Showing posts with label Lyme. Show all posts
Showing posts with label Lyme. Show all posts

Wednesday, February 12, 2014

Awards Presentation!

Presentation of Awards for Invisible Illness, Visible God
I'm honored and humbled to receive a Bronze Medal for the Devotional Category of the Illumination Book Awards. My husband Dave has been disabled by an “Invisible” Illness for 13 years now (he was eventually diagnosed with chronic Lyme disease). In fact, I find it staggering that nearly one in two Americans has some kind of invisible illness—something they deal with on a daily basis that others can’t really see, whether it’s cancer, asthma, learning disabilities, anxiety, depression, Alzheimer’s disease, chemical sensitivities, or any number of other conditions.

Sometimes a diagnosis comes quickly, and other times we can search for years, trying to find out what’s wrong with ourselves or a loved one.  Either way, the answers can come as a crushing shock. One day our world comes to a screeching halt—but the rest of the world continues on, largely oblivious.

In some ways, many more of us have an “invisible illness.”  Not all hurts come with a diagnosis. Anyone who has lived with the pain of broken dreams, unmet expectations, the death of a loved one, regrets, fears, worries—has lived with a private pain that the world just can’t see.

But God sees. God understands. God cares. And Jesus continually intercedes and acts on our behalf with power.  He is:
…one who has become a priest not on the basis of a regulation as to his ancestry but on the basis of the power of an indestructible life…
~ Hebrews 7:16
When I first read this, I was blown away because I realized that since Jesus is in me, then this power of an indestructible life is in me, and I could rest in that power. Something more powerful than my emotions, a peace that passes understanding! And since we are in Christ—this peace is a sure refuge. This inspired me to write Invisible Illness, Visible God: When Pain Meets the Power of an Indestructible Life.

We are not powerless. 

Jesus is our priest on the basis of the power of an indestructible life—an immense power to overcome immense pain. On our own we drum up despair, depression, thoughts of death—and he comes to save us with life-giving power. God offers us the ability to walk through the flames and come out more beautiful. God enables us to choose life over death, and to choose love over bitterness. We are weak, but his power rescues us. He is the better hope by which we draw near to God.

Often we want the physical miracle, the visible one—and sometimes instead he makes himself and his love visible to us. Pain meets the Power of an Indestructible Life, full on, face to face—and God calls us to fix our eyes on him.

The power of an Indestructible Life

His love endures forever—Psalm 107:1
His faithfulness reaches to the skies—Psalm 108:4
His righteousness endures forever—Psalm 111:3
His salvation lasts forever—Isaiah 51:6
His covenant is everlasting—Ezekiel 37:26
He betroths us to him forever—Hosea 2:19
He puts his Name on us forever—1 Kings 9:3
His sanctuary is among us forever—Ezekiel 37:26
He lives with us forever—2 John 2
He will swallow up death forever—Isaiah 25:8
He reigns forever—Psalm 9:7
He gives us his Holy Spirit forever—John 14:6
His word stands forever—1 Peter 1:25
He remembers his covenant forever—Psalm 111:5
He is a priest forever, he has sworn!—Hebrews 7:21

Imagine—Jesus never, ever stops interceding for you, his beloved, his delight.  He uses the greatest, most extraordinary power that exists on our behalf, to be our priest, our intercessor, our guarantee, our hope. He could condemn us and instead betroths us and unites us with him.

Indestructible life.  Forever.  That is the surety, the rock, of his covenant with us.

His mighty power encouraged me in my darkest days, and I pray that you also will draw strength from his power.

Invisible Illness, Visible God: Illumination Bronze Medal Winner


Wednesday, March 21, 2012

Lyme Disease - Back to Life

by Deborah Luce

 Isaiah said, “I have labored to no purpose; I have spent my strength in vain and for nothing.”  ~Isaiah 49:4
Job said, “ My life drags by -- day after hopeless day . . . I give up; I am tired of living. Leave me alone. My life makes no sense.”  ~Job 7:6,16
“Hope is as essential to your life as air and water.”  ~Rick Warren, The Purpose Driven Life 

I am an art teacher and first started noticing something was wrong when my hands and feet hurt all the time.  I thought that the reason that I was often tired was because I have a job and four kids, but then I was tired on vacation too.  I got worse and worse; I would lose my balance and suddenly get very tired, and it felt like I would throw up if I didn’t lie down.

