Durham, North Carolina
PACC is a parent driven support group that has been developed in collaboration with the ARC of Durham County. PACC is committed to empowering families with children with communication impairments and disabilities. PACC holds monthly parent support meetings that address parents’ individual and collective concerns through open and confidential group discussion. Further, it will provide parents with educational and learning tools that will enhance their understanding of communication impairments and disabilities through guest speakers, videos, books, etc.
A Service of:
North Carolina Central University's
Department of Communication Disorders

Contact Info

Contact Info:
bbpacc2010@gmail.com

Tuesday, May 10, 2011

What is a Learning Disability?

What is a Learning Disability and What Does It Mean?



The links above aim to provide information about what learning disabilities are, including signs and symptoms. The last source is a checklist to see if your child, client, or student is exhibiting signs of a learning disability.




The links above provide information about treatment of learning disabilities including the roles of speech therapist involved with language based learning disabilities.


Information provided by Amanda Carter and Blanca Segovia

Links of Resources Related to Learning Disabilities

The National Center for Learning Disabilities

Organization, which aims to extend services and provide information about learning disabilities. Pictured below is a learning disability check list to see if your child, student, client, or loved one is exhibiting signs of a learning disability:



LDA- Learning Disabilities of America 

Since 1963, this organization aims to help enhance the lives of people living with learning disabilities, their parents, teachers, and other professionals.

ASHA Article: Secondary to Postsecondary Education Transition Planning for Students with Learning Disabilities

American Speech-Language Hearing Association's position on continuing education in regards to learning disabilities.


NSSHLA Article: Improving Communication in Adolescents with Language/Learning Disorders

Information provided about adolescent development including  resources about communication and building relationships, which promotes success within therapy. The article also focuses on service delievery to adolescents and how it differs from service to other populations.  The experience of the speech therapist should exhibit strength working with this population and provides an insight into the role a speech therapist should have in the lives of adolescent children.

GreatSchools: Transition Planning for Students with IEPs

Provides information on Transition Plans, including times, discussions, IEPs, student involvment, documentation and community resources to inform the student and parent of their rights to plan and persue education after high school.


Information posted by Amanda Carter and Blanca Segovia

Autism: Observing and caring for your child

Posted by: La'Toria Elliott and Devin Reynolds

     Raising a child can be a difficult task for parents of any age. Parents and caregivers have to deal with work, their personal lives, and tending to the needs of their child. All of these tasks can quickly overwhelm new parents who are still adjusting and accepting the change in their lifestyle. As the parent watches their child grow, they may often compare the development of their child to other children their age. Sometimes, when a child misses developmental milestones the parent may assume that their child will eventually "catch up", and not be concerned about it. However, if a child consistently misses developmental milestones, careful observations should be made.


     Although parents may feel the word Autism is overused, it has become widespread in our society today. Autism is a developmental disability that usually occurs in an individual by age three. According to Autism Speaks, Autism occurs in one out of every 110 children. Autism can affect a child’s social and communication skills as well as their behavior. It is important to remember there is a wide range of characteristics that may be exhibited by individuals, but vary among each person. Below are some characteristics of an individual that may have Autism that are often overlooked:
  • Avoidance or lack of eye contact
  • Sensory Issues
    • The child may need additional stimulation.
  • Sensitivity issues
    • The child may not tolerate bright lights or loud noises.
A tip for parents who have children with disabilities:
    
     In the worst case scenario if you were to pass away, have you ever wonder if your child’s new caregiver would know how to take care of your child? They may know the basics, but would they know the things that makes your child unique. For instance, your child may only eat certain foods or they may need to be read a book before they can fall asleep at night. We suggest creating a “Care Notebook.” In this notebook, you can include basic tips and ideas for taking care of your child and even unique tips like your child only eats macaroni and cheese with ketchup on it. A care notebook is just a good way to make sure child is taken care of properly and in the same manner you take care of them. It can also be helpful for babysitters and nannies to use as well.



