The crowd began to build by about 6:30 this evening...and eventually grew to over 1,000 people.
Wednesday, October 14, 2009
Fields of Faith
The crowd began to build by about 6:30 this evening...and eventually grew to over 1,000 people.
Tuesday, October 13, 2009
A Praise and a Prayer Request
Now the prayer request...Bethany has been asked to share her testimony tomorrow night at a Fellowship of Christian Athletes-sponsored event called "Fields of Faith". She has shared her story several times, but this will be by far her largest audience. The event will be held at a football stadium in Hot Springs, and there should be a big crowd there. There will be several speakers throughout the evening, so she will not be the only one, but she is understandably nervous about the event. Please pray that God will give her the words she needs to say, and that the students will hear what He wants them to hear. I will try to take some pictures and post them tomorrow night!
Monday, October 12, 2009
Through the Valley
Thursday, October 8, 2009
Sorry, Mom!

...and Betty Kapteyn (then)...
...the happy couple on October 10, 1959...
...and the happy couple now!
I think they look great! This picture was taken on their recent trip to the Canadian Rockies, where they went to celebrate their anniversary. I took this picture from my mom's Facebook page (that's why it's so small...I tried to make it bigger and it just got blurry) and I figure if she uses it as her Facebook profile picture, it's okay to post it here! They had a great time on their trip to Canada, and my brothers and I are sending them to the Lodge at Mount Magazine for a couple of days, where they will engage in one of their favorite pastimes...fishing!
Their marriage has been a wonderful example for their children and grandchildren, and we are so proud of them. I know that I am blessed beyond measure to have a mom and dad who love the Lord and each other. Thank You, Lord, for Christian parents!
P.S. Some people have asked how to post a comment...just click on where it says "0 comments" or "1 comment" or "2 comments" (you get the idea!) and it will link to a place where you can leave a comment.
Monday, October 5, 2009
Comforters
A few days before the ballgame, it was announced that Dave Dravecky would be making his major league comeback on August 10th. Dave Dravecky was a very successful pitcher who had been sidelined by cancer in his pitching arm. He underwent surgery, a series of cancer treatments, and extensive rehab before making this very well-publicized comeback. We had seats right above the bull pen where we were able to watch all of the activity, and were amazed at the amount of press coverage that this game was generating. As a matter of fact, we were interviewed by a San Francisco TV reporter who was amazed that we had come all the way from Arkansas for this ball game...little did he know that we had bought our tickets six months before! Of course, as a huge baseball fan, Brad was loving every minute of this. The crowd went crazy as Pete Rose got thrown out of the game, and even crazier as Dave got the win. The really cool thing was that Dave Dravecky was an outspoken Christian, and he used this opportunity to very openly share his faith and give glory to God. We listened to all the post-game interviews on the radio as we sat in the parking lot stuck in traffic for what seemed like hours, and his testimony was just amazing. We headed home from our vacation a couple of days later, still talking about Dave Dravecky's story.
The next time Dave Dravecky pitched, his arm broke with a resounding crack that was heard all over the stadium. His cancer had returned, and his arm could not be saved. His arm and shoulder were eventually amputated. Years later, he wrote a couple of books about his experiences called, "Comeback" and "When You Can't Come Back." His wife, Jan, struggled with depression for years, and has also written some excellent books. Together, they have founded a ministry called "Outreach of Hope" (http://www.outreachofhope.org/) which is a designed to be a source of encouragement for those going through the cancer journey. It's a wonderful ministry, and they put out some great free literature as well.
Back when we were watching Dave Dravecky pitch and listening to his story of overcoming cancer, we didn't even have children, and we certainly never dreamed we would face the kind of situation we faced with Hannah. But his story, and his determination to give God the glory in his circumstances, made a huge impression on us...and I truly believe that our presence at the ballgame back on August 10, 1989, was divinely orchestrated. Isn't it amazing how God works in our lives, even when we're completely unaware?
