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Torts
LIF Toddler
Member since 9/10 494 total posts
Name:
me
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I finally have some answers
Although it isn't great, it is something.
I had the recurrent m/c panel done- as per MY request (if you remember my doctors said there probably wasn't anything wrong since I already have 1 DC). I went in to go over my blood work results and it turns out that I have the MTHFR gene mutation. The doctor did not give me specifics but said that I have 2 copies of the less severe one strand(?????). I have NO CLUE what that means, even though I asked for the name he didn't give me the technical term so I don't know what I'm dealing with. I do know that when the time comes that eventually see a HB on a sono, I have to start Lovenox. My folic acid was also increased and I was put on a vitamin to fix my homocysteine levels. My dr also said that I probably saved myself 3-4 more losses by pushing for the blood tests. I'm so happy I did.
I did a search and saw that a lot of women here have MTHFR so at least I am in good company.
If you made it this far, thanks for reading! I'm so thankful that I can move forward. Now I feel like I have something to work with.
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Posted 1/25/11 5:06 PM  |
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JavaJunkie
Someday, Somehow
Member since 6/05 5857 total posts
Name:
Lois
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Re: I finally have some answers
I have no experience with this but I'm glad you got some answers!!
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| Posted 1/25/11 5:32 PM |
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curiousO
he is here.. thank you God
Member since 10/07 2344 total posts
Name:
Me
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Re: I finally have some answers
glad you got your answers.
I also have MFTHR. I wonder why your dr did not mention anything about baby aspirin and metanx??? these are the first things that REs give for it.
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| Posted 1/25/11 5:33 PM |
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Torts
LIF Toddler
Member since 9/10 494 total posts
Name:
me
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Re: I finally have some answers
Posted by curiousO
glad you got your answers.
I also have MFTHR. I wonder why your dr did not mention anything about baby aspirin and metanx??? these are the first things that REs give for it.
I'm already on baby aspirin for my Antiphospholipid syndrome 
I also have to take some homocysteine b-6 formula vitamin. He didn't say anything about the metanx. I didn't see an RE for this b/w. Maybe that's why
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| Posted 1/25/11 5:41 PM |
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prunepie
LIF Adult
Member since 7/06 4357 total posts
Name:
jennifer
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Re: I finally have some answers
yes i take baby aspirin too and metanax....actually the generic is folgard or folast...you may want to ask your pharmacist or doc again :)
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| Posted 1/25/11 7:18 PM |
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Torts
LIF Toddler
Member since 9/10 494 total posts
Name:
me
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Re: I finally have some answers
I just looked at my papers. The homocysteine formula vitamin my doctor prescribed is a folic acid/b-6/b12 combo. I looked up Folgard and Metanx and they all appear to be the same thing, just different manufacturers. Phew!
I'm ready to just start the meds and be done with it.
Are there any other complications with MTHFR or is primarily with pregnancy? I googled (I know!! I shouldn't) and I found different forum topics where women were diagnosed after numerous embolisms  What I saw was scary!
Message edited 1/25/2011 7:43:02 PM.
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| Posted 1/25/11 7:42 PM |
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classc1
LIF Adolescent
Member since 6/10 805 total posts
Name:
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Re: I finally have some answers
Hi,
Glad that you got answers. It sounds like you have a less serious version of MTHFR than I have...I have one copy of each mutation. That is called being compound heterozygous MTHFR. It sonds like you have two copies of the A mutation. You should find out exactly which form you have and if your homocysteine levels are normal. I'm curious as to why you will be put on Lovenox if you have one copy of each mutation. That is usually treated with Folgard and BA unless your homocysteine levels are not normal although some do take Lovenox in an excercise of caution. Just an FYI, I was told to take one Folgard tab daily for each copy of the mutation so I normally take two Folgard tabs which are 2.2 grams each I believe. Also, ladies on the internet suggested that I switch to a pre-natal where the folic acid is more bio-degradeable such as Neevo.
There is a great yahoo group on MTHFR that you might want to join.
Message edited 1/25/2011 8:35:48 PM.
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| Posted 1/25/11 8:32 PM |
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ricaim
LIF Adult
Member since 8/09 1201 total posts
Name:
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Re: I finally have some answers
Posted by curiousO
glad you got your answers.
I also have MFTHR. I wonder why your dr did not mention anything about baby aspirin and metanx??? these are the first things that REs give for it.
Not necessarily. I only had baby aspirin and increased folic acid. I think it depends on the mutation you have and other factors possibly.
