A life impacted, but not defined by Multiple Sclerosis: Bibianne’s story
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- Опубліковано 11 вер 2019
- Bibianne Yu was a piano teacher all her life - until 2016.
That year, she sold her beloved piano, eight years after she was first diagnosed with multiple sclerosis (MS). The disease affected the agility of her fingers and gradually took away her ability to enjoy one of her life’s greatest passions.
MS is a degenerative disease that impacts the central nervous system by breaking down nerves’ protective layering and causing damage.
MS is “Canada’s disease,” with one of the world’s highest rates of the condition. One in every 385 Canadians are living with the disease.
St. Michael’s, where Bibianne receives care, is the country’s largest MS centre, with more than 8,000 patients receiving treatment at its clinic. The hospital has a unique opportunity to change the trajectory of MS for its patients through world-class, specialty care and leading research and innovation.
This is Bibianne’s story.
READ MORE: features.unityhealth.to/ms/ - Наука та технологія
I am from ALgeria.. 29 years old..i have this illness...i am teacher and i have a little daughter.....i beleve in God and his mercy....so...no place for sadness☺☺☺☺
amen
You’re making my heart hurt. I am looking at a possible MS diagnosis and this is killing me. I hope to have your strength.
Brian Walsh II Me as well. I’ll pray for you! I’m worried because I’m also a pianist
Brian, you're gonna be okay. Please come and check out a Facebook group called The MS Gym. There is so much love and support and hope in this community.
WHAT EVER THE OUT COME DONT GIVE UP u have a community here 4 u if u need us... ✌️✌️✌️😘😘😘
I was diagnosed with ms at 14. You just gotta fight through it.
Brian, I know it's scary right now. You're probably having a ton of emotions right now, that's normal. I've had multiple sclerosis since 2011 and I'll be straight up. It might refine things for you but it certainly won't define you. There are so many people with ms with amazing quality of life and are very able. You don't have to do something like me and become a nationally qualified bodybuilder just to prove that but I promise you that you can grow and love the new almost way cooler version of you! ❤️ my hearts with you
Thank you for sharing your story. I also have MS and was diagnosed 12 years ago in 2008. I have also decided to tell my story on here to to help support others newly diagnosed or going through MS. I wish you well
I pray for you and everyone with MS. I was diagnosed a few months back. I had been in a very dark place but also trying to be positive and seek inspiration from others and my support group.
I just got back from my 2nd brain scan where they found white matter that suggests MS. 2 other family members have it so I’m not giving myself false hope. This was the first story that popped up for me after searching and I’m a piano player as well. I needed to listen to her and witness her spirit. Thank you.
If you're newly diagnosed or still undiagnosed, please seek out positive stories. There are many. #pugyoums #ppms
Thanks for sharing your story
You are so fortunate to have such a wonderful clinic. We have little here, a couple MS physicians and no support. It is very frustrating to not have information and resources. I watch Dr Aaron Boster on YT, I’ve learned more about this disease from him than the past three doctors I’ve had. Keep your spirit!
My ex suffer from MS.
I daily use to pray for her.
Unfortunately she left me for some other guy.
I know this sounds selfish but I am 18 I really hope not....I don’t want to have to be brave
Please could I share this story on my IG to raise more awareness? X
Adaptive Behavior with indigenous treatment modalities!
Musicians Against Multiple Sclerosis@ salutes you!
MWM
I pressed too hard while massaging my neck, but now my muscles tremble and weaken, and my eyes hurts a little. Can it be multiple sclerosis? What should I do?
God bless you you are an amazing woman ! be strong I also have MS and you give me hope you make me strong thank you 🙏❤️
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Does anyone have any info in any new treatments or things that help with secondary progressive MS? My mother is deteriorating and is nearly bedbound. She can’t change herself anymore or take care of herself. She can’t use the bathroom and it’s just so sad. She is getting so tired and has talked about wanting to die if she continues this way. I’m desperate any info would help. She’s confined to the chair in our living room and has basically given up. She was diagnosed in 1996 the year i was born. Any info would be greatly appreciated 🖤
I know of great Dr who can help her
Now listen to me carefully Aimee.
Just type on UA-cam "Dr Terry Walsh"
She is a doctor and also a MS patient.
She tells her journey from wheelchair to walking & how that became possible and what are the things that made it possible.
My MS diagnosed since 2018
Same for me
Words ain't enough to express how grateful I am to Dr Madida for his assistant in resolving and treating my aunt's Parkinson Disease.
I have MS. I felt way worse on copaxone. I quit after 18 months. No drugs for now. I have too many other health problems to handle MS meds. I wish the system would investigate things like chronic bacterial infection, but they can’t make money off that.
How r u now
was recently diagnosed - bacterial infection in the gut system?
yes watch be aware of movements of mind body stay alert study
Hi i am 10 years old and i am also diagnosed with ms
May the good lord bless you how are you doing now ❤️
That’s really young. I’m sorry you got the disease at such a young age. You’ll be okay man. I have it myself.
How are you doing Nasir?
I've been diagnosed with MS since 2017. I wasn't able to move my feet I'm 24 years old from the Philippines.
I’m sorry to hear that.. May i know what is your first symptoms?
I will be praying for you
Im from philippines 🇵🇭 to 10yrs ago i have ms to but now leave in Japan hoping youll be better and im praying you god blessed us !
I love her spirt 💕
ME TOOOO I LOVE MUSIC AND PIANOS and I can imagine how hard it was to give it up... im a flight attendant and the day I have to leave my profession for good is gonna devastate me cuss I love my job and all my coworkers!!! #mssucks
got finally diagnosed in 1998 but I trace it back to about 1993.... and been flying since 1997
Thank you for discussing your problem as it explains everything indetail and quite easy to understand as well....for a very long time I thought I am the only one suffering from the disease but is one of the best video as I had been suffering from same problem....for a while I thought that I am never gonna get better until someone told me about Planet Ayurveda and that has helped me a lot.
My sister is 32 years old and she has suffered from meniere disease for years and she always complains to me that I had to bought her Dr Madida herbs I saw on UA-cam and she is telling me last month that she is cured completely and don’t long have the symptoms like vertigo or dizziness, feeling of fullness in the ear or ringing, hearing loss, imbalance, motion sickness, nausea, or nystagmus
Aw
Canada consumes alot of caffeine! I wonder if there is a connection to MS as the USA also has high MS rate 🐱
NO.
I heared that who ms they don’t live long only 20 years after ms diagnosed that’s really?
Milagros Garcia my question that ms patients don’t live long life , does ms head spinning too ?
untrue - life span is only 5 years less than average and that is based on old data... people dying now had MS for 30 yrs+ and didn't have access to the treatment we do today. So perhaps MS patients today will have a very similar life span who knows...
Wake up...Drugs just stop relapses they don't stop progression. From dx people with rrms and no diability will only live 20-43 years.