Well, that was a much longer introduction than I meant to give...I was really just going to post a poem that I found in one of the Outreach of Hope publications. I found it last night as I was reading through some of their materials, and I thought some of you might be able to relate to it. I actually think it could apply to a variety of situations, not just a cancer diagnosis. I'll close with it:
When I Was Diagnosed With Cancer:
My first friend came and expressed his shock by saying, "I can't
Saturday, October 3, 2009
Report from Indonesia

These are my precious nieces, Julia and Katie. And yes, though they are exactly two years apart, they are nearly the same size! Julia is very petite, and Katie is...well...not. You may remember from a previous post, Julia is the one who always called Hannah "Arnie". My brother told me a story about her tonight that I thought was so cute. He said that she has begun pretending like she's flying a plane to "mecca". At first they were very confused (and probably a little concerned!), wondering why she wanted to go to there, but they finally realized she meant "America"! What a brilliant child!
Thursday, October 1, 2009
Thought Life
That's no longer necessary (although I became quite good at it and can still do it, such as when I'm in a group of moms who are talking about prom or senior pictures), and I now find myself thinking a lot. The problem is that my thoughts seem to always settle on the really bad memories of those final weeks...wondering what we might have done differently to make things easier for her, remembering those final few moments, and regretting the things we maybe should have talked about that we didn't. And, you know, for some reason I usually don't recognize this for what it is...an attack of Satan.
There's a verse I've heard all my life, but it's just recently taken on new meaning to me: "...Whatever is true, whatever is honorable, whatever is just, whatever is pure, whatever is lovely, whatever is commendable, if there is any excellence, if there is anything worthy of praise, think about these things...practice these things, and the God of peace will be with you." Philippians 4:8. The thoughts that I mentioned certainly don't fit this description. So, with God's help, I'm working to focus my thought life on the good memories...and there are many. I am so thankful for the almost 17 1/2 years we had with Hannah...one of the greatest blessings of my life!
Tuesday, September 29, 2009
Cousins!
First, I wanted to post a couple of pictures that were taken over the weekend by my sister-in-law, Maria. On Saturday, all of the Sullivan cousins, including baby Faith, were at the "deer camp" in Briggsville, which is in rural Yell County. (Actually, I think all of Yell County is rural!) Maria, who is a great photographer, took the opportunity to get some family photos. Here's Bethany (top right) with all of her cousins...yes, they're all girls on this side of the family!
Hannah was the oldest of the cousins...she was fortunate enough to be the first grandchild on either side! As such, she definitely got some special treatment!
And another picture...here's Bethany in her "country girl" pose:Hannah loved spending time at the deer camp with her cousins. So much so, that when we had to make a decision regarding where she would be buried, there was no question that it would be at Briggsville. There's a small cemetery there where Hannah's great grandparents are buried, as well as several other Sullivan family relatives. It's a beautiful place, and I will share more about it in an upcoming post.
Monday, September 21, 2009
Anchor of Hope Cancer Ministry
Up until the time Hannah was diagnosed with cancer, I had very little idea what life with cancer was like. I had always thought that when a person was diagnosed with cancer, they spent the next several months or years in bed, too weak and sick to do anything. I had no idea that most people with cancer still live full and active lives, in spite of chemo treatments, hair loss, radiation, bloodwork, etc.! Of course, as Hannah's journey unfolded, I leaned that firsthand. And as I looked around that room tonight, I saw people living life, and loving Jesus. What an amazing experience!
"We are afflicted in every way, but not crushed; perplexed, but not driven to despair; persecuted, but not forsaken; struck down, but not destroyed; always carrying in the body the death of Jesus, so that the life of Jesus may also be manifested in our bodies." II Cor. 4:8-10
Friday, September 18, 2009
God's Infinite Wisdom
The first few days after Hannah's death are pretty much a blur to me. There are some isolated moments that stand out clearly in my mind, but not very many. It's funny...at the time, I felt that I was completely lucid, and things seemed very vivid in my mind...but when I look back at it now, it's very foggy. I do remember feeling very numb, and honestly not feeling a lot of pain. But after the visitation, after the funeral, after the burial, and after all the family left, it was time to get back to "normal life." And that's when the pain hit in earnest. This may be a strange word picture (okay, it IS a strange word picture), but as I walked through each day, every little reminder (and EVERYTHING was a reminder early on) felt like a plastic knife being shoved into my chest. By the time I got into bed each night, I felt like my chest was literally bristling with plastic knives. Why plastic knives? They are not too sharp...sharp enough to cause a lot of pain when they are thrust into your chest, but not sharp enough to kill you. If anything, the number of knives and the depth of their penetration increased over the next several months.
