#181 Blessings from China

Photo by Jeff Rogers 

I have had it on my heart to adopt since I was a young child. After having two biological children, my husband and I began to prayerfully explore adoption options. Our idea was to adopt a healthy baby because we felt like we couldn’t handle special needs, and didn’t think we could do foster care. We started the international adoption process but faced one closed door after another. After becoming pregnant with our third child, we just assumed the adoption idea was over.

A few years later my husband told me about studying John 15:13, “Greater love has no one than this: to lay down one’s life for one’s friends.” My husband said, “we don’t have to die for someone to lay down our lives. I think we should look into adoption again.” I was all in! That very day I got an email from Rainbow Kids who helps to find families for kids all over world who are hard to place. There was a little girl from China who caught my eye. When I looked deeper I realized we fit every adoption qualification for China at the time, though we didn’t those few years back. We started the process and there were lots of details that can only be explained as God’s work. Although we had said we couldn’t handle an older child or a child with special needs, we realized those were false barriers. It didn’t have to be a healthy baby. We could do anything with God’s help! Our beautiful daughter was revealed to us in September 2015, and when we saw her date of birth, we knew she was ours despite her special needs. She was born the very week my husband and I had the first conversation about moving forward with adoption again. God was in this!

When we traveled to China to adopt our daughter, we were privileged to visit the foster home she had lived in for the past 6 months. What a blessing that was! But my heart went out for the children still there. One little boy with the same special needs as our daughter specifically tugged at my heart. After we left, I begged my husband with no avail to let us go back and get him. I continued to pray for him, and he was eventually placed with a good family. But it was still in my heart that we needed to go back to China.

The following year, our adoption agency began looking for volunteers to help with a camp for harder to place children in a Chinese orphanage. The idea was to get to know the children beyond their picture and information on a paper and advocate for them. The agency asked me to go. I went and spent two days in the orphanage with these precious children. One of these was a sweet 10 year old girl with Down Syndrome. My best friend (who is a special education teacher) had seen this little girl’s picture before I left and told me to pay special attention to her because it had always been her dream to adopt a child with Down Syndrome. She was the first child I met…and I knew she was special! I knew my friend would love her but I couldn’t tell her to adopt the child. I didn’t want to force or seem pushy. When I got home I told my friend, “you would love her but I’m not telling you what to do.” Adoption is difficult and expensive. But with the support of our community, my friend went to China and brought her home! She is truly a blessing to so many. Also during that time, I had another friend who adopted another little boy from our camp. He is now my little girl’s best friend and is an amazing child!

Months after my trip, my heart was still breaking for one particular boy in our camp. He was about to become ineligible for adoption because he would “age-out” at age 14, and we were having no luck finding him a family. He was fun, smart, and super brave. He didn’t talk much, but he smiled a lot. He was a great kid—but who was going to adopt him? I read the story of Moses telling God that he wasn’t good enough to go face Pharaoh in Egypt but how God promised to be with him to help him. And I realized something. God wanted me to go back for this boy. I wasn’t equipped for this job, but God would be with me. After having major conversations with our children because we didn’t know what to expect about adopting an older boy, they simply said, “he needs a family. He will be our brother.” We raced to get him home with us before time ran out. That was in 2017, and he has now been home with us a year and a half. It is evident God is blessing us with this young man. I am unbelievably thankful God wanted me to be his mother.

When looking back over this story, I realize it is far from over. I really feel like I’m in the middle of it. God continues to teach me important lessons. I have learned that sometimes we simply limit ourselves and God helps us go beyond what we think we can do. Sometimes you just have to step out and let Him work. I have also seen God shapes us through the difficult times, and we can help other people because of our own struggles. I have also learned to be patient and trust God. God delays our requests for reasons we don’t know or understand until later. Most of all, I’m thankful for my children and that God protected them while they were in China and protected us in all of our travels. The children bring us much joy! They have a hope and a future and they are loved.

A Million God Stories is a Christ-centered ministry which offers a platform for Christians from all streams of Christian faith to give praise for how God has worked in their lives. Christ heals in infinitely creative ways and we acknowledge that His way of helping may differ from person to person.

#180 Thankful Nevertheless

 Photo by Jeff Rogers

I met Rick my freshman year of high school. We dated in high school and married young. I was saved and baptized in January of 1980, and three years later, Rick was saved. The first time I heard him share his testimony, he said he couldn’t figure out why I would go to church not just once, but twice on Sunday, because that was our only day to be together since he worked six days a week. Rick said he wanted to know more about this man called Jesus who I loved more than I did him.

