Gene Mutation

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Jeanie
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Gene Mutation

Post by Jeanie »

I have just sent in a saliva test to 23&me for MTHFR. I wonder if anyone has this mutation.

Jean
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tex
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Post by tex »

Jean, I've never had a test for that mutation, but I have a hunch that many of us (probably including me) have one or more of those mutations.

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It is suspected that some of the hardest material known to science can be found in the skulls of GI specialists who insist that diet has nothing to do with the treatment of microscopic colitis.
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Gabes-Apg
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Post by Gabes-Apg »

Jean,
There are a few members that have confirmed MTHFR gene mutation results.

Mcnomore, JoAnn, mbombarder, come to mind. If you do a search for MTHFR, you will see recent discussions.
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Pat
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Post by Pat »

Had that test recently and I do not have any mutations. I keep testing for different things and the only thing that has come up is I have no Aldosterone.

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Post by Grahm »

Should we be testing for different things? I've only done the enterolab and vitamin B one.

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Post by Grahm »

That should be vit d:)
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Gabes-Apg
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Post by Gabes-Apg »

Connie,
if wellness eludes you, or if you have multiple AI issues and are struggling to get good management of those AI issues, then I would recommend investing in the gene mutation testing. For those with multiple AI issues there is a good chance that gene mutation is a key part of the root cause.

In saying that, a big part of the fix the fix for the MTHFR gene mutation, and Pyrrole gene mutation is healthy digestion, balanced systems in the body, and correction of nutrients/mineral deficiencies.
If you are:-
-following low inflammation, gut healing eating plan and lifestyle;
-nurturing the adrenals, immune, thyroid systems;
-Listen to your body and decoding its messages;
-taking good quality supps that your body needs; you are doing 80-90% of what is needed.
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Grahm
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Post by Grahm »

Thanks Gabes, your awesome!!

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Gabes-Apg
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Post by Gabes-Apg »

Connie, (and anyone else interested)
A PS to my post above....

If your children are having:- allergy symptoms, Ie asthma / skin issues / IBS / hormone issues for females. Then I would recommend getting the gene testing.

For females with these issues, early knowledge and implementation of the right protocols will minimise hormone and thyroid issues (especially conception/pregnancy issues)

In all cases, early implementation of the right eating plan, keeping inflammation in the body at a minimum, the digestion healthy, avoiding mineral/nutrient deficiencies will protect against diabetes, depression and anxiety, IBD's, AI conditions, etc etc issues that can become chronic quickly.
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ldubois7
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Post by ldubois7 »

Jean,

I just received confirmation that I have the MTHFR gene mutation.
Im just starting to research it. I'll pass along anything I find.
Linda :)

LC Oct. 2012
MTHFR gene mutation and many more....
Jeanie
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Gene Mutation

Post by Jeanie »

Linda,

Best wishes to you. I am still waiting to hear. If I do have it, I certainly do want to find out about it.

Jean
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Jeanie
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Gene Mutations

Post by Jeanie »

I got the results back from 23&me and they just do the raw data so I sent it along to LiveWello. I have 12 homozygous mutations plus the heterozygous for a total of 74 mutations! Wow, I wasn't expecting that many. I do not have the big ones for MTHFR but I do have several in that category. My homocysteine was high so that's why my doctor suggested I get tested. If the folate doesn't get in at the cellular level, it causes problems. I don't know how much of it I understand but I surely have done a lot of reading! I figured I must definitely have mutations because of the number of problems I have had. I am still waiting to get in to see my doctor.

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Jean
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Gabes-Apg
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Post by Gabes-Apg »

Jean
it is like another language hey!! (or another planet even..)

If you have some in the MTHFR category, Methylation is a highly probably issue, best to take active forms of B6 and B12, and to observe symptoms for other deficiencies, ie magnesium, zinc, etc.

We dont have to understand it all! a bit like MC, just follow the main principles and tweak things to suit the individual.

I am just waiting for my next welfare payment and I will be getting the 23andme testing.
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Jeanie
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Mutations

Post by Jeanie »

Gabes,

Thank you for your response. I have been L5 MTHF for several weeks now. My doctor put me on that before I even took the test. I am also taking magnesium and several other supplements. There are six doctors in Minnesota that know anything about methylation and fortunately my doctor is one of them. It certainly is a foreign language. It seems that the average doctor knows nothing about mutations. I had one of them tell me everybody has mutations and there's nothing you can do about it anyway. Does that sound familiar?

I will be anxious to hear what you find out when you get your test.

Jean
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Post by Hopeful »

As usual, Gabes has some valuable information. I was mentally putting off research into this gene mutation stuff since I'm just getting good eating habits for my MC under my belt. But! My daughter has MANY of the issues that you talk about. She's 36 and has given up on having a child after so many problems through the years.

Now I will do the research for her sake...
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