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It’s a Wrap!

This is the final installment of Life Happens – Jesus Answers and “Journey of Transformation.” God is bringing changes to the PWOCI blog so it is time to say goodbye. Change is good when it’s God directed and I trust that He has many blessings in store for us as we Shine in the Light of His Glory.

To begin, I’m including the final paragraph from the July 1, 2010, entry for context:

By September 2002 my health disaster was out of control. Clearly, there was more than lupus ravaging my body. The time had come to take my health care to the next level. I needed answers and I needed them fast. Fortunately, God had an awesome rheumatologist waiting in the wings.

By October 2002 I was wheelchair bound. I needed assistance with eating, bathing, dressing and walking. I was carried up and down stairs. I was bedridden. The excruciating pain, weakness, and burning in my arms prevented me from using them except for balance. The slightest exertion exhausted me. Infected ulcers burrowed to the bone on my elbows. This was a new level of torment.

By the grace of God I landed in the office of Dr. Michael Baker and my search for genuine help was over. I slumped in the rented wheelchair, head adorned with a ball cap covering my unsightly mane, and tears streaking my red, swollen, disfigured face. Both Dr. Baker and my husband carefully lifted me out of the chair and led me toward the examining table. Not only was I nearly paralyzed, I was breathless from exertion, and virtually lifeless.

After a physical examination, lab tests, and a muscle biopsy, Dr. Baker concluded that I had a form of muscular dystrophy called dermatomyositis. This life-threatening autoimmune disease attacks skin, muscle, and connective tissue – basically, the entire body can be affected. Only a small percentage of lupus was present by comparison. The other autoimmune diseases were Sjogren’s Syndrome, Raynaud’s Syndrome, and hypothyroidism. Treatment was prednisone and intravenous immunoglobulin (IVIG) infusions derived from human plasma.

With this new information came the time to update my Exceptional Family Member Program (EFMP) data including the fact that I had only a five-percent chance of survival. Without treatment, or if treatment didn’t work, I would have died. Years later while my dad was dying I learned that I could have received hospice care because my diagnosis and prognosis were so critical. This is something more people should know in case they have gravely ill family members who aren’t necessarily terminal.

Once I was officially diagnosed with a neuromuscular disease I became one of “Jerry’s Kids” and received a custom-fit wheelchair compliments of the Muscular Dystrophy Association. I still have it to this day and intend to keep it as a reminder of the depths to which I plummeted and the brink from which God saved me.

In spring 2003 a knowledgeable army dermatologist gave me a remedy for the infected ulcers on my elbows. One part vinegar to one part water. You heard me right. I was so angry to have suffered for eight months with this torture and all I would have had to do was soak my elbows in vinegar and water! Of course, the remedy was just as excruciating as the ulcers themselves. So I took oxycontin an hour before soaking because the burning pain was too much to bear.

By July 2003 the ulcers were gone but they left permanent, hideous scars. I was able to drive by this time and managed to get myself to PWOC. I had to sit during the entire program and went straight home and back to bed after. In March 2004 I was able to discontinue taking prednisone but continued the infusions.

The promise I received from the Holy Spirit back in 2001 about this trial lasting about five years came to pass. From the time I began getting symptoms in January 2000 to the end of 2004 the ordeal was largely over. Five years. After that the recovery process began.

In January 2005 I began weight training for the first time since 2000 and could lift only 10 pounds on the leg extension machine (quadriceps). I’m still working my way up to 90 pounds which is what I lifted before the disease set in. My quadriceps and biceps were the most severely affected muscles in my body.

By May 2005 I no longer needed oxycontin and phenergan for pain and nausea, and I finished the IVIG infusions after 27 months of treatment. It nearly took a miracle for me to receive these costly infusions but God worked it out. By August 2005 my hair had grown back completely. In 2006 I continued serving at my local PWOC.

In October 2007 my rheumatologist declared me cured of dermatomyositis. I stood in front of the PWOC body and gave an impromptu testimony about my healing, and proceeded to cut up the handicapped plaquard once displayed from the rearview mirror of my car. It was an act of faith.

As I recall 1999 when I walked around our Germany apartment praying for God to transform me by the renewing of my mind (Romans 12:2) I had no idea how He would answer that prayer. I certainly didn’t expect Him to take me down a dark and tangled road. Having endured all this and more, I am convinced we are far better off not knowing the future. Anticipating suffering of this nature would render many of us immobile.

Having persevered and arrived on the other side, I understand why God chose this path for me. It was effective. He used my physical anguish to produce an inward cleansing and strengthening of my heart and soul. As a result, I am free from many old habits, mindsets, and strongholds that kept me from living free in Christ.

