Monday, April 1, 2024

All I Can Do Is Everything Humanly Possible

I was so thrilled when it came time to schedule my IUD removal. To think, either we’ll have a baby in the near future or we’ll decide we’re finished trying- which would mean a vasectomy for Kevin and I never have to worry about an IUD again 🙌🏻

For some reason the removal was extra painful and made me feel all emotional. It’s so easy to forget how intense pelvic pain can be, and for me it brings back a lot of bad memories from the past decade. I left with a bit of dread hanging over me; knowing I had an SSG and endometrial biopsy ahead of me still. The doc tried to encourage me saying, “You’ve had vaginal deliveries, you can handle it!” But is that really the pain threshold we want to set? Childbirth? Woof.

I had to wait five weeks after the IUD removal for the biopsy. Kevin and I got all our ducks in a row regarding all the supplements and meds we’re supposed to be taking starting now. It’s a lot. Definitely hard on the stomach. If I’m lucky, maybe my hair will get thicker🤞

I completed my initial full-time contract at work, which felt like a huge accomplishment. I’ve been at this hospital for about a year and a half and I didn’t sign a contract right away. I wasn’t sure how to work full time nights with kids at home, plus I was still in school for my BSN. But we needed the money that came with it. I signed the contract and was financially relieved, but pretty devastated emotionally knowing we would have to wait even longer to try for a baby. I already felt anxious to start the testing process after I graduated with my RN. I was nervous to put it off again for an entire year. In spite of the mixed emotions, it feels great to know what I’ve accomplished this year for my family. Both financially and career-wise. It was the right choice and I’m relieved that the pressure of fulfilling a contract is off. Though, I am still full time for the foreseeable future.

I met with my neurologist and my OB; they were both so supportive and hopeful for me, which was wonderful. My OB said I didn’t need to “draw a hard line” at 35 and thought I had a few good years left. Putting biology aside, I think I need to draw a line at some point for myself. After all we’ve been through, having started my reproductive efforts at 20 years old, it’s been a lot of my life dedicated to this. It’s not as if we’ve just been waiting on Mother Nature to do her thing, it’s always a long and expensive process. It’s a lot of collaborating with several doctors. 

It has to come to an end sometime soon. I remember the exact day the doctor confirmed my pregnancy with Jack, because it was 1/1/11. To think that was over 13 years ago. I don’t want us to put more of our lives on hold due to a “just in case.” Closing the door after a tenth pregnancy, no matter how it ends up, will open more doors for us in the long run. More experiences for our children, more financial planning, and more peace.That’s not to say I’m not scared of losing another baby. I worry about falling back into that dark place. I find myself already making a “Plan B” list of things to be hopeful or excited about if a baby doesn't work out. I’m discovering what other goals I could dedicate my efforts towards.

My OB approved my plan to stay on a couple meds during a pregnancy. Also, I can continue all my medications while trying to conceive, which is a huge sigh of relief. It eases the stress and pressure if it takes a long time to fall pregnant. At least I won’t be suffering with chronic pain sans meds.


Lots of notes from appointments on how to try to preserve a pregnancy

Looking at our plan can feel overwhelming and like a Hail Mary attempt. I keep telling myself: All I can do is everything humanly possible.

I will try to give life a chance to grow and accept the fact that I likely have very little influence over the outcome. Most factors are entirely out of my control. Maybe that's also a good thing? If all was healthy, I likely could do very little to accidentally hurt a little life growing.

I try to take courage in the fact that my body has always done everything it knows how, to the best of its ability, to protect new life. I’ve successfully produced a son and daughter, despite all the odds. I'm trying not to live in traumatic moments of the past. Who's to say the next pregnancy won't be perfectly normal and complication free? It's absolutely in the realm of possibility. I’m trying to have faith that “life finds a way” ;)


Appointment day was rough. I felt a little crazy. Why not stay up through the day, then work all night, then stay up into the next day to drop a grand on what feels like having a hole punch eat through your uterus? Why the hell not.

The biopsy was so much worse than I remembered; electricity was just shooting up my spine. Like literally are you sampling my vertebrae in there 😭 I had a harder time with the recovery too, it almost felt post op. I had to splint while walking or coughing and wasn’t allowed to take any hot baths which is my go to for pain management.

The SSG was more manageable and the NP said it was the most “perfect and beautiful uterus” she’s seen in a while. At least I have that going for me.

In 2019 when I was first diagnosed with endometritis, they gave me the choice of doing two weeks of antibiotics with a follow up biopsy, or doing a month of antibiotics with no follow up (because it was like 98% successful.) I couldn’t afford a second biopsy so I did the month of meds and it was just miserable. I know the protocol for treatment has changed in the last five years. We were never able to get pregnant after the antibiotic treatment before we took a long break from trying to conceive, so I was never totally sure if the endometritis cleared up. 

As horrible as the biopsy was, it would be completely worth it if the results came back negative! While waiting on results I put all the vibes out there- please please please be negative. Then the results came in.



And my reaction was somewhere around here:


I instantly felt dread just thinking of the constant nausea from the antibiotic treatment. I was prescribed Cipro and Flagyl and told to take both, twice a day, for two weeks. RIP my gut flora. I am taking a probiotic in between doses to minimize side effects, but I am just so freaking sick. It reminds me of morning sickness but worse, and my head is just spinning all the time. Work has been difficult because when I have 10 patients it’s hard to just run off sick and hide in the bathroom until the cold sweat stops. I will be taking antibiotics until the 10th of April, followed by another biopsy to confirm effective treatment. If I survive that long. The flu-like symptoms seem to get worse every single day of meds. 

My sweet friend just happened to stop by within 20 minutes of me getting the crummy news and brought flowers that she just happened to buy because they reminded her of me. Such an angel. She saved me from spending the afternoon crying.


Endometritis is caused by an infection in the uterus and can be due to several different types of bacteria. It is more likely to occur after a miscarriage or childbirth. It’s also more common after a long labors or a C-section. The incidence of chronic endometritis is very high in patients with unexplained infertility. 

From a scientific standpoint I think all of this advancement in understanding the endometrium at the cellular level is really exciting. Secondary infertility is more common than primary infertility and I wonder how frequently this is a contributing factor. Especially since the treatment is relatively conservative and easy with a high success rate- the data really speaks for itself.

