This Gymnast Is Literally Allergic to Everything, Even Exercise
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- Опубликовано: 4 окт 2024
- Natasha Coates has a rare condition called mast cell activation syndrome. Anything from sweating to laughing can set off a life-threatening allergic reaction, and she is hospitalized at least every two weeks. Coates hasn’t let her condition hold her back. An accomplished athlete, the elite disability gymnast has won 22 British titles and 38 British medals. Her condition makes training and competing challenging. But that only makes the victories that much sweeter.
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Dude imagine your body wanting to kill you at any time possible and being a pro championship winning gymnast. Mad props to her.
@Linna ! y.o I WANT S !!!! DON’T OPEN MY VIDEO !!!! THIS IS NOT THE TIME, I HAVE SEEN 4 OF THIS KIND OF COMMENTS T O D A Y, INCLUDING YOURS!
AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
VSCO Memer Bro what?
@Charger kun why?
Mee-aw Because of Healthcare.
god once said, "lets make her allergic to ATP because why the hell not" (atp is basically what you'd call energy, or something similar)
She isn’t allergic to winning though
What's with your channel name
Or is she?
💌💟😍😍
Your username makes me uncomfortable
Genius
She took “I’m dying laughing at this” to another level
😐
@@darshanb6916 what are you trying to say? Can't take a joke eh?
@@kpp28 who you talking to?
E it was either a bot or they deleted it
Was that supposed to be funny?
This just goes to show that we take literally everything for granted as a society. Be grateful for what you have people.
Wtf did these replies come from
She's such a sweet heart. But who are these six pack dudes on the block next door :
ruclips.net/video/mNSaZbXW5us/видео.html
Ewwww....
🌹💙💚😍💕
Tf are these bots. I think these are bits report them
If she was in America she would not be able to afford all those hospital visits
I was wondering how her American friends can afford that. I'm not sure if I'm right, but it would sound like constantly using EpiPens and those are expensive...
I thought exactly the same thing. People who are against social health have never been really sick before. Money worries is the last thing you need when your ill.
@yOuR dOg sPeAkS cHiNeSe?? But not to the extent in the UK. In the UK there is a national health care system. In America if you don't have insurance, or aren't on Medicare and welfare its extremely expensive. And even with those, it gets super costly really fast
Achoo! Careful, Natasha may also be allergic to socialist bullshit.
Perseverance is the key to bravery. But who are these six pack dudes on the block next door :
ruclips.net/video/mNSaZbXW5us/видео.html
This person is living on hardcore difficulty and trying to 100% it
We all are living on hardcore difficulty
@Naireals delete that
@Naireals Okay. Sure...
_Sweating might kill her - competes in a physically straining sport anyway_
The thought alone is making ME sweat, literally
P she only competes in tournaments held in north pole or around
Ok
666th like
I'm sweating too it's hot in here I had to turn on the fan-
Weak
Crazy, I use to have the same illness as well. Allergic to sweat, even miniscule amount, like bearly even a drop. You won't believe how easy it is to trigger such a reaction unintentionally. Laughing, showing strong emotion, any bit of exercise. Even in cold weather where you'll think you never sweat, it will still affect.
Only difference with mine is that it's not lethal. But it causes excruciating pain, like being poked by a million needles all over.
yikes!
Hey, the same thing happens to me, though I don't think it's sweat, it only happens when my blood heats up, it is really painful, it is usually on my wrists, ankles, back and chest
@@batatadoce3025 That sounds like it sucks. Hopefully there's some way to make it go away or just get less annoying.
Woah. That sucks. What is that called?
@@adrienneislost1320 I'm still not certain what causes it, but it usually happens when it's cold, working out, getting angry, even listening to music that gets me hyped triggers it.
Looked up to Natasha for so long! She's truly an inspiration and such a talented and resilient person ❤️
Damn, it would be crazy expensive to have that disease in the US.
