I’m trying to put together a post on MTHFR. It’s been difficult to figure out what I want to say and what medical information is important to give.
Let’s start with my personal brand of MTHFR
According to my lab work, I am compound heterozygous for MTHFR mutations. “Right…” You say. “What does that mean?” It basically means my body can’t absorb Folic Acid. I can’t metabolize it or Vitamin B9. Does that make any more sense? Not to me. Not even almost a year after diagnosis. I still don’t understand.
What do I do to treat my MTHFR? I take Folic Acid and baby aspirin. Oooohhh, big deal, huh?
From the research I’ve done in the past 11 months and from what the doctors have told me, it seems like something that is life altering. Yet, my life doesn’t seem that different. In fact, most days I wonder if taking this extra folic acid and aspirin are really helping. And helping what? I don’t feel any different. I’m 31weeks pregnant. I can’t stand taking pills. After taking 3 folic acid pills a day, I missed a couple and nothing happened. So, I put myself down to 2 folic acid pills a day (and the baby aspirin). Still don’t feel any different. I guess right now it’s a waiting game. I’m wondering if I should get retested after the baby is born. Maybe there was a mistake? Maybe I really don’t have it?
According to some websites, MTHFR can cause pre-eclampsia, placenta abruption, IUGR, stillbirth, having a baby with chromosomal abnormalities, recurrent pregnancy loss, clotting problems, strokes, hypertension, and heart disease. They say this is all hereditary. Yet, nobody in my family has these issues… except me. And the only ones I’ve had are miscarriages, possibly mild pre-eclampsia, and IUGR with one of my pregnancies. My other three full term pregnancies were fine. I was born with a heart defect, but I don’t think it’s connected.
People with MTHFR are supposed to be on a blood thinner when pregnant. My doctor recommended Lovenox injections. I refused. I took the chance that my body would take the extra folic acid and aspirin and do what was needed with it. And so far, it has.
So, were my tests wrong? Or am I the only one in my family to have MTHFR? Are there other family members suffering from it, but not sharing the information? And what would happen if after I have this baby, I stop taking the medicine? Do I really want to risk stopping medicine and end up having a stroke? No. But, do I want to keep taking these pills for the rest of my life? No. But, I am lucky that this is the only thing wrong with me. I am blessed to be so healthy.
