Відео

❤️

You look good!

DR ALAHO OLU on UA-cam Channel you’re indeed a great and trusted traditional and holistic herbalist, he cured me and my wife from Multiple Sclerosis, he also has cure for HPV, HSV, HIV, FIBROID, ALS, CANCER, LUNGS DISEASES……….

DR ALAHO OLU on UA-cam Channel you’re indeed a great and trusted traditional and holistic herbalist, he cured me and my wife from Multiple Sclerosis, he also has cure for HPV, HSV, HIV, FIBROID, ALS, CANCER, LUNGS DISEASES……….

Thank you. I needed this.

Thank You

Hi Anna-Maria- 1st time viewer and happy to hear you are doing well. I am an MSer's as well on Kesimpta for 2 years so far. I am so grateful to be doing well on this and love the flexibility of taking it from home 1x a month. I wish you continued success and plz keep us updated on your journey. love from the US

Who Knew?? #BloodFlowMatters Supplying Oxygen and Nutrients to every Cell along with clearing toxic brain waste, what is the role of CCSVI Venous Hypertension and proper/improved Cerebrospinal flow, impacting neurological symptoms regulating mood and cognitive Senescene Psych issues? #CCSVI #BloodFlowMatters With age, blood flow to the brain decreases b/c blood vessels produce less nitric oxide, a gas that expands blood vessel walls. Such disruptions contribute to changes in cognitive function that occur with age. #Exercise increases nitric oxide & boosts blood flow to the brain. #Urgent #BloodFlowMatters Keep in mind! Arteries are nothing without a Heart, and a Heart is nothing without Veins! Treatment improving Arterial Circulation is permitted and common, all treatments that improves Circulation in Veins are not widely available. #CCSVI Horizontal sleeping causes Reflux of De-Oxygenized blood towards the stenosed Hypoxic brain, which after years results in MS Sleeping is a Silent threat to mankind! Keep in mind! Arteries are nothing without a Heart, and a Heart is nothing without Veins! Treatment improving Arterial Circulation is permitted and common, all treatments that improves Circulation in Veins are not widely available. #CCSVI Help facilitate Neurovascular Disease Research Best chance for longevity quality of life depends on availability Neurovascular Disease Research Collaboration. '“When we age, one of the common things that happens within our brain is that the blood vessels do become compromised in part because of chronic conditions,” it is said. “And when that occurs in normal aging, what happens within the brain is … silent strokes.”' As much CCSVI has been Scientifically established to have a role/part in 43 so Neurological afflictions including Dementia and so called MS 'There is evidence to suggest COVID-19 impacts the same blood vessels that feed the brain. If the virus is damaging those vessels, which could speed up aging, this, in turn, means some survivors might be at risk of getting early-onset dementia.' Time for Learning Science #BloodFlowMatters Apparantly nothing else matters critical Healthcare So happens CCSVI a TREATABLE Congenital Science Confirmed Recognized Med Condition STUDIES show causative factor so called Multiple Sclerosis & role/part 43 other SO called Neurological Afflictions Incl. Migraines, Asperger Autism Dementia/Alzheimer's Aphasia Optic Neurtis Tinnitus Transverse Myelitis Ect! facilitate collaboration defining the path forward establishing the understanding and treatment of Neurovascular disease organizing unified clarity in Science knowledge and progress!