Perplexed but not Driven to Despair
"But we have this treasure in jars of clay, to show that the surpassing power belongs to God and not on us. We are afflicted in every way, crushed; perplexed, but not driven to despair; persecuted, but not destroyed; always carrying in the body the death of Jesus, so that the life of Jesus may be manifested in our bodies."
2 Corinthians 4: 7-10
January
2019 was an intense month for the Winkelmeiers! Influenza A struck the members of
our home with a vengeance and it got to me, Dave, first. Last year I had gotten
it three times, Type A twice and Type B once. If there was a Type C, I was
bound to get it. All the members of the family got it as well last year
and everyone recovered with no major hiccups. However, this year, Angela seemed
to be hit the hardest and went from having the Flu to having a long bout with
walking pneumonia. The Doc gave her 2 rounds of antibiotics and things seems to
clear up except this little nagging cough that occasionally gave excretion. We
assumed that she was still battling pneumonia. She also had some chest pressure
and feeling a little more fatigued in the evening, which is common when someone
is sick.
On the
evening of April 16, 2019, we were doing life like normal. I was driving Eden back
and forth to Jiu Jitsu and she was hanging out at the house with the kids and a
couple extra girls to watch while their parents were getting training to be
foster parents. Angela is always helping others and that night was no exception!!
She was working hard to keep up with them while I did yard work. I came in from
doing yard work and noticed her coughing and holding her chest. She said her
chest hurt her more that evening than times before. She just looked more tired
and fatigued. Grant it she pushed herself at the gym that day and had, what she
called, “a good workout”. To me a good workout is painful. It always is bad when
I walk out of a gym and I’m hurting. Angela is often sore because she works out
at the gym five days a week and that includes running 4-5 miles on the treadmill
and other intense cardio. We attributed that some of the soreness she was experiencing
in her chest to her workouts because she’s intense and often sore. That night
was different though. She was bent over and looked really concerned, which got
me concerned!! I told her that she needed to have a chest X-Ray done soon.
Two
days later she had her late afternoon appointment to get the X-Ray at Metro
Imaging. After the appointment she called me with some concern in voice. She told
me that the Radiologist said that she had an “abnormality” in her right lung
and suggested that she get a CT Scan to get a better Idea of what’s going on in
there. Like I mentioned, it was late in the afternoon I told her to let her
doctor look at it in the morning and he would tell her what to it is. I’ve been
through hundreds of X-rays and know that an abnormality is a vague term that
could mean many different things. We still had in our heads that she was still
dealing with pneumonia and pneumonia shows up as abnormal on an X-ray. I’ve
been there done that. After she left Metro Imagining I told her to call her doctor
on his cell to let him know and she did. He’s also was a friend of hers, dating
back a few decades and who is great Christian man. He reassures her that it
could be anything and reminded her that she had been sick with pneumonia and the
influenza. Of course, our minds are still concerned, but continued to trust God
with it. He’s the one in charge and on His throne.
Friday,
April 19, 2019, my 8-year anniversary for my lung transplant, will have a
totally new
The left side of the picture is actually the right side.
The tumor is pushing her heart over to the left.
Both lungs should look like the side with the cursor.
|
After processing,
or trying to, Angela decides to go to the gym to run on the treadmill to
process it. It’s a happy place for her to release stress. I tried to talk her
out of it, but she persisted. I don't think I would be comfortable with a grapefruit size mass bouncing around in my chest. She ran about 4.5 miles that day!!! She
came back from the gym smiling and satisfied. We did more praying and she got
her bloodwork done which came back perfect!
Over
the weekend, it took everything we had to keep our minds focused and not deterred
by fear. We went along our normal weekend activity and went to the CT Scan at
3pm on Monday, April 22, 2019. The call from the doctor with the results came late in the evening we thought that we were going hear from him in the morning. At 9:38pm, the phone rang, and Angela
answered it with nostrils flared and taking deep breathes. My heart also raced as she put the doctor on speaker phone. There was little small talk because we
wanted the facts and that was it. Unfortunately, the news was much worse than
we could have imagined. Not only did Angela have the large mass in her right
lung that was pushing against her heart in such a way that it could eventually
affect the circulation of blood throughout her body, she has 4 other spots in
her body that were detected. Angela and I can’t believe what we’re hearing. Dizziness
from the adrenaline took over. The doctor goes on to explained that the other
small masses are 1-2 centimeters in diameter, and she has one on the T3 vertebrae along her spine that's embedded in the bone, a mass on her liver, and one small mass on each
lung. Needless to say that we got off the phone with he doctor with more
questions than he could possibly begin to answer. One of the most comforting
parts of the journey is that he asked if he could pray with us before getting off
the phone. He took us to Jesus because Angela had a problem he could not fix.
However, he and his office staff started moving like a fine tuned machine and God
used their urgency and assertiveness to get a biopsy scheduled for her in less than
36 hours. The doctor asked me what hospital I wanted her at and I promptly replied,
“Siteman Cancer Treatment Center at Barnes-Jewish”, which he was happy with the selection
as well. He said that he would speak with an oncologist there and get the ball rolling.
