Medicaid is a joint program funded by both the US federal government and several states; he provides medical care for low-income Americans. Thanks to this powerful program, as well as over a million young people aged 21 and younger, both critical medical services and long-term care are available to approximately 52 million Americans (about 1 out of 7 US citizens). More than 20% of the population of disabled youth receive Medicaid, including 7 out of 10 low-income children with disabilities.
These disorders have a wide range, including both physical conditions, such as cerebral palsy or congenital blindness, and mental states, such as dyslexia or autistic spectrum disorders. The main channel for reaching disabled children with additional income for safety (SSI & nbsp; disability), in the first place, is children with primary mental disabilities, such as disability or emotional distress.
Because Medicaid is faked between federal and state governments, both have an opinion about how this works. The federal government establishes basic eligibility requirements and broad recommendations on benefits, but each state determines exactly what ranges of income can be qualified in their territory and what services they will offer. However, in order to support children's health, the federal government is much more strict about child benefits, forcing states to accept children with much higher income levels than most of them prefer to accept adults, and to offer them much wider coverage and a better quality of services, than for adults.
The first and most important service provided by the federal government for children with disabilities is called early and periodic screening, diagnosis, and treatment (EPSDT). This benefit begins at birth and is responsible for paying for all hearings, vision, dental, mental / emotional and physical exams that your child receives for free from your school and medical provider, and also pays for immunization. If a child has a genuine medical problem and has a low income, a part of the program kicks to pay for any form of standardized treatment that the state provides to them.
... and the introduction of "Aging"
All this is absolutely amazing ... until the child is 19 years old (21 in some states). At a time when a person with a disability is no longer a teenager, they suddenly find themselves absolutely ineffective in terms of Medicaid benefits if they cannot qualify for one of the disability programs. Even those who really claim to be an adult-oriented Medicaid program often find that their new program (no longer complying with federal rules for children) is substantially lacking in support compared to their old one.
This sudden decline in support and benefits is known as “Aging,” and this is the most difficult problem that many American parents of disabled children will struggle with during their child’s transition to adulthood. Over the next few messages, we will examine the effects of aging from the EPSDT and into the normal state. Medicaid, and offer some of our best tips on how to deal with the transition if you are a parent with a disabled child.
