people.. Thnk u so much for posting
this inspired me a lot... my diagnosis came out just a month ago and it really stress me out because i'm from a country where this type of disease was a kind of rare. i really wish to meet other who suffer ms so that i can hear their experience and also share mine. i cant help but crying when watching this video. will mine be worse than they?? >
Amazing video! It's not just Europe though... Millions of people worldwide are affected by this disease. But we can do something about it. March happens to be MS Awareness month. MS is not something to be taking lightly, and spreading the world might be the one deed we can do for the rest of us. There are tons of organizations, striving to research and raise awareness for MS. There's MS Society and even MSAA (Multiple Sclerosis Association of America). It's never too late to start.
My neurologist specifically stated that the Extavia may halt the progression of the disease. It will never be gone, but it could possible prevent my MS from getting worse.
Madde there are so many meds that you can inject to help halt the disease. It doesn't mean your life is over. You found it early and the possibilities of living a "normal" life without MS is certainly a possibility. Don't give up!!!
I am getting tested after this covid is over... I’ve had symptoms for years and no doctor has taken me seriously because I am now turning 17 with all these symptoms. I have every symptom of MS to a T. No more no less. I am terrified. I don’t want to panic until I am tested. Can I ask if anyone in the comments has it and has had it since a young age/ how you guys deal with it?? I really don’t want to end up in a wheelchair or physically unable to do what I love... my passion is training animals, I love working with large dogs. And to train a pulling 100+ pound dog I have to have strength. :(
Kiara Ellis I don’t think there is a symptom on the list I don’t have. But I will stick to the main ones. I have had extreme fatigue for years- had to drop out of public school and sports I loved. I have bad hip and joint pain and feel like I pull a muscle if I turn wrong on a daily. I also get really bad spasms- in my legs to the point I can’t move in fear of my whole body spazzing they get so tight. I also have really bad “ restless leg syndrome “ at night- for hours on end where I can’t sleep, it is in my left arm too and they will randomly jerk. I also get lots of pins and needles and my hands go numb. Like right now when I text- my hands go stiff, equal to if someone were trying to text in the freezing cold I describe it.
Kiara Ellis another main thing I struggle with is heat intolerance. I can not function. Even if driving in the car with the sun I get so weak, nauseas and get the worst migraine. It’s impossible going anywhere in summer.
my sister last year died she had MS she the aged of 37she was bed ridding she couldn't walk she had horrific uncontrolled head shaking where it put her spin out of shape I would want anyone to have this disease it is a cruel disease
My school used to do (or I think they still do now) a thing called MS Reading Challenge. A person will sponsor you so much an amount of money for every book you read and all of the money would go ahead to find a cure for MS. I wish I joined it *sigh*
My left thigh muscle is very weak and fatigued the last 3 weeks and I fear I may have ms. Not just the disease, but how much it could cost me just to get any diagnosis, and how long it could take to secure financial aid even if the coronavirus panic wasnt wrecking our economy. In america, if cant afford healthcare or ins, you are fucked if one thing goes wrong.
I think the hardest for me is waiting for diagnosis. You can't join a support group, and they will not speak to you either, until you have a definitive diagnosis...which can take YEARS. It's been 6 years for me so far. I don't have any support from any organisation. This needs to change as many people, like myself, are left in the wilderness to figure it out for themselves. You can join an online discussion group, which helps, but nothing physical like a group you can go out and chat with.
Broxine I will do thankyou. It's taken a long time here due to lack of neurologists where I live. We only have one and he has to cover several counties so waiting for an appointment to see him takes, on average, 6/9 months. X
P.s. Because when I last had the tests for MS there wasn't enough evidence to definitively say I've got MS, they were waiting for me to have further relapses to get more evidence. X
I don't have children. The past 5 years have been unreal, sometimes. It was as if I was in a haunted house. I just have ear pain now. It comes and goes. I feel so much compassion for people like me who did have children. It makes me think. Why don't I just give up? Sit in a chair before my time. Use sign language. My English writing skills have declined. I speak always the clown. Well I aspire to be as perfect as my critics.
My mom went to the doctor for dizziness they said it’s likely she has MS. Doing blood tests tomorrow and they wnat her to see a neurologist ASAP. Scary to think there’s s good chance this will be my moms life now.
sergioortizz covid kinda put a hold on testing but she showing more and more symptoms and her doctor is almost certain she has it just wants to confirm it.