Additional Information

Support Groups for Parents and Siblings of Children who are Autistic


Triangle Parents of Children with HFA, Aspergers, or PDD-NOS
Contact info: http://www.meetup.com/TriangleAspies


Autism Raleigh
Contact Info: http://www.meetup.com/Autism-Raleigh/
Organizer: Amy McCalla


The Wake County Autism Society
Contact Info: http://www.wakecountyautismsociety.org/supportgroups.htm

Eastern North Carolina Autism Network

This organization hosts a number of workshops and also has support groups.
Contact Info: http://enc-autism.org/2010/11/01/smithfield-nc-and-johnston-county/

The Sibling Support Project

The goal of the Sibling Support Project is to increase peer support and education programs for brothers and sisters of children with special health and developmental needs, providing training, demonstration Sibshops and technical assistance to agencies and organizations wishing to add a program for siblings to their existing services. For more information, contact: The Sibling Support Project, Children's Hospital and Medical Center, PO Box 5371, CL-09, Seattle, WA 98105-0371,(206) 368-4911.

Children with Learning Disabilities/Post Secondary Scholarship Information

A list of scholarships specifically for children with disabilities to help aid the transition to college or technical schools:


Who:
What:

National Center for Learning Disabilities
Two $10,000 awards given to high school seniors with an identified learning disability (LD) who are pursuing an undergraduate degree.


Two $1,000 scholarships for students with LD, one of which is designated for a student pursuing an education and/or a math degree. One ADD/ADHD scholarship will also be awarded.

A renewable $750 award available to high school students with physical, learning, cognitive, hearing, or vision disabilities.

Three $6,000 and three $2,000 awards available to high school seniors with LD who demonstrate leadership skills, scholarship, and a high level of service to others; must be a member of Recording for the Blind and Dyslexic (RFB&D).


A $1,000 award for a student with LD and/or ADHD who has demonstrated initiative, talent, and determination resulting in a notable accomplishment in any field - including art, music, science, math, athletics or community service.




Available to students with disabilities with financial needs who enroll in a State University System of Florida institution.




General Scholarship and Financial Aid Information

What
What
A list of scholarship programs available to students that are categorized by topics and special interests.



Allows students to search for scholarships that match their personal profiles and needs.


A list of grants, scholarships, and funding links and resources for students.



A widely used resource on money for college, financial aid, and more.


Federal Student Aid, an office of the U.S. Department of Education, ensures that all eligible individuals can benefit from federally funded financial assistance for education beyond high school


A list of books, web links, and specific scholarships and loans that address financial aid opportunities for students with disabilities.


In the search bar on the right, enter "Financial Aid" for links to scholarships for students with LD.

Information and resources to assist students with the financial aid process.

State funding information for post-secondary education.

Financial aid from the U.S. Department of Education, including information about Pell Grants, Stafford Loans, PLUS loans, and more.




Information posted by Amanda Carter and Blanca Segovia


Autism Spectrum Disorder From the Viewpoints of: Melissa Ross and Erika Ramos

Autism:
Autism is a developmental disorder that appears in the first three years of a child’s life and affects thebrain’s normal development of social and communication skills. Is it a physical condition linked to abnormal biology and chemistry in the brain. The exact causes of these abnormalities remain unknown, but this is a very active area of research.

