Doctor explains Stiff-Person Syndrome after Celine Dion's announcement about her diagnosis
Vložit
- čas přidán 7. 12. 2022
- Dr. Ritesh Ramdhani discusses the symptoms, risks, and more about Stiff-Person Syndrome, after Celine Dion's recent diagnosis. 7ny.tv/3P9Wscy
Check out more Eyewitness News - abc7ny.com/
Find us on social media:
FACEBOOK: / abc7ny
INSTAGRAM: / abc7ny
TWITTER: / abc7ny
TIKTOK: / abc7ny
We’re abc7NY, also known as Channel 7 and WABC-TV on TV, home to Eyewitness News, New York’s Number 1 news. We hope you love us on CZcams as much as you do on television!
NEW TIPS:
Online: abc7ny.com/submit-a-news-tip/2...
Email: abc7ny@abc.com
About WABC-TV: abc7ny.com/about/
#nyc #news #otv-breaking-news
I’m so sorry for her one thing after another
Celine our prayers are with you
We're all on borrowed time, love every moment...gratitude every day.
Amen amen n amen!!!🙏🏽👍
Amen…🙏
Amen 🙏🏼
THIS DOCTOR GIVES ME HOPE
Yes still there a patients who get healing so its a good news
It’s progressive
|--|=======-----------...
Prayers for the wonderful and kind CeLine.
My heart goes out for her now. Celine is an amazing person and has given so much to the world and I do hope she feels better with the options of treatments menitoned by Dr. Ramdhani. ♥
Our human bodies are miracles of nature...but they are not perfect. Many of us have conditions we must learn to live with. Though her life will be different, she will learn to thrive in new ways. We will always have videos and recordings of her amazing voice!!
Amen..🙏
My heart is breaking for Celine, she is a wonderful person and a wonderful singer, my prayers are with you and hope you will get back to good health soon 🙏 ❤️ xx
She is a witch
The curtain closes, a new life begins! Thank you for the wonderful years of entertainment Celine….Prayers.. 🙏🙏🙏. We are all going to get old…acceptance is the key..
My heart goes out to her, as I to suffer from stiff person syndrome.
Stem cell transplants can cure autoimmune diseases. They do them in other countries w great success. The evangelicals & pharmaceutical companies do not want stem cell transplants in the US. There is no money in it for them. I have stiff person syndrome. I need 58k to go to another country to get it. Unbelievable isn't it. I wish Celine the best. She can bring attention to the cure. Blessings.
|--|======-----------...
If you’re in CT or close, I know a place that does stem cells and they’re from another country. I wish I could remember which.
update?@@EmberFfin
Mineral deficiency comes to mind. Months ago I had high stress and digestive issues. My prior job was causing the high stress and an eating disorder was causing the digestive issues. I remember getting eye spasms and then horrible leg cramps along with breathing issues, hypertension and periodic constipation and dehydration. Doctors couldn't figure it out and kept dismissing it as anxiety but I felt like it was something more so I started doing lots of online research about my symptoms which lead me to diet. So, I started a anti-inflammatory diet which after 1-2 months did help a good bit but it wasn't until I did what I call a "gut reset" that I got completely better. I basically cleaned my intestines/bowels out and then started drinking protein drinks with minerals and vitamins along with my anti-inflammatory diet and after a month or so, all of my symptoms were completely gone. Oh, and my last totally blood count levels came out optimal so my method must have worked in my case. I don't know if a "gut reset" along with a clean, high nutient diet would help Celine but my doctors didn't know what was causing my issue either so I had to fix it myself. Of course, I wouldn't suggest doing what I did without consulting your doctor first just incase it's not right for you.
❤
I understand completely what Celine is going through. I Have generalized Dystonia and it affects all my muscles and my voice too.
But there is hope for you Celine.
I am sure your neurologist and doctors have discussed DBS
Deep Brain Stimulation.
Dystonia is located in the deepest part of the brain, basal ganglia.
I don't know what part of the brain your condition is located, but I hope and pray that you will be a good candidate for this surgery. There are medications that help too.
I was diagnosed at 48 yrs. I m 68 now and the DBS helped me tremendously.
I'm no longer in a wheelchair and living a much better life.
My Dystonia will never define me.
And I want you to know that you are in my thoughts and prayers. Never give up on Hope.
I know you will be singing 🎶 again.
God be with you.
Hi! How are you? Hope you're feeling well or better!
May I ask you these questions?
What were your symptoms? And how was your diagnosis? What tests were performed?
Thank you
Blessings 🙏🏼
@@lillyrocks2011
I had to have cognitive testing done and an MRi done to rule out any other diseases.
