MS, Vitamin D and Viruses...a MUST SEE!
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- Опубліковано 26 гру 2011
- www.DrKrupka.com Dr. Krupka gives a detailed account of how Multiple Sclerosis (MS) is affected by vitamin D levels and Viral history. This is some serious content and worth watching more than once. If you have an autoimmune disease or know someone who does, grab your pen and paper to take notes and change your life!! Pass it on to your friends. • MS, Vitamin D and Viru...
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I did not walk nor could hardly use arms for two years from Gluten binding up and not absorbing nutrients. I now take 10,000 IU a day D - 3 and went to grade school SKATING party tonight :)
So glad to hear that you're doing better. Hope the skating party went well!
this is wonderful.
I found out a few months ago I have Lyme disease! took nine years to find out!!! Turns out the vitamins, like D, saved my life more than I realized :)
+Sara Star I was dx with MS and Lyme in November. I can't find a dr to treat lyme. what treatments have you done for it
Hi Brandie, hope I can help some! It took me 9 yrs to find lyme literate doc who know right away I had Lyme. I too cannot find a doc w/my insurance and pay him cash, but low costs. I am lucky I had high Candida yeast overgrowth and changed my diet to kill candida, which inturn saved my life. check out www.candidadiet.com for food to eat and not eat, this is number one start. Supplements of all kinds to rebuild nutrition stolen from bacteria. Pure water important, spring is best. I just got an oxygen concentrator to put ozone in body, doing very slowly since not monitored by a doc. From research done so far and knowing a doc who knows about ozone, I doing 35 % food grade hydrogen peroxide w/distilled water. Research it. I connect w/other Lymies and those that have had oxygen have said it has helped. I found my concentrator on craigslist for 1000 less than new. If you like me, you broke now from being broken, Lyme is expensive when cannot function and work.... I do many natural antibiotics and rotate them.. Silver, olive leaf extract, oregano and wormwood will kill some of it and keep immune stronger to deal w/all the infections we can get. more in head, but hurts to type. ask me more if wish, good luck!!!
this guy has a gift for explaining things
here's a few things for treating ms at home
Make sure you eat plenty of fruit and vegetables (preferably organic).
Make sure you have enough vitamin C
Do some exercise eg walking, yoga etc
make use of herbs with infection fighting properties including dandelion root and burdock and others including huang qi
(I discovered these and the reasons they work from Denelle Multi Care website )
You gave me more insight than my neuro did when he diagnosed me with MS in January. Thank you!
Why does a chiropractor sound better than my GP? Like this Dr.
Dr John Bergman explained it in one of his videos: chiropractors are trained to focus on health and medical doctors are trained to focus on disease.
Marcus Kool I call bullshit!
Coz he can say whatever he likes, because he's not a doctor.
bcide medical doctors are just that, medical= pharmaceutical.
Doctors know what the drug reps tell them. Drug reps tell Dr's how to treat symptoms not the problem causing the symptoms.
My vitamin D3 levels have been low for years and I insisted that my levels be checked twice a year.
Now I have MS.
Dear my doctor... Pay attention to your patients.
This is very interesting because I fell into a depression and rarely left the house for nearly a ten year period and suddenly started experiencing symptoms of MS. I even had a swollen optic nerve, and had mri, lumbar prosedure wihich came back normal. I was referred to a neuro, and I told them to go to hell, because I didnt want to get on meds. I started walking daily and taking in the sun, and voila! symptoms dissapeared. My optic nerve hasnt been swollen since, Its been 4 years!
My husband has MS got diagnosed 2 years ago I shared this video with him !! Thanks for the info!!
What a GREAT transformation you've made! I hope your story can inspire others to make some of the difficult changes you've made. It certainly sounds like your enjoying the benefits of all of your hard work!
Thank you doctor. I was D/Xd in June of 2011 and I can't tell you how informative this clip was to me. Keep them coming please.
Thank you for taking the time to make this video. I am just now diagnosed with MS and in the throes of a horrible exacerbation and am starving for ways to help myself. My vit D level was 9 and I'm only prescribed 5000IU daily otc ....nothing else has been said about working on increasing that level. Instead I've been given high dose steroids among a sack full of other neurological meds and honestly I'm terrified of what is happening to my body. Thanks again for this insight.