Signs and Symptoms:
Most parents of autistic children suspect that something is wrong by the time the child is 18 months old and seek help by the time the child is age 2. Some symptoms may present itself as moderate to severe. Children with autism typically have difficulties in:
  • Pretend play
  • Social interactions
  • Verbal and nonverbal communication
Some children with autism appear normal before age 1 or 2 and then suddenly "regress" and lose language or social skills they had previously gained. This is called the regressive type of autism.
People with autism may:
  • Be overly sensitive in sight, hearing, touch, smell, or taste (for example, they may refuse to wear "itchy" clothes and become distressed if they are forced to wear the clothes)
  • Have unusual distress when routines are changed
  • Perform repeated body movements
  • Show unusual attachments to objects
Communication problems may include:
  • Cannot start or maintain a social conversation
  • Communicates with gestures instead of words
  • Develops language slowly or not at all
  • Does not adjust gaze to look at objects that others are looking at
  • Does not refer to self correctly (for example, says "you want water" when the child means "I want water")
  • Does not point to direct others' attention to objects (occurs in the first 14 months of life)
  • Repeats words or memorized passages, such as commercials
  • Uses nonsense rhyming
Social interaction:
  • Does not make friends
  • Does not play interactive games
  • Is withdrawn
  • May not respond to eye contact or smiles, or may avoid eye contact
  • May treat others as if they are objects
  • Prefers to spend time alone, rather than with others
  • Shows a lack of empathy
Response to sensory information:
  • Does not startle at loud noises
  • Has heightened or low senses of sight, hearing, touch, smell, or taste
  • May find normal noises painful and hold hands over ears
  • May withdraw from physical contact because it is overstimulating or overwhelming
  • Rubs surfaces, mouths or licks objects
  • Seems to have a heightened or low response to pain
Play:
  • Doesn't imitate the actions of others
  • Prefers solitary or ritualistic play
  • Shows little pretend or imaginative play
Behaviors:
  • "Acts up" with intense tantrums
  • Gets stuck on a single topic or task (perseveration)
  • Has a short attention span
  • Has very narrow interests
  • Is overactive or very passive
  • Shows aggression to others or self
  • Shows a strong need for sameness
  • Uses repetitive body movements
***Information courtesy of http://www.ncbi.nlm.nih.gov/***
Resources:

Autism Speaks
www.autismspeaks.org/

Autism Support and Advocacy Center
www.ausupportandadvocacy.com/

TEACHH Autism Program – UNC
http://www.teacch.com/
 Autism Society of NC
http://www.autismsociety-nc.org/

 Blog for parents who have children with Autism
The Mariposa School for children with Autism
 
*** Remember early identification is KEY***

Attention Deficit Hyperactive Disorder

Posted by Jonet Artis and Sara Hopson

Attention Deficit Hyperactivity Disorder (ADHD)

Description
Attention-deficit/hyperactivity disorder (ADHD) is described as being levels of “inattention , distractability, and/or hyperactivity and impulsivity that are not developmentally appropriate.” (Glanzman & Blum, 2007) These characteristics can possible cause difficulties for the child to adapt functionally in a variety of locations including home and school. 

Diagnosis
According to the American Psychiatric Association, 3-7% of school-age children are diagnosed with ADHD
(as cited in Salmeron, 2009). Children can be diagnosed as having ADHD at earliest the age of 3 however; generally the diagnosis occurs between the 8 and 9 years old. 60% of children with ADHD continue to have significant symptoms as adults. The American Psychiatric Association state that the diagnosis of a person as having ADHD is based on five criteria. These five criteria include, “number and severity of symptoms, age of onset, setting where impairment occurs, clear evidence of impairment, and exclusion of other causes." (as cited in Salmeron, 2009)

Intervention
Currently behavioral interventions and/or stimulant medications are used to treat children and adolescents with ADHD
(Raggi & Chronis, 2006). Although stimulant medication has been found to be effective in areas of academia within the classroom for a short time period, for longer periods there is no evidence if it is just as effective. Behavioral parent training and behavioral school interventions are said to be successful in improving classroom behavior but not specifically to academic performance. Academic interventions seek to enhance behavior and academic outcomes A type of academic intervention is peer tutoring. Peer tutoring is a type of intervention where children with ADHD receive a tutor/helper from their class that helps them to learn academic material. This type of intervention utilizes a one-to-one instruction which means that the instruction can go at the pace of the student and “be tailored to the child’s academic ability.” (Raggi & Chronis, 2006) Through this instruction the child will have to actively respond to the peer tutor because of the one-to-one instruction and the peer tutor will be required to provide immediate feedback.

