This is the Story Of Daniel

This page is a work in progress to be completed eventually ...

Daniel was Born June 13, 1993 ~

Vaccine Injured on October 1993  left him autistic but unknown to me at the time. He seemed to recover from the high fever  and almost comatose state, except looking back i know there were changes.

Diagnosed March 1996 ~ Gloom and doom diagnosis from a Dr. that said he would never do anything but sit in a corner staring into nothingness, he would never be toilet trained, he would never communicate, he should be institutionalized so i could get on with my life. The Dr. was wrong. Today Daniel is toilet trained, he communicates thru sign language and PECs, he is learning to read and type, he smiles alot and finds pleasure in many things. Daniel's life is not normal in any sense of the word but he brings happiness to those he touches.

Began School September 1996 ~ Back then I trusted people to do what was right and according to law. It didnt take long to learn that school districts couldnt be trusted and felt they were above the law. Daniels first school experience was nothing short of tortuous. He cried for weeks before they informed me how unhappy he was, they tried to force feed him foods that he didnt want. It was horrible.

The Battle of the Schools Begins ~ Finding the internet I learned some things that might help Daniel. ABA particularly. When i suggested this to the school special education teacher he stated, yes that might help Daniel but the school wont pay for it. Schools are required by IDEA to do what is appropriate, ABA is the appropriate methodology for children with autism. This was to become the first of many battles with the schools to provide what was promised by law.

Move to New School District to Avoid the Closet  ~ The school built a small room not bigger than a large closet to teach Daniel in. It was in the basement far removed from his normal classmates. The smells of the kitchen permeated this room.  He would grab the door frame to keep from going into this room. It was horriffic to watch. Office of Civil Rights said it was big enough. Our family decided to move so that Daniel wouldnt have to endure this room.

School District Denial of FAPE ~ We moved to a neighboring town, being promised wonderful things by a special education teacher who said she would give Daniel what he needed. Several months later it was apparent how false her promises were. He basically rode a tricycle around the gym all day. He was given none of the instruction promised on his IEP. This was the first of many Due Process Hearings I had to endure to provide Daniel appropriate education.

2 Years of Progress and Bliss ~ Things went fairly well for 2 years after the judge ordered the school to do what was appropriate. Daniel made excellent progress, he learned things many they had said previously that he couldnt. He proved them wrong.Amazing what appropriate education can do to a child with autism.  School was a great place for him to be, he loved going there, being with the kids. He learned to communicate.

Changes Bring Low Expectation Teacher from Hell ~ A new special education teacher  brought unwanted changes. I knew from the first day i met her that it was going to be bad. She had such low expectations and preconceived notions that i knew it was going to be awful, and it was. Daniel no longer made progress, he no longer wanted to go to school. He was unhappy. This person (and i wont give her the title of teacher, she doesnt deserve that title)  blamed Daniel for her inability to teach. She blamed Daniel for her ineptitude.

Change Schools Hoping for a Miracle ~ After 2 years of no progress and this person's continued lazyness and ineptitude it was suggested that I bus Daniel 50 miles away to an autism classroom. I met the teacher and all seemed idealic.It appeared to be good.  He went there and was happy again. He made friends, he was learning, he got to swim every day. This was in the spring of 2005. All seemed right in the world again.

No such thing as Miracles ~ Something changed at the beginning of the 2005 school year (September). Still don't know what happened. Daniel no longer wanted to go to school. He wasnt happy at school. It was reported he screamed alot. I am not sure if this is true or if they just didnt like my asking questions about the rights they were violating. I personally believe they were trying to intimidate me into accepting less than the law provided, accepting what they were willing to provide. And Daniel deserved to not have his rights violated. They forced me to medicate him. To put him on drugs to make him more manageable. I did comply and felt horrible. It also began my renewed research into the treatments of autism and for that I am grateful. I learned a great deal in the month of October. I learned there was hope for a cure.

Coming Home ~ On October 20, 2005 The school district kicked him out of school.In addition to this being a violation of our rights, it   hurt more so because things had gone so well in the spring, but it   also came as a blessing in disquise. Daniel was now back in his old school, with the kids he grew up with. A few miles away instead of an hour away.  And with a new teacher that expected great things and is willing to work with me to provide Daniel what is appropriate.


