Systemic diseases such as lupus may include some sort of oral involvement. And, good regular dental care with a trusted dentist can help discover and alleviate any problems that might arise.
Finding Firm Ground: When Lupus Affects the Feet
By Laura Putre
Jacklyn Cantu’s lupus symptoms began in her feet, when they swelled and turned blue six years ago. “It was mainly in the evenings after a day of work, and I really didn’t think much of it, but it gradually got worse and worse,” says the 26-year-old human resources associate from Bryan, TX.
She tried to ease her discomfort with over-the-counter medications for six months or so. But by January 2007, “I was at the point where I couldn’t do anything on my own anymore,” she says. “My boyfriend at the time was having to dress me [and] drive me to work. We lived in a second-floor apartment, and I could barely get up and down the stairs.”
She eventually saw a doctor and was diagnosed with lupus, and she’s been in remission for four years. Even though treatment has helped, her feet won’t let her forget that she has lupus. Every day, they swell and ache due to arthritis and turn blue from sensitivity to cold—a marker of a vascular disorder called Raynaud’s phenomenon, which is fairly common in people with lupus. The autoimmune system attacks small blood vessels, causing them to constrict with exposure to cold.
David Baek, D.P.M., a podiatrist who specializes in wound care at Shady Grove Podiatry in Gaithersburg, MD, sees many people with lupus or other autoimmune diseases. Their most common symptoms, he says, are swelling and pain from arthritis in the foot and ankle.
The second most common complication is Raynaud’s phenomenon. “The smaller digital vessels—fingers and toes—are very sensitive to temperature changes,” Baek says. “Even in cases where on hot days we have the AC running, we’ll take a patient’s socks off, and in front of my eyes, I can see their toes blanching and turning white, turning purplish from the constriction of the vessels.”
Besides numbness and discomfort, those with more severe cases of Raynaud’s may develop ulcers on their toes. In the most extreme cases, a person can develop gangrene, Baek says.
With the lesser forms of Raynaud’s, the treatment is mostly palliative. “We tell them to watch the temperature, especially in the wintertime,” Baek says. “In the summer, watch the amount of exposure in air-conditioned rooms. Wear socks in the evening. Obviously, watch for any type of skin breaks, signs of infection, and severe redness.”
People with chronic health conditions need to be especially careful about foot problems. “For healthy people, a blister is going to heal fine, but for anyone else, it’s usually recommended that they see their general practitioner. If they’re on an immunosuppressant, they’re at high risk for developing a worse infection because their immune system is suppressed,” Baek says.
Karin Ewing, 26, an e-learning and instructional specialist in Cincinnati, OH, was diagnosed with lupus six years ago and has had Raynaud’s phenomenon in her hands for some time. About nine months ago, it showed up in her feet.
“It just started off as an intense pain on the balls of my feet and my toes,” she says. “Then I started to get ulcers on the tips of my toes, and those became very deep and very painful.”
Ewing says that her ulcers don’t heal quickly. “What might take one person a week to heal, it takes me two months. They become infected and my toes swell,” she explains.
Her feet also swell and hurt from arthritis. “One of the biggest things is trying to find a balance between being able to go on with my daily life but also being able to manage the pain,” she says.
Medications—Aleve® and sometimes Vicodin®—don’t always help. And she often has trouble sleeping because the pain is worse at night. “You kind of have to take it day by day and manage the pain as best you can,” she says. “That’s what gets me through.”
Ewing tries to limit her walking on bad days and sometimes takes the morning off from work. She also leans on family members and a few close friends. On a recent fairly bad morning, her boyfriend took her dog for a walk, made her a pot of coffee, and packed her a breakfast to help her get going. “He takes such good care of me,” she says.
Cantu’s family helps her, too. She also plans ahead for days that require lots of walking—like a recent trip to Sea World—by resting for a day or two afterward.
But she only has to travel as far as her closet to see the adjustments she’s made for her feet. It used to be filled with high heels and now is full of flat styles.
To her dismay, her younger sister was recently diagnosed with lupus—so she tries to share everything she has learned so far. “We had no idea what lupus was when I was diagnosed,” she says. “But my sister has me, so it’s been a little easier for her.”
The difficulty in knowing if a certain symptom is due to lupus, a side effect of medication, or something else entirely stems from the nature of the disease.