I was just diagnosed today and I’m trying to cope so prayers are welcomed.

I was diagnosed in 2018, my entire right side was seized up and unusable, balance was thrown off and could hardly stand. With physical therapy, modern medicine and dietary change I was able to get back 100 percent health. Doctors thought I would only regain around 50 percent strength. A message to all MS'ers stay positive, don't get down on yourself. STOP eating processed foods. START to meditate and exercise daily. This disease doesn't make you weaker than the average person, it actually makes you much stronger, and can give you a much deeper appreciation for life.

Love this! I have had MS for 45 years now and am back at work in my late 60s because I can! We need these success stories with the emphasis on life style changes.

I got MS when I was 15, at first I was so scared but and now I am 23 and feel good because I believe nothing happens without reason. God never gives you something which you cannot handle. God bless you all.

My mom was diagnosed with multiple sclerosis in christmas of 2011, within a week. She felt some of those symptoms, the tingling in one of her legs and the loss of sensibility in one of her hands. She always felt something wrong with her hand but the doctor said it was nothing... For years! In 2011 she felt those symptoms intensified, so me and my brothers made her go to hospital because it wasn't very usual. She was diagnosed with multiple sclerosis and came out of hospital in 24th of december. It was a very difficult journey for her. She had to change her treatments for two or three times because her disease was getting worse after the flare-ups. She stopped working because my father thought it was better that way and because that option was possible (fortunately my father has a stable job). Today she is a very healthy and strong woman, she faces life with an huge and strong smile. She goes almost everyday in long walks, she is an excellent and active grandmother, she eats very healthy and, most important, she tries to run away from stress and big emotional changes. I'm very proud of her. She's the person I love the most in my life. Because of that, now I'm studying Biomedical Sciences and I want to take my PhD in Neuroscience and understand better this disease, because my mother always lived for me and always gave me everything, so if there's a chance I can try to make up for everything she has done for me, I will sure do it. I wish the best of luck and very strenght to every person with this disease, and remember, there will always be someone in labs and hospitals trying to find a reason why, a better treatment, a cure... We are out there! :)

I feel like I might cry. Battling MS is hard and unpredictable, sometimes it gets me all in tears and asking "why me?". It is hard even trying to explain why I'm so tired, why I sometimes walk without coordination and why sometimes I don't really feel my left hand. You know what? I'm tired, but I'm alive. I'm walking weird but I'm walking. I sometimes don't feel my hand but I'm capable of moving it. Not gonna let this defeat me, MS is my new bestie and I'm more inspired to live and appreciate my best life than ever, as mentioned by amazing speaker.

I was dxed in 2000 (the Friday before my spring break. Yeah 🤦). There were 3 drugs for MS at that time. I go to a neurologist now who is a world renowned specialist in MS (his mother had it bad, and so he made it his passion). Last time I saw him, he said there are now 30 something treatments for MS, with more on the way. He also said that within my lifetime I will see treatments that reverse the damage. Then the next time I saw him, he said, "remember how I told you you'd see this within your lifetime? Now it's more within a decade". So this isn't a life ending disease. Help is on the way.

I think the toughest part of MS, for me, is not knowing what the future holds. And it makes me question everything from the past.

Her opening minutes was the last three years of my life, i'm trying to be ok with this.

“and you still did this to me” i’m crying... acceptance is one of the hardest parts of any illness. she’s amazing for talking about this.

Newly diagnosed and this is exactly what I needed to see.

I only had 19 years of young health. I was married at 18 and diagnosed at 6 months after marriage. Was told do not have children, just raising them will take a toll on you! I was young and stubborn enough to fight back. I m now 62 and still fighting with Ocrevus and the help of my family Thank you for the story of your experience.

My 32 year old daughter was diagnosed with MS 2 weeks ago. We are still in shock and I feel completely devastated for her. However, we are trying to stay positive and optimistic but geez its really tough. Luckily we live in Australia and most of her medical care is covered through Medicare and her medications will also be covered under our country's PBS. I do really feel for our friends in the US who are not adequately covered through their private insurance - very unfair. We are trying to take each day at a time....but as her Mum, I can't help but be very worried about her future. Wishing you all the best of health and happiness.