Thomas Sweet yes, it is. I have broken down crying in front of Drs /pharmacist because I needed a drug treatment that would have cost over 2thousand dollars a month, and we didn’t think my insurance would cover it. Thankfully, it is covered (my Dr was surprised, she said her other MCAS patients have to pay). Unfortunately, the therapy doesn’t do much to make me feel better yet, but it’s helping. I was really hoping that I would have felt a big difference, like some.🤷🏼♀️
To be very real with you she likely wouldn't still be alive if she lived in the US. The health care is awful even if you can afford it.
Trust me, it is. I live with it. My reactions are only occasionally life threatening, unlike this brave girl, but when everything you eat, wear, and touch could make your body panic - it requires being careful. Most doctors here haven’t even heard of it. 🥲
@@tsulehisanvhisystem9352 Yeah. We claim to be this amazing country with all this first world stuff but as someone I talked to said once, America is actually just a third world country with a Gucci belt
And it shouldn't be. But obviously Europe is just full of socialists...🙈🙈🙈
She didn't let her condition stop her in her tracks. She's an inspiration to so many. Anything is possible if you just believe
Wtf are wrong with these replies!!!!
Dude wtf are all these?
You are literally everywhere
@@subifyouhatetiktokandreddit234 Was about to say the same thing lol see him everywhere.
I have MCAS too, though not as bad. It, and the conditions she doesn’t mention that nearly always go along with it, are really hard. Currently bedbound but getting stronger every day 💪🙌
Best of health to you!
Good luck, dude
Good luck on your journey >:D
So here's my question: How can SHE be doing all this gymnastics bullshit? I'm not even downplaying you, I'm saying...is she lying? I don't believe that just being alive can cause her so much discomfort...and yet she goes into gymnastics. She could be doing a million other things.
@@9to5Drone the fact is that she’s doing what she loves period. It’s most definitely not even in question about what other things she could be doing. That’s what makes her strong willed! She even says she may very well die from this complication/disease yet she won’t let it interfere with what her heart and soul loves to do. It’s a fire that won’t be burned out in her heart and soul due to her shear determinism!!!!!!! May she keep doing what she does cause she is definitely strong in my heart/soul/ and opinion! May you live a long healthy wealthy and happy life!!!!!!! :) :D
I have MCAS too! I’m in Australia. I’m so excited to see this being spoken about.
Sending a big virtual hug to Natasha. Watching you fly through the air is so beautiful. You’re an incredible gymnast. Thank you for sharing your story with us. ❤️❤️❤️
❤️❤️❤️
❤❤❤
She is so damn inspiring .... I hope she live a long and happy life
amiin
@@juliet5585 she literally posted on her instagram 4 hours ago... please stop spreading false information.
She literally competes in a form of gymnastics for people who are held back meaning she is literally being held back. We can do the positive message without trying to act like a severe disability that causes dozens of hospitalizations a year doesn't hold you back from doing anything.
True. It's important to not misrepresent the situation. Especially bc it can set unrealistic expectations. The true situation is just as inspiring, if not more, bc it would seem less like the "1 in a billion special person who you have no chance of being" and more like "a possibility for you if you have the means and the dedication"
Much love for her and anyone else who Suffers from a chronic condition that not many understand. She's one of many people who I look up to when dealing with my own invisible problems ❤
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!💖🖤❤️今後は気をライブ配信の再編ありがとうです！この日のライブ配信は、かならりやばかったですね！１万人を超える人が見ていたもん（笑）やっぱり人参最高！まさかのカメラ切り忘れでやら1かしたのもドキドキでした,.
💖🖤在整個人類歷史上，強者，富人和具有狡猾特質的人捕食部落，氏族，城鎮，城市和鄉村中的弱者，無`'守和貧窮成員。然而，人類的生存意願迫使那些被拒絕，被剝奪或摧毀的基本需求的人們找到了一種生活方式，並繼續將其DNA融入不斷發展的人類社會。.
