I am a patient of Multiple Sclerosis living in Korea. I was diagnosed with the disease at the age of 19 and it's only been a year now. I still don't know. Why I got this disease. But I want to overcome it. Even though I have a disease, I am doing my college life and preparing for a certificate and working hard. However, there are often many difficulties in everyday life due to illness. I hope God gives me strength to overcome. I hope the same patients with multiple sclerosis will cheer up. Thank you. Have a nice day.
Oh hi we're at same age and suffering from same illness 🤗 I hope you're doing great and don't stress too much coz it can cause relapse and it already happened to me ahaha yea it's hard but we need to overcome it no matter what ..urrgh
Please check out the Medical Medium Daily Celery Juice protocol! It has been such a miracle for my digestive issues that I want to share it and help others as well! It can help MS symptoms as well!
God is with you through all of this! ALWAYS AND FOREVER! He states in His Word, that vs does not give us more than we can bare. He knows us better than we even know ourselves. Just think through your life and look at all that you've been through and thought you couldn't make it through, but you did. He ALWAYS also has help available as well read a way out. And most times, the way out of a storm is going through it! It's not easy to hear, think, say or do! As Les Brown would say, "it's simple, but it ain't easy." Thank you for your courage in sharing this. God will bless you as long as you stay true to Him and keep striving for the best! May you keep working hard on all aspects of your life! And may God bless you in all you do. I'm here because my wife, got admitted into the hospital yesterday. She had eye pains for at least 3 days of not longer, and we couldn't figure out what was going on. It was hurting her when she moved it around, kind of a burning/ itching feeling. We trying lubrication eye drops, but that didn't do much. She undergoing an MRI as I'm typing this, and I'll be hearing from her later how that goes. A bit of background, her mom has MS, but doesn't hit all the markers, and after annoying her, I told my wife to ask if her grandmother on her mother's side, or any other family member had MS. Turns out my wife's paternal grandmother had MS. When it comes to health, it is best to look into family history of things. I will keep you and others here in prayers. I don't know what will happen, but I'll ready to educate myself as much a I can while staying faithful and true to God! As He is the ultimate rock and healer. Whatever path He puts us on, we will accept and be as diligent and good and faithful servants as we could! God bless you all!
got diagnosed with this today & can no longer continue to serve in the army. i’m beyond devastated, but these little animations put a smile on my face through it all. thank you. * UPDATE it’s been four years since my diagnosis, and i was discharged from the army one year upon the discovery. i sought out treatment, & got on top of my condition. it has been a tough journey, but i am making it!
@@HealingIsHolistic please stop, this is not correct, detoxes or cleanses most likely won't help. It's a serious disease, stop spreading conspiracy theories.
Hey man, I'm also serving in the army, national guard for my state and I have so many MS symptoms, I got a doctor appointment tomorrow to discuss it further and I'm very scared. I hope it gets easier for you
i hope your ok i don't mean to sound mean but think of it this way just learn to accept it and there is nothing you can do about it but there is something you can do and that's to think positive you got this don't give up god bless you 👊
Dude this channel is doing more than helping people study ....this channel is carrying on the tradition of understanding biological processes to make the world a better place. It's people like this who make today...today
I want the general public to know how this great man called Dr Orede cure me and my sister from HIV with the gotten from Dr Orede he cures other diseases too like STDS，My own was worst I have suffered from Human papilloma virus HPV）for 2years he cure me too。he have a medicine that is 100％percent assured to cure any type of disease and you don't need to spend so much money anymore。On ARV or any other。You are contact him on WhatsApp：+2349049521615 Email：drorede884@gmail.com。Com Contact him now 👇👇👇 @Dr Orede
I was just diagnose with MS 3 days ago spent 5 days in the hospital... My walking got so bad I thought it was over for me... I thought I would never walk normal again... I have a long road ahead of me... But I REFUSE to let this disease beat me! Prayer for Us All dealing with this illness
@@colleenstack210 Wow so sorry to hear that... I basically lost the function in my legs... I couldn't stand for short period of times I was literally dragging my right leg behind me with every step & had drop foot type symptoms... My whole lower body felt locked... Spasms & Trimmers in the right leg... I got out the hospital on the 10th... How are you feeling?
So freakin' amazing, a lot of people would take an hour or 2 to explain MS in a way everyone can grasp, but not only have you explained it so easily, you've done so in just over 10 mins! Too good 🙌🏼
Multiple sclerosis is an autoimmune disease in which the body's immune system attacks its own tissues. Best solution: EDUCATE the immune system to BALANCE and support immune system response.
my grandmother struggles with this disease and this video really helped me understand what she goes through on a daily basis. thank you for educating people like me about this horrible disease.
I'm studying neuropsychology for my Master's level and picked multiple sclerosis as my term paper topic. I'm always very keen to understand a topic before I get into writing the actual paper and this was very helpful. Thank you!
To all of you who have been diagnosed with multiple sclerosis: Stay strong, research developments are progressing. Maintaining a positive attitude is fundamental
sitting in a hospital bed right now , they are saying that they strongly suspect MS because of my MRI and my symptoms... my spinal tap is tomorrow too confirm. Im really scared. this video helped me understand what is going on.... thank you
@jax raven Your story sounds similar to mine. Docs thought I was dying when I went to the ER with blindness, loss of feeling in my left arm and lower half, and walking issues. They did a cat scan, MRI, spinal tap, and massive blood labs on me, but the MRI showed lesions through my brain, brain stem, and spinal cord. Apparently, I've had it a lot longer than my diagnosis, but what can ya do? My best advice that helped me get back to functional (never 100%, sadly) was 1) Check your diet. What you eat is a big deal. I used the Swank Diet. 2) Exercise. I'm not saying like the Incredible Hulk but just hit the gym. I found water work was perfect. I can't swim, but Aqua therapy was the best thing I ever did. Added weightlifting afterwards. 3) LAUGH! Learn to laugh at yourself. I told my family to make fun of me and it helped all of us out! I wish you the best! Take care!
Please don't get upset regarding it. Every turn has both a positive and a negative impact on your life. It just depends on how you take it. I was effected with MS when I was 12 and now I'm 17. Better medication can be expected soon. Cheer up.
Currently at the hospital with my 15 year old niece who’s been diagnosed with MS 😞 I’m so heart broken for her. Watching this helps me understand what’s happening but it also puts into perspective the scope of how serious this is. My poor girl 🥺
I want the general public to know how this great man called Dr Orede cure me and my sister from HIV with the gotten from Dr Orede he cures other diseases too like STDS，My own was worst I have suffered from Human papilloma virus HPV）for 2years he cure me too。he have a medicine that is 100％percent assured to cure any type of disease and you don't need to spend so much money anymore。On ARV or any other。You are contact him on WhatsApp：+2349049521615 Email：drorede884@gmail.com。Com Contact him now 👇👇👇 @Dr Orede
MS patient here. Thanks for a great and informative video! However, I feel like when you listed the most common symptoms you left out one that 70-80% of patients suffer from, and that greatly influence our lives (for most patients), namely fatigue. It is an extremely common symptom, and one of the most difficult ones to have your surroundings understand, as "we all get tired sometimes". MS fatigue is in a whole other league, and one of the main reasons, that many MS patients can't work full time jobs.
- Pumpkin seeds and almonds are high in magnesium which can help regulate catecholamines ( these contribute to chronic stress leading to more pain and fatigue). -Sardines are packed full of goodness which supports melatonin production ( good for myelin proteins to recover nerves) and contain vitamin D. -Figs are good for producing oxytocin which can help relieve symptoms. - legumes are important to actually digest the fibre from leafy greens and receive the full benefit. -Lions mane is thought to boost NGF which might help restore nerves. - Water hyssop has an element called Bacoside which showed some effect on demyelination in white matter in a nice model.
@@Beannin so magnesium inhibits norepinephrine so it’s going to be working against the Modafinil. Maybe try stopping the magnesium and see if you improve. Do you take vitamin B? It seems some people struggle with fatigue and others struggle with anxiety attacks and then quite a few people go in bouts of both so I think it’s just finding the balance.
I'm 29 and I am positive this has been whats been happening to me for the last 15 years. I usually end up in the ER and get sent away, but from that pattern I can tell that those ER visits were all relapses or flare ups. Recently, i have peripheral neuropathy out of nowhere, my arm and leg will be numb, tingly, "asleep" feeling and painful forever. ER sent me away this time saying I need to ask my primary for an MRI since they determined it's not a stroke. Thing is, Primary Care Drs never listen and never care. But maybe now that I have 15 years if evidence they will start treating me. Sorry for ranting in a youtube comments section about it, it just really sucks and doctors in America are so very out of touch with reality.
I have ms also and my first bout was my left side going numb. The neurologist that was treating me for a car accident had been telling me that my right side was losing nerve signal. But when my left side went numb he told me that I was having a stroke and to get to the er. It stayed 10 days and went away. So I got an appointment with a family dr who did a full panel blood test and it all was great. So he told me to get a neurologist and I found a different doctor and he did an mri. When I got home the phone was ringing and it was the mri place wanting to know if I could come back and re test with the dye and it showed that I had six lesions and I was diagnosed with with rrms. When I started treatment with copaxone I lost my vision and I got the first round of steroids that cleared it up and added 40 lbs. Now I am partially paralyzed on my right side and my left is numb again with pins and needles. I have started using acreavus and it has been good. Every 6 months and a couple times Acthar.
@@whodo4893 That's good. There's good evidence that rituximab works much like Ocrevus (ocrelizumab) and is significantly cheaper. FYI. Perhaps worth checking out.
Water hyssop can help regulate nerve signals, here’s a full diet plan to address the MS; - pumpkin seeds and almonds are high in magnesium which can help regulate catecholamines ( these contribute to chronic stress leading to more pain and fatigue).
3:50 4 types of multiple sclerosis incl progressive with bouts cycles with residual issues 6:49 eye movements symptoms 6:58 intention tremors: plaques along motor pathway: muscle weakness, spasms, balance issues, worst cases incl paralysis 7:21 plagues in the sensory pathways from skin: numbness, pins/needles, parenthesias (tingling, itching, burning) 7:49 plaques in autonomic nervous system: bowel/bladder symptoms, GI issues bloating/reflux, valves ex esophageal, swallowing errors, blood vessel/pressure, palpitations, breathing hurdles 8:01 affect higher order activities (mind): poor concentration, critical thinking, anxiety, depression 8:11 MS suspected when multiple neurological symptoms are spread out over time (bouts) and space (different areas in nervous system). MRI: white matter myelin plaque cerebrospinal fluid: high levels antibodies visual evoked potential: measure nervous system response to visual stimuli 10:09 treatment: increasing interest in vitamin d as viable
my aunt has this! she was trying to explain this and i understood most of it when i related it to the synaptic, axon, and nervous cells. I am learning about these medical terms in Vet tech and I was excited when i ran into this video today. I was concerned about my aunt's condition because, I do help her alot when it comes to going to the store and running errands together every now and then as we enjoy each other's company. Thank you for this explanation. this helps alot!
