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Color Changes in Fingers, Toes May Cause Wintertime Blues

November 16, 2009

DANVERS, Mass., Nov. 16 /PRNewswire-USNewswire/ — For an estimated 5-10 percent of the population, the wintertime blues are more than a state of mind.

Cold weather triggers a painful and sometimes debilitating disorder for millions of Americans who suffer from Raynaud’s disease (also known as Raynaud’s syndrome or phenomenon). Raynaud’s is an autoimmune disorder in which spasms in the blood vessels can interrupt blood flow to the fingers, toes, nose and ears. Exposure to cold triggers the spasms, typically causing the affected area to turn white, then blue, then bright red. Emotional stress can also cause an attack.

During an attack, Raynaud’s sufferers experience tingling, swelling or painful throbbing. Episodes may last from minutes to hours. In severe cases, the area may develop ulcerations and infections, which — if left untreated — can potentially lead to gangrene.

According to the Raynaud’s Association (www.raynauds.org), only one out of five sufferers seeks treatment. Both men and women suffer from Raynaud’s, but women are nine times more likely to be affected. “Some researchers estimate as many as 20 percent of all women in their childbearing years have Raynaud’s,” says Lynn Wunderman, chair of the Raynaud’s Association.

“Too many Raynaud’s sufferers dismiss their symptoms as being due to ‘poor circulation,’” Wunderman says. “In a sense that’s true, but there’s a medical cause for their poor circulation — and sometimes it can be serious.”

In some cases, Raynaud’s symptoms may indicate a serious underlying disorder such as scleroderma, lupus or rheumatoid arthritis. Robert Riggs, CEO of the Scleroderma Foundation (www.scleroderma.org), notes that more than 90 percent of people diagnosed with systemic scleroderma also have Raynaud’s. “In most of these cases, Raynaud’s is the first symptom.”

These patients are considered to have “secondary Raynaud’s,” meaning another associated disease is present. Fortunately, however, most Raynaud’s sufferers have the more benign “primary” form. The Raynaud’s Association and the Scleroderma Foundation advise individuals with symptoms to consult with their physicians, who can perform simple blood tests to determine whether or not antibodies associated with other diseases are present. Rheumatologists — physicians who specialize in the diagnosis and treatment of arthritis, Raynaud’s and diseases of the joints, muscles and bones — may be consulted.

At this time there is no cure for Raynaud’s, although research is underway. In the meantime, sufferers are advised to avoid cold temperatures as much as possible, effect lifestyle changes (skiing may not be advisable, for example) and protect the affected extremities with gloves, hats and other such measures. The Raynaud’s Association website, (www.raynauds.org), maintains a product review section that covers everything from warming creams to microwaveable mittens.

“Obviously, winter presents the biggest challenges,” says Wunderman. So, should Raynaud’s sufferers move south for the winter? “Well,” she concludes, “that might help somewhat, if you can avoid all of those frigid air conditioned places — not an option for many sufferers in their daily lives.”

About the Raynaud’s Association:

The Raynaud’s Association, Inc. is a national non-profit (501c3) organization whose mission is to provide support and education to the millions of sufferers of Raynaud’s disease, an exaggerated sensitivity to cold temperatures. The Association seeks to educate the general public about this condition, which can be very painful and, for some, may cause serious blood vessel damage.

About the Scleroderma Foundation:

The Scleroderma Foundation, Inc. is a national non-profit (501c3) organization that provides support and education to people and families coping with scleroderma and related conditions, such as Raynaud’s. The Foundation also funds medical research to find the cause and cure of scleroderma and related conditions.

    Raynaud's Association          Scleroderma Foundation
    Contact: Lynn Wunderman        Contact: Robert Riggs
    Phone: 800-280-8055            Phone: 800-722-4673
    Fax: 914-946-4685              Fax: 978-463-5843
    Email: lynn@raynauds.org       Email: rriggs@scleroderma.org
    Web Site: www.raynauds.org     Web Site: www.scleroderma.org

SOURCE Scleroderma Foundation


Source: newswire



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