說到食物，不要以為那些被拒絕的人只吃垃圾。相反，他們學會了在被忽視的肉類和蔬菜中尋找營養。他們學會了清潔，切塊，調味和慢燉慢燉的野菜和肉類，在食品市場上被忽略的部分家用蔬菜和肉類，並且學會了使用芳香的木煙（如山核桃，山核桃和豆科灌木 來調味g食物煮的時候 1618753721
She really takes "yolo" seriously.
No one is immune from death, Make the most of what you can do now. ❤
The animation in this episode is incredible! Props
Me: Reads the title
*visible confusion*
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》》 𝙊𝙣𝙡𝙮 𝘼𝙙𝙪𝙡𝙩 《《
在整個人類歷史上，強者，富人和具有狡猾特質的人捕食部落，氏族，城鎮，城市和鄉村中的弱者，無`'守和貧窮成員。然而，人類的生存意願迫使那些被拒絕，被剝奪或摧毀的基本需求的人們找到了一種生活方式，並繼續將其DNA融入不斷發展的人類社會。
說到食物，不要以為那些被拒絕的人只吃垃圾。相反，他們學會了在被忽視的肉類和蔬菜中尋找營養。他們學會了清潔，切塊，調味和慢燉慢燉的野菜和肉類，在食品市場上被忽略的部分家用蔬菜和肉類，並且學會了使用芳香的木煙（如山核桃，山核桃和豆科灌木
來調味食物煮的時候%^%^ 1618758487
Very inspirational she didn't let her condition stop her chasing her dreams God bless her and protect her❤❤❤❤❤❤❤
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!💖🖤❤️今後は気をライブ配信の再編ありがとうです！この日のライブ配信は、かならりやばかったですね！１万人を超える人が見ていたもん（笑）やっぱり人参最高！まさかのカメラ切り忘れでやら1かしたのもドキドキでした,. 💖🖤在整個人類歷史上，強者，富人和具有狡猾特質的人捕食部落，氏族，城鎮，城市和鄉村中的弱者，無`'守和貧窮成員。然而，人類的生存意願迫使那些被拒絕，被剝奪或摧毀的基本需求的人們找到了一種生活方式，並繼續將其DNA融入不斷發展的人類社會。. 說到食物，不要以為那些被拒絕的人只吃垃圾。相反，他們學會了在被忽視的肉類和蔬菜中尋找營養。他們學會了清潔，切塊，調味和慢燉慢燉的野菜和肉類，在食品市場上被忽略的部分家用蔬菜和肉類，並且學會了使用芳香的木煙（如山核桃，山核桃和豆科灌木 來調味g食物煮的時候1&!/ 1618744053
WATCH MORE VIDEO F.U.L.L H.D 💓 CLICK HERE : livegirls19. com
!💖🖤❤️今後は気をライブ配信の再編ありがとうです！この日のライブ配信は、かならりやばかったですね！１万人を超える人が見ていたもん（笑）やっぱり人参最高！まさかのカメラ切り忘れでやら1かしたのもドキドキでした,. 💖🖤在整個人類歷史上，強者，富人和具有狡猾特質的人捕食部落，氏族，城鎮，城市和鄉村中的弱者，無`'守和貧窮成員。然而，人類的生存意願迫使那些被拒絕，被剝奪或摧毀的基本需求的人們找到了一種生活方式，並繼續將其DNA融入不斷發展的人類社會。. 說到食物，不要以為那些被拒絕的人只吃垃圾。相反，他們學會了在被忽視的肉類和蔬菜中尋找營養。他們學會了清潔，切塊，調味和慢燉慢燉的野菜和肉類，在食品市場上被忽略的部分家用蔬菜和肉類，並且學會了使用芳香的木煙（如山核桃，山核桃和豆科灌木 來調味g食物煮的時候1&!/ 1618770366
My daughter suffers from an over zealous immune response that makes her life unbelievably difficult. Her life is a balancing act. She’s such a fighter, like you. We always say that you get to a point where you learn to find joy wherever you can -wring the joy out of life. Life is so fragile. You can’t let yourself live in fear too much. It takes bravery, and you have to have it to live inspite of the sometimes really scary. You already know this. You’ve learned to make the most of each day. You’re learning at a young age what it means to really live. I admire your courage❤️❤️❤️
Dude people like you make this world a beautiful place to live in, you are a legend a living inspiration and it doesn't matter how much years you live what actually matters how much you live in those years so chill you can do it!