My husband loved basketball and coached a little league basketball team. He coached two little boys, Todd and Earl Reed, who went to my church. Every Sunday, between Sunday School and church, those two little boys would run to the church office and call Rick and ask him if he was coming to church. The boys were in two separate Sunday School classes, so they would both make calls to Rick as soon as they got out of Sunday School. They kept calling every Sunday and didn’t give up. They knew they were waking Rick up, but they didn’t care. They just wanted him to come to church. I cannot tell you how thankful I am that God placed those two little boys in our lives.

Rick was saved during a revival service at our church in 1983. He promised the two little boys that he would come to that revival service. When he came in the door that morning, they flocked to him and wanted to sit with him. When the preacher gave the invitation to come forward and accept Christ, he asked that we bow our heads and close our eyes in prayer. Rick shared with me later that he bowed his head, but he didn’t close his eyes. During that invitation, he saw one of those little boys, Earl Reed, pointing to him and then pointing toward the altar in the front of the church. Rick told me that was Earl Reed’s way of praying that he would give his life to Christ that morning, and he did! The Bible says a little child will lead them, and those two little boys did lead him. Rick got involved in church right off the bat, mainly working with the Youth. We didn’t have children of our own, so we had the time to devote to them.

My husband was a wonderful, selfless man, always putting others before himself. He was all about helping and ministering to people. He went on two mission trips a year; one with World Changers, an organization that goes all over the United States helping people who can’t afford the needed work on their homes, and one with Joshua Land Ministries to help build churches in Kentucky. In 2011, he was working with a crew to help put a roof on a new church in Mt. Sterling, Kentucky, when he fell off the roof and landed on his head. There didn’t seem to be any indication that he tried to catch himself, so we think he passed out before he fell off the roof. They flew him to the regional university hospital, and he stayed there approximately two weeks. He never regained consciousness and had two strokes during that time. After about two weeks, the doctors told me Rick’s brain was dead, and that I was going to have to make the dreaded decision to take him off life support. Immediately after the doctors telling me I was going to have to make that decision, my pastor called to check on us. I asked him, “How do you make a decision like that? I feel like I’m taking his life.” He told me, “You’re not taking his life. If it’s God’s will for him to live, even if you remove the life support, he’ll live.” God knows what we need and when we need it, and I needed to hear that. Rick’s family and I made the decision to remove the life support. The doctors explained to us that, after we took Rick off life support, it was possible he would live for a few days because, even though his brain was dead, physically he was very strong. He lived almost a week. I got to bring him home to our local hospital under Hospice care, and he passed away on July 17, 2011.

It was really hard and very lonely for me, but God was always there. You don’t know God is all you need until He’s all you’ve got. My family, Rick’s family, and my church family were wonderful, and my work family was too. They stayed with me at the hospital during Rick’s illness and for a couple of weeks after his passing. My church family came by often to see if I needed anything and tried to keep me busy. My job gave me a reason to get up every morning. But, it was during those times by myself, especially in the evenings and at night, that were my loneliest times. It was just me and God. At the end of the day, I would pray, “God, I made it through today. Tomorrow is another day, and I’m going to need you to help me through tomorrow”. In the mornings, I would say to God, “Your Word tells me that your mercies are new every morning and your grace is sufficient. I need your grace and mercy today.” I grew more spiritually during that time than I ever had. I know God was with me every minute. At night when I was lonely and sad, I would open up the Bible and it would give me comfort. I drew such strength from God’s promises.

“For I know the plans I have for you,” declares the Lord, “plans to prosper you and not to harm you, plans to give you hope and a future.” (Jeremiah 29:11)

Be strong and courageous. Do not be afraid or terrified because of them, for the Lord your God goes with you; he will never leave you nor forsake you.” (Deuteronomy 31:6)

In September 2013, more sorrow began. My middle sister was diagnosed with cancer. She went through various treatments and surgeries, and we had to watch her suffer terribly. She passed away in February 2015.

Then God, in His infinite wisdom and perfect timing, sent someone to me. I had bought a new car and someone hit it in the parking lot of Food City right after I bought it. I called my current husband, who owned the body shop and had repaired cars for me before, to repair my car. We were married in January of 2018. He’s a wonderful man. God has blessed me doubly – with a whole family! My husband has two children, a daughter and a son, who are both married, and we have two grandchildren and one on the way.

I have so many things to be thankful for. First and foremost, I am thankful for my salvation. I’m thankful for the time I had with my first husband and for my new husband and new family. I’m thankful for the closeness I have with my mother, father and my sisters; for Rick’s family with whom I am still close today; for my church family; and for my job and my work family. God has given me many people to love, and who love, support and encourage me. He is so good!