Sheila Colburn write to me, I've answers...
@@Ultamami have MS as well as low vitamin D.
Can you please help?
Perfect video and what a great teacher! thank you so much!
I really appreciate this video. You're very good at explaining these issues. Thank you!
Thank YOU! My wife has MS and we have taken steps to learn Vitamin D Levels, but the explanation of powerful impact is most helpful.
Awesome video! Thank You for taking the time to put this information out there!
Totally agree. I live in northern WI where direct light is less than average, I went to California for 10 days and came back like a fully charged battery. Getting out in sun is a challenge for me because I need someone with me to help and the availability of help is limited times. Going to listen to this guy and try to improve my health.
Thanks, lordboston05, I'm really glad you liked it!
I'm an athlete, and I learned a lot knowledges of nutrition after watching your videos. thank you so much. and please keep producing more videos about health. I want to become stronger and healthier naturally.
I just wanted to say thank you 😊 for sharing this . This has changed my life I have had severe crohns for over 20 years . My dr always said vitamin d didn't really matter . The swelling on my joints is getting better . I think you so much I owe it to you . Thank you for taking the time . Please continue to do this . You have changed my life to happiness.god bless your soul !
Try the coimbra protocol
Thank you for sharing your knowledge.
I'm 68 and got MS in my early 40s but it wasn't diagnosed till my early 60s., took that long to get it diagnosed. It went into remission for years and for a time I was a fitness trainer and became a certified nutritionist. It got a bit worst in my 60s and I have balance and a walking gait problem and now use a cane. I was told by my neurologist that I needed to be tested for my Vit. D levels so I got tested and they were low. So now I take 2000 i.u. of Vit. D3 a day plus other D3 in Cal-Mags and my multi-Vitamin and from other food sources. I only eat clean, fresh mostly organic veggies and fruits, no wheat any more and no cow's milk only almond milk I eat a mostly Paleo/Wheat Belly eating plan and have never smoked and drink wine/champagne and an occasional fun martini on rare events like a birthday. I do yoga and have a stationary bike and am not taking any prescription drugs as I don't like their toxic side effects so I'm trying to do everything as natural as possible and handling this holistically. I sleep well and try and keep stress to a minimum after raising a family for decades and care taking for my late husband who died from Diabetes type 2. He was on 9 different prescription drugs and insulin and from what we both could see nothing really worked for him...he had a very stubborn case of it and probably could have also benefited from Vit. D as well. I also take B Complex and B12 as some of the symptoms from B12 deficiency mimic the same symptoms of MS, interestingly enough. I found a functional chiropractor in my area, only one there is and he's way too expensive and doesn't take my insurance and he acted like a real snob to me when communicating with me...guess only for the super rich around here since I live in a relatively affluent seaside resort. Other than that, I would like to try your raindrop therapy and add that to my list of healing modalities which also includes meditation and tapping! I'm trying every possible positive thing I can try and the way to manage one's MS is to be pro-active. Thanks for your great informative video...I'll check out your website! Hope to watch more of your videos!
@Henry Stoneking lol, yoga is good for calming you down. its good to relief stress. Deamons... pff
@Henry Stoneking
I believe in God. But if God is our heavenly father, why does he take away the health of some people, and make them suffer. As a father I will never treat my son that way. I had for years feel abandoned by God, and still suffers emotional and physical. People and Christians had prayed for me, I had read the bible. I do pray but no comfort or help, only guild by doing alternative things to heal my body and mind.
Yoga its a stretching exercise, that is bollucks what you claim.
Why wait for a God and Jesus to rescue you, when obvious they only answer with silence.
I use EFT, EMDR and meditation to heal my childhood trauma and adult trauma. I use qi qung exercise to balance my body, and has included wim hof methode. I still pray, but for 15 years I had suffered from anxiety, later chronich fatigue when my son was small. No God or Jesus has comforted me, while I have seen my life got stolen from me and my friends has enjoyed there life.
It is understandable that people try all types of exercises and therapy, even that very conservative Christians call it evil and demonic.