"What Ifs"
I reached the point where it seemed like I was spending all my time dwelling on the "What Ifs". And God had to gently remind me that this was not how I should be spending my time. Instead, I needed to give him the "What Ifs" and begin savoring every moment I had with Hannah. Not that it was easy...it was not easy at all...and it required a continual, conscious decision to put the "What Ifs" into His hands and live one day at a time. I had never really understood the concept of "one day at a time", and had certainly never lived it, until that point. As Hannah's health deteriorated, it became one hour at a time, and sometimes even one minute at a time. I really think it was that focus that made the last couple of months of Hannah's life not only survivable, but even, at times, enjoyable for us.
People often commented on our "strength" during Hannah's illness and death, but as I've said before, this is a misunderstanding of God's grace. What appeared to be strength was actually human weakness bolstered by total dependence on God. A couple of weeks ago, we had the privilege to share Hannah's story at a church in Mountain Home, and after the service we visited with a gentleman who had lost his wife to cancer after many years of marriage. Our visit was brief, because there were many others waiting to speak to us that night, and a few days later, he emailed us to share a little more of his story. He ended his email with this statement:
Monday, September 14, 2009
Go Panthers!

Sunday, September 13, 2009
One Year Ago Today
Last year's concert featured David Cook (the winner) and David Archuleta (the runner-up), along with the other top eight contestants. I didn't order the tickets right away (I believe they went on sale at the end of May), because I just wasn't sure how Hannah would be feeling. As the summer went on, though, she was doing well...she had completed her radiation treatments and was handling the oral chemotherapy with no real problems. She had had an MRI every two months since her surgery, and she had gotten an "all clear" every time. So, probably in July, I ordered tickets for the three of us girls (Brad never seemed to want to go with us...don't know why! (o; ) We were excited about the concert and were really looking forward to it. Hannah was a David Cook fan, and we had a special interest in him because his brother was battling brain cancer.
We spent that weekend with Brad's mom and dad, who live in Van Buren, so it would be a shorter drive to and from the concert in Oklahoma City. This was a blessing, because the weather was awful that weekend. The remnants of Hurricane Ike were blowing through Arkansas and Oklahoma, and we drove to Oklahoma City in heavy rain and strong winds. I remember that Hannah was somewhat tired when we left Van Buren that day, but that was not unusual, as the primary side effect of her chemo was fatigue. It was too rainy and yucky to do our usual "stalking" that afternoon, so we went out to eat instead. I noticed that Hannah actually seemed relieved that we would not be "stalking", even though she had been talking excitedly about it in the days leading up to the concert. We finally arrived at the concert, and showed our tickets to an arena worker, who directed us to the stairs. As we walked up the stairs, Hannah mentioned that she felt a little dizzy. This also was not really unusual...the radiation treatments had left her with a constant feeling of being "off balance"...her world was never completely level. We finally found our seats...in the very top row of the arena. And I mean the top row...the only thing behind us was the wall. We were definitely in what you would call the nosebleed section. As we sat waiting for the concert to start, Hannah again mentioned that she was dizzy, and we attributed it to the dizzying height at which we were sitting. She was very quiet during the concert...not singing along and yelling for her favorites like she usually did...and right about the time David Cook came out (the winner is usually saved for last at these concerts), she asked if we could leave. We immediately got up and left...and what a long ride back to Van Buren that was. We still had the incredibly heavy rain and the tropical storm force winds, and now it was pitch dark. But that's not really what made the trip so long.