⁰⁰ Critical Healthcare Research addressing Neurovascular/Cardiovascular Disease including Heart & Brain function Amygdala Dopamine/Serotonin related Mental Health Depression Vascular Disease issues! #anxiety #VascularDepressionConsensus FB Group: MultipleStenosisSociety t.co/7JNmFD7W4l Apparently What is the role of CCSVI Venous Hypertension and proper/improved Cerebrospinal Blood flow Impacting circulation and homeostasis balance? #CCSVI #BloodFlowMatters #spasticity #perfusion Horizontal sleeping causes Reflux of De-Oxygenized blood towards the stenosed Hypoxic brain CCSVI is Science Confirmed Recognized Medical Condition STUDIES show causative factor MS Varicose Veins Fatigue Atrophy Inflammatiion Thyroid issues Covid-19 Heart function matters Cramps Mental Health problems Bowel & Bladder affairs insomnia Senescene Psych unusual behavior! Studies have shown that mostly ineffective often harmful or poorly tolerated Pharmaceuticals that 'TREAT' so called Multiple Sclerosis (M$) $20-40Billion W/a B/yr industry! Living with the Symptoms of Multiple Sclerosis is torturous tortuous tumultuous utter misery! Chronic Cerebrospinal Venous Insufficiency CCSVI/Neurovascular Disease CCSVI is a Treatable Congenital Scientifically Confirmed Recognized Medical Condition, Established Causative Factor in Multiple Sclerosis SymptoMS, AND plays a part 43 other so called Neurological afflictions! CCSVI may be impacting yourself right now and you are unaware! #CCSVI Apparently the Sooner a Person Receives Venous Angioplasty for Treatment of CCSVI! best possibility eliminating cause of MS Symptoms and easing or disappearing! So Called Multiple Sclerosis is more important to some than others Pharmacists, The M$ Society, Neurologists 'so called MS experts', Cane Manufacturing, Scooter and Power Chairs companies, etc Etc ETC So Called Multiple Sclerosis (MS) is/HAS been a MYSTERIOUS elusive UNPROVEN Autoimmune THEORY solely based on SYMPTOMS! STUDIES show Pharmaceuticals That 'TREAT' so called MS only 20-40% Effective DO NOT slow Progression of the Disease Often have Harsh Corrosive Side Effects sometimes DEATH! #CCSVI So Called Multiple Sclerosis (MS) is/HAS been a RUBBISH UNPROVEN Autoimmune THEORY Based Solely on SYMPTOMS! #CCSVI Venous Hypertensiono >microbleedings >iron >free radicals >neurodegeneration #multiplesclerosis M.S. - Mystery Solved Mysterious Autoimmunity = CCSVI Hypertension M.S. - Mystery Solved Mysterious Autoimmunity = CCSVI Neurodegeneration Keep in mind! Also venous hypertension ➡️ impaired CSF absorption ➡️ reduced G Lymphatic drainage ➡️ interstitial peptides accumulation ➡️ neuro inflammation #CCSVI So happens, to mention apparently, Neurogenesis and Homeostasis, are often side effects of Venous Angioplasty treating CCSVI!! Apparently sooner treatment best possiblity Symptoms easing or disappearing. 1/1 #CriticalHealthcare_Research #CCSVI Neurogenesis is the process by which new neurons are formed in the brain. Neurogenesis is crucial when an embryo is developing, but also continues in certain brain regions after birth and throughout our lifespan. qbi.uq.edu.au › brain-basic Homeostasis is an internal feedback system that stabilizes and balances our body's chemistry, so that our organs work smoothly and efficiently with each other. Sickness is the disruption of homeostasis, which doctors treat with medicine.Oct 20, 2016 www.bmj.com› bmj.i5643 Blowing the Whistle on Corrupt Pharmaceutical Industry by Gwen Osen FB Group: MultipleStenosisSociety facebook.com/share/p/jQxWX5Ce6sZgzmky/?mibextid=oFDknk