Maybe I’ve had endometritis for a long time. I had 6 miscarriages in between Jack and Aidia. Jack was a long labor (like 28 hours) and a rough delivery. Maybe I developed it after giving birth to Aidia. Or after my miscarriage after her in 2019. I also had IUDs inserted and removed several times through all those years. I do have pelvic pain often, but with fibromyalgia it’s really hard to distinguish actual clinical symptoms when it comes to pain. A biopsy looks at the cellular level so it wouldn’t be surprising to me if chronic endometritis often flies under the radar with no symptoms. I imagine women who unknowingly have endometritis are often diagnosed with unexplained multiple losses or infertility. Even if I wasn't having any more children, I want to treat this to keep my own risks down.

Here’s a Link if you would like to read more about it.

Life will always throw curveballs and we just have to learn how to handle them. My hospital was just purchased by a new company and it really threw all my plans for taking a maternity leave out the window. Losing benefits randomly is scary and it just confirms that all we can expect is the unexpected. I really hope that also means unexpected joyful news. Thanks for all the love and support. Send me all your favorite foods to eat when you can’t eat anything without getting sick ;)

In the meantime, I’m going to do tough girl stuff. Like going to therapy.


Sunday, February 4, 2024

Forced Perspective

    January is at least 49 days long and is just miserable, but on the bright side we’ve had several test results come in. Kevin’s first analysis came back normal, which was totally expected as this test has always been normal and I don’t usually struggle to conceive. But, he’s ✨35✨ now so I guess we’re getting old in fertility years. Every test that comes back with fantastic results is a huge sigh of relief. 

    Mostly, we were concerned about his DNA fragmentation results and oxidative stress. Just under a decade ago, his results in those areas were so bad that it gave us a “poor” chance of a live birth. These tests don’t show up on a normal analysis and have to be processed at a special lab across the country. I stayed pretty optimistic because a year after his surgery in 2015, his numbers did return to normal and were still great in 2019. But deep down, I just felt like the results would not be good news and all of this would be over. I was patient until it was time for results to come in. I tried not to compulsively check for results. Then we got a message saying the results were going to be delayed for up to two more weeks due to the storms on the East Coast 🙃. Frustrating, but at least it helped me relax while waiting. 

     In the meantime, I went in for my baseline ultrasound and blood draws. I did have a cyst on one side (shocking I know 😑) so they had to run an estradiol on my blood to make sure it wouldn’t affect any test results before sending blood off for my Ovarian Assessment. Luckily, it was not in a place that would affect results and the only inconvenience was the extra bill. 

    My ultrasound showed good news, I had ten little follicles waiting to mature on both sides! I felt so proud of the way my body was working properly, especially after all we’ve been through. My ovarian assessment results actually were sent off and returned while we were still waiting for Kevin’s results. My egg supply score was in the “excellent” category. My AMH was high: 88th percentile. I haven’t heard from my doctor regarding this specific test, and it’s not a diagnostic test on its own. But high AMH is often associated with PCOS. I dabble frequently with ovarian cysts, but my OB told me a few years ago she didn’t feel I had enough symptoms of PCOS to explore the idea further.

    At last, Kevin's DNA fragmentation/oxidative stress results came in. I took a deep breath before opening the file, knowing that if results had backslid, it would likely be the end of the journey.

    The relief and joy I felt seeing this! I was surprised, I really was prepared for a poor outcome. It has been 9 years since Kevin's surgery and I am thrilled that the results have held. The reproductive urologist wasn’t even sure if that surgery would accomplish anything. The only treatment for Kevin going forward is taking supplements to support healthy fertility and keep oxidative stress in check. I'm getting started on some of my supplements also. I need to take quite a few more than Kevin. A new one this time around is Selenium, which has been shown to possibly reduce Hashimoto's antibodies and thereby reduce the risk of miscarriage. My Vitamin D levels also came back at vampire level, so I've started on Vitamin D again too.  

    My IUD will be removed in a couple weeks, and after waiting 4-6 weeks for the inflammation to decrease, I'll have my repeat endometrial biopsy. If it comes back positive again for endometritis, I'll have to do treatment again. I really hope it's negative. The month of hard core antibiotics almost killed me last time. Absolutely brutal. 

    The last test to complete is the sonohysterography to make sure everything still looks good and there aren’t any physical issues with my womb that need addressing. After that, we should be able to make a decision about moving forward. I just need to save up another cool million dollars for these tests. Just kidding. But that's what it feels like. Especially since the discouraging news regarding a payroll error which has resulted in us owing hella taxes. Just one more frustrating setback. The good thing is, I feel sure that this is the last time. The last initial consult; the last battery of tests. Once it’s all paid for and plans are in place, it’s either going to work, or it’s not. And I think that will be the end of it. 

    I’m thankful we’ve overcome the impossible before, because even if it doesn’t work out again, I still get to glimpse the impossible watching my rainbow baby. You never know when something is going to bring up emotions, and a couple weeks ago it happened in one of the weirdest places. Aidia needed a renal ultrasound to double check her kidneys (everything’s fine). During the scan I was looking at all the little perfectly working structures in her kidneys and I almost started crying! It took me right back to my ultrasounds during my pregnancy with her; seeing her perfect heart and all her organs functioning like a beautiful machine with all their intricate parts. She is perfect and incredible and I still am in awe that she exists. 
 
    I also see the impossible while watching Jack, who was a miracle even before I knew that he was. He’s an exceptional person; talented, ambitious, and driven in a way that I didn’t know children could be. Maybe not in the traditional honor student way, but in perusing his passions (and everything else be damned). He reads long biographies of Einstein, Hamilton, Elon Musk, and Steve Jobbs. I see how he relates to people with dreams that most people weren’t ready to understand. I don’t always understand him, but I want to support him, and somehow still parent him in any way that I can (wish us luck).

    Therapy has been so helpful in unraveling all my different motivations and emotions that have mixed together through the years. It’s been very healing to do “parts work” (Look it up, it’s not as weird as it sounds). Therapy has helped me feel more settled regardless of the outcome and it’s brought more peace. I have a lot more grace for myself, specifically for my younger self. I was doing the best I could without knowing as much as I’ve worked out now. I’m starting to believe that a person can find peace even in painful circumstances when you do enough internal work. I am thankful to age because of the growth that has come with each year of life. I want to put in the work to change any circumstances that control over. Doing this fosters an environment of peace. I don’t think I ever really believed that before.
 
    I’ve been learning how to work through trauma in therapy. I came to my current therapist having previously been diagnosed with PTSD by two other therapists, and still felt guilt over the trauma label. Like I was being dramatic. My therapist explained that most of us automatically assume “real” trauma is rape or war, and that’s it. But in reality, trauma is not an “event.” If you want to read more about this, I highly recommend this Article I found online.

    This year is really the first time I’ve ever truly considered the risk to my own health and life. Especially considering the involvement of blood thinners, etc. Maternal mortality is a terrifying and awful thing. For the first time, I got scared. I realized I could never leave the two children that I have. Fortunately, no doctor has suggested that it’s too dangerous for me to try for another child. I just don’t want to push it too far.   

