Best biomarker for PFS & Are there Portuguese in the forum?

no prob but i wasn’t asking you if i should do it, that’s something i ask myself. i just wanted to know how much sucess you had. i’ll read that thread better, and your posts, but thanks for helping me! :slight_smile:
i moved to belgium actually! for me it’s all the same really, uk, be, elsewhere, as the place i’d like to be is back home… if not possible in the south then in lisboa
it’s a beautiful place , i’m glad you liked it!
no one expected it to happen really…but i’m positive, i think we’re getting better , i think this year there will be a turnaround in the markets and maybe in few years we’ll be able to see change. and then maybe i can go back home :slight_smile:

just got active b12, folate and p5p.
i also got d3 vitamin…
i will start with b12 folate and p5p only as soon as i get them. in the long run i may add d3 as i live in a not very sunny place and im from a sunny place originally

will let you know. i hope this will not be another € spent on supplements withouth any return. i read the theory and it makes sense to me.

i would like to run a genetic test too, because of MTHFR, because in my family my uncle had anxiety/depression/insomnia issues, my grandma has also nervous system issues, my mom had a couple epileptic crises, like me, and has anxiety/depression…(low grade depressions, we’re fully functional).

my mom’s epilepsy crisis showed up after a vaccination and mine showed up after a medication.
my muscle spasms also showed up after a medication.
could be i have chemical sensitivity…