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Fibromyalgia & LDN

Posted , 8 users are following.

TeresaJS
TeresaJS

I've been on LDN for 2 weeks now. Started at 2,5mg increasing 0,5 a week, now at 3,5. I see some improvement. wink Anyone's taking it?

1 like, 35 replies

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  • TeresaJS
    TeresaJS

    Posted

    Cort Johnson has an amazing web site about FibroM and CFS’s alternative therapies one of them being LDN. Maija Haavisto is one of the site’s contributors  and a young women who’s been on LDN for over 8 years now. She actually wrote a book about her journey. She became an expert and alternative treatments advocate. There’s a really interesting interview with her at the site.  
  • TeresaJS
    TeresaJS

    Posted

    To let you all know: 

    I've been on LDN for 2 and half months now and couldn't figure ou the right dose yet. I got serious shoulder inflammation meanwhile and because of some menopausal bleeding (I guess) I became very weak. Blood work found that I was low in ferritin, had severe vit. D deficiency, a number of undetermined oddities in the thyroid besides adrenal dysfuntion. I also had some  excruciatingly painful cramps and meanwhile my walking became weird. I'm borderline panicky with any prospect of having MS. It's even hard to say it but ther it is.

    I don't know what LDN is doing for me (it started well though) but it seems to hav opened the Pandora's box. 

     

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