Local Support Groups for ADHD

Family Advocacy Network (FAN) “Meet the Experts” Support and Educational Series
  • Designed for parents of school age children who have emotional and behavioral challenges or other mental health issues. Refreshments available. Childcare provided with advance registration.
  • Meets on the 3rd Saturday of each month, 9:30-11:30 at the Orange United Methodist Church, 1220 Martin Luther King Jr. Blvd. Chapel Hill, NC 27516.
  • Support group meetings to be held one hour prior to educational clinics.
  • For updates, visit http://www.fan-mhaorangeco.org/
  • For more information contact Julie Bailey at 919-942-8083 ext. 2 or email her at julie@mhaorangeco.org.

Also NOTE: FAN additionally offers a 4-week parent support/education series three times per year entitled, “Parenting Wisely,” an interactive computer software program for small group or individuals needing assistance with basic parenting skills.
For details, contact Linda Boldin, Family Advocate, at Linda@mhaorangeco.org, or 919-942-8083.

NC Support Groups for Parents of Children with Special Needs
Wendy Ward at (800) 962-6817 ext. 35 Chapel Hill, NC:

Additional Resources

Exceptional Children's Assistance Center (ECAC)
This is a training and information center that provides free information and assistance with educational issues to parents of children with disabilities. They offer a lending library, newsletter, and a Parent Info Line answered by parents. Telephone toll free 800.962.6817 or 704.892.1321.

Family Support Network of North Carolina (FSN)
Family Support Network of North Carolina promotes and provides support for families with children who have special needs. A directory is provided that enables families to search for national and state organizations. Telephone toll free 800.852.0042.

IDEA Partnerships – The Families and Advocate Partnership for Education
The Families and Advocate Partnership for Education (FAPE) is a project funded by the U.S. Department of Education to provide parents, administrators, service providers, and policy makers with information about the implementation of IDEA '97.

References 
Glanzman M.M., & Blum, N.J. Attention Deficits and Hyperactivity. In Batshaw, M. (2007). Children with disabilities. (p.345) (6th Edition). Baltimore, MD: Paul H. Brookes.
Raggi, V.L., & Chronis, A.M. (2006). Interventions to Address the Academic Impairment of Children and Adolescents with ADHD. Clinical Child and Family Pyschology Review, 9(2), 85-111.
Salmeron, P.A. (2009). Childhood and Adolescent Attention-Deficit Hyperactivity Disorder: Diagnosis, Clinical Practice Guideline, and Social Implications. Journal of the American of Nurse Practitioners, 21, 488-497.

Epilepsy Defined with Resources

Posted By : Laura Taylor Eaddy and Erica Thomas

There are multiple definitions of Epilepsy, and the definition can change depending on the physician, the patient and the situation. The most common definition is Epilepsy that it is a neurological condition, which affects the nervous system. Epilepsy is also known as a seizure disorder. The seizures in epilepsy may be related to a brain injury or a family tendency, but most of the time the cause is unknown. The word "epilepsy" does not indicate anything about the cause of the person's seizures, what type they are, or how severe they are. Epilepsy can also be referred to as an expression of a chronic neurological condition of which one manifestation is recurrent seizure, or a self-limited condition that resolves over several years. It can also be described as a chronic condition characterized by recurrent seizures that is an expression of an underlying brain abnormality