I have MS, I have been diagnosed with it last year. It doesn't even feel like I have it. I discovered it when I got temporary blind from my left eye. I thank God every day, that I'm able to live normally like this disease isn't growing inside of me.
@@nununies thank you for replying x I am feeling scared. I am on 2 weeks since my vision in my right eye has rapidly deteroriated. Did you have any other signs like fatigue and inflammation but not full body debilitating symptoms? Thank you
@@rerootedearth11 I'm so sorry to hear that! I hope you get well soon! I actually had a terrible headache on the left side of my head, which is where my m.s is located, and I felt my tongue and the tip of my fingers tingling. The fatigue and other symptoms only started after I was diagnosed.
@@osmosis hello! I recently got this symptom, I ran today for 30 mins for about 4kms and noticed foot drop in my left leg, I was unable to lift my left leg as much as my right leg. However, there was no pain at all and it became normal in about 2-3 minutes. However, for those 2-3 minutes, the heaviness/numbness in the foot and being unable to lift it fully was very evident. My dad has PPMS and I'm worried I have it now too. What do you guys think?
Was diagnosed at 21 and Ive lived with it for about 5 years now. The hardest part is feeling it get worse and worse over time. And I fear for the future... I don't want to end up in a vegetative state later in life. There are promising studies involving stem cells but they're so expensive. Hopefully they figure out an affordable cure within our lifetime.
I'm terrified I might have this because I've been having a lot of the neurological symptoms associated with this disease for the past year. Do you think, with all the technology advancements we're having, that in the next 20 years this thing will be cured?
I was diagnosed with MS at 26 years old, 13 years ago. I had the same fears that you have, valid fears. MS is very unpredictable but I will tell you what my neurologist told me the day I was diagnosed. This is the best time in history to be diagnosed with MS. It is understood and new treatment options are being released every year or two. A cure is possible in our lifetime. Remylenating medicines are also a realistic possibility. Tell your doctor about any new symptoms quickly.
I'm in my first year of diagnosis. Last year I had an otic neuritis followed 3 months later by a nystagmus. It's sometimes easy to forget the severity of this condition, because at present the worst I endure is some residual vision blurring, brain fog, and fatigue. I have been on Tysabri for 10 months and haven't had an attack for that whole time. Videos like this are very informative and necessary, but they get me worried about the future again.
Including these things in your diet should help; Sardines are packed full of goodness which supports melatonin production ( good for myelin proteins to recover nerves) and contain vitamin D. -Figs are good for producing oxytocin which can help relieve symptoms. - pumpkin seeds and almonds are high in magnesium which can help regulate catecholamines ( these contribute to chronic stress leading to more pain and fatigue). - legumes are important to actually digest the fibre from leafy greens and receive the full benefit. -Lions mane is thought to boost NGF which might help restore nerves. - Water hyssop has an element called Bacoside which showed some effect on demyelination in white matter in a nice model.
@@Callummullans thanks for the tips. Do you mind if I ask your credentials? I'm just wondering if your advice comes from research in your own time (in which case could you point me in the direction of your useful sources)? Or are you a qualified doctor/nutritionist?
@@adammurray6015 I mention catecholamines because people with chronic fatigue have higher levels, catecholamines also inhibit oxytocin receptors but magnesium can control catecholamine levels.
Thank you for this video, very informative. I just got diagnosed about a month ago and I’m still trying to come to terms with the fact that I have it. My entire right side fell paralyzed, it’s so scary. I remember reading about Lou Gehrig’s disease and being terrified and now I have something very similar.. thankfully physical therapy and steroids have helped me regain most of the control I lost back though. :) I again thank you for breaking it down like this because understanding my body is key in managing this cruddy disease.
Thank you for making this video. I have had ms since I was 13, and this video told me more than any doctor I have been to. Over last 4 years, the doc just gave me death sentences and no meds.
I'm not in the Medical profession nor am I training to be, I just find the subject so interesting and I love these videos. You explain them so well and in a way that are understandable. I am glad I found this channel and I thank you for making the videos. 😄
I want the general public to know how this great man called Dr Orede cure me and my sister from HIV with the gotten from Dr Orede he cures other diseases too like STDS，My own was worst I have suffered from Human papilloma virus HPV）for 2years he cure me too。he have a medicine that is 100％percent assured to cure any type of disease and you don't need to spend so much money anymore。On ARV or any other。You are contact him on WhatsApp：+2349049521615 Email：drorede884@gmail.com。Com Contact him now 👇👇👇 @Dr Orede
Kiki, it seems these days most professions are compartmentalized , you don’t have those restrictions, which could be an asset for understanding outside the box, questioning and sharing information his always helpful to a lot of us , stay healthy, peace
I was once a former athlete and now I have both Multiple Sclerosis and Epilepsy, however a piece of advice I would give which has helped me is to start supplementing with Vitamin D and Magnesium. I take approx. 20,000iu Vitamin D daily along with 200mg Magnesium capsules *(Note for some strange reason different doses and different brand have a different impact on me, so it can be trial and error)* Also following an anti-inflammatory diet has helped a lot (avoiding things like red meat, dairy products and coconut oil etc). I find that living a healthy lifestyle can (on many occasions) have such a better impact than any drug can - Although if yours is really bad I wouldn't advise avoiding medical treatment. One more side note: Turmeric and fish oil combined is usually a great recipe for preventing cancer.
I want the general public to know how this great man called Dr Orede cure me and my sister from HIV with the gotten from Dr Orede he cures other diseases too like STDS，My own was worst I have suffered from Human papilloma virus HPV）for 2years he cure me too。he have a medicine that is 100％percent assured to cure any type of disease and you don't need to spend so much money anymore。On ARV or any other。You are contact him on WhatsApp：+2349049521615 Email：drorede884@gmail.com。Com Contact him now 👇👇👇 @Dr Orede
I found out a week ago. I had drop foot and left arm hurt to the touch. I'm 30 years old but I am going to get on those vitamins you recommended and rx. My Dr subscribed 50k vitamin d and take once a week. Any other advice sir?
I have my first neurologist appointment upcoming today, and I am 99% that this is what I have been feeling for almost two decades (I am 50). I have done a lot of research, and I am scared shitless about a positive diagnosis. This video helped me understand a bit better what causes it and specifically helped me to identify my inbound sensory symptoms (specifically the electric shock when touching my jaw to my chest😰). I wish this symptom was spoken about a bit more, it has been years I have been searching and I would get the same "pinched nerve" response from primary doctors, chiropractors, massage therapists, physiologists, and the Internet. Wish me luck, guys. 😞🤞🙏 EDIT: After two MRIs, a spinal cord lesion was found between C1-C2. But also a severe Vitamin B12 deficiency was found. B12 deficiency can cause nerve damage. I am not vegetarian but only ate animal protein about twice a week. I was put on B12 shots once weekly and also daily pills by mouth. It has been two months, and I have stopped feeling the pins and needles on my toes, and my toes are feeling less numb. Lhermitte sign is still there but much less "electric." Of course, I am very happy with the diagnosis and WORD OF CAUTION TO VEGETARIANS: TAKE A B12 SUPPLEMENT. B12 DEFICIENCY MAY CAUSE DEMYELINATION OF NERVES IN THE PERIPHERAL AND CENTRAL NERVOUS SYSTEM AND CAUSES NEUROPATHY AND LOSS OF SENSATION. IF YOU ARE EXPERIENCING SYMPTOMS SIMILAR TO MS DO HAVE YOUR DOCTOR CHECK YOUR B12 FIRST, BEFORE GOING INTO THE FINANCIAL EXPENSE OF AN MRI. GOOD LUCK AND MUCH HEALTH, EVERYONE!!
B12 deficiency is no joke! It can be lethal if it goes on too long, and nerve damage can be permanent even if B12 levels are recovered. If anyone is experiencing brain fog, tingling toes or hands, confusion, fatigue or anxiety attacks, HAVE THEM CHECK YOUR B12!! The level at which they consider it “too low” in the US is significantly lower than most countries, and you could experience harmful and permanent effects even in ranges that are “borderline” where doctors won’t think it’s the issue. I know this from first hand experience. They were testing me for every neuro-degenerative illness they could think of including MS, Lou Gehrig’s disease and others while I was wasting away, on the brink of losing my job and in a wheelchair because I could barely walk anymore. On every health forum online there was someone posting about this book called “Could it be B12?” And I was peeved that they were trying to peddle their book to people who were struggling for their lives. Finally, when the doctors were out of options and I had all but accepted that I might be dying, I purchased the e-book version of it… and it saved my life. Yes, it WAS B12 😢. After THOUSANDS of dollars in tests (some quite painful) and months of fear and worry, all I needed were B12 shots. (I also used Sublingual Methyl B12 tablets to get started). I strongly encourage anyone suffering from the symptoms above to do more research on B12!
World MS Day today, coming back here since I was diagnosed at 17 years old a couple years ago and to wish fellow diagnosed people the strength and courage we all need. We're more than this disease.
I've never been in a hospital before and have been diagnosed with ms and coronavirus. Went blind in one eye seemingly overnight. I care for my health, am active, and will get through this. Thoughts and prayers from loved ones help me so much to keep up my morale.i have a number of large brain lesions. I have not lost my motor skills, memories, personality, or inner voice, which is a blessing!
@@user-be3be5cp2h sure, for a whole week every time i relaxed my right arm and leg and then move them i immediately feel spasms that my muscles involuntarily contract so hard and it's painful then it goes away after few seconds and comes again when i move, i also feel so lazy and get so tired even tho i did nothing at all and sleep alot it's called fatigue, i also have poor concentration, anxiety and depression however someone who doesn't have ms can still have them, those are my symptoms so far, i made an MRI test it showed scars (lesions) in my brain and v.e.p test but it was good nothing wrong and finally had a csf spinal tap and it showed a high percentage that i might have ms so now i just started taking a medicine for it, also there are many and many diseases that might be mistaken for ms because they're all problems from the immune system i even until now not 100% sure i have ms i gotta wait for more time to be 100% sure..