No one, want to suffer there all life, while waiting for the empty promises of Jesus or God
you are amazing!!! My GP stated to me 4 years back, because of my symptoms, that he suspects a nerve condition being the underlying reason. Now, I am suffering my fourth flare up inside 6 months. After prayer last night, I awoke this morning to the Holy Spirit saying MS brain. I googled it and now I know what I've been dealing with. Then I was lead to YOU and your wonderful informative video. I will go get the testing. Thank You!!!
I am well aware of the implications of food sensitivities in the development of autoimmune disorders, but once antibodies are created, even if you get rid of the trigger (gluten, dairy, grains etc.) you still have to modulate the immune response. Sometimes removing the triggers has a calming effect on the disease progression, but other factors like vitamin D deficiency (and intestinal permeability, viral issues, emotional issues) need to be dealt with for a patient to go into full remission
Thank you for making this complicated matter very easy to understand. Looking forward to more lecture from you.
I was involved with 3 very bad car wrecks. First one 1975. Slammed the right side of my head against the dashboard after a drunk driver slammed into the back of my fiance's 65 Chevy Nova. No seat belts back then unless it came from factory.
11 months in neck brace and traction for "whiplash!" No MRI or Cat scams then.
Here is the story of my luck--we were sitting in the road in front of my parents house. Waiting to make a left turn into driveway. Oncoming traffic was heavy. Suddenly I heard my fiance say, "Oh s=%t!! We are going to...."
Cane too with me on the floor of the car and I could see my dad, my fiance, my neighbor, & a cop.
Guy who slammed into us was drunk as a skunk!
After #2 wreck in 2004, I ended up in the ER. MRI showed not only brand new ruptured discs, but the Dr found very old ruptured and cracked discs--from the 75 wreck.
After the 2004 wreck, I was left with pain up and down left arm and partial numb of right arm. Lady ran a stop sign & slammed into the right fender of my car.
Wreck #3 in 2006. MRI showed a lot more disc ruptures and damage. Now the left arm is pain 24/7 while right is numb.
In August 2005, I started to pass out and went to the ER. BP was sky high. Admitted and diagnosed with Graves disease. Found a primary care doctor and they had problems finding a BP medication that I was not allergic too. Add in finding a dose of Graves medication that would work.
In 2008 I got bronchitis which turned into pneumonia. During a coughing fit, I heard a POP in my neck and pain shot up into my head and down into my neck.
MRI showed a piece of disc that had been cracked had totally broken off and was touching my spinal cord.
I was left unable to work due to threats from the center manager of a MAJOR freight company!
He fired people for being a minute late for work!!!
He bullied any person who missed work more than 1 time.
The doctor had me apply for disability.
On March 18, 2013, the process server came to hand me papers for foreclosure on my house. I was having "thyroid storms" which is when Graves disease goes nuts. Anytime I stood up, I would pass out.
Guy banged on the door. I should have taken my time, let his butt wait, instead I rushed. I opened the door and passed out--falling down the steps and slamming the right side of my head on the concrete driveway.
Thyroid storms cause the temporary loss of speech, hearing, & sight.
When I came too all I could hear was tapping. When the sight returned I was staring at a pair of mens shoes--the one was tapping impatiently.
Then I heard, "So how long are WE going to play THIS game!!"
What a jerk. I told him leave the papers. He threw them down and left me.
In June 2013, I found a low cost clinic. I was "living" off my credit cards. The doctor wanted an MRI of my neck to see how bad it got. When I mentioned hitting my head in a fall in March, she ordered another MRI of my brain.
I got a call the day after I had the MRI's. It was the nurse at the clinic. They wanted me in the office the next day--BEFORE any patients were there!
She started with the neck and said it looked like a jig saw puzzle.
What I did not expect--the head MRI!! I thought I had cracked my skull since I still had a big lump.
She says see this white thing in the brain?? Yes.
You either have Lyme disease, ALS, or MS. She left the room.
I collapsed on the floor, sobbing.
Couldn't get disability and I knew no job would hire someone who passed out all the time.
Finally after 5 1/2 YEARS, almost losing my house, my savings gone, and finally got disability.
The test for Lymes was negative. That left ALS or MS.
My specialist said it was MS.
They asked all kinds of"symptoms" questions. Since my symptoms ALL came on instantly after accidents or illnesses, I have no idea what is from the wrecks.
