What Is Multiple Sclerosis?
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- Опубликовано: 7 май 2013
- Check out 23andMe: bit.ly/13zNPet
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Millions of people around the world suffer from MS, but what is it? Lets shine a light on this disease in an effort to increase awareness. Please share, if you can :)
Written and created by Mitchell Moffit (twitter @mitchellmoffit) and Gregory Brown (twitter @whalewatchmeplz).
TWITTER: / asapscience
FACEBOOK: / asapscience
Mitchell Moffit
www.mitchellmoffit.com
/ mitchellmoffit
/ mitchellmoffit
Gregory Brown
/ www
/ whalewatchmeplz 
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I have MS and I'm only 15 so it's hard to find people who understand what I'm going through but it's nice to know people really do care.
+damarius ingram hey man, i'm a few years older than you (21) and I may have an impending MS diagnosis. Just letting you know you're not alone and stay strong.
I just saw your comment and I just wanted to say thank you it means a lot knowing someone understand.
+damarius ingram how long have u had ms if u don't mind me asking ... i hav ms too
+Cuh xD Not to long I was diagnosed in June. At the time I was 14 when it all started
i have MS, i was diagnosed when i was 13 and yea it can be hard for people to fully understand what you have but they try. At least they supply support for you and they do care they really do and since i am 18 now, you will meet amazing people who understand the pain you and i have gone through, just try stay positive and keep a smile :)
This video made me cry, I am part of the small percentage that has MS and is a teen. So the fact that AsapSCIENCE took the time to make this video to raise awareness is greatly appreciated
Kerrie Hamilton me too 😥
Get stem cells. Dr Neal Riordan
I have MS too. This has inspired me to start my owm RUclips journey. Please check out and support.
it's so sad that each comment in this video either have ms or know someone who does... I hope you all get well guys and I hope they find cure for it .
This video made me tear up. My mom suffers from MS and it is horribly debilitating. It is just as bad if not worse than many diseases such cancer, because there is no cause or cure. Yet diseases like cancer get much more publicity in the effort to end it. It's sad to think that if people gave as much publicity to MS they might be closer to finding a cure if not just something to help with pain and symptoms. I am truly thankful that the people from ASAP Science took the time to bring some light on this disease.
I know a doctor who can give you some information that could save your mom. Would you be interested in hearing what he has to say?
I would be interested to hear what he has to say. Where is he located?
Sierra Peterson He's from Seattle I believe. Anyway, shoot me an email at wilrho20@gmail.com and I will give you the link to the presentation he did explaining what MS really is all about and what you can do about it.
wilsonsmanz can you message me on google+ about that doctor
I feel so sorry for you... I really hope they find a cure soon and help your mother
My wife has MS. I love her dearly. We got married a year after she was diagnosed because we realized then and there that we couldn't know how our future was going to look; she had to live the life she deserved and I wanted to help her.
Bless the meek, and the sick. We live our lives as best we can, but never forget those that suffer.
I hope everyone who has this disease finds some peace.
My thoughts are with you and a big hug for you and your wife
Christopher, your words touch my heart, I too suffer from MS...ruclips.net/video/XmhSRaRIB4w/видео.html
How is your wife doing now?
My wife also has ms. Its been 5 yrs now. Seeing her suffer everyday made me crazy. I felt the world against us. I love her very much, i also wanted to eased the pain she felt, i wanted to help her but i cuoldnt. I took care of her, i always tell her that everything will be alright, im seeking who can help us. It started after giving birth of our first child, and she cant take care of our child.. we from philippines, and until now we are trying to figure it out how to overcome this struggles in life. Shes very strong, fighting everyday. I cannot supply sometimes of her needs, for lack of finances.
My mom has MS and she always has trouble walking and thinking. Her hands/fingers get incredibly numb and right now she's in a really bad state. I just hope they will find a cure for MS one day.
