Hi. I'm trying to narrow down the countless treatment options for MCS. My reactions seem different than most. I am reacting to foods ( I only have 6 safe foods), supplements, chemicals etc,,
What type of reactions would you get to supplements? Since my reactions are more with the autonomic nervous system , do you feel the Carrick Brain Center would be helpful?
Any insight is greatly appreciated as I am determined to heal. I don't want to take supplements or do IV treatments that will make me worse.