Eva, I agree with MrsD and know enough about Methylfolate and have talked to you. If you are taking the 15mg that is a very high dose. I have a friend who takes close to 2mg and I'm right there with her, I take a little less, but we both make sure our B12 is sufficient. We buy both otc. Can only wish you the best.

I do not trust OTC med or vitamins for that matter

Let me ask you something
Do you know anything about this body
Did you even do any homework on a thyroglossal duct cyst
Something this body had been suffering with
An active one
I came to NT FAILED CERVICAL SUGERY and have been around
I find it amazing that the school would put the kinds of food for our youngsters to start life off with a unhealthy bang
Always sent my children to school with a balanced meal
And would put an extra serving for another students in the class
They would eat Corissa's lunch

The help I am looking for is something many WILL NOT UNDERSTAND
However I expect common knowledge
to be exactly that
I had many different variants to look at
This mutation is just another thing to put on the list of problems
As my cyst is active
And I have been to three reputable ENT SPECIALESTS WHEN I HAD PRIVATE INSURANCE
by the way
A person in this country could DIE before they could get health insurance
This a disgrace
I now in a difficult place

Yesterday at my OBGYN
He had the decency to tell me Eva
I have limited knowledge of genetics

Since seeing three ENT's
THESE ARE THE THREE RESPONSES
1st one told me it does not LOOK like you have one
2nd one told me it is something I need to keep an eye on
3rd one asked why did the neurosurgeon not have it removed when he entered my neck anteriorly this ENT NEEDED TO CLEAR ME FOR SECOND SURGERY
do you even know what it's function or purpose is of how I acquired it
The third ENT said
It should have been removed
Did you know that goiter is prevelent on my mothers side
My mother and all her siblings three of four has them
Members of my lineage have died as a result of complications
To much iodine when doing the surgeries so the story is via my mother
After my first ACDF 5/6-6/7 and failed to fuse
I had no choice in the matter

My surgeon asked me
Why would I return to him to fix the job
My response was this
Dr. Peterson why would I go to another person
Isn't what you did "YOUR ART WORK"
"ONLY YOU KNOW WHAT YOU DID"
WITH THAT NOT A WORD AS HE DRAINED THE HEMATOMA THAT GREW OVER NIGHT"
I trust nobody
Including the OTC meds
Since my failed second surgery
I was reduced to wearing a soft collar all of the time
Until about a year now
My cyst has become bothersome
Why do I bring this up
HORMONES another reasons doctors are misdiagnosing
Another biggie as diet and proper nutrients are to ones body

I will continue to post
And let others know how things are going
May all who look for help
Do your homework
Thoroughly
I do not believe everything I read or hear on television

How about this

There is a neurologist who is cunducting a study
His name DR. KEVIN TRACEY OF NEUROLOGY
based out of NYC my back yard
"Believes" and has proven that all things such as inflammation
be the VERY FIRST SIGN of something gone wrong
He believes and so do I doing extensive research
LIKE I SAID WITH THIS BODY EVERYTHING "IS" interconnected
He has a site if you type in his name and state
You will find a site called
"CAN THE NERVOUS SYSTEM BE REBOOTED"
A LARGE pharmaceutical COMPANY WANTED IN AND GAVE HIM
A HUGE SOME OF MONEY FOR HIS REASEARCH
THAT SPOKE "VOLUMES TO ME"
THERE IS MONEY TO BE MADE
AND THEY WANT IN
BECAUSE
WHAT THIS DOCTOR PROPOSES
NO MEDICINES
ESPECIALLY FOR THOSE LIKE MYSELF
allergic reactions
Deadly side affects
Not any different then the DEPLIN
Always everything with caution and knowledge
HOMEwork this I have done
As it is what is left of this dying body
It is rotting before my doctors
And "they don't give a turd"
INSTEAD IT IS
WHERE'S THE MONEY
A sad country it has become
I came to this country at five
My father had some idea that the western world
The only world I know
Is way ahead of itself
Me

TESTED POSITIVE
FOR THE MUTATION
just spoke with her
her doctor will be doing more tests

AS IT EXPLAINED
not only is more than 50% of the population
is affected


it would be great to get more info
on the mutation on the forum

There is already much information on the NT forums.
Just search MTHFR ... lots of posts on the PN forum.

i hope my two cents
should help
this is new to me
and i went through the site
not broad enough info
as there are many interconnecting
ingredients and the lack of
and so on


I arrived

JUST TOOK MY FIRST TABLET
with my multivitamin 50 plus
will continue to post

a site i yet to look at
thank you MrsD
ME

how long it's been i have slept through the night

it was four in the morning
to void liquids
it was that gut feeling
i had anticipated
waiting for it
as i returned to bed and wondered
when i would be visited by doom
and with that i fell back to sleep
7:01 A.M. i awoke
this to me is greatest thing ever
for this body has a chance to feel just a bit better
i'm going to share it
me

Good news Eva, hope it continues for you. I can't imagine how horrible it is not to sleep. I've had some bad nights in my life, but not anymore.

TESTED POSITIVE
FOR THE MUTATION
just spoke with her
her doctor will be doing more tests

AS IT EXPLAINED
more than 50% of the population
is affected
it would be great to get more info
on the mutation on the forum

just some FYI
happy
knowledge
i was put on a high dose as i am at the extreme
side to the mutation
i Should benefit from
this


http://www.balancingbrainchemistry.c...epression.html