All of these stories everyone is sharing makes me feel so much less alone. Im 17 and my mom has it, my aunt has it, and a few days ago I was just diagnosed with it. I'm surprised at how many other teens also have it. I hope you all stay strong
Update?
My dad has multiple sclerosis... It's very hard to live with but luckily enough, the medication he takes works, only slowing the progression of the disease. Having lived with it for well over 14 years, he's done remarkably well. Please do take part in the spread of awareness of this terrible, and life crippling disease.
Isaiah, Thank You for your encouragement..ruclips.net/video/XmhSRaRIB4w/видео.html
People don't understand how we are effected. Everything is slower.healing, movement and everything else. Personally, I cannot even wake up. It fucks you up. You feel great one second and next you feel like shit, not able to do much, not able to move much and fatigued. Pain which come with it is like an add-on.
Salaam bro. I know exactly what youre going through. And i'm saying this because I have MS too.
may God help us
My mom has MS I wish the best to y'all may god help you 🙏🏽
with the not being able to wake up part, do you mean that literally? cause i have some times where I am totally (temporarily) paralized for a few seconds so minutes. I also have other MS symptoms but I haven't been diagnosed yet. I'm going to the neurologist soon. could that be a sign of MS?
Thanks! Hope all is well for you too!
My grandad had it and passed away two years years ago. He couldn't move he couldn't speak he couldn't do anything. Please help fight this dreadful disease. RIP GRANDAD❤️❤️❤️😭😭🇬🇧🇬🇧
:(..
i am so sorry my mom has it know she had it since she was born and i feel really bad for her but she is still good she hasn't slowed down yet
Edward Roberts mine died to cancer...
God Bless You and your family! I hope you are feeling better.
It's so sad that all there videos have around 9mil views, but this one doesn't even have one million
How?
Agree, no offense but the Anaconda music video was stupid, but it got millions of views. Videos like this are important, and if people don't raise awareness for certain diseases like this, it might be too late. I'm saying it's not too late, or it can't be too late in our generation, but it could happen. Asap SCIENCE needs more suscribers, I'm talking about like wayyyyyyyyyyy more. I'm also a supporter for Asap SCIENCE. I hope the world will change and will not only raise awareness for diseases like these, but rely less on getting drunk and getting laid almost everyday to make themselves feel better, and instead they should help the world become a better place than it already is.
MS sux!!! I know because...I have it but, it doesn't have me!
This comment just made my day😭
I know this is a little late but that's the spirit.... Never let that decies winn over you. I myself have ms to... I was half paralysed when it was at it's worse. Today i can walk normally again and are actually a beast in the gym to.... Keep on going and keep on training.. It helps. It also helps if you get 150% of your daily does of vitamins... Especially D vitamins
I love your confidence in not letting your disease take control of you! Although I don't have it nearly as severe as you do, I do understand what it's like to have to fight with a serious illness. I hope you do well in the future! ❤️
Proud of you☺🌸
I was just Diagnosed last December, I'm now on my Fourth Neurologist and I've been Hospitalized 5 Times Since January. Thank you for this Video so I can Show my Family what I'm fighting.
How are you doing now M. Dobb...ruclips.net/video/XmhSRaRIB4w/видео.html
My mum suffers from MS and it's really hard seeing her struggle to do the simplest tasks as her legs just do not work. I wish there was a cure.
Its the same for my mother... I really want to see her healthy and happy 😔
Today is my mom's birthday and she said she didn't want us to buy her anything so my dad decided to donate the money to ms research :)
my mother has multiple sclerosis 😞
it's really hard for her 😢😢
Same
Hello. You might find interesting the book and website called Overcoming Multiple Sclerosis. You might also want to watch the youtube video about Multiple Sclerosis on a youtube channel called Mic the Vegan.
itea I lost all sympathy when you used emojis
Youngster Joey
Stop with the negativity and the bitterness. You're not going to find happiness that way. Just be good kid. Stop with this "bad boy" thing you're trying to be. I know you'll probably just write something nasty back at me, but just think about what I'm saying. Life doesn't have to be an ugly thing. Peace.