    I have a hard time with the idea of not wrapping up my family on my own terms with a nice little bow, but that’s rarely the way life works. It is hard not to know when it’s the “last time.” Last baby. It’s hard to imagine finding out my baby was, in fact, my last baby when she’s already 7 years old. But that’s part of being human, being mortal. We never know when something is the last time. As my anxiety so often reminds me, you never know when it might be the last time you see or speak to someone. We only have the moment! 

    I’m grateful I enjoyed Aidia’s babyhood, preschool years, and all the early “firsts” because I knew she was my miracle baby. I soaked it in and savored it as much as I constantly could. At least I didn’t take her for granted. My miscarriages started when Jack was only 13 months old, so I filled his baby and toddlerhood with everything I could, too. It may be a forced perspective but I’m thankful that I have loved each stage with my children. I’m going to do my best to continue that. It helps to remember that I have lots more to look forward to, even if I have to adjust my expectations about having any more children. 
 
    I continue to filter many conflicting thoughts. I’m 16 months into night shifts and I’m definitely feeling the shift work sleep disorder. I don’t dare start on a med for insomnia right now when I’m about to try to quit all my meds. I love my job and want to stay at my current hospital for now. But, I worry if progesterone supplementation would be enough to balance out any issues with hormone regulation and circadian rhythm problems. With fibromyalgia, I depend so much on medicine to make it through the day (and night) and wonder if I would really survive not taking anything. But would I survive never trying for a last baby? I don’t think so. 

    I probably need to take some of the responsibility off myself. If a pregnancy is healthy, it’s pretty hard to hurt the baby accidentally. If I lost one, it would probably be due to factors beyond my control. Most moms have to continue working through pregnancies and push themselves through hard shifts. I think I have to remove some of that guilt and anxiety that working would make me lose an otherwise healthy baby. All these thoughts reaffirm to me that this is what I want right now. More than travel, more than financial freedom. One way or another I’ll be able to close this chapter and focus on all the other exciting things life has to offer. No more living in limbo. Thank you everyone for your kind thoughts when reading this very personal journal I post on the internet, I will keep the updates coming. 😉

Monday, January 1, 2024

The Journey To Peace

Well, I’m back. It’s only been 4+ years since my last post! I went to nursing school and have been working as a nurse for a little over a year, and recently graduated with my BSN. I work at a hospital on the pediatric floor, mainly in long term acute care. Basically, I get to hang out with all the babies who are ventilator dependent, and I adore them. I’m significantly healthier than I was 4 years ago, when we decided to take a nice long break from anything fertility related. I’m also still playing with Skyward Symphony, so my music degree isn’t going to waste!

RN, BSN, summa cum laude 


My gorgeous family in 2023

Looking back, it was definitely the right choice to pause fertility treatments; we needed to focus on Jack’s needs for a while. He ended up being admitted to the state hospital in 2020 and stayed there for 7 months. He is now doing a million times better and just finished his first semester of 7th grade. He fixes all of his teachers’ computers. I’m so proud of Jack! Aidia is the most wonderful ray of sunshine and is excelling in first grade. She just turned 7 years old! She is the biggest cat lady I’ve ever met in my life. I continue to feel lucky every day for my rainbow baby.


I’m sure from the outside it looks like we settled long ago on being content with the son and daughter we have. In a way, we were content enough to focus on other things. But ever since our 7th loss in early 2019, I’ve been swallowing down the ache for one last baby to complete our family. Please don’t mistake that feeling for one of ingratitude. I know I’m beyond lucky to have any children at all.

I imagine the relief of our family being complete but can’t seem to find that peace without at least exploring the possibility of one more. This phase of our lives has lasted a long time. I was pregnant with Jack at 20 years old and we've been trying to build our family since that time. I'm now 33. I’ve tried to lie to myself and say I’m content to be “done” with 2, but it’s just not what I actually want. I wish it was!  Maybe that sounds selfish, but you can’t say I haven’t put in the work over the years to deserve a chance. I don’t necessarily think it’s a bad thing to want a 3rd child, obviously lots of people do, but for some reason since my chances are so poor- I get the vibe that I should “just be thankful” for what I have. Like, “Girl, sit down. You got your miracle.” Simultaneously, we STILL get asked when we will have another baby. I feel how I feel. I don't want to apologize for it on my own blog. I'm the one who will have to take the toll of all of it- regardless of how it turns out. My heart shatters for people who struggle with infertility of any kind; my personal hopes or wishes don’t negate that.

I can’t believe my baby just turned 7. Time is going too fast. The days are so long but the years are short. Like every other mother, I'm worried I'm missing it and not doing enough for my children- not teaching them enough.



I always told myself that age 35 would be my cut off from trying for any more babies because my risks are already so high. It just used to seem so much further away. It took 5 years to get Aidia, so it feels like it’s now or never.

I don’t know if this journey will be one that leads to another miracle, or if it is a journey to acceptance. I can only hope that it is a journey to peace and that my soul can rest with whatever is in store for this area of our lives. 


I went back to therapy nearly two years ago. I’ve been much more careful with myself as we’ve discussed the possibility of trying for a baby, as I now know how traumatic this tumultuous journey can be. I had specific goals to accomplish before I was willing to dive into anything fertility related again. Therapy has been a huge thing for me- I’ve tried to engage in a healing process, instead of crawling back to therapy after exposing myself to even more trauma. I’ve been slowly working through what I’ve experienced, and unraveling how it might affect the decisions I make now. 

 

I’m trying not to get too emotionally invested in this process or outcome either way. I just want to take baby steps and see what everything is looking like. See what our chances look like on paper. It’s too much emotional pressure otherwise. Right now, a baby is still a pipe dream. There have been many months where I’ve gone back and forth between “maybe, maybe not.”

 

It’s not the same economy that Jack was born into. I work full time nights as an RN. I would be lying if I said I didn’t grit my teeth and wonder how we would hypothetically manage. How would I go part-time? What about childcare, breastfeeding? Pumping at work?! How would I work overnight if I had a baby, or ever sleep during the day? Wouldn’t working dayshift be even harder due to childcare? Would I even survive working nights without caffeine? I now have one child in junior high and one in first grade. Their expenses and needs have expanded over the years. Do I want one child in high school and one in diapers? A 3rd child would mean less room in a 3-bedroom house, and less of Mom to go around. It would mean less money for upgrades, first cars, college, or vacations. It might stretch us to our limits.


