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How are you navigating the financial strain of Friedreich’s ataxia?
Even with my husband and me both having health insurance, we feel like something always comes up where there are extra costs involved when it comes to medical-related needs.
For example, my scooter was not covered by insurance, or making adaptations in my home to make it more accessible was not covered by insurance either.
How are you navigating the financial strain of FA? Do you feel that you have access to the care that you need?
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