yup I heard about the vit D insufficiency so am taking it, B12 I find hard to take as wonko has said,maybe I will try sublingual .. good thread I have wondered what to ask my health food store to get for me..
Taking Vitamin D supplements is surrounded by some controversy. I'm just now doing some reading that applies to it ... the general theme is that having low Vitamin D is a symptom and result of Lyme activity, and by supplementing, the Lyme bugs are strengthened and fed. I just got and am reading a book by Bryan Rosner called The Top 10 Lyme Disease Treatments and will give a brief review of it when I'm done reading, and he talks about Vit D.
I was told I had very low Vit D before I was finally diagnosed with Lyme, and I resisted taking huge doses of Vit D, because it just didn't make sense to me: I'd rather go sit in the sun and make my own Vit D. (There is a HUGE medhelp forum on Vitamin D and if you want to read posts by some very ill people who have been sick for a long long time, that's the place to go. Makes the bunch of us here sound almost healthy.)
The short story from the Rosner book (and other places) is: Vitamin D is not actually a 'vitamin' like Vitamin C -- it was misnamed long ago. Vitamins are necessary in the diet to have good health and are gotten through food intake, but Vit D is not normally gotten through food, only through exposure of the skin to sunlight. Rosner's book says Lyme bacteria and cell wall deficient (CWD) bacteria interfere with the body's balance of converting Vit D to a usable form called 1,25-D, by causing *too much* conversion from D to 1,25-D, which in turn suppresses the immune system and keeps your body from killing the bacteria. Therefore the more Vit D you take when you are sick with Lyme/CWD, the more 1,25-D the bugs can create and the more they suppress your immune system and produce inflammation and keep themselves alive.
Okay, I'm not sure I buy this theory, which is why I'm reading up on it. There is a Dr in So.Calif. named Trevor Marshall who has invented something called the 'Marshall Protocol', which has a point of view that you stay OUT of the sun and don't take Vit D (among other actions) in order to cure Lyme/CWD infections. I looked at their website a year or so ago and found it a bit cult-like but keep running across mentions of it, like in this Rosner book (which I find very wordy).
Drs insist that everyone take a bunch of Vit D, and with Vit D added to milk and all sorts of foods, it's hard to avoid -- never mind avoiding sunlight. One of my very nice and highly trained (nonLLMD) Drs insisted that I must 'refill' my empty tank of Vit D with 50,000 IU pills, which made no common sense to me, so I didn't do it -- I said I'd go sit in the sun instead. Those folks over on the medhelp Vitamin D forum keep taking tons of Vit D and so far I keep reading it's not working for them, their levels drop back immediately upon ceasing intake of it, and they are still sick as dogs and don't know why. Bottom line: taking Vit D might not be as good as the drs think.
Usual apologies for the looong post. My review of the Rosner book will follow eventually.
Personally, I don't buy it. I looked into it before and discussed it with my LLMD. And from my own experience (or what's most important to me, hehe) I do better supplementing D.
But there are others who say it makes them feel worse, so caution may be key here.
I also have avoided the huge doses of D. Perhaps a reasonable approach to this is to get tested. If you are low, start with a small dose supplement (I started with just 400 IU) and see how you do. I'm now up to 1000 IU bid, and am waiting for my latest blood work. Of course, always ask your doctor too.
Agreed, definitely talk to your doctor(s) before deciding what to do.
I DO go sit in the sun for a bit when I can, and I feel better afterward, so either Marshall's theory is wrong overall, or the theory is wrong for me (but not necessarily for others) .
It may well be that the Vit D thing working or not depends on what kind of bug(s) one has. So much not known ...
What I have not seen is any statement by any MD anywhere (please forward data if you have it!) as to WHY there are people including me with such terribly low Vit D levels. That's why I didn't wolf down the big amounts the nonLLMD gave me...there has to be a reason why my levels are low.
Copyright 1994-2017MedHelp International.All rights reserved. MedHelp is a division of Aptus Health.
The Content on this Site is presented in a summary fashion, and is intended to be used for educational and entertainment purposes only. It is not intended to be and should not be interpreted as medical advice or a diagnosis of any health or fitness problem, condition or disease; or a recommendation for a specific test, doctor, care provider, procedure, treatment plan, product, or course of action. Med Help International, Inc. is not a medical or healthcare provider and your use of this Site does not create a doctor / patient relationship. We disclaim all responsibility for the professional qualifications and licensing of, and services provided by, any physician or other health providers posting on or otherwise referred to on this Site and/or any Third Party Site. Never disregard the medical advice of your physician or health professional, or delay in seeking such advice, because of something you read on this Site. We offer this Site AS IS and without any warranties. By using this Site you agree to the following Terms and Conditions. If you think you may have a medical emergency, call your physician or 911 immediately.