With my history, I have to entertain the possibility that I might be too sick or too high risk during a pregnancy to continue full time work. I take around 7 prescription meds to manage chronic conditions, and I would need to stop all but 1 or 2 if pregnant. That’s going to feel like it’s going to kill me all on its own. It is hard to imagine making it through a 12+ hour shift without at least an Aleve. I’m willing to push through the pain I go through fibromyalgia sans medications, but I am worried about how difficult it will be. This is less important, but I’ve spent over a year working hard to reach my goal weight. What if a pregnancy wrecks all of that work? My likelihood of gestational diabetes returning is also high. It’s a lot to consider.


Working at night affects your circadian rhythm, which regulates hormones. The research on working nights while pregnant being associated with miscarriage, pre-term labor, gestational diabetes, intrauterine growth restriction, etc is terrifying (though they haven’t proved causation). I remember when I first started nights my period was all over the place for a couple months as my circadian rhythm was adjusting. The risk scares me a lot. Rearranging my whole life to reduce the possible risk also feels terrifying. 


Babies must be on Aidia’s mind also. She asks me for a “roommate” at least twice a week. I explain that it’s not always easy for everyone’s body to have a baby and she tells me to pray harder! I love her sweet little spirit and optimism. She came bursting in my room the other morning and explained that she had solved the problem and we could just ADOPT a baby! Like it was as simple as driving down to the animal shelter. She told me she didn’t even care if was a boy instead of a girl. She would definitely be the world’s best big sister. 



Though we’ve been trying to focus on “baby steps,” our consultation with my RE cost a few hundred dollars and THEN it felt like “oh ok this is for real.” My doctor wanted to repeat a bunch of tests. I’ve been working with this same doctor since our 4th loss and trust him completely. He said I was brave after all we’ve been through to come back and even try for one more baby. I don’t know if I’m brave or actually just stupid. He emailed me a copy of his notes and I can’t believe the pages and pages of tests and procedures we’ve had in the past 13 years. I almost forgot what it took to get Aidia here. 

 

One of the hardest thing with fertility testing is figuring out billing. Usually insurance isn’t contracted so we opt for self pay prices. I call around with CPTs but companies get confused and you get bounced between representatives forever. Sometimes the nurses at the fertility clinic will get on the phone with 3rd party labs and try to figure out costs for me, which is amazing. At the end of the day, you usually have to decide to either take a gamble, or, pay the self pay price and know what you’ll pay. The first blood panel I needed cost $600 out of pocket to run. Insurance covers the CPTs but not the 3rd party lab. So you can bill insurance and hope they cover it, but if they deny it, you’ve lost your chance at the self pay price, and now that $600 would turn into $2000. I was a bit stressed about paying for the blood panel, but in the same week I was offered 3 extra partial shifts with call in pay which basically paid for it. That was kind of amazing timing.


The blood panel was a lupus/ antiphospholipid syndrome extended panel. Despite the autoimmune cesspool which is my family history, I actually tested negative for lupus and APS way back with a hematologist over ten years ago. I had read enough about APS to know it can be really brutal on pregnancies, but always felt relief that I had tested negative and ruled that issue out. I was fine redoing the test if that’s what the doc wanted. I decided to start with that test because I was confident it would be negative and I could mark that off the to do list easily. 


Then I learned that APS antibodies can be transient. 





I was completely shocked that I tested positive. Granted, looking at my history it makes a lot of sense. Not sure why these things still surprise me but this one really did. This one hurt my feelings because I was so sure it wasn’t going to be an issue. 


Just to be clear, I don’t have lupus, just the APS antibodies (which occur more commonly when you have lupus). This is the third condition found in my blood that increases the risk of blood clots. I sat in a stupor and wondered- how did I ever have children at all? How have I never had a blood clot? Should I be taking baby aspirin all the time, like starting yesterday?! How many dormant autoimmune issues do I have that are yet to be discovered? 


Basically, antibodies in my blood are mistakenly attacking cardiolipins (which are a fat important for blood clotting). These antibodies can lead to impaired blood exchange between mom and baby, cause placental insufficiency, possible impaired hCG release, and can lead to repeated miscarriages or stillbirth.


I just can’t believe we have another diagnosis working against us. It feels like we have all the top risks for miscarriage. Hashimoto's, endometritis, MTHFR, APS, and Factor V Leiden. Plus on Kevin’s side there is a history of high oxidative stress and DNA fragmentation. I look at that list and I feel deflated. But we’ve beaten the odds before. 


The treatment for APS is aspirin and Lovenox in pregnancy- which I did with Aidia anyway until I had a subchorionic hemorrhage with her. At that point I stopped the Lovenox injections and continued aspirin. Since I have other clotting issues here’s a good chance that I would be doing aspirin and Lovenox anyway. Especially with 7 previous losses. So this news doesn’t really change anything, it was just a bit triggering. Bad news never feels good. As far as the idea of going on more blood thinners in a pregnancy…I’m scared of having another hemorrhage and losing a baby to overcorrecting the risk of clots. Aidia survived a hemorrhage. It just feels like the worst game of “guess and check.” 


Though it may be brave to face the infertility world again, I also know it is equally brave (if not more) to know when to stop. I’m just not sure which hurdle I’m facing yet. 


I read an article online where a psychologist talked out the traditions we have around women, like bridal and baby showers, and how they celebrate the “beginning.” She said “It makes sense that that’s what we anticipate. When we’re done having kids, our perception of ourselves changes. We must navigate the expansion and contraction of ourselves in relation to who we thought we were, what we expected to become, and the reality of who we are…women who don’t firmly ‘close the door’ - be it mentally or physically- can be tormented for years, never letting themselves feel complete or enough.” 


I love working in pediatrics. My goal is to someday transfer to working in a NICU and get certified for critical care in that setting. Right now, it feels like there’s this big hole in my heart and I hope that I will be able to heal it to the point that I could work in a NICU without feeling triggered by my own traumatic experiences. The envy can be biting in some situations. I have more work to do before I’m ready to pursue that goal. I always thought that if I could settle my feelings and complete my family, I could be at rest with those emotions and give my all to help others. It probably all runs deeper than that, and tying things up with a nice little bow won’t solve everything. I don’t know what this year is going to look like, but I’m hopeful that I can face it with a little less fear, and a little more commitment to finding peace and satisfaction no matter the outcome. 

 

Sunday, December 1, 2019

Pressing Pause

.