No more sad 'how/when/why I was first diagnosed' stories. No more glossy magazines and advertisements for/about raising money for a cure (and please it's not money to keep these magazines alive!). A CURE! Come on! I've had MS for 21 years, it's now progressive. I know MANY INTELLIGENT CREATIVE DOCTORS, please make a medical discovery as your past cohorts did with something like discovering antibiotics!!! - no more talk, CHANGE! NOW.
@@victorgomez6330 , @mobley Mobley I am ok , after the optic neuritis i never had any subsequent attacks 6 years after, I do take Avonex. It looks like it was a single event for me so far . But that optic neuritis left a bit scared i see differently with that eye
I have learnt one important thing after the diagnosis: "Stop being a damn weak p*ssy!!!" Despite of the "diagnosis" I feel myself totally healthy and I refuse any medical treatment and give a sh*t what my "doctor" says! I don't suffer from symptomes, because I changed my whole lifestyle. There is always one phrase in my mind: I'm not sick!!
Please! I've been ill for 5 years- I was diagnosed with chronic fatigue- but this is simply a number of symptoms for over 6 months. Has anyone had MRI that have not shown lesions? How reliable is MRI and spinal tap for tests? I have so many symptoms of MS and continue to decline. Please respond if you have info or have also had a difficult time getting diagnosed for issues.
I'm 15 and just found out that i have MS.. i dont know, my life is over. And that there is nothing to do. Just accept it and live whit it. it's hard you know? I dont know what to do anymore. All i can say is my life is over..
@@sergioortizz Right now I'm fantastic! I am feeling great and happy! I was scared and worried about it at first, cause i did not really understand what it would do. But really at the end of it all it made me into who I am, it actually helped me to love myself! Sorry if my English is a little of. Typing on my phone and autocorrect is set on Swedish! :D
I was 17 went I woke up blind in one eye. At least these people can seek medical treatment. In the Caribbean you are pushed about because doctors have little or no experience with treating an MS patient. Only the very few can. I am lucky to be treated by one such doctor. But for the others in my country...I can't say.
I m also suffering from ms problem from last 3 mnths......my age is 24.....in starting my legs were not working.....and numbness in hands.....still there is numbness in my hands.......i try to live my life again.....please someone tell me is it a serious problem????
Well. I think you can't describe what MS is. Its a different reality and completely different disease from patient to patient. Long story short.... This is my story.... When I was 5 I ve been diagnosed with diabetes (type 1). When I was 27 years old (3 months after I got engaged) I got my present. MS. Anyway I am 37 now, I got married (same woman), and I have 2 children. I am happy enough I could say. Of course I do face some difficulties on a daily base. Could I be happier? Of course. Could it be worst? Of course, this is fu****ng life. Keep calm and live everyday the perfect day. Oh excuse my English
I have no faith left in the medical profession. Drugs have existed for as long as I have had MS but they won't prescibe them because of cost. They could have helped me but they chose not to.
unclevroomvroom #ms #findAcure I myself have relapsing remitting ms im just trying to find people to talk 2 that can relate because honestly no one knows how it feels unless ur actually living it ...... I’ve made only one ms video hope you have time just to check it out I’m sure ur extremely busy but I’m just trying to reach out for some support. th-cam.com/video/9VekoY7PiGE/w-d-xo.html
Madde, I was diagnosed when I was just 11 years old, I'm 19 now. At the time I was too young to realize what it could mean for my future and it only really hit me this last year. I have had the same thoughts, that theres nothing I can do and its very frustrating. Its ok to be upset about it for a little while but eventually we have to keep living our lives. I most often use it as a motivator for my physical fitness. Gotta use it while I gotta it. I'll be doing a 5 mile mud run for MS this week!
Beautiful people. They are happier than us with our stupid problems, they appreciate more the things they have left. The cute, Spanish girl brought me to tears- what a beautiful soul, an angel.
