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Northern Lights: How My Husband Helps Me Deal With My Multiple Myeloma
By: Nancy Shamanna; Published: November 20, 2020 @ 7:46 pm | Comments Disabled
Late last month, a sudden cold snap swept down from the Arctic and caused temperatures here to plunge to almost 30 degrees Fahrenheit (15 degrees Celsius) lower than normal. From a nice warm autumn, with lovely golden leaves and even some flowers still in bloom, a heavy snowfall blanketed the land and caused a sparkly landscape. The problem was that it was really cold. We scrambled to find our parkas, mitts, hats, and boots.
We had winter tires put on one of our vehicles, and my husband Dilip got out the snow blower we bought a couple of years ago. ecause of the injuries I sustained many years ago due to myeloma, I am not supposed to lift heavy items, so I didn’t help to lift tires on rims or clear the winter walks.
This recent incident reminded me of the many other things Dilip does for me to make my life with multiple myeloma easier, especially now with the raging Covid-19 epidemic. In our area, the number of Covid-19 cases is now higher than it was in May.
Since my current treatment of Darzalex (daratumumab), Revlimid (lenalidomide), and dexamethasone causes me to be immune compromised, I have been even more cautious about going out now that the epidemic is raging. I wear a mask in public and talk to friends outdoors from a safe distance. Dilip now does all our grocery shopping. He takes advantage of the early-morning “seniors hour” to lower his risk of exposure to the virus. He still works as a physician at a stroke rehabilitation unit, but is very careful to avoid getting this virus.
Dilip is also very considerate about helping me with the side effects of the drugs I take. The current treatment has proven to be very effective in treating my myeloma; I am getting close to a remission again, it seems. However, the dexamethasone may cause what I would describe as confusion, so I am not too efficient for a couple of days a week. He drives me places, and also is good at any sort of computer or technical work, where I tend to make mistakes.
In addition, the Revlimid can cause me to have gastrointestinal issues, especially towards the end of the 21-day treatment cycle. Even though I take Olestyr (Questran, cholestyramine for oral suspension), a bile acid inhibitor, and at times also Imodium (loperamide) to manage the issues, it can mean that I don’t feel like going out (such as going for a walk or seeing our grandchildren) at the same time that Dilip does, or that I am slower to get ready in the morning. He is very understanding, and we accommodate to our differences in schedules.
My dear spouse also reminds me to take my medications, which now are quite a few since I’m currently also on maintenance therapy for breast cancer. Even though I keep a chart of medications to take, I need to be reminded sometimes because I noticed that I have become a little more forgetful over the years. Occasionally I would completely forget to take my medications if he didn’t remind me.
The fourth week of my treatment cycle, which I call ‘treatment week,’ is a little hectic for both of us. On Monday I take blood tests, Tuesday I have an appointment with the oncologist, and on Wednesday I get the Darzalex infusion at the treatment center. Dilip takes me to all the appointments. Due to the Covid-19 pandemic, he does not always come into the cancer center with me, but it still takes a chunk out of his day to just shuttle me back and forth.
As you may know by now, I have an extensive hobby of needle and fiber arts. I have an unending supply of projects, it seems, and I am always working away on a few of them simultaneously in my spare time. These projects provide me with peace of mind and give me a sense of accomplishment. Dilip is supportive of my hobby, which in turn is a blessing to me. If it makes me happy, he is happy.
At the same time, I recognize that I am feeling a lot better than at some previous times in my ‘myeloma journey.’ I therefore try to remember that he can get tired too and make more of an effort to help him out more also. For example, I have been trying to de-clutter our home more lately since simplicity is helpful for efficiency. If things overall are running smoothly in our household, we will have more time for the activities that we enjoy.
In addition, I try to give Dilip space to live his own life, since he is not a cancer patient. He is so sympathetic that he can get too caught up in my problems sometimes.
We have been together for almost 46 years now, and I don’t know how I would cope without him. We reminisce about all of the wonderful times we have had together. We try to skip over times that were not so good, such as the medical problems during the myeloma decade. But even the last decade has brought us much joy, since our family has expanded to having five grandchildren and two wonderful sons-in-law. We work together as a team to be grandparents, and are known as ‘Nana and Tata.’ We could not think of a nicer lifestyle.
I am really glad to be in a lifestyle where I am appreciated even though I am coping with cancer treatments. I certainly appreciate the other kind people in my life, especially my husband. I really don’t know how I could manage half as well without him helping me.
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The quotation for this month is from Scott Adams (1960 – ), the creator of the Dilbert comic strip, who said: "Remember there’s no such thing as a small act of kindness. Every act creates a ripple with no logical end."
Nancy Shamanna is a multiple myeloma patient and a columnist at The Myeloma Beacon. You can view a list of her columns here [1].
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