21 Tips for Living With Lupus

Living with lupus can be a tedious ordeal. Systemic lupus erythematosus (SLE) can be a scary diagnosis as it can wreak havoc on all parts of your body, such as the skin, heart, joints, and kidneys. There are estimated to be over 1.5 million people in the U.S. who suffer from this chronic illness. There is currently no cure for lupus, but there is still hope. Here are 21 ways to make it easier to overcome the challenge of living with lupus to help you live a full and happy life.

1. Do research if you’re living with lupus and teach others

Learning about your disease can take away a lot of the mystery and fear that lies behind it. Sharing that information with close family and friends will give guidance and understanding to those you care about.

2. Eat a healthy diet

While there is no special diet for lupus, a healthy diet is best for the body to be in peak condition to fight off any illness. Try to make sure you are eating a balanced diet and talk to your doctor about any changes you feel could help.

3. Exercise

Exercise is always an important staple for a healthy body and mind. Walking a couple of blocks, swimming a few laps, or doing some yoga can be just what you need to get your blood pumping and to reduce joint pain.

4. But don’t overdo the exercise

While light aerobic exercise will help a lot, try to avoid high-intensity workouts. Specifically, don’t do them when you have joint pain or you could exacerbate an already painful experience.

5. Ice, ice, baby

Cold therapy can be a good choice when joint pain first rears its ugly head. Ice slows the pain response to the brain and reduces swelling by reducing the blood flow to an area.

6. Hot! Hot! Hot!

A helpful tip to kick joint pain in the long term is to try a warm bath, shower, or a heating pad. This will loosen up your tight muscles and reduce the soreness by increasing blood flow and circulation. Heat also has a pleasant reassuring quality that can help you relax a little mentally.

7. Avoid alcohol

Some alcohol use won’t generally be bad for people with lupus, as long as their doctor has approved it. Alcohol can have some other side effects, like reducing medication effectiveness or create new medical issues. Those with depression should also be extra cautious when imbibing, as alcohol is a natural depressant and can make depressive thoughts worse.

8. Track your flare-ups

Knowing early warning signs or what causes flare-ups can greatly increase the chances of mitigating or even preventing them.

9. Minimize stress

Find ways to avoid stress as stressing the body only makes living with lupus worse. Strategize with a doctor or find ways for friends and family to really help out.

10. Make time to destress

It might be difficult to pursue some hobbies because of lupus, but finding time to destress is of vital importance. Find something you enjoy and take time to do it, whether it be listening to music, reading, or cooking.

11. Practice good sleeping habits

Sleep deprivation has also been linked to increase pain sensitivity. If you’re living with lupus, you know it can wipe you out like nobody’s business. Fatigue is definitely something to be aware of, so making sure you get a healthy amount of rest each day is a smart move.

12. Watch out for the sun

Sensitivity to ultra-violet light is very common in those who suffer from lupus. It can trigger flare-ups, which can really ruin your day. Make sure if you go out in the sun that you use at least SPF 30 sunscreen, which provides protection from both UVA and UVB rays.

13. Artificial light can be a problem

Indoor fluorescent light gives off UV rays just like the sun. You might want to try covering your lights with light shields.

14. Just don’t smoke

Smoking has been linked to all kinds of negative health effects, like cancer and heart disease. But for those living with lupus it increases inflammation, can cause flare-ups, and worsens other symptoms.

15. Prevent infections

Patients with lupus are more susceptible to infections so try to avoid those who are already sick and contagious. Always make sure to wash your hands and ask your doctor about keeping up on vaccines.

16. Beware of lupus fog

This mental impairment can confuse you, mess with your memory, and be very frustrating. Make sure to keep a journal of your activities and write down important information for safe-keeping to help counteract these issues.

17. Get a massage

Massages increase energy levels, reduce stress, and can help with muscle soreness. Try a local licensed massage therapist and see if it works for you.

18. Know your limits

Don’t push yourself too hard. If you are tired or in pain, know when you have to cut back hours at work or take time away from others to rest and recuperate.

19. Ask for help

It might be hard to admit at first, but everyone needs help sometimes. Those with chronic pain conditions are already highly-susceptible to anxiety and depression, so it is always good to have an emotional support structure to make sure you are well taken care of.

20. Record new symptoms

Keep a list of your symptoms and questions you want to ask your doctor. It is always a smart idea to inform your doctor immediately of any new symptoms that arise.

21. Acknowledge yourself

You are not your disease. Just remember that you have lots to offer the world and you have friends and family that want to see you happy. Focus on what makes life great rather than the battle you have with lupus.

Living with lupus is a challenge that can be overcome with resilience and dedication. Do you have any tips or tricks you use to manage your condition?

2 thoughts on “21 Tips for Living With Lupus”

  1. Thank you for passing this information. I have been battling with SLE for 11 years now. And unfortunately the doctors I’ve seen so not understand SLE completely so they always seem to just blame everything on the lupus and offer no solutions. You need to educate yourself and know your body. But doctors also need to acknowledge that SLE is really not like anything else. Not even like any other autoimmune disorders and each patient should be treated as individuals. I cannot tell you how many times I’ve heard “wow, I’ve never seen this reaction/symptom/or this type of problem in someone so young. Yes my rheumatologists have kept me alive for 11 years, but they do not listen to me. I’ve been hospitalized many times and it does not seem to matter to them. This city would really learn from other countries and the east coast/Midwest because of their lupus clinics. Because SLE can attack every system in the body, we should have more than 1 doctor (under 1 roof) that can collaborate on our treatment and wellness. I’m tired if just surviving and seeing 12 different specialists who do not communicate about my care, or even understand SLE. At least I see some glimmer of hope in articles like this. Please keep it up.

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