As I drove through that stormy weather, a storm was building inside of me. That night, for the first time, I began to realize that Hannah might not survive this. At the time, as far as we knew, Hannah was cancer free. But deep down inside, I knew something was not right. It was the first time that I began to feel like we were losing her. We returned home to the Hot Springs area the next day and within about a week, Hannah developed what we thought was a stomach virus. After several days of nausea, the doctor ordered an MRI (about 10 days before her next routine scan was scheduled) and it revealed that the cancer had returned with a vengeance. There were now two tumors on her brainstem, and so many tumors up and down her spine that the doctor referred to them as "snowdrift" tumors. With tears in his eyes, he explained to the four of us that he believed Hannah had less than a five percent chance of survival at this point. Wow...what a blow! He did explain some treatment options, including a combination of chemo drugs that had shown some success with glioblastoma tumors, but really didn't give us much hope of cure. As the four of us drove home that day, we decided that we were just going to ignore that number...we knew that our God didn't deal in percentages. But, at the same time, we were just beginning to realize that God's plan for Hannah may not include earthly healing.
This post has become much longer than I intended it to be...I will share more on this topic another day...but I did want to mention what a wonderful time we had at Shady Grove Baptist Church in Prescott this weekend. They had a "Faith, Family, & Fun" emphasis this weekend, and we had the privilege of sharing our story both last night and this morning. What a precious fellowship of believers! This church has followed our story basically from the beginning, and took us in just like a part of their family. Of course, we are brothers and sisters in Christ, and it was apparent this weekend. They truly blessed us with delicious food, beautiful music, and wonderful fellowship. Thank you, SGBC!
Tuesday, September 8, 2009
Reunions & Remembrances
Most of my former classmates had heard about Hannah's story, but there were a couple of awkward moments when those who did not know asked me how many children I had. I still haven't figured out how to answer that question without making people uncomfortable. I usually say that I have one daughter who's 14 and one who's in Heaven. This usually results in a shocked, jaw-dropping response, accompanied by a mumbled, "Oh, I'm so sorry..." This is the point where I usually get choked up and am unable to say anything else. Thankfully, this weekend, I was able to retain my composure and share a little bit of Hannah's story. Another sign of progress in this grief journey.
If you are really my friend,
Speaking of Hannah's name...my 2-year-old niece, Julia, has always called Hannah "Arnie." Yesterday, I got an email from my sister-in-law in Indonesia (they are doing well) and she told me that she was telling one of their fellow missionaries about how funny we always thought that was. Her friend suggested that she look it up and see what the name Arnie actually means. Well, she looked it up, and here's what she found:
Friday, September 4, 2009
A Touching Tribute
"Dear Panther Fans:
Welcome to another exciting year of Panther football. Last year's team finished 8-4, and with the return of 12 seniors, this year should be another good one. The kids have been working hard since the beginning of July for Friday night football.
You may have noticed on the back of our helmets is a sticker with the letters "HS" and a gray ribbon. This is in honor of Hannah Sullivan who was promoted to heaven on February 26, 2009, from brain cancer. Hannah was a manager for the girls' basketball team and would have been a senior this year.
Instead of honoring the passing of Hannah, I would like for us to honor her life. She was my role model. As Hannah battled "her storm," three parts of her life stood out: her faith, belief, and love for God. The year-long battle only made these characteristics stronger in her life.
As I watched Hannah react in such a positive way to all this adversity in her life, I could only think how great it would be if the Panther football team could learn from Hannah and use these traits during the season. I challenge our players to have faith in one another and to work as a team and not as individuals.
I challenge the players to not only believe in their teammates, but also in the coaches and the many decisions they have to make during the season. Finally, I challenge the players to love their team despite any differences they may have.
I especially challenge the team to demonstrate these characteristics during the "rough times" of the game and the season. I encourage them to let their faith, belief, and love stay strong, and to continue to battle and be positive, no matter the outcome. Finally, I challenge the team not only to be like Hannah on the field, but also to model her life off the field.