I didn't have any lesions on my brain.
I don't know if you have been diagnosed yet with some type of Dystonia.
If you have, I probably could help you more.
Sharon Mazurek
My thoughts and prayers are with you
@@lillyrocks2011 my thoughts and prayers are with you.
Am broken down because of this news.God above all.Celine b strong.
Millions of people are suffering NEUROLOGICAL injuries from covid vaccines as well as miocarditis and heart attack. Can we please talk about the truth.
This condition has been around a lot longer than Covid-19 and the vaccines to prevent Covid-19 infections.
@@josephbennett3482 Yeah well now the cases are multiplying, go figure, perhaps it's a new other disease with similar symptoms catching up just faster
Thank God! A recovery is still possible 🙌🏼💙💪🏼
Nookie! Its called Nookie! She's been without a mans errr touch for so long Cobb webs have caused her pelvis to Stiffen and so it spreads throughout her body.... Women need Men to loosen them up...
@@saywhat951 SPS is real.... my best friend may die this week from it. I also have stage 4 cancer. Normally I would've laughed, BUT maybe tomorrow.
Sorry To Hear About your problems with your voice please get better soon
My husband's 1st wife was diagnosed with " stiff person syndrome" she was giving 5 years after her diagnosis and lived 5 years and 5 days. No cure sadly.
Oh no...
Praying
Get wellcelinea will pray for you
I pray she achieves remission. 💙🙏🙏🙏💙
I could see why she is not performing. The stress alone could cause another attack. It's best avoided I totally agree. Muscle spasms in part of the body hurts enough so image the entire body which is what she is going through. With this disease the entire body goes into a muscle spasm. My heart really breaks for her and I so hope they finally find a medication that works. This women sings about love in every song song she has. She has brought us so much love through her music. I am so fortunate to have her CD's and Music video CD. She even made videos of her music videos for us to purchase. When I was a kid it took so long to record these music videos and collect them and now we can buy them right on. Your so loved Celine.
I have the same syndrome as Celine Dion's. What helps me is that when my muscles get stiff, or spasm, or cramp, I take 400 mgs. Of the Garden of Life brand of magnesium citrate gummies. Shortly thereafter, All of my muscle symptoms go away. Also I drink fruit juices which relax my muscles, And I keep hydrated which relax my muscles. Sometimes I take one or two tablets of aspirin which also relax my muscles. Sometimes I take 0.5 milligram of Ativan which relaxes my muscles because it is a muscle relaxant. Sometimes I'll take 1 mg. Sometimes I'll take 10 mgs which is the lowest dose that it comes in of Ativan. It relaxes my muscles because it's a muscle relaxant. Sometimes I'll take 1 mg. And sometimes I'll take 10 mgs, which is the lowest dose that it comes in of Atarax. It relaxes my muscles because it's a muscle relaxant. Sometimes we'll take 20 mg. I take everything with fruit or other food.
The mortality rate in general is 100%
Yes. It's only question of time.
Prayers of repentance to Celine.. can’t go against the Almighty God when He blessed her with an amazing voice .. run to God Celine He has the last word..
Everyone will eventually get sick and die. But most will not have the money to receive proper treatment though. Life is harder for poor people.
Awful lot of folks coming down with neurological disorders… myocarditis…. Rubbery “clots” forming in the veins. They made a movie about this oddity.. you can’t find it on CZcams… but you CAN find the documentary “Died Suddenly” on Rumble
Seeing photos of an emaciated Celine a few years ago i thought muscle spasms would be in the cards for her because when there is no more fat to consume the body begins to eat away at the muscles. Stiff person disease is a million to one condition, but mis-diagnosed patients is considerably more common.
Hi! I think you're right, it's easy to misdiagnose or not getting the right diagnosis or confuse it with another.
Are you doctor? Thank you
Probably after loosing her husband her body experienced so much stress and pain that peace is needed in her body
Celine has gone through hell with her Stiff Person Syndrome (so rare!) ...A new video to raise awareness was just released. We love you
If you ever encounter a tubal pregnancy, you will encounter is very stiff body as well. You will collapse and not be able to get up & the entire midsection is stiffen. It Is also extremely painful!
Fibromyalgia needs more attention ❤
Dymealition
Anyone else gonna ask if it’s related to the jab??
She was vaxed otherwise she couldn't do concerts
|--|=======-----------...
Why ask, You already know
@@eaglez9518 No She was not jabbed; just her systems collapsed due to overwork and late nights
@@chavale2 If she did not vaxed she was not allowed to work / overwork. vax was compulsory for any concert and singing, Justin Bieber was vaxed as well.
