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I know MS it started as a. Kid but went away but came back. Can’t take. The. Heat. Or. Cold .💙🕊️💖🌈🦋😇✝️🛐

How old were you

Thank you for sharing this information

I have all this and my Dr says I am not quite sure. I’m like you have to be kidding me. Help me while I still am able to go. The bug crawling is weird. I constantly hit my legs. I see falling stars when I close my eyes at night.

TREATMENT WITH BENFOTAMINE. A FAT SOLUBLE FORM OF B1 THAT WILL PENETRATE THE MYELIN AS WELL AS LIONS MANE MUSHROOM

I’m really interested in this device

You're very knowledgeable and great at explaining everything. I was diagnosed with M.S 6 years ago. You must be an M.S Doctor. I'm glad i found your channel. 🙂💖

Wow!! I love it. Its frustrating when people dont understand.

Wow curious which do you pay for out of pocket?

Are you on infusions? Thanks. Ocraves?

Could having a harder time gripping things be a subtle symptom?

From one Vickie to another ❤ Thank you 🙏🏼

Hi thanks for the great video, We should avoid Gluten bt the bread you were eating doesn't it contain Gluten? or you can eat Glute?

You are amazing at doing research, phenomenal at speaking and EXCELLENT at citing your sources! Thank you for providing such great content!

My lesions are actually closing. My last MRI, was good. I started taking a mushroom supplement. Lions main, mushroom pills. Try them

I was Dx June 15th 2023. My Dx came FAST and HARD. in January 2023 I went blind in my right eye… and it was Whirlwind of specialist and appointments. I knew I had MS by March but didn’t get the official Dx until June when u heard it from the MS clinic.

Thank you for the wealth of information that you explain so clearly.

I've learned all I know about MS watching RUclips, because my doctor is terrible. She will not tell me anything or refer me to other specialist for my "secondary MS" symptoms, like incontinence. Thanks for the video.

You are a good speaker and have chosen an important topic to address. My neurologist said (I got diagnosed january of this year) that my life expectancy will not be shorter, so that’s really positive. Are you in the Living Well Hub with OMS? I recently joined and feel like it’s such a positive community! I will follow the Pathway program soon and am very curious about it. Thank you for making these videos, you feel like a friend to me! 🌷

This is a difficult topic. Wasn’t sure I was going to watch it, because I don’t like to think about it, but I’m glad I did. Thank you for this video. 🧡

Happy Mothers Day & thank you for sharing this video on a tough subject. While I have no reason to be suicidal thanks to the unconditional & loving support from family and friends, I am however not thrilled with the idea of living longer. I say this thanks this MonSter in us. Half of my fatigue stems from the fight i give to remain positive & active in my own life. I do eat very well thanks to being a professional chef & researching what foods are good and not good, thankfully I enjoy enough of the healthy foods & I'm strong enough to limit what we shouldn't really have to maintain a healthier life. I do drink water mostly every day & have learned the importance of drinking the recommended Early in the day & less as I get closer to bed time. What I & I'm sure most everyone may prefer, Quality over quantity, if they can reduce or even Better, Eliminate symptoms Before extending average life span then to me That would be far better.

Not good news to me!I’m suffering with progressive MS and have no quality of life. So I wish I could die now at 60 yrs of age. Having to keep existing on my own with all my horrible symptoms is inhumane & beyond cruel! It’s torture!

I'm 39 living with RRMS my neurologist is very optimistic about my MRI scans and neuro exams and I'm hoping to live with a normal life expectency. Plus I also have to manage living with bipolar disorder so with having two chronic conditions. We'll see how long I live.

Thank you for being the friend I like to listen to. You make having MS easier to live with and function, especially being on my own. I don’t have to explain why I feel the way I do to anyone, you get it. Thank you!

I look forward to your weekly videos they are so informative. Keep up the awesome work.

I kinda thank God I won't live as long. Waking up daily in this jail is hell. I like sleeping because I dream I'm walking again. Sorry to be so pessimistic but it's the truth. My son is my caregiver i have guilt everyday because he can't do the things he wants to do.

Thank you for addressing this tough subject. The day i was first told I probably have MS was a terrible day. I was so terrified of what was to come. I thought it was a terminal disease. My Mum said "you can live a long life with MS". This was in 1998, a long time ago! She was obviously right, as Mums often are! There were no drugs for MS back then. As you say, exercise, staying hydrated, eating well, and so on are all things we can do to help ourselves stay healthier. I only wish that back in the day that I could have seen this video. My anxiety would have reduced straight away! You have such a wonderful channel, which is so informative. Keep up the good work! x 👏

Thank you for all your dedication and research. This gives me hope!

Thanks so much for this video. 😂This gives me hope that I'll live 30+ more years.

Hi, Thank you for your video. Best wishes and Happy Mother's day. ❤

*Suicide Hotlines:* United States 988 Australia 131114 Canada 1 (833) 456 4566 United Kingdom 0800 689 5652 Other Countries: blog.opencounseling.com/suicide-hotlines/

Drinking alcohol minimal with Tony Montana as a guess are the only off label medications that work for me. Have tried everything.

I'm wondering if estrogen injections would help with MS

This is my goal, my MS keeps me home bound right now. Not forever.