Hate this disorder. Had a really bad episode a couple weeks ago. Great job on this video. I think I'll show my friends this. Tired of explaining it haha.
@luv life Personally my mother has had it for around a decade (secondary progressive.) On good days you would never be able she was sick, sadly on these days she pushes herself too hard and the stress causes a flare up. This can cause slurs and sometimes she forgets how to talk or use a limb. I know she has bladder issues and seizures. She also has horrible migraines and pins and needles, sometimes she has delusions that she can't remember. She has horrible cramps that have progressed from her feet to her legs and now she has esophagus cramps. It's one of the worst things ever, I've never seen her in so much pain. Obviously these aren't all the symptoms, loss of sight, confusion, horrible fatigue and others are a part of our lives. But still I love my mom and no matter what she thinks I have no problem helping her and I'm happy to do so. If God only gives us what we can handle my mom is a superhero and honestly, I wouldn't have it any other way.
Iam a patient of ms living in Pakistan iam 20 years old 9 months back I was diagnosed with this, iam a student of psychology iam studying hard with this disease it is difficult sometimes with this but iam trying my best, thank you so much for guiding us❤️
What helped me alot is double my vitamins. Double C, B D etc. A few years ago I couldn't walk, talk, eat, couldn't do anything for myself. Today when I start to feel sick I drink 3x more vitamin B and extra other vitamins. My last relapse was in 2016. Was very bad. When depression takes over, drink more vitamins. Visit friends. Never be alone. What also helped me is to stay busy. Never sit and do nothing. Keep your brain busy. Do extra work etc. Just stay positve. It helps alot.
My heart goes out to everyone with MS. It’s really unfair and messed up. You didn’t deserve this, and I’m so sorry you are forced to walk this path. Pray we find a cure.
I have had this disease for 11 years (Since I was a baby) and it’s not as Bad as most people but it really effects physical activity. It also effected my eyes, causing the inside of my eyes to be swollen. You get so tired very easily. Once I rode my bike around a very short block and I was tired halfway through. It is really hard for me to see without my glasses, which are super strong it could blind someone, and even my glasses now are not strong enough...
This sounds similar to cushings disease for the eye swelling which is caused by a build up of catecholamines which is also a problem in MS. Maybe try to increase the amount of magnesium in you diet with seeds and nuts. Here are some other suggestions; Sardines are packed full of goodness which supports melatonin production ( good for myelin proteins to recover nerves) and contain vitamin D. -Figs are good for producing oxytocin which can help relieve symptoms. - pumpkin seeds and almonds are high in magnesium which can help regulate catecholamines ( these contribute to chronic stress leading to more pain and fatigue). - legumes are important to actually digest the fibre from leafy greens and receive the full benefit. -Lions mane is thought to boost NGF which might help restore nerves. - Water hyssop has an element called Bacoside which showed some effect on demyelination in white matter in a nice model.
Hi I am from Hong Kong, 26 years old. I want to get rid of this disease completely because I just got the diagnosis. Treatments not started yet because it is early stage diagnosis, symptoms including dizziness, slow writing on the right hand especially, numbness in tongue, and unclear visions. Any suggestions from your side?
I hope from the deepest of my heart that everyone will get better 🙏 Just today my life's best friend and brother was diagnosed with it. Stay strong Brother and Sister you are not alone ❤ 💪
@@CharlotteKate-wm2db where this this doctor? Anywhere near Germany? And do you have any further details about him ? Name usw... Because honestly I don't know of you did got what kind of illness is this but till this moment there is no cure, they use only cortisol on patient to stop the symptoms from getting worst.
I want the general public to know how this great man called Dr Orede cure me and my sister from HIV with the gotten from Dr Orede he cures other diseases too like STDS，My own was worst I have suffered from Human papilloma virus HPV）for 2years he cure me too。he have a medicine that is 100％percent assured to cure any type of disease and you don't need to spend so much money anymore。On ARV or any other。You are contact him on WhatsApp：+2349049521615 Email：drorede884@gmail.com。Com Contact him now 👇👇👇 @Dr Orede
Thank you for the time and effort you've placed into making this. It was incredibly informative. May you be blessed with millions of views and subscribers.
I want the general public to know how this great man called Dr Orede cure me and my sister from HIV with the gotten from Dr Orede he cures other diseases too like STDS，My own was worst I have suffered from Human papilloma virus HPV）for 2years he cure me too。he have a medicine that is 100％percent assured to cure any type of disease and you don't need to spend so much money anymore。On ARV or any other。You are contact him on WhatsApp：+2349049521615 Email：drorede884@gmail.com。Com Contact him now 👇👇👇 @Dr Orede
I want the general public to know how this great man called Dr Orede cure me and my sister from HIV with the gotten from Dr Orede he cures other diseases too like STDS，My own was worst I have suffered from Human papilloma virus HPV）for 2years he cure me too。he have a medicine that is 100％percent assured to cure any type of disease and you don't need to spend so much money anymore。On ARV or any other。You are contact him on WhatsApp：+2349049521615 Email：drorede884@gmail.com。Com Contact him now 👇👇👇 @Dr Orede
My best friend got diagnosed with this about a month ago. I've spent hours reading/watching videos about this and every time I do it says the same thing - it happens mostly to people that are 20-40 years old and people who don't live near the equator. She's 14 and lives in the middle east so she gets plenty of sun. None of her relatives have it so I don't think it's anything genetic but she IS a female and females usually get it more than men. I never wanted to become a doctor but now I do because I'm determined to try and find a cure for this. Thank you for this video it really helped me understand multiple sclerosis a lot more.
i was diagnosed with MS this year and i went to the hospital 3 weeks before my 14th birthday it attacked my whole left side and i couldn't walk, raise my left arm my eye sight was even off i spent weeks in the hospital i had 6 MRI's done 2 cat scans before they diagnosed me it was torture then i had to get a lumber puncture (spinal tap) and it hurt like hell they then put me on steroids and i got out 3 days before my birthday i then had to get glasses and physical therapy i wasn't in school for a whole month my relatives never had it either i dont know how i got it
Heya, you should consider a career also in science. Often they would be able to spend more time doing the research that leads to a treatment/understanding the disease, compared to doctors. Science needs motivated people like yourself! Good luck! :)
Just been diagnosed with PPMS, this video explains a lot in terms that are easy to understand. My Neurologist is awesome and very supportive, however this allows a person to go over it at their own pace.👍
Dear MSers, i have MS and it's a moderate case but it's characterized by SEVERE anxiety , i also have heavy fatigue, brain fog, body weakness and all of that. I take tecfidera but the anxiety and the fatigue and balance was getting worse. I decided to finally take the popular diabetes drug metformin and the results are fantastic, everything is better, balance, movement, leg strength and most importantly anxiety, im still suffering but things are getting a lot better. It's up and down as always but now the overall path is up. Bless your hearts everyone
Love your videos- as a visual learner this helps me retain and better understand various disease processes. The subtle humor is amazing. This osmosis video, in particular, is one of my favs!
Thankyu god for showing me the osmosis...it was a suggestion. You guys have no idea how it is helping me in clearing the concept. The no 1 channel in you tube....♥️♥️
My mom had MS. For the past 3-4 years my arms have been going numb. I can only sleep on my back at night. Even my tongue has gone numb trying to sleep on my stomach. I wake up and all day my joints in my hands and feet hurt so much and are very stiff and swollen when I wake up in the mornings. My memory is garbage and my digestion is terrible. I hope I can get my doctor to take me serious and find out.
My wife was tested recently and we're waiting on results, however, the Neurologist stated she has seen this enough to know it's MS. I am very worried for her (recently went blind in one eye, and losing her balance), we're basically waiting on what type of MS she has. This explains her constant being sick, and many other issues that have taken place over the last two years.
@@boychub1830 - Not really. She has MS attacks every few months, tons of lesions in her brain and down her spine. She is now in a power assist wheel chair as needed and often times she is sleeping. She has PPMS. The brain lesions have caused her personality to change a lot and can become very mean. She does not realize what she is doing most of the time. The problem with MS is that it's different for everyone. So, I wouldn't read into what I had stated too far. I met a lady a couple months back that has been living with the same MS as my wife for the last 30 years. She stated that sleeping a lot is a part of MS, especially PPMS, and has tons of lesions on her brain as well. She was more mobile than my wife though.
@@boychub1830 - I believe that it did come back after some time or at least partially come back. I have not talked to her much about it for a couple of years.
Sardines are packed full of goodness which supports melatonin production ( good for myelin proteins to recover nerves) and contain vitamin D. -Figs are good for producing oxytocin which can help relieve symptoms. - pumpkin seeds and almonds are high in magnesium which can help regulate catecholamines ( these contribute to chronic stress leading to more pain and fatigue). - legumes are important to actually digest the fibre from leafy greens and receive the full benefit. -Lions mane is thought to boost NGF which might help restore nerves. - Water hyssop has an element called Bacoside which showed some effect on demyelination in white matter in a nice model.
I believe most degenerative diseases can be traced to the HPA axis, there’s a lot pointing to this area/ function. Here’s some stuff to help in diet; Sardines are packed full of goodness which supports melatonin production ( good for myelin proteins to recover nerves) and contain vitamin D. -Figs are good for producing oxytocin which can help relieve symptoms. - pumpkin seeds and almonds are high in magnesium which can help regulate catecholamines ( these contribute to chronic stress leading to more pain and fatigue). - legumes are important to actually digest the fibre from leafy greens and receive the full benefit. -Lions mane is thought to boost NGF which might help restore nerves. - Water hyssop has an element called Bacoside which showed some effect on demyelination in white matter in a nice model.
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I was diagnosed last year (2019) in the middle of the night on my 17th bday I had a seizure. I woke up in the hospital so confused. I was in the hospital for 9 days and I even had to have my birthday party in the hospital. I have gotten used to it by now but I dont want to live with this for the rest of my life. I hope a cure is found.
I also got my diagnosis at my party when I was 17, that's more than two years ago for me.. but if I can tell you something it's to enjoy life in the ways ur able to and never push yourself ever, everyone has bad days, things will hopefully be a bit brighter soon
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Multiple sclerosis is an autoimmune disease in which the body's immune system attacks its own tissues. Best solution: EDUCATE the immune system to BALANCE and support immune system response.
My mum has this and I want to understand more on why she takes so many prescribed pills and why she has bad headaches and won't talk sometimes. Thank you for helping me!