I was close to hitting rock bottom. Mentally. Which, by the way, is a hard thing to admit to the internet. It wasn’t just the fact that we were trying to conceive and I had to be patient about it. It was taking hormones for two weeks out of every month and then stopping them suddenly. Temping every morning, two LH tests a day, documenting all of it. Stopping my medications for migraines, sleep, and anxiety for a period of time every month, just in case pregnancy occurred. It was trying to get my thyroid back to a healthy number with my new, higher dose of thyroid medication. It was the fact I’d been off my antidepressants for 11 months, and got worse every month. It was trying to test for pregnancy early, according to days past ovulation, not a missed period, in case we needed to adjust the progesterone dose right away, but not knowing for sure when ovulation happened because of multiple peak LH tests. It was my cycle being all over the place for the first time in my life. It was having no energy to function or cope with daily life or stress. Kevin and I had the discussion often, where is the tipping point? When does it get bad enough that I have to stop? I thought I was close to the breaking point already, and then last month happened.

At the start of my cycle at the end of October, I went in for an ultrasound to confirm our suspicions that I possibly had an ovarian cyst. Sure enough, on my left side, there is an ovarian cyst about 4 times larger than the one I had rupture on my right side in January. It made sense to me, gave an answer for the random pain I had been experiencing for a few months, and explained why my cycle was so irregular for the first time. We didn’t get a blood test at the right time to confirm that it was a hormone producing cyst, but it was likely, considering the changes to my cycle. The cyst wasn’t quite large enough to require intervention; they wouldn’t go in and drain it or anything, because it was not large enough to cause an ovarian torsion. It would either rupture, or resolve, and we could keep an eye on it every few months to make sure it didn’t get bigger. I walked away feeling like I had a bomb inside of me. I was just waiting for it to rupture. Considering how painful the small cyst rupture was, I could only imagine how severe it would be with a large cyst.

cyst
The clinic said while they wouldn’t do any interventions with an active cyst, like prescribing ovulation meds, etc, but I could still try to get pregnant naturally. It might just be more difficult, and harder to track my cycle. Adjusting to that news was stressful, but to top it off I had insurance issues and was charged over $600 for the ultrasound, despite having already met my deductible. The hospital had coded it for infertility (even though I do not meet that medical criteria) instead of diagnostic imaging. I’ve spent hours on the phone trying to get it re-coded, and it’s in the review process now.

I tried to work through my options, in what was one of the hardest counseling sessions of my life. I cried through nearly the whole session. I was having so many breakdowns in my daily life, I knew I wasn’t well. But I didn’t feel brave enough to stop trying for a baby, to take the time to get well. Aidia turns 3 next month and I so desperately wanted to give her a sibling who she would be closer in age to. For both her and the younger siblings’ sakes. When she starts first grade, Jack will be in Jr High School. I thought it would be best for her and our final child to be closer in age; playmates, school mates. I just really dreamed of that for her. And if I stopped trying, on purpose, I would watch her grow older, and watch that gap widen. If it takes another couple years for another rainbow baby to arrive, assuming it’s possible, I would always be in so many different phases at once. I imagine Jr High, elementary school, and a baby at home. My kids love each other so much, but they don’t play together in the same way that kids closer in age do. Sometimes I watch them play with their cousins and tears well up. They get lonely, at home. They both always want Mom’s attention so that someone will interact individually with them on the level they want. That can be a high demand on me.

I had so much fun playing with siblings close to my age growing up. I don't know why I can't give my kids that. It's hard not to feel like it's my fault, but I always knew it wasn't.  Until we decided that a break might be necessary. The idea of waiting on purpose felt like it had fault attached to it. Sometimes, at the school pick up line, I watch three kids pile into the same van, and my mind is blown that you could have all your kids close enough that they could go through school together. It actually breaks my heart. I’ve sat in the van and cried over it. Mourning this idea, this dream, that I wanted to give my family. I'm slowly accepting the fact, that even being able to have one more baby would be an absolute miracle, even if all my children turn out to be more than 5 years apart. I went through this same painful process during all the years we were trying for Aidia and Jack was getting older. I didn’t think I would have to do it again. I tell myself that as long as we have love in our family, all will be well, no matter what happens. But it still hurts. It’s a total paradigm shift. I explained to my counselor that stopping didn’t feel like an option, because time was against me. And I don’t want to be stuck in this phase for another ten years. We wanted to get our last baby here, and move forward.

I couldn’t keep enduring these mental breakdowns, though. My anxiety had reached a new level. I felt afraid of the moments I used to crave. Any time there was any quiet or peace, where I should take a moment to relax, or meditate, my stomach lurched and acid jumped up my throat. Because I'd “forgotten” for a moment to worry, constantly. To be on an endless loop of my worst moments, my fears, things I'm ashamed of, embarrassing days that were last week or decades ago.

I had developed a new kind of performance anxiety with the symphony which just pissed me off because literally i joined the group to do something good for myself. To feed my soul. I started playing percussion in 5th grade, I know what I’m capable of, but I felt out of control. Whenever I had a critical moment in front of a huge rehearsal crowd, my heart would beat as if outside my body, my hands sweat, I felt dizzy, I would visibly shake. I certainly didn’t have the confident calm that I needed to actually perform music. I would make silly mistakes because my body felt like I was running for my life. Fight or flight. The thing is, I've been in performance situations a lot in my life. I have a Bachelor's in music. I've done juries and ensembles and traveling performances. I've had great and terrible performances. What I'm doing now is relatively low pressure and fun. I couldn’t understand why my responses were so disproportionate. It was beyond frustrating. (As a side note to anyone wondering, I was able to get control of the new-found performance anxiety, and had one of the most wonderful experiences playing our oratorio to 4 sold-out shows. Rough journey, but happy ending. I’m so thankful.)

My counselor asked me if all these waves of panic I'm getting through the day, have like a "color" to them. I told her no, they are electricity. Literally a jolt in my heart and a simultaneous stab in the stomach- as if you were to look up from walking down the railroad tracks, and suddenly realize is a train immediately in front of you. But I get that physical lurch because I suddenly realize that I forgot to be upset or worried for a minute. It's a battle with myself. I couldn’t seem to get out of that cycle.

I told her my due date with Vincent was the next day, and it almost feels like your body remembers. She was discussing the possibility of EMDR. I was less than thrilled at that idea. I would rather not go back and revisit everything that could have possibly traumatized me. But I also know it's highly effective treatment. In the meantime, she wanted me to have more self compassion and recognize the pain I’m in. I agreed to try and affirm to myself something along the lines of “It’s ok to be ok” when I get those horrible anxiety pains, touch wherever it is that I’m feeling the pain: chest, stomach, etc. She counseled to try and let myself have peace occasionally. It’s ridiculous how hard that can be sometimes. We talked about how some of my biggest problems are totally out of my control, so I kind of turn obsessive about making the few things I am somewhat in control over perfect, but that's still not possible, which results in anxiety and depression. I get stuck in an obsessive loop in my head about how something should have happened or how I should do something in the future.

