Відео

fantastic

Hi, Thank you for your video and advice. Best wishes to you! ❤

quite large for typical residential living spaces.. i've been looking at UPwalker to ?keep me upright and mobile..

I take meds for it. I'm fine I'm not dead 😮

Ive had MS for twenty years now.

Love the “little voice”. God was speaking to you! Blessings.

Be mindful that in northern latitude places like the UK have little sun and when we do everyone covers up with clothing or sun screen. Best bet always supplement with vitamin D3 daily. Also it's actually nearly 80% of those in the USA who are deficient in vitamin D3! I take a daily supplement of 10,000 i.u. of vitamin D3 following George Jelinek Overcoming multiple sclerosis program. Feel amazing ❤

I have been walking and meditating with the sun and that has tremendously improved my mood❣️ and energy😍As always you are so amazing friend 💕

There are people who are sticking to a carnivore diet because it keeps their MS in remission .

We're all MTHFR , one snp or both.

In everything that you think is bad is same thighs good to… so watch out !!!😊😊😊

I cant tolerate Humidity , so draining , i hate it . Colder weather is the best .

Hi, Thank you for your video and advice. Best wishes to you! ❤

This is a hard sell when it’s over 90 degrees and 50% humidity-but you are 100% correct! Sunrise bugs or sunset bugs are the Florida options for vitamin D. ☀️

Get your free download of the health benefits and tips for safe sun exposure benefitsofsunlight.getresponsesite.com

I signed up with Teladoc Registered Dieticians , its very convenient since we can talk over the phone. The only problem is teladoc changes access to your R.D. every few months so there is little continuity of care. Also I need a supplement specialist as the R.D's can only advise in a limited way for supplements. They recommended some great ones , but there are others that I researched and wanted to add . The amounts of supplements,finding reputible manufacturers , and testing for supplement results is more something a supplement specialist can provide more guidance with in my case. And since I do not drive , I need someone who can meet over the phone or P.C.

Thank you for this valuable information ❤ God bless you Always 🙏 He will see that you help us and he will help you for sure. 🌟

Tamping down inflammation is so scary at this time in life because it lowers your immune system. Covid is still out there. The flu and chest colds can be so dangerous for those taking any treatment for anything that reduces your immune system. But what other choice do you have?

I live in Brazil and would like to know the price? I found it very interesting because I have a fallen foot.

My diagnosis was quick, within 2 weeks. It started on my 34th birthday(21 years ago), I couldn't turn a magazing page, my fingers on the left hand wouldn't grasp a piece of paper. Thought maybe I slept on it funny, but everyday after was worse. My Dr. was on holiday so I went to walkins and got same answer, maybe a pinched nerve. Then I had a lightning bolt up my left arm and it went numb, I went to a dr. in my clinic and she told me to pack a bag and go to hospital where I would be seen by a neurologist. I had an MRI, lumbar puncture, tons of blood work and by this time I had lost use of my whole left side, totally paralyzed. The started agressive steroid treatment and physio, I had MS. Was told if I got out of a wheelchair the best I could hope for was walking with a walking aide...I told my neurologist to watch, I would walk on my own again. Six months later I was walking(without an aide)and working out the gym. I've been off meds for almost 20 years as the side effects where terrible. At that time there were only 3 drugs to choose from. Now I'm a fitness trainer and nutritionist specializing in living a Blessed with MS life. If I hadn't been diagnosed with MS I know I wouldn't be as healthy as I am now.

Ditched seed oils, processed foods, sugar, and increased animal based fats, and fatty protein, feel tremendous.

I am age 74. I have been walking into doorframes since my 40s.

Achieve Healthy Hydration!

Why not make assumption on symptoms, the doctors are not doing any better. They just want us to keep coming just to fill their coffers

Thank you so much 😊😊 Im so much confident now than ever before with ms. Also could you please make a video on "how to prevent disability with MS"

He describes exactly my problem what I’m dealing with. I had a stroke 11 years ago

Nice video. Glad you are doing well after 18 years with MS, and hopefully you will continue to thrive for years and decades going forward.