I feel you same
i'm going to become a medical student, and MS is one of the things i really wanna study and contribute to curing
yilin Dr Terry Walhs cured herself of multiple sclerosis, her videos and testimonial are on the internet.
that's amazing!
Easy, just don’t eat pork. That’s the main source which contributes to MS.
I was diagnosed with MS last year when I was 18 and it was the scariest thing I ever dealt with. Knowing that there are creators out there using there platform to spread awareness is just really great to hear.
Hey man I hope you’re doing good. I was just diagnosed in January I’m 17. It’s also been the scariest for me too.
I got it the day before the summer school break when i was 11, i woke up being almost 50% blind because it was blurry and the summer weather(brighty) and TV's and Supermarkets killed me. It was my first relapse/MS Symtoms and it lasted for roughly 2-3 months(not fun when you're that age)
the MS Kicked in real hard later when i was 13-14 and i had a tendency to fall to the floor right after standing up from bed in the mornings and i was numb bottom-down and then after a year of monthly IV treatment with Tysabri i got immune to it, So now i have to take 6+ Hour long injections of Rituximab(Also used to treat leukemia) 4 Times a year.
Just leaving this here.
Somebody may read it, Or maybe have been in a similair situation or something
Im a male, if thats good to know.
Hey dear how are you now. My doctors also going to start rituximab injections next month .
I got diagnosed with MS at sixteen but my doctors said the illness probably started when I was only twelve so this video by a channel that is so dear to me and many other younger people is something I'm incredibly grateful for 🙏
My mother was diagnosed with MS about five-eight years ago and because there is no cure for it, it's pretty much become chronic. It's hard just being her kid because there's a lot more to it than it seems. People think, oh just hire a care giver. Well care givers for one don't spend the night, and two none of them ever stay. And just imagine, not being able to walk, but watching your children walk. Depressing. Oh yeah, she has that too. That's depressing. They need to find a cure because this is way too stressful for EVERYONE.
Hey my ms warriors, I love you
I got MS when i was 13 and i have to take shots 3 times a week to prevent future attacks. This really means alot thanks 💞
Love you Ali!ruclips.net/video/XmhSRaRIB4w/видео.html
@@suwaydaj8203 bro can you tell me what are your symptoms before getting diagnosis ? My left side muscles of my body are in pain and shrinking size with left eye little blur than right. I'm going to a neurologist soon but I'm really anxious how my future would be. I'm just 19 😔
I received the diagnosis of MS at 17 but I had the first symptom at 15. I also had a tumor this year and I defeated it with chemo and radiotherapy. Now I have 21 years old and I have a clear vision of what I want in life and I will not let my health or my social anxiety prevent me from achieving my goals. We must be strong, stronger than anyone else!
My father has ms and is staying as strong as ever, i am glad to call him my dad as he's fought it for 14 years and never once given up. :) Sometimes you just gotta stay positive!
I'm Gonna have it all my life and I'm still 19
It happened when i was in College and my left eye suddenly turned black.. Then I took medicine till today..
And if I stop taking medicine.. The MS is going to hit another body part
me too! Idk if this is weird but can we be friends of something? It's hard finding someone with ms at my age.
Your Devine Destinee heey im really happy you wnna be friends :)
+DontQuitYourDayDreams I have it too! I got diagnosed today.
dkahmedkhalaf glad people are bonding over something like this. It really gives me hope for the human race.
My mom has a serious case of MS and she can hardly even see.
Three years ago, my aunt died because of MS. After a while from her death and from nothing, I started feeling difficulties in walking and balancing. I broke my leg because of that. After 7 weeks I removed the splint and it took me almost a week with the same earlier difficulties in walk. After the diagnosis in the hospital, they told me that I probably have MS. I immediately remembered my aunt and what she went through. I didn’t believe what they said about me. I went to another hospital hoping they were wrong but, they weren’t. Now I’m 23 yrs, I can go to school, I can go out with my friends, I can go to the gym, I can travel, laugh, eat whatever I want, I can do anything just like a normal person. Maybe I got the disease, but it will never ever get me.