I was diagnosed with multiple sclerosis in 2018. I was 21 years old and in that year I had lost a family member and went through my first heart break. For the past 3 and a half years I have been a Latin dancer which has been a passion for a long time. I have performed and competed on stage for the past 2 years. Last year I tied for second place for my salsa pro/am freestyle. I also won my bachata pro/am freestyle!

So glad I found this talk. Diagnosed with MS last year. I am 28 now, a CA finalist, it still kills me to think that i m not able to walk properly. My condition is progressive in nature though I have not given up. I am positive each day n believe me it is no easy. But i m not giving up.

So touching. I cried my eyes out when you were talking about your pains. I recently got diagnosed with multiple sclerosis and i can say I'm going through a lot these days. Wishing everyone with multiple sclerosis a healthy and easy life.

I was diagnosed at 18, which was just 5 years ago. I find this talk very comforting to me. It reminds me that just because I have MS, it doesn't mean my life is over. Thank you so much for your inspiring words ❤

Great talk! I am 38 and have had RRMS since I was 21, but officially diagnosed at 27. It’s a roller coaster ride and still is. I was on Tecfidera from the start, and currently taking Vumerity. I also may be switching over to one of the newer infusion drugs in the near future. I am blessed to still be athletic, but there are times I have my days where I am weak and my brain fog creeps up. If you are newly diagnosed, do NOT ignore treatment. It’s one of those illnesses where you need to incorporate western medicine, along with a good diet and exercise. Those three go hand in hand, and if you follow up with them, you will be fine 😊. I am confident that within the next 10 years we’ll have better medicine to slow it down more or even halt it. I hope scientists find a DMT that only nukes problematic B cells instead of all of our B cells 😅

I got it when I was 17 and I was sad at first but then Allah guided me.

Very inspiring, so added it to my fav's... I, was diagnosed with RRMS 15 years ago I'm now 45 and at the age of 30 I felt my whole world come crashing down but just like Robin, I had to accept my fate & what was now my new norm & granted "it's been tough" but I've "changed my attitude" towards so many things & kept the faith alive, and I keep on going through all adversity... Coz once you're defeated mentally, you're defeated spiritually & ultimately physically even without the aid of "chronic illness!" So I say that to say this... Be strong all my newly diagnosed MS warriors & stay positive in your mindset & don't allow the challenges you face define you it's not the end; far from it. And to my veteran MS warriors, keep on keeping on... God Bless you all peeps... Love & light!!!!

A huge embarrassment is doing a side step while walking. The tag line is true, "we're not drunk, we have MS" applies. I have had to say that a few times in the last 20 years!

I was diagnosed with MS when i was 12 years old. Im 22 soon 23. And my first symptom was central vision blindness. I was very young and my third attack was very scary. It took everything away from me. MS made me sacrifice things I didn’t want to from making friends, talking walking or feeling like a normal human. It caused Bipolar disorder and because of its immune system killing itself ms caused other diseases too. To this day, im suffering but im glad i can see again.

Was so proud I made it to 30 minutes on the elliptical … then the next day at 30 minutes my legs collapsed and three men had to help me up. Of course I cried out of embarrassment but I should have laughed. I did 30 minutes two days in a row. The elliptical is a replacement for not being able to walk without a limp. It’s a godsend.

Truly amazing! My wife was diagnosed in 2009.Thank you for sharing your story!

I recently started working in neurology department, and meeting patients with MS made me realize how much I should appreciate life and everyday blessings like being able to run. Big respect for all you guys, and never give up on yourself! Keep fighting this battle and enjoy as much as you can, because I promise, you aren't alone on this journey. ❤️

Great presentation. I found out I had MS at 51. I asked not Why Me but rather Why Now. Weren’t we supposed to retire and have it easier? Instead of starting out on a new battle at 51. Then I flipped to gratitude. I Had Had 51 healthy years with career, travel, family etc. Thank you for explaining the battle and the mental strength needed to stay strong.