Who cares about her performances. Let's hope and pray for her LIFE.
What causes it 2:29 they don’t inow… anybody can have a stiff neck … is it something autoimmune or nuero related dymealituon …. If they don’t know what causes how can. They effectively “Treat it “
I think it is mandatory for this condition to have a medical card like person with Epilepsy just in case not to be mistaken as a heart disease of origin or syncope in the public.
What is the person's body temperature
Wow some of these comments are brutal ... we were all deceived, we are all suffering 💔
What kind the question is that mess about her future for now we all have to pray for her .
it's signature of vaccines injury .. may she be healed soonest
Not rare and not at all one in a million. Just look at the size of the sps support community. Currently the number of patients is huge. And many believe vaccines triggered / caused this.
Its like every US doctor is giving interview to get Celine in as patient.
I hope she can get IVIG
Am not a doctor but this has to be a brain disorder.....my brother had an accident hit his head big-time was in coma for over 1 month and he went through Spasticity and spasms....there are medications that relaxes muscles....the amazing thing was when he would sleep muscles would totally relax....and would be very flexible
This is called the doctor, not the Newcastle. Since I want to be something in special education, working on my masters to get there, can people with cerebral palsy also get FPS in the future? Evidently, CP (as cerebral palsy is commonly known). might have muscles best to be involved. I think that would be high, local con, or maybe lol I can’t remember. However, more importantly, can SPS, big diagnosed in children? I really hope not, but if it is, it is.
Didn’t mention the jab, how odd
Didn't happen that's why
Because thats irrelevant.
She was vaxed otherwise she couldn't do concerts
|--|=======-----------...
They will never mention LOL
Funny
@@Birdbike719 what you mean? Did you took the JAB!!!!!!!
As CEO for Cymatrax, Inc., We have one trial showing how our technology progresses better signaling to the brain for PTSD and Autism while listening to filtered digital audio. I would love to find a way to get this to her.
Have you looked at CRISPR technology?
contact Celine Dion's management team so that u can get it to her & tell them ur CEO of Cymatrax
What a coincidence. I have had stiffness in some of my muscle/nerves for years and fortunately, It is going away just in these times. I feel like a new person.
I hope this door which is opening right now, can be worthy for others too.
|--|=======-----------...
The doctor: um, im, um, um, um,um,um,um
Is this similar to sciatica symptoms? Those are also extremely debilitating 😢. I pray for her and her health 🫶
No.
Sciatica is a nerve condition in the lower back and lower extremity. As for the similarity in the symptoms for this ailment and the stiff person disease no
It's a NMD
Sounds more like an MS or ALS type disorder
😢😢😢😢😢😢😢😢😢😢
We all fear the day when Celine will no longer be among us. (not click baited)
Accept Jesus
‘$afe & effective’ & ‘fully te$ted’ tho !
i just have been diagnosed with boring- person syndrome
HA HA HA
Is there cure?
Your comment is pretty entertaining tho 🤣
YEP GhoulSyndrome
She has the money for treatment. Many dont have that advantage.
❤️❤️❤️🙏🙏🙏
🙏
Clot shot has consequences
So does your do nothing approach 🙄
Because a vaccine that's only been around 2 years can cause a disease that's bern around so long they've had to change the name. Critical thinking is your friend
So does you bogus comment. Should we call it the clot virus? It did that. About 900,000 times more than vaccine.
🙏🙏🙏🙏🙏🙏🙏🙏🙏
They don't know what causes it, but yet, they have a drug to treat it.
Which suggests they do know, at least a little, about what causes it.
@@Schaemia he said they don't know the cause.
@@hankwarren198
But they know the symptoms and they know what it is. Just not what causes it. It's like MS or RA
The drugs are meant to relive the symptoms, they won't cure the main cause of the disease.
I'm disturbed that there are no word about what might be causing the disease. In science experiments we see that something affected the object, we go few steps back to start looking the reason and make conclusions according to what was done with the object. But when it comes to real people and their health problems, the vaccines are excluded immediately without any second thought. Yet she started having health issues after getting her shots. Surprise, surprise.
My father has SPS. It's an inflammation in the brain causing spasm. Just because the cause for that inflammation isn't known doesn't mean the inflammation itself cannot be treated. It cannot be cured though, only the symptoms can be alleviated.
What about real people that have it that can't afford treatment,I mean really she can afford any type of treatment, she doesn't have to rely on government assistance or anything like that. And she's not the only one that has it .