Ive lost mt sight throughmy left eye with m,s

I appreciate you so much for speaking about your experience. The first many years I was in such horrible cog fog, I lost my livelihood, and was then a 31 y/o mama of a 3 y/o. I had just begun dating my now husband 6 months prior to my symptoms.. I'm really late to the game of taking better care of myself, that self talk has been a def struggle. I love how you break it down to thinking of the person you really love and thinking how you'd want them taken care of, loved... As moms we are often drained taking care of others, or maybe just me.. I am 16 years in, living with primary progressive, working on a major diet and attitude shift. Thank you!

“You always have something”. That’s what I heard from my parents and my husband. Years and years I’ve had subtle symptoms and the GP didn’t find any explanation. So, finally I didn’t go to a doctor anymore, it all must be stress, I thought. Well, it happened to be MS. Thank you for sharing your story, mine is quite the same.

I have scoliosis never wore brace or anything

What is the actual price of this item if I wanted to purchase it right now outright

I am about to get my first MRI. Ive been asking for 4 years of having relapsing symptoms and the doctors have finally agreed! Im excited yet terrified.

Yes, it took me 8 years to figure out about the pain in my legs and arms. ...and yes I was in my late 50's and they said, age? neuropathy? slow blood flow? ugh!!!!!

I have all of these problems but I feel like my doctor will think Im crazy. Everytime I go with a symptom to my dr i feel like they brush it off and just want to focus on one problem per visit. I have an array of problems but im tired of complaining with no one is listening.

I had asthma as a child. I wasn’t diagnosed till I was 12. I outgrew it. My son has it now. I also had bad headaches and still do. My MS symptoms get better no leg or hand pain, and better mobility when I’m on my period. Less leg heaviness. But I still use a walker and a wheelchair.

Numbness in left arm (from hand to elbow).

For my last MRI I was in my sixties in age. I honestly feel it's silly not to be able to just sit still & get the MRI done, but..... something in brain takes over and I get so anxious I have panic attacks really severely. So for the last MRI my doctor wanted to make sure I felt nothing anxious at all about being in the MRI machine, so he gave me 2 Ativan pills about 45 minutes before the MRI was to start. Then about 15 minutes before the MRI he had me take 1 more Ativan, I am overweight so maybe that's why he went to 3 pills total. I remember getting on the table, and don't remember one thing after that, I kind of went to sleep I guess. ha! I tried an open MRI machine once & even it was horrible for me. I can't explain why it bothers me so much but I will never get into a MRI machine without plenty of medication. ha!! Hope things get better with you. I see the word Multiple Sclerosis listed next to your name, based on your age it appears you are one of the lucky people that can handle the disease pretty well. It affects people so differently from person to person. My brother died of MS at the age of 56. His disease was terrible, he was bed ridden the last 5 years of his life, I hated the day he passed but I was so glad he didn't have to endure the pain anymore. I know other people with MS much older than him and they do very well, you keep that up too! Take care.

ah, yes. . . foot drop. . . for me too the demanding call to figure out was going on. . . . . . . .neurologist. . . mri. . . brain and spine lesoins. . . . . . . . . . . . . . MS! 4years ago at this point. . . .

Can do you know if MS has anything to do with bladder issues? My daughter has had been diagnosed with a weak bladder. She does have left sided weakness and has leg pain in one leg only. She does has a neurologist for migraines and we are seeing a neurosurgeon to rule out spinabifida.

Tell me, how do you take this exercise when your whole body is screaming in pain. Don't get me wrong. I'll push myself. I still do some exercising. I am not a baby. I have been suffering pain in the central nervous system for over thirty years from MS. The advice given is for everybody Not something special for ms patients to follow. But it would give you your best chance the same as everybody else

My neurologist told me that it was very unusual to get MS at age 60. He thinks that I might have had it for years, and just didn't know it. Looking back, I see things that may have been a symptom. I now use a cane or walker when outside of the house.

I still waiting on diagnosis, it started 2 years ago, I woke up shaking at 330 , 5 episodes, drop foot, right side weakness, hot showers I thought I was having a stroke, slurs words numb face. Dr wahls level 1 as a vegan has helped me alot