I saw a neurosurgeon after my 2006 wreck. He said he wouldn't touch me because I was a "walking paralysis case waiting to happen!!"
In March of this year I went to my primary care place. The PA blurts out that my blood work showed I have RA and Lupus!!
What the crap!! Four autoimmune diseases for a person who, up until the 2004 wreck was an active person!! I had been a 5 to 10 mile per day runner as well as I loved to dance at rock bars.
And to add to my damaged neck, in 2016 I was slammed into at a stop sign. The last 2 areas of my neck, left sides of C3 & C4, now had cracks too!!
Now I do not know what symptoms are from the 4 wrecks and what is from what of the 4 autoimmune diseases.
The lousy health insurance charges me a $50 per visit copay for a specialist!!
This is in addition to deducting $134 a month out of my check.
I have to see my one specialist so that is $50 that month.
I have already signed a DNR in the event of paralysis. I refuse to "live" paralyzed!! My family is all dead.
I am hoping this vitamin d helps.
Hi Suzie, how are you as of now ?
Suzie Phillips What a misfortune! I hope the vit D helped. How have you been lately? Any updates?
This is an AWESOME video! ThankU so much...
Thanks, Starmamma, It's great to get sources for Raindrop Therapy listed here. Keep up the good work!
Fabulous video. Clear, logical, and informative. Thanks!
I found your video very informative. I was diagnosed in 2009 but feel I had MS since my teens. This gives me a little more hope on controlling my MS.
Dr Krupka
wow this was amazing thanks so much, i have just been diagnosed with ms and am really grabbing at straws now , with my one eye......this made sense .......strangely i feel i need to have this checked out, i wish i lived closer!!!!
i will however run tot the shop to stock up on some vitamins i wont go overboard and i will have my self tested, i don't really take anything currently so i guess a start would be good
many thanks for this rather inspiring video!!!!!!
regards from africa
great stuff.. am a med student myself.. hav been readin abt these dugs for ms but never knew things as basic as vit d can b so useful..thnks for uploadin such good info
Fantastic video! See....Coimbra Protocol.
Thank you.. I will certainly tell my Fiancee tonight.. ASAP.. about Vitamin D benefits.. It makes me feel lot better. Thank you for your help..
Thanks, Dawn!
very informative,had my full attention,i am from trinidad &tobago.thank you for the information and look forward to more of your information...great job!
THANK YOU THANK YOU THANK, i INCREASED my vitamin, D I take 10,000 ius daily and am off all meds but Nuerontin I could not handle the side effects anymore, it has been 2 years and no activity I am officially in remission with my MS and my ANKYLOSING SPONDYLITIS..
ALSO I HAD AN EXTREME CASE OF chicken pox as a child.
Winter Star yes, i had vaccinations, and so did my kids, because i thought i was doing the right thing, well, i wish i didn't do it, cause i have ms arthritis diabetes and 2 of my children have autism, one mild and one severe. i blame the vaccines.. i also agree with everything you said here, thank you,
Karen smith in 5th grade, we were forced to cattle-call thru the cafeteria at school to get the Polio vac. ...days later, my stepmom showed me a tiny article on an inside page of the paper, saying the vaccine was contaminated, and being recalled. Officials determined to cover that up, by forcing us all to get 're-vaccinated' using the killed virus. One was a sugar cube, the other was injected. But i realized, from that process, and observing how things were reported, discussed, etc., something was very wrong.
If I had known then, what I learned later, my kids would not have been vaccinated, either. There are a few ways to avoid them, but it requires dedicated help from licensed practitioners to do it. If I'd known, I'd has tried very hard to find that. But it's too late for most.
And, Industries that profit from vacs as we know them, are rabidly passing legislation to force everyone to get vac'd, no matter what.
So the situation will get much worse, before those are stopped for crimes against humanity. Vaccines CAN be done right; we just don't live in that world.
Meanwhile, it's really important to learn everything we can, about how to use nutritional and natural methods, to minimize damages, and optimize our remaining abilities...a daunting task, as good information is so badly tangled with bad information, maliciously, deliberately funded by those determined to mine humanity of every bit of profit possible, no matter what the consequences...there's gotta be real special places in he!! for those, whether anyone believes or not.
@@Jesusfreak3378 I have Ankylosis Spondylosis .I am suffering alot .. medication like saazo i.e, conventional medicine by Rheumatologist do not work .
