Special Education

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Special Education is a broad field of discussion depending upon your child's needs. Each child is different and therefore, so are their requirements.

Some children have emotional problems, some physical, some mental development, while others may have a combination. You know your child best, which means you should take an active role in your childs progress. While experts in the field of special education are made available to you, know that it is you who must be their advocate. If you feel a method of teaching or tools being used are not helpful to your child, let your opinion be known. Sharing your knowledge of your childs likes, dislikes, fears, needs, and all the information you can with your child's teachers will often make their tasks easier and your child's development faster and more successful.

This Website For Guidance

Our website is not the know all, tell all website. No website or book is. We are here only to provide free information and suggestions. A guide for those who are seeking answers and solutions that may not be available from other sources. If we can assist just one child or parent, we are pleased to do so.

Our Recommendation

Parents of children with special needs should visit a lawyer and set up a Special Needs Trust. A special needs trust is set up allow use of property for the beneficiary without losing access to essential government services and benefits. As it stands now a person who is disabled cannot inherit more than $2,000- it will interrupt his or her government benefits. Especially important are long-term care and nursing home benefits under the Medicaid welfare program.

Government benefit programs are now recognizing that family contributions can only improve a disabled person's life. As long as the family's contributions are supplementary and do not duplicate government benefit programs, they are allowed. Some current government benefit programs do let the family to provide some supplementary income and resources to the person with a disability. However, government regulations are very strict, and they are carefully monitored for abuse.

Special Needs Trusts are frequently used as a way to receive an inheritance or personal injury settlement proceeds on behalf of a disabled person in order to allow the person to qualify for Medicaid benefits.

A special needs trust can be used to buy such things as:

* Uninsured medical and dental expenses, eyeglasses

* Maintenance of vehicles

* Insurance (including payment of premiums)

* Transportation (including buying a vehicle )

* Athletic training, gym membership or competitions

* Personal care attendant or escort

* Rehabilitation

* Essential dietary needs

* Materials for a hobby or recreation activity

* A computer or other electronic equipment

* Trips, vacations, concerts, or outings

* Things that add to quality to life: movies, video games, books, crafts , etc.

It is strongly advised if you are a parent of a special needs child that you speak with an attorney regarding the set up of a special needs trust.

For more free articles on a variety of subjects that deal with the needs of Special Education children, please click the blue "Free Articles" banner near the top of our website, or CLICK HERE.

A Quick Note From The Publisher... If you like the article above, you may be interested in the following article which is also related to Special Education... Your Special Needs Child--Coping After Receiving a Diagnosis As the parent of seven children, three with developmental delays, I have experienced both the heartache, and frustration as well as the joyful rewards that accompany any parent’s journey in helping their child succeed under trying circumstances. That gray, icy March day, over eight year’s ago, that my oldest son was diagnosed with Global Developmental Delays, possible Autism, still sits like a dark shadow on the corner of my heart. My husband and I certainly were not expecting such a harsh diagnosis. Our sweet 2-year old son was simply not talking, we just wanted to know how we could get help from a Speech Language Pathologist, not an entire team of Neurologists, Phds, Occupational Therapists, Social Workers and Educational Specialists. We knew our son was delayed in speaking, but nothing could have prepared us for the extensive testing they put him through, or the scrutiny we would be placed under as we were interviewed endlessly by social services and others on the review team. It was the beginning of a journey that neither of us anticipated, however, we learned far more than we could’ve imagined we would during the process, and over the course of the past eight years, we are grateful that we have been able to guide other newly-diagnosed families on how to better cope and how not to waste time indulging in too much self-pity along the way. Here are some guidelines that we established for ourselves once we came to terms with our son’s situation. We’ve followed these for two of our other children that were also diagnosed with the same label, Global Developmental Delay, possible Autism. After Receiving the Diagnosis: 1. It's okay to grieve. No parent ever expects a child that is born healthy to face any type of significant developmental delay. ...