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You have a beautiful spirit. I pray you have a wonderful week!!

Have you tested your vitamin d level? Many people report huge improvents in ms fatigue and other symptoms after correcting deficiencies both in vitamin d, magnesium, b-complex vitamins and zinc. Dr Aaron boster has some amazing where explains the importance of combining disease modifing therrapy with vitamin d, lifestyle and diet for ms progression. Wish you all the luck and strenght!

Love your videos - pls keep updating us with other life matters. Congrats

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Dear Lii I have watched some of your posts for the past year and want to tell you, you are a strong and positive woman and thats the only way you can cope with a life changer like this. I got my MS Diagnosis a year ago and Im already 52 years old. Things started to make sense after diagnosis and now I know why Im just not myself anymore. Fortunately my kids are in their teens by now so I get more rest and quiet now. Having small children with MS your stage is really challenging. I was diagnosed with RRMS but a year after, no new lessons on MRI but my walking and especially fatigue and cognitive situation is getting worse so my diagnosis was now changed to SPMS. I’m also trying to handle challenging myself with cognitive training and handling the fatigue. I crochet and love it very much. The touch of the soft wool the (silent) sound of the needle and the process of creating something beautiful either for myself or family and friends makes me happy and relaxes me. I also am a spiritual person always have been and now Gods word has become even more meaningful and soothing to me than before. Dear Lii, stay as positive as you are, you are a wonderful person! Love from your MS-sister Jules

Lovely to hear You speak many languages to the children, do they speak swedish? _ Greetings from Finland ( Uleåborg ), snowing' slowly ' here right now and it's beautiful to watch 🩵 -- Yes, it's very important to find things that bring us joy, hope and happines, like caring of plants and whatever one enjoy doing. Finding balance with lower capability is hard and frustrating at times- i know 😒😊 Take care 💫💚

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Congrats on getting married this year!

all the best to you

So good to see you out and about! Love your videos. I don’t have MS but have other chronic illnesses that are hard to deal with. You are an inspiration and help me so much! God bless you ! Hang in there!❤

I don’t want to start a new subject for you, as your hands are full. However, people as yourself always have a right to know so that you can’t be taken advantage of. You should check up on this, investigate it, get checked. This doctor on RUclips is from the UK and he had this to report about MS and the covid vaccine hype. ruclips.net/video/I9S2jooTxkQ/видео.htmlsi=xdGHnTualhDBEATV

Happy Birthday Hector. From Jodie and family in Melbourne Australia 🥳🐨

Happy birthday Hector 💙💙

Is it still considered rrms what you have or has it transitioned?

I have has PPMS for 6 years. I'll be praying for you.

Hi!! Have a good day!

Beautiful family! He looks so happy! Good job Mom. (on the tomatoes too!)

Beautiful family 🎉🙋‍♀️🇬🇧

🎂❤️🙏🏾

Happy Birthday to your Hector. I pray you have a great week!

What you could do is buy the toys for his birthday during Christmas shopping and save till birthday if it’s hard to find anything after Christmas

Lii, you are an amazing person. When I watch your vlogs I feel inspired by your strength and Grace. I do not live with a chronic illness, and yet you are more able to deal with life with more grace and strength than I ever could. If only our best wishes could cure this cruel disease. Keep doing what you are doing to make the most of the life you have and enjoy your beautiful family

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Hi lovely ,i cant thankyou enough for your videos. So much detail in symptoms. Its past midnight in the uk here and iv been watching a few of your videos this evening. I feel like i have MS im 35 and these sgmptoms have been getting worse last two years. Tonight my right leg feels heavy tingly and like i have been sat on my legs for ages. Have brain fog fuzzy lips,feel like one side of my mouth is not having a full smile. Before christmas i had like an electrical pulse/shock of the left side of my face and it felt numb right upto the side of nose on the left side. The tiredness is emmense. I wish my doctor would listen. My children went back to school this week and iv had to get taxi as i dont feel like i can make that walk there and back. My headaches are so bad and getting me down. Do i go to another doctor and seek advice again? Feel so fed up. I have subscribed to you as your so relevant to me right now. ❤

I was wondering if there is anything a service dog might be useful or helpful for you?? Just a thought? Getting things or maybe detecting changes in your body and alerting ?