Blood tests, a CT scan, an MRI . . . family doctor, infectious disease specialist, gynecologist, endocrinologist . . . I continued to work as a very absent-minded tired art teacher.  The students probably thought that I was just a very strange art teacher, but really I was a very sick lady.

A friend of mine, to whom I owe my life, told me about a doctor she and her husband were going to for her husband’s lyme disease.  I was at the end of my rope and so I said fine, let’s drive across the country -- what do we have to lose?  It turned out that the doctor is in my health insurance network.

I was tested for lots of things and it turned out that I had Lyme Disease with some other virus that I got from teaching high schoolers for years.  I started on the antibiotic treatment and lots of supplements in April of 2002 and I did not go back to work after spring break. God provided financially throught the sick bank at work and I was able to keep my insurance.

I would lie in bed and say ok... God, take me, I am worth nothing ... He said “No.”

I have continued treatment for over a year now and have improved a lot.  I'm thinking more clearly and am regaining my motor skills.  I have gone from sleeping 14+ hours a night/day to 9 hours, my vision is no longer blurry, and my muscles and eyes don't twitch anymore.

But there are a lot of ups and downs. I have to constantly turn to Christ because you can not brace yourself for the downs--you just have to cry out to God! He is in the business of restoring souls, and that is what I need regardless of the state of health I happen to be in at the moment.

I think I had to realize that I could turn to God afresh every day and yesterday was past anyway ... I could not remember it any way! It is very important to use what energy I have on relationships with my family ...  A three year old can fold their own clothes and we only think paper plate is all they make.... Cereal is sometimes a dinner food.  That's ok.

I have learned and am still learning to turn to Christ through the ugliness of Lyme and He always meets me where I am and restores my soul if I have the guts to cry out to Him and not just melt into self pity.  Christ has mercifully given me my life back through long-term antibiotic treat ment.  I wanted to be better yesterday but God has his timing.
“So we fix our eyes not on what on what is seen but what is unseen. For what is seen is temporary, but what is unseen is eternal”
~II Corithinians 4:18

Deborah is an art teacher and mother to 4, and continues to get stronger each year.

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Wednesday, February 29, 2012

Dave's Perspective on Lyme Disease

I love those moments when I get to hear how God is working in Dave's life.  This was one of those times.


Question: 
 How has Lyme Disease changed the way you think about your life?

 Answer: 
 Life is short-honor God with all of your time.

 I need to BE more and not just DO.  Doing must come out of who we are in Christ.

 God has broken me and is letting me start over.  Will I let him use me as a vessel for His glory?

 God has kept me around for a purpose--I have been close to death three times:

  • Rupturing my spleen in 1979 
  • Lyme undiagnosed for 15 years that started affecting my heart 
  • Lost half of my blood in 2003 due to undetected slow-bleeding ulcers 

 So, what is this purpose of God's? Am I willing to be used?  I want to be willing to say like Isaiah, "Here am I, send me."

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See Lyme Resources

Wednesday, February 22, 2012

A Caregiver's Hope for Lyme

December 10 years ago, 1 am:  I woke up and Dave was not in bed.  I was used to Dave’s strange hours, but the house seemed eerily quiet.

1:30:  I went to the bathroom, the house was dark.  I looked out the window, no car.  Dave was gone.  I woke every hour after that, still no Dave.

8:00:  Got up with the kids, still no sign of him.  “Where’s Daddy?”  my almost five-year-old son Zach wanted to know.  “He’s out, he’ll be back later.”  What else could I say?

Noon came and went with still no sign of him.  Why hadn’t I continued hiding his keys?  Where could he be?  Do I call someone for help?

2:00 pm:  Dave called, he was in the next city about an hour away, and would be home when he could, but wasn’t feeling good.  He had gone to Menards, sat in the parking lot until the store opened at 7, then went to Border’s Books to read, although he could never read more than a paragraph.  The words would jumble and he read the same paragraph over and over.  Suddenly he couldn’t remember where he was, what he was doing there, why he had come—or how to get home.  He sat in our car until he remembered, and then called me.  He stopped on the way home to sleep a bit, and then made the rest of the drive.