I have now found out 42 diagnoses when 33 were. All in different scattered sclerosis flows, I stopped writing to be able to write, with the coordination of nonsense. Now I communicate with people with this diagnosis already that I walk myself without a stroller is good

i hurt so many people with my attude and mood swings i didnt understand that ms was making me be someone that was very unlikable, but i recognize it now and know how to handle my self better by resting properly exercising and eating healthy foods

I am 46 and currently amid testing to see if my issues are MS. Love this talk as tears run down my face. 💚

I was diagnosed Jan 2021, with RRMS, EDSS 1. By September 2021 I declined to EDSS 3.5. I thought my world was over.. I had numbness in my hands, legs, nausea 24/7, bouts of dizziness, the MS Hug, lower back pain, couldn't make it past a bathroom and the list goes on. I was fortunate that my mobility wasn't impacted. I found out about HSCT and went in October 2021 in Monterrey, Mexico to get it.. unfortunately, this treatment is still stuck in clinical trials phase 3 in the states. It has an estimated ~85% chance to halt RRMS. My last MRIs showed no new activity! I work 40+ hours a week and I only take vitamin D once weekly. I have enough energy to cook dinner when I get home, too! I wish this was offered as a frontline treatment for everyone with MS.... I am forever grateful for my second chance at life. Best wishes to everyone battling this horrific disease.

You 14:28 r Amazing!! I am 47 years old and I was diagnosed with M.S. in 2010 relapse remitting. It was a complete Surprise for me when I was diagnosed, being that from the age of 2 I was a gymnast, and from 2nd grade all the way through high-school I cheered the I became a competition coach for both. I try to remain positive, but it's hard. M.S. is incredibly painful. Thank you for sharing your story. Stay Strong, Heather Buszka 14:28

my brother was diagnosed during covid, he lost his job, his fiance left him. I want to help him get back on his feet and be there.

you are my hero. I have watched this over 40 times. f ms. you go girl. all power to you.

I'm 29 years old and have been living with MS since I was 23. I've been struggling more so recently because I'm wanting to start a family and I'm worried about starting medication. We are in no position to start a family at the moment and I'm worried about going on a medication to have to get off of it in a year or so. I've also been extremely scared about my health. I haven't had an episode since my first diagnosis but I feel like a ticking time bomb. Sorry for the rant, I just wanted to say you are a huge inspiration to me. Your positivity is exactly what I needed. Thank you so much for doing this TedTalk.

I got diagnosed 2 weeks after my 20th birthday. It’s been 2 years and I’m still grieving every day.

I am in the process of getting an MS diagnosis. I’m so lucky to be in the UK where treatment is free. I feel for people who have to stop at medical bills.

Im diagnosed in 2019 and ALHUMDOULILLAH proudly fighting

My dad has MS and I’m here searching for anything to be able to help him 🥺 I love him so much and I’m afraid he’s giving up on himself and it’s devastating ! I hope I can get better knowledge and insight so I can try and help my dad 🥺 if any one has any advise or things that help them in their everyday life please share with me , thank you so much and I’m sending healing light and energy to each and everyone reading this !

Everyone's MS journey is different. You can't look at other people's experience and make assumptions about your own health. Best wishes for everyone who has a MS diagnosis. Keep healthy and keep fighting. I am so lucky to live in Australia where my medications are free. Every day we show up we are winning.