There is nothing like a life-threatening illness to get you in a position of dependence, humility, and focus. It creates sober reflection and laser sharp awareness of what really matters in life. The things I thought were important gradually fell away while life itself shone through as the most significant thing of all – that is, eternal life. “Turn your eyes upon Jesus, Look full in His wonderful face, And the things of earth will grow strangely dim, In the light of His glory and grace …”

God taught me many things through my journey of transformation thus far, but rather than sharing some of them in my own words I’ve chosen to let the Word of God speak:

Before I was afflicted I went astray, but now I obey your word (Psalm 119:67).

Blows and wounds cleanse away evil, and beatings purge the inmost being (Proverbs 20:30).

I was pushed back and about to fall, but the Lord helped me. The Lord is my strength and my song; he has become my salvation (Psalm 118:13-14).

And the God of all grace, who called you to his eternal glory in Christ, after you have suffered a little while, will himself restore you and make you strong, firm and steadfast (1 Peter 5:10).

(More: Romans 12:1-2; 2 Corinthians 12:8-10; Hebrews 12:1-2; Psalm 103:1-5; Psalm 116:1-7; Psalm 119:71, 75, 92, 116-117; Isaiah 40; Isaiah 55:8-9; Isaiah 61:1-4.)

THE JOURNEY ENDS

It’s my hope that this Journey of Transformation has been a testimony of God’s ways, power, love and grace. I pray that the Holy Spirit used this story to encourage, to educate, and to challenge you. Never cower in the face of grave difficulties, but trust in God’s sovereignty, goodness, and mercy even when everything in you cries out against them. Because when Life Happens – Jesus Answers. May Jesus lead you gently through your own Journey of Transformation.

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Clash of the Specialists

It was November 2001 when I landed in the dermatologist’s office. Dr. Honl was kind, compassionate, professional, and deeply concerned about me. Days later I ended up in the rheumatologist’s office. Dr. Linney (name has been changed) wasn’t so concerned.

The battle of the specialists began.

The first time I visited Dr. Honl she carefully examined my skin. When she noticed my shins she asked, “Do you ever use lotion?” I replied, “Yes, but it takes too much energy to get down there and apply it. I don’t do it often.” The skin looked dry and scaly, almost with a marbled, shiny appearance.

She looked at my fingers and toes. Apparently the ulcers that were forming on the bottoms of my big toes did so because circulation was lacking. The Raynaud’s Syndrome was kicking in more and my hands and feet often turned purple. It was hard to keep them warm. The calcifications and burning sensations on my knuckles and finger tips definitely suggested a serious autoimmune problem.

After assessing me completely Dr. Honl announced, “I think you have a connective tissue disease called dermatomyositis. The skin lesions and muscle weakness are consistent with that.” I told her that other doctors stood firm on the diagnosis of lupus. She was certain that these new eruptions were not signs of lupus although there could possibly be some lupus mixed in. Was she correct?

An official diagnosis had to come from a rheumatologist – a specialist who deals with autoimmune diseases. I’d been here before. The rheumatologist I saw in Bowling Green, Kentucky, who seemed more interested in collecting his fees than he was in helping me, was the guy who gave the “official” lupus diagnosis. But now maybe I would have a doctor who would exert some effort in nailing down this mysterious disease process.

Tri Care assigned me to a rheumatologist named Dr. Linney who happened to be the same one my sister saw. Some doctors are better than others and both of us struck out with this one. After examining me he affirmed the standing diagnosis, “You have lupus.” I said, “Dr. Honl, my dermatologist, thinks that I show definite signs of dermatomyositis.” How did he respond?

Dr. Linney’s cold demeanor nearly made me shiver. There wasn’t a hint of warmth or concern in his expression. With a determined arrogance he refused to give Dr. Honl’s diagnosis a second glance. Something was wrong. I sensed in my spirit that this guy was putting his pride before his patient. It was clear to me that he stood firm on his opinion because he couldn’t handle conceding to a dermatologist – a female dermatologist at that. After all, he was the big rheumatologist and he had to be right! But was he?

Power and control. That’s what it was all about. Where did that leave me? I revisited my Merck Manual and read about dermatomyositis. It sounded scary. It could put me in wheelchair. It could take my life. But for the time being, lupus reigned.

A year from this point I finally would have the right answers, but until that time God had more things in store for me – a visit with a naturopathic physician was on the horizon.

