Пікірлер

• 
  @willkahok82463 күн бұрын

  Why don't you send a kiss to the people in Gaza they would really appreciate that and they need you

• 
  @aemp12 күн бұрын

  Υπάρχει μια καταπληκτική επίκουρος καθηγήτρια Νευρολογίας στο Αιγινητειο Νοσοκομείο η κ.Ανδρεαδου Ελισαβετ που με παρακολουθεί γιατί έχω σκληρηνση κατά πλάκας κ με έκανε κ περπάτησα γιατρέ ! Αν έρθετε Ελλάδα παρακαλώ πολύ επικοινωνήστε μαζί της είναι εξαίρετος επιστημον κ άνθρωπος

• 
  @hanan_adnan12 күн бұрын

  ليه مافيه عربي

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  @donnapower902015 күн бұрын

  I have progressive MS and have become a little cynical... Do you really think 'big pharma' will give you a drug to stop progressive MS?! Did you not hear how much money each organization got? Funding disappears if there's nothing to research... And ask each MS society around the world how much from each dollar donated actually goes toward research...only 5 cents per dollar goes towards R&D in Canada. And after 50+ yrs 'they're' no closer to knowing the cause of MS or having any effective long term treatment? But hey, can come up with a cv vaccine in six months that's going to save the world...🤔

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  @CM-um5miАй бұрын

  2:30 pm 😅

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  @annarosagaspari1078Ай бұрын

  Il mio commento e' sparito! Grazie YUOTUBE 😂

• 
  @plonker2505Ай бұрын

  Thanks to all the speakers for a very enlightening discussion demonstrating that the ailment is receiving attention, it is very encouraging 🙏

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  @plonker2505Ай бұрын

  Thank you for a very heartening and open discussion on what is being done. Could brain elasticity figure in any way to retrain parts of the brain that may not be affected where lesions have affected certain functions?

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  @CM-um5miАй бұрын

  I have such pain tapping on my side or 6” goes through my body so bad I can’t antagonize to die, now I have no place to live, I’m homeless .

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  @fatimamirza24082 ай бұрын

  Thank you for this information

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  @dianefresca68962 ай бұрын

  Taking abugio for PPMS.

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  @al7rnkch3 ай бұрын

  ❤❤❤ Ok

• 
  @casperience244 ай бұрын

  Cheers

• 
  @sharathchandra13234 ай бұрын

  Damage control? Solutions. Drugs. Any injections? Tired of hearing stories!🤷‍♂️

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  @adithyavikram75 ай бұрын

  Role of stem cell therapy in multiple sclerosis.

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  @adithyavikram75 ай бұрын

  Role of inhibition of CD40L with Frexalimab in multiple sclerosis.

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  @Robin-me8fe5 ай бұрын

  Thank you all.

• 
  @stevend17525 ай бұрын

  thank you

• 
  @timothyjohnson-wi4mx5 ай бұрын

  I am enjoying listening to this podcast but it cutout as Dr. Fox was discussing new treatment options. :-(

• 
  @SorenArouet5 ай бұрын

  I have a son, I wanted to hike with him. But here I am losing every fight and still wanting to get back on the ring everyday.

• 
  @danutgerebenes62287 ай бұрын

  Recent am fost diagnosticat și eu și am fost inițiat în program național să încep un tratament cu pastile timp de 2ani care trebuie să iau în fiecare zi o pastilă ,acesta este un tratament în fază de studiu adică nu se știe ce eficiență o să aibă dar acum am o problema cu analizele că zice că am hepatită activă și nu poate să inceapă tratamentu ,vreau să zic că cîte cazuri am văzut în spital este de groază atîta de tare ma afectat că sînt distrus total atîta de milă îmi este de colegii de suferință ,și nu prea am văzut pe cineva să se laude că a avansat spre bine ,din contră mai spre rău ,visavi de Medicu meu Neurolog nu am reproșuri pentru că știe meserie și este super sufletistă și dedicată meseriei pe care o face eu aștept să văd ce o să fie ,eu doresc multă sănătate la toată lumea de aici din ROMANIA.

