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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 💭
Great Bend, KS

I was diagnosed with lupus back in 2017 and had a rheumatologist because I was on Medicaid or Medicare or whatever you call it and I lost it after I turned 18 and was out of school. Then I became pregnant and so I had it again and I did see a rheumatologist while I was pregnant, but I did not like them. They did not hear me out. I feel like so. I did stop going. I moved to a different town and was getting my life back on track after having two kids. I have finally seen a doctor for my… read more

April 9
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A MyLupusTeam Member

You can go to a free clinic. There's a lot of health clinic that has services for ppl with no insurance. Or you can go to you Department of Social Services and apply for medical, you should qualify.

April 9
A MyLupusTeam Member

Consider writing a letter to the rheumatology department at the nearest university affiliated hospital. Tell them your situation and a copy of your records or write an overview of your health history. Perhaps a rheumatologist would be willing to see you pro bono on a limited basis. It wouldn't hurt to try.

Here's some resources from the Lupus Foundation as well.

https://www.lupus.org/resources/financial-assis...

April 9
MyLupusTeam

How can you access rheumatologist care without insurance for lupus treatment?

Accessing rheumatologist care without insurance can be challenging, but there are resources available to help. The Lupus Foundation of America provides information about assistance programs that can help with healthcare-related costs, including Show Full Answer

How can you access rheumatologist care without insurance for lupus treatment?

Accessing rheumatologist care without insurance can be challenging, but there are resources available to help. The Lupus Foundation of America provides information about assistance programs that can help with healthcare-related costs, including medical care and equipment.

Here are some options to explore:

* Contact the Lupus Foundation of America for their list of resources specifically designed to help with healthcare costs when you don't have insurance
* Look into patient assistance programs (PAPs) offered by drug manufacturers, which provide free or discounted medications to people without insurance
* Talk to your local hospitals about financial aid programs - many offer assistance to cover some or all of medical bills for those who qualify
* Ask about sliding scale fees at community health centers, which adjust costs based on your income

Your primary care provider may also know about local resources and programs available in your area. Don't hesitate to reach out and explain your situation - healthcare providers often have information about assistance programs that aren't widely advertised.

Financial concerns shouldn't prevent you from getting the lupus care you need. Taking the time to research these options can help you access treatment while managing costs.

April 9

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A MyLupusTeam Member asked a question 💭
Bryant, AR