Northern Lights: Notes On Nutrition

We are currently in the peak of summer, and fresh fruit and vegetables are plentiful and in a great variety.
This made me realize how much my diet and nutrition has changed since I was diagnosed with multiple myeloma.
The first change that indirectly impacted my eating habits was having vertebral fractures in the spring of 2009. I was immobilized for at least a month and took a lot of medication to manage the pain. My activity levels plummeted to almost nil and so did my appetite. I just couldn’t bring myself to eat much.
Then, I started induction chemotherapy with Velcade (bortezomib) plus dexamethasone (Decadron), which lasted for three months. During that time, other nutritional issues appeared.
I was told not to ingest ‘antioxidants’ such as vitamin C or green tea so that Velcade could work effectively. Although ‘antioxidants’ are widely regarded as cancer fighting compounds, they have been shown to diminish the effectiveness of proteasome inhibitors. Thus I swore off my vitamin pills, green tea, and even any citrus fruit or juice. I desperately wanted the chemotherapy to work as quickly and effectively as possible. I reasoned that I could always catch up on my usual healthy eating with the antioxidants later, which I do now that I’m no longer on chemotherapy.
Another issue was that dexamethasone was causing food cravings and keeping me awake at night. I would be prowling around the quiet house at midnight, looking for snacks, preferably junk food, such as potato chips and granola bars. After a while I realized that this was not helping me to keep a healthy weight, so I tried to control those impulses.
At the same time, Velcade was causing nausea. I received the anti-nauseant granisetron (Kytril) intravenously before my Velcade injection. Granisetron slowed my digestive system down to a crawl, which lead to my having to take a natural laxative to counteract those effects.
I still felt a bit nauseous and couldn’t handle any heavy meals. All I really wanted to eat was home-made soup, particularly the ones that a kind neighbor prepared for me. During that time, I also consumed a lot of ginger-based products, such as ginger ale and ginger candies. I even drank calorific, non-alcoholic ginger beer.
Looking back, I think that my eating habits were very disrupted during induction therapy.
Then came the stem cell transplant, which caused a period of food avoidance. I had to stay away from any foods that might carry bacteria or fungus since I basically had no immune system for awhile and my gastrointestinal tract was also compromised. Trips to a salad bar were not on the menu for me during this time. I could only eat mild foods and got quite nauseated by my unusually enhanced sense of smell. I had lots of stomach upsets and was just generally quite sick and exhausted.
However, 100 days after the transplant, my blood counts were climbing back to normal levels and I felt quite a bit better.
I then started a year of Revlimid (lenalidomide) maintenance therapy, which also affected my digestive tract, sometimes causing stomach flu-like symptoms.
Having weathered that storm of 20 months of treatments, I have the greatest of admiration for myeloma patients who deal with these treatments year in and year out because I found those 20 months to be quite stressful.
Once I was finished with treatments, I could better focus on eating a good diet again.
Of course, I am highly motivated to try to stay as healthy as possible, and I am interested in eating a diet that is ‘anti-cancer’ in nature.
As a myeloma patient, I am also interested in bone health because of the weak condition of my bones. My age and gender, of course, also play a role.
For my bones, I am taking calcium supplements with added vitamin D. I am also trying to get plenty of calcium in my diet from milk, yogurt, cheese, leafy green vegetables such as spinach, as well as canned fish with bones, such as salmon. I realize that taking calcium supplements is a topic that needs to be discussed with one’s doctor because some myeloma patients have too much calcium in their blood and probably wouldn’t want to take supplements.
To help prevent a recurrence of any sort of cancer, I am now eating lots of cancer-fighting foods, which are high in antioxidants. These foods are quite similar to those generally thought to be healthy. They include berries, such as acai, blueberries, and blackberries; other fruits and vegetables with vibrant colors such as tomatoes, broccoli, carrots, and red grapes; garlic; green tea; and whole grains. My husband is a wonderful cook of south Indian food, and we eat quite a lot of dishes using lentils and whole grains.
I am also striving to use organically grown foods when available. I started to browse the ‘organic’ section of my supermarket and was surprised to find a large variety of vegetables, meat, eggs, fruit, and dairy products there.
For protein, I drink milk and eat yogurt, fish, chicken, eggs, in no particular order or amounts. I still eat red meat, but rather infrequently now.
Foods high in omega-3 fats, such as fatty fish, walnuts, omega-3 enriched eggs, and flaxseed, canola and soybean oils, have been shown to be heart-healthy and to play a role in decreasing cancers. I regularly eat salmon, nuts, and eggs that are enriched with omega-3. In addition, we use canola oil in cooking.
Although I haven’t tried taking any kinds of supplements (except for calcium/vitamin D and a multivitamin), we use fresh-frozen turmeric, which contains the active compound curcumin, in Indian cooking at home.
I try not to eat too many desserts any more, since they really are just ‘empty calories.’ I also don’t bake much anymore. I like baking but with all of the other healthy foods we are trying to consume now, there just isn’t much room for desserts in my diet anymore.
My beverage of choice is water. I try to drink lots of it and not so much juice as I did previously. As a choir singer and exerciser, I often have a water bottle with me. In winter, I add hot tea, coffee, and hot chocolate to keep me warm and hydrated.