• 
  @Velkro50007 ай бұрын

  After training myself to avoid inflammatory foods, sleeping and exercising regularly, my MS has been very manageable.

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  @braedenmckean3757 ай бұрын

  My mom has had it for 25 years. These last 5 have been hell. This is a family disease that affects everyone in the household. My mom can't do anything anymore, and now she's losing the ability to stand up with her walker, so it's getting scary for everyone. It's been really hard having to grow up watching my mom deteriorate right in front of me.

• 
  @korisnikk42087 ай бұрын

  Prevod hrvatski

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  @Jamila_Turkeyy997 ай бұрын

  ربنا يشفس كل مريض يارب متقلقوش هتكونوا بخير ان شاء الله اطمنوا ربنا معانا كلنا...😢❤

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  @user-ig3kn2ly2x7 ай бұрын

  Cc: Okay, so let's see what we've got: From the information as stated in 2023, the disease is being brought on by at least One Virus; Epstein Barr. Now, it appears, at least in my case, {another virus} Triggered the development of the more obvious symptoms we see as MS. Then, most of what ive seen since the late 90s, showed / shows the slowing down of the symptoms, but no effective treatment or cure; only the management of the decline. Outcomes from 97 - 17 amounted to therapies but no real reverse of the disease; why..? Answer: The inability to Manage Viruses. Seems my 1989 bout with Mono, and sudden diagnosis of MS in 2016, came about 4 Months after being given Oral Herpes by my girlfriend at the time. So: It does appear, One Virus; Epstein Barr causes the Fatigue, Lethargy, etc. The Other Virus; HS1, is causing my Optic Neuritis, as the girlfriend was experiencing Her own Neuritis and vision loss in her right eye as well. Was taking her to the doctor for it as I recall, come to think of it. Conclusions: So what I see taking place, is the body's attempt to rid itself of at least Two Viruses, that become endemic, fusing and blending into the body after many months and years, that to the body... ' it would appear that the body would / is attacking itself, quite correct. Answer: What we now need, is an approach or treatment, that Nullifies both Viruses, so the body no longer is forced to attack itself. Thank you. Peace. ❤

• 
  @user-ig3kn2ly2x7 ай бұрын

  Okay, so let's see what we've got: From the information as stated in 2023, the disease is being brought on by at least One Virus; Epstein Barr. Now, it appears, at least in my case, {another virus} Triggered the development of the more obvious symptoms we see as MS. Then, most of what ive seen since the late 90s, showed / shows the slowing down of the symptoms, but no effective treatment or cure; only the management of the decline. Outcomes from 97 - 17 amounted to therapies but no real reverse of the disease; why..? Answer: The inability to Manage Viruses. Seems my 1989 bout with Mono, and sudden diagnosis of MS in 2016, came about 4 Months after being given Oral Herpes by my girlfriend at the time. So: It does appear, One Virus; Epstein Barr causes the Fatigue, Lethargy, etc. The Other Virus; HS1, is causing my Optic Neuritis, as the girlfriend was experiencing Her own Neuritis and vision loss in her right eye as well. Was taking her to the doctor for it as I recall, come to think of it. Conclusions: So what I see taking place, is the body's attempt to rid itself of at least Two Viruses, that become endemic, fusing and blending into the body after many months and years, that to the body... ' it would appear that the body would / is attacking itself, quite correct. Answer: What we now need, is an approach or treatment, that Nullifies both Viruses, so the body no longer is forced to attack itself. Thank you. Peace. ❤

• 
  @LaylaFamily20247 ай бұрын

  Your honesty is appreciated

• 
  @tedteddy18027 ай бұрын

  I also have primary progressive multiple sclerosis I was diagnosed 10 years ago, my neurologist back, then told me I would be bedbound or dead in 10 years. I’m still driving and cooking for myself, because I took my health into my own hands after he threw his hands up in the air and said there’s nothing more I can do for you, I said thank you and walked away and now I tell people this disease is a blessing, and a curse a curse, because it is so hard to even stand up a blessing because now I know how the human body works. I know exactly what I did to myself to come to this state, God bless anyone out who is suffering from any debilitating disease God bless you always calculate your next move and take it one day at a time. Happy holidays, everyone