A Million God Stories is a Christ-centered ministry which offers a platform for Christians from all streams of Christian faith to give praise for how God has worked in their lives. Christ heals in infinitely creative ways and we acknowledge that His way of helping may differ from person to person.

#179 Chance Encounters

 Photo by Jeff Rogers

When our son was born, he was normal. At three months old it was like a switch was flipped. He started throwing up. Our first child had problems with lactose intolerance, so we thought that was it. We went to the doctor and he changed his formula. But he didn’t get better. Months later we spent six days in the children’s hospital running tests. They came up with a diagnosis of failure to thrive. This is basically a diagnosis that they give when they don’t know what is wrong but they know something is wrong. We battled this for four years. It was back and forth to hospital doing feeding studies and running tests. At four years old he was well underweight at 20 pounds. Every time he would gain weight, he would get sick and lose weight. The only thing that would stay down was his formula in the bottle. We stopped going to the hospital because it wasn’t helping.

It is amazing how God works. When our son was five he started going to a Methodist preschool. The mom of another child started talking about a severe illness her child had. As she described his symptoms, it sounded just like what our son was going through. We told her about our son—about his illness and all that he had been through. She said that she felt sure he had the same disease as her son, a rare disorder called eosinophilic esophagitis (EE). Not long after this, their family moved away. Her husband was a microbiologist and had taken a job at the college in our town but was only there for two months and then they moved away. But two months was long enough for us to have the conversation with his wife. There is no way we would have found out about the disease if we hadn’t met her.

We took our son back to the doctor at the children’s hospital. We told him that we thought our child had eosinophilic esophagitis. Turns out this hospital has the number one clinic in the world for eosinophilic diseases! After several months on the waiting list, we were finally able to get our son an appointment in this clinic, and they diagnosed our son with eosinophilic esophagitis just as we suspected. They told us to eliminate the 10 foods that most commonly cause allergies. We did this for several months, but the results of his scope came back worse than the first time. What could it be then? The doctor called me personally and said the results of his scope were very bad. He said our son had to have a feeding tube or he would die. They told me how they do the feeding tube and how they cut the stomach and put it in. I was so upset that I cried, but it seemed we didn’t have a choice. In 2011, he got the feeding tube. It was so hard on him because for four days he laid in the bed and he normally has lots of energy and is a people person. I worried that he was shutting down.

The feeding tube bypasses the esophagus (the tube that takes food from the mouth to the stomach) and goes directly into the stomach. For three months, he wasn’t allowed to have any food by mouth. All of his nourishment went through his tube into his stomach. We put a special formula into the feeding tube to feed him. In three months, he gained 10 pounds and his esophagus was healed so he was approved to eat some things by mouth. But what he took in by mouth was not providing his nourishment. We were still putting special formula into his feeding tube, and this is what provided the nourishment he needed to live.

We had another problem. The formula cost about $1,500 per month. Insurance wouldn’t pay for this and I had lost my job in 2015, so money was tight. We couldn’t afford to buy the formula.

I had read about a law passed in Illinois that mandates insurance companies to pay for the formula for EE patients who need it in their tube feeding to survive. In my mind, this was no different than insulin for a diabetic patient. Our child had to have this to survive.

Our state representative helped to get a bill passed in our son’s name that would ensure Kentucky insurance companies would pay for the formula needed for survival in EE patients. As a part of this process, our family testified before the state legislature’s insurance committee. There was a unanimous “yes” vote in that committee. A unanimous “yes” vote had never happened in that committee. We also testified in a House of Representatives committee and a Senate committee. So many prayers were being said. Everything fell into place, and the bill became a law in only two months!

Life is still hard for our son. He is 60 pounds at 13 years old and has had 27 scopes in seven years. But even after everything our son has been through, he is still is so joyful. God made him an independent and positive person, and we are so thankful for that. He loves people and sings and plays the drums. He is a blessing to many people.

Through all of this, we have realized how many people have prayed for our son and how God has answered prayers. One day we were at a rest stop and a woman saw our son and said, “I have been praying for you.” She was from another state, and somehow her church found out about our son’s struggles and he had been on their prayer list. At critical moments in our life, God has provided in some way—the mother at the preschool, the specialty clinic at our hospital, the law that passed in two months when we were out of money and couldn’t afford the formula. God’s provision and timing have amazed us again and again, and we are so thankful.

A Million God Stories is a Christ-centered ministry which offers a platform for Christians from all streams of Christian faith to give praise for how God has worked in their lives. Christ heals in infinitely creative ways and we acknowledge that His way of helping may differ from person to person.