If this video served you please share it so it can help more people who are dealing with chronic illness. ♡

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That numb feeling, started at your toes, is called stocking parathesis, and can be caused by MS. I've had it twice, mine went from toes to just under my belly button...very scary, and mine took a few weeks to go away. I have MS too.

Today, is December 31, 2024, 5:28PM. My continued research as promised, Pam. Here you go. Seems to be working, sans the damage done to the Balance system with most MS patients, thus the problems, Mark :) " -------- Although I do not know the specifics of the stem cell procedure, when I ask the question about the existing health of one's red blood cells when donating blood, I often see and read about the way red blood cells are treated in order to preclude and prevent infections, which can be easily transferred from one person to another. For this reason, it does make sense, that if Biologics or Viral Agents were and are [somehow responsible] for the onset of Infection, then it does make sense to see how and why a stem cell therapy / procedure, just might accomplish the reset the body needs for as long as it can last, so as to have a person appear to be making a recovery. But: Most folks just cannot afford the high cost of that type of treatment. Don't ask Me how I know. So instead, I researched the problem from the other side the equation, that if the Virals and Biologics could be mitigated to eradicated, that one could improve substantially from the effects of MS. See Below my research and efforts from diagnosis in 2016 to what I am doing in 2024: FYI/FYR: Status Update: December 27, 2024: Findings: Experiencing [Substantial Improvement] as of December 15, 2024. Effort to Outcomes: 'This week, 'So much regained function in lower extremities, I feel as my Feet are Literally [Glued To the Floor, as Full Contact Clearly has Been Regained, Pam]. Further: Experiencing signs of [Substantial Balance Improvement, as Steadiness reaction to balance changes can can be coped with in real-time. ' Yes, I the combination of what appears to be regrowth and cessation of biologics, which appear to cause decompensation are leading me to believe, that this method and approach is [Substantial]. Here you go. Status Update: It's December 26, 2024 months post my own guinea pig study, for I do not have the time to sit and wait for yet another group of individuals who will do whatever, only to have more and more people suffer in silence, as they decompensate from the effects of MS. Nay.., I felt it necessary to do some research on my own, and test my outcomes in real time, saving perhaps years of guessing games, for at the end of the day, the only thing that will likely happen, is that people like Terri Garr will be diagnosed and pass from the disease without an effective treatment or possibly a cure. 'I developed my own augmented tincture solution, and I am finding it be [quite beneficial]. Opinion: Knowledge should not be held back and folks forced to pay substantial monies, just to regain function. No.., so sorry, but I took action after seven years of my own research. It does appear my Tincture is helpful. This is what I am doing in 2024, and when I just stood up, my footing was So Solid, [.. I feel as if I am glued to the floor -""the signal via the increasingly obvious restoration of the Meyelin in my lower extremities, et. al.., - "is so robust once again"]. ------------------------------------ Here you go, Dear Pam. I am feeling fine once again. Having a 160 IQ does make the impossible just time consuming. Here you are. Went again to Walmart last night. Spoke to the clerk. She began asking me is the Tincture resolves MS Symptoms permanently. Said to Her: ... 'I don't know but there's no real reason it wouldn't continue working; -..it's a daily therapy as far as I'm concerned..' ...Later, I think, 'when I went back, she seemed a bit upset, as she uses a cane herself, and appears impaired, while I now, am now beginning to walk around again the way I did before the 2016 MS diagnosis. Go with God: As promised, and Merry Christmas, Mark ❤ @melissacreighton7653 Honestly, I realize I am at a point, where, from Guinea Pig experience, what is actually working and effective, but if and where I provide the precise formula, experience tells Me my augmented Tincture will be Buried into Silence. But, I'll try anyway: Augmented Tincture I am.using 3 times per day and now can see, walk, and manage the balance issue, hoping for a complete recovery: Tincture Formula: 2 Oz. Black Walnut 1 Oz. Wormwood 1 Oz. Clove Oil 1.5 Oz. Liquid Stevia 1 Oz. Berberine (24) 10 mg. Zrtec, liquid 1.8 Oz. Chinona Bark, finely ground, Fill grinds, just over grounds with regular Southern Comfort, Cover grounds and sit in refrigerator for 72 hours. Then: Remove from frig, filter til only 1.3-1.5 oz. from the rendered chinona grounds remains. Then: Pour extracted Chinona Bark liquid into 4-6 ounce glass, add black Walnut, Wormwood, Liquid Cloves, Liquid Stevia, Liquid Berberine, liquid from 24 Zyrtec liquid pills, then Stir and Fill (3) 2 Ounce Bottles. Then: ( Eyedroppers worth 3 Times per day for 26 Weeks.). And there you are.