I was diagnosed in 2016, but my symptoms started in 2013. It takes so long just to get a diagnosis. It started with my left thigh going numb while walking and running. Then i woke up one morning and could not see good. I just wanted a reason for this it took so long. My vision got better with treatments my thigh isn't numb anymore. you wake up every morning and dont know what your condition is going to be like today. Heat and stress is my major things that bring on my attacks. When i was first diagnosed i was grateful for the answer and wanted treatment. The doctor was so surprised i turn down the narcotics. I have a family and ms hasnt slowed me down. I make myself get up some mornings, but i think my health could be worse. I am not dying and if you watch what brings on your attacks and take care of yourself you can live normal and just as long. it just depends on the type you have and if you are health conscious. When people find out i have it its like "oh im so sorry". Thats why i dont tell many people I say dont feel sorry for me it could be worse. My doctor does research and im on a clinical trial they watch my health really closely and so far no attacks in over 2 years. I couldnt walk the drunk test before I started now i can i was having the balance issues now i dont that was so embarrassing i would always make sure i had a shopping cart to hang on too. The spinal taps arent fun but i have done them with no calm down meds. Im in this trial because i want to make a difference I want to help people like me and future generations. i just dont get in the heat and am very aware of stress. Dont think its the end of the world and never give up.

I don't have MS but chronic asthma and it has turned my world upside down this video was definitely the encouragement I needed ❤️

I got diagnosed with MS 1 week ago. I'm 31 with 2 young boys, thank you I needed it.

Loved your attitude towards MS, having MS myself for over 23 years has caused me to appreciate life more than ever . We all have ups and downs, but bouncing back and realizing this life is short helps to maintain a positive attitude on what is out there for us to embrace. GOD bless you and hope to see more of what you have to say.

Thank you for leaving MS sufferers with the hope that longevity is not as bad as told. The harder part of MS is that people appear fine when they are actually internally suffering. for this reason they are dismissed and ignored and even blamed for the illness. Changing eating habits is a major contributor to coping better with MS. People this can change your life: consume raw green leafy produce, avoid sugar, starches and meats at all cost; drink lots of water and move, breath, pray or meditate, these new ways are life-changing but worth the effort. To your health!

Her story is mine😥😥 i was just diagnosed and iam bawling. Word for word she gas said everything i feel. Ty for your story. Sylvia from texas

I’m so glad I made it here. This disease is so unpredictable . When I’m not experiencing symptoms really I feel hopefully, then when they occur I think is this it? Is this where I’m going to lose my ability to move my arm completely? So much uncertainty BUT this speech was so empowering. KEEP FIGHTING!

I have MS since 2021. I'm a Filipino living in the Philippines where healthcare is far from the US. My neurologist is not covered by my insurance as well as my tests and treatments. I just hope that someday our healthcare will improve. I cry a lot thinking about my future and my family don't understand this disease. They only see it as if I only have a flu or I'm just stressed out. I'm young and I want to have my own family someday but I don't want to be a burden to my future child and husband. I want to keep my balance, I want to keep my ability to walk to continue climbing mountains. Oh how I hate this disease. Thank you for this inspiring video. I will do my best to live my best life. God bless you all.

This was so good. Thank you for your honesty.

With or without MS, we do not know when we will die. It’s best to live life and appreciate living every single day.

I may have MS. My neurologist appointment is tomorrow, and I'm nervous but ready for whatever comes my way. This TED talk made me cry however because I had been "woe is me". But whatever is going on with me isn't a losing battle, just a new way of living life for me. I don't know what the diagnosis will be. Could be temporary and curable. Could be life long. But whateve it is, I'm ready to fight for myself.

Thank you for sharing your MS journey...you have inspired me to tell my story in front of everyone and honestly I feel very good. This definitely has given me the confidence that I needed and made me capable enough to start my own channel, I wanna grow with you all and proud to call myself a MS warrior !!

Diagnosed 3 months ago. Feels like my prior self has died. I am still grieving the loss of who I was an am fearful of my future. I am still young and already blind in one eye. This disease is horrific.

I was diagnosed at 17, now I am 20 with PPMS

Robin, I loved listening to your talk. I was dx with MS almost 21 years ago when I was 20. I have learned so much about life and my inner strength while living with MS. I totally agree that staying positive is important as well as exercise and nutrition! Thank you for sharing your story. 🧡

Great job, Robin! Very proud of you

Robin, this is beautiful. Your are a great spokesperson for those with our disease - Thank you

I am so grateful that my insurance covered all of my medicine and tests through this journey. I realize that I've never let myself mourn over this diagnosis. I spent the whole summer of 2020 undergoing tests while battling relapses. This wasn't the diagnosis I wanted but this video brought me closer to peace. I feel better knowing that we're all battling together and that we got this.

