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Cluster Headache Help and Support >> Getting to Know Ya >> Old/new member http://www.clusterheadaches.com/cgi-bin/yabb2/YaBB.pl?num=1448132596 Message started by Kim Dawn on Nov 21st, 2015 at 2:03pm |
Title: Old/new member Post by Kim Dawn on Nov 21st, 2015 at 2:03pm
Hi all! I'm Kim. I was on this site a long time ago, I believe my ID was kimmiedawn8199. Well, looks like the beast is back, after almost 4 years hiatus. Not really good timing since I just gave birth 2 weeks ago. Just trying to make sense of the Vitamin D3 regimen.
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Title: Re: Old/new member Post by Mike NZ on Nov 21st, 2015 at 3:18pm
Hi Kim and welcome back, although sorry your return is from CH returning.
Congratulations on the new arrival too. D3 can work wonders for preventing CH, with some of us having gone multiple years CH pain free as a result. Send Batch a PM and he'll update you with everything you need to know about D3. |
Title: Re: Old/new member Post by Kim Dawn on Nov 22nd, 2015 at 1:30pm
Unfortunately that wasn't me who was a success story 4 years ago. I'm hoping I can be a Vitamin d3 success story very soon though :)
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Title: Re: Old/new member Post by Batch on Nov 22nd, 2015 at 8:47pm
Hey Kim,
You're correct... it was another Kimmie... sorry about the confusion... The other Kimmie lives in Texas... On top of that there's at least one more Kim that I've worked with on vitamin D3 and oxygen. Her CH returned two weeks after the birth of her latest child... Take care, V/R, Batch |
Title: Re: Old/new member Post by Batch on Nov 23rd, 2015 at 2:04am
The latest from GrassrootsHealth on Vitamin D3... Good stuff...
Take care, V/R Batch Daily Dosing How is vitamin D absorbed and used in your body? Vitamin D3 enters the body through sun exposure, diet or a supplement and goes into the blood stream where much of it binds to the vitamin D binding protein (VDBP) -- a protein that carries vitamin D compounds into circulation. From there, vitamin D3 functions within two systems in the human body - the endocrine system and the autocrine/paracrine system. #1 - The Endrocrine System - for skeletal health The endocrine system - this long studied system for action by vitamin D - is where calcium homeostasis and bone health are maintained. Vitamin D3, from UV exposure or diet, is delivered to the liver, converted to 25-hydroxyvitamin D, or 25(OH)D, and moved into circulation where it has a half life of approximately three weeks. As necessary, 25(OH)D is then transferred to the kidney where it is further converted to the active form of 1,25(OH)2D which has a half life of only a few hours. This active form can then help control calcium absorption and bone health. All the successful studies on vitamin D and bone health have benefited from the long half life and availability of 25(OH)D. For bone health, the important thing is the amount of 25(OH)D available, rather than direct intake of vitamin D. #2 - The Autocrine/Paracrine System - for autoimmune health What has not been appreciated until relatively recently is that in addition to being delivered to the liver for conversion to 25(OH)D, vitamin D is also delivered directly to all tissues of the body. Many of these tissues, such as breast, colon, prostate, and brain, can convert vitamin D to its active form within the tissue. It is through this process that vitamin D can help enable the cells to fight against infections, disease, and autoimmune disorders. Vitamin D has a half life in the autocrine system of roughly 24 hours, so in order for it to have a meaningful impact on cellular functions, you need a new supply of it every day. This new understanding means that frequency of dosing matters when testing for disease reduction and immune control - large monthly or quarterly doses that are effective for bone health will not show positive results for disease reduction. For disease prevention and treatment, daily dosing (food, sun, supplement) is very important! Do nursing mothers need daily D3? Without daily dosing, breast feeding mothers could have 50-60 ng/ml of measurable 25(OH)D in their blood but no measurable vitamin D3 in their breast milk. After vitamin D3 has been turned to 25(OH)D it cannot enter the breast milk. The only way to get vitamin D in breast milk is by dosing daily - either by sun, diet or supplementation. Dr. Hollis' research indicated that 6,400 IU/day was necessary for breast feeding mothers to attain sufficient vitamin D (to the value of 400 IU/day for the infant) in their breast milk. Why does this matter for clinical trials? Most of the clinical trials conducted in the past 40 years have focused on the endocrine system and have consistently shown the positive effects of vitamin D on bone health regardless of dosing regimen (from daily to quarterly). In the past 10 years, many new clinical trials have focused on non-skeletal outcomes such as autoimmune disorders, cancer, cardiovascular disease and infections. These new studies have also used various dosing regimens--but have yielded inconsistent results. Those with adequate daily vitamin D inputs have largely shown positive results while those with longer dosing intervals have shown no vitamin D effect. While 25(OH)D levels are maintained in these studies, it is the vitamin D3 levels that are essential to these systems. Therefore, it is necessary to design a clinical trial based on the physiology of the system of interest in order to accurately assess the effect of vitamin D in the body. Conclusion "Circulating vitamin D, the parent compound for tissue vitamin D activation, likely has an important direct physiological role beyond what was originally anticipated through the local tissue autocrine system." Schedules for vitamin D dosing could have profound effect on health outcomes. (Edited to add my editorial below...) Most of the RCTs in the last year that used vitamin D3 as the intervention failed to give it at a phamacological dose of 5,000 IU/day to 10,000 IU/day. Only one of these RCTs used a vitamin D3 loading dose and all of these RCTs treated vitamin D3 as a mono-therapy, i.e., no cofactors... Here are the examples from queries on clinicaltrials.gov listing vitamin D3 Cholecalciferol as the intervention covering the last year (received on or after 11/01/2014 | updated on or before 11/01/2015). 47 studies found for: Vitamin D3 /day cholecalciferol | Vitamin D3 Cholecalciferol i.e., a daily dose of vitamin D3. 5 studies found for: Vitamin D3 4000 IU /day cholecalciferol 1 study found for: Vitamin D3 5000 IU /day cholecalciferol 1 study found for: Vitamin D3 7000 IU /day cholecalciferol No studies found for: Vitamin D3 10000 IU /day cholecalciferol 1 study found for: Vitamin D3 4000 IU/day Cholecalciferol plus a Multivitamin None of the above studies included the vitamin D3 cofactors: magnesium, zinc, boron, vitamin A (retinol). When you read through these RCTs you come to the conclusion that nearly all of them were poorly designed to investigate the autocrine/paracrine role of vitamin D3 in genetic expression... This was either do to ignorance of vitamin D3 pharmacokinetics and pharmacodynamics, or... these RCTs were intentionally designed this way in order to ensure inconclusive results... Big Pharma likes vitamin D3 RCTs with inconclusive results... and for good reason... It would be very bad for their bottom line to have 12 cents worth of USP vitamin D3/day found to be more effective in treating a medical disorder than a patented monoclonal antibody costing ≥ $5000/month... Sooo... for those of us taking the anti-inflammatory regimen with 10,000 IU/day vitamin D3 and the vitamin D3 cofactors to prevent our CH... and stay a lot more healthy in the process... we're way out in front of the vitamin D3 intellectual power curve... Take care and keep on trucking... V/R, Batch |
Title: Re: Old/new member Post by blacklab on Nov 23rd, 2015 at 11:53pm
What a great read Batch, thankyou
colin |
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