Epilepsy can develop in any person at any age, although people with certain conditions may be at a greater risk. About 75% of people with epilepsy had their first seizures in childhood. Epilepsy affects about 2.0 million Americans, and in 2010, nearly 140,000 new cases of epilepsy were diagnosed in the United States. Epilepsy results in an estimated annual cost of $15.5 billion in medical costs and lost or reduced earnings and production. About 10% of people will experience a seizure sometime during their lifetime and about 3% will have had a diagnosis of epilepsy by age 80. It is estimated that about 75% of people with epilepsy had their first seizures in childhood. More than 30 different types of seizures have been described. Some researchers have estimated that as many as 500 different genes could be linked to epilepsy. It is usually diagnosed after a person has had at least two seizures that were not caused by some known medical condition like alcohol withdrawal or extremely low blood sugar. Sometimes, according to the International League Against Epilepsy, epilepsy can be diagnosed after one seizure, if a person has a condition that places them at high risk for having another. Treatment of epilepsy is diverse and ranges from medical intervention, to special diets, to brain surgery and removal of affected tissue. While some of these treatment techniques can prove effective in the maintenance and reduction of seizures, there is no known cure for Epilepsy.

Resources For Children with Epilepsy:

North Carolina Department of Health and Human Services


www.ncdhhs.gov/disabilities/



Centers for Disease Control and Prevention.

www.cdc.gov/epilepsy/



Epilepsy Foundation of North Carolina

www.epilepsyfoundation.org


Beyond Academics

www.beyondacademics.org

http://beyondacademics.blogspot.com/ (videos)

Developmental Delay and Hypotonia


By: Cierra Harris and Michelle Harris

Developmental Delay
            A developmental delay is defined as a child's not reaching his developmental milestones at expected times. It is an ongoing major or minor delay in the process of development. Delay can occur in one or many areas, for example, gross or fine motor, language, social, or cognitive skills. Developmental delay is most often a diagnosis made by a doctor based on strict guidelines. Usually the parents are the first to notice that their child is not progressing at the same rate as other children the same age. Developmental delay can have many different causes, such as genetic causes, like Down syndrome, or complications of pregnancy and birth, like prematurity or infections. Often, however, the specific cause is unknown. Some causes can be easily reversed if caught early enough, such as hearing loss from chronic ear infections, or lead poisoning. 


Hypotonia
            Low muscle tone, or hypotonia, is one of the physical problems often associated with developmental delays. Children can have generalized hypotonia or it may affect just specific areas such as the hands or upper body. It is clinically significant because in severe cases the muscles are literally too weak to perform important tasks such as holding a pencil or sitting without slumping in a chair. In milder cases, stamina or precision is affected.

Treatment
            The multi-disciplinary treatment approach is usually utilized in order to provide intervention for developmental delays. This approach consists of pharmaceutical intervention, special education, counseling and applied behavior management. These approaches focus on assumed neurological and observed behavioral, language, psychological, and academic deficits, not their possible causes. The ultimate goal of treatment is to eliminate undesirable behaviors such as hyperactivity, attention difficulties, anxiety, depression, mood swings, agitation, self-injurious behavior, insomnia, perseveration and impulsivity, while increasing desirable outcomes such as relatedness, eye contact, self-control, attention span and confidence. Determining appropriate treatments and their sequence requires knowing the multiple causes of symptoms in each patient. Hypotonia can be treated by increasing the amount of nutrients available for transport and by trying to regulate the naturally sluggish dispatch system.
            Early intervention is a key part of intervention for children with a developmental delay. It is important to detect a developmental delay early so that early intervention can begin. The type of intervention that is appropriate depends on the type of delay and what areas need to be addressed. Generally, children need to learn developmental skills in a consecutive fashion. For example, a child needs to learn to sit up on her own before she will be able to stand up, which is why it is important for early intervention to occur. Also, early intervention helps a child advance in all areas of development. Sometimes if a child has a delay in one area (e.g., speech), the delay can affect other developmental areas (e.g., social and emotional). Therefore, it is vital that a child receive early intervention as soon as possible. Finally, early intervention is critical for the child to develop good self-esteem. Without early intervention, a child's self-image may suffer and his may become avoidant of school. For example, a child who has a language delay may feel embarrassed to speak in front of his peers and teacher at school. Early intervention can help prevent these embarrassing moments for a child before he begins school.

