I'd also get your DNA tested for the MTHFR mutation.

Errors in methylation, as I quoted to you last week, and Marlene
suggested just recently, may explain your intolerance to Niacin.
(You were not using Niacin BTW, but non flush version called
inositol hexanicotinate). The latter retains some vitamin actions, but is not Niacin and should not cause flushing at all.

This post:
http://neurotalk.psychcentral.com/post1059073-12.html

COMT is a methyl transferase and a genetic mutation in this enzyme involves methylation failures.

If you google, "methylation errors", or "under methylation", or the Pfeiffer Institute as qualifier you will find more.

I would also think getting a heavy metals screening might be useful when you get your testing done at the doctors.

Stacy, I am glad you are a little better and I hope you continue to stop swelling and you find a good doctor that knows what do to.

I hope they can do the testing Mrs D talked about. Some of those problems are very common.

I cant believe how good I am doing, well relatively speaking. From death to life, like a light switch turned on. I have been drinking chlorophyll to clean my blood out as I have believed niacin was the culprit and as fast as this left I think I am correct.

MrsD I will take your advice to heart and I copied your post. I was reading about EM last night and it talked about metal toxicity.

Thank you MrsD for always helping out.

And thanks Sally!! Im praying I am on my way to find some answers. I have avoided this as I feel in the end all it will lead to is a lot of bills and no answers and just pain meds, but it is time to do it anyway.

Here's a case study on how niacin can upset the balance of things. Even though your issues are different from the patient in this link, it's a good example of how quickly things can be imbalanced when you have one or more of the mutations.

Mrs. D suggestion to tested for MTHFR mutation is probably a good idea. It's all very complicated and knowing what you're dealing with can help you manage your supplements.

Glad you're coming out of this tailspin.

http://mthfr.net/overmethylation-and...dy/2012/06/27/

Thank you Marlene I will put this on the table when I go to the doctor. Every little thing helps to put the pieces together.

You didn't include a case study?

Just added it to post....thanks

That is a nice link, Marlene...the subject is complex and difficult to understand. I think many doctors are clueless about it too.

I had a DNA test several years ago just for kicks and it references the MTHFR gene here:

We evaluated the following markers:

Gene: MTHFR

Marker: rs1801133

Your Genotype: T/T

Does anyone know what this means? I hope DNA test results have become easier to decipher than when I did mine.