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Posts Tagged ‘living through chronic illness’

By Bob Chrisman

An old friend called on her way back home from a weekend with her partner, son, and grandson. “I have some bad news and some good news. Which do you want to hear first?”

“Let’s get the bad news out of the way. Maybe the good news will soften the bad.”

“I didn’t expect you to say that. Here goes. The doctor found that I have endometrial cancer, undifferentiated. They have caught it at a very early stage.”

I stopped listening to her for awhile. The “C” word causes my stomach to clinch and the muscles in my neck to tighten. I’ve heard it too often in conversations with my women friends. Lost two of them to aggressive tumors that spread throughout their bodies.

But I focus too much on the losses and not on the wins. A friend diagnosed with breast cancer has remained cancer-free for 12 years. Other women have recovered completely from cancer of various organs. I’m thankful for those successes, very grateful.

My mind returns to the recurrences I’ve seen. A woman twelve years post treatment for a brain tumor has learned within the last two weeks that her cancer has returned. This time the doctor said she will die, but that’s what he said the last time and she lived for another twelve years.

Why all this focus on death at a time of year when the world screams with life and beauty? Why must death occur during these spring months when the earth bursts forth in new life and beautiful shades of yellow-green, when flowers of all colors open and scent the air, and when we can say, “Winter is gone for at least seven months”? Why?

Maybe all this life and beauty replaces the darkness and depression of the winter and I want no more of it. Give me life in all of its forms and beauty. I suffer enough during the winter and I’m over it, but I’m not, it seems.

I notice the beauty and revel in it because I know the bleakness of winter. Joy returns to my life because I know that the good times may not last forever. The friends I carry in my heart as the treasures of a lifetime will die. I must rejoice in their being while they are with me and not put that off for a change in the season or the approach of death.

How is it that the richness of life requires us to know the poverty of despairing times? Does it work like salt on cantaloup or watermelon? The saltiness makes the sweetness that much sweeter as death makes life more precious.

If I could stop death and dying, would I? No, I would let things happen as they must. I might even bring death to those I love earlier if they desired it, but that’s not my place in life. Sitting next to the bedside of a friend who’s dying makes me aware of the value of the time we had together and what a loss their death will be. If they must die (and they must), I can spend the final days and hours with them and carry them and those times in my heart until I pass from this earth.


NOTE: WRITING TOPIC — DEATH & DYING is the latest Writing Topic on red Ravine. Frequent guest writer Bob Chrisman joined QuoinMonkey in doing a Writing Practice on the topic.

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By Louis Robertson

 
 

This list is a work-in-progress and represents some of the lessons life has taught me. I started it as a “gift” to my children and wanted it to be something they could return to again and again to help put things into perspective and to add focus to their lives. QuoinMonkey, whose opinion I have always trusted, encouraged me to share it with a larger audience. I agreed hoping that the readers of red Ravine may find something in this they can use.

 
 
 

Things I Wanted You To Learn

 
 

1 – As long as you remember me I will stay alive in your memories. You are my legacy, my magnum opus.

 
 

2 – I am very proud of the person each of you has become. Although I did not say it as much as I felt it, you are the source of my joy and pride as a father.

 
 

3 – You can achieve anything! If you can imagine it, you can do it, but it will take hard work. It will not come easy, but if you believe in your ability to achieve, know you have the desire to see it through and persevere, then it can happen. Oh, and a good plan helps.

 
 

4 – Everyone has worth! Even the marginalized — especially the marginalized — have something to contribute to your life. You need to work beyond the visceral feelings, put yourself in their place, and look for the lesson.

 
 

5 – You are constantly being presented with opportunities to learn and grow. God doesn’t give things to you, rather he allows opportunities to be presented to you and it is your responsibility to recognize them, learn from them, and grow.

 
 

6 – Don’t get stuck in the past. What happened, happened. No amount of rehashing, bitching, complaining, or wishing will change the fact that it happened. Look for the lesson and move on, but understand that sometimes it may take years for the lesson to present itself to you.