FYI/FYR: Status Update: December 27, 2024: Findings: Experiencing [Substantial Improvement] as of December 15, 2024. Effort to Outcomes: 'This week, 'So much regained function in lower extremities, I feel as my Feet are Literally [Glued To the Floor, as Full Contact Clearly has Been Regained, Pam]. Further: Experiencing signs of [Substantial Balance Improvement, as Steadiness reaction to balance changes can can be coped with in real-time. ' Yes, I the combination of what appears to be regrowth and cessation of biologics, which appear to cause decompensation are leading me to believe, that this method and approach is [Substantial]. Here you go. Status Update: It's December 26, 2024 months post my own guinea pig study, for I do not have the time to sit and wait for yet another group of individuals who will do whatever, only to have more and more people suffer in silence, as they decompensate from the effects of MS. Nay.., I felt it necessary to do some research on my own, and test my outcomes in real time, saving perhaps years of guessing games, for at the end of the day, the only thing that will likely happen, is that people like Terri Garr will be diagnosed and pass from the disease without an effective treatment or possibly a cure. 'I developed my own augmented tincture solution, and I am finding it be [quite beneficial]. Opinion: Knowledge should not be held back and folks forced to pay substantial monies, just to regain function. No.., so sorry, but I took action after seven years of my own research. It does appear my Tincture is helpful. This is what I am doing in 2024, and when I just stood up, my footing was So Solid, [.. I feel as if I am glued to the floor -""the signal via the increasingly obvious restoration of the Meyelin in my lower extremities, et. al.., - "is so robust once again"].

GE, Friends. I decided to work to solve a critical problem that unfortunately ended my older Friend and Mentor's Life in 2017. Worse: I too was diagnosed in Early Spring, 2016. Thing Is: Nobody gave Me [any medicine], as I was completing the self-imposed study on Poverty, so I understand what many people have gone thru. So: I was well motivated to solve the problem, and I think I figured out the cause, and how to treat it. Below are my notes and what I am working on to help Everybody. ' Happily, Because I have developed an Augmented Tincture Solution, Combined with a simple medication anybody can buy, turns out' The Damm Stuff Actually Works. -Fact. 'The Closest Thing to a Miracle Cure as I have seen in Decades.' *As of "this weekend, I'm beginning to feel and function almost normally once again." *I will keep you posted on my research efforts to outcomes. My Best, MDM, JD Candidate \\//

Im just waiting for results on my mri scan how long did u wait for mri results on brain ? Do u get a burning sensation? My hands and feet buzz and throb