I can't promise you, the fans, a state championship, or even a district championship if the team follows Hannah's example; however, I can promise you that at the end of the season we will be a better football team, better players, and most of all, better individuals! Panther Pride Runs Deep!
Thank you,
Coach Efird"
I have nothing else to add...Thank you, Coach.
Thursday, September 3, 2009
Safe Arrival
Wednesday, September 2, 2009
A Series of Tremors
It seems to me that losing a child to cancer must be a very different experience. Rather than one enormous earthquake, cancer consists of a series of tremors of different intensities. In our case, there was the initial shock of the brain tumor, the shock of the cancer diagnosis, the shock of hearing the devastating list of treatment side effects, the shock of seeing our child wearing a radiation mask and bolted to a table, the shock of the cancer's return, the shock of seeing our child bald, the shock of watching chemo drugs drip into our child's veins, the shock of each worsening MRI, the shock of hearing the doctor say there is nothing else they can do medically, the shock of entering hospice care, and the final shock of our child's death. Even though you reach a point where death is expected without a miraculous intervention from God, there is still a period of shock.
You know the feeling you have when you've been punched in the stomach? That is the feeling I had the entire time Hannah was sick. Our belief that God was in complete control of the situation, and our knowledge that He truly is good all the time sustained us and gave us an unexplainable, deep-down peace, but to be fully honest, I have to acknowledge that my feelings did not always line up with my beliefs. And I think that's okay...God created us with feelings and emotions and I believe He understands that human part of us, because He was human, too.
"For to this you have been called, because Christ also suffered for you, leaving you an example, so that you might follow in His steps." I Peter 2:21
Tuesday, September 1, 2009
Glioblastoma Multiforme
When Hannah was first diagnosed with cancer, it was such an incredible shock that for a few days, I just couldn't mentally process it. At first, Hannah didn't want anyone to know that she had cancer...we finally convinced her that we needed to let people know so they could pray for her. She also did not want anyone to know that she was going to have chemotherapy, so when I sent that first email explaining her diagnosis, I said that they were going to treat her with radiation and "medication." Of course, most people figured out that meant chemotherapy, and eventually, Hannah relented and allowed me to share more details. I remember when I sent that first email explaining her diagnosis, we received many, many wonderful, supportive responses. In those first couple of days, we also received emails from children's cancer support groups, some friends who had lost children to cancer, and someone who told me about where to get free wigs for cancer patients. I remember reading those emails and thinking, "No way...this is not for us...not for Hannah!" After a little time passed, I was ready to hear from those folks, but not immediately.
We got the diagnosis about ten days after Hannah's brain surgery. We had gone in to get her stitches removed, and knew that we would probably receive the results from the pathology report. I remember that Hannah climbed up on the table, the surgeon did a brief exam of her incision, and then he told us that the pathology report indicated that Hannah's tumor was a glioblastoma multiforme. He had told us the day after the surgery that these tumors are rated on a 1 to 4 scale, with 4 being the most serious (he never used the word cancer). Brad asked him what Hannah's tumor was, and I clearly remember him saying, "This is a Four." Those words reverberated inside my head for quite some time. Then he introduced us to our oncologist, who entered the room accompanied by three other people. He gently explained the fact that glioblastoma multiforme is a very aggressive brain cancer with a nearly 100% fatality rate in adults. He also explained that Hannah's youth and the fact that it had been removed put her in a more favorable position. He outlined the course of treatment...radiation and oral chemotherapy...and left us with these other people, who I later figured out were social worker/counselor type people. I guess they figured we would each need one of our own after hearing that news. The one who appeared to be the head counselor offered Hannah an assortment of ugly teddy bears, and I remember that she chose what I thought was the ugliest one. As if a teddy bear would fix the problem. We were stunned by the news, but the peace of God was upon us because we had already put Hannah in his hands, and I don't think we even cried while we were there. Once they saw that they were not going to need to scrape us up off the floor, the counselors left too. Then, after all this, Hannah had to roll over onto her stomach and let them pull her stitches out...all I really wanted to do was hold her at that point, but I had to settle for just holding her hand. We left there that day, went to Firehouse Subs, and prayed over our lunch, again putting Hannah's future in God's hands.