 
 

7 – When someone has the ability to really irritate you, either by their actions or beliefs, step back! Try to identify what is bothersome and put a new face on it. For example, that person who is always butting into your conversations? Ask yourself, What purpose does this serve to them? Are they lonely, feeling marginalized, friendless, or just trying to get noticed? Then wonder what their self worth may be to have to do this to feel alive, noticed, or a part of something. Maybe even wonder how things must be at home for them. Now ask yourself “How can I help them feel better about their life?” But also remember, sometimes people are just jerks.

 
 

8 – Always remember that you are loved and have a large family to fall back on when things are tough. Don’t be afraid to ask for help; it is not a sign of weakness. It took me 43 years to realize that allowing people to step up and take some of the burden from me is often a gift to them.

 
 

9 – Remember the lesson I taught you as a kid about power. You have a reservoir of power that you control. Be stingy with who you give it to. That kid that knows he can make you mad by calling you fat is taking away some of your power. To get it back you need to be aware of your reaction and change it. This will not only help you with your personal interactions but is essential when trying to break a cycle of reactionary behavior. Once you fall into a pattern, the pattern will repeat itself until something changes. Changing your reaction will make the interaction more real and will cause you to look at it from another perspective. Once you change the pattern it will either fall apart or create a new trigger to a new pattern. Listen to that little voice that says, “Why do we always have the same argument over and over?” and use that pause to look for the pattern, and then change it.

 
 

10 – Make at least one person smile every day. Find something to compliment them on. Do something unexpected for them. Tell them they are important to you. Some days it may be the catalyst that changes their lives or the start of a chain reaction of passing the smile on. When you are given the choice, make a positive impact rather than a negative impression.

 
 

11 – Challenge yourself to be the best person you can be! Don’t settle for okay, strive to be great! Do each task to the best of your ability. Make it a game or a challenge. Don’t just do the job to check it off a list, do it so you can stand back and say out loud, “I did that!”

 
 
 
 

∞ ∞ ∞

 
 
 

About Louis: Louis Robertson (R3) is a divorced father of two teenage children who lives in South Central Pennsylvania. His day-to-day life centers on his children and teaching them about responsible living. He earns a living as a computer systems consultant.

Louis has experienced medical challenges since he was a teenager. After his first liver transplant in 1993, his perspective on life became more focused and his appreciation for the little treasures life grants increased. When he learned he needed a second liver transplant, his focus moved to preparing his family and children for a future without him. He now is a candidate for a third liver transplant and lives his life watching for life lessons he can pass on to his children.

 

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by Judith Ford


actor-jude-suffering

Actor “Jude” Suffering, dramatization of author Judith Ford in Discovery Health Channel series Mystery ER, photos © 2008 by Judith Ford. All rights reserved.




Last April, when Discovery Health Channel contacted me, I’d been working on my book, Fever of Unknown Origin, for over 15 years. I never intended it to be what it turned out to be—a 600-page manuscript with multiple plotlines and themes. It started out as a way to come to terms with a serious illness that put me in the hospital for most of the summer of 1990.

But while I wrote, my life kept happening. My parents got sick and died; their stories seeped into the book. What I thought and felt about my illness, about illness in general and about death, changed. I did countless rewrites. In 2003, I launched a website, www.judithford.com, expecting I’d be ready to market the manuscript within a year. That didn’t happen. I got discouraged and quit writing more than once, each time returning weeks later with renewed vision, scrapping whole chapters, restructuring and polishing what remained. Fever and I had been alone together too long; I’d lost momentum.

And then I received the Discovery Health Channel email. Bill, a “finder” for the network, found my website. He was looking for stories for a new TV series called Mystery ER. “Yours would be a great story for us,” he told me, “and free publicity for you.”

I didn’t jump at the offer. I’d watched Discovery Health Channel once or twice and knew that it aired stories of real people dealing with dramatic medical issues. I wasn’t sure participating would be good for me or for Fever. I told Bill I’d think it over. He sent me a CD with samples of Mystery ER.

The first opened with a woman having energetic convulsions on an ER gurney. The second involved an orthodox Jewish boy who’d contracted trichinosis, somehow, without ever having eaten pork. He collapsed in an ER doorway. While the stories were presented with respect for the patients and what looked like medical accuracy, I didn’t see how my book would fit. It contained no scenes of me passing out or seizing.



more-silly-yoga-poseMy illness had developed in slow motion, starting in 1979 with bone-numbing fatigue, low fevers, and an odd prickly rash. I went to doctors who theorized hypoglycemia, spider bites, allergies, chronic mono. None had treatment suggestions, so after two years of feeling like hell, I created my own plan. It included lots of sleep, no refined sugar or white flour, daily lap swimming, dance classes, yoga, and meditation.

