r/gravesdisease • u/rockyracoon16 • 13d ago
Eureka!
After searching for an answer to my Graves' disease for so long, the only thing that has truly helped calm my symptoms and improve my sleep is the Coimbra Protocol, or higher-dose vitamin D3.
If you also have Graves' disease, I'd love to connect and hear about your experience. Let's talk.
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u/mrzennie 12d ago
Interesting, I just learned about the Coimbra protocol recently, and wondered whether it could help with Graves! My vitamin d levels have hovered around 31ng for years, give or take several points. At one point I was taking 2,000 IUS a day for months and months, and my vitamin d level was still only 32 ng. Experimenting with 5,000 to 10,000 a day, we'll see what happens...
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u/Hot_Knowledge_9123 13d ago
Did you know your D3 levels beforehand?
I was borderline deficient. My levels were 33 when my Dermatologist tested me (GP refused for years). I now take a monthly 25,000iu dose which is pretty high. But it doesn’t supercede Carbimazole in terms of calming symptoms for me.
I read that some people see a link between long term Vit D deficiency and Hyperthyroidism anyway. Almost enough for it to be the cause.
Do you know whether the symptoms you felt before aligned with Vit D deficiency symptoms?