4:30 pm, Dave came home, oblivious of the chaos in my mind, and went to bed.

Thankfully we haven't had an experience like this since the early days of Dave's illness.  Dave had to go on medical leave from his position as the children’s pastor at our church in June of 2000, but was undiagnosed at that point.  In October of that year we learned he had late stage Lyme disease.

We traced his symptoms back 15 years to his college days when he began having trouble thinking of words and writing.  He had two extended flu-like illnesses, characteristic of early Lyme disease, but no one suspected what was wrong.

Over the years he had joint pain, dizziness, headaches, eye twitching, and problems stuttering.  Eventually he developed chemical sensitivities and food allergies, then sensitivity to light, sound, motion, and smells.  For four months our church brought us meals because the smell of cooking made him pass out.  Then we learned he had Lyme, and began long-term antibiotic treatment.

Dave did 16 weeks of IV Rocephin, but discontinued because his insurance wouldn’t pay for it.  Then he started a variety of oral antibiotics along with supplements to build his immune system back up.

He wasn’t able to go to church, or to engage in a meaningful conversation, and he slept about 16 hours a day.  Our kids were 1.5 and 3.5 when he went on leave, and I felt like a single mom—and a widow with a husband.  I couldn’t talk to him, couldn’t discuss decisions with him, and yet there he was real, but not all there.  Where was he?  What was happening in his mind?  God, will he ever get better?

I remember praying, God, heal him, or take him home to you—but don’t let him continue on like this, living but not able to live.  I prayed that way for months until I finally demanded, God, what are your intentions towards Dave?

And God replied, Merry, what are your intentions towards Dave?  What will you do if nothing changes?

I knew my intention was to love him, to stand by him, to care for him.  How could I make it through this ordeal?  I went back to the basics of my faith—God is sovereign, God is good, God is loving. These truths didn’t seem to make sense in our circumstances, and I had to choose—who will I believe?  Will I believe what the world and my circumstances reveal to me, or will I believe God?  I chose God, and struggled to hang on to my convictions.

The first Christmas came and went, and then the second, with little improvement.  I was able to cook in the house again, but that was small consolation for me.  Then in September of the second year I saw a window into Dave’s soul.  For one glorious week he was able to read, to talk, to discuss things again.  I had seen brief windows before, windows of an hour or so where he would ask what was happening to him, how long had he been sick—did he still have a job?  Then he would slip back again, occasionally grabbing his briefcase and asking, “Do I have a meeting tonight?”  No, my dear, no.

I let my hopes grow because a week was so long—but slowly he slipped back into Lyme-land again, and again was unable to communicate.  The pain he felt seemed horrendous, and I felt helpless to know how to comfort him.  He used to be comforted by my touches, but since his medical leave they seemed to increase his pain.

I prayed, “Lord, protect our marriage.  Don’t let my heart wander from him.  Let him still love me if he comes out of this.” Amazingly I began to love Dave more.  Truly, and deeply, love not dependent on what he did for me, but because God considered him worthy of my love.

In January of the third year we again switched antibiotics, deciding the last down-turn was due to antibiotic failure.  His painful “herx” reaction lasted a month this time, but for once had a definite ending.  Always before I could never tell the difference from one herx to the next—they all seemed to run together with no discernable pattern.  But this time it ended, and the Dave I’d had for that week in September was back again.

We seemed to be moving into a new phase and getting to know each other again.  He could read for about 20 minutes at a time, and when I saw his passion for reading God’s word again, such a precious gift that had been taken away—my heart rejoiced.

For several months, these improvements continued.  We believed we were heading towards a remission.  He still had a lot of pain, required about twelve hours sleep each night, and continued to be very sound and motion sensitive.  But he was able to come to church again, and taught Adult Sunday School for about nine months.  He sometimes couldn't make it through both Sunday School and church as it was too exhausting, but to be teaching again, which is his passion, gave him a new excitement about life.