Ten Tips for Improving Parent Participation in an IEP Meeting
We found that parents are sometimes uncomfortable at IEP meetings. Listed below are tips that will help parents feel more prepared for the meeting and more comfortable during the meeting.

1. Prepare and plan for your meeting. Look at the current IEP. Think about what is working well and what isn’t. Review recent evaluations and assessment information that you have. Do you have copies of the most recent assessment information done by the school district? If not, ask for it. Make a list of questions you want to ask at the IEP meeting and points you would like to make.

2.Do you have someone who can help you plan for the meeting and attend the meeting with you? If possible both parents should attend an IEP meeting, but it is also very helpful to take someone else as an advocate or support person. It is hard to advocate for yourself. Having someone to brainstorm with you ahead of time, take notes in the meeting, and ask questions can reduce your anxiety and help you participate more effectively. 

 3.  Look at the notice inviting you to the IEP meeting. The notice should tell you who the school district intends to have at the IEP meeting. Are there additional individuals that you would like to attend the meeting? You have the right as a parent to invite other individuals who have knowledge or expertise about your child’s special needs. For example, perhaps your child receives speech therapy or other therapies from a provider in private practice. Would you like that professional to attend the meeting to make recommendations to the other members of the IEP team? 

 4.  Are you and the others you would like to attend the IEP meeting available at the time scheduled? You have the right to have the meeting arranged at a reasonably mutually convenient time. If the meeting is not scheduled at a time that works for you, you should contact the appropriate school staff to reschedule. 

5.While at the meeting make sure you ask all of your questions and get your questions answered. Educational professionals often speak in their own language. If you don’t understand something that is said, don’t hesitate to ask that it be restated in more understandable terms. It is part of an educator’s job to communicate effectively to parents and others. It is important that all team members understand what is being recommended in the meeting.

6.Communicate what you would like to see in the IEP. As the parent you are a member of the IEP team and as the parent you have important information about your child’s strengths and needs that should be shared with the other members of the IEP team. While wanting to provide appropriate services, school staff can sometimes forget whose child it is. You are not just the parent. You have an important perspective to share and you do not have to just agree with what other members of the team recommend.

7.  Make sure the meeting focuses on developing a program to meet the unique needs of your child. Special education is specially designed instruction to meet the unique needs of a child with a disability.  If the needs of other students or the administrative needs of the school staff creep into the discussion the meeting can get off track and result in a poor plan. These other needs may be important but should not influence your child’s IEP. The IEP should be designed to meet the unique needs of your student with a disability. 

8.   Make sure issues are discussed sufficiently and the meeting does not end without completing the task. Sometimes it takes longer to complete the IEP than the time the school has allotted. For example, the IEP meeting is scheduled from 3:00 to 5:00 and the discussion becomes rushed as five o’clock approaches. Or, sometimes the meeting runs long and individuals cannot stay for the entire time. There is nothing wrong with scheduling another meeting to complete the IEP when all the needed team members can be available. 

9.  Keep your cool. Try not to take comments about your child personally or encounter disagreement with anger. That can be difficult. You may be justified in your anger, but  the views of parents who become too angry can sometimes be discounted. So, try to keep your anger in check and keep cool. 

10.   Finally, review the IEP document to make sure that everything agreed to in the meeting is written into the document.

Therapy Sites for Children
The website below provides therapy tools for children. These are free tools that parent can utilize to provide their children with additional support at home.

