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what can you do if you have lupus but no insurance and very little money. Are there programs out there to help people like me?

i do go to a local program for employed uninsured people but they seem unequipped to handle lupus as i see very sweet family doctor who has little experience with autoimmune diseases. currently on plaquenil 600 mg but still have the occasional flare.

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You can contact your nearest Lupus Foundation of America chapter to get referral information on certain agencies that may offer financial assistance. The foundation itself does not provide any monetary assistance. You'll also get to know about these agencies from your county's Department of Social Services.

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Try applying for government assistance.

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