I'm 26, and my whole right leg went numb 6 months ago. Then I woke up speaking like I was drunk, handwriting deteriorated, and my balance was off, so I was taken to the hospital for a possible stroke. My speech and writing have come back, but I now get strange brain attacks(which I can now feel coming) where if I'm speaking I suddenly sound like someone has slowed my speech down to 20% speed or very slow motion Those typically last about 5-15 seconds. I'm so scared. Now, in the past 4 days, all 10 toes feel numb, and my right thumb becomes numb randomly through the day. I have 2 MRI'S of the brain wednesday, and 2 more on Thursday. This is so hard to live with, and I haven't even been diagnosed yet(I just know it in my heart), but I know we can all get through this, one day at a time. 🙏✌💕
+saraev1119 Please check videos about Vitamin D deficiency, especially "Vitamin D protocol". You can be healed for sure!
+goranvu Don't say "for sure"; that is not fair. Nothing is for sure.
we're here to keep each other up and going #together
saraev1119 look at Dr Coimbra protocol on TH-cam I am starting it getting test done now
saraev1119
today i was suppose to get my diagnosis and he said i dont have enough lesions to diagnos me with MS yet ive been found positive for Lhermitte's sign and my upper neck hurts wayyyyy to much... alot of the symthoms that i hear on youtube match my symthoms im having... still i have to go through MRI and perscribed me a pain killer so i wont feel the pain in the nerves and shaking of the thumb.. i get numbness more often than usual.. I praying to my Lord Jesus Christ that he will cure me from this disease what ever it is... Im raising my 4 children alone and its terrifying dealing with all this and feeling fatigued while your at it.. Im Hopeful God will do a miracle and I will be a living testimony that He cured me from this and any other disease
2012 my diagnosis came after a visit to a pre booked ophthalmologist sent me to neuro because I had gone blind in one eye 4 times, after MRI I was later told I had rrMS. 6 months later I had relapse that almost wiped me out. I was 42, I got better, I worked like crazy to fix myself, I still have some pretty bad symptoms but with copaxone (dmt) and some other meds it's okay and I'm still living a normal life. Huge thanks to all who have treated my MS.. It makes it possible to be okay.
David 7 look at video about Dr Coimbra protocol Vitamin D protocol
David 7 how are you today?
Makes no sense how there is no cure for this by now
ok now really the 7 people that disliked this video plz tell me why these people are opening there hearts to us and trying to sit there and tell us how they got it and what they are going through!
Maybe they were very very, very annoyed by the horribly pathetic piano soundtrack. Just imagine that you were diagnosed x MS, and, already losing hope in having a happy future, you stumble upon this pathetic realitytv drama... Imagine 2 sec. Sheep.
I think they are probably thumbing down MS.
I love this video. After 25 years of MS, watching this video is inspiring and heart breaking. I relate with each of them, but MS has been easier and harder for me.
All we can do is make the best of life. Pain is inevitable, but suffering is optional. I try my best to live in other people's world if I'm not digging mine at the moment.
Dulci Hill Dr Coimbra protocol Vitamin D protocol video on TH-cam
@@DulciHill how do you feel now? Has it gotten any better or eased up for you?
My neurologist has moved away now. The new doctor has not returned my calls for nearly 2 weeks. I know I am a stubborn guy in his 60s, but this is hard. My wheelchair is broken and I do have a new one on order but the supplier hasn't called me. Living alone is the hardest thing for me really. Forgive me my whining please and be strong.
Dave Wolfgang aww . be strong .i hope u bcm okay . tc
i am 41 and i now i ive got ms this last 8 months. i have the same feeling, and know with the help of my family i continue my life how i can . i know its not that easy but keep it up god help you
I also have Multiple sclerosis and its been yr.I'm not at all enjoying this.Being subjusted to wheelchair,blind or paralysis are the this I fear the most.
my cousin-in-law carolene was diagnosed when she was still a student in manchester. 30 years on and she needs full time carers, which my cousin is lucky enough to afford. it's the slow progress of the disease that fools people into not really believing it, in a way; some of them lack empathy and if they can't see physical symptoms then they fool themselves into thinking that it can't exist especially since it doesn't affect them!
