Phoenix Rising supports the Millions Missing global day of protest
Phoenix Rising is delighted to support the demands being made in the ME/CFS community’s first-ever global day of protest …
Discuss the article on the Forums.

Mucuna Pruriens - Anyone tried it?

Discussion in 'Alternative Therapies' started by shepard515, Dec 6, 2013.

  1. shepard515

    shepard515

    Messages:
    9
    Likes:
    0
    Boston, MA
    I was recently reading up on the mutations in my methylation pathway and the best protocol moving forward when I stumbled on mucuna pruriens in some of Dr Amy Yasko's literature. I've been struggling with severe depression for a number of years (I believe as a result of my methylation being messed up) and this looked like it could be a beneficial supplement to take. I am currently on Methyl B12 and will be adding in methylfolate this weekend. The methyl B12 has been helping with energy, mood and overall health issues I've had but still have a long way to go. This post is mainly directed at whether or not anyone has used mucuna and if it has been beneficial for them. Thanks in advance!
     

See more popular forum discussions.

Share This Page