Before I go into any details I want to let everybody know that we are VERY lucky in that Brycen qualified for waiver services and Medicaid insurance shortly after he received his official dx from U of I! Shortly after Brycen qualified for the Intellectual Disabilities Waiver which includes the Medicaid, respite and SCL services, this waiver was full and now others are on a waiting list. The other three waivers that are available depending on the child's dx are also on waiting lists which is not fair to those parents that are battling to get insurance to cover necessary appointments, testing, and therapies. One 1/2 hr speech appt is billed at $77! Can you imagine trying to afford to pay for those appts out of your pocket...much less usually 4-5 appts a week are needed?!
So how our insurance works is that every dr appt and therapy appt are run through our private insurance (Blue Cross Blue Shield) first and then Medicaid will pick up the amount that is left. We were initially told by the therapist and a doctor at U of I that BCBS would not cover any of his therapies, which is what made getting Medicaid so important to us. With Autism, studies have shown the earlier a child receives consistent intervention, the decrease in services they will need later in life and during school. Why the heck would insurances NOT cover this then? This has been a hot subject in various state's governments lately.
Anyway, surprisingly to us...Brycen's speech for May WAS COVERED by BCBS! I'm not sure of all the details, but my understanding is that prior authorization is needed and since Brycen's doctor gave an order for the therapy and because his records and treatment plan demonstrate that he is not talking and far behind other children his age, this was the reason it is covered. The extent of coverage is not known at this time, but we are guessing about 20 appts each calendar year which we know Brycen will have burned through in two months, but Medicaid will pick up the rest of the speech appts which is AWESOME and they currently pay the 10% coinsurance for each of the first 20! The OT is the same way in that they will cover 20 appts each year and since he started later with OT and only goes twice a week, very little will need to be paid by Medicaid for this year.
We are some of the lucky ones and compared to some other states, Iowa is far better with more waiver spots and also other ways of getting Medicaid before a waiver spot if income is low enough. Of course, Iowa is not the best state...but I have been told that moving to MN would really decrease the amount of services we would get and we would be placed back on a waiting list. That is not acceptable as we definitely can't afford to pay out of pocket for the therapies he needs without going far into debt...what hard-working family could? The reason I need to work is to pay just the bills we have now and the groceries and diapers we need now...there is not extra money to pay for that cost, much less I couldn't work more hours to help with that since I would need to be available to take him to all the therapies and appts. I really feel bad for those families that are battling this right now in Iowa, all other states, and across the world that aren't qualifying for insurance that will cover what is needed for their child. As if these parents of children with autism and all other life-long disabilities don't have enough to handle!
"When one door of happiness closes, another opens;
but often we look so long at the closed door that we do not see the one which has opened for us."
Helen Keller
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Autism and Our Family
"Autism"----It's one word that can change the life of a child and family in so many ways. Autism Spectrum Disorders are being diagnosed at a rate of 1 in 68 children currently. If you do not already know someone that has been diagnosed, the statistics say it won't be long before you do.
Our son developed typically until around the time he turned 2 years old. We heard words...we saw him play with other kids...we watched as he played with his toys appropriately...we made eye contact with him...overall we understood his wants and needs. In a matter of a few months, that was all taken away from him. He began lining up toys, lost all of his words and signs except for one word "ball", ignored other kids, could not sleep through the night, lost eye contact and the ability to follow directions, and he had no way of letting us know what he wanted or how he felt. It was heartbreaking to see something happening to our child that we couldn't stop!
Brycen began receiving home therapy 1-2 times per month for about 6 months before we realized it wasn't just developmental delays. We knew it was Autism...we just didn't want to say it outloud to anyone. He was officially diagnosed with Autism (classic form and regressive), as well as Mental Retardation in August 2009 by the University of Iowa Hospitals and Clinics.
We continue to learn as we make our way through this journey with Brycen and we will continue to share this journey with you on this blog! The blog has been a great therapy for us to be able to vent our frustrations and struggles with accepting that we have a child with special needs, while sharing how blessed we are to have a child teach us what life truly means. It has also been a great way to inform others of his progress and changes over the last couple of years.
Thank you for your support of Brycen and our family! We hope you are able to learn something through this blog no matter if you are a parent of a child with special needs or a neurotypical child, a teacher or therapist, a family member, or just someone that is interested in the journey that a family goes on as they learn their child is battling a life-long disorder.
Our son developed typically until around the time he turned 2 years old. We heard words...we saw him play with other kids...we watched as he played with his toys appropriately...we made eye contact with him...overall we understood his wants and needs. In a matter of a few months, that was all taken away from him. He began lining up toys, lost all of his words and signs except for one word "ball", ignored other kids, could not sleep through the night, lost eye contact and the ability to follow directions, and he had no way of letting us know what he wanted or how he felt. It was heartbreaking to see something happening to our child that we couldn't stop!
Brycen began receiving home therapy 1-2 times per month for about 6 months before we realized it wasn't just developmental delays. We knew it was Autism...we just didn't want to say it outloud to anyone. He was officially diagnosed with Autism (classic form and regressive), as well as Mental Retardation in August 2009 by the University of Iowa Hospitals and Clinics.
We continue to learn as we make our way through this journey with Brycen and we will continue to share this journey with you on this blog! The blog has been a great therapy for us to be able to vent our frustrations and struggles with accepting that we have a child with special needs, while sharing how blessed we are to have a child teach us what life truly means. It has also been a great way to inform others of his progress and changes over the last couple of years.
Thank you for your support of Brycen and our family! We hope you are able to learn something through this blog no matter if you are a parent of a child with special needs or a neurotypical child, a teacher or therapist, a family member, or just someone that is interested in the journey that a family goes on as they learn their child is battling a life-long disorder.
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