Please help me how you are free from AS disease .
Great video! Thank you so much for sharing that amazing information.
I like the way he explains everything.
great video thank you dr.patric,great information
DrPatrickKrupka You are a hero for me.
Since i`m 19 years old i start drinking alcohol (liver), start drinking a lot of coffee (kidneys), and never go into the sun (skin/ vitamin D.).
Two weeks ago i get my MS diagnosis and this video was one of the first i watch about MS. Now i know the symtoms and i see the MS starting with (round about) 21/ 22 years in my live. My motoric is really good because im alwas working in the steel factorys. So i have everyday to use my feets and hands to "build perfection" and don`t fall into the mashines.
my MS was more on the psychological symtoms (depressions, angryness, suicidal ideation,oblivion,bafflement, change of character,....).
PLUS: 2 weeks after my last cannabis use i have my first bad push (i don`t pause it so long usually :-) after the 4th week, i feel so bad (strange walk,gaucheness, bad view with my left eye for 2 days.....) and i get strong headache and i decide to go into the hospital.
Now the "specialist for MS" (he don`t believe my MS diagnosis at first because i have a good walk again) order me to use "copaxone" and i decide this morning, to ask another doc (i hate injections too much to make that every day and i doubt the most parts of the mainstreammedizine!!!).
Many of the diseases today are "only zivilisationdiseases!!!"
We sit on the couch, stay in the dark, don`t move our lazy bodys and drive every mile with the damn car. Cancers, heartattacks, MS and so many other things that we can avoid with a little bit of movement in our allday.
Sorry for my gramer and Thank You really much DrPatrickKrupka :-D
You're very welcome!
DrPatrickKrupka
When i make a video about MS in german, i have to put this link into the discription.
Thousand thanks and greetings from europe,...
A wonderful video, I so enjoyed it. Very Informative, can't wait for your next video. We need more Doctors like you showing another path. Thank you and please keep those videos coming. Oh by the way your drawing isn't great, but I did get the message! lol
I love this video. shared it prob 20 times in different MS grouos. thank you for making this
Very interesting. Thanks for the information. Look forward to learning more on your rain drop therapy
good presentation thank you for info
Thanks for this video.
good stuff. thanks for mentioning Jodi B. She has gone to Calgary.She whipped the GP and neuro guys into line after 3 years of nonsense to get a definitive diagnosis . Her main recommendation was D3.8000units a day. It also helps with the uptake and utilization of calcium for bones. Important stuff when falling is an issue.Good info on your video. Cheers.
I live in the famous Northern province of Saskatchewan ,Canada.I am of european decent and live (and grew up) in the central to northern provinces of Alberta,Sask and Manitoba.The Hot Spot of the world .I refuse to believe that ,but that is my own humble,yet honest opinion.Thank you for all the info,keep up the good work!!!!
Thanks for sharing buddy.
Excellent video!
Easy to understand, you should be a artist, lol. I have not taken any pharmaceuticals in 18 years. I do take vitamin C & D and in those 18 years I have not had a cold or flu, no matter how many ill people I am around. Swear by Chiropractics, my nephew in Utah has a practice, Dr. Jay Shetlin. Use oils when needed, great post! Came by to learn about this issue, thanks!
Thank you for this Sir.
I was diagnosed with MS in 1994 and am now considered a paraplegic. Since 1994, I switched from one MS disease-modifying med to the next. Each one ended up making me feel horrible and did not stop the progression of my MS. Several years ago, I said no more of these drugs. Since watching your video, I am very interested in increasing my vitamin D3 dosage with my doctor's input. My vitamin D level a few years ago was considered "normal." All the different schools of thought on vitamin D usage is quite confusing. Thank you for sharing this important information.
Hi, I think that the advice of the doc at the end of the video is very valuable: find yourself a functional medicine doctor: he can help you with the Vitamine D and possibly other deficiencies.
Thank you so much! Your explanations have helped me immensely.
I have been taking 120,000 for 1 year. My blood level has gone from 18 to 65!
Will check blood again level soon. Someone mentioned to care, now, due to possible damage by calcium hardening the arteries?
Any videos explaining this phenomenon?