Today, is December 31, 2024, 5:28PM. My continued research as promised, Pam. Here you go. Seems to be working, sans the damage done to the Balance system with most MS patients, thus the problems, Mark :) " -------- Although I do not know the specifics of the stem cell procedure, when I ask the question about the existing health of one's red blood cells when donating blood, I often see and read about the way red blood cells are treated in order to preclude and prevent infections, which can be easily transferred from one person to another. For this reason, it does make sense, that if Biologics or Viral Agents were and are [somehow responsible] for the onset of Infection, then it does make sense to see how and why a stem cell therapy / procedure, just might accomplish the reset the body needs for as long as it can last, so as to have a person appear to be making a recovery. But: Most folks just cannot afford the high cost of that type of treatment. Don't ask Me how I know. So instead, I researched the problem from the other side the equation, that if the Virals and Biologics could be mitigated to eradicated, that one could improve substantially from the effects of MS. See Below my research and efforts from diagnosis in 2016 to what I am doing in 2024: FYI/FYR: Status Update: December 27, 2024: Findings: Experiencing [Substantial Improvement] as of December 15, 2024. Effort to Outcomes: 'This week, 'So much regained function in lower extremities, I feel as my Feet are Literally [Glued To the Floor, as Full Contact Clearly has Been Regained, Pam]. Further: Experiencing signs of [Substantial Balance Improvement, as Steadiness reaction to balance changes can can be coped with in real-time. ' Yes, I the combination of what appears to be regrowth and cessation of biologics, which appear to cause decompensation are leading me to believe, that this method and approach is [Substantial]. Here you go. Status Update: It's December 26, 2024 months post my own guinea pig study, for I do not have the time to sit and wait for yet another group of individuals who will do whatever, only to have more and more people suffer in silence, as they decompensate from the effects of MS. Nay.., I felt it necessary to do some research on my own, and test my outcomes in real time, saving perhaps years of guessing games, for at the end of the day, the only thing that will likely happen, is that people like Terri Garr will be diagnosed and pass from the disease without an effective treatment or possibly a cure. 'I developed my own augmented tincture solution, and I am finding it be [quite beneficial]. Opinion: Knowledge should not be held back and folks forced to pay substantial monies, just to regain function. No.., so sorry, but I took action after seven years of my own research. It does appear my Tincture is helpful. This is what I am doing in 2024, and when I just stood up, my footing was So Solid, [.. I feel as if I am glued to the floor -""the signal via the increasingly obvious restoration of the Meyelin in my lower extremities, et. al.., - "is so robust once again"]. ------------------------------------ Here you go, Dear Pam. I am feeling fine once again. Having a 160 IQ does make the impossible just time consuming. Here you are. Went again to Walmart last night. Spoke to the clerk. She began asking me is the Tincture resolves MS Symptoms permanently. Said to Her: ... 'I don't know but there's no real reason it wouldn't continue working; -..it's a daily therapy as far as I'm concerned..' ...Later, I think, 'when I went back, she seemed a bit upset, as she uses a cane herself, and appears impaired, while I now, am now beginning to walk around again the way I did before the 2016 MS diagnosis. Go with God: As promised, and Merry Christmas, Mark ❤ @melissacreighton7653 Honestly, I realize I am at a point, where, from Guinea Pig experience, what is actually working and effective, but if and where I provide the precise formula, experience tells Me my augmented Tincture will be Buried into Silence. But, I'll try anyway: Augmented Tincture I am.using 3 times per day and now can see, walk, and manage the balance issue, hoping for a complete recovery: Tincture Formula: 2 Oz. Black Walnut 1 Oz. Wormwood 1 Oz. Clove Oil 1.5 Oz. Liquid Stevia 1 Oz. Berberine (24) 10 mg. Zrtec, liquid 1.8 Oz. Chinona Bark, finely ground, Fill grinds, just over grounds with regular Southern Comfort, Cover grounds and sit in refrigerator for 72 hours. Then: Remove from frig, filter til only 1.3-1.5 oz. from the rendered chinona grounds remains. Then: Pour extracted Chinona Bark liquid into 4-6 ounce glass, add black Walnut, Wormwood, Liquid Cloves, Liquid Stevia, Liquid Berberine, liquid from 24 Zyrtec liquid pills, then Stir and Fill (3) 2 Ounce Bottles. Then: ( Eyedroppers worth 3 Times per day for 26 Weeks.). And there you are. --------------------------------------------- FYI/FYR: Status Update: December 27, 2024: Findings: Experiencing [Substantial Improvement] as of December 15, 2024. Effort to Outcomes: 'This week, 'So much regained function in lower extremities, I feel as my Feet are Literally [Glued To the Floor, as Full Contact Clearly has Been Regained, Pam]. Further: Experiencing signs of [Substantial Balance Improvement, as Steadiness reaction to balance changes can can be coped with in real-time. ' Yes, I the combination of what appears to be regrowth and cessation of biologics, which appear to cause decompensation are leading me to believe, that this method and approach is [Substantial]. Here you go. Status Update: It's December 26, 2024 months post my own guinea pig study, for I do not have the time to sit and wait for yet another group of individuals who will do whatever, only to have more and more people suffer in silence, as they decompensate from the effects of MS. Nay.., I felt it necessary to do some research on my own, and test my outcomes in real time, saving perhaps years of guessing games, for at the end of the day, the only thing that will likely happen, is that people like Terri Garr will be diagnosed and pass from the disease without an effective treatment or possibly a cure. 'I developed my own augmented tincture solution, and I am finding it be [quite beneficial]. Opinion: Knowledge should not be held back and folks forced to pay substantial monies, just to regain function. No.., so sorry, but I took action after seven years of my own research. It does appear my Tincture is helpful. This is what I am doing in 2024, and when I just stood up, my footing was So Solid, [.. I feel as if I am glued to the floor -""the signal via the increasingly obvious restoration of the Meyelin in my lower extremities, et. al.., - "is so robust once again"].