I was 16 , my whole right side of my body was paralyzed 😭😞
+Omar Lopez
Have you seen this info? here is a link.
nutritionfacts.org/video/treating-multiple-sclerosis-with-the-swank-ms-diet/
this is inspiring I don't have ms but a lot of my family does.I am inspired to keep faith still
i have MS since 2012 and undergone treatment last 2015..my 2nd Nuero Doctor said that I should maintain corticosteroid Prednisone so I did,. i became fat and pimples spread all over my face.I was feeling okay so I took the drug for 5months and then here comes a month were i didn't have a period so i thought that I am pregnant.I consulted an OB and find out that steriod is not good for the baby..She said I should ask my neuro.my 1st nuero saw me and ask what happened to my face i said my 2nd nuero told me to maintain steroid.He said Steroid is not for maintenance so He change and give me a multivitamin with Iron..Its been a month since I stopped steroid and take multivitamins with iron and I felt just the same when i was taking steroid but felt relieved knowing that multivitamins was good for me.(after i consulted an OB my peroid came...false alarm)
BE STRONG AND HAVE FAITH WE HAVE GOD TO BE WITH US ALWAYS!!
eldy look at Dr Coimbra protocol on TH-cam Vitamin D protocol showing good results
eldy which vitamins?
How are you today my dear?
Yes thank you :-). With me it's my right leg that is paralysed. I really do appreciate your kind words. There are still so many people in ignorance about the disease. If you can't see it on the outside than you must be fine on the inside. Thanks for your concern.
I hope it continues for you. I too was diagnosed and refused to accept it because I didn't have symptoms and felt totally healthy as you do. Well after about three years it did hit me HARD and it has been downhill since. I should have been on injections when I was diagnosed and maybe it might have been different.
I was diagnosed with primary progressive ms in 2012 1st symptom 2003 used cannabis oil in 2017 and after 3 doses neuropathic pain stopped as did spasms in both legs and arm havnt had them since
Sending strength to all of you .
My mom is suffering from dis.. N my biggest fear is dt i might lose my mom soon evn b4 i cud fulfill hr every wish.. Evn though new technology r still producng day by day.. Bt no cure is still there for n it breaks my heart.. Aftr watchng dis video now i knw dt my mom os nt d only 1.. Feel a bit encouraged aftr watchng ol dis people.. Thnk u so much for posting
my cousin and some people i know have this terrible disease. all power to the people who courageously live with it
this inspired me a lot...
my diagnosis came out just a month ago and it really stress me out because i'm from a country where this type of disease was a kind of rare. i really wish to meet other who suffer ms so that i can hear their experience and also share mine. i cant help but crying when watching this video. will mine be worse than they?? >
nasuha zaidi
Hi where are you from?
Amazing video! It's not just Europe though... Millions of people worldwide are affected by this disease.
But we can do something about it. March happens to be MS Awareness month. MS is not something to be taking lightly, and spreading the world might be the one deed we can do for the rest of us. There are tons of organizations, striving to research and raise awareness for MS. There's MS Society and even MSAA (Multiple Sclerosis Association of America). It's never too late to start.
BRAVE ONES - WE ARE A BEAUTIFUL HEROES AND FIGHTERS! GOOD LUCKY OK!!!!!!!!!!!!!!!!!!!!!!!
My neurologist specifically stated that the Extavia may halt the progression of the disease. It will never be gone, but it could possible prevent my MS from getting worse.
Madde there are so many meds that you can inject to help halt the disease. It doesn't mean your life is over. You found it early and the possibilities of living a "normal" life without MS is certainly a possibility. Don't give up!!!
I am getting tested after this covid is over... I’ve had symptoms for years and no doctor has taken me seriously because I am now turning 17 with all these symptoms. I have every symptom of MS to a T. No more no less. I am terrified. I don’t want to panic until I am tested. Can I ask if anyone in the comments has it and has had it since a young age/ how you guys deal with it?? I really don’t want to end up in a wheelchair or physically unable to do what I love... my passion is training animals, I love working with large dogs. And to train a pulling 100+ pound dog I have to have strength. :(
May I ask what you have been feeling?
Kiara Ellis I don’t think there is a symptom on the list I don’t have. But I will stick to the main ones. I have had extreme fatigue for years- had to drop out of public school and sports I loved. I have bad hip and joint pain and feel like I pull a muscle if I turn wrong on a daily. I also get really bad spasms- in my legs to the point I can’t move in fear of my whole body spazzing they get so tight. I also have really bad “ restless leg syndrome “ at night- for hours on end where I can’t sleep, it is in my left arm too and they will randomly jerk. I also get lots of pins and needles and my hands go numb. Like right now when I text- my hands go stiff, equal to if someone were trying to text in the freezing cold I describe it.