God has a greater plan for all of us !!!!
“Nothing is impossible” she is a true example. God bless you dear 🍀
I have a very similar condition, but it is limited to my lungs. My auto-immune system attacks my lungs 2-10 times a day, every day, for absolutely no reason. More hospital visits than I can count as well.
It's tough. I can sympathize with this woman. Major kudos and respect to her being an Olympian.
This women achieved her victories and beating that allergic reaction god bless this women
Seeing stuff like this makes you feel terrible for moaning about the trivial things in your life. Inspiring
True, but sometimes even the little things can be valid. If you don't deal with them because of this feeling that 'other people have worser things to deal with' sometimes they build up and overwhelm you.
Good. I wish I knew that more before I got sick. I have this and the illnesses (yes plural, it usually co-occurs with other illnesses) make things really hard.
That's interesting! I love seeing people doing amazing things despite difficult conditions.
I find it amazing that Coates can be out around all those people. I'm sensitive to chemicals and can have cytokine storms (mast cells gone crazy), which have damaged my lungs and kidneys. I have to be so incredibly careful not to be exposed to fresh paint, pesticides, most cleaning solutions, perfumes. That won't likely kill me if I'm careful. I've also been periodically sensitive to heat and am allergic to over 20 foods and most trees, grasses, and flowers (and cats and mold and so on). I've only once had a bad case of angioedema where we were unable to find the trigger and that was very frightening, though in my 20s the left side of my face would swell with frequency (and we never knew what that was about). Given how sick I get when exposed to paint (and a few other things), I can imagine the terror she lives with. I also understand the drive to be out in the world despite illness. I did my best--was fully employed in a professional position (had to be accommodated my entire adult working life)--until that was cut nearly 20 years short with disability. That said, I can't imagine my own emotions being a threat to my life. I wish her the very best. And I hope some things shift for her as time goes on... I have less trouble with allergens that are found outdoors now, which has been such a blessing. At least I can be outside without being afraid (save for yellow jacket wasps).
Mad respect to her,she's amazing.
Shes incredible its astonishing how much she has endured I hope she continues to live long
man and I thought that normal gymnastics was hard...
@@animalover734 ik that its hard (I did it for a long time) but like I can't imagine living with that yk
@@animalover734 yea except if she starts crying from almost breaking a bone she might die
Mad respect to this girl
This woman is so strong! I wish her the best and I hope that a cure is found! 💜💜
Thanks for showing her story- very inspiring, terrible disease. I have mild MCAS (So far... still haven’t needed an epi) and it sucks... always itchy/rashy feeling exhausted from the constant reactions. And so so many antihistamines/treatments to keep track of, it’s maddening. My life basically fell off a cliff ten years ago when this all started to activate, my career as an artist has taken a huge hit, but I’m still fighting and I go to my studio every day...even if it’s just to check the locks. so tough to explain to everyone, even doctors
Oh my gosh! I haven’t found another person with MCAS who hasn’t needed an epi!
What a beautiful and strong woman! Keep pushing, you're so inspiring and so brave!!
Natasha is truly a warrior. ❤
Best of wishes for her.
I was born with a rare genetic condition, Spondylocostal Dysostosis, that got worse when I turned 22, I'm 28 as of September this year. Like you with gymnastics I have done karate since I was 7, and I teach now. Let's keep it up and inspire others to adapt and not just give up too ❤💜💪👊👍
Man she is one of the strongest of the strong because I know if I had this condition I don't know if I would make it let alone do what she does
Such an inspiring human being, Big ups to you Natasha
I saw her from a documentary a long time ago and seeing her with hair was such a joy! she looks lovely either way but seeing how far she become is truly amazing ❤️
Thank you for your courage. I have struggled with this also. It is poorly understood by the medical establishment here in the US which makes it all the more difficult.
