Today John and I met with Dr. Mooney. John finally got to meet the new RE! It was a happy day, but a sad one too.
Let me start by saying that I am SO grateful to the two women who suggested I speak with Dr. Mooney at RG. THANK YOU. Because of these two women, I feel I am in better hands than I unfortunately ever was at ORM, and I've only met this doctor twice now.
The results of my blood work came back. Some of the things made me happy...my fsh and tsh levels are great. Even my fasting insulin was very good. But then we got to the Recurrent Pregnancy Loss panel that was run on my blood. First I found out that my body does not harbour any antibodies of the immune system, so that was good. Then Dr. M started to talk about the tests they ran to determine if any of my genes were normal or abnormal. Two tests came out normal, and three came back abnormal.
The three which came back abnormal are the MTHFR 677, PAI 1, and the Factor XIII. Basically, these are heterozygous status which means I got the "bad" gene from either my mother or my father. With these genes missing, and from what I understand, I am at a higher risk for: early miscarriage (possibly why nothing has implanted so far), preeclampsia, IUGR (Intrauterine growth restriction is a term used to describe a condition in which the fetus is smaller than expected for the number of weeks of pregnancy), and pre-term delivery. We can deal with these issues by giving me baby aspirin and heparin after an egg transfer, but the reality is that this isn't something that is easily fixed. Likewise, just because I get an embryo to stick doesn't mean that I won't have serious complications later on in a pregnancy.
I left the Dr. M's office feeling three things: sadness for the new found diagnosis, anger that Dr. S at ORM never thought to test me for these things (and when I did ask for additional blood work he told me they weren't needed) and lastly, a bit of relief that we FINALLY have an answer. No, it isn't the answer we want but it is AN answer. Now I don't have to ask "what if". What if we tried another IVF and the embryo's would be transferred into me? What if we used baby aspirin and heparin?
Now I can begin to ask...when do I get to take the next step on the road less traveled?
Walk of Hope Week!!!!
10 years ago
10 comments:
Hi, I got in late on your post, so I thought I would send some love here. I am sorry about the news, but I just know that the happy ending will happen for all of us. It may not happen the way we expected, but it will happen. Also, did insurance cover these tests? I am thinking I should be asking for these. ((Hugs))debdebtx
I'm sorry for your diagnosis, but glad you got some answers. Goog luck on moving forward.
I'm sad for your actual diagnosis, but so happy that you have some answers and can move forward, knowing this information. I'll be here for whatever you need and can't wait to see where this journey takes you!! ((HUGS))
I am sorry to hear the news, but glad you finally have some answers! Here's to the next step - GL!!!
Kristen - I'm glad to hear SOME news about what's going on. I know that answers (no matter how bad) are often more comforting than the unknown. Do you know what your next steps will be?
((HUGS))
I'm sorry to hear your news. I'll be keeping you in my prayers for your next step. ((hugs))
Hi Kristen, I am glad you finally got some answers although I am so sorry they brought you sadness. Good luck on your next steps, I am always thinking of you.
Karen
I have PAI-1 and was put on Lovenox the day of my transfer...worked like a charm!!!!
I am so sorry you're learning about this now. I swear, more and more I am questioning ORM, if we go down this road again. I hope your new found information helps make your choices easier!
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