Thank you for this! So helpful for me and I'm sure for others.

Just got diagnosed and I want to say thank you for the honesty

Really well done! Your description of this disease is great. I love your attitude. We have to stay positive.

You are a super star. Thank you for sharing this much important story!! Love you, lady!!

I was diagnosed 1yr ago. It sucks that we have this. So thankful for you speaking, encouraging, and letting me know I'm not alone!!!

She said everything I am feeling. Thank you! Great Ted Talk.

Thank you for being so courageous! What an example you are to your teenagers and to us all! I have a dear friend with MS, and I want to know how best to come alongside her! You've helped me more than you can know! Blessings to you and your family! 💜💜💜

I was diagnosed a little over 18 years ago but my health has gone downhill VERY rapidly in the last 3 years. I can honestly say that this is the first talk that I have seen that makes me feel better. I'm lucky to have a wonderful husband and family that would do anything for me. However, I still get depressed about everything I have to deal with so I'm very glad I listened to this video!

Really u r a ms star!!! Loved every word...so inspiring n encouraging!! Thanks for sharing!!! Robin, u r a very fine lady. You will definitely live a very happy n satisfying life.👏👏👏👏👏

Bless you this is so relatable and I appreciate you so much. Stay strong.

Oh God, I just came across your video. You are so beautiful! Ms changes us 😌 We finally glow.

Great talk and simple explanation of MS outsiders can understand without trying. Resistance is futile, acceptance is the best way forward. Embracing this insidious dx is my superpower. It prompts me to learn and laugh. And not just about MS. Ruminating on the future wastes the present. No one gets out of here alive.

Thank you for your energy and clarity. My brain/cog fog/word finding issues because of MS are so bad that I gave up public speaking. Dx at 48 10 yrs in and happy to have aggressive treatment to "save my brain".

Got diagnosed in 2009… I was 22. 13 years after I have 30+ lesions just in my brain, and had 5 time ON, twice bilaterally. I’ve had three kids and had to start Tysabri, even if JCV+. I hope I’ll be able to do stem cell transplant one day, when I’ll have the money. Hopefully they will find a real cure for us all.

Newly diagnosed , extremely grieving , and very emotional .

This is my life every day. What a well spoken Talk. 💥💛

very good to listen to her speak. My daughter was diagnosed with MS just recently so it is a big adjustment and coming to terms with things. AS with serious health conditions you do not have awareness or understand till things are closer to home.

I was diagnosed with RRMS in 1997 and then SPMS in 2018 I have been bedridden since 2020 and I don't know what to do but I'm grateful and optimistic every single day "NOW".

These are the real heroes we shall praise. blessings!

I have MS and I truly appreciate the way you explained this too the world. Most don't understand the struggle and feel your symptoms maybe imagery. I've so much hatred toward MS these feelings are real and when I was diagnosed 5 years ago my thought process was OMG I've a disease that hate me as much as I used to hate myself👿. Im a working process but with God, my family, my medical Angel's I see my life as complete. No time to give up on me, my boys, or my family. Yasssss I've too always laugh to keep from crying....but I've alot of days I do cry. I know when there's darkness light will shine through🌝🌝🌝🌝

I have cried, laughed and cheered during this amazing talk Im newly diagnosed and have adopted this attitude as its the only choice we have thank you 😘💝

Thank you for your inspiring story that you shared with us. I myself living in Europe (thankfully we do not worry about our health-bills, since it is funded through taxes) am suffering from PPMS. After getting the diagnosis I went through the same thoughts you went through. It took and still takes a lot of effort to accept this disease. I am only 45 and have still a whole life before me. I am of the opinion that our stay on earth is a gift and we should make the best of it. I try to carry on the life as it was before the diagnoses. Thinking positive in not giving up the battle gives me the strength to go on and being happy.

