Tuesday, February 28, 2017

Week 24 of 4K

This week she brought home her Valentine's Day project that she had worked on last week:

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It was "D" week this week!
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On February 24, it was Dads and Donuts at school! We were a little nervous all week as we weren't sure if Mark would be able to make it or not. But he told us nothing would stop him from going, even if he wasn't feeling good. He was able to go with her! You can see from this picture, the smile says it all:
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She also made this for Daddy:
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It says "I love my dad because he takes me to the pool!"

We were going to a hotel that weekend and she was so excited to go. It was the only thing she could talk about all week. :) So I'm pretty sure that was how she got her answer. :)

Thursday, February 23, 2017

More on my plate

Well, I've decided with all I have going on, I really should add another thing: I'll go back to school.

Yep, I'm back in school.

I've been a medical transcriptionist for about 14 years now, 10 of those years I've worked from home which has been a huge lifesaver for us many times.

Unfortunately with voice recognition and many doctors now doing their own transcription, the future of transcription is very bleak. In fact, I'm very fortunate I still have a job.

I always knew I would eventually try to get more into the medical coding aspect as the future of coding is very strong and it's something I can eventually do from home which is a goal of mine (I love working from home!). But with Mark's health up in the air and Hannah still not in school full-time, I wanted to wait a little bit before adding on going back to school.

Well, it appears the time has come sooner than I thought and I'm now enrolled in school to become a medical coder. I didn't want to be in the position where I lose my job and had no choices. I need to think about my future and the future of my husband and daughter.

But, wowzers, I'm a bit panicked.

However, I feel God is leading me to do this. I enrolled in school, paid the tuition and the minute I hit "submit", I panicked What am I doing? How am I EVER going to fit this in when I have trouble doing it all now?

Then I got a text from a friend that said When can I come and sit with Mark and Hannah so you can have a break?

I got tears in my eyes. I felt it was God telling me I was taking the right step.

It'll be a lot of late nights, lots of studying whenever I can...but I have a feeling this is what I need to do for my future and the future of my family.

I admit I'm a little bit stressed about getting all this schooling done in my "spare" time and what I'm going to do when I won't be working from home for awhile....but I'm going out on faith.

It'll all work out....right? Please?

In the meantime I sure could use some prayers. :)

Tuesday, February 21, 2017

Week 23 of 4K

This was a busy week. Not only was it Valentine's Day week but also our school was doing a Cents for CF Awareness Week and Hannah was able to participate in the dress up days.

Tuesday was Valentine's Day.
Here is a picture the school posted on their Facebook page:

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Here is her bag that she made for all her Valentine's she received from her friends at school:
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She also brought treats for her class. She decided to bring cupcakes. She decorated them herself and she and Grandma put them into a heart and a card. I think she did a great job!
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Wednesday was blue and yellow day for dress up. Blue and yellow are the colors of the Cystic Fibrosis Foundation:
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Thursday was favorite team jersey/sweatshirt. Hannah loves the Packers---we don't. Mark and I are Vikings fans. She wanted desperately to go in Packers colors. So, we let her wear her Packers socks and Packers hair bow---that was enough. :) We had to draw the line there. :) She was super excited though!
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Friday was Super Hero day. While I'm sure this meant more like Superman or Batman or someone with a cape, Hannah isn't really into them. Her "super hero" is Cinderella. :) So she dressed in her Cinderella dress:
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We're happy to report that Cents for CF was a big success and the school was able to raise about $1000 for the Cystic Fibrosis Foundation!

Hannah also brought home her letters from this week (N and X) and a penguin she made:
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She also brought home an assignment where she colored the healthy snacks and crossed out the unhealthy snacks. I was very impressed that she knew what was healthy and what was not----like, there is no way that a girl raised by us would know healthy versus unhealthy :)----then she informed me that the teachers helped her. Ah-ha! Now that's more like it.