Receptive and Expressive Language Delay

Miriam Featherstone and Tyler Johnson

 Language Delay Overview
             A language delay is the failure to develop language capabilities at the expected time for the child’s chronological age. The child is progressing through the expected developmental milestones but he is acquiring the relevant capabilities several months after his typically developing peers. If a child has a receptive language delay, he is having trouble comprehending language. It is usual for receptive language skills to be in advance of expressive language skills because development is progressive. One has to understand language before one can use it effectively expressively. Therefore, it would be unusual for a receptive language delay to be greater than any co-occurring expressive language delay. These delays occur in up to 10% of children.
Receptive Language Delay
            A receptive language delay involves difficulty with comprehending language at the expected developmental milestone for the child’s chronological age. The child most likely has difficulty understanding longer utterances that include simple nouns that are combined with adjectives, verbs and prepositional phrases. Understanding spoken language is a complicated process, and all children will not be able to meet the milestones at every age. Developmental milestones are a set of functional skills or age-specific tasks that most children can complete at a certain age range.  Pediatricians use milestones to assess the development of a child.  Although each milestone has an associated age level, the actual age when a normally developing child reaches that milestone can vary because every child is unique. 

Tips for teaching a child with a receptive language delay:
                Teach words in context and generalize across many contexts (if you are talking about the word "shoe", use the word when you are tying your child’s shoes, when putting one your own shoes, when going to a shoe store, etc.).
                Break down multi-step directions into separate parts.
                Shorten your sentences when giving directions and asking questions.
                Model the answer to teach the child appropriate answers.
                If your child does not do something when told, show him and then if necessary physically assist him
Expressive Language Delay
An expressive language delay is evident when expressive spoken language is below the appropriate for the child’s age but his language comprehension is intact. By age two, the expressive vocabulary of children with an expressive language delay is often twenty words. However their typically developing peers generally have approximately two hundred words. An expressive language delay may be manifested in a child’s limited ability to produce two-word combinations by age two.  According to Rescorla and Schwartz, as these children age, a number of them will continue to have problems with the syntactical structure of their sentences. The children may be able to produce sentence with the appropriate semantics to convey the correct meaning, but they lack the ability to use the correct morphemes to lengthen their utterances.
Although other significant cognitive, motor, sensory, or social and emotional disabilities may not exist, an expressive delay in language development that is untreated until the child begins school may put a child at a very considerable risk for long-term language, academic, and social deficits. These young children are at particular risk for persistent language problems and learning disabilities along with emotional and behavioral disorders.

Tips for teaching children with expressive language delays:
  • Reflect the child’s messages and add one more word.
  • Choose 5-10 words to highlight during daily routines and play activities, and repeat them often
  • Use “fun” words and sounds like “uh-oh”, “Shhhhhhh,” or  “pop-pop-pop!”
  • Pair words with gestures to help your child attend to and learn the word. Encourage the child to use gestures; these will eventually help to cue the words.
  •  Be patient with the child.
  • Don’t pressure your child to talk – this only creates more frustration. Accept their communication.
  • Gently model the words for them.

Friday, April 29, 2011

Resources for Parents/Families

http://www.ecac-parentcenter.org

ECAC is North Carolina’s Parent Center. It provides information and services for parents, students, educators etc. There are three parent education programs:  
1.      1. NC Parent Training & Information Center (PTI)- information provided to best parents/families advocate
2.      2. NC PIRC, a Parent Information and Resource Center- provides information in Title 1 schools with emphasis on No Child Left Behind.
3.    3. NC Family to Family Health Information Center (HIC)- provides information and support to families with children who have health care needs (i.e. insurance)

http://www.uhccf.org
This non-profit foundation addresses the health needs of children despite insurance restrictions. Here, families can find coverage for the gaps in their health benefits.
http://www.modestneeds.org

This foundation offers grants to children and families who need services, but may not be financially able to do so. They offer Self-Sufficiency, Back-to-Work, Independent Living and Non-Profit Grants.

http://www.beyondacademics.org
UNCG presents Beyond Academics, a four year certification program, for children with developmental disabilities. The course of study educates these students to follow their career, becoming advocates, and living in the community independently.

This foundation targets inclusion and equal education for children with severe communication and physical disabilities. An assessment is administered to establish the child’s abilities and needs to perform adequately in the classroom.  

http://nc.eastersealsucp.com
This resource is called the Easter Seals UCP North Carolina and Easter Seals UCP Virginia. It provides information on services addressing each individuals need.