Do you feel unfairly judged for using government assistance?

Hello everyone,

How are you doing?

In the US, chronic illness patients often rely on government programs like Medicaid, Medicare, or Social Security Disability Insurance (SSDI) to manage healthcare costs and daily living expenses. For many, these programs are essential in covering medical treatments, medications, and sometimes even housing. But there can be a strong stigma attached to using these forms of government assistance, with the perception that relying on such support is a “handout.” 😔

In a country where self-reliance is often praised, there are so many misconceptions about who deserves aid. Media and political rhetoric can sometimes paint those using government assistance in a negative light, contributing to feelings of judgment or even guilt for needing help. Many people with chronic illnesses already face barriers in accessing proper care, and being unfairly labeled as “taking advantage” of the system adds emotional and mental stress.

Have you faced judgment for using programs like Medicaid, SSDI, or food assistance? How do you respond to or cope with this stigma? Are there people in your life who understand the necessity of these programs, or do you feel the need to justify your reliance on them?

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We’d love to hear your experiences and strategies for dealing with these societal judgments. Let’s support one another!

Take care,
Somya from the Carenity Team 🌼