Slowly that Fall, though, the improvements melted away again, and by April of the fourth year, the improvements were all but gone again.  Over the next 2 years I slipped into a deep depression.  To have Dave and lose him again was surprisingly more painful than the first time I lost him and it wasn't until the spring and summer of the seventh year, that I came out of that again, found my ability once again to hope in God rather than in cures, to trust God again, to again remember that circumstances don't define God's love for us.

I don’t know what the future holds for us, but I do know that God can be glorified even in something as tragic and life-changing as Lyme disease.  There have been other windows, other glimpses...but the roller coaster continues.  Somewhere in the middle of all of this I quit demanding that God do what I wanted (although I continue to pray for Dave’s healing), and I began to submit myself to God and ask, “Lord, change me.  Make me willing—and able—to bear up under this strain, and to walk with you.  Be glorified in my life and in our family—and in Dave.”  God has faithfully answered that prayer and drawn me nearer to him.  He has softened my heart and made me willing to follow Him, no matter what happens in our lives.

I felt I could thank God for the blessing of knowing him more deeply through Lyme—but not for the Lyme itself because that hurt Dave so.  But one day Dave told me that he thanks God for the Lyme—not because of what was lost or the pain it’s involved—but because he is changing too.  If there was no God, Lyme would just be an awful tragedy.  But God can work for our good even in the midst of a tragedy, bringing something meaningful out of an otherwise meaningless and destructive illness.  We can look at the almost twelve years and maybe more lost to Lyme—or we can put our hope in a God who can bring good out of nothing as He created the world out of nothing.

*     *     *

For more information about Lyme Disease, check out the links on my Lyme-Illness-Disability Resource page, or email me (see the bottom of the About Us page).

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Friday, February 3, 2012

Invisible Illness, Visible God - Finished!

Some of you know that I've been working on a book for the last 10 or so years (longer if you count the years early in Dave's illness that I journaled, before I ever thought of writing a book).  In between taking care of Dave and the kids, homeschooling, working part time, and trying to breathe, I found snippets of time here and there to work on it.  Some years I worked on the book a lot, some it lay dormant, like a seed in the ground.  Cold, dark, resting--waiting to grow.

Last fall I attended a Women of Faith convention, and learned about a contest that WestBow Press was sponsoring.  The deadline gave me just under 4 months to finish up, and I wondered if I could do it.  I prayed and God cleared my Thursday afternoons and many Saturdays, so I set those aside for writing and revising.

My original journals went through several evolutions.  The first draft was mainly for me.  Sometimes I joke that I "unwrote" a book because my journals were so lengthy!  During the second draft I was trying to find my way...could this be a book that might interest and help others?  Two trips to Write-to-Publish and countless conversations, prayers, and experiments later, I settled on a devotional format.  Last fall I had a revised draft of about 2/3 of the book finished, and I spent the last 4 months finishing the final third and reworking the whole.

This week I finished, and entered the contest.  You can find a "sneak peak" on the page at the top of my blog:

Invisible Illness, Visible God
When Pain Meets the Power of an Indestructible Life
101 Devotions for Those with Chronic Illness and their Caregivers

The Grand Prize, of course, is publication of the winner's manuscript courtesy of WestBow Press, with the option that Thomas Nelson might decide to pick up the book.  Hundreds of people enter, and last year's winning entry looks like a quality book (I love Marcia Moston's title:  Call of a Coward).  The winners will be announced on March 31st.  While I'd love to win, my prayer is that a quality book will be chosen that glorifies God, and that whether through this opportunity or another, my book will be published.  I'm so thankful to be finished, and truly appreciate the support and prayers that many have given us.  The encouraging emails kept me going when I wondered if I should give up on such a big project.  Thank you!

Monday, January 30, 2012

Lyme Disease Epidemic Message on the Superbowl Jumbtron - ILADS

Hopefully one day there will be a cure. Merry
Lyme Disease Epidemic Message on the Superbowl Jumbtron - ILADS

Super Bowl just the ticket for Lyme disease education.

The International Lyme and Associated Diseases Society is running a powerful public service campaign to create greater awareness of the misdiagnosis of Lyme disease on a JumboTron outside the XLVI Super Bowl at Lucas Oil Stadium.


