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Michigan • Rare/Genetic
People with Cystic Fibrosis in Michigan may qualify for federal and state disability benefits, including SSDI, SSI, Medicaid, and State Disability Assistance. This guide explains eligibility, how to apply, and what support is available.
To qualify for federal disability benefits like SSDI or SSI, you must have a medical condition that prevents you from doing Substantial Gainful Activity (SGA). For 2025, the SGA limit is $1,620 per month for most people, or $2,700 if you are blind. Cystic Fibrosis is listed in the Social Security Blue Book under respiratory disorders, so if your symptoms match the listing, you may qualify. You must also meet work and income requirements for SSDI or SSI.
Both programs require regular medical reviews to keep benefits.
Source: SSA Disability Work, 2025
In Michigan, adults with Cystic Fibrosis may qualify for State Disability Assistance (SDA) if they meet medical and financial criteria. SDA is for adults who cannot work due to disability and have limited income and resources. You must be a U.S. citizen or qualified immigrant and live in Michigan. SDA is not available if you receive cash assistance from another state.
Michigan also offers Medicaid waivers for home and community-based services, which can help with care needs related to Cystic Fibrosis. These waivers may cover therapies, home care, and other supports.
Source: Michigan.gov SDA, 2025
Source: SSA Disability Work, 2025
Source: Michigan.gov SDA, 2025
Michigan offers ABLE accounts, which let people with disabilities save money without losing SSI or Medicaid benefits. You can use ABLE funds for housing, education, transportation, and other disability-related expenses. To open an account, you must have a qualifying disability that started before age 26.
Source: Michigan.gov Disability Resources, 2025
Source: SSA Disability Work, 2025
Source: Michigan.gov SDA, 2025
You must report changes in income, work, or health to avoid overpayments. If you get too much, you may have to pay it back. Report changes online, by phone, or in person. Keep records of all reports.
Contact a Michigan Benefit-to-Work Coach for free help with applications and work incentives.
Yes, if your Cystic Fibrosis meets SSA criteria and you have enough work credits. The SSA Blue Book lists Cystic Fibrosis under respiratory disorders. You must also meet the income and work limits.
The SGA limit for 2025 is $1,620 per month for most people, or $2,700 if you are blind. If you earn more, you may not qualify for SSDI or SSI.
You can apply for SDA at your local MDHHS office or online. You must meet medical and financial criteria and be a Michigan resident.
Yes, work incentives let you earn some income without losing benefits. The SGA limit is $1,620/month in 2025. Report all work to SSA.
An ABLE account lets people with disabilities save money without losing SSI or Medicaid. You can open one in Michigan if your disability started before age 26.
Yes, you must report changes to avoid overpayments. Report changes online, by phone, or in person. Keep records of all reports.
Michigan offers Medicaid waivers for home and community-based services. These can cover therapies, home care, and other supports for people with Cystic Fibrosis.
Disclaimer: This guide is for informational purposes only. Always check with official agencies for the most current rules and eligibility.
Children with Cystic Fibrosis may qualify for SSI or SSDI if they meet SSA criteria. Benefits may continue into adulthood if the disability persists.
If denied, you can appeal within 60 days. An attorney or advocate can help with the appeal process.
SSA reviews your case regularly to make sure you still qualify. Report any changes in your health or income promptly.