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Wednesday, February 15, 2017

Week 22 of 4K

This week was "V" week

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She also brought home her Humpty Dumpty project she did:

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She also had her first accident at school. :( She banged her head on the hill when she was sliding down. She had a pretty good bump on her face and near her eye, right by the eye we had so much trouble with earlier in the year. I didn't think to take a picture. She milked it for a few days and then she seemed to forget about it.

Yep, first accident. Not too bad. :)

Tuesday, February 7, 2017

Weeks 20 and 21 of 4K

I'm combining a couple weeks here as week 20 there just wasn't much going on.

Okay, that and I just didn't have time to post.....but I will now. :)

Week 20 was "W" week:

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Her teacher encourages the kids to sound out words that begin with that letter so all week we kept hearing "W-w-w-wondra". She was excited that our last name started with a W. :)

She also got a new shirt and couldn't wait until Valentine's Day to show it off. :)
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Week 21 was a big week for Hannah as it was "H" week which she refers to as "her" letter. :) She was sooooo excited!!

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It was the end of January (where does the time GO?), so she was able to bring home her January Journal
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She was to draw ice cream and while most kids just drew a regular ice cream cone, she drew her favorite ice cream, Superman ice cream, from her favorite candy store. :) Superman ice cream is an ice cream of many colors---obviously. :)

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She drew a snowman.

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Here she is sledding down a hill with our dog, Doogie. And at the bottom of the hill is a ghost----her imagination cracks me up!

Also during H week, they learned about animals that hibernate (or as Hannah says "H-h-h-hibernate!!)
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She also brought home a project they had made, a snowman. :)
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Friday, February 3, 2017

Closing thoughts

Life for us continues to be a rollercoaster. We deal with struggles every day with Mark’s health. Diabetes is so much more than shots and watching your sugar intake. It affects the whole body and creates so much stress in the lives of the diabetic and their family.

Mark’s vision is severely decreased due to his diabetes. He has no peripheral vision and only tunnel vision. He says it’s like looking through a straw. This has forced him to give up his driver's license and it is possible he may become blind in the next few years.

As I talked before, he has a very weak heart due to the diabetes.

He has stomach issues due to the diabetes where his stomach doesn’t work like it should. When he has flare ups of this condition, he has intense nausea and vomiting which can last for days at a time and is in the hospital.

Then there's the horrible nerve pain called neuropathy. Diabetes damages the nerves and I can't even begin to describe the pain I've heard my husband in. Imagine 100 pins constantly poking your feet at the same time and trying to walk. I've heard my husband screaming in agonizing pain from nerve pain. He says it's much worse than any heart attack he's had. It really flares up at night and it’s hard for him to get rest at night.

Recently he’s been dealing with swallowing issues when many times while eating and drinking he has severe burning in his throat. Sometimes he’s unable to swallow and ends up vomiting food and even just water. We found out the middle of his throat basically doesn’t work because of the damage of diabetes.

These complications are only a handful of complications my husband deals with because of his diabetes. He has constant lab and doctor appointments, specialist appointments and constantly dealing with reactions due to high or low blood sugars. He takes 4 insulin shots a day and takes about 60 pills a day.

Mark has pain when he eats, sleeps and walks. I can’t imagine the constant struggle and having pain with every day things that so many of us take for granted.

But, not surprisingly God has provided yet another miracle for us. Mark has lived over 30 years past his life expectancy and even doctors that treat Mark now are amazed he is still with us. I give God all the glory.

Like all things I look back and can see that God is faithful. These are times that I otherwise wouldn’t have experienced had I not been struggling. I consider it all blessings. I mean, I got to witness the miracle of a transplant! An organ from another human being was put into my husband so he could live! A miracle! And I got to experience God’s helping hand in providing $10,000 in one month to help bring my daughter home. A feat we thought impossible but proved to us that NOTHING is impossible with God.

I am so grateful I have gone through this journey.

I’ve cried more, BUT I’ve smiled more.

My faith has been tested, BUT I’ve learned so much more about God, I’ve realized He has a plan and He will always provide.

At times there has been more stress and strain in our marriage, BUT it has also made us stronger and we’ve learned to lean on each other more. I can’t imagine going through this with anyone else but Mark right by my side.

