LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Medical Questions » NEWS flash!!! Do you have MTHFR?

 - UBBFriend: Email this page to someone!    
Author Topic: NEWS flash!!! Do you have MTHFR?
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
Can you believe my doctor checked me for it and it's NEGATIVE!??

He was shocked, his nurse was shocked, I was shocked. I think they were more shocked than me!

Hahaha.. even more shocking was that my doctor's was positive~!

So now on to the 23andme .. I need to get busy getting my results interpreted.

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
WPinVA
Frequent Contributor (1K+ posts)
Member # 33581

Icon 1 posted      Profile for WPinVA     Send New Private Message       Edit/Delete Post   Reply With Quote 
Well, that's good. One less thing. There are lots of other mutations though, so perhaps you have one of the other ones.
Posts: 1737 | From Virginia | Registered: Aug 2011  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
I know .. I figure I have plenty of others.

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
Robin123
Moderator
Member # 9197

Icon 1 posted      Profile for Robin123     Send New Private Message       Edit/Delete Post   Reply With Quote 
I don't understand what you mean by your doctor checked it for you. For me, I did the 23andme test, interpreted by geneticgenie, and the results were clear as day, showing some MTHFR gene mutations.
Posts: 13116 | From San Francisco | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
WPinVA
Frequent Contributor (1K+ posts)
Member # 33581

Icon 1 posted      Profile for WPinVA     Send New Private Message       Edit/Delete Post   Reply With Quote 
You can also have it checked with a blood test ordered by a doctor.
Posts: 1737 | From Virginia | Registered: Aug 2011  |  IP: Logged | Report this post to a Moderator
ukcarry
Frequent Contributor (1K+ posts)
Member # 18147

Icon 1 posted      Profile for ukcarry     Send New Private Message       Edit/Delete Post   Reply With Quote 
I am not sure what he means by 'it'? I have eight results for MTHFR alleles and 99 results under the heading of methylation.

The two that are normally regarded as being the most crucial are MTHFR A1298C and MTHFR C 677T ,especially. the latter, so perhaps he was referring to that? If so, it is good not to have any mutation n the latter, but it doesn't mean that all is plain sailing. In fact I am 'normal' for C677T too, but have a lot mutations in the methylation category and am homozygous (ie both genes are mutations) for A1298C.

The FUT2 results, for example, have bearing on your B12 status.

Have your 23andme results come back yet, Lymetoo?

Posts: 1647 | From UK | Registered: Nov 2008  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
Yes, I have my results but have not had time to connect with livewello or other sites. I've been really busy. I may be able to do some of that today.

My doctor just did a blood test.

Any tips on getting this done?

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
ukcarry
Frequent Contributor (1K+ posts)
Member # 18147

Icon 1 posted      Profile for ukcarry     Send New Private Message       Edit/Delete Post   Reply With Quote 
For livewello.com, the instructions were quite good as to how to upload your 23andme. You need to use a laptop or desktop rather than tablet and after payment, you get lists of results under headings, methylation being one such heading. You can see at a glance, as the homozygous results (mutations from both parents) are highlighted in red, and the heterozygous ones(mutation from one parent) are highlighted in yellow. We printed these results, but they stay accessible on Livewello's site.

You can access on the site info about your ethnic ancestral makeup and any inherited condition in your genetic makeup. Yoy can also read about some health conditions in relation to your results, but you need to pay the extra annual subs, as I finally did yesterday, to get some of the info on health conditions (personalised). I think, if you use Livewello, that it is worth doing that, but probably not straightaway. Give yourself time to navigate the site a bit.

Frustratingly, I have yet to make many changes, as the person I sent my stuff to and had a Skype consultation with is very busy (she is probably the most experienced UK person so far as this is concerned), so I still haven't received my report from her a month after that consultation! She was good in the consultation thogh, so I would advise you to work with someone experienced who can steer you through any supplement/dietary changes etc that might benefit you.

Because a mutation/polymorphism isn't necessarily causing you a problem, it is likely that a practitioner will want you to have at least a test that will evaluate your nutritional status, so that they can cross reference your genetic results with that to identify problem areas.

Don't try to read too much at once, as if you are anything like me, you will get befuddled! Good luck!

Posts: 1647 | From UK | Registered: Nov 2008  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
I thought Livewello was one of the ones that were free?

Poo ...

I need to get my printer working.

THANKS!

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
sixgoofykids
Moderator
Member # 11141

Icon 1 posted      Profile for sixgoofykids   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Genetic Genie is free and will show the methylation genes.

I am homozygous for the MTHFR gene C677T. No surprise there. I've been taking Methyl Guard since I found out a couple weeks ago and I think it's helping. Too early to know for sure. I've also started on DAO for histamine and have gone on a low histamine diet. That is helping for sure.

I liked the results I got from Promethease and it was only $5.

--------------------
sixgoofykids.blogspot.com

Posts: 13449 | From Ohio | Registered: Feb 2007  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks, sixgoofy!

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
maritzap
Member
Member # 11146

Icon 1 posted      Profile for maritzap     Send New Private Message       Edit/Delete Post   Reply With Quote 
Dr Amy Yasko offers free analysis and supplement recommendations
Www.knowyourgenetics.com

Posts: 75 | From San Diego, CA | Registered: Feb 2007  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.