Naturally, I had a huge panic attack when I got home after counseling, where I couldn’t make my lungs take in air. It was basically at that point when Kevin and I decided, painful as it was, that if I wasn’t pregnant that cycle, that we would take a break, and focus on me getting well for a while. As much as we want to finish our family and put this whole phase behind us, it doesn’t help anybody if mama ends up in the loony bin and can’t even take care of the children we have. We wondered if I would even be able to handle a baby right now, if I had one. Admitting that felt like a personal failure, but sometimes the hardest and bravest thing to do, is to realize we are not superhuman, and there is a limit to what we can endure. It's a hard pill to swallow that I am worth enough to get help, even if it means putting everything else off. It’s not quitting. It’s not selfish. Even if it feels like it.

I don't write about it often for his privacy, but for several years Jack has had problems that require an extreme amount of intervention. Special needs that often drain us, financially, physically, emotionally, mentally- trying to make sure he is taken care of. Some weeks are harder than others, but it is such a strong underlying current in our day to day lives, that any little thing can suddenly become "the last straw" where I feel incapable of dealing with anything else that day. And yet feel sick to my stomach about the situation all night, and can't rest.

Any parent who has a child with special needs and required interventions will tell you the same thing. It's more than we can handle, but we continue to handle it every day. Because that's what parents do. But putting our dreams of finishing our family on hold for my own sanity felt unimaginable.

When life gets really hard like this, and you feel defeated, you realize life breaks you down for a purpose. I felt ready to accept basically anything, if I KNEW it was the right thing. The hard part is, you rarely know for sure what the right choices are in life. If God told me we weren’t supposed to have any more kids, I could probably accept that answer eventually. If He told me it would take five more years, fine. At least I would know. It’s the not knowing that is hard. And if the answer is “pause and get some help for yourself,” that answer is nearly impossible to hear. Moms don’t put themselves first.

My very wise friend said when you feel your mental health deteriorating like this, and you're putting off getting help, it doesn't just stay where it is and wait for you. It continually gets worse. Putting a dream on hold in the pursuit of wellness sounds worthwhile, but I wondered how much a break would really help me, if I truly felt sad the whole time.

I couldn’t help but consider the situation the manifestation of a tender mercy. For so many years, I told God I would rather not be able to get pregnant if the baby wouldn’t survive. Just don’t let it happen until we can conceive a healthy baby. And as hard as it has been, I feel thankful for that. Maybe He’s protecting me from an 8th loss. From a psychotic break. I think it all comes down to fully, surrendering our will and trusting Him. If we are meant to have a 3rd child, they will come, somehow, someday. Just like Aidia did. I can’t explain her, her birth makes even less sense now than after she was born. When I thought we could explain how it happened. She’s purely miracle. Being able to accept His will brings peace, even in pain. I hope I can deepen my connection with God to be able to be led where I need to go. And for life to be happier despite challenges.

Just when I was settling my mind down, and becoming as content as I could be with our decision to move forward, I started feeling really sick at work one day. I was down, because the two coworkers I was working with that day had BOTH announced they were pregnant. What are the odds of that? I was already struggling so I felt like the “ok it’s official, the universe hates me.” The baby conversation was constant through the day. Painful. And the cramping I was feeling kept getting worse, along with the nausea. I was sure it was the cyst. But my coworker convinced me that cramping and nausea were indeed pregnancy symptoms, and I should go home and take a test, just in case. I didn’t want to, because I was settled with our plan to move forward once my period showed up. But in the end I agreed. I went home in the afternoon and took a test. It wasn’t first thing in the morning, which is when you are supposed to test when you test early. I didn’t do a “four hour urine hold” to let any hCG build up, so I was sure it would be negative. And just as I was about to toss it in the trash, I noticed the faint second line that showed up. It was very fine, very faint, but still a line. Not stark white like the other negative FRER tests I had taken. My heart about fell into my feet. I was totally shocked. I wasn’t confident with calling it a positive test, because of how faint it was. When Kevin got home that night, he could see it too. So I flipped my perspective back again. Ok, here we go, now it’s actually happened right when I gave my ultimatum, and I’ve got to be ready to be pregnant now. With my other pregnancies, when I would get a faint line like that, it would be noticeably darker by the next day. So we would know for sure by the next morning.

The next morning came, and I took another test. But it wasn’t darker. It was, at most, the same as the first line. This was concerning to me, but after all, it had been less than 24 hours, and urine dilution matters a lot at that stage. And still, both tests had lines. I was a little nervous at the idea that I was possibly having a chemical pregnancy, basically where a pregnancy tries to take, but never grows. You could get a positive one day, and a negative the next, when that happens. But I still couldn’t be totally convinced they were positive. What if they were just really bad evap lines? Those days, I was totally in limbo. Maybe it was just too early.

The third time I got that same, very faint line, I decided to call the clinic. I didn’t know what was going on. I couldn’t call them positive, but they weren’t white negative tests either. They definitely weren’t getting darker. The clinic sent me in for blood work. I felt confident that my number would be low, since it was early, but that we could track it through bloodwork and see how everything was doing. I was absolutely gutted when the beta came back, not low, but negative.

I had been told by two separate friends, that their doctors had said cysts can cause little lines to show up on home pregnancy tests. I was starting to wonder if that was what was happening. My nurse had never heard of that before, but I knew whatever lines I was seeing were not accurate. Because I saw that little line just two hours away from my blood test. Even with a chemical pregnancy, evidence should have been stronger on my blood test than a urine test, since it was such a short amount of time between the tests.

So we accepted those extremely faint lines we were seeing were either evaps, or caused by the cyst, but weren’t really positive after all. And we shifted our mindset yet again. I wasn’t pregnant. It hurt all over again, but I was relieved at the same time, because that would not have been a promising start. It was time to go back to my doctor and get some help, start on my SNRI again.

It was a difficult appointment with my doctor (who I adore.) My mental screening was poor enough that they had me do a second, more in depth screening related to suicide. I guess that was validating that I needed to be there. My doctor agreed it was time to go back on the meds I had been avoiding since we had been trying for a baby. But he also wanted to convince me that if we were determined to have another child, I could stay on my meds. Some people just have to. But I am not most people, my risks are not most people’s risks. Especially with neural tube defects. I couldn’t imagine putting anything in my mouth that I knew might possibly harm my baby while I was pregnant. I know the common side effects are that the baby has to withdraw from the meds after being born. They can shake and be colicy, maybe struggle learning to feed, or have minor breathing problems. Even though that’s not the most serious of side effects, I can’t imagine doing that to my child.

