Showing posts with label SSI. Show all posts
Showing posts with label SSI. Show all posts

Tuesday, June 4, 2019

Four Ways to Qualify For Medicaid


I routinely get calls about families with children with autism and other disabilities needing more therapy or to see specialists that their insurance doesn’t cover.  It could be speech therapy, occupational therapy, ABA, etc. 

At some point the conversation works its way around to if their child had Medicaid it might help with some of the things the child needs that the family cannot afford above and beyond insurance.  Many families are surprised to learn there is more than one way to qualify for Medicaid.  You have four ways you might be able to qualify for Medicaid if you have a child with a disability that I know about.

The first way is to apply for Medicaid.  This sounds strange but many times parents are told by friends and professionals that they will not qualify when they do.  Medicaid takes strange things into account when you apply.  For instance they take into consideration all those medical bill you are paying out of pocket right now.  My experience with parents and Medicaid workers is the Medicaid worker will try to ask you about things you might not of thought about or might not know about as best they can if you explain your situation. 

The second way is what in our state is called the Family Opportunity Act.  It might be called something different in other states.  Louisiana has a program at the Medicaid office for families to be able to ‘buy in’ to Medicaid if they have a child with a disability.  There are other qualifications too.  If the person who answers the phone does not know about this specific program ask for a supervisor as this is a small program.  From what I understand from other parents the fee is very nominal especially compared to what they are or could be paying out of pocket. 

The third way to get Medicaid is if your child can get SSI.  In our state and some other states part of getting SSI is also getting the Medicaid card.  Parents are told from the beginning that income is a consideration and it is, but they should apply anyway.  The child also has to have a severe enough disability. Think about it like this.  If a child qualifies for even $5.00 of SSI they get a Medicaid card.  The cash assistance may not be encouraging to you but the Medicaid may be a big help.

The final way I know of to get a Medicaid card is though the state’s Community and Family Support Services.  These services are at your area Human Service Authority if you are in Louisiana.  If you are in another state ask at your state’s Office or Department of MR/DD.   If your child’s disability is severe enough your child could qualify for what is commonly called a Waiver.  One of the services you get as part of the Waiver is a Medicaid card.  The important part here is that if your child qualifies for the Waiver it is regardless of your income. 

I am sure there are other ways to qualify for a Medicaid card.  These are just the ones I know about for a child with a disability.  Some of these include adults with disabilities.  You have to ask though.  Do you know any other ways to qualify for Medicaid? 

Wednesday, October 31, 2012

Complications of Aspergers

So I sort of alluded to the fact that I'm having problems with the second daughter, the one that has Aspergers.  I hate talking about her but as I believe I said this is my life too.  I'm at a loss as to what to do to help her other than go meet her and lead her through the things I want her to do.  Maybe this is part of parenting a child with ASD and I don't know it. 

She is having problems with budgeting.  I know alot of young men and women do have problems.  I also know it can be done - even on her small social security check (SSI).  I know this becaus it is done and done well with my oldest daughter's check by the provider agency.  My oldest daughter has what she needs and quite a few of the things she wants. 

The second daughter as close as I can figure out has a couple of problems.  I'm not sure if it has to do with the Aspergers or not.   The first thing is that she has difficulty planning for the entire month with one check.  She has difficulty anticipating her needs for a month. 

The second thing is she is busy taking care of other people, including her boyfriend, and gives/loans her money.  She loans money to the boyfriend's family and then doesn't get paid back.  Therefore her bills don't always get paid. 

Once again the only thing I can figure out to make it work is to take the day off from my job and go meet her to help her get things paid.  Of course that means I miss work.  And then there is the figuring out how to do this without making her so angry she doesn't cooperate.  I wonder if things are supposed to be this way?  Anyway that is my plan to go to her and make sure the important things get paid.  Then make sure she has food.  

Did I mention that it came out sometime during the past month that she had been going through the trash for food and picking up shorties for the boyfriend?  It just sort of popped out of her mouth at different times in the past month.  Do you see why I'm so conflicted? 

At the same time that I can see that she needs to be able to make her own choices and her own mistakes....  Is this one of the things meant by Independent Living Skills?   What do you think?  No one ever answers these questions but I keep asking? 

Saturday, July 2, 2011

Aspergers and Confabulation

She does not lie and she is not lazy.

I went to the psychiatrist for my second daughter's SSI. It brought up all that anger from all those people, usually teachers, over the years who used to tell me she lied or she was lazy.