I’ve met people in my life who I otherwise wouldn’t have met.

I’ve realized not everything comes easy and that I take a lot for granted.

I’ve also learned to trust in God’s timing. His timing is always perfect even if it means sometimes waiting much longer than we would like.

As hard and painful as this journey has been at times, I’m glad God chose us to go through it. I’m honored this has been my cross to bear.

A few years ago, myself and some other adoptive mothers came together and wrote a devotional book about adoption called “Adopted For Daily Life”. I wrote a 5-day part on hope. I have copies of what I wrote here and if you would like a copy, please take one. While it is focused on adoption, it can also be tailored to everyday life and I hope and pray in encourages you.

To close, I’d like to say thank you again for having me here and allowing me to share my story. What I want you to take most from my story is that God does have a plan, He does perform miracles and if He is making you wait, it isn’t necessarily a bad thing.

And I encourage you to look back and see how faithful God has been. He is faithful every day, even by things we don’t think about, like the rising and setting of the sun and the food He provides. I’m sure you can think of many times in your life when He has been faithful and provided.

And know whatever you’re facing right now or will face in the future, He is able.

Thursday, February 2, 2017

Mark's brain bleed journey

A few years ago, tragedy struck our community. You may know the story of the Milberg family. Kari Milberg was involved in a terrible car accident, taking the lives of Kari’s daughter and 2 nieces and Kari fighting for her life with a severe traumatic brain injury.

I didn’t know the family at the time but their story touched my heart. I couldn’t imagine what they were going through. A grandma losing 3 granddaughters and having a daughter in critical condition. And each of the sisters losing a child. The heartbreak they were dealing with was too much to fathom.

I joined their memorial page on Facebook and would occasionally reach out with some encouragement, Bible verses or anything that touched my heart. I didn’t think I was doing much. But when I eventually met the family, I was touched by how much I really did help them and stood by them.

We continued to keep in touch and became closer. I remember one day when I was talking with Kari’s sister about Kari’s traumatic brain injury. She said "A brain injury affects everything. It's not on the surface so people do not see it as a disability. But from my learnings and experience, it's one of the WORST disabilities. Each and every day is different for her".

I'll never forget that. I remember closing my eyes and literally thanking God that with all the difficulties Mark had, he didn't have a brain injury. I just couldn't imagine that.

Unfortunately I do now.

About a year ago, Mark was dealing with balance issues with bad dizziness. He had already been struggling with this because of his diabetes but it seemed to be getting worse. I had brought him to the ER one time and brought him into another doctor afterwards with no real answers. They thought maybe it was damage from the diabetes or some medication side effects. In my heart I just had this feeling something was more wrong. He was having more difficulty, more twitching, balance issues, and more falls. I honestly thought it was more than nerve damage or side effects from the medications but I didn’t pursue it. Now I wish I had.

I had taken a week off of work in May to celebrate our 15th wedding anniversary. The original plan was to go on our annual vacation to the North Shore where we spent our honeymoon. However, with Mark not feeling the best, we decided to stay at home and get a few things done and then spend one night in the Cities at Hannah’s favorite hotel.

We went down to the hotel one night and had a wonderful night. Hannah was in her glory at the kids pool.

The next morning at 4 a.m., Mark woke me up with uncontrollable shaking in his right leg. He said to immediately call 9-1-1: Something he rarely tells me to do so I knew it was serious.

He was brought to the U of M where he had his kidney transplant. By the time I got Hannah and I packed up and out the door, we were about 20 minutes behind the ambulance. When we arrived to the ER, almost immediately Mark started having seizures that were getting to be uncontrollable and I was asked about his code status, whether he wanted life saving measures or not. Luckily Mark and I have talked about it several times and I knew he wanted them to do whatever it took to keep him alive. They had to put a tube down his throat right away to protect his airway. Watching all this happening was like watching a movie. It didn’t seem real and it was happening so fast. The nurses and I were trying so hard to keep Hannah’s mind off of it by giving her Popsicles and candy at 6 in the morning and giving her markers and sheets to color, but it was a lot for a little girl to witness.

