I need a little help and some of you may now where I can find this information.
Now that our adoption is complete, I feel the strong desire - along with my husband - to make some changes in CPS's system. I know its a long road but it needs to be done and SOMEONE has got to do it.
Even our Attorney Ad Litem thought this was ridiculous! She couldn't believe that the subsidy paperwork stated "Not based on Race,Religion,Age,etc" but then the qualifications were as follows. She did say before the adoption that she would be in support of this and would help in whatever way she could. Just currently I need a starting point!
We would like to start with the qualifications for continueing Subsidy post adoption. Currently a child only qualifys if they are:
- Severely handicapped (most states mean that the child must not be able to move on their own, must have at least some form of minimal lifesupport)
- Be part of a Sibling Group
-If they are a minority they must be at least 2yrs of age.
- If they are white they must be at least 6yrs of age.
To us - ALL of the children in CPS's custody have been abused and/or neglected in one way or another. They have ALL experienced the trauma of seperation from the life and family they knew. They ALL have medical futures that are shady (I think the latest statistic I could come up with was 88% of them recieved poor prenatal healthcare as well as poor healthcare postnatally). It is our feeling and belief that medicaid should be something open to ALL these children. Not just the minorities, not just the siblings, not just the disabled. These children are ALL at risk and can have lingering health issues.
Our daughter for instance is a 4.5yr old white child. She had OT 2 times a week for sensory processing disorder. This WAS covered by her insurance but since we adopted and they dont consider this a disabling condition we didn't keep medicaid as a back up. We have great insurance however they do not cover her therapy. We had to stop therapy as it would cost us a minimum of $600 a month.
She also has sleep apnea. Its chronic and non-obstructive. But its not enough.
Both her parents have severe mental handicaps. Her birth father is bipolar, severe ADHD and Schizophrenic. He was institutionalized most of his life.
We are having to get genetic testing for DD due to finding out her siblings both tested positive for MSUD. Which means their bodies do not process certain amino acids in protein and can cause grand mal seizures, mental retardation,developmental delays.
None of this means a thing to CPS. All that mattered to her was the color of her skin.
We would like to fight to get ALL the children in child services equal rights. ALL of these children (no matter their skin color,age,disabilities going in) deserve to have health care. Obviously - those that have actual disabilities should be getting their continued stipends and such. Im not against that at all). ALL these children' may not need the extra money (we dont need the money we actually make a decent living), but ALL should have the health care available to them.
Where and who can I talk to in order to get changes done? I dont even know where to begin.
***Disclaimer - please dont think this is about race. Its not - CPS has made it that way but like I said - All these children have had bad starts to their lives - they deserve to have the care needed to bring them around to healthy, happy, well adjusted and loved children!***
Now that our adoption is complete, I feel the strong desire - along with my husband - to make some changes in CPS's system. I know its a long road but it needs to be done and SOMEONE has got to do it.
Even our Attorney Ad Litem thought this was ridiculous! She couldn't believe that the subsidy paperwork stated "Not based on Race,Religion,Age,etc" but then the qualifications were as follows. She did say before the adoption that she would be in support of this and would help in whatever way she could. Just currently I need a starting point!
We would like to start with the qualifications for continueing Subsidy post adoption. Currently a child only qualifys if they are:
- Severely handicapped (most states mean that the child must not be able to move on their own, must have at least some form of minimal lifesupport)
- Be part of a Sibling Group
-If they are a minority they must be at least 2yrs of age.
- If they are white they must be at least 6yrs of age.
To us - ALL of the children in CPS's custody have been abused and/or neglected in one way or another. They have ALL experienced the trauma of seperation from the life and family they knew. They ALL have medical futures that are shady (I think the latest statistic I could come up with was 88% of them recieved poor prenatal healthcare as well as poor healthcare postnatally). It is our feeling and belief that medicaid should be something open to ALL these children. Not just the minorities, not just the siblings, not just the disabled. These children are ALL at risk and can have lingering health issues.
Our daughter for instance is a 4.5yr old white child. She had OT 2 times a week for sensory processing disorder. This WAS covered by her insurance but since we adopted and they dont consider this a disabling condition we didn't keep medicaid as a back up. We have great insurance however they do not cover her therapy. We had to stop therapy as it would cost us a minimum of $600 a month.
She also has sleep apnea. Its chronic and non-obstructive. But its not enough.
Both her parents have severe mental handicaps. Her birth father is bipolar, severe ADHD and Schizophrenic. He was institutionalized most of his life.
We are having to get genetic testing for DD due to finding out her siblings both tested positive for MSUD. Which means their bodies do not process certain amino acids in protein and can cause grand mal seizures, mental retardation,developmental delays.
None of this means a thing to CPS. All that mattered to her was the color of her skin.
We would like to fight to get ALL the children in child services equal rights. ALL of these children (no matter their skin color,age,disabilities going in) deserve to have health care. Obviously - those that have actual disabilities should be getting their continued stipends and such. Im not against that at all). ALL these children' may not need the extra money (we dont need the money we actually make a decent living), but ALL should have the health care available to them.
Where and who can I talk to in order to get changes done? I dont even know where to begin.
***Disclaimer - please dont think this is about race. Its not - CPS has made it that way but like I said - All these children have had bad starts to their lives - they deserve to have the care needed to bring them around to healthy, happy, well adjusted and loved children!***












Also, the subsidy rates in Maine have recently been chopped, but only for those with the highest needs kids-
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