1 King: Research Project: Key Assessment
1 King: Research Project: Key Assessment
1 King: Research Project: Key Assessment
King
Emma King
Program Y is an agency that is local to Region M. This agency provides children’s and
adult services to people with developmental disabilities or acquired brain injuries and their
families. Program Y offers children’s services to people ages birth through 21 years of age,
however, this section will primarily focus on the Family Centered Early Supports and Services
(FCESS) birth to three program within agency. Program Y serves 34 towns within Region M and
employs about 11 professionals within the children’s services program. The entire organization
serves about 600 families within Region M (Program Y 2, 2020). Region M is a rural region that
Program Y’s mission is “to work toward inclusion, participation, and mutual
relationships for all people who are at risk for isolation from the community” (Program Y 2,
2020). This FCESS program within the organization works with infants and toddlers with
disabilities and their families. Program Y provides services to families that involve early
intervention. Early intervention is a system of services for children ages birth to three with
developmental delays or disabilities and their families (Brilliante, 2017). Early intervention is a
process that will lead young children and their families to developing an Individualized Family
Program Y offers many different services for families based on their individual needs
(See Appendix A). The services that Program Y offers are as follows: developmental evaluations,
that helps to link families with information about community resources, assistance with
transitioning from early intervention, advocacy groups, feeding and nutrition programs, special
Region M is a rural area that has a population of approximately 76,100 people. This
Region has a 10.2% poverty rate, with about 40,000 of the region’s people being employed
(DATAUSA, 2017). This region has a median property value of $188,700 (DATAUSA, 2017). The
state that houses the region had 476 drug related deaths in 2017, and in 2014, the percentage
of people needing addiction treatment but not receiving it was at 88% (Opioid & Health
Program Y serves a population of 600 families within the entire organization. The main
focus of the FCESS program within Program Y is families with children ages birth to three who
have or might be at risk for developmental delays or disabilities. This also includes children who
may have been born with an exposure to opioids or alcohol. The state that houses Region M
had a 3.9 percent of newborn infants in 2019 who were being monitored for opioid or alcohol
exposure (Albertson-Grove, 2020). The program also serves children who have a developmental
delay of at least 33% or have an established condition. The program may serve children and
families who do not have the resources for private help, as Program Y is funded by family’s
private insurance, Medicaid and State and Federal programs so that families do not need to pay
each family based on their need. Program Y is an organization that wishes to work toward
inclusion and participation for all the people who are at risk of isolation from the community
Model explains that the world of the child consists of five systems of interaction: (1)
Microsystem, (2) Mesosystem, (3) Exosystem, (4) Macrosystem, and (5) Chronosystem (Swick &
Williams, 2006). Each of the bioecological systems depend on the child or individuals’ life and it
grows and changes through every system as the person grows (Swick & William, 2006).
Program Y helps to build up children and adults with disabilities entire systems by helping them
gain more opportunities in their communities, schools, churches, which help to compose their
microsystem. The children and adults with disabilities will also become a part of their
exosystem and macrosystem. The exosystem is the relationship that an individual has with the
parts of the community that involve the neighborhood that the child lives in, local politics, and
media. The program also helps to put a new lens on the macrosystem that an individual is a
part of (Exploring Your Mind, 2020). This is the culture and its attitudes. This gives the culture of
The Individuals with Disabilities Education Act (IDEA) is a law that has four connected
parts, Part A, Part B, Part C, and Part D. Part A of the IDEA law sets the foundation for the entire
law by outlining the general provisions of the law which includes the purpose of the law, the
effective date of each amendment and the definitions of terminology that is used throughout
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the law. Part A also outlines details such as the employment of individuals with disabilities, and
how each individual state can administer the IDEA law (Individuals with Disabilities Education
Part B of IDEA includes the provision that explains the use of grants that assist states to
provide special education for children ages 3 to 21 with disabilities (IDEA, 2004). Part B states
that a free and appropriate public education is available for all children with disabilities (IDEA,
2004). This part of the law states that each U.S. state administers its own program for children
with disabilities, and the regulations outline each of the eligibility requirements and the
procedure for the referral process as well as the Individualized Education Program (IEP) process
(Brilliante, 2017). Part B of IDEA provides procedural safeguards which allow the child and their
family the safeguard of being guaranteed a free public education (IDEA, 2004). Lastly, Part B
offers the provision of monitoring, technical assistance, and enforcement of the law (IDEA,
2004).
Part C of IDEA includes the provisions that explain the use of grants that assist states to
provide early intervention services to children ages birth to two years of age and their families
(IDEA, 2004). This section includes the reasonings for including early intervention for infants
and toddlers as well as definitions on the terminology used throughout the law. Part C covers
who is eligible for early intervention services, how grants work and the state’s requirements for
the system (IDEA, 2004). Part C of IDEA covers the Individualized Family Service Plan (IFSP), the
referral process, assessing the infant or toddler, periodic reviews and the content of the IFSP
(IDEA, 2004). Like Part B, Part C also explains the uses of funds and procedural safeguards.
Lastly, Part D of IDEA covers national activities to improve education of children with
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disabilities. This part of the law explains the federal government’s obligation to support
activities that contribute to a positive education for children with disabilities (IDEA, 2004).