Kiara Ellis another main thing I struggle with is heat intolerance. I can not function. Even if driving in the car with the sun I get so weak, nauseas and get the worst migraine. It’s impossible going anywhere in summer.
Shay Rose how are you now??
my sister last year died she had MS she the aged of 37she was bed ridding she couldn't walk she had horrific uncontrolled head shaking where it put her spin out of shape I would want anyone to have this disease it is a cruel disease
My school used to do (or I think they still do now) a thing called MS Reading Challenge. A person will sponsor you so much an amount of money for every book you read and all of the money would go ahead to find a cure for MS. I wish I joined it *sigh*
Very good film. We have many films about people affected by MS in the UK that you may find interesting!
- MS Society UK
My left thigh muscle is very weak and fatigued the last 3 weeks and I fear I may have ms. Not just the disease, but how much it could cost me just to get any diagnosis, and how long it could take to secure financial aid even if the coronavirus panic wasnt wrecking our economy. In america, if cant afford healthcare or ins, you are fucked if one thing goes wrong.
I think the hardest for me is waiting for diagnosis. You can't join a support group, and they will not speak to you either, until you have a definitive diagnosis...which can take YEARS. It's been 6 years for me so far. I don't have any support from any organisation. This needs to change as many people, like myself, are left in the wilderness to figure it out for themselves. You can join an online discussion group, which helps, but nothing physical like a group you can go out and chat with.
BevsArtsandCrafts why does it take so long?
Please search for coimbra protocol to try to get your sympthoms under control
Broxine I will do thankyou. It's taken a long time here due to lack of neurologists where I live. We only have one and he has to cover several counties so waiting for an appointment to see him takes, on average, 6/9 months. X
P.s. Because when I last had the tests for MS there wasn't enough evidence to definitively say I've got MS, they were waiting for me to have further relapses to get more evidence. X
BevsArtsandCrafts damn. Wish you the best for 2019!
Broxine and you too xx
I don't have children. The past 5 years have been unreal, sometimes. It was as if I was in a haunted house. I just have ear pain now. It comes and goes. I feel so much compassion for people like me who did have children. It makes me think. Why don't I just give up? Sit in a chair before my time. Use sign language. My English writing skills have declined. I speak always the clown. Well I aspire to be as perfect as my critics.
Stay strong.
I got to know that I have MS two weeks ago and I’m a Norwegian 16 year old girl.
My mom went to the doctor for dizziness they said it’s likely she has MS. Doing blood tests tomorrow and they wnat her to see a neurologist ASAP. Scary to think there’s s good chance this will be my moms life now.
How did it go??
sergioortizz covid kinda put a hold on testing but she showing more and more symptoms and her doctor is almost certain she has it just wants to confirm it.
Grey Heart what symptoms?
sergioortizz honestly couldn’t list them for you. It’s too many and I just got off work so my brain is all over the damn place.
Why do people dislike I don’t get it
can you guys check my short film about MS to see if it is well represented
No more sad 'how/when/why I was first diagnosed' stories. No more glossy magazines and advertisements for/about raising money for a cure (and please it's not money to keep these magazines alive!). A CURE! Come on! I've had MS for 21 years, it's now progressive. I know MANY INTELLIGENT CREATIVE DOCTORS, please make a medical discovery as your past cohorts did with something like discovering antibiotics!!! - no more talk, CHANGE! NOW.
Mandy Harbison you tried coimbra protocol?
How are you today?
i am 32 i have it too ... just found out :( . it s started with optic neuritis
How are you doing now dan?
How's it going?
@@victorgomez6330 , @mobley Mobley I am ok , after the optic neuritis i never had any subsequent attacks 6 years after, I do take Avonex. It looks like it was a single event for me so far . But that optic neuritis left a bit scared i see differently with that eye
I have learnt one important thing after the diagnosis: "Stop being a damn weak p*ssy!!!"
