Okay sorry for so many posts just freaking out about this peyronies disease..
I’ve been taking ViT E 400iu (AC GRACE UNique E) a few times a week for last few months but urologists can recommend up to 800IU a day for PD for 6 months. Although it’s not well known to have a massive helpful effect i guess it’s better than nothing.
It’s well known here it shouldn’t really be taken everyday, I don’t know if thats because the quality is not where it should be or what ever but what is bad about taking it everyday and in my situation with Pey disease is it worth giving it a go everyday?
:)
I’ve been taking ViT E 400iu (AC GRACE UNique E) a few times a week for last few months but urologists can recommend up to 800IU a day for PD for 6 months. Although it’s not well known to have a massive helpful effect i guess it’s better than nothing.
It’s well known here it shouldn’t really be taken everyday, I don’t know if thats because the quality is not where it should be or what ever but what is bad about taking it everyday and in my situation with Pey disease is it worth giving it a go everyday?
:)