New era for ME/CFS research as top cytokine study attracts media headlines
The immune systems of patients who have recently developed ME/CFS look markedly different from those who have been ill for much longer, according to a major new study from Drs. Ian Lipkin and Mady Hornig at Columbia University. This shift in immune function hadn’t been seen before.
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Any experience with Phosphate formulas?

Discussion in 'General Treatment' started by SaraM, Oct 3, 2011.

  1. SaraM

    SaraM Senior Member

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    I am thinking of trying Cal, mag, and potassium phosphate supplements for reducing muscle pain. The only supplements I could find are manufactured by Hyland's homeopathic. Somebody on this forum once mentioned having good results with phosphate minerals. I do not eat dairy, and I am probably phosphorus deficient. Any experience with phosphate?
     
  2. SaraM

    SaraM Senior Member

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    I tried Cal, and Mag phosphate made by Hyland's with no positive or negative effect. Then I started taking dicalcium phosphate by Carlson lab. The daily dose is 3 caps ( 1000 mg Cal and 774 phosphorus). I can take 1 cap with no problem, but when I take 2, I get a severe headache- I am not a headache person. It seems that I have a problem with phosphorus or phosphate and I wonder why, because my diet lacks foods rich in phosphorus. Does this mean CFS patients have problem with this mineral?
     

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