Keep in mind #BloodFlowMatters #CriticalHealthcare_Research Horizontal sleeping Who Knew?? #BloodFlowMatters Supplying Oxygen and Nutrients to every Cell along with clearing toxic brain waste, what is the role of CCSVI Venous Hypertension and proper/improved Cerebrospinal flow, impacting neurological symptoms regulating mood and cognitive Senescene Psych issues? #CCSVI #BloodFlowMatters With age, blood flow to the brain decreases b/c blood vessels produce less nitric oxide, a gas that expands blood vessel walls. Such disruptions contribute to changes in cognitive function that occur with age. #Exercise increases nitric oxide & boosts blood flow to the brain. #Urgent #BloodFlowMatters Keep in mind! Arteries are nothing without a Heart, and a Heart is nothing without Veins! Treatment improving Arterial Circulation is permitted and common, all treatments that improves Circulation in Veins are not widely available. #CCSVI Horizontal sleeping causes Reflux of De-Oxygenized blood towards the stenosed Hypoxic brain, which after years results in MS Sleeping is a Silent threat to mankind! Keep in mind! Arteries are nothing without a Heart, and a Heart is nothing without Veins! Treatment improving Arterial Circulation is permitted and common, all treatments that improves Circulation in Veins are not widely available. #CCSVI Help facilitate Neurovascular Disease Research Best chance for longevity quality of life depends on availability Neurovascular Disease Research Collaboration. '“When we age, one of the common things that happens within our brain is that the blood vessels do become compromised in part because of chronic conditions,” it is said. “And when that occurs in normal aging, what happens within the brain is … silent strokes.”' As much CCSVI has been Scientifically established to have a role/part in 43 so Neurological afflictions including Dementia and so called MS 'There is evidence to suggest COVID-19 impacts the same blood vessels that feed the brain. If the virus is damaging those vessels, which could speed up aging, this, in turn, means some survivors might be at risk of getting early-onset dementia.' Time for Learning Science #BloodFlowMatters Apparantly nothing else matters critical Healthcare So happens CCSVI a TREATABLE Congenital Science Confirmed Recognized Med Condition STUDIES show causative factor so called Multiple Sclerosis & role/part 43 other SO called Neurological Afflictions Incl. Migraines, Asperger Autism Dementia/Alzheimer's Aphasia Optic Neurtis Tinnitus Transverse Myelitis Ect! facilitate collaboration defining the path forward establishing the understanding and treatment of Neurovascular disease organizing unified clarity in Science knowledge and progress!⁰⁰ Critical Healthcare Research addressing Neurovascular/Cardiovascular Disease including Heart & Brain function Amygdala Dopamine/Serotonin related Mental Health Depression Vascular Disease issues! #anxiety #VascularDepressionConsensus FB Group: MultipleStenosisSociety t.co/7JNmFD7W4l Apparently What is the role of CCSVI Venous Hypertension and proper/improved Cerebrospinal Blood flow Impacting circulation and homeostasis balance? #CCSVI #BloodFlowMatters #spasticity #perfusion Horizontal sleeping causes Reflux of De-Oxygenized blood towards the stenosed Hypoxic brain CCSVI is Science Confirmed Recognized Medical Condition STUDIES show causative factor MS Varicose Veins Fatigue Atrophy Inflammatiion Thyroid issues Covid-19 Heart function matters Cramps Mental Health problems Bowel & Bladder affairs insomnia Senescene Psych unusual behavior! Studies have shown that mostly ineffective often harmful or poorly tolerated Pharmaceuticals that 'TREAT' so called Multiple Sclerosis (M$) $20-40Billion W/a B/yr industry! Living with the Symptoms of Multiple Sclerosis is torturous tortuous tumultuous utter misery! Chronic Cerebrospinal Venous Insufficiency CCSVI/Neurovascular Disease CCSVI is a Treatable Congenital Scientifically Confirmed Recognized Medical Condition, Established Causative Factor in Multiple Sclerosis SymptoMS, AND plays a part 43 other so called Neurological afflictions! CCSVI may be impacting yourself right now and you are unaware! #CCSVI Apparently the Sooner a Person Receives Venous Angioplasty for Treatment of CCSVI! best possibility eliminating cause of MS Symptoms and easing or disappearing! So Called Multiple Sclerosis is more important to some than others Pharmacists, The M$ Society, Neurologists 'so called MS experts', Cane Manufacturing, Scooter and Power Chairs companies, etc Etc ETC So Called Multiple Sclerosis (MS) is/HAS been a MYSTERIOUS elusive UNPROVEN Autoimmune THEORY solely based on SYMPTOMS! STUDIES show Pharmaceuticals That 'TREAT' so called MS only 20-40% Effective DO NOT slow Progression of the Disease Often have Harsh Corrosive Side Effects sometimes DEATH! #CCSVI So Called Multiple Sclerosis (MS) is/HAS been a RUBBISH UNPROVEN Autoimmune THEORY Based Solely on SYMPTOMS! #CCSVI Venous Hypertensiono >microbleedings >iron >free radicals >neurodegeneration #multiplesclerosis M.S. - Mystery Solved Mysterious Autoimmunity = CCSVI Hypertension M.S. - Mystery Solved Mysterious Autoimmunity = CCSVI Neurodegeneration Keep in mind! Also venous hypertension ➡️ impaired CSF absorption ➡️ reduced G Lymphatic drainage ➡️ interstitial peptides accumulation ➡️ neuro inflammation #CCSVI So happens, to mention apparently, Neurogenesis and Homeostasis, are often side effects of Venous Angioplasty treating CCSVI!! Apparently sooner treatment best possiblity Symptoms easing or disappearing. 1/1 #CriticalHealthcare_Research #CCSVI Neurogenesis is the process by which new neurons are formed in the brain. Neurogenesis is crucial when an embryo is developing, but also continues in certain brain regions after birth and throughout our lifespan. qbi.uq.edu.au › brain-basic Homeostasis is an internal feedback system that stabilizes and balances our body's chemistry, so that our organs work smoothly and efficiently with each other. Sickness is the disruption of homeostasis, which doctors treat with medicine.Oct 20, 2016 www.bmj.com› bmj.i5643 Blowing the Whistle on Corrupt Pharmaceutical Industry by Gwen Osen FB Group: MultipleStenosisSociety facebook.com/share/p/jQxWX5Ce6sZgzmky/?mibextid=oFDknk causes Reflux of De-Oxygenized blood towards the stenosed Hypoxic brain, which after years results in MS Sleeping is a Silent threat to mankind!