Thank you, you shared a lot of very helpful information for those of us trying to understand MS. I had a few small symptoms that were mild, but two years ago I had Lyme Meningitis, which was a nightmare in itself, which seems to have caused the MS to speed up. After one week in the hospital and three more weeks of antibiotics I still tested positive for Lyme. Thankfully I have a couple of wonderful doctors.
@@swingwizard now i am writing you Arthur. Please explai me if you have had MS and if you have cured, how you feel now? I need to know for my mother. From where to find silicium if I understand you correctly. Did it help you?
In my master's level neurobiology studies, I've chosen Multiple Sclerosis as my term paper topic. Could you please suggest a book that can help me understand the pathophysiology of this disease? Thank you for your assistance!
Thank you so much for this information. My dear friend who is 76 yrs. Old is suffering from ms. Understanding ms a bit is the best tool I can use to help her. 🙏🏻❤️
I know this has been on UA-cam for awhile, but I've been diagnosed (Merry Christmas, right?) and am trying to learn everything I can. Thanks for being so informative!
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My mother became a paraplegic then quadriplegic and eventually dead from this terrible and cruel disease. I pray this among other conditions become a thing of the past.
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I have PRMS officially diagnosed in 2019 this came up on my feed to watch very informative I'm definitely getting worse I can feel the difference over the years which is scary
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Smoking is common in patients with Multiple sclerosis. It has general negative health effects, but in addition has been shown to have direct links to MS disease activity. Smoking is thought to be a risk factor for developing multiple sclerosis (MS). The habit is also strongly associated with having a worse disease course and with decreased effectiveness of MS treatment. Even children exposed to secondhand smoke are more likely to develop MS later in life than their peers
I'm at a stage where I don't study medicine topics until I watch a video on that topic from ur channel !! Ur explanation helps me understand what's written in the book ! Thanku from a medico :)
My close friend recently got diagnosed and she has been using cortisols for some time now. I came here to learn more, thank you so much this was a very informative video and it was easy to understand.
Thank you for the video, it helped me understand this sickness. I was diagnosed with MS-RR a year ago and I've been trying to find alternative methods to control it, from changing my diet to meditation. I didn't want to follow any treatments since all of them carry damage to other organs and if in the end, like you explained it, doesn't really have a cure, I will only be further damaging my body than curing it by taking any of those treatments. I do think genetics play a part on the development of this deseace but also stress and not following a good and healthy way of life. My mother has lupus and my great grandmother got paralyzed from the waste down at the age of 25 and unfortunatelly 5 years after that, she died and no one knew why, so my neurologist told me that possibly she might have had MS only the most agrassive type. Now, living with MS is not so difficult when the disfunctions are cognitive and not motor/physical, like mine... but, I know there will come a time when I will have to face the uglier side of this sickness and I can only hope by then, modern medicine has found a way to stop its progression. Cheers!
i have lots of these symptoms like panic attack ,fear,anxiety ,depressions,terrified,high pitch sound in loud environment,confusion,feeling like i am in a dream when walking on street,spinning wheel flash or tv dots which affect vision,trembling of hand and legs,difficulty to breath ,difficulty to concentrate,mind disorder,cold or warm ice piercing my left shoulder bone and in extreme case the muscle around it start to feel like bubble of air poping,and i also once got the symptom of drops of water falling inside my head which was very disturbing situation...
I am a patient of Multiple Sclerosis living in Korea.
I was diagnosed with the disease at the age of 19 and it's only been a year now.
I still don't know. Why I got this disease. But I want to overcome it. Even though I have a disease, I am doing my college life and preparing for a certificate and working hard. However, there are often many difficulties in everyday life due to illness. I hope God gives me strength to overcome. I hope the same patients with multiple sclerosis will cheer up. Thank you. Have a nice day.
Hello let me recommend you to Dr Okolo who has herbal medicine to cure MS.. he cured my Dad completely from ALS
Oh hi we're at same age and suffering from same illness 🤗 I hope you're doing great and don't stress too much coz it can cause relapse and it already happened to me ahaha yea it's hard but we need to overcome it no matter what ..urrgh
Please check out the Medical Medium Daily Celery Juice protocol! It has been such a miracle for my digestive issues that I want to share it and help others as well! It can help MS symptoms as well!
God is with you through all of this! ALWAYS AND FOREVER! He states in His Word, that vs does not give us more than we can bare. He knows us better than we even know ourselves. Just think through your life and look at all that you've been through and thought you couldn't make it through, but you did. He ALWAYS also has help available as well read a way out. And most times, the way out of a storm is going through it! It's not easy to hear, think, say or do! As Les Brown would say, "it's simple, but it ain't easy."
Thank you for your courage in sharing this. God will bless you as long as you stay true to Him and keep striving for the best! May you keep working hard on all aspects of your life! And may God bless you in all you do.
I'm here because my wife, got admitted into the hospital yesterday. She had eye pains for at least 3 days of not longer, and we couldn't figure out what was going on. It was hurting her when she moved it around, kind of a burning/ itching feeling. We trying lubrication eye drops, but that didn't do much. She undergoing an MRI as I'm typing this, and I'll be hearing from her later how that goes.
A bit of background, her mom has MS, but doesn't hit all the markers, and after annoying her, I told my wife to ask if her grandmother on her mother's side, or any other family member had MS. Turns out my wife's paternal grandmother had MS. When it comes to health, it is best to look into family history of things.
I will keep you and others here in prayers. I don't know what will happen, but I'll ready to educate myself as much a I can while staying faithful and true to God! As He is the ultimate rock and healer. Whatever path He puts us on, we will accept and be as diligent and good and faithful servants as we could! God bless you all!
More power to you! ✨
That two seconds of club music for the T Cell going through the blood/brain barrier is the best thing that happened to me all week.
Nicole B Garcia 😊😊
1:08
very fukin true
Lmfao
So true 😂
got diagnosed with this today & can no longer continue to serve in the army. i’m beyond devastated, but these little animations put a smile on my face through it all. thank you.
* UPDATE
it’s been four years since my diagnosis, and i was discharged from the army one year upon the discovery. i sought out treatment, & got on top of my condition. it has been a tough journey, but i am making it!
@@HealingIsHolistic please stop, this is not correct, detoxes or cleanses most likely won't help. It's a serious disease, stop spreading conspiracy theories.
Hey man, I'm also serving in the army, national guard for my state and I have so many MS symptoms, I got a doctor appointment tomorrow to discuss it further and I'm very scared. I hope it gets easier for you
i hope your ok i don't mean to sound mean but think of it this way just learn to accept it and there is nothing you can do about it but there is something you can do and that's to think positive you got this don't give up god bless you 👊
@@AthosRespecterhow did it go???
are you able to update on your condition?
Dude this channel is doing more than helping people study ....this channel is carrying on the tradition of understanding biological processes to make the world a better place. It's people like this who make today...today
So deep bro
It also helps people like me with MS understand what is actually happening to my body
@@taittinger1092 awesome
I want the general public to know how this great man called Dr Orede cure me and my sister from HIV with the gotten from Dr Orede he cures other diseases too like STDS，My own was worst I have suffered from Human papilloma virus HPV）for 2years he cure me too。he have a medicine that is 100％percent assured to cure any type of disease and you don't need to spend so much money anymore。On ARV or any other。You are contact him on WhatsApp：+2349049521615 Email：drorede884@gmail.com。Com Contact him now
👇👇👇
@Dr Orede
Try siyag sidh yog cure ms because many aids patient cure
I was just diagnose with MS 3 days ago spent 5 days in the hospital... My walking got so bad I thought it was over for me... I thought I would never walk normal again... I have a long road ahead of me... But I REFUSE to let this disease beat me! Prayer for Us All dealing with this illness
Hi . I'm here in hospital day 5 just diagnosed to. Praying for you 🙏
@@colleenstack210 Hi, If you don't mind me asking? What are your symptoms? & sending positive vibes your way & prayers Up!!! 😘🙏
@@Ms.Tucker89 hi I kept falling for 4 days and hit a car thinking I was hitting the brake. Numbers n tingling in both my legs. How about you?
@@Ms.Tucker89 I had buzzing in my lower spine when I sat thats all I could feel another sign
@@colleenstack210 Wow so sorry to hear that... I basically lost the function in my legs... I couldn't stand for short period of times I was literally dragging my right leg behind me with every step & had drop foot type symptoms... My whole lower body felt locked... Spasms & Trimmers in the right leg... I got out the hospital on the 10th... How are you feeling?
So freakin' amazing, a lot of people would take an hour or 2 to explain MS in a way everyone can grasp, but not only have you explained it so easily, you've done so in just over 10 mins! Too good 🙌🏼
Wow, thanks! Appreciate the feedback, Pranav! 😊
Please tell me Phone number of doctor treating ms
@@osmosis This channel is life saver!!!!!!!!! Guys you are UNBELIEVABLE!!!!! 🙌🏼🙌🏼🙌🏼🙌🏼🙌🏼😮❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️
I am an MS Warrior❤The hardest thing I have ever faced in my life is being diagnosed with Multiple Sclerosis.
Multiple sclerosis is an autoimmune disease in which the body's immune system attacks its own tissues.
Best solution:
EDUCATE the immune system to BALANCE and support immune system response.
@@swingwizard prove it
It's scary ❤️
@@swingwizard Can we talk please
@@swingwizard I sure will, I literally feel like I'm stuck between life and death. What is this trial oh God.
This looks horrendous. My heart goes out to all those suffering with this.
gabor ap my mom has this :(
It’s manageable. I’ve been symptom free for a year now!
Its not walking I. The park
gabor ap Thanks for your kind words.. Blessings to you..
It’s a slow but horrible disease
my grandmother struggles with this disease and this video really helped me understand what she goes through on a daily basis. thank you for educating people like me about this horrible disease.
Check out the Wahl's Protocol!
I'm studying neuropsychology for my Master's level and picked multiple sclerosis as my term paper topic. I'm always very keen to understand a topic before I get into writing the actual paper and this was very helpful. Thank you!
Best of luck! Glad to be able to help you out! 😊
To all of you who have been diagnosed with multiple sclerosis: Stay strong, research developments are progressing. Maintaining a positive attitude is fundamental
sitting in a hospital bed right now , they are saying that they strongly suspect MS because of my MRI and my symptoms... my spinal tap is tomorrow too confirm. Im really scared. this video helped me understand what is going on.... thank you
@jax raven Your story sounds similar to mine. Docs thought I was dying when I went to the ER with blindness, loss of feeling in my left arm and lower half, and walking issues. They did a cat scan, MRI, spinal tap, and massive blood labs on me, but the MRI showed lesions through my brain, brain stem, and spinal cord. Apparently, I've had it a lot longer than my diagnosis, but what can ya do? My best advice that helped me get back to functional (never 100%, sadly) was 1) Check your diet. What you eat is a big deal. I used the Swank Diet. 2) Exercise. I'm not saying like the Incredible Hulk but just hit the gym. I found water work was perfect. I can't swim, but Aqua therapy was the best thing I ever did. Added weightlifting afterwards. 3) LAUGH! Learn to laugh at yourself. I told my family to make fun of me and it helped all of us out! I wish you the best! Take care!