Love this 💪🏻 I also have MS and can relate a lot to what you are saying. Keep fighting, your attitude is so inspiring 🧡

This video is a Good vibes. I’m with this MS since 2 years now ,completely imbalance total collapse.the best thing that happened is I delivered a boy baby .with this multiple sclerosis I was so worried but finally I got pregnant and now healthy baby is delivered.this is my victory against this multiple sclerosis .thank god thank u so much for the love you shower on me

Doing your disease , your best partner . MS is like my alarm when I forget taking care of myself .

She is very honest and so strong being able to cope living life. I am happy that she has and continues to overcome this.

Brilliant. Brilliant talk. I can relate to what you shared practically 100% as an MS warrior myself. Thank you. I feel inspired right now and my 'mind over matter' morning had just been beaten. I'm attaching my to-do list!

I was diagnosed 2 days ago, randomly don’t have any of the symptoms but my MRI confirmed it, this really helped me as I go through how the rest of my life could be.....just turned 23 never thought I would be where I am with this diagnoses

good luck I was Dx 1996. Still walking (albeit w/ a cane/rollator), still working-on and believing or knowing that I am going to Heal completely and reclaim lost functioning *faith*. You got this!

You lady made my day. I have been recently diagnosed with MS and am still on my way of accepting it. I can't really tell how I feel, I just don't know what challenges life would bring me in future. How I am going to reschedule my daily routine, how it will affect my work and overall quality of life, it still beats me. But your positive share of thoughts makes me feel happy to the fact that I am still alive and not hopeless, that I am still capable of achievements. It is really emotional for me at the moment to have experienced the diagnosis, and your example has tremendously cheered me up. Today I have agreed with the doctors to be signed on a treatment programme that should help me maintain my health. That makes me hopeful. Thank you sincerely for your inspiring speech. I can't tell you enough how much I needed that

Everyday I fight my disease it's a challenge but I continue to stay strong and battle with it.

I'm scared , but now I know I'm not alone thank you .. I loved how you expressed your anger towards your immune system .. I'm angerry but I will survive and never give up I definitely will make use of my tool belt ☺️ Thank you ❤️

I am newly diagnosed and this is so inspirational. Thank you!

Robin, if you see this-Thank you for sharing your story. Your layman description of this terrible disease was concise and comprehensive. More people need to be aware of how MS impacts your cognitive process. Take care of yourself!

Loved it, and great that MS is getting more visibility. But even when people are giving visibility to MS I feel left out. I have Primary Progressive MS. It has nothing invisible to the world, but I do feel invisible in the MS community. Would appreciate that even in a great personal experience exposition like this it would be mentioned that other more aggressive forms of MS exist.

i was 48 when i was dx 2010 i dont take anything for my ms i do have damage on my right side thats why i joined the ms fitness challenge gym on fb it has help me get stronger and I ALWAYS SAY NO MATTER WHAT IM GOING TO LIVE MY BEST LIFE . and I DONT WORRY ABOUT WHAT I CANT DO I THANK GOD FOR WHAT I CAN DO .love april

My wife is 25 and I'm 26 and she just got diagnosed with ms and I'm sooo worried that she won't walk again ... im so scared for her 😔 we had so much plans on traveling and life just hits us so hard so quick .. I cry everyday

I needed this, thank you 😊

This really helped me out so much. My name is Dawn. I'm writing from my boyfriend's youtube page, and am helping him understand also what I'm going through with my ms. It's not only my battle in life. It's our battle together. He is truly a gift from god! Our love is so strong as ONE!

When you said sinus infection I immediately started balling. I’ve suspected I’ve had ms for a year now and can’t get anyone to listen to me. I had sinus infection after sinus infection and they kept saying I had vertigo but I knew more of my body was having excruciating symptoms. I’ve recently gone to a spine doctor for pain who put me in physical therapy which I am doing now. Still on the journey to diagnosis but that spine doctor was the first person who listened to me.

i do not wish this upon my worst enemy...

This made me cry I had to tell doc what to rest for they kept saying I had fibromyalgia

At my lowest times this is where I come