Living every day with a life-changing illness is discouraging enough, but Maryam Hosseinzadeh is one of 400,000 people in the United States battling multiple sclerosis, a disorder that by changing the brain's makeup appears capable of generating the secondary ill of depression.
Hosseinzadeh credits medicines, immune-modulating therapy and the ongoing support of neurologist Nancy Sicotte, MD, for keeping the potentially debilitating symptoms of MS and depression from dominating her life.
Sicotte, director of the Multiple Sclerosis Program at Cedars-Sinai Medical Center, recently received a three-year, $506,000 grant from the National Multiple Sclerosis Society to study brain changes in MS and underlying causes and potential treatments of MS-related depression.
In 2004, after bumping a wall while parking her car, Hosseinzadeh had her eyes checked for blurry vision. She also had noticed her right leg dragging for a couple of months, but hadn't paid much attention.
"When I went to see the doctors for my vision, they said, `It's not blurry vision. You have double vision, and that's one of the symptoms of MS,'" said the 35-year-old West Los Angeles resident who spent nearly two weeks in a hospital undergoing tests before the diagnosis was confirmed.
In patients with MS, the immune system attacks myelin, the material that surrounds and protects nerve fibers in the brain and spinal cord. Loss of this "insulation" prevents the fibers from conducting signals correctly, leading to symptoms. Nerve cells also die, causing long-term deficits. The disease typically attacks body systems in haphazard, unpredictable patterns.
"One day I woke up and I couldn't feel my legs; from the waist down, I couldn't feel anything. One day I woke up and I couldn't taste any food. I couldn't smell anything. It's weird because the disease can affect your nerves anywhere," noted Hosseinzadeh, who earned her bachelor's degree in electrical engineering in Iran but studied animation after moving to the United States in 2002. She now works for a movie studio, creating animation for cartoons.
Hossienzadeh first was treated with high-dose steroids, which improved her vision. "But I still had problems walking. I was wobbly, and I couldn't control my balance. I had to use a crutch, then a walker, and I ended up in a wheelchair. In one year, 2005, I was hospitalized six times, each time for two weeks. My symptoms worsened every two months," she said, adding that a nine-month series of chemotherapy treatments finally began to ease her woes.
Now, taking a daily injection of a drug and a monthly infusion of immunoglobulin to boost her immune system and energy, she can hike and do yoga, but skiing, one of her favorite pastimes, remains out of reach.
"I was on other medications before, but the combination of chemotherapy, Copaxone and IVIG (intravenous immunoglobulin) changed everything," said Hosseinzadeh, who, like many patients with MS, battles a recurring cycle of depression: Having to deal with the physical, financial and emotional aspects of the disease is difficult, but becoming depressed makes the disease's symptoms worse.
"If you can cut out the stress and depression, you can deal with the MS better," Hosseinzadeh said.
But managing depression is not easy, especially because mood alteration appears to be a central part of the disease, Sicotte said.
"Depression in various forms is common during the course of MS and can have a major impact on quality of life, thought processes and long-term health," commented Sicotte, a member of the Department of Neurology who directs the Neurology Residency Training Program.