Home Forums General Discussion L- Arginine – Raynauds

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  • #302162
    BrendanG
    Participant

    Hi

    Has any one used L-Arginine for treatment of Raynauds?  I note that there is quite a bit of web info suggesting it is helpful,  but also a caution that it may contribute to renal fibrosis.

    Brendan

     

     

    #329186
    JOJO19551
    Participant

    Brendan, I have not tried this but I do use Grape seed extract tablets every day and what a difference!!  Jo Ann

    #329187
    MaryP
    Participant

    I generally avoid arginine rich foods and supplements as I've read that mycoplasma thrive on them.    Here's one article.  http://www.rain-tree.com/myco.htm .  It's ok to link an article, isn't it???

    #329188
    Maz
    Keymaster

    [user=53]MaryP[/user] wrote:

    I generally avoid arginine rich foods and supplements as I've read that mycoplasma thrive on them.    Here's one article.  http://www.rain-tree.com/myco.htm .  It's ok to link an article, isn't it???

    Hi Mary,

    Thanks for asking – yes, perfectly find to use links! 😀 RBF just has to be careful of whole articles being cut and pasted into posts, as this might incur copyright infringements. Quoted material is fine, like a few lines or a paragraph from an article, as long as the link to the article and full credit is given to the author.

    Hope that explains things?

    Peace, Maz

    #329189
    Trudi
    Participant

    [user=53]MaryP[/user] wrote:

    I generally avoid arginine rich foods and supplements as I've read that mycoplasma thrive on them.    Here's one article.  http://www.rain-tree.com/myco.htm .  It's ok to link an article, isn't it???

    Great article.  I'm actually on l-arginine for blood pressure; something else to discuss with the doctor!!

    Trudi

    Lyme/RA; AP 4/2008 off and on to 3/2010; past use of quinolones may be the cause of my current problems, (including wheelchair use); all supplements (which can aggravate the condition) were discontinued on 10/14/2012. Am now treating for the homozygous MTHFR 1298 mutation. Off of all pain meds since Spring '14 (was on them for years--doctor is amazed--me too). Back on pain med 1/2017. Reinfected? Frozen shoulder?

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