Either way, I believe she lives in Canada. I know she's Canadian. Canada has universal healthcare
Just to clear the confusion for the world ....when doctors diagnose someone with anything and place the word "syndrome " wich technically means we don't know what causes it or what is the mechanism of action ... .I wish I can tell Celline that are alternative real medicine not conventional approaches available. If I would take a wild guess she suffers from massive chronic mainly mineral deficiency for a while now.
I agree! I believe that's what was causing my leg cramps, twitches and digestive issues, breathing issues, etc. Doctors couldn't figure it out so I did my own research. I cleaned my intestines and bowels out (gut reset) , started an anti-inflammatory diet and drank protient drinks with 21 minerals and vitamins. My symptoms went away!
Maybe the deficiency is at a micro-level which may be why doctors can't properly diagnose.
Except perhaps Down's Syndrome, which is a chromosomal issue.
Maybe eyewitness news should’ve dug a little deeper into the ads that this woman was pushing for her clothing line, and what it represented, just short of being a Balenciaga scandal…wake up people!
116th Commented 💙
Looks like another clot shot casualty to me.
No more ADRENOCHROME
Oh, get your booster people otherwise this could happen to you.
Unrelated to COVID or the booster.
@@Hgood1 😂 you’re stiff too. 🍹
Its absolutely true millions are suffering neurological injuries and miocarditis all you have to do is research CDC own website
This likely happened BECAUSE of the booster
@@sabine3769 everybody are sleeping they are not even do little research before put experimental drugs on their own body. just following main stream media
New stem cell treatment ?
I doubt Celine will be back on stage.
Eating disorders that’s what I think it years of eating problems could cause it in some
She got it after COVID vaccine :(
*GET YOUR BOO$TERS!!!* 💉💉💉
I suppose if someone farts it's jab always the jab stop making up bs 🙄
@@thomasmatthewharris1980 they will blame vaccinations for everything whether it makes sense or not simply to advance their stupid agenda. God, practice some critical thinking people!
*Singer Celine Dion was disabled from a KNOWN SIDE EFF*CT of the* 💉
She has been diagnosed with Stiff Person Syndrome, which is so rare, it’s only found in 1 in a million people. Did she just get unlucky? Nope. She got 💉'd.
Thanks to Amy Kelly of daily clout, we know that SPS was reported in Pf1z*r’s postmarketing documents on page 37, which is also page 8 of Appendix 1. Being in this document indicates that Pf1z*r was aware of it no later than 2/28/21, and the FDA knew about it no later than April 2021. So the FDA and Pf1z*r clearly know and *told the public nothing!*
Pf1z*r knew about SPS in February 2021 and the FDA knew about it on Aprile 2021. But the FDA isn’t going to warn anyone about all these side effects because that would create V "hesitancy"
Celine should team up with Justin Boo$ter Face...
call it The 💉 1njured Tour!
It seems like an aging disease.
mRNA blood brain barrier breach..
Performance as a singer? What about just being a person? This is horrible .I'm a big fan..I didn't take that comment well
Ok great As I hypochondriac I have yet ANOTHER disease to worry about!
First question - the most important - how many of the mRNA jab did he take already ....?
Yall believe anything tgese celeb show or tell yall
I wonder if her xtreme weight loss / malnutrition played a role....
Overweight people are more like to get this disease. Stop wondering a. Yikes.
Vax
Gut reset - carnivore diet
I just wonder if she had the Covid vaccine and boosters?
She is very thin. Maybe a small dose of steroids and light weight training might get her to heal.
She got the COVID vaccine 🚩🚩🚩
I’ve had stiffness more than 4 hours once after taking a blue pill.
wen he says "underlying malignancy," does he mean Celine Diom drained newborn baby infants of their blood for her adrenochrome consumption ?
Look at her. Seriously...just stop.
Stupid comment
@@thomasmatthewharris1980 its a question 😂
SUGAR
I understand completely what Celine is going through. I Have generalized Dystonia and it affects all my muscles and my voice too.
But there is hope for you Celine.
I am sure your neurologist and doctors have discussed DBS
Deep Brain Stimulation.
Dystonia is located in the deepest part of the brain, basal ganglia.
I don't know what part of the brain your condition is located, but I hope and pray that you will be a good candidate for this surgery. There are medications that help too.
I was diagnosed at 48 yrs. I m 68 now and the DBS helped me tremendously.
I'm no longer in a wheelchair and living a much better life.
My Dystonia will never define me.
And I want you to know that you are in my thoughts and prayers. Never give up on Hope.
I know you will be singing 🎶 again.
God be with you.