I want to look into raindrop therapy now! Thanks again!
Do you have any explanation-videos about Methylation , especially when phase 2 is not working properly?
Susie, I didn't give a blanket dosage suggestion because each patient is different. Dosages in my office usually range from 2000 IU per day up to 15,000 IU per day depending on the severity of the case and what their labs reflect. THe 40,000 IU dosage was just referenced from the research article, not a suggestion from me.
Thank you for making this video. I have been on Vit. D supp of 100,000 units per week and it was just increased to twice a week for the past 8 months(per my neurologist). Over the Winter some of my symptoms seemed to get better and now that it is hot again they are back. I have had HPV for years and know one ever mentioned that it could be the cause of my Vit. D levels not going up. I will see my MD this month for a follow up and ask about the Rain Drop therapy. Thank you again for the info.
Really well made video. Thanks !
great work as always Pat...Spot on with my research...anyone listening to u should certainly see improvement...a few points that i would add would be:
1. cholesterol and saturated fats are extremely important to keep in sufficient amounts for anyone with this condition, and really for almost any condition for that matter, particularly brain conditions
2. Vitamin C and Glutathione (IV or Liposomal) will also help very very much with any Viral Conditions, but there may be a precursor needed for blood brain barrier i forget at the moment...Vit C for extracellular viral load, and Glutathione for within the cell...
3. THIS IS THE MOST IMPORTANT ISSUE FOR MS PATIENTS I CANNOT STRESS THIS ENOUGH... U MUST AT ALL COSTS GET A VENOGRAM FOR CCSVI...
ALMOST EVERY PERSON ON THE PLANET WITH MS HAS CCSVI...AND WHEN U GET THIS TAKEN CARE OF UR MS MAY VERY WELL GO AWAY IN LITERALLY 1 DAY...THEN SIMPLY FOLLOW PATS ADVICE HERE SO AS NOT TO RELAPSE...
ok take care guys...I guarantee that as soon as u research ccsvi ur gonna have a smile on ur face...i can see it now...ur welcome...i work as a research analyst in medicine and science...and let me tell u ppl like pat are good to know...
What procedure are you suggesting people do with ccsvi?
Great Info.
Very informative. Thank you.
Thanks so much for the video
Excellent Doc. Thanks.
Thanks a lot,, your video is very helpful.
learned a lot thank you very informational
Thanks for the information! Very helpful :) Gotta find out about that raindrop therapy - never heard of it before.
Brilliant video
Excellent explanation; and very nice to see that someone is addressing at a deeper level, the implications and causes of low Vitamin D levels. Viruses have been the elephant in the room. Unfortunately, this is the case due to the average doctor being synonymous with K-mart, or Walmart, or Target. What I mean by this is that you can have an associate "manning" a particular department, but that doesn't mean such an associate is truly an expert in that field (neurologist, endocrinologist, etc.). Most doctors today are sheep, essentially learning what was presented in books, which were manufactured by man, whom do not (inherently) cover 100% of the variables that play into any disease, pathogen, or scenario. Call me crazy; but unless you have a series of profoundly debilitating conditions, and continually get the runaround and/or arrogance + ignorance from doctors (e.g. "it's all in your head"), you might as well hang up the opinions -- unless you are intimate with the experiences expressed by someone you care about that is severely effected.
must thank-you for making videos!
Excellent info
Im always willing yo listen to good advise, i wish the afflicted would...hard convincing people to do the right things...
This was what i had suspected, when I was first diagnosed. It is part of the reason I switched neurologists, because the first one said there was no ties between the symptoms i was having and the non-existent vitamin D level, but he was treating me with prescription amounts of vitamin D for 3 months instead of me just going out and buying it over the counter. The MRI said I had MS out right, so we changed doc's. Thank you for this info, I will go to my doc now well informed!!
Thank you!
Even with lots of sunshine therapy I have been consistently low in D3 verified by blood work.
It's in my family.
I was diagnosed with MS about 3 weeks ago.
Been taking my D supplements every day morning and night.
I already feel better with my depression.
My PCP said "oh most people are low in Vitamin D it's not a big deal"
She the MD said that.
I see neurologist tomorrow and see primary care doctor in a week.
