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IN SICKNESS AND IN HEALTH

For one woman, that vow has been a test of commitment for over 37 years.

BY:ANNE HOSANSKY

IN SICKNESS AND IN HEALTH image

photography by Fran Collin


Rebecca and David Otterness met while students at Gustavus Adolphus College in St. Peter, Minnesota. She was studying to be a nurse, he to be a minister. They'd go on long strolls around the lake, but Rebecca noticed that David had difficulty walking. "I just thought he wasn't in shape," she recalls. A physician offered a more serious reason: multiple sclerosis.

"David told me the truth right away," says Rebecca, now 59. "He said I was free to leave him. But we'd both promised God we would marry." As an Evangelical Lutheran, she told David that leaving "isn't who I am."

Rebecca searched through her textbooks, but they had little on MS, just two paragraphs explaining that the symptoms come and go and the person could remain ambulatory for 20 years. "I thought, I can handle this for twenty years," she says. "In my family, we believe God gives us the strength for what He calls on us to do."

She and David married in 1969. A year later, he was ordained and became the pastor of a small parish. But he had to use a cane, and Rebecca thinks the congregation saw chronic illness as a "sign of sin." So they moved to a different parish, along with their baby son, Peter. But David's balance was so shaky that every time he gave a sermon, she says, "I'd sit in the pew holding my breath, wondering if he would fall." He never did.

A physician told her she'd know when David got worse because there'd be a "drastic change." Instead, the changes were so gradual she says she couldn't pinpoint their occurrence. The couple later found out David had progressive MS, "but doctors didn't have a clue about how to treat it" aside from prescribing vitamins and hormone stimulants. Rebecca found her nursing training useful, noting that "they didn't have to teach me how to give shots."

In a few years, David had to stop working. "The congregation said his disability made it impossible for him to be the minister they needed." So he and Rebecca moved back to St. Peter, where her family lived and she could find work as a public-health nurse. Under the federal Disability Income Program, David was in a three-month program to train as a hospital chaplain, but his health deteriorated and he was never able to serve in that capacity.

"The literature said MS doesn't affect the brain or personality, but I saw cognitive changes and difficulties in problem solving," Rebecca says. There also were, she adds frankly, "communication conflicts." She'd tell him something and he'd say she hadn't.

Finances were becoming an additional strain. David was getting Social Security and Church Disability but, Rebecca explains, "I learned to be very frugal." Then, in 1980, she got a job on a resource team at Immanuel-St. Joseph's Hospital/Mayo Health System, in nearby Mankato, where she now works in obstetrics. ("It's a great fit for me," she says. "If I worked with families who were sick, I'd burn out.") She worked an early shift so she could be home by the time Peter got back from school. She'd set David up in a recliner with a tray of food, and her mother came each day to help him.

Although it was increasingly difficult for him to move from room to room, David refused to use his walker. "He was angry and frustrated. It was a hard time." And even after he fell and broke his hip in 1984, he resisted using a wheelchair.
"I had to step outside my normal self and be hard," Rebecca says. "I'd yell at him, ‘Safety is a priority! If you fall, I'll have to get you up. That will hurt my back and I won't be able to help you.' When he did fall, I'd stand over him and say, ‘You'll have to figure out a way to get up.'" She'd leave for about five or ten minutes, then come back to a David sheepishly willing to let her help him into the wheelchair. "It wasn't comfortable for me to act that way, but he needed me to be firm."

In the past few years, David, now 62, has developed severe problems with chewing and swallowing, so Rebecca must puree everything. "That takes more out of me than anything else." The liquids have to be thickened, but since David now has diabetes, he can't have carbohydrate thickeners. Rebecca found a non-carb gel thickener, Hydra-Aid, which they order from California. "I order six one-gallon jugs at a time, that's a six-week supply. With postage, it comes to about $150." Their insurance company refuses to cover it.

With David no longer able to get out of bed or turn over by himself, she tried various lifting mechanisms but couldn't position him properly. Researching online two years ago, she found the Voyager Portable Lift, which is much easier for her to maneuver. It hooks into ceiling tracks she had installed in the bathroom, bedroom and living room at a cost of $6,000. "That's less than a month in the nursing home." Insurance didn't cover the lift, either, but the Minnesota MS Society provided 25 percent of the cost.

The nursing home is sometimes a necessary alternative when Rebecca wants to visit her siblings. She tries to take David and his wheelchair in their ramp-equipped van, but when her niece got married in a mountain meadow last year, the chair would have been impossible. "David knows how important it is for me to go to family things, so he told me to go."

Rebecca managed to find time to get a Master's in Nursing from the University of Minnesota in St. Paul in 1995. It took eight years to complete the program because she could only do it part-time. If her situation were different, she says, she'd use the degree to become a full-time nurse practitioner or to teach. But, for now, she keeps her limited part-time schedule so she can be with David as much as possible.

An aide now comes four mornings a week to bathe, dress, exercise and feed him. "This is a tremendous help to me," Rebecca says, "and wonderful for David's morale," which has remained amazingly good. David even jokes to Rebecca that at least he isn't "wandering in bars."

