yisucks;52418 wrote: Impossible– I have an appointment with Armine on the 10th. He went through all my results and defintely sees some issues. I sent him my report through mthfrsupport.com and he is seeing issues with mold, IgE which could be causing these MS symptoms, and me being having “significant mitochondrial dysfunction.” He spoke of some other things, like me being estrogen dominant, difficulty with breaking down free radicals, being prone to anxiety disorders (which is 100% right on), etc. I really like him…he’s funny and has a great attitude. It’s expensive for a first consult, but the price drops after that.
I actually asked him if he has any concerns about the FDA and 23andme and he gave me a really good, honest answer. There are people out there that don’t want folks having access to their raw data. Also, this information is dangerous for doctors because, sadly, they profit when people are sick.
I am hopeful that by working on my methylation, as well as continuing my supplements for yeast via raster’s ND, my diet, etc, I can really start to heal my body, because it obviously is working against me with all the defects I have. This is all totally makes sense and is why I try and try and try and can’t get better. Here’s to hoping for a better, healthier 2014.
Thats awesome. Data is power and you hit on a bunch of it. All of those things you mentioned can contribute to ms like symptoms in one way or another. The one other test to keep in mind for the future if you still run into dead ends is for mold illness. I would think Dr Armine would be on top of all of that. You’re in good hands. Im really excited for you, you have to keep me updated.
Make sure you download and save a couple copies of your raw data somewhere safe. In paint cans even (emf). Some day we’re probably not going to be allowed to do stuff like this. Being normal american citizens, we are probably in the golden age of medicine, real medicine, and the powers at be are not going to let it stay that way for very long.