Thank you for explaining this so clearly. I've been a MonSter fighter since 21-Oct-2008. I always share items during MS awareness month to bring our illness to the forefront to make people aware of our struggle. I will be using this video for the next month. ❤
My grandfather and cousin suffer from MS.
Just found out I've ms
Terrified on the inside
Being a soldier on the outside😵
Thank you so much for making this video. My mother suffers from this disease and some days moving is the world hardest task. she always powers through ut and its nice for it to be explained to me in a simple way.
What's multiple sclerosis?
My dad's MS has revealed itself out of the blue. My aunt's MS got revealed after her daughter was born, (the female body gets horribly weakened during childbirth). My dad is dead, but my aunt is still fighting.
I personally believe that MS is a genetic matter, and that you're born with it. It just gets stronger with time.
I am 18m I got diagnosed by ms 3 months ago I ignored it for a month due to me being ignorant until I couldn't read move well tend to fall often extremely numb and cant taste stuff bc of my ignorance it got worse now its progressive and a second attack can paralyze me, now I was living alone in dorm lazy careless obese etc and antisocial and had to drop my semester now after sleeping in hospital for 2 weeks going back to uni my life is changing now, its only been a few days since im back and im numb righth now but ive been eating healthy except chocolate bc its love getting vitamin D going to the gym as I aim to lose 50 pounds , and more social tho im a bit shy so while ms is a drag if I stay motivated forever like I am right now I would be glad for ms as I could've turned out t o be a failure in life, fellow people with ms don't give up! everything happens for a reason and ms could bring positive stuff into your life stay strong everyone :)
Just want to hug you after reading this. I'm so sorry you've gone through and are going through this.
This is so horrible this illness, you hear about cancer all the time which is terrible also but there are other illnesses to which are just as devastating, like this one yet you hardly hear of it!!!!
The singer Don Van Vliet passsed away in 2010 from this awful illness. :(
My dad might have MS and will have to have tests to see if he does , watching this video made me understand what it is and how it will effect him , he already has health conditions and i am his carer . This video has brought some light on this disease , thank you for doing this video x
My mother has some form of MS. I'm glad you guys are covering it.
I think I may have it, but i have had 2 MRI scans about a year apart. Brain/ cervical/ thoracic spine. And they are neg. Its just hard to believe. Not sure what to do or how to treat myself at this point
omggg I love your videos!!! now I can finally make people understand what ms is when they ask me weird questions I just said umm it puts scars on my brain or something? XD
My dad has MS and it’s really hard for him but I’m glad to go to camps that help me and and show me that I’m not the only one with a parent that deals with this too.
I’m 17 (born female) and was diagnosed at 15. MS relapsing-remitting. I went from one day feeling completely normal to waking up with my body numb and tingly, like when your foot falls asleep. In less than two full months I got my diagnoses. At the time I couldn’t even put my hair in a bun because I couldn’t really feel the left side of my body. The following months I spent walking down my small town high school hallway with a walker constant getting stared at.
I’ve come so far but I still struggle every single day. Living in constant pain and missing out on activities because it could cause a flair up. Not to mention the mental trauma this diagnosis caused.
God I would never wish this Olin my worst enemy.
I think I have MS and it was thought to have been fibromyalgia for the past 20 Years almost the same symptoms.I recently had a brain scan that is saying its most likely MS.I am going to go to Stanford to find out for sure.(waiting on approval) they said there is medication that can be taken to help. as this is very debilitating.there has been time where I haven't been able to Stand up for weeks.my legs just wouldn't work,and the pain everywhere else is so bad.I pray that they find a cure others don't realize when you are so fatigued and can't even get out of bed from it.I hope everyone gets the pepper diagnoses and treatment.
they must be having treatment as far as I've studied in my medicine books, you will be given pulses of steroids most probably methylprednisolone, however you should remember that its a treatment/ management, NOT a cure, so you will have to comply with long term follow-up care in addition to taking vitamins (vitamin D especially) and calcium supplements while you will be receiving methylprednisolone. hope you can find what is best for you.....