Gradually, I got well and stayed well until 1990, when all the symptoms returned, this time with higher fevers. I also developed anemia, systemic inflammation, and eventually, ulcerative colitis. All dramatic enough to compel me to write but not, I thought, material for a TV show. How could Mystery ER dramatize a fever of 106, an itchy rash, abnormal liver function, and an enlarged spleen? And how in the world could they condense what had become a story about my life into thirty minutes?

“Not to worry,” Nora, the producer, told me. “We’ll just deal with your illness, not the rest of the book, and we’ll write it in a way that’s compelling and authentic.” She offered to come to Milwaukee to interview on camera me, my husband, Chris, and one of my doctors. The show would include clips of our interviews interspersed with dramatizations, played by actors. “And,” said Nora, “we’ll let you mention your book on camera.” It was the promise of book publicity that made me say “Yes.”



chris-ford-and-a-producerThe morning of the filming, the lighting and sound guys took over my friend Judy’s downtown Milwaukee condo. They banished her, her four-year-old granddaughter, and three dogs to the master bedroom. The TV crew moved furniture, set up shades to block the floor-to-ceiling windows, and demanded absolute silence. Each interview was two-and-a-half hours long, including breaks to deal with shifting light, the phone ringing, and the grandchild slinking out to lean adorably—but distractingly—against the wall to watch us.

At first, I enjoyed being asked detailed questions about my illness. What was my life like when it began? Busy, way, way busy. Had I believed my first recovery, in 1981, had happened as a result of meditation and dietary changes? Yes, I thought I’d been mentally and physically amazing. But as we got more deeply into the summer of 1990, my energy flagged. Frankly, having written in so many ways and in such detail about my suffering, I was bored by it.




                                                                chris-ford-anxiously-waiting-for-his-interview
                ruby-and-bear-less-than-amused




I perked up when we got to the part about my friend and former teacher, Dick, coming to the hospital to do a healing hypnosis two days before I was scheduled to have my colon removed. The night after the hypnosis I slept well for the first time in months. The colon symptoms abated and the colonectomy was cancelled. I went home five days later.

Nora perked up, too. “So when the medical people had given up on you, this other form of healing cured you?” Um. No. The medical people had far from given up; they were pumping me full of IV Prednisone and Demerol. They drew my blood many times a day. They’d hooked me up to a chest tube through which I was getting all my nutrition. My turn-for-the-better was sudden and wonderful, but it wasn’t magic, nor was it complete. It took two more months before I could go back to work. I had a serious relapse in 1997.

I explained this to Nora but her fascination made me worry that she was going to spin my story in a direction I didn’t want it to go.

“Did you feel that this was divine intervention?”

“Not really,” I said.




actual-jude-being-interviewed





The questions about what causes and cures disease are big and wide and controversial. My exploration of those questions is central to Fever and impossible to capture in sound-bites. Before I got sick in 1990, I would have told Nora that health was a decision, that most people could make themselves well with a combination of focus, relaxation, right thinking, and right eating. My 1990 relapse, eventually diagnosed as Adult Onset Stills Disease, blew all that certainty and bravado to bits. The only thing I knew for sure afterwards was that life is unpredictable, uncontrollable, precious, and brief.

At the end of my interview, Nora asked me what message I’d like to send to other people struggling with mysterious illnesses. I laughed out loud. “I spent 15 years and 600 pages on that,” I told her. “Give it a try,” she said.

I responded with something generic, like, “Every person who gets sick has to come up with their own sense of meaning.” Later, I wished I’d talked instead about how the illness changed me. How it humbled me. How it taught me to let go.

My doctor, Dr. M, was interviewed last. Just before her session, she whispered to me, “I don’t think I should be here. I don’t think what you had was Stills Disease.” She thought my diagnosis was ulcerative colitis, despite the fact that three other doctors had suggested the Stills label, conjecturing that the colitis had been caused by a drug reaction. I hadn’t had a colon symptom in 18 years. I reminded Dr. M. that even the gastroenterologist had rejected the colitis theory. “No,” she said, “I’m certain.”