There wasn’t
much sleep for me that night as I held Angela in my arms until she slipped off. While, I spent most of the night watching her breathe as I prayed that God would give it to me instead. She managed
to sleep 5 hours and woke up refreshed and with a great attitude. Of course,
things were still on our minds as we made phone calls to our close friends and
family. We kept the normal daily routine other than me staying home to keep an
eye on her and help her with the kids. I did have to see my pulmonary specialist for some annual Lung Transplant check-up. Unfortunately, my lungs had really
taken a beating this year from a nasty virus I’ve never had. My lung function
is down to 30% from 36%, I’ve lost 30 pound in 16 months with no real explanation
and I’ve been having shortness of breath in normal daily activities like
getting dressed. I was assuming that with all my health issues with lung rejection that I would at some point have something happen to put me back on the transplant list. I think we were all kind of preparing for that in our minds, but never did we think Angela would have something like this!! She has always been the eat well, take supplements, and exercise
kind of person. She’s never smoked, done drugs or anything that would be potentially
harmful to her body. She always has her seatbelt on reminding, everyone else to
get them on.
5 hours in the ER. |
The biopsy
was scheduled for Wednesday morning at 8:30am. We got our hustle on and delivered
our 2 little guys over to the babysitter and pulled in at Barnes St. Peters
right on time. The weather totally carried the mood that morning with this
persistent drizzle and a cold chill. The biopsy went smoothly and Angela, as the
doctor report, did great. He did have a heavy expression of concern on his face
as he spoke with me privately. He told that he strongly believes tumor was cancerous
as he formed a shaped his hand like he was holding a ball. My heart continued to
sink even deeper because this is coming from a radiologist whose hundreds of these, if not
thousands. I didn’t want to tell Angela about my conversation, but I think she
needed to here it. As the radiologist was making his rounds to check on her in
recovery area, I asked him in front of her why he believed it was cancer and he explained
that is could have been a variety of things, but this mass had characteristics he’s
seen before in cancer. Once again, our hearts sank even further. We were becoming
more and more perplexed but not driven to despair!!
On our
way back to pick up the kids, Angela’s doctor called to inform us that he spoke
with an oncologist at Siteman who agreed with our doctor that we needed to move
quickly and get Angela admitted into the hospital immediately. This was not foreseen
by us and again threw us into panic and fear. We had to figure things out for
where our boys would stay before we could go down to Barnes-Jewish emergency room
to be evaluated and admitted. God had that worked out already and our friend who
had the boys already was able to take them for a couple of days. Our baby has
to be watched by a qualified foster-parent and she was just what we needed in our time
of need. God continued to show himself in the valley of the shadow of death. He was showing himself in even the small details throughout this journey. We
started at 8:30am and by 10pm she was admitted and settled in a room.
Thursday
was a day of a few more test and waiting to be moved over the oncology floor.
By that evening she had a new room with an incredible view of Forest Park which
made it easier. We think it was sent from God to comfort us. Her parents
also came in early from vacation as well as her sister, Amanda, who lives in
Perry, MO. Friday was a rough day as she started off with a PET scan and had to
have the hard talk with the Dr. Brian Van Tines who is overseeing her case! He
came in with an urgency in his voice and told us that Angela was in SERIOUS
trouble, which I think we already knew. It’s just a hard hit to your faith when
a professional tells you that your illness is very serious. Angela was crying
and shaking her head in unbelief as her sister held her. My brain took over as it
went into “business mode” as I had to fight off the feelings of shock and unbelief as
fear oozed its icy way through my veins. Dr. Van Tines is one of leading
sarcoma specialist in the world and is the Director of the Sarcoma department
at Siteman. He doesn’t mince words and is straight to the point. He said that
he believes that the cancer inside Angela is Leiomyosarcoma (LMS). He was
seriously concerned that the mass in her right lung was pushing against her heart
in such a way that it could cause obstruction of the major veins. He also had
serious concerns about the tumor on her spine and how it was compromising the
integrity of the strength of her vertebra. He then went through what he
believed was the course of action. Dr. Van Tines said that he ordered that she
have a Port Catheter placed in the right chest area to have easier access to
her circulatory system and that she was going to start chemotherapy immediately which would span for 4 days while she was in the hospital. He also
proceeded to tell us of all the horrible side effects that were to come. It was
overwhelming, to say the least!! The nurses were sent into a frantic pace after he
left the floor to catch a flight out of the city. We were left puzzled and
confused. But there was a resolve in our hearts that God had given us favor by getting treatment from the best doctor!!
The
next four days of chemo were rough on Angela. The side effects started immediately.
Nausea, neurotoxicity and fatigue crashed her world. The drugs were making it
hard for her to even
think straight. Saturday, the day after her first
treatment was the worst. She had retained so much fluid that her appearance was
definitely altered. Each day was its own set of challenges. She did not get the
port as soon as we would have liked. She had to have several IV lines started
in her arms which left them bruised and sore until they placed port in chest on
Monday morning and she received her last chemo treatment that evening. Tuesday was
a day of rest and recovery before they had a surgical procedure on her spine.
The procedure and the experience of it is something we may share later. It
was successfully completed, and she was released from the hospital on Thursday
evening.
Fatigue and Nausea after 4 days of Chemo |
Our
lives have been forever turned upside-down, as you can see, but we know God is in complete control. We are hearing from him in new ways as we walk through this. Your prayers
are greatly appreciated. OUR GOD REIGNS!! HE IS KING!! HE IS OUR ROCK!! The storm has come and we are standing on Him as our foundation. ---Dave
Please know that I will be fervently praying for Angela. I am so very sorry to hear this.
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