He basically told me, if I had a child born with a birth defect, we would never really know if it just happened, or if it was due to the medication, since the inherent risks are about the same, and the question I needed to ask myself was- could I live with myself knowing it could have possibly, though not likely, been the meds? No. I don’t think I could. Some studies say SNRIs double your chance of miscarriage. Other studies concluded there was no added risk. But studies also agree that being clinically depressed highly increases the chance of miscarriage. So what is a depressed mom to do? Risk the baby by not taking meds and staying depressed? Risk the baby by taking meds that might help or might harm? It’s an impossible choice.

I wasn’t on antidepressants for any of my pregnancies, and I survived them. But I do wonder if I was also adding risk by not staying on them. Which is why we were taking an official break, so I can be on my meds long enough for them to help. They are the hardest type to get back off of (as my doctor reminded me.) I knew that, since I went through that hell last time I stopped them. Sick as a dog for two weeks. This is the reason I didn’t just try to take a break and take the meds for a month or two, it needs to be worth going through the process. My counselor advised me to try not to set a timetable for it, rather, have goals or ways of measuring what “feeling better” looks like. I do have a lot of those landmarks to identify when I’m doing better, but we are thinking it will need to be at least a 6 month break.

It’s hard not to blame yourself for losses when the first thing doctors would say to me was “maybe I should have started my Lovenox injections sooner, or the aspirin sooner, or hormones later, etc.” They make it sound as if it’s in your control. Causing huge amounts of anxiety about anything I consume while trying to get pregnant, or during pregnancy. Can I have any caffeine, is this prenatal ok, what time should I take my blood thinners? No one ever sat down and told me “This is not your fault. Nothing you could have done would have prevented this.” I just can’t take risky medication while pregnant after what I’ve been through. I love my doctor, but could a man ever really understand what it’s like to carry around something so precious and so fragile within you? I’ve already lost 7. No more extra risks.

I picked up my meds, ready to press forward. But that night, I felt crampy, nauseous, and was nervous about taking the meds since I still hadn’t started my period. I decided I would take an internet cheapie test, since I had never seen a fine false line on one of those. To ease my mind. So I took the test at night, no urine hold, anticipating the negative result would comfort me. It was a dark positive. I stared at it, refusing to believe it. Oh my gosh, it really was just too early before. This is for real. I wondered if it was a bad test, so I took at second one about 15 minutes later. It was the same, if not a little darker.

We again switched our mindset. Ok. Here we go. I was so unbelievably happy. But the number of plot twists felt like too much to handle. This was in the middle of opening week for symphony. I had a run through rehearsal, a dress rehearsal, and four shows within a week. I was there at least 4 hours a night, and one day was about ten hours, and I tried to deal with what was happening at home in the mornings.

The next morning I took another FRER, expecting it to light up super positive since the cheap ones did. Can I even explain my emotions when it was very clearly negative, not even a hint of a line? I had to get off this roller coaster. I couldn’t take it anymore. So I took another cheap test, also negative. In desperation I called my clinic, thinking I must be having a chemical pregnancy. They sent me in for blood work. I was expecting low numbers, which would probably drop to zero over the next few days. Instead, it was negative. So, to recap, faint barely there lines followed by negative blood work a few hours later (Wednesday). Then two dark positive tests late Thursday night, followed by negative tests and negative blood work early Friday morning. So we knew with two negative betas less than 48 hours apart, it wasn't a chemical.

So how do I explain those two dark tests? Turns out, the brand Wondfo had recently recalled more than 60k tests, for showing dark false positives, even if they were dipped in water. I left a scathing review on Amazon. I cried. Honestly the mental anguish of those days. I had been pulled back and forth, I was angry, I was defeated. And if there had been any doubt in my mind before, I knew now. I can’t do this anymore. I started my meds. And finally two days later, my period showed up. WHY did this have to happen? I had accepted it wouldn’t happen that month and was ready to move forward, but instead I had to have one last heartbreak.

When we decided “that's it, that's all we can take for now,” it felt like a huge weight was lifted off my shoulders, so much extra stress gone. But at the same time, this immense sadness settled on me.

We've been through about one year and suffered one loss since deciding to have a third and final child. We went through 5 years and 6 losses before we were blessed with Aidia. I'm going to have to be patient through the sadness, and not put my body and mind through more than I can tolerate. Patience can pay off. My body needs a chance to heal. I would rather start a pregnancy in a healthier state.

Whenever we are ready to try again, I will call and schedule a follow up ultrasound to check on any cysts, and will have a repeat uterine biopsy done to check for any recurring endometritis. But until that time, I can focus on my two wonderful and amazing children that I already have. They are the sunshine in my life. My job. My role in the Symphony. Trying to improve myself, with better sleep, better exercise. Have some happy around. I know I will still feel sad. I wish I could say I will be content with my current family size, and we can be done for good, but I would be lying to myself. We feel like there is one more baby that needs to come. But at least I will know what the plan is for now, and why.

Monday, October 21, 2019

New Challenges

It's something we've always said, when looking for the silver lining. "If we figure out the cause of the losses, at least we can get pregnant on our own and don't have to worry about that part." 8 of my 9 pregnancies were conceived the first month trying, and one was the second month of trying. That's a pretty telling statistic. With a history like that, you know you're going to be pregnant if you try to be. My worry was always if the baby would survive or not.

Because of my history, when I last wrote that we were gearing up for a baby, after treating the endometritis, I fully expected to be back on the blog writing within a month, hoping that the treatment would allow for a healthy and long gestation. July came and passed, and I wasn't too disappointed when we didn't fall pregnant. We knew the timing may have been off because of when we met with my doctor and got the “go-ahead” to conceive. it was a close window. Although I was still a bit surprised.

I actually was so sure that we would be pregnant, because in the past it always happened right away, that I started to have some pretty bad anxiety. I would suddenly remember that I might be pregnant that month, and my arms and legs would literally go numb. It was like a “going into shock” kind of response. I think it's just that fear manifesting itself physically, the flashbacks that I have from losing 7 different babies. You feel like once you're pregnant, there's no way off the roller coaster ride. You're at the top of the hill, and there's no escape other than to follow the path straight down. I talked to my counselor about it, and worked through it the best I could. It's almost impossible not to feel like loss is inevitable. And if I was pregnant, I knew it wouldn't be possible for me to just not love a baby to avoid getting my heart broken. I bond right from the start.

I felt like I had equal and opposite fears. Fear one being that I will never have another healthy baby and will need to give up for sanity's sake. (But we only want one more. And I'm only 29. So really the question is, how long can I push it until I have some sort of mental lapse?)
My opposing fear is that I do have a third child, and have no idea how I could keep my job, or how we will manage. But I try to trust in God to work out that part. It always has so far. 
 
