Reducing Holiday Stress - Treating Raynaud's - Genetics and Lupus - Travel Checklist

Managing Lupus and Holiday Season Expectations

The holidays are typically a time of celebration, traditions and quality time with family and friends — but it’s hard to enjoy the celebration if you have a lupus flare. So, it’s important to recognize that the holiday season can be especially exhausting and stressful for people with lupus. There are many ways you can reduce stress and prepare for holiday obligations without becoming overwhelmed — and still have fun. Learn more

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Understanding Lupus Genetics Recent genetics research about lupus has led to more discoveries of how genes can affect lupus development. If research advancements continue, medical experts might one day be able to look at a person’s genetic profile, predict their risk for developing lupus, and maybe even stop the disease before it begins. Read more Spirit of Giving The holiday season evokes a spirit of giving as people around the world rally together to support the causes they’re passionate about. Explore the many ways you can give back during the holidays — from fundraising events to creative ways to donate — and help bring us closer to solving the cruel mystery of lupus. Learn more

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Sharing the Journey: Avoiding Raynaud’s During the Winter During cold weather, symptoms of Raynaud’s phenomenon tend to strike people with lupus. Find out how other people with lupus try to keep this painful condition in check. Get cold weather tips Common Questions About Kidney Transplants A kidney transplant can be an important and sometimes necessary option for someone with severe lupus kidney disease. Our lupus experts address your questions.  Get answers Your Lupus Travel Packing Checklist Planning on heading out of town for the holidays? Check out our handy lupus packing list full of key travel essentials to help you manage your health wherever you go.  View checklist Resource Center Adds More Educational Content in Spanish ¿Hablas español? Hemos agregado 75 nuevos recursos de lupus a nuestro sitio web. Te invitamos a verlos. Haga clic aquí

Special thanks to EMD Serono, a 2017 Lupus Foundation of America supporter.

“We’re never as alone as we think we are.. sending love to everyone who’s fighting their battles.” -Katiuscia M., Facebook

Lupus Foundation of America 2121 K Street, NW, Suite 200 Washington, DC 20037 Phone: 202-349-1155 | Fax: 202-349-1156 | info@lupus.org Our mission is to improve the quality of life for all people affected by lupus through programs of research,education, support and advocacy.
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