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| Posted 1/25/11 8:34 PM |
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Torts
LIF Toddler
Member since 9/10 494 total posts
Name:
me
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Re: I finally have some answers
Posted by classc1
Hi,
Glad that you got answers. It sounds like you have a less serious version of MTHFR than I have...I have one copy of each mutation. That is called being compound heterozygous MTHFR. It sonds like you have two copies of the A mutation. You should find out exactly which form you have and if your homocysteine levels are normal. I'm curious as to why you will be put on Lovenox if you have one copy of each mutation. That is usually treated with Folgard and BA unless your homocysteine levels are not normal although some do take Lovenox in an excercise of caution. Just an FYI, I was told to take one Folgard tab daily for each copy of the mutation so I normally take two Folgard tabs which are 2.2 grams each I believe. Also, ladies on the internet suggested that I switch to a pre-natal where the folic acid is more bio-degradeable such as Neevo.
There is a great yahoo group on MTHFR that you might want to join.
My doctor explained it to me by saying instead of having 1 copy of each mutation (strand) I have 2 copies of 1 mutation.. but he didn't specify. I'm going to call my regular OB tomorrow (I ADORE him) and ask him to call me and explain it to me in terms I actually understand  I know my OB personally so I know that I can ask him a million questions and not feel like a moron.
I do remember that he said I have a less severe mutation. SO that in itself is a good thing.
I'm going to find the yahoo group now! Thanks for the info :)
ETA: The Lovenox will be used in future pregnancies because of the MTHFR compounded by the Antiphospholipid syndrome that I also have. Blah....
Message edited 1/25/2011 8:42:16 PM.
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| Posted 1/25/11 8:40 PM |
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Phoebee
LIF Adult
Member since 11/06 1623 total posts
Name:
Michelle
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Re: I finally have some answers
YUP, that was one of my issues too.
Lovenox and baby asprin was what the Dr. ordered for me!
After 6 losses, I'm scheduled for Friday to have 
hang in there... you have answers now and hopefully on your way to 
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| Posted 1/25/11 9:08 PM |
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classc1
LIF Adolescent
Member since 6/10 805 total posts
Name:
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Re: I finally have some answers
Posted by Torts
Posted by classc1
Hi,
Glad that you got answers. It sounds like you have a less serious version of MTHFR than I have...I have one copy of each mutation. That is called being compound heterozygous MTHFR. It sonds like you have two copies of the A mutation. You should find out exactly which form you have and if your homocysteine levels are normal. I'm curious as to why you will be put on Lovenox if you have one copy of each mutation. That is usually treated with Folgard and BA unless your homocysteine levels are not normal although some do take Lovenox in an excercise of caution. Just an FYI, I was told to take one Folgard tab daily for each copy of the mutation so I normally take two Folgard tabs which are 2.2 grams each I believe. Also, ladies on the internet suggested that I switch to a pre-natal where the folic acid is more bio-degradeable such as Neevo.
There is a great yahoo group on MTHFR that you might want to join.
My doctor explained it to me by saying instead of having 1 copy of each mutation (strand) I have 2 copies of 1 mutation.. but he didn't specify. I'm going to call my regular OB tomorrow (I ADORE him) and ask him to call me and explain it to me in terms I actually understand I know my OB personally so I know that I can ask him a million questions and not feel like a moron.
I do remember that he said I have a less severe mutation. SO that in itself is a good thing.
I'm going to find the yahoo group now! Thanks for the info :)
ETA: The Lovenox will be used in future pregnancies because of the MTHFR compounded by the Antiphospholipid syndrome that I also have. Blah....
Ah...now I get the Lovenox use. Wow...thank goodness you insited on testing!! Since you will be using Lovenox, there is another great group on Babycenter called Lovely Lovenox ladies. I went there when I first found out about my diagnosis as I wanted to make sure that I did not need Lovenox. You should check out that group..lots of good info.
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| Posted 1/25/11 9:21 PM |
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BigSmooch
LIF Adolescent
Member since 12/10 747 total posts
Name:
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Re: I finally have some answers
I saw your post on Pregnancy/Miscarriage...
It really is a good thing you pushed for the tests
I think I am going to be tested for the same thing. I only had 1 loss at 9 weeks but because they found nothing abnormal with the genetic testing the peri I saw suggested we check my antibodies and also my progesterone mid cycle. He said it can't hurt to check these things out before my next pregnancy if it will prevent another loss. Are those tests part of the miscarriage panel I hear people chat about on here?
I wish you the best of luck
Also, are antibody issues common? Or are they pretty rare? Just wondering because I saw a lot about it on the internet after researching.
Lots of luck Torts
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| Posted 1/28/11 3:37 PM |
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