What You Don’t Know About Supplements May Be Hurting You

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50 thoughts on “What You Don’t Know About Supplements May Be Hurting You

  1. Thankyou very much for getting ‘down to the specifics!’
    World reknowned neurologist Dr. Roy L Swank Oregon Health Sciences U found our
    plasma is abnormal, and our redbloodcells clump together. Prooven by his RBCM=
    Red Blood Cell Mobility test.
    I eat 15 grams of fat per day and supplement with olives and Avacado for energy. I have learned about linolic and linoleic acid needed for energy and oil for our nerves in our diet.
    Thankyou for getting to the nitty gritty regarding supplements!
    I am 30 years diagnosed with M.S. and 33 years a Registered Nurse still working!
    Teresa Fridley R.N.
    tafrn10@gmail.com
    I can’t wait to get my Vitamin D3 et al!!!

  2. I am greatly encouraged by this webinar! I already take 2000 mg of D3 and niacin. The niacin lowers my cholestrol so I was able to stop taking the statins. I can’t wait to try the other supplements!

    I have not had an attack since I started taking the D3! I have been close to an attack, but just sleep it off.

    Thank you for the straight answers! My neurologist is a noted research scientist, but does not tell us these things! At last, someone is telling us the truth!

    Barbara Holoboff
    Edmonton, Alberta

  3. I really enjoyed listening to Dr Rudy Cartwright giving us details on the various
    supplements available to help with MS.

    I have already started to take Vit D3 and I will work through the other supplements outlined in the webinar.

    I also listed to the webinar on calcium and now I am cutting it out and taking a substitute.

    Can I thank Dr Rudy ,his son and yourself for making this information available to us in an understandable format.

    Kind regards Geoff

  4. I HAVE MS SO YOU ARE SAYING I SHOULD HAVE SOME SUNLIGHT TOO.I’M WONDERING IF I WOULD BE WRONG TO MOVE TO FLORIDA. I GET TO HOT I HAVE HARD TIME BREATHING. I HAVE A LIMITED MOBILITY PROBLEM. HOW MUCH THIMINE SHOULD I BE TAKING.WHAT IS THE WEBSITE

  5. low dose naltrexone, what is known and what can it do for people suffering from ms?
    Very happy to be able to hear or see information about it, so thank you very much!

  6. wow everything you have said on here makes sense. I was on drugs for my ms paying 2000 a month. My boyfriend has gotton me off the, and I went on natural pills. And I feel exactly the same as I did on the drugs.

    Thank you very much for this information
    Patricia Kucybala

  7. Thank you so much Dr. Cartwright for your valuable info. Are you going to provide an essential blend in 2 weeks time? I thought I heard a comment to that end.

  8. Thank you so very much ! ! ! Please continue. I find that I want to learn all I can and wonderful people like you both are very helpful! What was the modification drug you spoke of at the end – MS Therapies? Calcium is bad?
    Take care,
    Thanks again,
    Karen

  9. I HAVE HAD TREMORS IN MY LEFT HAND FOR NEARLY SIX MONTHS!ON TOP OF THAT I WAS BORN WITH ONE HAND(RIGHT HAND MISSING) WHICH MAKES IT VERY HARD TO WRITE AND EAT. I HAVE BEEN WITH MS FOR ABOUT 5- 6 YEARS.MY FIRST CASE WAS OPTIC NEURITUS IN MY RIGHT EYE THAT CAME BACK ABOUT 75 PERCENT!WHAT SHOULD I BE DOING TO HELP THIS SITUATION I AM IN!I AM A INSPIRATION TO PEOPLE,BUT THIS IS MAKING THINGS VERY DIFFICULT!

  10. So incredibly helpful. I reached a point a while back where I felt I’d covered all reading, on every different approach. I had sorted the supplements that made a difference, and while the odd alternative exploration proved useful for one reason or another, after a while those I had felt so beneficial seemed to be left wanting recently. This webinar has opened the possibilities again. There are so many more ‘supplements’on the market. And possibly the essence of what I’d like to ask is something many would like the answer to.
    As best possible I avoid stressfull situations and life proceeds smoothly, but what to do when, as has happened to me, your sister dies. All seemed under the control of the supplements. What now? Melatonin stole the sleep and ran off with it. How to stay calm. Stop the trigeminal creep. So many with Multiple Sclerosis are prescribed anti-depressant medications. Would supplents suffice? Could one use GABAtropin?

