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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.
July 2, 2018
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A MyLupusTeam Member

You can write your story on your page. You can add people to your team. If you go to the top where it says meet others and click on it then you can put in your city and it will bring up people in the same city or town. It also shows people in other towns or cities close to you. When you see other people's post hit the arrow down on the post you wrote and you can add that person. That is the way to get to know people more. Just start adding especially in your area.

July 2, 2018
A MyLupusTeam Member

Visit the site as often as you like. Read what people have to say. You can mark the like or hug if you choose, you may also comment on the subject. You can add anyone you choose to your team you might relate to one of their stories, have same interest in common, like their personality etc. I hope this helps a little!.

July 2, 2018
A MyLupusTeam Member

I am new but am learning by just tinkering and stumbling around.

July 2, 2018
A MyLupusTeam Member

I find this site to be very helpful. I'm 70 and have Lupus, I've had Fibro for over 30yrs and 2yrs ago I got Lupus. I have to tell you if you talk to any 2 people with Lupus I believe they won't have the same reaction. The one thing we all have in common when we have a flare we have a lot of pain and extreme exhaustion. But for me I get a lot of support when I can share what kind of day I'm having and I hope that I'll be there for someone else to help them

July 2, 2018
A MyLupusTeam Member

I just jumped in and blundered my way around.

July 7, 2018

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A MyLupusTeam Member asked a question 💭
California, CA