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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.
A MyLupusTeam Member asked a question 💭
Mooresville, NC
8 hours ago
 · 
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A MyLupusTeam Member

Ive alwats seen mine every 3 to for i changed rheumatologist this time last when i had ti go 9!monthi was in a flair they didnt my Dr was on maturnity & no one took her place so i was going every 3 ti 4 months with nowim going out 6 month, she one of the doctors i was going to call today because of the way i feel i never call in even whrn i go into a flair , ill call her monday

7 hours ago
A MyLupusTeam Member

Used to be every 2 months, but as my symptoms have calmed down we've cut back to every 6 months. She's always available via her practice's online portal if I get sick or have increasing pain.

7 hours ago
A MyLupusTeam Member

Ive had SLE since I was 10 years old and no one knew what was going on. I would never wish the disease on anyone else but this is not a disease you play around with. It's been challenging but I get through. It can be a painful disease when joints, and other areas become involved. Find an accredited reumstologist and see him/her every 3 months or sooner when things are active. Find a physician to follow you religiously.

8 hours ago
A MyLupusTeam Member

I see mine every 3-4 months. If I am in a major flare or having other issues.

8 hours ago
A MyLupusTeam Member

Because my husband has lupus nephritis and is on heavy medication, he sees his every 6 weeks to monitor labs (as well as his nephrologist) and make adjustments. But his doc also has a great portal and replies within 24-48hrs of msgs, so he gets a lot done by just shooting a msg (dose change, inquiry, referral)

2 hours ago

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