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Real members of MyLupusTeam have posted questions and answers that support our community guidelines, and should not be taken as medical advice. Looking for the latest medically reviewed content by doctors and experts? Visit our resource section.
February 11
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MyLupusTeam

Do cold, numb fingertips happen with lupus?

Yes, many people with lupus experience cold and numb fingertips. This is often caused by Raynaud's phenomenon, a condition commonly linked to lupus where blood vessels in your fingers and toes constrict in response to cold temperatures or stress, reducing blood flow.

A MyLupusTeam Show Full Answer

Do cold, numb fingertips happen with lupus?

Yes, many people with lupus experience cold and numb fingertips. This is often caused by Raynaud's phenomenon, a condition commonly linked to lupus where blood vessels in your fingers and toes constrict in response to cold temperatures or stress, reducing blood flow.

A MyLupusTeam member shared, "I also have Raynaud's. Very often my hands hurt and my fingers get numb and tingle." Another member mentioned, "My hands and feet are always ice cold."

During a Raynaud's episode, your fingers may turn white, blue, and then red as blood flow returns. You might also experience tingling or a warm sensation as circulation normalizes. For people with darker skin, these color changes may be less noticeable.

What can help?

Here are some strategies to manage cold fingertips:

- Dress warmly and wear insulated gloves, especially in cold weather
- Avoid sudden temperature changes (like grabbing items from the freezer)
- Warm up gradually with gloves or warm (not hot) water if your fingers feel numb
- Keep your whole body warm, as overall body temperature affects circulation
- Manage stress, which can trigger episodes

If your symptoms are persistent or bothersome, talk with your doctor. They may recommend medications or other treatments to help improve blood flow and reduce episodes.

February 11
A MyLupusTeam Member

Yep, I've got Raynaud's and my doctor gave me Nifedipine for it. It's a calcium channel blocker that, for me, caused hot flashes, so when I was taking it in the summer it was horrible. I talked to my doctor about the hot flashes in summer and he told me that many patients go off it in the summer for that reason and only take it in the winter. I get headaches from it also, so I usually take mine every other day in winter.

February 11

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