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Posted by jblral (Member # 8836) on :
 
Has anyone ever had their Vitamin D levels tested? Interesting article in the LA Times about Vit. D deficiency.

The complete article can be viewed at:
http://www.latimes.com/features/health/la-he-vitamind12jun12,1,5420197.story
 
Posted by Lisianthus (Member # 6631) on :
 
Yes, I've had mine tested, and I was low. I now take a supplement and by docotrs orders I have a nice tan [Big Grin] I sit in the sun every morning and read and have my forbidden coffee. [Wink] It just feels really good to soak up the sun.

Thanks for the link to the article jb. I didn't realize vitamin D did all that [Eek!] Very interesting.

My son was tested too and the doc gave him cod liver oil with vitamin D in it. (I prefer the pills)

Lisi
 
Posted by dguy (Member # 8979) on :
 
Since Lyme bacteria consume the form of vitamin D measured by the standard blood test (25D), most Lyme patients are found with low levels. Taking vitamin D supplements before getting the infection under control will only give the bad guys more fuel to work with.

The proper blood test for us also measures 1,25D which is what the bacteria are busily converting the 25D into. If you don't know your 1,25D levels (often too high in Lyme patients), taking in more D via diet or sunlight may be doing more harm than good.
 
Posted by sofy (Member # 5721) on :
 
dguy

My D is low & my endo just told me to boost my intake of D3.

I would like to show my lyme & endo docs this info. Can you give me a source where I can find this info that a doc will look at?

I trust your statement but docs want something more that just a post from someone on a lyme site.
THANKS
 
Posted by dguy (Member # 8979) on :
 
This describes the involvement of vitamin D:
http://www.marshallprotocol.com/forum2/4062.html

This tells about how to test D levels and interpret the results (fairly easy to read):
http://www.marshallprotocol.com/forum2/366.html

This describes the science, and involvement of vitamin D (warning: somewhat technical):
http://www.marshallprotocol.com/forum2/2810.html

The site also has a section reserved for professionals that your doctor can access.
 
Posted by pq (Member # 6886) on :
 
Some things to consider with respect to vitamin D:

Raw Numbers at: http://lassesen.com/cfids/raw_survey_results.htm
Simple form at: http://lassesen.com/cfids/protocols.htm

http://health.groups.yahoo.com/group/CFSProtocol/messages/1 at this link,the reader is referred to the first 10 messages which give links to abstracts and studies on vitamin D; its role in the body as such, is discussed by group members.
http://health.groups.yahoo.com/group/olmesartan/
http://www.lassesen.com/cfids/MarshallProtocolRisks.htm

http://www.lassesen.com/cfids/marshall.htm

http://impnvestigator.chat.ru/

[ 21. June 2006, 12:54 AM: Message edited by: pq ]
 
Posted by pq (Member # 6886) on :
 
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[ 20. June 2006, 01:16 PM: Message edited by: pq ]
 
Posted by dguy (Member # 8979) on :
 
In fact it was a chart (since removed) on the anti-MP lassesen.com site that convinced me the MP was a good thing to try. This particular chart graphed the success rate of the MP vs vitamin D ratio.

The chart showed the MP was rarely successful for people with a 1:1 ratio of 1,25D to 25D. But the success rate increased steadily as the vitamin D ratio did, up to about 80% at the 3:1 ratio, the ratio that many Lyme patients have.

My 3.5:1 ratio is so extreme, it was off their chart, off the chart in the direction of increasing success. So, even the detractor's site was saying the MP was very likely to be a cure for me and many other Lyme patients.

The other links pq listed above are mainly attacks on TM. If you spend timing reading TM's posts on the marshallprotocol site, you'll quickly see why he has detractors. I try to ignore TM's attitude and instead concentrate on the science, and I'm convinced there's something to the protocol. I think it's worth a look by anyone with abnormal vitamin D ratios.
 
Posted by pq (Member # 6886) on :
 

 


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