NEW! Ask each other what to do for MTHFR. Share your experiences, thoughts, protocols from other doctors and how it is working for you. I want this to be the most active forum. You are living with MTHFR mutations and your experience must be shared with others to provide them insight. Thanks!

Please locate a Topic that is similar to your situation and add your question to it. There are already over 58 Topics here so possible to find a similar one. This helps us all find information quickly. If you do not find a similar Topic , please create a new one: 1) Title the new Topic with the type of MTHFR mutation and main concern. [Ex. "MTHFR C677T heterozygous and chemical sensitivity'] 2) Ask your question clearly and extensively. PLEASE FEEL FREE TO SHARE YOUR THOUGHTS and experiences to others. You may respond to anyone if you feel you have useful information to share.  

What is your MTHFR protocol? Is it working for you? Be specific! What are you taking? How much? How long have you been doing it? Did you have to ease into taking what you are now? Who is your doctor?