Arthur Schagen correlation sadly doesn’t mean causation
@@swingwizard I wonder where the aluminum accumulation came from. But this is a good deduction.
How are you doing now?
Me too
Thank you for this my doctor is saying that I might have this and I'm only 16 and this helped me understand it more so it seems less scary
You are welcome Meghan. Thank you for your comment. Best wishes from the Osmosis Team.
Meghan Whitney Damn, I'm sorry. I can't imagine what you must be going through. Stay strong.
Thanks I'm trying
Please don't get upset regarding it. Every turn has both a positive and a negative impact on your life. It just depends on how you take it. I was effected with MS when I was 12 and now I'm 17. Better medication can be expected soon. Cheer up.
Can I ask you if you got the HPV vaccine before you got the diagnose?
Currently at the hospital with my 15 year old niece who’s been diagnosed with MS 😞
I’m so heart broken for her. Watching this helps me understand what’s happening but it also puts into perspective the scope of how serious this is. My poor girl 🥺
I’m a medical student and we have an exam tomorrow about demyelinating disorders. Thank you for this video!
I want the general public to know how this great man called Dr Orede cure me and my sister from HIV with the gotten from Dr Orede he cures other diseases too like STDS，My own was worst I have suffered from Human papilloma virus HPV）for 2years he cure me too。he have a medicine that is 100％percent assured to cure any type of disease and you don't need to spend so much money anymore。On ARV or any other。You are contact him on WhatsApp：+2349049521615 Email：drorede884@gmail.com。Com Contact him now
👇👇👇
@Dr Orede
MS patient here. Thanks for a great and informative video! However, I feel like when you listed the most common symptoms you left out one that 70-80% of patients suffer from, and that greatly influence our lives (for most patients), namely fatigue. It is an extremely common symptom, and one of the most difficult ones to have your surroundings understand, as "we all get tired sometimes". MS fatigue is in a whole other league, and one of the main reasons, that many MS patients can't work full time jobs.
- Pumpkin seeds and almonds are high in magnesium which can help regulate catecholamines ( these contribute to chronic stress leading to more pain and fatigue).
-Sardines are packed full of goodness which supports melatonin production ( good for myelin proteins to recover nerves) and contain vitamin D.
-Figs are good for producing oxytocin which can help relieve symptoms.
- legumes are important to actually digest the fibre from leafy greens and receive the full benefit.
-Lions mane is thought to boost NGF which might help restore nerves.
- Water hyssop has an element called Bacoside which showed some effect on demyelination in white matter in a nice model.
I don't understand the relevance of your reply.
@@Beannin
Getting more magnesium in your diet might help with the fatigue.
@dorianGreysportrait I take a magnesium supplement every day and 200 mg of Modafinil. Still absolutely knackered.
@@Beannin so magnesium inhibits norepinephrine so it’s going to be working against the Modafinil. Maybe try stopping the magnesium and see if you improve. Do you take vitamin B? It seems some people struggle with fatigue and others struggle with anxiety attacks and then quite a few people go in bouts of both so I think it’s just finding the balance.
I'm 29 and I am positive this has been whats been happening to me for the last 15 years. I usually end up in the ER and get sent away, but from that pattern I can tell that those ER visits were all relapses or flare ups. Recently, i have peripheral neuropathy out of nowhere, my arm and leg will be numb, tingly, "asleep" feeling and painful forever. ER sent me away this time saying I need to ask my primary for an MRI since they determined it's not a stroke. Thing is, Primary Care Drs never listen and never care. But maybe now that I have 15 years if evidence they will start treating me. Sorry for ranting in a youtube comments section about it, it just really sucks and doctors in America are so very out of touch with reality.
Hi Zoe! Thanks for sharing your experiences. It's not easy, but we're rooting for you! 🙏🏼
I have ms also and my first bout was my left side going numb. The neurologist that was treating me for a car accident had been telling me that my right side was losing nerve signal. But when my left side went numb he told me that I was having a stroke and to get to the er. It stayed 10 days and went away. So I got an appointment with a family dr who did a full panel blood test and it all was great. So he told me to get a neurologist and I found a different doctor and he did an mri. When I got home the phone was ringing and it was the mri place wanting to know if I could come back and re test with the dye and it showed that I had six lesions and I was diagnosed with with rrms. When I started treatment with copaxone I lost my vision and I got the first round of steroids that cleared it up and added 40 lbs. Now I am partially paralyzed on my right side and my left is numb again with pins and needles. I have started using acreavus and it has been good. Every 6 months and a couple times Acthar.
Keep ranting, people need to hear your situation ❤
@@whodo4893 That's good. There's good evidence that rituximab works much like Ocrevus (ocrelizumab) and is significantly cheaper. FYI. Perhaps worth checking out.
Water hyssop can help regulate nerve signals, here’s a full diet plan to address the MS;
- pumpkin seeds and almonds are high in magnesium which can help regulate catecholamines ( these contribute to chronic stress leading to more pain and fatigue).
3:50 4 types of multiple sclerosis incl progressive with bouts cycles with residual issues
6:49 eye movements symptoms
6:58 intention tremors: plaques along motor pathway: muscle weakness, spasms, balance issues, worst cases incl paralysis
7:21 plagues in the sensory pathways from skin: numbness, pins/needles, parenthesias (tingling, itching, burning)
7:49 plaques in autonomic nervous system: bowel/bladder symptoms, GI issues bloating/reflux, valves ex esophageal, swallowing errors, blood vessel/pressure, palpitations, breathing hurdles
8:01 affect higher order activities (mind): poor concentration, critical thinking, anxiety, depression
8:11 MS suspected when multiple neurological symptoms are spread out over time (bouts) and space (different areas in nervous system).
MRI: white matter myelin plaque
cerebrospinal fluid: high levels antibodies
visual evoked potential: measure nervous system response to visual stimuli
10:09 treatment: increasing interest in vitamin d as viable
Ty!!
Thank you so much
I have a lot of these symptoms fuck
@@artythekot so do i, ima be talking to my doctor soon. I wish you the best of luck
@@sexyramen9504 Good luck to you too, I hope it's manageable. I hope I don't have it because it would destroy my life and all my plans completely.
my aunt has this! she was trying to explain this and i understood most of it when i related it to the synaptic, axon, and nervous cells. I am learning about these medical terms in Vet tech and I was excited when i ran into this video today. I was concerned about my aunt's condition because, I do help her alot when it comes to going to the store and running errands together every now and then as we enjoy each other's company. Thank you for this explanation. this helps alot!
I have MS, I have been diagnosed with it last year. It doesn't even feel like I have it. I discovered it when I got temporary blind from my left eye. I thank God every day, that I'm able to live normally like this disease isn't growing inside of me.
Did your eyesight ever recover?
@@rerootedearth11 Yes, it did! But at around 80% or so, and I have to use glasses now.
@@nununies thank you for replying x I am feeling scared. I am on 2 weeks since my vision in my right eye has rapidly deteroriated. Did you have any other signs like fatigue and inflammation but not full body debilitating symptoms? Thank you
Did they do blood work to say MS?
@@rerootedearth11 I'm so sorry to hear that! I hope you get well soon! I actually had a terrible headache on the left side of my head, which is where my m.s is located, and I felt my tongue and the tip of my fingers tingling. The fatigue and other symptoms only started after I was diagnosed.
Got diagnosed last year and doing well. Wanted to know more about it. Thank you for the information
Glad it was helpful, Erik! Wishing you the best of health!
@@osmosis hello! I recently got this symptom, I ran today for 30 mins for about 4kms and noticed foot drop in my left leg, I was unable to lift my left leg as much as my right leg. However, there was no pain at all and it became normal in about 2-3 minutes. However, for those 2-3 minutes, the heaviness/numbness in the foot and being unable to lift it fully was very evident. My dad has PPMS and I'm worried I have it now too. What do you guys think?
@@ShankyBady read the Wahl's Protocol
Was diagnosed at 21 and Ive lived with it for about 5 years now. The hardest part is feeling it get worse and worse over time. And I fear for the future... I don't want to end up in a vegetative state later in life. There are promising studies involving stem cells but they're so expensive. Hopefully they figure out an affordable cure within our lifetime.
I'm terrified I might have this because I've been having a lot of the neurological symptoms associated with this disease for the past year. Do you think, with all the technology advancements we're having, that in the next 20 years this thing will be cured?
I was diagnosed with MS at 26 years old, 13 years ago. I had the same fears that you have, valid fears. MS is very unpredictable but I will tell you what my neurologist told me the day I was diagnosed. This is the best time in history to be diagnosed with MS. It is understood and new treatment options are being released every year or two. A cure is possible in our lifetime. Remylenating medicines are also a realistic possibility. Tell your doctor about any new symptoms quickly.
@@corvoattano9303did you have it?
@lindaharsh6729 Thanks for your positive statement...but we are 13 years in time and still no impressive improvement
I'm in my first year of diagnosis. Last year I had an otic neuritis followed 3 months later by a nystagmus.
It's sometimes easy to forget the severity of this condition, because at present the worst I endure is some residual vision blurring, brain fog, and fatigue. I have been on Tysabri for 10 months and haven't had an attack for that whole time.
Videos like this are very informative and necessary, but they get me worried about the future again.
I'm so scared for the day i wake up without my vision or unable to feel my legs. I'm terrified. Its good to see some medicines do help.
@@SkarGig Bless you.
Including these things in your diet should help;
Sardines are packed full of goodness which supports melatonin production ( good for myelin proteins to recover nerves) and contain vitamin D.
-Figs are good for producing oxytocin which can help relieve symptoms.
- pumpkin seeds and almonds are high in magnesium which can help regulate catecholamines ( these contribute to chronic stress leading to more pain and fatigue).
- legumes are important to actually digest the fibre from leafy greens and receive the full benefit.
-Lions mane is thought to boost NGF which might help restore nerves.
- Water hyssop has an element called Bacoside which showed some effect on demyelination in white matter in a nice model.