New advances in the Treatment Of Autism  ~ The medication of Daniel, forcing him to be drugged, which he has since stopped taking, forced me to find new alternatives. I hated putting him on drugs, it was against my better judgement, but I didnt have a choice, it was drug him or he was out of this school. In the past his behaviors were controlled with behavior modification, not drugs. The drug was horrible, it gave him night mares, it made his skin cold and clammy. He looked drugged most the day. The drug was clonidine. Never again.  I started him on some supplements that have already shown benefit in his focus and ability to attend. He is calmer. He said mom (actually ma) for the first time in 9 years. I want so much to give him all the supplements and RX supplements (MB12 and Nystatin, and DMSA)  that are recommmended by DAN ! Drs. for the treatment of autism but they are expensive, so barring some donations it will be slow going, but eventually I hope  he will have all that is needed. I do feel he needs it now, while he still has a chance, and it is painful knowing I can't provide the things he needs.

11/21/05 ~ Daniel has been in his new program I designed for 2 weeks. He is enjoying going to school. . The teachers that have known him all say what a change they see in him .  They dont know  that this change is due to biomedical intervention. And its just the beginning. I see great things happening in Daniel's life with just a little help there can be hope.

2006 - The New Year looks to be  another one full of difficulty ....

When Daniel was kicked out of the out of district school in October and forced to return to this school district the bleakness of it turned to a blessing in that I was able to design his educational program and his learning atmosphere. It did seem like for the first time in a long time that Daniel would have appropriate education.

However the person they hired to assist him throughout his day was not qualified. Daniel had 2 wonderful paraprofessionals in this school previously- paraprofessional is the title of his educational assistant - and I had hoped the District would rettain one of these ladies to be Daniel's paraprofessional, but the District had other ideas (influenced by school political motivations and personal friendships with this person by the sped teacher) and hired someone with no experience at all.

I stated repeatedly this person wasn’t qualified and would never be qualified (my opinion after spending many days attempting to train this person) but they were determined to keep her. So I had to remove Daniel from school on December 16. Being in school with this person as his para was creating situations and behaviors that were making him regress and will be detrimental to Daniels future educational progress, as well as preventing him from learning. This person was incapable of implementing the program yet the District was adamant in keeping her, so I had to request a Due Process Hearing to force them to provide someone qualified.

Since then we had a resolution meeting - a new requirement of IDEA '04 - to try and resolve the issues but afteer being screamed at repeatedly by the special education teacher we were unable to resolve anything. They are determined to keep her, to try and cover their butt's for the violations of rights and Denial of FAPE that has occurred (its actually a very long and complicated story), they are determined to keep this unqualified person and they seem to think they wont be accountable for their actions. So we have to go to hearing on February 7th 2006 and until the Judge makes a decision it is looking like Daniel wont be in school at all ...which is taking its emotional toll on me for having to prepare for this hearing - I can't afford an attorney so its up to me to protect his rights - and the anguish of knowing he needs to be in school is extremely upsetting as well.

What makes it even more upsetting is that for probably the first time in his life Daniel's mind is out of the fog he has been in and he is very receptive to learning. BIOMED intervention has created new opportunities to reach him that are exciting and miraculous and yet he can't even have access to his birthright appropriate education because of this School Districts actions .....

Sure, I am capable of teaching him, but I do not have the resources the school has, nor does he have the contact of peers. And its a proven fact he learns better with a qualified paraprofessional than he does with mom.

So once again I am faced with a legal battle to fight for my son's life... forced to fight a system in a court of law against a qualified attorney, with the most complicated laws of this country. How fair is that ? I know I can do it, I have had to before and won, but I shouldn’t have to....

If this school would JUST do what is right, if ALL schools would just do what is right, without their little games and power trips, parents such as myself wouldn’t face this so overwhelming seemingly insurmountable task , a simple obligation a school has (that most take for granted) of providing education to a child.

So fight I must, time and energy wasted just to provide for my son what the law says he will have and the school has to be forced to provide…

On a brighter note Daniel was laying in his bed the other day and I went in and he said "Bye Mom"...... 2 simple words. Usually he would just wave bye bye, meaning “leave me alone mom” but now he has found his voice... thanks no doubt to biomedical intervention, and told me in typical preteen fashion to leave him alone....


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