They did a CT scan of his head right away and that was where they found a subdural hematoma (bleeding on the brain). They said at this point it could go either way. We had a 50/50 chance of him surviving.

My mom came down to stay with me while my friend who is like a sister to me came down to take Hannah to her house. Being separated from Hannah at that time was one of the hardest things I’ve ever had to do but I also knew this was not the place for her to be. She knew the seriousness of the situation. As we hugged good-bye, her sweet eyes filled up with tears and she said “I love you Mommy”. I told her it was okay to cry and she sobbed into my arms. Knowing I couldn’t comfort my child when she needed it most and not knowing if she would ever see her dad alive again was so heartbreaking.

Mark was intubated for 3 days. He was nonresponsive for days. I was told the longer it took for him to wake up, the less likelihood of a recovery of any kind.

With each passing day, doctors prepared me that while it was too early to tell, the prognosis of a full recovery was very slim. They had no idea how much, if any, function he would get back.

I remember holding Mark’s hand and praying to God that if Mark wouldn’t make a recovery, to take him home. I knew Mark wouldn’t want to live this way. I knew Mark knew the Lord and eternity was so wonderful for him. I cried so many times “Please Lord, fix this or take him home.”

When he did first start waking up, there was concern as he was only moving his right arm and only smiling on the right side. We were told this may mean a deep brain injury and there was concern he wouldn’t gain function on his left side. When he started with speech therapy, he couldn’t even open his mouth and eventually we had to put a feeding tube in so he could get some nutrition and medications in.

It's hard to imagine sitting there watching someone you love not being able to do anything, having to literally have someone do everything for you. The not knowing was so hard. The doctors kept telling me it was too hard to tell what Mark would gain back and what he wouldn't.

So all we could do was wait. Wait and see what happened. He couldn't even smile. He couldn't squeeze his hand. What if that was the life of Mark now? What if he was totally dependent on me? I knew he wouldn't want to live that way.

Then we started seeing slow progress.

That first time Mark smiled---priceless.

The first time he said my name---priceless.

The first time he squeezed my hand---priceless.

The first time he stuck out his tongue---priceless.

Remember when I told you about the Milberg family? While dealing with this traumatic brain injury was new to me, it certainly wasn’t to them. They were such a rock of support for me, from the encouragement, to advice on which rehab facilities to go to and how to adjust when or if we did make it back to our house. God brought us together and their support was and continues to be a huge important part in our lives. God will often bring people into our lives to help guide us and I’m so blessed He brought the Milberg family to us in our time of need. I was able to comfort them in their time of need and they were able to comfort me in my time of need.

After 3 weeks he was stable enough to be moved to a rehab facility. There we spent another couple weeks with speech, physical and occupational therapy every day. As tiring as it was for Mark, it was the step he needed to come home.

Once we did get back home, Mark continued to do therapy 3 times a week. It certainly was a journey of grieving. Grieving the “old Mark” versus the “new Mark”. Grieving what Mark used to say or do without knowing what for sure he will gain back.

We had no idea how much he would get back. We have been very blessed that Mark has gotten so much back---much more than we thought he would.

Days are still so hard for him. He still has the balance issues which will never get better. He gets frustrated very easily and has angry outbursts---not the Mark before this brain bleed happened. In so many ways, he had to start over, having to learn new things, trying to remember things that came so easy for him. It’s still a daily struggle for him.

Yes, a brain injury is the worst disability I could ever imagine. It's something I would never wish on my greatest enemy. Every day is a challenge. Every day you wake up not really knowing what to expect.

I will look back and see that You are faithful.

When I look back on our journey with Mark’s brain bleed I can most definitely see God’s loving hands protecting us. When we were in the Cities at the hotel and had to call the ambulance, we were only about 15 minutes away from the U of M where he got his high-level care and has had his transplant. Had we been at home, he would’ve been an hour away from high-level care. Had we been in the North Shore, who knows what would’ve happened. Being so close to the U of M could’ve quite possibly changed the course of this journey. He may have had seizures longer and possibly more brain damage. He possibly would not have survived. As it was, it truly is a miracle he is even still with us. God had us change our plans for a reason.