THE JOURNEY CONTINUES:

Through life’s uncertainties I have learned to lean on Christ. If I never had any problems, if I got all the answers I wanted, and if everyone agreed and got along . . . I’d be living in Pleasantville where everything is black and white. Boring! I want color! I want vibrancy! I want to live.

Regrettably, living involves pain. Living involves unanswered questions. Living involves power struggles between people who won’t agree. Life is a big mystery held in the hands of a big God who has something bigger in mind than we can comprehend. Trusting and waiting are hard, but they are what I must do.

Since ancient times no one has heard, no ear has perceived, no eye has seen any God besides you, who acts on behalf of those who wait for him (Isaiah 64:4).

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Life Happens – Jesus Answers is a weekly column addressing the challenges we face in life, coupled with the presence and grace of Jesus, our One True Source of hope and peace. The column’s author, Laura Firtko, can be reached by email here: LifeHappens@pwoc.org

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Doctor! Doctor!

In July 2000 we packed our household goods, cleaned our apartment, moved into the Ray Barracks guest house, and eagerly anticipated our PCS to Fort Campbell, Kentucky. My “lupus” symptoms hadn’t changed. As far as I could tell, the condition remained isolated to my gum tissue, and I kept hoping it would go away.

By the end of August we were settled into our little rented house in Clarksville, Tennessee, and I began exercising. I felt fine and seemed relatively healthy except for the red rash that appeared across my nose and cheeks. I looked like Mrs. Tomato Head, especially after exercising. Needless to say, I was embarrassed to be seen at the fitness center.

In September the skin on my hands became extremely sensitive. It felt like third-degree sunburn each time I handled the window shade cords or attempted to tie my shoelaces. Any object with a ridged or slightly rough texture caused a burning sensation. When October brought three raised red bumps to my forehead, it was time to get this mysterious disease investigated more thoroughly. Unfortunately, my first few visits to primary care doctors and physicians’ assistants (PAs) resulted in frustration and serious doubt about the medical profession. The first doctor told me the skin changes would subside in a couple weeks and not to worry about them. One PA told me I had rosacea (reddening of the facial skin that usually occurs in older adults). My eyes got big, my anger rose up, my mouth wanted to yell, “You have got to be kidding me! This isn’t rosacea! You’re not serious, are you?” Instead, I simply asked, “Are you sure this isn’t something more like lupus? After all, that’s what other doctors have suggested.” Then she shot a wide-eyed gaze at me as if I had no business questioning her. Gimme a break. She couldn’t have been more wrong.

Eventually I landed in the office of a dermatologist who actually seemed to give a rip. Results of a skin biopsy led him also to “suspect” lupus. At this stage it only appeared to be discoid lupus – a less serious form that remains isolated to the skin. He did warn me, though, that it could become systemic, meaning full-blown Systemic Lupus Erythematosus (SLE). Hadn’t I heard that before from a certain periodontist in Hanau, Germany? Hmmm … I vaguely recall … Yes! Now two different doctors agreed with each other. In order to halt the progression of the disease, the dermatologist prescribed a drug called Plaquenil, an anti-malarial drug, interestingly enough. Did it help? I don’t remember, but I didn’t get malaria! Whew. Close call.

Following one of those uplifting dermatology appointments, I went to the restroom and examined my face in the mirror. Fear of the unknown swirled around within me as denial rose to the surface and evaporated. Reality was staring back at me. I inquired of the Lord, “Father, what’s happening to me? Is this rash going to scar me for life? Will it ever go away? Will I ever be the same? How long will this last?” The reflection in the mirror was of someone I never saw before and didn’t care to see repeatedly. I recalled the days when people complimented my skin. After this, could anyone bear to look at me?

God had the answers to my questions, and He chose to reveal them one step at a time, one symptom at a time, one day, one month, and one year at a time. The trial before me would be treacherous. It’s a good thing I didn’t know what was next.

TO BE CONTINUED …        

Women of PWOC, stay connected! In the coming weeks I will continue sharing my Journey of Transformation from being wounded and angry to healed and thriving. My purpose in sharing this story is to glorify God, to show the truth about Him, to display His goodness and provision in the midst of suffering, and to give you hope. No matter where you find yourself at this time in your life, be assured that God is trustworthy and faithful despite how you feel about Him. He does have good plans for you. “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” (Jer. 29:11).

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Life Happens – Jesus Answers” is a weekly column addressing the challenges we face in life, coupled with the presence and grace of Jesus, our One True Source of hope and peace. The column’s author, Laura Firtko, can be reached by email here: LifeHappens@pwoc.org

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