Hang in there Irene, it's very hard, stay strong...ruclips.net/video/XmhSRaRIB4w/видео.html
Pusha T/Drake beef anyone?
It’s crazy. I’m 17 and I have MS. It’s scary to see what is going to happen to me eventually. but I got this.
I really do.
I find this to be a serious medical condition that needs awareness spread, thank you asapscience, I don't see who could dislike this video, fortunately I do not no of anyone who has acquired this, and I am sorry fore people and families who have, I am glad you are spreading awareness of one of many not very well known, but harmful diseases, such as plastic anemia. THANK YOU ASAPSCIENCE
Here after the Pusha T diss on 40
Pusha brought me here 🙏🏼
My aunt has MS. Thank you for helping to raise awareness 💙
Thanks for making this video. I also suffer from this condition and its great that you are raising awareness. Also love your design style AWESOME!
My mum died of MS when I was 10
My moms dying from ms too
I'm sorry for your lost :( hopefully we will find a cure
I'm a very sorry for your loss.
U can die ms? I thought it is rare to die from it
i'm sorry for your loss katie.
My mom suffers from MS
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My auntie suffers from MS, this video really helped me understand what it is!
I am having a flare up of ms, and this video caused me to cry. I'm 19 and had treatment and treatment fail on me. I wish that people were more aware. I'm so greatful for this video to spread awareness
My dad has ms in his left leg and he can never walk again
MS is in the brain and spine not the limbs.Im not trying to be rude just informing you.
John Gabriele Your wrong. My father is also immobile do to this disease, and you havent a clue what your talking about. It effected his brain, which sends out signals to all of the limbs organs and such throughout the body. the nerves sending messages to the leg from the brain is where the immune system attacked the myeline. That's how. Please don't call people wrong when they are being effected like this on a daily basis and your just basing your facts off of a video you didn't understand completely
ec qwolf i know that it immobilizes your limbs but it attacks the brain and spine not the limbs.
ec qwolf I also believe i may have this disease so i may be effected by this but i hope not.
If you think you have the disease you need to go to a neurologist right noe
Pusha T sent me here
Thank you for making this. My mom has MS and is paralyzed from the neck down. Thank you for bring awareness to this disease!
My mom was diagnosed with ms in 2007 and I showed her this video and it made her dad
thank you for this video i've hered of m.s. but never new what the disease meant, I pray i don't have this, some days my body don't feel strong like doing any thing, I pray I don't have this, an I also pray for all those that do have it, thank you for the education teaching thank you.
My mum had ms and she was paralysed from head to toe couldn't speak either and sadly she passed a way on the 21st may 2015 and I want to help with other people going through this horrific incident
This video made me cry because my grandma had MS and when I would see her in the hospital she would be laying there sad and shouldn't move she could only blink,breath,drink, and eat and we would have ice cream then on December 11 of 2007 she died plz help MS do what ever you can one of the things I do every year is the MS walk if you read this thank you plz help MS
A lot of people forget about MS being chronic because it isn't terminal, they don't realise how bad it is physically or mentally. It annoys me how so many more illnesses are paid attention to but MS is just as serious and still gets ignored
My best friend was just diagnosed with this today and I’m hoping he will be able to completing high school with me and his other friends.
my mom has ms she had it for over 30 years she had screamed she had cryed and were a little bit pore were moving to a new house
My mom just got diagnosed with it and i had no idea what it was thanks for the explanation
Thank you so much. My mum has MS and people don't understand and just think she's 'lazy' when she's actually suffering. When I saw this video on my recommended I had tears in my eyes because there's people out there who actually care xx
yellow purple Dr Terry Walhs cured herself of multiple sclerosis. Her videos and testimonial are on the internet. She has got a book out called the Walhs protocol. It's regarding auto immune disease. Thought it was worth mentioning.