This made me cry so hard. God bless you angel and your friends and family and anyone else going through what you’re going through. I pray you all live long healthy, happy, and beautiful lives 👼
I smile everytime I see these types of videos because they are just so inspiring
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Leurs états de santé
respectifs les empêchent
de s'approcher trop
près l'un de l'autre.
在整個人類歷史上，強者，
富人和具有狡猾特質的人捕食部落，氏族，城鎮，城市~sae和鄉村中的弱者，無力防守和貧窮成員。
然而，人類的生存意願迫使那些被拒絕，被剝奪或摧毀的基本需求的人們找到了一種生活方式，並繼續將其𝔻𝔸融入不斷發展的人類社會。
說到食物，不要以為那些被拒絕的人只吃垃圾。相反，他們學會了在被忽視的肉類和蔬菜中尋找營養。
他們學會了清潔，切塊，調味和慢燉慢燉的野菜和肉類，在食品市場上被忽略的部分家用蔬菜和肉類，並且學會了使用芳香的木煙（如山核桃，山核桃和豆科灌木）來調味食物煮的時候 1618786047
Thank you... I’m suffering from some health condition too but it’s not as serious as this one is, I had a surgery once but I was, and till now, still freak out for anything could happen to me everyday. I became paranoid at any single symptom and panic about it, but compare to her case, mine is just a small fly. Thanks for letting me know this amazing girl and I’ll try to be as brave as like her
Imagine the healthcare bills if she lived in the US
How much does health care cost in Americ!?!?
@@animegirl8033 bad enough that it’s the number one reason Americans file for bankruptcy
@@nartnir oh wow
Never mind health care costs, I doubt they would be able to diagnose her properly. They would probably say she had hysteria or something
As someone whos in a wheel chair alot of the time, i can confirm that now any moment of free, flowing, fast movement is elating.
Never has the phrase "I died from laughing" been more alive
Who could dislike this video?
RIP Great Big Story- so sorry to see you go :c
What an inspirational person! Hope she lives a long, happy life!
As an American, I know for a fact - she would have just died with the kind of healthcare we have. Live your life girl, bless you
What a legend.
From a Buddhist perspective, every relationship we have will eventually end in parting and sorrow, we just don't usually think about it. 🙏🏻 She is an impressive competitor and a beautiful human, and I wish her all the best.
I hope the girl is doing alright. That's insane..
she's still freaking amazing!
It's so sad to hear that..
But in positive ways you can handle it..
Love you hope you all the best..
My husband has this condition. Doctors can never find what he is allergic to. I feel really bad because he is always swelling, itchy, and in pain. It takes a lot out of him.
I have a condition that sounds similar to this (Chronic Colanergic Urticaria) where whenever my body temperature rises or I get excited, nervous or exercise my body releases histamine and I get small bumps all over my arms and my chest gets very red.
RIP Great Big Story 2015 - 2020
This girl is actually able to say I’m dying of laughter.
Courage + strength = Natasha Coates
Me: *holds up a piece of paper that says "exercise" on it*
This person: AAAH
Thank you for sharing our story! There are so many masties all over the world whom doctors think are crazy. Every little bit is education helps!
The one thing she's not allergic to is Raid Shadow Legends.
This comment was sponsored by raid shadow legends
Raid shadow legends is a new RPG game with high-quality graphics
Raid is is my only allergy.
bruh wtf
Oof
Great spirit, could die any day and still compete in sport , What a warrior.
And then there is me.....
SALUTE to you girl! People like you inspire me to be a better person every day! May the universe let you live a happy and contented life, you deserve nothing but the best. Lots of best wishes ❤
Wow this is a strong message, no one will have carrot
RIP TAYLOR ❤️❤️❤️
I met a woman who had this at my work! Everything sets her off. It’s an incredibly rare condition. Amazing story!