Well done. You have a positive attitude and that will help you so much.

music too loud compared to voice

Hope you're doing ok. We're all here with you 🧡

Do you know if there is a clinical study in my city

Thank you for posting this, I really want it. I need someone to contact me in Rio de Janeiro😊

Wany

Doctors do more effort for insurance companies than patients obviously

Your more supported in groups online, than you are with family and friends 😢

Thank you.

I was diagnosed Sept 19 this year. MRI’s contrast and no contrast of brain and spine. 8 brain lesions and three spinal 😢numbness and tingling began last month. A year before that I had heat sensitivity and fatigue. No answers at the time for that. Now I know. I’m in my 40’s. I’m thinking of Tysabri if I’m not JC positive. I feel like my life is over

Oh sweetheart you're such a beautiful lady this shouldn't be happening to someone like you. Lots of love and hugs.

I haven't been tested for MS yet but I do have a lot of the symptoms for it. I plan to get tested soon but while that happens, I've been trying to learn more about MS. One thing that's been happening to me recently is that whenever the sky is gray (meaning very cloudy and looks as if it's about to rain), I get very anxious and I don't know why but I just don't feel well. I don't know if this can somehow be related to MS (if it iS MS that I have). I've read online that anxiety can be a symptom of MS.

The last sentences made me tear up: "You are loved and there is hope!" Thank you so much for uttering those words as they really made me believe them! Thank you so much! 💕💖💛💖💕💖💛💖💕