• 
  @user-ig3kn2ly2x7 ай бұрын

  Okay, so let's see what we've got: From the information as stated in 2023, the disease is being brought on by at least One Virus; Epstein Barr. Now, it appears, at least in my case, {another virus} Triggered the development of the more obvious symptoms we see as MS. Then, most of what ive seen since the late 90s, showed / shows the slowing down of the symptoms, but no effective treatment or cure; only the management of the decline. Outcomes from 97 - 17 amounted to therapies but no real reverse of the disease; why..? Answer: The inability to Manage Viruses. Seems my 1989 bout with Mono, and sudden diagnosis of MS in 2016, came about 4 Months after being given Oral Herpes by my girlfriend at the time. So: It does appear, One Virus; Epstein Barr causes the Fatigue, Lethargy, etc. The Other Virus; HS1, is causing my Optic Neuritis, as the girlfriend was experiencing Her own Neuritis and vision loss in her right eye as well. Was taking her to the doctor for it as I recall, come to think of it. Conclusions: So what I see taking place, is the body's attempt to rid itself of at least Two Viruses, that become endemic, fusing and blending into the body after many months and years, that to the body... ' it would appear that the body would / is attacking itself, quite correct. Answer: What we now need, is an approach or treatment, that Nullifies both Viruses, so the body no longer is forced to attack itself. Thank you. Peace. ❤

• 
  @BattlesCinematics3 ай бұрын

  Can yo u elaborate on wh at you did to help yourself? I'm e xpecting a diagnosis at just 29 years old. I'm terrified.

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  @truthseeker54967 ай бұрын

  What stands in the way is the treatment to slow the symptoms costs $87,000 twice a year. Why would pharmaceuticals want to create a cure and lose that income?

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  @sksk-ir5fo7 ай бұрын

  You are so right. I have ms for 7 years and have not touched ms drugs nor will I ever. Doing ok with diet and exercise

• 
  @gregp10037 ай бұрын

  Thank you

• 
  @shura-827 ай бұрын

  My 53-year-old husband's PPMS (diagnosed in 2022) manifests itself in an incredibly extreme cognitive decline that I have not seen addressed anywhere in MS literature or research, including this webcast. He can no longer remember his age or address, cannot find his way around anywhere, or follow even basic instructions or perform simple household tasks. It is not the "cog fog" usually referred to in MS literature, but something like a combination of dementia, brain damage and learning difficulties. No strategy training can help him as he is blissfully unaware of his symptoms and feels fine. Is this presentation something the webcast participants have ever encountered and do they have any advice?

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  @redefiningmyself85985 ай бұрын

  @shura-82 please consider having your husband evaluated at a university hospital by a neurologist and a neuro-psychologist for his cognitive decline and to get a second opinion 🙏🏼

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  @shura-825 ай бұрын

  @@redefiningmyself8598 He has been seen by a neuropsychologist twice, as well as by multiple neurologists.

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  @hydelake2247 ай бұрын

  turn loose AI and Crispr on this disease and see a cure in 12 months. We lack only the will.

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  @user-ig3kn2ly2x7 ай бұрын

  Exactly. I am now seeing various medical professionals who seem to be making substantial progress on how to treat, slow, and halt the disease. Honestly, so tired of hearing ' we don't know. '

• 
  @shawnmcanthony57248 ай бұрын

  Soon no one will say i am in jehovah gods new world here on earth isiah 33:24 like in the garden of eden. This is a fact world conditions are deteriorating more crimes decaying morals eg. The acceptance of same sex marriage. Jehovah god acted in the time of Sodom and Gomorrah and he will act soon. Speak with one of Jehovah's witness to find out more❤

• 
  @user-wq3uz8uv1r8 ай бұрын

  I Daniel McCoy M S .about a year ago I can still use all my limbs. I will begin to start trimming. I hope I found a cure.

• 
  @flannershirley8 ай бұрын

  Thank you! I wanted to ask about GAIT. I have this and unfortunately there is no medicine from what I understand from my neurologist. Is this true?

