We have made it to 14 weeks! This is the point where most of the world starts to worry less and enjoy the pregnancy more. I'm trying to do the same- but it's easier said than done. I am, however, thrilled and humbled to be in my second trimester. I have begged God in countless prayers over the years to help me at least get to this point- and now that it's happening, I have a hard time believing it.
Baby is at least as long as a lemon now, but since he or she measured about 14 weeks at our 13 week appointment- their true size now is probably closer to an orange. We have hit a major growth spurt- baby's weight should nearly double each week at this point. Baby's neck is longer now, so he or she is "standing up" and looks even more baby-like. Our little one is probably sucking their thumb- and is now experimenting with all kinds of facial expressions!
Baby at 14 weeks development |
Round ligament pain is now a daily occurrence for me. It's funny how those sharp pains reassure me that everything is growing properly, and make me worried at the same time. Sometimes it's a real shock how much everything can hurt if you stand up too fast. I've had lots of issues with my SI joint moving around too much, especially this early. It's extremely painful and sometimes makes it so I can't put weight on one of my legs until everything pops back in. It's likely from the back issues I have pre-pregnancy combined with Relaxin and my expanding belly. Fortunately I have my almost-graduated physical therapist husband to help. He can usually pop everything back into place even through my screaming and crying at him. He has some stabilization exercises ready for me as soon as I feel up to doing them. Other life issues have arisen that have stressed me out to the max this week- but I have great support and I'm learning how to deal. Life is what it is. We go on and we'll make it somehow, no matter what!
I have been pondering quite a bit this week regarding low dose aspirin therapy near delivery time. When the MFM talked about stopping it at 34 weeks, everything inside me screamed NO immediately. During my time in support groups, researching, and networking- I have met many women who deal with MTHFR in addition to other risk factors- like me. Many of these women (and I would say a disproportional amount than a normal sample from the public) have had unexplained stillbirths. Ever since I was diagnosed with MTHFR, stillbirth has been a fear of mine. Now, it's becoming a stronger, more real fear. I found that often these babies would have no obvious cause of death. "Just a fluke. The heart just stopped." I'm convinced that MTHFR, when in combination with other risks, causes more issues, and specifically stillbirths, than has been accepted by science currently. It's happened twice in my own family.
My doctors are not concerned with MTHFR. I have two copies of the same mutation- the rarer type at that. But many people can have some form of MTHFR and have no complications or knowledge that they have it. I've had to go with my gut this whole pregnancy- and everything leading up to it. I think in combination with Leiden Factor V, the MTHFR becomes more dangerous. I feel confident that I have a healthy baby right now- but I don't want to take a sudden turn for the worse. I HAVE to treat the mutation the best I know how. That includes a simple regiment of baby aspirin. I took it through delivery with Jack- it seems like a tried and tested method to me. The MFM said if I were going to get a clot in the cord or something- that aspirin likely wouldn't prevent it anyway. That doesn't seem like a good enough reason to me not to take it! I think the risk of hemorrhage or placenta abruption doesn't compare to the risk of small clots near delivery in my case. Especially with baby aspirin- I'm not on Lovenox anymore. It just seems like near the end of pregnancy, there comes a point when baby will be safer outside of me than inside.
Gotta have that cider |
My doctors are not concerned with MTHFR. I have two copies of the same mutation- the rarer type at that. But many people can have some form of MTHFR and have no complications or knowledge that they have it. I've had to go with my gut this whole pregnancy- and everything leading up to it. I think in combination with Leiden Factor V, the MTHFR becomes more dangerous. I feel confident that I have a healthy baby right now- but I don't want to take a sudden turn for the worse. I HAVE to treat the mutation the best I know how. That includes a simple regiment of baby aspirin. I took it through delivery with Jack- it seems like a tried and tested method to me. The MFM said if I were going to get a clot in the cord or something- that aspirin likely wouldn't prevent it anyway. That doesn't seem like a good enough reason to me not to take it! I think the risk of hemorrhage or placenta abruption doesn't compare to the risk of small clots near delivery in my case. Especially with baby aspirin- I'm not on Lovenox anymore. It just seems like near the end of pregnancy, there comes a point when baby will be safer outside of me than inside.