I can't wait to see her face to face with all my complaints about fatigue, back pain, headaches, falling due to leg weakness, chronic ankle swelling and so much more ...Im going to ask her if I can record the session.
I will report back here with her response to my MS diagnosis.
Guess what? The neurologist ordered vitamin D3 levels and I am 32!!!
I have never been above 29.
That's because I increased my dose from 5000 to 10000 in 2 doses per day.
Tomorrow o see that primary care doctor who said vitamin D3 levels are not a big deal and most people are vitamin D3 deficient
WOW this video is Amazing.. so much useful information... I'll make sure to write about Vitamin D in my research paper. Thanks Doc.
Thank you! I found your video very insightful and helpful! Being from the Seattle area, (highest MS per ca-pita) I truly believe that our lack of Vitamin D plays a huge part in our MS.. Thank you! :)
Thank you for the video it was very informative. What about GcMaf what would it be effective in treating MS. What about Autism and its autoimmune effects? Would it be possible to post a future video on the inflammatory cytokine pathway of that disease?
You have made this so easy to understand, I have been taking vitamin D for a few months now, but I had no idea why I was taking it, just my Doctor said I should, now I understand why one other thing I have always I am able to go to sleep without tossing and turning for a couple of hours. Thank you, Doctor.
MrTman, I'm not currently aware of a commonly available test for that anomoly, but for all practical purposes, just testing your vitamin D levels and supplementing if necessary should handle the issue. Regardless of the issue leading to the decreased vitamin D levels, restoring them and maintaining your level is the most important goal.
Hey Doc. hope all is well. I have Secondary Progressive MS, I think. LOL . .and this was hands down one of the best videos I have seen in a long time. Thank you VERY VERY much. New Sub
Tim Man how's the vitamin D working for you
Pretty decent,I am early in restarting my vitamin D regime ,but its helped a lot in the cpl weeks.Thanks :)
I enjoyed your video. Wish i had a doctor like you at the VA Hospital . I was diagnosed with fibromyalgia and now they are doing tests my vitamin D level was extremely low. Lived in Germany for 3 years one of those years I was deployed to Iraq. The heat over there is overwhelming I got sick alot. every year i have to get my eyes checked (dry eye),and when i did get my glasses it does not work and it is frustrating. I think these doctors are really missing on what is really going on with me. My pain is getting worse and I am getting tired of taking medication.I am taking 1000 unit Vit D3. I cant sleep they gave me meds for that to. I have TMJ, getting botox for that and my headaches. I am suicidal because my body is going through this. I use to run track a long time ago. I really did enjoy the video ( female veteran medically retired)
+Carla Valmont
I am so sorry to hear all your troubles, Carla. Sometimes, I wish I had a magic wand and with it I could just make all these sufferings vanish in one gesture....
Have you ever thought of doing yoga? Hatha yoga, that is, and also meditation? These two very natural practices help you help yourself, and there are no side effects! Good luck to you!
Awesome.
I am on the Coimbra Vitamin D t herapy for MS. About a month after diagnosis my mother sent me your video. I started going to a massage therapist regularly.
How do I know my viral load reduced? I had a wart on my leg about the size of a pencil eraser. When I was diagnosed with MS the first stupid thing MDs do is out the patient on steroids. Then I went to my primary care physician to discuss reducing the root cause of MS, ie, my viral load. I also asked to have wart removed. She said that wounds won't heal well while steroids are in my system, so I could not have the wart removed.
After a month of Raindrop therapy (oils placed on big toe and spine only), the nasty wart on my leg just shrivelled up and fell off. My Massage therapist was as excited as I was. She could feel energy changes in me, but other than that we had no proof that anything antiviral was occurring. I was so excited to show her my leg wart was gone, saying "can you imagine if the treatment did this to a virus on the outside of my body, what changes are occurring inside?
This treatment works!!! YL oils...the treatment is recommended with a carrier oil if the patient can't tolerate the oils put on "neat" (direct to skin with no carrier oil). I had no problem with the oils "neat" and have been doing the treatment for a year!!!