Is Sedrate and or CRP elevated with MS? My husbands sed is 116 and crp is 11.1 .. just started autoimmune disorders

I was diagnosed with MS yesterday , I’m 67. I was 29yrs old, when I had nerve conduction tests & a lumber puncture. The neurologist said probable MS come back when you get new symptoms or symptoms worsen. I tried to do that , but there was always a 3mth wait for the appointment so by the time it came around I was back to normal so I canceled One time I was at a urologist, my leg went to sleep and when he called for me I fell. The urologist said I should be seeing a neurologist not him when he found out about the other symptoms & that I I’d had similar symptoms a few months earlier. He immediately rang the neurologist & 15 min later I’m seeing the neurologist. He said the urologist told him I had the same symptoms in January, why didn’t you see me then? I explained , I rang for an appointment in January but appt was in March, just before that the symptoms went away so I cancelled. At the same time I was reading about "yuppy flu", chronic fatigue syndrome. My symptoms seem to fit this condition so I went to see a specialist in CFS. She diagnosed me with CFS/ME. For 15 yrs I knew I had CFS/ME, but I also had a lot of MS symptoms that didn’t fit CFS/ME (I was a registered nurse). At that time I saw a physician who had a special interest in ME/CFS. He told me to return to a neurologist as soon as possible as possible because he believed I had both MS & ME/CFS, that one could be secondary to the other.. I went back to the neurologist who had I’d seen 15 yrs earlier & he did another set of nerve studies & sent me for an MRI. He said it was inconclusive. Over the years since then I’ve had many flare ups, at first the symptoms would go away each time, but then I stopped going back to normal after every flare up. My legs have got weaker, I have lots of permanent numb parts of my body & the fatigue has taken a toll on my quality of life. I had to stop working, then going out and now my world has shrunk to my home. Last week I had 2 falls, then I thought I had an UTI, then left sided weakness, tremors & parasthesia. My left foot, left arm (from scapula to hand) & thighs are numb. I can’t put my pants, socks or shoes on. I’m having a lot of trouble walking, my gait is off, I feel off balance like I’m going to stumble & fall plus I have to concentrate on how I place my feet as I keep tripping over my toes. This has happened multiple times over the years. Apart from an 18mth period around 2004, I had these sort of symptoms twice a year they last about 6weeks. I went to see my doctor a few days ago wearing a dress & thongs (flip flops), she remarked on my clothing seeing we are going into winter here. I told her about not being able to lift my legs or control my legs enough to wear pants or shoes & socks. That lead to me telling her about all my other symptoms at the moment. Next thing I’m having a brain & spine MRI. First time I’ve ever had tests while I’m in a flare. It’s 50 yrs exactly since my first symptoms & 38yrs since a neurologist said I had possible MS. I would have been diagnosed far earlier if I hadn’t stopped seeing the neurologist or if I had actually told a doctor about ALL my symptoms. I didn’t want to sound like a hypochondriac so only mentioned the symptom that was bothering me most at the time. I only ever told a doctor all the symptoms I was experiencing at the time I saw them 3 times. Funny how all 3 of them thought I had MS. I was my own worst enemy, I now wonder if I would have had a better quality of life if I’d been diagnosed and treated earlier.

Thank you for your video. You are a beautiful person. I have been very sick Thank you

It’s the sugars that attack the brain and nervous system.

How do you find a physiatrist who has interests outside of sports medicine?

Thank you for this video! I feel like each of us can feel when certain foods are not right for us. For example, I feel my symptoms worsen when I eat gluten or use sunflower oil specifically. Carbonated drinks also make me bloated and give me inflammation almost immediately

Thank yoooouuuuu !!! ❤ I had a hard time trusting “plant based” meats … so I just switch to fruits veggies and water! It’s working out so far.

as always agree ❣️ 💯 🙏🙌

Yes, yes, and yes, Ms. Vicky ❤ I love it and agree with everything that was said here, and I also feel like my mental health has very much benefited from the improvements I've made to My diet! I see you making these great content out here 🙋‍♀️

Wow OK I Please need some sort of answer to this, I believe this can fully work for the body functions, but what about eyes?? I have been told my Optic Nerves have been so attacked the myelin is depleted and I have atrophied Optic Nerves!. No one has answers for my, my vision is poor and fully legally blind in my right little better in my left, I am so scares, can my eyes be helped?? Thank you

I really love your outlook, I was diagnosed in 2022 finally after years of not knowing what the hell was going on with me. Ive probably had MS for about 10 years! I'm 32 with 2 little ones and no father involved so it is a big challenge having this disease, but I need to remember I'm not dying from it, I'm here, it has however taken much of my sight😢

Thanks. About 20 years ago i had an OPEN MRI in Germany for low back (L5-L3). Brought the film back to UCSF (san francisco) and my doctor said they were very good images. The MRI was truly open, and my claustrophobie did not act up. The machine looked like the hitachi oasis tesla 1.2.

Thanks. You are not alone, nor are you there to sell the machine or pooh pooh "patient comfort".

We should be able to get B12 from bread. Bread? Yes, Bread. Slow rise bread made from nutrient-rich ancient whole grain, using natural multi-strain sourdough fermenting agent. But few of us are able to get or make highly nutritious bread now, sadly. Most of our bread is made using highly hybridised grain, loaded with chemicals & stripped of its nutritional powerhouses, the germ & bran. What is left is then made into ‘bread’ using additive ‘improvers’ & made the fast-track Chorleywood way - churned out within one to two hours which does not allow for the much longer ferment needed to generate all the extra nutrients, including B12. It also only uses one strain yeast ‘Saccharomyces Cervisiae’ which generates carbon dioxide for rising, but not all the lovely B Vitamins.

👋 Thank you! Did you take a communications course? You have amazing communication skills and you’re very knowledgeable in MS. It is really helpful to me because lately, I’ve been on bed rest. I’ve just about watched half of your videos. Thanks for helping us!

Thank you 👋 😊