I know that there isn't enough research on my side here. My doctors don't really hear these concerns. Have I argued with my doctors before? Absolutely. I haven't always been right- but it's brought me this far. I'm just trying to make the most informed decision possible. Some of my doctors still don't believe that Kevin's surgery had any effect on the fact that we know have a baby with healthy DNA (??!!???) I have had to fight for every test, every diagnosis, and every new treatment plan through all six miscarriages. I'm sure as hell not going to stop advocating and researching for my baby now that there is a good chance of survival. It's not just about my brain and the science- it's a matter of the heart. I'm their mother.
I've been gently reminded not to drive myself crazy. There is risk in everything. Most things are out of our control. This is totally true. I don't keep my almost-five-year-old in a bubble all day- that's no way to live. Life is scary and fragile but you have to keep living anyway. However, I think you have to keep researching and getting opinions when you have a strong feeling about a specific treatment. Do you have any idea how crazy pregnancy after multiple losses makes you? Literally crazy. No denying it. You don't trust anything anymore. Nothing feels simple. You worry about your baby staying alive. All. The. Time. Talk to anyone who has been through it. Every heartbeat check, ultrasound, doctor appointment- you just fight through the fear. The innocent faith of "Oh everything will be fine" is lost. Because that is not your reality. No matter how many people try to tell you otherwise- you know better. The risk is real. BUT- so is the hope. The hope is real. So you cling to it.
I've found help in talking to women in my specific situation. Their support is invaluable. They totally get it. They make me feel less crazy. One of the most valuable pieces of advice was given to me by my counselor last year. When I told her all the reasons I shouldn't feel like this. She said, "You are going to feel what you're going to feel. You can't change that." So simple but so profound. These emotions are what they are. But I can choose how I handle them. After all the research and all the debate- there comes a point where it becomes an issue of faith. That's the point I need to turn it over to God and ask for peace. That is where I'm at now. I'm trying to learn how to do just that. In two weeks I have my next OB appointment. I want to clarify their position on the aspirin- since they are the group delivering me and honestly- the only opinion I even care about. I hope we can come to an understanding and I can breathe a little easier after that. I know God is watching over us, and I know all of you, our loved ones are standing by to help!
I've been gently reminded not to drive myself crazy. There is risk in everything. Most things are out of our control. This is totally true. I don't keep my almost-five-year-old in a bubble all day- that's no way to live. Life is scary and fragile but you have to keep living anyway. However, I think you have to keep researching and getting opinions when you have a strong feeling about a specific treatment. Do you have any idea how crazy pregnancy after multiple losses makes you? Literally crazy. No denying it. You don't trust anything anymore. Nothing feels simple. You worry about your baby staying alive. All. The. Time. Talk to anyone who has been through it. Every heartbeat check, ultrasound, doctor appointment- you just fight through the fear. The innocent faith of "Oh everything will be fine" is lost. Because that is not your reality. No matter how many people try to tell you otherwise- you know better. The risk is real. BUT- so is the hope. The hope is real. So you cling to it.
I've found help in talking to women in my specific situation. Their support is invaluable. They totally get it. They make me feel less crazy. One of the most valuable pieces of advice was given to me by my counselor last year. When I told her all the reasons I shouldn't feel like this. She said, "You are going to feel what you're going to feel. You can't change that." So simple but so profound. These emotions are what they are. But I can choose how I handle them. After all the research and all the debate- there comes a point where it becomes an issue of faith. That's the point I need to turn it over to God and ask for peace. That is where I'm at now. I'm trying to learn how to do just that. In two weeks I have my next OB appointment. I want to clarify their position on the aspirin- since they are the group delivering me and honestly- the only opinion I even care about. I hope we can come to an understanding and I can breathe a little easier after that. I know God is watching over us, and I know all of you, our loved ones are standing by to help!