Despite of the "diagnosis" I feel myself totally healthy and I refuse any medical treatment and give a sh*t what my "doctor" says! I don't suffer from symptomes, because I changed my whole lifestyle. There is always one phrase in my mind: I'm not sick!!
locoopupy . how r u ?? i love ur way of talkin and motivation. i pray to GOD to cure all the people with MS
Please! I've been ill for 5 years- I was diagnosed with chronic fatigue- but this is simply a number of symptoms for over 6 months. Has anyone had MRI that have not shown lesions? How reliable is MRI and spinal tap for tests? I have so many symptoms of MS and continue to decline. Please respond if you have info or have also had a difficult time getting diagnosed for issues.
If your MRI scans and spinal tap are coming back as negative then you probably don't have it.
How are you now??
I'm 15 and just found out that i have MS.. i dont know, my life is over. And that there is nothing to do. Just accept it and live whit it. it's hard you know? I dont know what to do anymore. All i can say is my life is over..
How are you now?
@@sergioortizz Right now I'm fantastic! I am feeling great and happy! I was scared and worried about it at first, cause i did not really understand what it would do. But really at the end of it all it made me into who I am, it actually helped me to love myself! Sorry if my English is a little of. Typing on my phone and autocorrect is set on Swedish! :D
@@typcute I use tecfidera tablets.I was ms when i have 19 years..now..i have 32.
you're welcome. i hope you are ok.
I was 17 went I woke up blind in one eye. At least these people can seek medical treatment. In the Caribbean you are pushed about because doctors have little or no experience with treating an MS patient. Only the very few can. I am lucky to be treated by one such doctor. But for the others in my country...I can't say.
+whaaat2
Have you seen this info? here is a link.
nutritionfacts.org/video/treating-multiple-sclerosis-with-the-swank-ms-diet/
i got same attack in my left eye
I m also suffering from ms problem from last 3 mnths......my age is 24.....in starting my legs were not working.....and numbness in hands.....still there is numbness in my hands.......i try to live my life again.....please someone tell me is it a serious problem????
I found out like 2 weeks ago i have 29y! They sey that i have 6y that disease!
14 Years and counting..
15here
Gracias y bendiciones!
Most people with MS live far from the equator (close to the sun) Vitamin D levels low
+Trkn56 Africans also get MS. Middle Easterners do too.
+Dimensions100 I still think it's oxygen problems (oxygen to the brain) where responses aren't being fully sent to parts of the body.
Trkn56 look at Dr Coimbra protocol high dose vitamin D
this music is too sad put it out please
Yes please. We are sad enough without the music.
Asa nu vreau sa fiu
good video :)
A wonderful video
you might want to check out a new product for self dressing "Miracle Dressing Aid" @ Sheri D Bean Co
Annoying repetitive music notes... can't watch it all...
Thank you, means a lot :-)
@ MS Society making a lot of money out of us aren't you!
Cannabis is how I deal with multiple sclerosis.
Well. I think you can't describe what MS is. Its a different reality and completely different disease from patient to patient. Long story short.... This is my story....
When I was 5 I ve been diagnosed with diabetes (type 1). When I was 27 years old (3 months after I got engaged) I got my present. MS.
Anyway I am 37 now, I got married (same woman), and I have 2 children. I am happy enough I could say. Of course I do face some difficulties on a daily base. Could I be happier? Of course. Could it be worst? Of course, this is fu****ng life. Keep calm and live everyday the perfect day.
Oh excuse my English
I hate ms can’t do as much any more tears most days
Why? I don't have ms but I don't think what you said is true.
I have no faith left in the medical profession. Drugs have existed for as long as I have had MS but they won't prescibe them because of cost. They could have helped me but they chose not to.
she is gorgeous. im sorry i just had to get that off my chest.
Thank you for this. Very informative. I just uploaded my Brother's PPMS story. Please check it out if you have time.
unclevroomvroom #ms #findAcure I myself have relapsing remitting ms im just trying to find people to talk 2 that can relate because honestly no one knows how it feels unless ur actually living it ...... I’ve made only one ms video hope you have time just to check it out I’m sure ur extremely busy but I’m just trying to reach out for some support.
th-cam.com/video/9VekoY7PiGE/w-d-xo.html
amazing people xx
Living with Microsoft isn't easy for anybody.
i am doing the same