I love her attitude: allergic to giving up!💓
Here before this gets recommended 5 years later
Natasha you are so strong and resilient in every way, keep on doing what ur doing and also your so so beautiful inside and out❤️
Jules JJ awww🥺 rip
*Damm, imagine literally nearly dying of laughter*
"Disability is not inability." - Comfort Yeboah, to her son Emmanuel Yeboah the night before she died.
Emmanuel, who was born with a deformed leg, would raise $50 000 cycling across Ghana in 2002 to support the disabled in his home country (who are often looked down upon or left to die).
Let tales of personal triumph like Emmanuel's and Natasha's inspire you to never give up and defy the odds
This is the woman my asian dad would compare with lol. Coz I can't do a cartwheel also and I have no dangerous illness
the animation is amazing!
GOOD JOB GIRL, YOUR A LEGEND FOR THAT REASON!
Moments like this make me both grateful and ashamed
Thats awesome!!! You goooo girl!!! God, I cried watching this episode!! More power to you!! ❤❤❤
Can relate to her on some level as I have cholinergic urticaria.
imagine going to hospital over and over again and losing best friend.i can't
Hi great big story,love your vids
Is great big story really being shut down by CNN? I LOVE great big story for what it does and what it represents. Honestly hope it can continue. It offers some of the most beautiful, meaningful and humanitarian showcases...the videos are some of the most beautiful I've seen.
I have problems with pizza and dairy and also nasal congestion , every body has its flaws , but we can adapt to them
This young lady is living proof that all my problems are not problems.
Good thing I never complain about the same problem but without the serious effects, only scratches, sneeze and crying; still a really great and inspiring history :O
If she was sad she can't even cry without risking her life, Huge respect to her!
She is AMAZING!! very inspiring
I to a certain extent know how she feels, I suffer from a condition similar called I.G.G.E, Immuno Gamma Globulin E disorder, my reactions aren't as severe as hers but it does have it's ups and downs, inoculations don't always take and as an example I got whooping cough as an adult, it was horrendous. I can't stand being to hot or to cold as either sets off allergic responses in my skin. In your blood is the substance called I.G.E which regulates a substance on your skin, two little I.G.E and this substance attacks the skin causing irritation, to much I.G.E ( as in my case ) and it destroys this protective layer which then leaves you vulnerable. Most people have an I.G.E level between 0 and 150, mine was 1219, the worst case I have heard of is over 25,000 he can't even watch television without reacting.
You made a name for your-self, be proud!
Wow, what an inspiration ♡
I hope she's safe during the pandemic ☹️
Same here ☹️
(the condition isn't really that rare actually, but she does have a form of it that is quite uncommon)
"I've nearly died from laughing too much with my friends" i hope i die like this with friends
inconsiderate
The fact that she is able to be a professional gymnast and have all these allergies is amazing. People who power through things like this are legends. ❤️
i have a similar case, too, but not as life threatening as hers. i have a severe case of hyperhidrosis where i can start sweating without any triggers. there is not a viable cure for this one- except cutting some nerves or taking injection shots, but once you start taking these you can never stop. it is hard in summer, cause of the heat of course, but it is hard in winter, too. in winter, the sweat glands produce sweat, but the skin is tight and dry so it has no way out, and it gets stuck under skin and forms bumps which can trigger bloody itching (sweat, if left on too long on skin surface, more so under the skin, becomes an irritant. this happens under the nails too, so when these bumps form it starts to literally peel the nail away, but it is not painful after the right medication. i am thankful that i don’t have a life threatening illness and i am so happy that, despite this inhibition, Natasha is working hard to achieve her dreams. i will always support you.
We humans are unbelievably strong. Don't give up.
make a movie about one of these people
"literally everything" winning doesn't count though.
This is terrifying, glad she has the necessary healthcare