No DMDs for me...in fact, I was bullied into them for 4 months by my neurologist and other MS sufferers who called me a fool. (All of them, bar the neurologist, had major relapses since chatizing me and had to switch DMDs and gained more disability. The DMD experiment was a total failure. I could barely function. I didn't want to live. My mind was foggy. My Massage Therapist asked me one day why my energy was no longer beight and healing, but dar k amd depressed. I told her I started DMDs. After fouur months of the side effects, I was frustrated and my Massage Therapist spends 1.5 hrs every week doing Raindrop. She said, I know you're conflicted about this and I'm not a doctor, so I can't give medical advice. But, I know your Neurologist has never put her hands on your body, not once (I had told her this). I touch your body every week and I feel your energy. Ever since you started taking those drugs, your energy us low. Low energy is not healing energy. Go home and pray and in your gut, you will KNOW.
I have not taken a DMD since! My vitamin D healing AND my Raindrop treatment were negatively impacted by the DMDs. Almost like starting from scratch.
I am so excited to share vitamin D therapy, but most people think 10,000 IU/day is A LOT of D. With MS, that's a paltry dose. Doses need to start at 1000IU per kg body weight to cause permanent remission of MS in 95% of patients.
Concurrent use of Raindrop Therapy and Coimbra High Dose Vitamin D therapy, has given me my life back!!!!
thats great to hear. How are you today ?
Hi Dr.Krupka.
Thank you for making this video. It was so easy to understand what Vitamin D really means for us with MS.
I live in north of Norway. ( at about 68' north ) so the sun is only here for about 3-4 months a year. My level of Vitamin D dropped from 120 in mars last year, to 82 a week ago. Even after I started with regular Vitamin D 10µi(?) from the pharmacy!! :(
I`ve started with Holistic D3 vitamin 4000 µi now and hopefully I get up again. :)
So Thank You. ;)
Thanks for the vid. I'd love to hear you expand on viruses. Can vIL10 level be tested?
Our local chemist recommended me a 20,000IU dose - Neurophysiology two years ago found Active-Denervation, I have just had a follow up EMG and no Active-Denervation was found....Taking vitamin D for the past two years sort of speaks for itself in renewing nerve myelin sheath...Thank goodness for our local chemists advice.
awesome. How are you today?
Excellent. Educative. Inspiring. Particularity; to those having progressive MSA like me. Wish u all the best.-Gyan, India
What are your thoughts on amygdalin (B17)?
Great Video.
THX for the video
I broke my hip, and was told to take 2tablets of vitamin D as well as Cacium.after 2 years, I just take I tablet of vitamin D.. It probably helped with my MS too and didn't know it. I will try to get more sun shine. Thank you for the information!
Great videos, thank you so much for the invite:)
Thank you for such a clear explanation. I was diagnosed MS this year and have been taking Vitamin D supplements (and eating healthy - no gluten, low fat, no dairy, fruit/veggies) for 7 moths and am feeling REALLY good. I just shared this on my Facebook Page. Everyone should watch, learn and act on your insights. Again, thank you :-)
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I can't seem to find the video about Raindrop therapy that you said you have. May I please have the link? Thank you. Loved this video, btw.
Do a youtube search there are tons of videos about it. Young Living has videos at their website.
I didn't give a blanket dosage suggestion because each patient is different. Dosages in my office usually range from 2000 IU per day up to 15,000 IU per day depending on the severity of the case and what their labs reflect. THe 40,000 IU dosage was just referenced from the research article, not a suggestion from me.
D-metabolites Vitamin D has several metabolites (forms). For practical purposes, this explanation is limited to two metabolites: 25-D (inactive) and 1,25-D (active). 25-D
Thank you So much!! Now I understand it all..I have ms..recently dx with SPMS...with chronic Deficient Vitamin D.....NO matter what i do..we cant keep my vitamin D up to healthy levels...your video has helped me understand vitamin D and MS! Thanks...
thanks so much .
So is this helping?
What or who is a functional medicine dictor? Definition pls, ty 4 sharing your knowledge. Wonderful video. What is your thought about anxiety as well as endocrine disease. Would these play in any part of ms or deficiency of vitamin D
Very interesting
DCs are physicians in most states, and have a number of sub-specialties (including orthopedics, neurology, internal disorders, nutrition, functional medicine, pediatrics, radiology... etc.)
Dr. hello I want you to tell us about illness ankylosing spondylitis biologic therapy Do you support this treatment and if so what is proposed for the age ways of biological treatment.