Hi sweetheart, I was dx at 17 in 1994 - 30 years ago next year. The diagnosis is a bereavement- it’s a mental possible loss of your future perfect health, career plans, parenting plans, everything your mind can torment you with..BUT Like a bereavement, THE FIRST 2 years are the Worst I promise you❤️🙏🏼😊 I had 3 bouts of numbness from 1991 that were put down to trapped nerve, atypical migraine, stress…!? I also had a bout of vertigo that was so bad that I had to crawl on my hands and knees to the bathroom as the whole world span if i lifted my head from horizontal that lasted 9 days. When the vertigo resolved I had double vision I was finally dx when I had a further bout of right sided numbness including my head and lost joint position sense at the shoulder. There were no treatments back then. And like you the MRI terrified me and I cried all the way through it! I didn’t have a DMT until 8 years later in 2002, 11 years after my sx. I’ve just come out of a relapse after a 7 year remission off DMTs- still all sensory- New lesion at C7/T1 which caused numbness down left side, loss of joint position sense at knee (that’s why you get that dragging leg-it’s still a sensory symptom) Now 95% recovered without steroids after 5 weeks and am starting Kesimpta in July I still get that utter Euphoria when my symptoms remit, and my heart & soul are full of gratitude for everything that my body can still do so well. I feel like every movement and sensation is miraculous ❤️🙏🏼 Back to now. I’m still RRMS and have got my degree, had a family, a great career, my EDSS is only 4 so I’m doing really really well!! When I was dx I wish an older person had gifted me with telling me what things would be like in the future as uncertainty is our burden. Everything will be ok my darling as our prognostic factors are identical Young, female, visual,sensory symptoms at onset You will achieve all your dreams and become more Resilient, Resourceful and Compassionate than 🎉would ever believe You’re going to be ok xxxx

At least they admitting they made a mistake. Mine wouldn’t.

I took mavenclad this past year for my MS. I didnt realize how sick i was until i got better. The chemo made me very ill. But because of MS i did not think anything of it. Than my body recovered from it. I havent had any MS symptoms since. I hope it worked. I never felt so alone

I have MS... dx,d 2002. I was called lazy,a drunk, a drug addict, lost everything job house family. Homeless not eatting. It sucked.

Thanks for your clear, concise explanation - best wishes 💃🌻

Hi Anna,thanks a lot for that valuable video! I really wonder whats your current EDSS ? How did your doc decide to apply alemtuzumab? thanks a lot!

Thank you for sharing your story ✌️

UA-cam Alan MacDonald : MS is a parasitosis ua-cam.com/video/EHVXJpDBcmU/v-deo.html

I just discovered your channel and would like to follow you on instagram. I will be starting lemtrada in a few months. More videos!

You Tube Alan MacDonald MS is a parasitosis

I have some symptoms of MS. I had a my MRI a couple weeks ago and the neurologist gave me results today saying they were clean but he didn't show me the picture and or explain anything to me. I haven't felt well since I caught mono at 17 and now I'm 31. Drs. always tell me it's my anxiety and since I'm young, and most of my blood work comes back normal that I shouldn't have anything wrong with me. Last blood work my Vitamin D was low and high white blood cells that come and go. They can't figure out why my white blood cells are elevated on and off. Also, I've been on vitamin D for about a year now and feel no difference. My symptoms are extreme tiredness! All I wanna do i sleep. Black dot in the middle of my vision and other floaters, flashing lights. Constant twitching on my top and bottom eyelids..sometimes in the corner of my eyes. Ringing ears and muffled hearing. I have a hard time swallowing..like my throat muscles are too weak to push my food down normally. I constantly feel like I have a lump in my throat. I've felt twitching inside the front of my throat. I thought it was my thyroid but I've had MRI on my throat and apparently it's fine and thyroid blood levels. Numbing sensations in my face and scalp, the back of my neck. I feel like it's in my brain too. I've felt the right side of my brain jolt or something, scraping sensations and other weird unexplainable sensations. Bad headaches. All four limbs get numbness but my left foot is almost all the time and it goes up to my knee. Vibrations in my chest. Elevated heart rate. Sharp pains in my fingers. No sex drive. I feel like I have sore throats all the time too. And severe dry eye. Muscle spasms all over. I feel like my brain is slow.. I stumble on words and pronounce them wrong or can't get the word out. I'm forgetful all time. Swollen painful lymph nodes that come and go. Mostly in my neck and along my jaw. Frequent urination and sometimes I can't hold it or very little pee comes out. I'm not sure if all these are symptoms of MS but I've seen quite a few Drs. So far and been to emergency rooms for all my strange symptoms. They can't seem to find anything. Last time I went to the E.R they sent 60 different blood tests and have ruled out about 70/80 percent of diseases etc. Idk what to do. I feel like I'm crazy at this point and never gonna get a diagnosis. 😭😭😭 Does anyone else have any of these symptoms? Or a suggestion on what it can be?