Still, she's frank about how different loss can be when it's your husband who's disabled, as opposed to a parent. "You lose your partner and the hopes you had, as well as the protection a wife gets. You're a widow with a husband." There's also the frustration of trying to communicate. "I know David loves me and is proud of me, but if I want to know what he's thinking, I have to make up five or six responses and he lets me know which is closest. It's like having a conversation with myself."

For many years, she mourned these losses. "But I got tired of grieving. If life were a balance scale, chronic grief would be on one side with resilience on the other. I needed to look at the resiliency factors that make it possible for me to do all this, so I jotted down my strengths. I ended up with thirty!"

The "incredible supportiveness" of her mother and three siblings is high on the list. Her father, who died nine years ago, had been a wonderful male role model for Peter. Her sister Ruth lives in Wyoming; her other sister, Reneé, is in Seattle; and her brother, Tom, lives in Salt Lake City. "I know if I call any of them and say I'm at my wit's end, they'll be here the next day. That's is a safety net under this tightrope walker!"

Her son and daughter-in-law, Jenny, who live nearby, substitute for Rebecca's mother when she isn't available. Peter even taught Rebecca how to use tools, and she boasts that she can do most of the home maintenance herself, "like staining the porch steps Peter built for us, and painting the house."

Supportive as her family and colleagues are, Rebecca finds there's no substitute for talking to other caregivers. "They understand what you're going through because they're going through it themselves." She exchanges e-mails with a man in Alaska whose wife has MS, whom she found through the Wellspouse Association's Internet bulletin board. They give each other tips, such as how to travel with a disabled spouse.

The "foundation" of her strength, she finds, is her unshakable faith. It sustains David, too. "I've never heard him blame God for his illness," she says. "I think David would tell you that one of the ways God has shown His love was by providing me to take care of him."

 

Comments

Inspiration

I've known Becky for about four years now and she's been an inspiration to me. My wife has progressive MS and is in about the same stage of progression as David. I had to quit working three years ago to care for my wife as she now requires 24/7 care. Becky has been a life saver! I live in Fairbanks, Alaska and there is no care giver support group and very little other help avilable. I'm pretty much alone and way out on a limb. I don't know how I'd have managed without Becky's efforts to provide care giving tips, encouragement, and support. During the times of deep dispair, Becky was just an email away. She's always instilled courage and gave me hope. I'm glad you featured this remarkable woman in your magazine.

Spouse caregiving

I've been caring for my wife for 5 and a half yrs now after a car accident left her disabled. I know what it means to honor our wedding vows. She is unable to walk and lost the use of her right arm. We suffer through seizures and depression and everything else that comes with this life as it is now. We met on a blind date at 15 yrs old. Married at 20 and now soon to celebrate our 25th wedding anniversary . God helps us through our trying time. I would love to share more. God Bless
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Rebecca

This is a beautiful strong of personal inner strength and resilence. My husband is 37 years old and has been diagnosed with primary progressive MS. He has become pretty severly disabled over the last five years. We were married the same year he was diagnosed. At first, I tried to tell myself this wasn't his illness, it was he and I against the MS. As he continues to progress, it has become more and more difficult to maintain that attitude. My comittment hasn't wavered, but my resilence seems to be being tested and it was nice to read this story to know it is possible to keep going. I do have to work on making myself strong so that I can keep up the marathon. I am also an RN, by the way.

My spouse has multiple sclerosis

I'm writing this comment on our 22nd wedding anniversary. My husband was diagnosed over 20 years ago. He has been bedfast now for over six years. His condition has deteriorated rapidly in these six years to the point where he can't move anything except his neck a little bit and blink his eyes. He has no short term memory and speaks in one or two word sentences. He spends his day watching tv and talking to our cats. I am several years older than he is, and when we married I used to joke that I would soon retire and he could take care of me. Boy, how off base that was. I retired early in 2000 (I just now turned 69) because he could no longer get himself up when he fell. My faith keeps me going, because I believe that God gave me this job to do, so I try to do it to the best of my ability. My husband has been on home based care with the VA for a year now, and that helps me tremendously. I don't have to load him up and take him 15 miles over to Hampton to the VA; the nurses come to the house.

As I read the comments from other MS caregivers I am reminded how similar our situations are. It helps to know I am not alone. There are others out there who know how I feel. I would love to hear back from others.

David my Husband

My husband was diagnosed with MS 21 years ago. He is now confined to a wheelchair and his bed. It has been 8 years that I have been a caregiver. My vow to my husband on our Wedding Day, was in sickness and in health; (I will be there). Our faith in God is my strength each and every day. I also have the help of our two sons and their families who live on each side of us. We have 7 of our 9 grandchildren next door!! What a BLESSING!!

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I have Multiple Sclerosis and have had it for 20 plus years, I know how hard it is for someone to make the commitment to care for someone with a chronic serious illness. It is hard enough going through the non believers, the you don't look sick (while your dying inside) etc. When you find someone that is caring and puts your needs before their own you are blessed.

I found that person in my second husband Paul, I know that there is a lot that he doesn't understand or fully comprehend yet, but he is my Angel here on Earth. So don't give up, don't feel sorry for yourself and most of all be good to your Care givers be it a husband or a family member or Home Health.

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