And of course, the Milberg family whom God brought into our lives. Even to this day, we lean on them for support and encouragement as dealing with a traumatic brain injury truly is a daily struggle.

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Hannah helping Daddy at rehab

Tomorrow--closing thoughts

Wednesday, February 1, 2017

Our infertility and adoption journey


When Mark and I first got married in 2001, we weren’t planning on having kids. To be honest, when we first got married, I thought with Mark’s health, I didn’t think he would survive long and we would be lucky to be married 5 years before he passed away. Being with Mark and taking care of him was my first priority, not having kids. I wanted to cherish the time I had with Mark while I could. I had always wanted to be a mom, but since marrying Mark, I didn’t think it would be possible and although I was disappointed and sad, I figured being Mark’s wife and taking care of him was what God chose for me.

But God chose differently for us.

As time went on, the longing to have a baby increased for both of us and we decided we wanted to try to have a baby.

Never in a million years did we think we would have trouble conceiving….never. My mom had no problems at all and actually had twins. My sister would just look at her husband and get pregnant.

But God had a different plan.

At first when we started our journey to have a baby, we were nervous but oh so excited and hopeful! We figured it wouldn’t take long at all before we were announcing to our family and friends that we were having a baby.

Month after month went by. We were living life in 2-week intervals. Anxiously awaiting the perfect time and then 2 weeks later anxiously awaiting to see if we were pregnant.

After months of not becoming pregnant, excitement of trying to have a baby, turned into frustration, sadness, helplessness. Although we always felt some hope at times, it was getting harder and harder to remain positive. When we first started our journey to have a baby, we had decided that if having a baby didn’t happen the “natural” way, we weren’t going to talk to doctors. We thought if God wanted us to have a baby, we would have one the way we were intended and we didn’t want to seek a doctor’s help.

God changed our hearts.

After much prayer, we decided to seek a doctor’s advice after a few years of not being able to become pregnant. It certainly wasn’t easy, especially for Mark. He had a hard time talking about my monthly cycles. He could easily talk about motorcycles but any other kind of cycles was difficult for him.

With a doctor’s help, we went through a procedure called artificial insemination where the sperm was placed into my uterus to help fertilization. My doctors really got to know me. I felt like I had no privacy at all. We were in constant contact talking about my body and when we thought I was ovulating as we had to try to pinpoint the best time for the procedure to take place for our best chances. We were living our lives in 2-week intervals again, only this time doctors were living it with us. There was a constant circle of emotions from hope to devastation.

After the artificial inseminations weren’t successful, we were encouraged to look into in vitro fertilization. This was quite an expensive, emotional process. It would involve giving myself shots of hormones every day, going into the doctor’s office almost every other day, lots of blood work, and a procedure that would require me being put under anesthesia. Our health insurance wouldn’t cover any of it and it would cost about $10,000. It was a big step to make and a big decision. In the end we decided to take a leap of faith and try it.

It wasn’t easy to go through it. It was hard to give myself shots. I was bloated and tired all the time and making so many trips to the doctor’s office was hard. But I knew this was our best chance to have a baby.

Unfortunately, it didn’t turn out the way we had hoped. During an in vitro cycle, embryos are created in which the sperm is inserted into the egg to fertilize it. Our embryos we had created during our in vitro cycle had fertilized but had stopped growing which was very unusual. After running some blood tests, it was found that I have a rare genetic disorder. My eggs could fertilize, but once fertilized, would just stop. Our doctor had been working in the infertility field for over 30 years and he had only heard of this happening to 2 other women. I would never be able to have a baby with my eggs.

It was beyond devastating news to me. I felt like such a failure. Failure as a woman, failure to my husband, failure to my friends and family. I couldn’t understand how this was happening. I honestly didn’t think Mark would want to be married to me anymore. I felt like damaged goods.

Of course Mark wanted to still be married to me and neither one of us felt like giving up. Our hearts desire was to have a baby and as long as the desire was still there we felt God was leading our hearts to keep trying, just to go in a different direction.