  11. This was a very informative webinar – i listened to the replay because i was off my computer for a week and was unaware of this webinar – thank u so much Dr. Cartwright!

  12. I’VE BEEN DX WITH MS SINCE MARCH ’08. I’M 27 YEARS OLD AND I’M CURRENTLY A LPN. WHEN I WAS FIRST DX WITH MY CONDITION I DIDN’T TAKE IT GOOD AT ALL. I LOST ALOT OF WEIGHT AND CRIED DAY AND NIGHT, HAD SUICIDE THOUGHTS AND DIDN’T GIVE A DAMN ABOUT ANYTHING IN THE WORLD. BUT ONCE I STARTED PRAYING AND TAKING BETTER CARE OF MYSELF I FELT SO MUCH BETTER!

  13. I want to know more about the Essentials and what’s in them. I have following the Dr. Klenner protocol and want to start on the Essentials.
    God Bless you both and also Sue Ellen for all your help.

  14. Well, I’m trying to get a D3. I’ve heard about it a long time ago. Here where I am now, Europe-Bosnia they have it in a form of something called BETAGLUCAN 500. It was told that in that pill is the biggest concentration of D3. So, what can you tell me about that, I mean is it in the same form back in States or they got something different? And I also need to inform you that I recently got out of the wheelchair. At that time I was using pills called Germanium 132. But the key thing about it is that this Germanium is organic. Not chemical, thank God!

  15. I can’t make out if it is vit B or D, and the vit for the nervous system I can’t make out either, but this is all so interesting. I am on Tysabri can I use these things.

    Regards
    Pat in London

  16. Thank you so much. My computer has been down, so I have only just listened to your webinair. Really informative. I have PPMS. A bit of a battle at the moment, but I do see my struggling at a “blip” and I know I will beat it.

  17. I ordered the essential today. Do i still take vim d3, capasin , alpha lopoic, and catalase together with the essentials i get from you guys.

    thank you foe all your help

  18. Very interesting &informative, I never thought how valuable supplements are.
    Thanks to you, I’ll make sure I’ll take more supplements especially b/c I have MS.

  19. I don’t have time to listen to the whole thing right now because I have an appointment at the hospital for the 2nd of 3rd dose of solu medrol. I have been seeing a homeopath and taking supplements for quite a while but also taking several prescription meds. I am trying to gain weight. (5’7″ 109 lbs) Thanks for listening.

  20. one of the family got m.s. but its called begin,.i hope i spell correct,.dose it mean it get worse at the moment he has not taking any medican with last year ,. i pray for him rvery day,.with god help that might leave him god bless

  21. Stumbled upon this website. Have had MS 20 yrs. Am 47 with SP MS. In order for vit. D to be effective and absorbed is it true that calcium be included with Vit. D?
    Thank you

  22. What brand of vitamin d3 should you buy… what vitamin can i take for ringing in the ears.. I do not have ms but my daughter do, and i take vitamin D3 and i will start giving this vitamin d to her…

  23. Hi
    When I read the label on a bottle of Catalase supplements,it contains wheat Is this a problem/ or is it a different type?

  24. Thanks a whole bunch for this great info. I know already that vit. D and Calcium is good for us with M.S. This I already take. I feel well, but I will try other products.

  25. i’d lik to no about kalawlla i’ve been on it 2 years i believe it hashelpedme but would like to hear from you bout it?

  26. what is the most important list of neutrants that should be taken in one day as I am taking all natural neutrant?

    John

  27. Hi, this is all very interesting to me (MS patient living in Dublin regularly in Ct.). Wish there was a way we could all hear the replies! A number of people have raised issues I would like to know more about. Thank you!

  28. I take vitD, daily, and inject myself with Rebif, 3x a week.
    But I think I am immune to my meication, as I do not notice
    any difference now. I have taken rebif for 5 years.
    I am now based in the U.K. and desperately want to get back to the U.S.
    where I had a brilliant neurosurgeon.
    I should never have moved away.
    Still have a house in Atlanta, GA.
    Where my daughter and son are based,and all my friends.
    But here in the U.K. they tell me not to drive?
    How do I get around then?
    U.K. doctors and neurologist seem happy to put me in a wheelchair.

  29. *Good evening Dr Cartright and Scott,

    I’ve been listening to your webinar and i have to say thank you for the so much information you provided. Now i have an understanding about what is going on with my MS. I hope with your help i will be able to turn MS around. May God be with you both and with all the Doctors who are there to help patients.

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