I hope that my column helps other myeloma patients to think about how they could be eating for best health too, at whatever stage of myeloma they are in.
Would anyone else like to share their diet or nutrition tips? I am quite sure that other patients and caregivers have given nutrition a great deal of thought.
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The quotation for this month is from William Shakespeare (1564 – 1616), English poet and playwright, who wrote "Our bodies are our gardens – our wills are our gardeners." (Othello, act 1, scene 3)
Nancy Shamanna is a multiple myeloma patient and a columnist at The Myeloma Beacon. You can view a list of her columns here.
If you are interested in writing a regular column to be published by The Myeloma Beacon, please contact the Beacon team at.
Related Articles:
- Northern Lights: How I Am Dealing With COVID‑19 As A Multiple Myeloma Patient
- Northern Lights: My First Six Weeks On Darzalex, Revlimid, And Dexamethasone
- Northern Lights: Myeloma Treatments And Tolerability
- Northern Lights: Learning About Others
- Northern Lights: My History With Myeloma And How Things Have Changed Since My Diagnosis
Nicely done, Nancy! Your column makes me realize I need to take a closer look at my own diet, my nutritional issues and challenges, and then try to do a better job at nutrition.
Thanks April! It was interesting to research for the column on nutrition, and try to put my thoughts together. It seems that the myeloma treatments can put one on such a roller coaster ride that it rearranges all of one's previous eating habits! I am enjoying my new eating style, especially the organically produced food, which is delicious!
Nice article Nancy, I would like to add that green tea keeps the bones from breaking down.
Thanks for pointing out the link between green tea and bone metabolism, Christina. On PubMed there is an article about that..another reason to drink green tea when not on certain chemotherapy drugs, such as velcade.
MM dix July 2012. Presently on Zelcade and Decadron every other week.
Just viewed a 2 hour video on cancer and treatments. Anti chemo and radiation. Diet and nutrition stressed. Vegan recommended with phrase......"animal protein is like fertilizer for cancer cells" repeated several times by several of the featured MDs. Does anyone know of any research or science to back this up?
Prior to be diagnosed, I learned about http://nutritionfacts.org/ - a great resource for learning about the benefits of a plant-based diet. Dr. Greger takes the latest research and shares the info in daily short videos. Hope this is helpful.
Dennis, I am unaware of research that is so disparaging of eating animal protein! I know that there are lots of opinions about that though. The reason that I don't eat much meat is that I need a lighter diet now, for my age and activity levels, and meat can be quite fatty. Also, my tastes have changed over the last four years and I prefer the lighter fare....still eat chicken and fish though! But this is just my personal outlook..am not a doctor.
Thanks for the link, Beth! That looks interesting too.
I enjoyed reading your article, Nancy. I finished my myeloma treatment back in June 2006 and I began looking at diet and nutrition. Our diets seem to be similar in most respects - I also love Indian style cooking. It's depressing that so many aisles in our supermarkets are now taken up with highly processed foods of one kind or another - I try to avoid all of them, including smoked and cured stuff, buying organic wherever possible.
I take green tea as a supplement, rather than a drink, simply because it's a convenient way of providing the equivalent of several cups of green tea each day. I think this might be helping to keep my myeloma in check as my paraprotein dropped from 0.2 gm/dl to non detectable levels shortly after I began taking it in Dec 2006. However, I've no way of knowing for sure. Perhaps I'm just very lucky. In recent years I've added calcium, vitamin D and curcumin supplements to my regime. If I should require further treatment I will, however, discontinue the supplements as I'd be worried that they could interfere with treatment.
Thanks Dorothy...it's great to hear your perspective as a long time survivor! I agree with you about the supermarket aisles...at least in our stores now there are sections for organic food, which I now gravitate to. I found organically produced milk to be tastier than the other milk, ditto organic bananas are sweeter than the regular ones. And I must say that 'organic, free trade' hot chocolate powder makes just yummy hot chocolate. Chocolate is also supposed to have anti-oxidant qualities, although of course one must use that in moderation!
So we live and learn and there are improvements being made all the time in availability of food. I had to chuckle the other day when I was picking rhubarb from my huge plants in the backyard...'this is organic' I said to myself! Organic food harkens back to when people had vegetable gardens grown without pesticides or herbicides, I guess, or to the era before the use of those chemicals. We also are growing pots of herbs on our patio to use in salads and cooking...again, organic!
I know that in the world's food production, chemicals must be used to get sufficient crop, but I am willing to pay a bit more for the organic food, when I can find it. I just feel that as a cancer patient (even when one is in remission from myeloma one is technically still a patient) I should do the best possible to avoid eating unnecessary chemicals, if that makes sense!
Thank you, Nancy, for this very informative article about nutrition. In the court of Inappropriate Eating I am pleading guilty as charged. You'd think after a million+ dollars worth of treatment, I'd spend more time in the appropriate grocery aisles. I will do better! Be well!
Thanks Sean...you be well too! I always enjoy reading your columns .. I am sure you would enjoy exploring new areas of the grocery store (and I am sure you could write it up in an entertaining way also!)
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