@@Callummullans thanks for the tips. Do you mind if I ask your credentials? I'm just wondering if your advice comes from research in your own time (in which case could you point me in the direction of your useful sources)? Or are you a qualified doctor/nutritionist?
@@adammurray6015 I mention catecholamines because people with chronic fatigue have higher levels, catecholamines also inhibit oxytocin receptors but magnesium can control catecholamine levels.
I've had MS for 15 years and this is the best explanation I've ever seen or heard. I've copied it to my children, grandchildren and friends. Thank you
Sorry, what treatment have you received? How you feel now?
How are you now ??? Is it a very serious disease.... I'm very much worried cause maybe i have this disease 😭
@@learninglifeoflabani0406 I hope you are doing well. Do you have any updates?
Thank you for this video, very informative. I just got diagnosed about a month ago and I’m still trying to come to terms with the fact that I have it. My entire right side fell paralyzed, it’s so scary. I remember reading about Lou Gehrig’s disease and being terrified and now I have something very similar.. thankfully physical therapy and steroids have helped me regain most of the control I lost back though. :) I again thank you for breaking it down like this because understanding my body is key in managing this cruddy disease.
Doctors have discovered by doing many autopsies that MS may be caused by parasitic worms and worm cysts in brain and other parts of the body.
Thank you for making this video. I have had ms since I was 13, and this video told me more than any doctor I have been to. Over last 4 years, the doc just gave me death sentences and no meds.
I'm not in the Medical profession nor am I training to be, I just find the subject so interesting and I love these videos.
You explain them so well and in a way that are understandable.
I am glad I found this channel and I thank you for making the videos. 😄
Gouty
I want the general public to know how this great man called Dr Orede cure me and my sister from HIV with the gotten from Dr Orede he cures other diseases too like STDS，My own was worst I have suffered from Human papilloma virus HPV）for 2years he cure me too。he have a medicine that is 100％percent assured to cure any type of disease and you don't need to spend so much money anymore。On ARV or any other。You are contact him on WhatsApp：+2349049521615 Email：drorede884@gmail.com。Com Contact him now
👇👇👇
@Dr Orede
Kiki, it seems these days most professions are compartmentalized , you don’t have those restrictions, which could be an asset for understanding outside the box, questioning and sharing information his always helpful to a lot of us , stay healthy, peace
ادعوا لامي بالشفاء من هذا المرض 🤲🏻
How is she now?
I was once a former athlete and now I have both Multiple Sclerosis and Epilepsy, however a piece of advice I would give which has helped me is to start supplementing with Vitamin D and Magnesium.
I take approx. 20,000iu Vitamin D daily along with 200mg Magnesium capsules *(Note for some strange reason different doses and different brand have a different impact on me, so it can be trial and error)* Also following an anti-inflammatory diet has helped a lot (avoiding things like red meat, dairy products and coconut oil etc).
I find that living a healthy lifestyle can (on many occasions) have such a better impact than any drug can - Although if yours is really bad I wouldn't advise avoiding medical treatment.
One more side note: Turmeric and fish oil combined is usually a great recipe for preventing cancer.
I want the general public to know how this great man called Dr Orede cure me and my sister from HIV with the gotten from Dr Orede he cures other diseases too like STDS，My own was worst I have suffered from Human papilloma virus HPV）for 2years he cure me too。he have a medicine that is 100％percent assured to cure any type of disease and you don't need to spend so much money anymore。On ARV or any other。You are contact him on WhatsApp：+2349049521615 Email：drorede884@gmail.com。Com Contact him now
👇👇👇
@Dr Orede
I found out a week ago. I had drop foot and left arm hurt to the touch. I'm 30 years old but I am going to get on those vitamins you recommended and rx. My Dr subscribed 50k vitamin d and take once a week. Any other advice sir?
Try siyag sidh yog cure aids cancer so this is little disease for sidh yog
Thank you so much for sharing, I have the exact same. 🙏 changing my diet has helped also with the epilepsy.
Read the Wahl's Protocol
Thank you guys! Once I graduate and Im no longer poor af ill definetly support you!
I have my first neurologist appointment upcoming today, and I am 99% that this is what I have been feeling for almost two decades (I am 50). I have done a lot of research, and I am scared shitless about a positive diagnosis. This video helped me understand a bit better what causes it and specifically helped me to identify my inbound sensory symptoms (specifically the electric shock when touching my jaw to my chest😰). I wish this symptom was spoken about a bit more, it has been years I have been searching and I would get the same "pinched nerve" response from primary doctors, chiropractors, massage therapists, physiologists, and the Internet. Wish me luck, guys. 😞🤞🙏
EDIT: After two MRIs, a spinal cord lesion was found between C1-C2. But also a severe Vitamin B12 deficiency was found. B12 deficiency can cause nerve damage. I am not vegetarian but only ate animal protein about twice a week. I was put on B12 shots once weekly and also daily pills by mouth. It has been two months, and I have stopped feeling the pins and needles on my toes, and my toes are feeling less numb. Lhermitte sign is still there but much less "electric." Of course, I am very happy with the diagnosis and WORD OF CAUTION TO VEGETARIANS: TAKE A B12 SUPPLEMENT. B12 DEFICIENCY MAY CAUSE DEMYELINATION OF NERVES IN THE PERIPHERAL AND CENTRAL NERVOUS SYSTEM AND CAUSES NEUROPATHY AND LOSS OF SENSATION. IF YOU ARE EXPERIENCING SYMPTOMS SIMILAR TO MS DO HAVE YOUR DOCTOR CHECK YOUR B12 FIRST, BEFORE GOING INTO THE FINANCIAL EXPENSE OF AN MRI. GOOD LUCK AND MUCH HEALTH, EVERYONE!!
Wishing you the best of health, Tanya! We're glad that our video was able to help 🙏🏼 ❤️ 😊
@Tanya Enid Has anything come of it yet? I do hope things are going well for you and that everything will be okay in due time. 🥺
Hi, I hope you are doing well. Do you have any updates?
Good luck, I hope everything worked well for you 🌹
B12 deficiency is no joke! It can be lethal if it goes on too long, and nerve damage can be permanent even if B12 levels are recovered. If anyone is experiencing brain fog, tingling toes or hands, confusion, fatigue or anxiety attacks, HAVE THEM CHECK YOUR B12!! The level at which they consider it “too low” in the US is significantly lower than most countries, and you could experience harmful and permanent effects even in ranges that are “borderline” where doctors won’t think it’s the issue. I know this from first hand experience. They were testing me for every neuro-degenerative illness they could think of including MS, Lou Gehrig’s disease and others while I was wasting away, on the brink of losing my job and in a wheelchair because I could barely walk anymore. On every health forum online there was someone posting about this book called “Could it be B12?” And I was peeved that they were trying to peddle their book to people who were struggling for their lives. Finally, when the doctors were out of options and I had all but accepted that I might be dying, I purchased the e-book version of it… and it saved my life. Yes, it WAS B12 😢. After THOUSANDS of dollars in tests (some quite painful) and months of fear and worry, all I needed were B12 shots. (I also used Sublingual Methyl B12 tablets to get started).
I strongly encourage anyone suffering from the symptoms above to do more research on B12!
Currently a nursing student studying for my med-surg exam and honestly these videos are so helpful, thank you!!
This 11mins video is so much easier to understand compared to my 1-hour lecture of Multiple sclerosis in class
World MS Day today, coming back here since I was diagnosed at 17 years old a couple years ago and to wish fellow diagnosed people the strength and courage we all need. We're more than this disease.
I've never been in a hospital before and have been diagnosed with ms and coronavirus. Went blind in one eye seemingly overnight. I care for my health, am active, and will get through this. Thoughts and prayers from loved ones help me so much to keep up my morale.i have a number of large brain lesions. I have not lost my motor skills, memories, personality, or inner voice, which is a blessing!
yesterday i was diagnosed with MS im 17 as well, im so so so scared 🥺
@@JiminPark-tz8so I just got my diagnosis 2 weeks ago. My symptoms increase temporarily when I exercise which is annoying. Hoping to push thru it!
@@JiminPark-tz8so hi, sorry to ask but could you tell me some symptoms? i'm suspecting that i have this disease too...
@@user-be3be5cp2h sure, for a whole week every time i relaxed my right arm and leg and then move them i immediately feel spasms that my muscles involuntarily contract so hard and it's painful then it goes away after few seconds and comes again when i move, i also feel so lazy and get so tired even tho i did nothing at all and sleep alot it's called fatigue, i also have poor concentration, anxiety and depression however someone who doesn't have ms can still have them, those are my symptoms so far, i made an MRI test it showed scars (lesions) in my brain and v.e.p test but it was good nothing wrong and finally had a csf spinal tap and it showed a high percentage that i might have ms so now i just started taking a medicine for it, also there are many and many diseases that might be mistaken for ms because they're all problems from the immune system i even until now not 100% sure i have ms i gotta wait for more time to be 100% sure..
You are helping me get through Paramedics. Can't imagine all the physicians in training that benefit from your channel!
Keep pushing out content!!
Diagnosed in 2015. So depressed. I hate it. It took away my life. It took away my ability to be the mother I was supposed to be. 😢
what are your symptoms?
Hate this disorder. Had a really bad episode a couple weeks ago. Great job on this video. I think I'll show my friends this. Tired of explaining it haha.
Spyder1246 I'm also suffer from this MonSter..honestly I just want to die. I'm too tired..don't want to suffer anymore.
Renáta Foris how are you doing? Have you found methods to help you cope?
whats it feel like
@@renataforis4065 pls don't lose hope
@luv life Personally my mother has had it for around a decade (secondary progressive.) On good days you would never be able she was sick, sadly on these days she pushes herself too hard and the stress causes a flare up. This can cause slurs and sometimes she forgets how to talk or use a limb. I know she has bladder issues and seizures. She also has horrible migraines and pins and needles, sometimes she has delusions that she can't remember. She has horrible cramps that have progressed from her feet to her legs and now she has esophagus cramps. It's one of the worst things ever, I've never seen her in so much pain. Obviously these aren't all the symptoms, loss of sight, confusion, horrible fatigue and others are a part of our lives. But still I love my mom and no matter what she thinks I have no problem helping her and I'm happy to do so. If God only gives us what we can handle my mom is a superhero and honestly, I wouldn't have it any other way.