After the devastating news about my genetic disorder, we had a long talk with our doctor. We actually could try what they called an embryo transfer using donated or adopted embryos. These would be embryos that were created during another couple’s in vitro cycle. If the couple has a successful pregnancy with their cycle and no longer want to pursue having another pregnancy, they may end up with extra embryos. The couple can make decisions on what they would like to do with their extra embryos and sometimes they choose to donate to another couple in situations like ours which is similar to an adoption of a baby or a child.

I still had a very strong desire to be pregnant. My desire to be pregnant was just as strong as being a mother and having a baby in my arms. To some, that may not make sense but to me, feeling my baby inside of me was something I desperately wanted. I wanted to feel the morning sickness. I wanted to feel the baby’s kicks and hiccups. I wanted that feeling of being so uncomfortable. I wanted to go through labor. I so desperately wanted to go through a pregnancy. I wanted to see that positive pregnancy test and be able to tell people “I’m pregnant!”

My heart really wasn’t ready to give up the dream of being pregnant.

Not long after, a friend contacted me who was pregnant with twins after going through an in vitro cycle. They had some extra embryos from their cycle that they were wondering if we would like to adopt.
I was beyond thrilled! Of course we wanted to adopt them!

So we adopted the embryos and had them transferred into my uterus. Two weeks after a transfer, you’re scheduled for a beta test which is a blood test to determine if you are pregnant and if the transfer was a success.

My beta test was scheduled to be drawn on my birthday, April 18. I thought God was going to be giving me my best birthday present ever. There was just no other explanation and I was so excited! After all we had been through, I couldn’t imagine a better ending then being told I was pregnant on my birthday!

It turned out to be the worst birthday as the beta test on that day showed I wasn’t pregnant. The transfer was not successful.

It was the hardest thing we had ever gone through. We were devastated beyond words. I’d like to say I trusted God and knew He had a plan but I didn’t. I admit I was so disappointed in God. I was angry and I just couldn’t understand why we had to go through so much struggle and pain. First with the transplant and now with the infertility.

After the cycle didn’t work we talked to our doctor about our next step. He told us we could get on a list for donated embryos at our clinic. However, the wait was at least 2 years long. It didn't cost anything to do that so we got on the list, although in my mind, I knew we didn't want to wait that long.

In the summer of 2010, we started the long, drawn out adoption process, but I admit my heart wasn’t completely in it. As much as I desperately wanted to be a mom, I still had such a desire to be pregnant, too. I wanted so desperately to be pregnant.

You can imagine the surprise when in December 2010, we got an email saying there were embryos available for us. A 2-year wait had turned into a 6-month wait. A God thing.

I still had it in my heart to carry. So this news was so wonderful to hear. We put the adoption on hold and prepared to undergo another transfer. We underwent the transfer which ironically was so close to the previous dates of the transfer the year before. When I asked when the beta test would be, the nurse nonchalantly said "I think we'll schedule it for April 18"

My birthday. The beta was scheduled once again on my birthday.

I got real quiet. The nurse asked me if that would work out. I remember whispering, "Yes, that will be fine".

Truth be told, I was devastated. I thought it was a cruel joke God was playing on me. How could He do this to me? Two years in a row? And on my birthday?

Then, my attitude turned. Hello! It just had to be positive. After all, God would never allow that to happen again.

Would He?

The two week wait never felt longer than that two week wait. I went through so many emotions from being excited to scared to nervous to hopeful to doubtful. It was a rollercoaster of emotions.

Then came my birthday and the time for the beta test. I got a positive beta best on my birthday. God answered my prayers! I saw a positive pregnancy test---those 2 lines on the pee stick that so many women got to see and I finally got to see them! I was able to hear the doctor say “Tammy! You’re pregnant! Congratulations!” It was a dream come true!

I'll never forget the moments of that birthday in 2011. Never. I was floating on air. It was the best birthday ever and I hold onto that memory so dear.

