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Vitamin D again

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The whole vitamin D issue has me totally frustrated. I was put on

50,000 u of Vitamin D2 (thought, like others, that it was D3), then

100,000 U weekly. I just got my latest labs back. My overall level is

up at 93 with a reference range of 30 - 100. But when I look at the

breakdown my D3 is only 6 ng/ml while my Vitamin D2 is at 87 ng/hl. I

want to be in a healthy range for bone health - osteopenia being an

issue. I know the jury is out on whether increasing the D3 level makes

a difference after diagnosis, but it doesn't hurt to be on the safe

side for that reason as well. Do I continue with D2, add D3 as well,

or just take D3 and if that is the answer is dosing basically equal or

should I adjust up or down if changing from D2 to D3???????? I have an

appointment coming up with my primary care to discuss this and would

like to go into the discussion as informed as possible. She is very

open to input that relates to my CLL.

Any input appreciated!!

Pat

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Are these units right? 50,000+ IU? I thought a megadose was 1000 IU.

>

> The whole vitamin D issue has me totally frustrated. I was put on

> 50,000 u of Vitamin D2 (thought, like others, that it was D3), then

> 100,000 U weekly.

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I know several other people who were put on the same dose weekly, not

daily, and monitored closely until the D level went up. If you start

dong a lot of reading on this subject it's very difficult to know who

to believe. Suggested daily doses ranged from 1000 to 5000u. Most of

the articles I read suggest Vitamin D3 and all suggested making sure

your level is monitored, esp. if you are taking mega doses because you

are deficient. It seems we all have different needs as far as a

maintenance dose goes.

Pat

On 1/20/11, mschaeffer3 <mschaeffer3@...> wrote:

>

> Are these units right? 50,000+ IU? I thought a megadose was 1000 IU.

>

>

>>

>> The whole vitamin D issue has me totally frustrated. I was put on

>> 50,000 u of Vitamin D2 (thought, like others, that it was D3), then

>> 100,000 U weekly.

>

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My wife and I continue to take 5000 IU daily and have our

levels checked every 6 months. We're both in normal ranges

and feel well. I was originally taking 8,000 IU daily based

upon what my nutritionist told me. Minimum I would suggest

is 1,000 IU. D3

Best to y'all.

On Fri, Jan 21, 2011 at 9:10 AM, Beth Fillman wrote:

> my gp is adamant about D3 only, and finding the most

> absorbable 'brand'.

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Thanks for all the responses. If you are taking prescription Vitamin D

you should check with your pharmacist about whether it's D2 or D3. I

thought I was taking D3 - the label just said Vit D and the dose. It

in fact was D2 and I noticed that when I refilled the prescription the

label specified D2, so maybe all of this taught my pharmacy something.

My pharmacist is wonderful and very careful about checking things like

drug interactions, appropriate doses,etc. He is a great backup to a

good medical team and the doctors in the area respect the fact that

he will question something that seems off (eg when the fact that I'm

on coumaden might be an issue with a new prescription).

I understand the issue of overall vit D levels being within a certain

range. It's the fact that the reports then break things down into D2

and D3 levels where I have a problem. Should the D3 level be within a

certain range or does it matter if it's much lower than the D2 level.

Thanks

Pat

On 1/21/11, Sharon - Medical <smodesti18@...> wrote:

> My wife and I are taking 50,000u 2x / month of pharmaceutical grade D that

> we received from her internist who is also monitoring her blood levels.

>

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Diagnosed in May 2010 I am on watch and wait; wbc 22,800. After reading the

importance of vitamin D on this forum I decided have my level checked. I was

surprised to find my insurance does not cover this as part of my routine blood

test! I decided to pay for it out of pocket (still don't know how much it will

cost) and found my level is 37, which is on the low side of normal (32 - 100). I

have been supplementing with 1000 iu of vitamin D3 per day since last

November, and my doc says to stay with that. I plan to have my level checked

again in a May by my general practice doctor, and I'm told insurance will cover

it then. Does this make any sense? Why doesn't insurance cover vitamin D

monitoring at my oncologist office?

Hollie

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Normalizing Vitamin D levels may or may not have any effect in CLL.

The recent Mayo clinical study was very clear on this.

" Whether normalizing vitamin D levels in deficient CLL patients would improve

outcome merits clinical testing. "

http://bloodjournal.hematologylibrary.org/cgi/content/short/blood-2010-07-295683\

v1

~chris

>

> Diagnosed in May 2010 I am on watch and wait; wbc 22,800. After reading the

importance of vitamin D on this forum I decided have my level checked. I was

surprised to find my insurance does not cover this as part of my routine blood

test! I decided to pay for it out of pocket (still don't know how much it will

cost) and found my level is 37, which is on the low side of normal (32 - 100). I

have been supplementing with 1000 iu of vitamin D3 per day since last

November, and my doc says to stay with that. I plan to have my level checked

again in a May by my general practice doctor, and I'm told insurance will cover

it then. Does this make any sense? Why doesn't insurance cover vitamin D

monitoring at my oncologist office?

>

> Hollie

>

>

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