Great, I thought. The whole show revolved around the Stills diagnosis. Would there be any show without it? Did I even want there to be a show?

While Dr. M was being interviewed in another room, I sat and worried over everything I had and hadn’t said. I wondered if I was doing my book a disservice, allowing it to be reduced to the one thin, unexamined plotline of my disease.

Nora took a break from Dr. M’s session to tell me, “Your doctor is driving me nuts. She’s giving me paragraphs of medical facts; none of our viewers will know what she’s talking about.”

“And,” Nora added, “she doesn’t think you ever had Stills disease.”

“Can we still do the show?” I asked, suddenly sure I did, in fact, want the show to go on.

“Oh yeah, we can edit out whatever doesn’t fit. It’s just annoying.”

And edit they did. The interview segments that took all day to film amounted to ten minutes of on-screen time.




actor-jude-looking-worrieda-doctor-actoractor-playing-jude-in-the-eractor-jude-throwing-out-junk-foodactor-mom-in-black-shawl-dyingactor-mom-saying-im-dying




“Inflamed,” my Mystery ER story, debuted on September 1. I expected the worst. What if they’d included my inane closing statement about “Everyone has their own meaning blah blah blah”? What if I looked old and dumpy? What if the editors made it sound like I’d cured myself with my mind? What if my story was no longer mine? I felt comfortable enough surrendering to the TV people at the time I signed release forms, yet as the Mystery ER logo lit up the TV screen I wanted to snatch my story back and protect it like the vulnerable newborn it suddenly seemed to be.

But really, the show was okay. More than okay. There were the requisite overly-dramatic bits – like a shot of my hypochondriac mother in a black shawl murmuring “I’m going to die,” and me in the kitchen frantically throwing out all the junk food when I was diagnosed as hypoglycemic. And the silly shot of me sitting in a yoga pose.

The interview sections, though, were fine. I looked okay and sounded smart enough to not embarrass myself. And, thank you very much, “everyone has to find their own meaning” ended up on the cutting room floor. As did all mention of my book. So much for the “free publicity.”

Now, two months later, I don’t mind losing the publicity. Much unexpected good has come of “Inflamed.” The friends who watched the show with me have gotten a lot of mileage out of doing imitations of my moaning mother. My sister-in-law has threatened to give me a black shawl for Christmas. Chris enjoyed seeing himself played by a handsome young actor with great pecs. My life-long running practice, an important theme in the book, made it into the script, and I loved seeing my actor-self running with better form than my own.

In the weeks since the show aired, all kinds of people—neighbors, former clients, the UPS man—have told me how much they liked the show, how impressed they were by the interview segments, and to ask if I’m well now. I am.

But here’s the really great part: Mystery ER lit a fire under me. It gave Fever more definition, more weight. It made me want to finish the book. It matters a great deal to me that a TV channel was interested in my story and that people who saw the show were touched by it.

This past summer, I went to a “How to sell your book” workshop at The Loft in Minneapolis and learned that a memoir doesn’t have to be completed before you market it. I hired a consultant to help me write the book proposal. She told me that mentioning Mystery ER in my cover letter would make busy editors and agents pay more attention. The proposal packets took most of August to write and assemble. Last week I sent out the first batch to eleven literary agents.

I’m doing the rest of the revisions with new enthusiasm, working every day. Fever and I aren’t alone together any more; I can feel my audience now, out there, waiting.




the-silly-yoga-pose

The “Silly” Yoga Pose, author Judith Ford in Mystery ER show
“Inflamed,” photo © 2008 by Judith Ford. All rights reserved.





Judith Ford is a psychotherapist and writer who lives in Milwaukee, Wisconsin. She was red Ravine’s very first guest writer, with her 25 Reasons I Write post. Reason #14: “I write to finish this damn book and it isn’t done yet.” (Remember that one, Jude? J)

You can eventually see the show, “Inflamed,” about Judith’s illness, as Discovery Health Channel re-runs all the episodes of Mystery ER. Check your local listings.

Oh, and all Mystery ER names have been changed.

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