Iam a patient of ms living in Pakistan iam 20 years old 9 months back I was diagnosed with this, iam a student of psychology iam studying hard with this disease it is difficult sometimes with this but iam trying my best, thank you so much for guiding us❤️
What helped me alot is double my vitamins. Double C, B D etc. A few years ago I couldn't walk, talk, eat, couldn't do anything for myself. Today when I start to feel sick I drink 3x more vitamin B and extra other vitamins. My last relapse was in 2016. Was very bad. When depression takes over, drink more vitamins. Visit friends. Never be alone. What also helped me is to stay busy. Never sit and do nothing. Keep your brain busy. Do extra work etc. Just stay positve. It helps alot.
Thank you
My hubby is too curious to know & trying to to explain my 12 years MS with hlp of dis video. He strongly Trust God & expects me to b okay someday.
To all my ms survivors I love you.
My heart goes out to everyone with MS. It’s really unfair and messed up. You didn’t deserve this, and I’m so sorry you are forced to walk this path.
Pray we find a cure.
I have had this disease for 11 years (Since I was a baby) and it’s not as Bad as most people but it really effects physical activity. It also effected my eyes, causing the inside of my eyes to be swollen. You get so tired very easily. Once I rode my bike around a very short block and I was tired halfway through. It is really hard for me to see without my glasses, which are super strong it could blind someone, and even my glasses now are not strong enough...
This sounds similar to cushings disease for the eye swelling which is caused by a build up of catecholamines which is also a problem in MS. Maybe try to increase the amount of magnesium in you diet with seeds and nuts. Here are some other suggestions;
Sardines are packed full of goodness which supports melatonin production ( good for myelin proteins to recover nerves) and contain vitamin D.
-Figs are good for producing oxytocin which can help relieve symptoms.
- pumpkin seeds and almonds are high in magnesium which can help regulate catecholamines ( these contribute to chronic stress leading to more pain and fatigue).
- legumes are important to actually digest the fibre from leafy greens and receive the full benefit.
-Lions mane is thought to boost NGF which might help restore nerves.
- Water hyssop has an element called Bacoside which showed some effect on demyelination in white matter in a nice model.
Hi I am from Hong Kong, 26 years old. I want to get rid of this disease completely because I just got the diagnosis. Treatments not started yet because it is early stage diagnosis, symptoms including dizziness, slow writing on the right hand especially, numbness in tongue, and unclear visions. Any suggestions from your side?
I hope from the deepest of my heart that everyone will get better 🙏
Just today my life's best friend and brother was diagnosed with it.
Stay strong Brother and Sister you are not alone ❤ 💪
@@CharlotteKate-wm2db where this this doctor?
Anywhere near Germany?
And do you have any further details about him ? Name usw...
Because honestly I don't know of you did got what kind of illness is this but till this moment there is no cure, they use only cortisol on patient to stop the symptoms from getting worst.
@@CharlotteKate-wm2db thanks that's very kind from your part...
But it's im not sending my number neither my mail to you just like that.
And if you care this much about others and it's not kindof BS just write here his Infos and share it with everyone!
I want the general public to know how this great man called Dr Orede cure me and my sister from HIV with the gotten from Dr Orede he cures other diseases too like STDS，My own was worst I have suffered from Human papilloma virus HPV）for 2years he cure me too。he have a medicine that is 100％percent assured to cure any type of disease and you don't need to spend so much money anymore。On ARV or any other。You are contact him on WhatsApp：+2349049521615 Email：drorede884@gmail.com。Com Contact him now
👇👇👇
@Dr Orede
@@se7li08 read the Wahl's Protocol
Thank you for the time and effort you've placed into making this. It was incredibly informative. May you be blessed with millions of views and subscribers.
I want the general public to know how this great man called Dr Orede cure me and my sister from HIV with the gotten from Dr Orede he cures other diseases too like STDS，My own was worst I have suffered from Human papilloma virus HPV）for 2years he cure me too。he have a medicine that is 100％percent assured to cure any type of disease and you don't need to spend so much money anymore。On ARV or any other。You are contact him on WhatsApp：+2349049521615 Email：drorede884@gmail.com。Com Contact him now
👇👇👇
@Dr Orede
Thank you! I have a neurology exam coming up and this made it so clear!!! Awesome video!
I want the general public to know how this great man called Dr Orede cure me and my sister from HIV with the gotten from Dr Orede he cures other diseases too like STDS，My own was worst I have suffered from Human papilloma virus HPV）for 2years he cure me too。he have a medicine that is 100％percent assured to cure any type of disease and you don't need to spend so much money anymore。On ARV or any other。You are contact him on WhatsApp：+2349049521615 Email：drorede884@gmail.com。Com Contact him now
👇👇👇
@Dr Orede
I just got diagnosed. Now i know I'm not crazy. So many weird symptoms. I finally have the answers.
My best friend got diagnosed with this about a month ago. I've spent hours reading/watching videos about this and every time I do it says the same thing - it happens mostly to people that are 20-40 years old and people who don't live near the equator. She's 14 and lives in the middle east so she gets plenty of sun. None of her relatives have it so I don't think it's anything genetic but she IS a female and females usually get it more than men. I never wanted to become a doctor but now I do because I'm determined to try and find a cure for this. Thank you for this video it really helped me understand multiple sclerosis a lot more.
Sorry to hear about your friend. Thanks for the feedback.
i was diagnosed with MS this year and i went to the hospital 3 weeks before my 14th birthday it attacked my whole left side and i couldn't walk, raise my left arm my eye sight was even off i spent weeks in the hospital i had 6 MRI's done 2 cat scans before they diagnosed me it was torture then i had to get a lumber puncture (spinal tap) and it hurt like hell they then put me on steroids and i got out 3 days before my birthday i then had to get glasses and physical therapy i wasn't in school for a whole month my relatives never had it either i dont know how i got it
Heya, you should consider a career also in science. Often they would be able to spend more time doing the research that leads to a treatment/understanding the disease, compared to doctors. Science needs motivated people like yourself! Good luck! :)
+Tercella King may Almighty ease out yout problems and mine aso
Good Luck being a Doctor
Just been diagnosed with PPMS, this video explains a lot in terms that are easy to understand. My Neurologist is awesome and very supportive, however this allows a person to go over it at their own pace.👍
We're glad that our video is able to help this way, Lisa. 🙏🏼
im going to cure my multiple sclerosis
It seems we are going through the same journey. Don't ever lose hope
Good luck to you! ❤️ I feel your pain, well I only have RR but it's horrible sometimes
Good luck with that!
@@laykantheealien5722 you only have RR for now
You can do it
I have multiple sclerosis, but it has been basically dormant for the last 10+/- years. I have problems with 'brain fog', but I'm still working.
Dear MSers, i have MS and it's a moderate case but it's characterized by SEVERE anxiety , i also have heavy fatigue, brain fog, body weakness and all of that. I take tecfidera but the anxiety and the fatigue and balance was getting worse. I decided to finally take the popular diabetes drug metformin and the results are fantastic, everything is better, balance, movement, leg strength and most importantly anxiety, im still suffering but things are getting a lot better. It's up and down as always but now the overall path is up. Bless your hearts everyone
The little faces and music made my learning experience much better
Love your videos- as a visual learner this helps me retain and better understand various disease processes. The subtle humor is amazing. This osmosis video, in particular, is one of my favs!
I'm a medical student & this video helped me alot for my class test tomorrow
Thank you 😊
We're so glad it helped!
Thankyu god for showing me the osmosis...it was a suggestion. You guys have no idea how it is helping me in clearing the concept. The no 1 channel in you tube....♥️♥️
My mom had MS. For the past 3-4 years my arms have been going numb. I can only sleep on my back at night. Even my tongue has gone numb trying to sleep on my stomach. I wake up and all day my joints in my hands and feet hurt so much and are very stiff and swollen when I wake up in the mornings. My memory is garbage and my digestion is terrible. I hope I can get my doctor to take me serious and find out.
My wife was tested recently and we're waiting on results, however, the Neurologist stated she has seen this enough to know it's MS. I am very worried for her (recently went blind in one eye, and losing her balance), we're basically waiting on what type of MS she has. This explains her constant being sick, and many other issues that have taken place over the last two years.
Hi is she okay now? This is also happening to my mother now
@@boychub1830 - Not really. She has MS attacks every few months, tons of lesions in her brain and down her spine. She is now in a power assist wheel chair as needed and often times she is sleeping. She has PPMS.
The brain lesions have caused her personality to change a lot and can become very mean. She does not realize what she is doing most of the time.
The problem with MS is that it's different for everyone. So, I wouldn't read into what I had stated too far. I met a lady a couple months back that has been living with the same MS as my wife for the last 30 years. She stated that sleeping a lot is a part of MS, especially PPMS, and has tons of lesions on her brain as well. She was more mobile than my wife though.
@@27Zangle thanks for the reply man. Is her eyesight cameback on the one eye?
@@boychub1830 - I believe that it did come back after some time or at least partially come back. I have not talked to her much about it for a couple of years.
Sardines are packed full of goodness which supports melatonin production ( good for myelin proteins to recover nerves) and contain vitamin D.
-Figs are good for producing oxytocin which can help relieve symptoms.
- pumpkin seeds and almonds are high in magnesium which can help regulate catecholamines ( these contribute to chronic stress leading to more pain and fatigue).
- legumes are important to actually digest the fibre from leafy greens and receive the full benefit.
-Lions mane is thought to boost NGF which might help restore nerves.
- Water hyssop has an element called Bacoside which showed some effect on demyelination in white matter in a nice model.
Great info... thank you. The more we learn about this, the better our chances of fighting it and finding the cause/cure.
I believe most degenerative diseases can be traced to the HPA axis, there’s a lot pointing to this area/ function. Here’s some stuff to help in diet;
Sardines are packed full of goodness which supports melatonin production ( good for myelin proteins to recover nerves) and contain vitamin D.
-Figs are good for producing oxytocin which can help relieve symptoms.
- pumpkin seeds and almonds are high in magnesium which can help regulate catecholamines ( these contribute to chronic stress leading to more pain and fatigue).
- legumes are important to actually digest the fibre from leafy greens and receive the full benefit.
-Lions mane is thought to boost NGF which might help restore nerves.