ILAD Superbowl Jumbotron





"Lyme disease is a silent epidemic in America. We want to alert and educate consumers about this disease, which is often misdiagnosed. Left untreated, it will become chronic and debilitating," said Leo J. Shea, III, PhD, President of the non-profit International Lyme and Associated Diseases Society (ILADS). "Tick-borne illnesses compromise your immune system and the diagnosis, which is largely based on symptoms, can be elusive unless a physician is Lyme-literate."
Open Eye Pictures and Burgess Communications partnered to create and edit a pro bono spot for the Ilads Super Bowl use. The thirty second spot was created by selecting and assembling footage from Open Eye Pictures' Oscar short listed movie UNDER OUR SKIN and sends viewers to the ILADS.ORG website for more information.
"After four years of research and production — and over 375 hours of footage, what we uncovered is a chilling tale of microbes, medicine and money," says filmmaker Andy Abrahams Wilson. "I want to show the horror of an illness and ill system that too long has been ignored."
Donna Weidel, President of Burgess Communications, adds, "I suffer from Lyme disease and from years of misdiagnosis. Finally I was tested for Lyme - and found a Lyme-literate doctor. Lyme is estimated to be growing faster than AIDS and has become a global health problem. This pro bono spot will draw more attention to the need for better diagnosis."
ILADS is a nonprofit, international, multi-disciplinary medical society, dedicated to the diagnosis and appropriate treatment of Lyme and its associated diseases. ILADS promotes understanding of Lyme and its associated diseases through research and education and strongly supports physicians and other health care professionals dedicated to advancing the standard of care for Lyme and its associated diseases.
DONATE TO ILADS EDUCATIONAL NON-PROFIT
ILADS Board of Directors is very appreciative of any financial support to further Lyme disease educational efforts.

Tuesday, January 10, 2012

"Eating Crow With Lyme"

Last fall I read this article, Eating Crow with Lyme, in the HSLDA Magazine. I was ecstatic today to find an online link to the article. Dr. Rodger Sayre states that he used to believe Lyme was hard to get and easy to treat...until a family member got it and couldn't get diagnosed, but was finally treated by a Lyme doctor. It's an excellent article, has great links at the end for people to use and he's humble about having to change his position on this.

Michael Farris Jr. was put on a task force by the gov. in Virginia to look into the Lyme epidemic in that state. (The CDC now reports that new Lyme cases are at least four times more common annually than HIV/AIDS cases. It's the most common vector-borne illness in the United States, with 29,959 reported cases in 2009.). I'm so thankful for their work, and for all those who are looking for a cure for Lyme. Several in Michael's family have Lyme disease; it's such a difficult disease to deal with, and my heart goes out to them.

Thursday, October 28, 2010

My Dad Does Great Things With Me
by Zachary Marinello (age 6)  © 2003

Once before he married mommy, he was bitten by a deer tick. Then it gave him his Lyme disease.  Then when he married mommy, after 9 weeks and I was a baby, He played with me.  And now he tries to do great stuff.

He walks with me, and we went to the secret garden.  When we were in the secret garden, we saw a statue, and me and Anna climbed on it.  It was a dragon with a man standing on top of it.  It was just a statue, and me and Anna knew that.  Dad wondered who could tell about it, and we saw a rock with words on it, so we read it.  Then we saw a bridge.  There was no river, but it was a bridge anyway.  I went on it, and then we left.  Before we went to the secret garden, we played pretend tennis and then baseball.  Then we went mini-golfing.

And when he does great stuff with me, I feel so good with him that I feel he is without his Lyme disease.  But he is still having a painful day today and I know that.  And Daddy talks to his friends when he meets them at lunch.  If he stays home and gets a rest, he’ll get better and better, and his prescription will help him get better. God will help Daddy and he preached so people would know more and more about Jesus.  I love Dad.

When Zach wrote this, he was in first grade and his favorite subjects (that week) were history and math.  This was his first composition, and he chose the subject.  He liked Rescue Heroes, wrestling with his sister, and being read to.

Mom's note--Zach was born 8 years after we were married, not nine weeks!  Zach is a wonderful reminder that the most important things we do are those we do together.

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