So as I said, July passed and we were set on August being the month for good news. Halfway through the month I stopped my medications for migraines, sleep, and anxiety. And started supplementing hormones. Which honestly is so difficult. Hormones make you crazy anyway, but without taking medication I have an extremely hard time sleeping, dealing with migraines, and not having panic attacks. And yes I know there are many natural remedies. I do the best I can with those. I go to counseling; I practice breathing and relaxation. But nothing works as well as normal medication to manage my struggles. Have you ever tried just breathing through a migraine? It doesn't work very well. Fear of hurting an unknown, unborn baby keeps me from doing a lot of things that help me. Hot baths, caffeine, etc. I have more anxiety than is normal for me when we are trying to conceive, but after all, after every loss I've had, the doctors discussed what I did or didn't do early in the pregnancy. So I have to start working to preserve a pregnancy before it even exists. 
 
August passed. and I was still not pregnant. At that point it felt, weird. But it would be silly of me to be worried after only trying a few months. September rolled around and I started ovulation tests to see if I was ovulating early or late or something. Using the digital tests I got days and days of high readings, but never a peak read. I did my best keeping track of everything, and held out hope that it would be the month. I didn't want to wait too long after the antibiotic treatment to conceive- worried that the endometritis could come back, or flare up. Just when I was feeling fairly confident that September was our month, I started my period 4 days EARLY. For the first time ever in my life. I started to worry. That seemed like a luteal phase defect. Why was I not getting pregnant, for the first time ever? Why was my cycle irregular for the first time ever? I confirmed with the fertility clinic that the supplementary progesterone I was taking 2 out of every 4 weeks would not be interfering with my cycle. 
 
So October, our 4th month trying, I started temping. Doing basal body temperatures is a lot of work when you combine it with taking LH tests twice a day mid-cycle, supplementing hormones morning and night, and taking a vitamin regimen. And stopping all your helpful meds. My BBT cycle looked accurate, up until the time of ovulation, it started slowly rising and then dropping all over the place. I couldn't see any confirmation of a healthy ovulation. Granted, I wasn't sure if my temps were accurate since I toss and turn at night, can't take them at exactly the same time every morning because of work, etc. But I called the fertility clinic to see if they wanted to do an ultrasound to check for a cyst, or to confirm if ovulation actually happened. 
 
I spoke with the nurse and she told me they don't rely on temping, because they have blood tests and hormone readings they can rely on. I'm hoping my BBT chart just isn't reliable. If I did an ultrasound mid-cycle, they wouldn't be able to tell if it was just the corpus luteum, or a different problem-causing cyst. So I was told if my current cycle didn’t take, I could get an ultrasound on cycle day 2 or 3, to see if I have a cyst. Then again on day 12 to see if there's an egg there, to see if I'm even ovulating. Fortunately, I'm already on progesterone, which is how they treat a luteal phase defect anyway. Of course it's better and more accurate to have the ultrasound done at the fertility clinic, but my insurance doesn't cover it there. So I'll need to do outpatient imaging at the hospital and hopefully it's good enough to tell them the info they need.

As the month came to an end, and my BBTs were soaring and dropping everywhere, I talked to some of the ladies in my support group. They suggested I get a laparoscopy for silent endometriosis, which makes it hard to get and stay pregnant. At this point I believe I basically have every diagnosis. One lady said she would lose 4-5 babies between every live birth, and finally doing IUIs somehow was much better, and brought her a couple healthy babies. But I could never afford a laparoscopy or IUI right now. There's no way.

I can’t control ALL these factors. Every year I feel like we get two new diagnoses. So far we’ve dealt with Leiden factor V, MTHFR, folate problems, low progesterone, Hashimotos, DNA fragmentation, endometritis, and now possibly a luteal phase defect? Or maybe just late ovulation? It’s so overwhelming. How do people have babies on accident?!

When my period hadn’t shown up today, I took a HPT and was very surprised to see a barely there faint line. I kept thinking I was imagining it, but every time I looked I could see it right away. I was worried though, that it was so faint, that maybe I got a test with a bad “evap line” which is where the test looks positive but it’s just because it was wet and then dried, leaving a shadow more than colored dye.

Well I wanted to know if it was real. I showed a few friends online and everyone saw a line worth going and testing. So my clinic ordered a beta HCG, TSH, and progesterone level.

I was gutted when the HCG came back at 2. Anything less than 5 is considered negative. But I still felt in limbo. In 2014 I had a beta come back as 2.2, that 3 or 4 days later was in the mid 80s where it was obvious I was actually pregnant. But after my loss this March, my beta gradually went down back to 2 as they monitored the completion of the miscarriage, so I could see that result still being negative too. After a few hours, my progesterone came back at only 7.6, despite two supplements a day. So I know it won’t be long before my cycle starts again. And we will move on to doing the ultrasounds to see if we can figure out what is going on.

I don’t know why suddenly I’m not getting pregnant for the first time ever. Now don’t get me wrong, I know 4 months is NOTHING when it comes to actual infertility, and I’m not trying to be insensitive to that. But also understand, we’ve been trying to have a houseful of babies since we first started trying in 2010 after we got married. That’s been a long time. And we did have Jack right away, followed by our losses starting the following year. I’ve been dealing with my personalized version of infertility my entire 20s. 9 pregnancies later, and I have an 8 year old and a 2 (almost 3) year old. We will never have a houseful of babies like we imagined. We are changed people, and want one more before we call it quits on our own terms. God willing.

It’s been a hard day. But mostly I was upset to find that my thyroid has been slowly declining this year. After my number today, I probably need to go on a higher dose of thyroid meds. Maybe that’s why I’ve felt like crap lately.

My arms ache to hold a new baby of my own. To complete our family. I don’t know why we’ve needed to have and treat so many different problems. I just hope we can overcome them one last time, and complete our family as our own choice instead of medical issues forcing that. I’m still learning that we really don’t have any control. It’s hard to completely relinquish that control, to give it all to God and say “I’ve done literally everything a person can do, for years, trying to prepare mentally and physically so a baby could survive. It’s not my choice if, or when we get pregnant, or if the baby will live or not.” I try to prepare myself for His answer, even though it has been “no” so many times, and 7 times He’s taken them back. I’ve also miraculously been blessed with two healthy children- so I’m not ready to give up yet. I look at my children and I know it's possible. I work in the hospital and go into the rooms of all these newborn babes, and think how simple and easy it seems. So painful- I’m just so worn out.

Jack, age 8.  Aidia, age 2