love you girl! I just wish I could see your face express more.... you're too beautiful for Botox ;)

Every group or person I hear talking about MS seems to have symptoms that are relatively mild compared to my daughter and can still live normal lives. I can’t find anything for someone like her … that has tremors in both hands so can’t eat or do makeup or clasp her bra etc, and trouble walking and standing and bipolar type behavior that is difficult for the one parent caring for her as an adult to deal with … I understand that living with MS is difficult and sad but no one addresses how someone fully caring for someone with MS is doing. We are invisible robots that never need rest or relief apparently? 😕

Thank you for the bottom of my heart for this video

Thank you for sharing

Hi everyone! Great video , thanks this is very informative. I am a clinical neuropsychologist with hospital practice. I don't like when people say MS is just a neurogenerative disease and that there is no cure, because imagine, you re there on a doctor seat receiving this news that impacts mental health and the whole treatment , that moment alone could destroy this person's future. And families are impacted as well. Today's reality is not just that, treatments are changing the course of MS and researches might bring the cure. INSTEAD ONE COULD SAY: It is a cronic disease that requires shared responsibilities and the cure has not YET been found but, in fact there are lots of ways to control MS that are helping people to live a much better life than decades ago. Reasons: 1- Nobody has total control of life, so everyone is at risk: fact. There is no need to create anxiety over the future. The need is to trust a good neurologist and to change into a healthier lifestyle. 2- Everyone goes through a neurodegenerative stage in life, actually it is part go the aging process. 3-There is good control of the disease, so concentrate on that. 4-Also concentrate on self-care, good exercise practise, have lots of friends as we all have a social brain that requires social connections. 5- Trust your neurologist, talk your doubts over, be the master of your brain health and share responsibilities with the ones you love and trust. 6-Be kind on you first.

Its funny when moneys involved then only then u get the correct mri results, shows the laziness of the hospital

I loose my eyesight too, and ive been given an mri of the head and it came ba k normal, but ive been getting tingling all over body

Very informative

I was homeless for awhile unable to get help. No one wants to help a grown man that looks healthy. I became homeless because of the MS and everyone said I was a liar. I lost everything I slept in gutters. I wanted to work but had no energy could not see well out of one of my eyes. Could not feel my legs under my knees. A nightmare try standing in a line with bad legs and MS fatigue f I r two hours for food. And told if you step out of line you need to go back to the end. Dx.d 2002 now I am 50 and am no where I should be in life because people do not like a healthy looking man trying to pull one over on the system. Then of course it's not fatigue your just depresses yes they call you nuts before dx a nightmare. To this day no one has ever helped me. But that's life

I was treated like a drunk a drug addicted bum. I was treated like I was just lazy lost everything. Years later I had a doctor tell me it might be something else years later. I was called a liar for a decade. Blind in one eye fatigue double vision. Finally got a MRI oh by the way for the last decade you were not lying its MS. Thank you veterans administration..... mavinclad young lady

Please keep up these videos, they're very helpful!!!

Thank you for this video. It is quite exceptional. I was diagnosed two days ago at age 47. Best from Germany

Thank you very much for this video. I'm almost 47 and was diagnosed a couple of days ago. My symptoms are dizziness, numbness and pins and needles in my right hand and arm, painful shoulder....the dizziness lasted for weeks and was just awful. I found good doctors and am looking positively into the future. It has still been a difficult pill to swallow as you say... videos like yours are very helpful. We are not alone! And that's such a good feeling! Will watch your other videos now. Thank you. Best from Hamburg, Germany (and by the way: your botox looks great)

That was very powerful and amazing. Just curious,since your diagnosis have you heard of any family members with it? I know you did say that there wasn't a family history of MS but that was in 2019. In our family my sister niece and three other family members (including a mother and daughter) have it that we know of - all female. Good luck I think that you are fabulous : )

❤️🙏

You be ok you are Beyuty ❤️

You inspired me though I have no MS but another one. lupus. You are beautiful, I love your videos. Without the background music, it will be easier to hear you, it’s not easy to process two sounds at one time for some people like me.