Two days later they tested my beta level again to make sure the levels were increasing and that the pregnancy was progressing as it should. I got the dreaded call that told me my beta level had dropped. I was miscarrying. I was no longer pregnant.

I literally fell to the floor in grief and tears. I spent days in bed. I didn’t understand. I’d like to say I was trusting in God and believed He had a plan, but I didn’t. I admit I was so incredibly angry with Him. How could He do this to us? We had already been through so much.

Why? Why me?

After a few days of laying in bed and crying, I finally prayed to God, “God I can’t do this. All I want to do is crawl into a hole and never come back up. I need You to help me get up. I need You to give me strength”.

It was then that I could finally slowly get up and move ahead. I’m not saying things magically got better. I had many tears for months and still had days where I just stayed in bed. But God gave me the strength to keep going when I asked Him to.

It was months before we felt we could move onto the next step in our journey to have a baby---adoption. Still, I admit it wasn’t easy. I knew in my heart we couldn’t keep moving on with trying to become pregnant. I had to grieve that loss of not carrying a baby. It truly was a loss I had to accept and grieve before we could take the next step. I took time to cry, to be angry, to “just be me”. While others tried to encourage me and help me “get through it”, I knew only I could truly help myself and I needed to move ahead in my own time, in my own pace and in my own way.

But I also felt God really did have a plan. My desire to be a mom was still there even if my dream of being pregnant didn’t seem possible.

So we went through the seemingly never ending home study for the adoption process. It seemed never ending. All the paperwork, background check after background check. Telling your deepest secrets and fears to a social worker. They really put you through a ringer when you want to go through the adoption process. I’m surprised they didn’t need to know my cousin’s ex-wife’s daughter’s dog’s blood type.

Not only was it a lot of work, it was also a lot of money. We had already spent about $30,000 on infertility treatment. I was working about 60 hours a week at my job to earn some extra money and had started coaching gymnastics to help raise more money for the adoption.

When we were going through the home study, we were required to determine our budget that we could spend on an adoption situation. Situations could cost as little as $15,000 or as much as $75,000 or even more depending on the situation. Our consultant wanted to make sure we could financially take care of a baby and not start out raising a baby in too much debt.

After going through all our financial records, our budget was determined to be $50,000. This was what was determined to be a safe cost of an adoption that we could afford while financially being able to take care of a baby as well.

It took us about 5 months to get all the paperwork and required tests done and then we were finally able to allow birthmothers to consider us as parents. We created a profile of ourselves, our family, and some information about us. If a baby became available we would be given a little information about the birthmother and the cost of the particular situation. If we were interested, we would tell the agency that they could give our profile to the birth mother as possible adoptive parents.

We submitted our profile to 7 different birth mothers, all without being chosen. It was very hard to remain focused and not become discouraged. We continued to pray but there were many days we felt no hope.

We felt like God would open up doors only to have them slammed in our faces. And it didn’t feel good at all.

Then a birth mother came up that we were given information about. The total cost would be about $60,000 which was $10,000 over our budget. We regretfully asked our profile not to be submitted. We confirmed twice that we did not wish for our profile to be submitted.

It wasn’t too long after that we were told the birthmother had chosen us.

I was so confused.

What had just happened? It was impossible that a birthmother could choose us when we hadn’t submitted our profile.

I called our agency. It turned out the agency had accidentally submitted our profile to this birthmother after we had asked them not to. At that point my heart sank. I thought for sure they were going to take our baby away because there was an error. The agency felt awful about the mistake and then asked we were still interested. I said of course we were if it was still okay. They said yes and that it was our decision.

Honestly, the minute she said we could still have the baby, there was NO WAY I was going to say no. That was our daughter.

But now we had a problem. We had about a month to come up with an additional $10,000 and it was Christmastime.

Yikes. How would we be able to do this?

I thought there was no way it would happen but I knew there was a reason our profile was submitted in error and this baby girl was our daughter. We could have said no to this situation but in our hearts we knew this was no mistake. God brought this little girl to us.