Wishing you and your family a wonderful 2025 🌸

Dear Lii! Loved to see your little ones and Caesar. Wishing you a Happy and Blessed New Year❤ Your experience at the children's school made me really sad. Sad because it reminds me how awful people could act even with people like us (how the heck could we tell them how struggling it is even when everybody looks helpful?!)

My dearest Lii, happy new year's eve and a great year! I am certain you will have a beautiful time because you are surrounded by a wonderful family! I have had many heartaches due to similar behaviors. I was even told once J should stay at home, and that was by a friend of 35 years. So imagine how considerate and sensitive your children are and will be (even more) towards special needs people, through your experience . A lot of people around me have been educated to consider the health and the human rights of someone like me. I guess it is a win all things considered. Have a great holiday!!!!

🙏🏾

Much love from australia

Oh my goodness! What a horrible experience at the kids school. I can’t believe parents would act like that!! Absolutely ridiculous and unacceptable. So sorry that happened to you😢

Holidays were not good. Sick during thanksgiving and got worse. Ended up in hospital for 5 days with double pneumonia!!!

Merry Christmas and a Happy New Year to you and your family. ❤

You have such a beautiful family! I loved seeing how excited the kids were when they opened their gifts. Merry Christmas and happy new year! ❤️

Wishing you and your family all the best in the new year :) <3

I didn't watch the video but just in case, look at fat soluble vitamin B1 Benfotiamine and TTFD - lectures by Elliot Overton!

مرحبا سيدتي لقد رايت بعض فيدوهاتك عن مرض التصلب المتعدد واردت ان اسالك انا اعاني من صعوبه بالمشي منذ ثلاثه اشهر اعرج وقد قمت باجراء الرنين المغناطيسي وضهر لدي نقاط بيضاء علا الدماغ ولكن دكاتره الاعصاب يقولون انه ليس تصلب متعدد ولكن اجريت البزل القطني للتاكد وضهرت نتيجه البزل انه لايوجد تصلب متعدد ولكن بعد البزل ساء المشي لدي اكثر من السابق فهل البزل القطني يؤثر علا المشي انا قلقله جدآ اليوم السادس بعد البزل لي وانا اعاني من ميلان في جسدي عند المشي

Hello , How are you doing ? I hope better and better . I wanted to ask if you have Ehlers Danloes Syndrome as well as the M.S? I have not got the chance yet to listen to more of your videos . I am blind with so many dxs it’s almost unbelievable . I don’t recall when I joined your channel but I am happy I got to listen to some so far . Thank you for caring and sharing important info . HAPPY HOLIDAYS TO YOU AND YOUR FAMILY . ❤Sissy US