More to come....
P.S. I have not yet heard from my brother in Indonesia. They are going to have to live with another missionary family in their new location, and may or may not have access to the internet. Thanks for the prayers...I'll let you know when we hear from them.
Monday, August 31, 2009
Smoky Season in Indonesia

Saturday, August 29, 2009
Hannah's Room
I'm sitting here on her bed, and I thought I would give you a description of some of the things in her room...just to give you a little window into Hannah's personality. When you walk into her room, the first thing you see (and the most gut-wrenching for me) is her letter jacket with "Hannah Joy" on the back of it hanging over the bedpost. In one of the most ironic events of her illness, she received that jacket the day we found out that her cancer had returned with a vengeance. That was also the day she ordered her class ring. What a strange thing that was...to receive those symbolic items of high school completion on the day we first began to understand that she may never finish high school. She had looked forward to receiving her letter jacket for a long time...and she actually only wore it a few times. Her purse is hanging from the other bedpost, with her driver's license and Hunter's Education card in the wallet inside.
Her bedroom walls are painted a dark red color...the room was this color when we bought the house, and she immediately chose this room as her own. Her bedspread is white and black, as you can see in the picture, and there is a black shag rug on her floor. The rug was necessary to cover up the Nike Swoosh that the former owners had painted on the floor...who paints a Nike Swoosh on a wood floor? We didn't know it was there until we moved into the house...they, of course, had it covered up with a rug.
To my left, hanging on Hannah's wall, is a framed poster of downtown El Dorado..."Arkansas' Original Boomtown". Of all the places we've lived, El Dorado was Hannah's favorite. She had such good friends there, and she absolutely loved that place!
Hannah's room has the best view in the house. We live in the country, on a hillside, and from here, when I look out the window, all I see is trees blowing in the breeze. Some of those trees we planted the year we moved into this house, and they have really grown over the past summer. For some reason, it makes me sad that I can't show Hannah how much taller they are now than they were in February.
On the floor beside her dresser, in a stand, is a porcelain doll which once belonged to Hannah's great grandmother, Frankie Stahl Owens. Hannah adored her "Grandma Frankie", who went to Heaven in July 2008, and during the last days of her illness, she was comforted by the fact that Grandma Frankie would be waiting to greet her when she got there.
Her dresser has a bunch of stuff on top of it...a funny little trombone player that her Aunt Sarah gave her back when she played the trombone in 7th grade; a picture of her and former American Idol contestant Ace Young; the wide headband she wore every day to cover up the bald patches from radiation; a stuffed animal she received from Arkansas Children's Hospital when she had to get platelets on Christmas Eve; a picture of the high school choir wearing their Alice in Wonderland T-shirts--a performance that she did not get to participate in due to low blood counts; an All-Region Choir patch; her sunglasses; some silk flowers sent by her good friend Paige after she died; and a picture of her and her friend Brittany.
To my right is what we jokingly called her "Wall of Fame". Hannah was a highly motivated student and was extremely proud of her academic achievements. On this wall is a group of plaques (shown below) which include the following: "Outstanding Student in Social Studies, Algebra I, and Career Orientation--2006"; "Outstanding Student in Health & Physical Science--2007"; and "Outstanding Student in Spanish I, World History, and Pre-AP Biology--2008". She also has a plaque for "Miss Congeniality" in the Miss Magnet Cove pagent in 2007; and the ones she was most proud of because they were voted on by the teachers..."Outstanding Freshman Student MCHS 2007" and "Outstanding Sophomore Student MCHS 2008".
One of these days, we're going to have to do something with all of these things. How do you do that, though? We've discussed making something special out of this room...a quiet, peaceful, inviting kind of room, a place where you can study your Bible, or spend some time with the Lord. I'm ready to open the shades, let the sun shine in, and keep the door of this room open again. But I'm not sure how to do it yet...we're still waiting for God's timing.