I love that more and more people are aware of MS. My dad has had it ever since before i was born and I know plenty of other people with it. It caused him to not be able to walk. Honestly it is really hard to deal with someone so close to you suffering so much. The only memories i have of my dad being able to fully walk without help are from pictures when I was a baby and before I was born.
What's the best way to get a diagnosis? MRI scan?
What is the best way to convince a doc to look into it?
My home room teacher has ms and she told us. She is always absent on mondays and I just wanna spread awareness
Ava piñam Dr Terry Walhs cured herself of multiple sclerosis. Her videos and testimonial are on the internet. She has got a book out called the Walhs protocol. It's regarding auto immune disease. Thought it was worth mentioning.
My friend has this, he is also adopted, and his mother is dead .. I feel bad for him😞
THANK YOU! my sister has been living with M.S. for about 11 years.. THIS IS HANDS DOWN THE BEST EXPLANATION ABOUT M.S. I HAVE EVER HEARD AND SEEN ... THANK YOU. THANK YOU. THANK YOU!
My mom has MS and after having a few episodes. She thought came from stress,so she tried not to be stressed for 5 years and she has not had any episodes, but she is also on medicine for MS.
Gaming Dave Dr Terry Walhs cured herself of multiple sclerosis. Her videos and testimonial are on the internet. She has got a book out called the Walhs protocol. It's regarding auto imunne disease. Thought it was worth mentioning.
I was diagnosed with it almost 10 days ago still have about a week before I start occupational therapy and get started on treatment..
My mother is a carer and works for a man with MS. It is in a whole half of his body and he is paralysed in a wheelchair.He is only in his early 40's. He has kids and they find it really upsetting.He has had MS for over a decade now.
I've got multiple sclerosis and I would like to say thank you for spreading awareness for the cause.
The best friend of my mother died from MS i think, She was paralyzed for over 10 years from the neck. I know it has something with sclerosis but i don't remember which one. ( in french is Sclérose en plaques )
My mom has MS. She lost her ability to walk 6 years ago. Its so hard to watch her deal with this. I wish more people knew about it and understood how bad it can be
Im 19 years old and I was diagnosed with MS about a week ago. Still trying to wrap my head around it. Its so strange to think that theres something wrong with you, especially when its something you dont fully understand
I am Diagnosed with MS from Egypt but the problem is that many neurologist still can't diagnose people with MS it takes a very long time to start your treatment and it costs a huge amount of money.
My grandmother died of this a long time ago, I remember that n the end she could only move her fingers and her head, it was so hard.
My neighbor had MS and she was always trying to move in order to not lose her independence.
I wanted to say Thank You! I have Progressive Relapsing MS and I was grateful for all of your information as well as a connection to 23andMe. God Bless you.
Just got officially diagnosed with MS today! It’s a bit bizarre suddenly being chronically ill and as I’m only 17 kinda terrifying but I’m thankful for the continuing progress of medical science and I hope one day we will get a cure!!
My friend has been diagnosed with it 4 years ago. I really hope that doctors find a cure for it
Hi I am gracie and I am nine and I have ms and I take shots three times a week.I have had symptoms like weekness lost of cordnation and numbness I suffer ms and it is not easy.my Nero said ms is very rare in kids but it is possible I got to the hospital a lot and have a lot of flair ups.please spread awareness of ms some people really need it!😊
my mom has been suffering with this disease for years and it's so hard to see her go through this😭 also praying that my siblings and I don't get it since its in our blood
I HAVE A QUESTION! - What are headaches and what causes them?-
My dad has multiple sclerosis and I'm 9 and he is 46
When I watched this I was crying and my head slowly went down
;(
hardcore gamer and vloger l My Mom was diagnosed when I was 5. I’m 22 now and although some things have changed she’s still happy and has a pretty good quality of life.