• 
  @kathleendonahue59557 ай бұрын

  Ampyra has helped me …. I think. I noticed my gait is worse without it. I’m grateful for whatever is being done but it’s very discouraging for me to listen to the first thing the man says is they don’t know what’s going on or what’s wrong so they couldn’t possibly know how to begin to treat or fix it I’ve lived with MS for over 20 years, but possibly more like 35 It just became undeniable after the birth of my first child more than 20 years ago

• 
  @vvt07128 ай бұрын

  I am a MS patient with RRMS, Dr Shanthi is my neurologist doctor. She is a very great and amazing doctor. Personally I like her so much. I will listen to her advice and be brave facing my MS disease.. #May God Bless Doctor Shanthi Stay Healthy.

• 
  @Catmandude8 ай бұрын

  KZread only has a thumbs up to represent that you appreciate or like the video. In a case like this I wish it was more like Facebook that had a sadness emoji.

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  @najialdhabyani6758 ай бұрын

  We hope that the statistics of patients with MS in Yemen will be included in the Atlas programme

• 
  @elinamirauskaite85188 ай бұрын

  ❤❤❤

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  @jennyo91209 ай бұрын

  Diagnosed 27 years ago and the past 5 years have been THE most challenging. It's a cruel disease.

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  @redefiningmyself85988 ай бұрын

  Yup, I'm 17 years in and it's now active secondary progressive MS. Stay strong 🙏🏼

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  @harrietisrael83519 ай бұрын

  I was so lucky to get rid of my Multiple Sclerosis (MS) after using DR ALAHO OLU on KZread herbal supplements for three weeks. He has medicine for HPV, HSV, ALS and MND…..

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  @najialdhabyani6759 ай бұрын

  Thank you, Joanna, for your comment about the importance of providing medications

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  @user-kn2wq1hz1i9 ай бұрын

  Rameshasalisexkannaba

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  @teserrano9 ай бұрын

  Es lo peor del mundo y todos dicen que es pereza y no entienden que cuando te da no eres capaz de dar dos pasos seguidos 😅😢

• 
  @bambisalmond76009 ай бұрын

  This disease stinks, never thought I would be diagnosed at 68. It’s changed my life was a runner, outdoor person & a dancer. My prayers go out to all who have MS 🙏

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  @RobdeKlerk-qg6lc7 ай бұрын

  How are you doing ?

• 
  @evekrawczyk6336 ай бұрын

  I was diagnosed in Oct 2022 at 69. What a surprise

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  @bambisalmond76006 ай бұрын

  @@evekrawczyk633 I know what u a dealing with, stay strong ❤️

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  @lesliea.m.53929 ай бұрын

  My 41 yr old daughter just got diagnosed with progressive MS 😢😢😢 it’s very depressing to not being able to do anything to help her , I pray constantly for her and try to just be here but she doesn’t contact me much 😢only by texts even though she lives only an hour away 😢😢 she doesn’t like anyone to visit 😢😢 if you could give me any insight to what I could possibly do to help her ….. please tell me 🙏🙏🙏

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  @Dasani_water_drinker9 ай бұрын

  You can do something. I know from experience

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  @koko_78 ай бұрын

  keep praying, she is may depressed coz of it, advice her to eat more greeny dark vegetables, eat more fish salmon, sardine, try to go out in sun and walk and take off course vitamin D daily along with vitamin K to absorb it, also omiga 3 pills, try to be happy it helps a lot, and a lot said Lion's mane mushroom pills help. and manuka honey..just be positive with her, share successful stories together.. it may help.. lets pray for each other every day.. God is great ❤❤👋🌷

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  @MohammedNomer8 ай бұрын

  If you have money try HSCT in mexico or russia my wife was diagnosed with ms six months ago we haven’t done it yet cuz of financial issiues but ill do it for her if it means ill sell my kidney

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  @sofiabanuelos49538 ай бұрын

  No please not sell your kidney

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  @maryanngames93538 ай бұрын

  @@koko_7yes she may very well be depressed! Keep praying, I will join with you in prayer for her🙏🙏❤️

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  @lindalovelace19649 ай бұрын

  Yes how are you doing? We are in the same boat.🙁

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  @dianefresca68969 ай бұрын

  I feel just like you . Its a horrid disease