What seemed impossible turned out to be possible. Our church at the time threw a benefit for us and many friends and family from all over the world gave. The total we were blessed to receive was about $9800---almost exactly to the dollar of what we needed.

Our daughter was born on December 20, 2011. Interestingly, Hannah's due date was only a few days apart from when my due date was had I not miscarried about 9 months earlier. We believe when we got our positive pregnancy test, it was God's way of saying we would have a baby in 9 months and indeed we were "pregnant", just not in the way we thought.

God can be sneaky like that.

We had to travel to Utah for Hannah’s birth but we were able to be in the delivery room when she was born. I was there the whole time holding the birthmother’s hand. I remember at one point she was in so much pain. I told her I was sorry and that I would trade places with her if I could. She said she knew I would. She understood.

I was able to cut Hannah’s umbilical cord and I was the first one to hold her. While it all meant so much to me, it was bittersweet as I watched Hannah’s birthmother cry tears of grief and sadness.

48 hours later, Hannah’s birthmother signed over her rights and Hannah was legally our daughter.

I will look back and see that You are faithful.

I often think back to that time. What if our profile wouldn't have been submitted in error? What if we would've said no for the third time? What if our family and friends wouldn't have come together and gave so generously so we were able to raise $10,000?

The answer to those questions is always the same: It was never in our control.

God was the one who decided the profile would be submitted.
God told us to say yes, not no.
God raised the $10,000 and opened the hearts of so many people.

When trying to determine how the mistake happened in the agency, they insisted that I called, explained we changed our minds and wanted our profile submitted to the birthmother. I know I never made that call and to this day I feel it was an angel who made that call.

From the time we started trying back in 2002 until Hannah was born in 2011, I prayed to God that He make me a mother. I would take any child but I secretly prayed for a daughter who looked like Mark. I can’t tell you how many times I hear that Hannah looks like her daddy---a constant reminder that God answers prayers.

It was always in His control and not ours. Hannah was meant to be our daughter, always was and always will.

We had to cross so many hurdles to bring her home and yet here she is today with us.

I went through a lot of grief and loss during our journey to have a baby. I have 10 angel babies waiting for me in heaven and I can’t wait to see them, hold them and tell them how much I love being their mother. But, at the same time, it’s so hard to not be their mother here on Earth. I grief that. I think of my babies all the time. I wonder what they would look like, what their personalities would be like, would they be boys or girls. I miss them. I think about them all the time, just like any mother does for their children. Some days I miss them so much I can’t stop the tears.

But I also know the loss I’ve felt and the grief I’ve gone through has been no accident. God has paved my way and my heart to become softer and more understanding for my daughter. My heart was broken so I could help my daughter with her broken heart. I know when Hannah gets older, she’ll have many questions. I know one day she will be sad and feel a loss for her birth mother. I know one day she’ll come up to me with tears in my eyes and say “Mom, I’m so sad my birth mother made such a hard decision”. I’ll cry with her and tell her that I’m so sad too. We’ll talk about how much her birth mother wanted her, how she didn’t “give her up” and instead “gave her a better life”, how much she loved (and love) her enough to give her a more stable life, how she is so lucky to have two sets of parents who love her so much while most people have only one.

She is a very lucky, blessed, loved girl and I’m so proud to be her mom. I’m so grateful God chose me to raise her. Hannah was named after Hannah in the Bible who struggled with infertility. I often thought of Hannah throughout our infertility journey. Her faith and love for God inspired me and helped give me strength when I needed it so much.

Hannah’s middle name is Dawn. She was given that name for someone special in my life who was with us during our entire infertility journey---through all the ups and downs, hope, disappointments. When I felt like giving up, she kept me going and kept my faith strong.

Hannah Dawn was name after our heavenly inspiration and our Earthly inspiration. We couldn’t think of a better name for our daughter.

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Hannah’s first picture. I was so blessed to be in the delivery room and be able to cut her umbilical cord.


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Holding Hannah for the first time. Yes, I’m on the phone! I couldn’t wait to share the news!

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Bringing our daughter home on Christmas Day 2011

Tomorrow--Mark's brain bleed