I have watched this child with Aspergers and now adult with Aspergers. She works ten times harder than any of my children to produce less than half as much work. I have watched it. I flat refused to let teachers or anyone else say any of those things.

Lying is a deliberate decision to tell something that is not true. She believes what she says. The psychiatrist today said what she does is a 'confabulation'. She believes it but it is not real or not really what happened.

I need to remember that word. I asked if I would get a copy. The psychiatrist said he did not think so because the federal government 'owns' it. Hmm I wonder how I can work on that.

Wednesday, February 2, 2011

SSI Check Amounts

My daughter tells me her boyfriend is supposed to get a check of $1000.00 to $2000.00 from social security. We were discussing it a little. She knows it is because he has seizures but isn't exactly sure of anything else.

I mentioned that the SSI checks in Louisiana, at least, were around $670.00. We also talked about whether he could be drawing on his dad for any reason. My daughter told me his dad had also had bad seizures.

It will be interesting to see how the change in finances in that family affects the way they live. Well and how they treat my daughter, especially when or if she returns from the hospital.

Monday, December 20, 2010

Aspergers On The Move

My second daughter, the one with Aspergers, tells me she is moving to Arizona or Minnesota with the boyfriend and his family. The boyfriend she just moved in with by the way. I'm not sure how to feel about that.

It's not the moving to a different place part. My second son already lives in Baton Rouge. Although this is another state. It's more about the fact she has Aspergers. She, not unlike others her age, believes everything anybody else tells her.

She just misses the social cues that could tell her different. There have been so many things that were supposed to happen with this family that have fallen through. I'm not sure if this is real.

The other thing is that we just got her Social Security started. I know she could get it in another state but those in between times can ge rough. I guess I also feel an argument coming because she will want me to give her the entire check at the beginning of the month to go. And I'm not. Am I wrong?

Thursday, December 2, 2010

First SSI Check

The first is the first SSI check my daughter is getting. She is also 18 on the first. At least right now the check comes in my name. My daughter is not happy about this. This is the second daughter, the one who has Aspergers. I'm trying to get her to understand she has to pay bills like rent. First. It's gonna be rough. Help. How has anyone else handled this?

Thursday, August 5, 2010

Social Security

I'm up in the night a bit nervous. I am going to start the process tomorrow to apply for the daughter with Aspergers social security (SSI). I suppose I am a bit sad too. Didn't want to need to do this. It will be a good safety net for her. Did I mention I hate forms? Really.

Saturday, February 27, 2010

Next Steps To Getting SSI

Well I guess if I am going to get SSI for Rose I need to do some things first. It has been awhile since she had an evaluation at school. I called last week for the second time. I got to speak to someone this time. They said they would send me the paperwork to sign.

I wanted to try to get what is called Mental Health Rehabilitation Services (MHRS). I tried to call and they told me no because one of her diagnoses is Aspergers. I need to investigate that.

I am still upset. I did not want to do this with this child. I am just putting one foot in front of another right now.

Tuesday, February 23, 2010

My Daughter With Aspergers...

I don’t very often write about this daughter. She is so different than the daughter with Autism She seems to understand and does understand a lot. She also doesn’t understand a lot.

We recently went to a doctor’s appointment. Rose turned 17 years old a couple of months ago. One of the questions I had for the doctor was about how we would be able to get and afford the medication she was on when we lost Medicaid.

I should say we have a really good doctor for my children. He has seen the last three more than the first two children and I trust him. We have gone to him for twelve or thirteen years now.

Anyway the answers to affording the medication were pretty good. Some of the medication could be gotten as generic for $4.00. (Has anyone not heard about this?)
Some were already inexpensive. Only one would be the problem and since the doctor had some kind of welcome at the local charity hospital we figured we might be able to use the drug program there. All good answers.

The I wanted to talk to the doctor with out Rose and he wanted to talk to me. Well the crux of the conversation was the same for both of us. Essentially—“And now what?”

What he said really hit me in the gut. He suggested we go apply for SSI. Oh my goodness. One of the therapists we saw when she was ten or eleven had said the same thing. I guess I never did it because I kept hoping I would not have to.

With my older daughter is was plain early I would need help. I just kept hoping with this one. I will post another time about what I have put in motion. I have just lost my breath over this.

Does anyone have a similar story? Please comment and let me know.