There’s so much new research out there that wasn’t available 20 or 30 years ago. She used to take weekly injections but now they have pills. Don’t be discouraged. MS is not a death sentence.
hardcore gamer and vlogger l l DR Terry Walhs cured herself of multiple sclerosis. Her videos and testimonial are on the internet. She has got a book out called the Walhs protocol. It's regarding auto immune disease. Thought it was worth mentioning.
M confused why 170 people UN liked the video . . .it's just educating people
I'm 24, and have been diagnosed with RRMS the 11th of December 2014. I'm looking for ways to handle this. Sometimes I feel great, the next day I feel like a mess, emotionally and physically... I want to wish everyone that has MS and their family members a lot of strength. I see how me having MS affects my family, and sometimes I wonder if they're struggling more than me...
My dad did a walk for MS. He raised over £600 and he did a walk across the whole of Hadrians Wall.
My brother has MS he likes playing hockey but in some games he has to be pulled out because of numbness in his legs
My mum has MS, She has had it for 20 years. Thankyou for helping me understand about her disease. :)
Adolf Oof. Dr Terry Walhs cured herself of multiple sclerosis. Her videos and testimonial are on the internet. She has got a book out called the Walhs protocol. It's regarding auto imunne disease. Thought it was worth mentioning.
My Aunt has this and it doesn't help that, no easy way to put it, she is pretty overweight and her husband doesn't help out much with the 4 kids they have. Although she isn't going to badly, she is going to get worse. Thanks for bringing light about this, I hope that she is cured.
my mom has ms, for a while the entire right side of her body was numb, she went to the doctor, got meds and didn't have a problem, she started to do more physical activity and is off the meds and she is doing very well now.
I'm 34 and suffer severe primary progressive multiple sclerosis. The outlook is that I will eventually end up wheelchair bound. As it stands right now, I can't get around without a walker. Been that way now for about a year. I was first diagnosed about 5 years ago, and have been going steadily downhill since the initial diagnosis.
A member of my family, who I will not tell, is half-blind because of multiple sclerosis, and must release all stress, because if not, the "unknown" family member will become completely blinded or paralyzed.
Me and Mom have it but I was recently diagnosed with it. My mom was diagnosed in 2011,and also I have allot of joint pain and when I am outside I can't stay in the heat to long.
I have MS I don't have my final diagnosis but the doctor pretty much told me
thank you :) I was gonna message you to ask you to do a video about MS but first searched your videos and found this ^.^ I am glad you guys covered it
Very recently diagnosed and I'm a strange case. I started having simple partial seizures at 18. My gp thought they were panic attacks until my mum reminded him that he diagnosed quite a few members of my family with epilepsy. He then referred me to a neurologist, which would have taken a few months to see if it weren't for one morning mum had to take me to a medical assessment unit after having loads of seizures, which to her looked a lot like TIAs. My neurologist sent for me soon after, gave me an MRI and evoked potential (to find my trigger, it is stress). I had to go into hospital for a couple of days for monitoring, blood tests and a lumbar puncture. Had to get tested for something called CADASIL (genetic :( ). Came back all clear, apart from altered wbc. Now, I have a clinically definate diagnosis, half of my face with altered sensation, painful leg spasms, some difficulty speaking and living on meds for my seizures. I'm 21 now and studying to be a nurse. It can be done, and I've always been told that I'm so strong for continuing as I am. All the MS warriors are strong, even at your weakest. (And the patients I've met that have MS are the most down to earth, genuine people I've met.)
I've had symptoms for 7 years and in 2014 I got my diagnosis of PPMS... Share this video and if you suffer from this monster don't let it win... fight it as hard as you can! Lifestyle changes (diet/exercise/having a positive attitude) helps a lot!
thx bro