- Water hyssop has an element called Bacoside which showed some effect on demyelination in white matter in a nice model.
i had a double vision problem and took me 2 months to to be diagnosed with the disease im 22 years old just guraduated from univ
Wish me luck
Really good study tool for my nursing school！thanks！
Rui Min ua-cam.com/video/IeZDWZ2kfF4/v-deo.html
I want the general public to know how this great man called Dr Orede cure me and my sister from HIV with the gotten from Dr Orede he cures other diseases too like STDS，My own was worst I have suffered from Human papilloma virus HPV）for 2years he cure me too。he have a medicine that is 100％percent assured to cure any type of disease and you don't need to spend so much money anymore。On ARV or any other。You are contact him on WhatsApp：+2349049521615 Email：drorede884@gmail.com。Com Contact him now
👇👇👇
@Dr Orede
I want the general public to know how this great man called Dr Orede cure me and my sister from HIV with the gotten from Dr Orede he cures other diseases too like STDS，My own was worst I have suffered from Human papilloma virus HPV）for 2years he cure me too。he have a medicine that is 100％percent assured to cure any type of disease and you don't need to spend so much money anymore。On ARV or any other。You are contact him on WhatsApp：+2349049521615 Email：drorede884@gmail.com。Com Contact him now
👇👇👇
@Dr Orede
I was diagnosed last year (2019) in the middle of the night on my 17th bday I had a seizure. I woke up in the hospital so confused. I was in the hospital for 9 days and I even had to have my birthday party in the hospital. I have gotten used to it by now but I dont want to live with this for the rest of my life. I hope a cure is found.
I also got my diagnosis at my party when I was 17, that's more than two years ago for me.. but if I can tell you something it's to enjoy life in the ways ur able to and never push yourself ever, everyone has bad days, things will hopefully be a bit brighter soon
Thankyou! It's helping me a lot in my nursing school.
I want the general public to know how this great man called Dr Orede cure me and my sister from HIV with the gotten from Dr Orede he cures other diseases too like STDS，My own was worst I have suffered from Human papilloma virus HPV）for 2years he cure me too。he have a medicine that is 100％percent assured to cure any type of disease and you don't need to spend so much money anymore。On ARV or any other。You are contact him on WhatsApp：+2349049521615 Email：drorede884@gmail.com。Com Contact him now
👇👇👇
@Dr Orede
This is the BEST explainer video I have ever seen on MS. You people are amazing and I'm extremely grateful you did this video.
Thanks for making my study session a little bit less painfull
Multiple sclerosis is an autoimmune disease in which the body's immune system attacks its own tissues.
Best solution:
EDUCATE the immune system to BALANCE and support immune system response.
My mum has this and I want to understand more on why she takes so many prescribed pills and why she has bad headaches and won't talk sometimes. Thank you for helping me!
I also think I might have it as my mother has it, my grandma has it and my great grandma has it so I think it's generic.
Thank you, you shared a lot of very helpful information for those of us trying to understand MS. I had a few small symptoms that were mild, but two years ago I had Lyme Meningitis, which was a nightmare in itself, which seems to have caused the MS to speed up. After one week in the hospital and three more weeks of antibiotics I still tested positive for Lyme. Thankfully I have a couple of wonderful doctors.
Thanks for the video. My sister was just diagnosed with MS and I needed to know more about it.
My friend just told me he has it, absolutely devastated for him
@@swingwizard so how you feel now?
@@swingwizard now i am writing you Arthur. Please explai me if you have had MS and if you have cured, how you feel now? I need to know for my mother. From where to find silicium if I understand you correctly. Did it help you?
In my master's level neurobiology studies, I've chosen Multiple Sclerosis as my term paper topic. Could you please suggest a book that can help me understand the pathophysiology of this disease? Thank you for your assistance!
Thank you so much for this video! im in need of simple explaination cause im running out of time!!
Thank you so much for this information. My dear friend who is 76 yrs. Old is suffering from ms. Understanding ms a bit is the best tool I can use to help her. 🙏🏻❤️
We're hoping that this helped! 🙏🏼
I know this has been on UA-cam for awhile, but I've been diagnosed (Merry Christmas, right?) and am trying to learn everything I can. Thanks for being so informative!
I want the general public to know how this great man called Dr Orede cure me and my sister from HIV with the gotten from Dr Orede he cures other diseases too like STDS，My own was worst I have suffered from Human papilloma virus HPV）for 2years he cure me too。he have a medicine that is 100％percent assured to cure any type of disease and you don't need to spend so much money anymore。On ARV or any other。You are contact him on WhatsApp：+2349049521615 Email：drorede884@gmail.com。Com Contact him now
👇👇👇
@Dr Orede
Read the Wahl's Protocol
My mother became a paraplegic then quadriplegic and eventually dead from this terrible and cruel disease. I pray this among other conditions become a thing of the past.
I might have MS (I have symptoms and am getting tests done) and I’m terrified✨
this is my go to video to help explain a quick and short explanation of MS
I want the general public to know how this great man called Dr Orede cure me and my sister from HIV with the gotten from Dr Orede he cures other diseases too like STDS，My own was worst I have suffered from Human papilloma virus HPV）for 2years he cure me too。he have a medicine that is 100％percent assured to cure any type of disease and you don't need to spend so much money anymore。On ARV or any other。You are contact him on WhatsApp：+2349049521615 Email：drorede884@gmail.com。Com Contact him now
👇👇👇
@Dr Orede
I'm surprised fatigue wasn't mentioned as a prominent symptom
is the cure not available yet? i'm still waiting for it. I stopped taking corticosteroid and my doctor just gave me pain reliever
There is no cure yet
This is the best channel in youtube
This has taught me more about my own disease than what I've learned from the past 3 years of treatment thank you
We're glad that our video was able to help! 🙏🏼
You're a genius, thank you so much for all your videos.
Qqq
I want the general public to know how this great man called Dr Orede cure me and my sister from HIV with the gotten from Dr Orede he cures other diseases too like STDS，My own was worst I have suffered from Human papilloma virus HPV）for 2years he cure me too。he have a medicine that is 100％percent assured to cure any type of disease and you don't need to spend so much money anymore。On ARV or any other。You are contact him on WhatsApp：+2349049521615 Email：drorede884@gmail.com。Com Contact him now
👇👇👇
@Dr Orede
Thank you osmosis... I truly wish you guys success!
Thank you, Miran! 💕
You men are amazing, Best medical youtube channel1
Thanks so much! It would be awesome if you could review us on our Facebook page. facebook.com/OsmoseIt/
Diagnosed in 1 patient right now, came for reviewing. Not much detail but Thanks a lot for upload👍🏻👍🏻
Dr Okolo herbal medicine formula will get cure completely from MS
A very direct clear video...excellent
You're welcome - It would be awesome if you and your friends could review us on our Facebook page. facebook.com/pg/OsmoseIt
I have PRMS officially diagnosed in 2019 this came up on my feed to watch very informative I'm definitely getting worse I can feel the difference over the years which is scary
These videos have helped me so much during nursing school!!!! Thank you :)
I want the general public to know how this great man called Dr Orede cure me and my sister from HIV with the gotten from Dr Orede he cures other diseases too like STDS，My own was worst I have suffered from Human papilloma virus HPV）for 2years he cure me too。he have a medicine that is 100％percent assured to cure any type of disease and you don't need to spend so much money anymore。On ARV or any other。You are contact him on WhatsApp：+2349049521615 Email：drorede884@gmail.com。Com Contact him now
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@Dr Orede
One of the best videos i have seen so far, if you want more info.
Thanks for the feedback! 😊
you guys are the best thanks for all your knowledge, from Mexico
I want the general public to know how this great man called Dr Orede cure me and my sister from HIV with the gotten from Dr Orede he cures other diseases too like STDS，My own was worst I have suffered from Human papilloma virus HPV）for 2years he cure me too。he have a medicine that is 100％percent assured to cure any type of disease and you don't need to spend so much money anymore。On ARV or any other。You are contact him on WhatsApp：+2349049521615 Email：drorede884@gmail.com。Com Contact him now
👇👇👇
@Dr Orede
I want the general public to know how this great man called Dr Orede cure me and my sister from HIV with the gotten from Dr Orede he cures other diseases too like STDS，My own was worst I have suffered from Human papilloma virus HPV）for 2years he cure me too。he have a medicine that is 100％percent assured to cure any type of disease and you don't need to spend so much money anymore。On ARV or any other。You are contact him on WhatsApp：+2349049521615 Email：drorede884@gmail.com。Com Contact him now
👇👇👇
@Dr Orede
Smoking is common in patients with Multiple sclerosis. It has general negative health effects, but in addition has been shown to have direct links to MS disease activity. Smoking is thought to be a risk factor for developing multiple sclerosis (MS). The habit is also strongly associated with having a worse disease course and with decreased effectiveness of MS treatment. Even children exposed to secondhand smoke are more likely to develop MS later in life than their peers
Hello I'm a patient of Ms at the age of 18.
Please bless me god will outcome from it too soon....😊😊🙏
I'm sorry for your suffering. I am in constant pain every day and often feel I can't take it anymore.
I'm at a stage where I don't study medicine topics until I watch a video on that topic from ur channel !! Ur explanation helps me understand what's written in the book ! Thanku from a medico :)
very well made introduction for MS, well done :)
This video explained this way better then my doctor did. And now I just sit in fear with my body tingling, double vision and (very intense) pain
Great video, as usual. MS can't be simplified more than that! Thanks a lot. :)
My close friend recently got diagnosed and she has been using cortisols for some time now. I came here to learn more, thank you so much this was a very informative video and it was easy to understand.
Read the Wahl's Protocol
Thank you for the video, it helped me understand this sickness. I was diagnosed with MS-RR a year ago and I've been trying to find alternative methods to control it, from changing my diet to meditation. I didn't want to follow any treatments since all of them carry damage to other organs and if in the end, like you explained it, doesn't really have a cure, I will only be further damaging my body than curing it by taking any of those treatments. I do think genetics play a part on the development of this deseace but also stress and not following a good and healthy way of life. My mother has lupus and my great grandmother got paralyzed from the waste down at the age of 25 and unfortunatelly 5 years after that, she died and no one knew why, so my neurologist told me that possibly she might have had MS only the most agrassive type.
Now, living with MS is not so difficult when the disfunctions are cognitive and not motor/physical, like mine... but, I know there will come a time when I will have to face the uglier side of this sickness and I can only hope by then, modern medicine has found a way to stop its progression. Cheers!
hi may i ask how is it going right now i mean it got better or worse
i have lots of these symptoms like panic attack ,fear,anxiety ,depressions,terrified,high pitch sound in loud environment,confusion,feeling like i am in a dream when walking on street,spinning wheel flash or tv dots which affect vision,trembling of hand and legs,difficulty to breath ,difficulty to concentrate,mind disorder,cold or warm ice piercing my left shoulder bone and in extreme case the muscle around it start to feel like bubble of air poping,and i also once got the symptom of drops of water falling inside my head which was very disturbing situation...