Okay so my Total D is 19, obese people seem to be challenged in producing Vitamin D through sun exposure and having had my gall bladder out, I may not be able to absorb the mega dose or the nutritionally available doses in the sardines, salmon, milk/yogurt, eggs, etc. Wondering if it is possible to be toxic/overdose on the way to trying to get my blood levels up. I've been living in mind-blowing, life-shattering pain for 7 months. None of my docs will even answer my questions about pain management. The rheumatologist won't see me until I've had 3 months of Vitamin D mega dose therapy (one pill a week for 12 weeks). I guess I understand that one...adequate Vitamin D levels will reduce inflammation and may change the rheum diagnosis picture. I just don't understand why we can't get me functioning muscularly/motor issues/neuro issues at a higher level so that I don't need the courage and faith of Gandi and the Dali Lama combined just to get through each moment. I'm getting 15 minutes of sun exposure without sunblock 6-7days per week (non-obese folks only need 2-3 days). I'm trying to keep my attitude up and my expectations reasonable but tonight I'm in too much pain to sleep and I'm frightened because despite all my attempts, the pain is getting worse and more constant.
I too am obese but suffer from migraine symtoms as part of my fibromyalgia which make me photosensative. Even with sun glasses on i struggle with sunlight. I have been on two pills a day for 6 months with barely a difference to my vitamin D levels.
I havent always had a vitamin D problem but the doctors arent sure when the problem started.. my Vitamin D levels were fine when the Fibro started two years ago but my blood wasnt tested again till january 2009 when it was discovered i had the problem.
I have been told today we are going to try 6 monthly vitamin D injections as well as the 2 daily pills to see if that increases my levels.
The really really odd thing is that i have been having my blood tested monthly and i went on holiday abroad to Cyprus for two weeks where i was outside in the sun sunbathing daily and it didnt effect my Vitamin D levels much that month.
I dont know much about the condition only what my General Doctor printed out... which was pretty handy... the link is http://www.patient.co.uk/showdoc/27001328/ its worth checking out.
I havent always had a vitamin D problem but the doctors arent sure when the problem started.. my Vitamin D levels were fine when the Fibro started two years ago but my blood wasnt tested again till january 2009 when it was discovered i had the problem.
I have been told today we are going to try 6 monthly vitamin D injections as well as the 2 daily pills to see if that increases my levels.
The really really odd thing is that i have been having my blood tested monthly and i went on holiday abroad to Cyprus for two weeks where i was outside in the sun sunbathing daily and it didnt effect my Vitamin D levels much that month.
I dont know much about the condition only what my General Doctor printed out... which was pretty handy... the link is http://www.patient.co.uk/showdoc/27001328/ its worth checking out.
Kelly
My doc said take 1000.
I did research online and found the Vitamin D Council recommends mega doses so 6000 it was.
I got retested 6 months in and my levels were 91 :D
Then I decided I would go back to 1000mg
The symptoms returned almost immediately
1000mg is simply not enough for Me. I should not be deficient due to my lifestyle but I am and suspect it may be genetic somehow.
Now I am taking 3000mg a day which is only 3 tiny capsules and I feel great.
The symptoms (sweaty face, exhaustion, weakness and night blindness) have gone.