Program Y uses Part C of IDEA for their FCESS program when determining eligibility. Part
C of IDEA and Program Y both state that in order for a child to be eligible, they must be under
three years of age and have a developmental delay or be at risk for a developmental delay in
one or more of the areas that they support which are physical, cognitive, social-emotional, and
adaptive development (Program Y 1, 2020). Program Y follows Part C of IDEA when connecting
families with the referral process. The program states that parents, caregivers and members of
the medical community can make a referral to Program Y for FCESS and the team will them
One of the main pieces from Part C of IDEA is the developing of the IFSP. Every state has
a referral process that connects with Part C of IDEA; however, some states the Department of
Education coordinates the FCESS and in others, the Department of Health and Human Services
coordinates the FCESS. There are six steps to the IFSP process which include the referral, the
reviews, and the transition to public school for children turning three (Brilliante, 2017).
The referral can be made by parents, caregivers, or medical professionals and this will
begin the eligibility process. During the process of determining eligibility, there will be a
their eligibility and what services they will have (IDEA, 2004). The state will also provide the
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family with their rights in an easy to understand format in their home language (Brilliante,
2017).
The writing and implementation of the IFSP is a process that involves the family, and
each member of the IFSP team. The IFSP will identify the services that the family is receiving,
and the services will begin within 30 calendar days after the family consents to implement the
IFSP (Brilliante, 2017). Once the IFSP is implemented, there will be 6-month and annual reviews
to see that the child is making progress with their services (Brilliante, 2017). Finally, children will
transition to special education at age three and the family and the interdisciplinary team will
develop an Individualized Education Program (IEP) which is covered under Part B of IDEA
(Brilliante, 2017).
Cerebral Palsy
Cerebral Palsy (CP) is a group of disorders that affect a person’s ability to maintain
posture, balance and mobility and is caused by abnormal brain development or damage to the
developing brain. CP is the most common motor disability in children (Hadders-Algra, 2014).
The symptoms of CP vary greatly from person to person, as there are four main types of CP
(Centers for Disease Control and Prevention (CDC), 2020). The four main types of CP are spastic
cerebral palsy, dyskinetic cerebral palsy, ataxic cerebral palsy, and mixed cerebral palsy (CDC,
2020).
Spastic CP is the most common type of CP and involves increased muscle tone, which
results in still muscles. People who have spastic CP can have one of the three types of spastic CP
which are described by the part of the body that is affected by it. Spastic diplegia is when there
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is stiffness in the legs when the arms are less affected by stiffness or not affected at all. Spastic
hemiplegia is when the stiffness is only present on one side of the body. Spastic quadriplegia is
the most severe form of spastic CP and it affects all limbs, the torso and sometimes the face
(CDC, 2020).
Dyskinetic CP affects the movement of the hands, arms, feet and legs, which can make it
hard for people with dyskinetic CP to sit and walk. The movement of the hands, feet and legs
can be fast, or slow and it varies between each person’s individual muscle tone (CDC, 2020).
Ataxic CP affects balance and coordination. It may be harder for someone with this form of CP
to write, reach or control their steady movements (CDC, 2020). Lastly, mixed CP happens when
Cerebral palsy in the past has been typically diagnosed around 12 to 24 months of age in
children, but early diagnosis at 12 weeks of age is possible for a percentage of the population.
CP can be diagnosed in children with a combination of best practice techniques such as learning
the risk factor history, providing a neurological examination, a standardized motor assessment
to learn the quality of the child’s movement, neuroimaging, and ruling out other diagnoses
(Novak, 2014). Children with CP will most likely be automatically eligible for early intervention
services, however, a child will still go through an interdisciplinary evaluation to determine what
specific services the child will be eligible for (Stern, 2020). Children with CP often receive the
greatest number of individual services and intervention compared to other children who
Assessment Process
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Children with CP can be diagnosed anywhere from an early diagnosis age of 12 weeks,
that the child can go through the assessment process as early as possible and find the
diagnosis-specific intervention that is best for them (Novak, 2014). During the assessment
process for infants and young children with CP, the child’s neurologist will most likely diagnose
the child with CP, then refer the family to an early intervention agency where they will begin
the interdisciplinary evaluation to determine the specific child’s need for services. If a
neurologist is unsure of the child’s diagnosis, they will recommend that the family seek an early
intervention agency that will accept family referrals, and then the interdisciplinary evaluation
will begin (Novak, 2014) for the Individualized Family Service Plan (IFSP).
The assessment process is used to determine the child’s present level of performance
(Conaster, James & Ledingham, 2013), and they are performed in the child’s natural
environment. Assessments for young children with CP should be used as a screening tool for
identifying the infant or toddler’s strengths and weaknesses rather than giving them a
numerical score (Conaster et al., 2013). A team of professionals who specialize in infants and
toddlers and the five areas of development will come together and assess the child’s
functioning in each of the five domains of development which are physical, cognitive,
communication, social and emotional, and adaptive development (Brilliante, 2017). Each child
important part of the early intervention process. For example, one child with severe spastic
quadriplegic CP may have mastered social, emotional and communication development, but
need to continue working on physical development (Conaster et al., 2013), while another child
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with the same diagnosis may need to continue working on cognitive development, but reached
a goal with physical development (Brilliante, 2017). There are many different assessment
strategies that are used from birth to age three to determine diagnosis and early intervention
assessment tool that is used to evaluate the five developmental domains with infants and
young children as old as five years 11 months (Voress & Maddox, 2012). The assessment was
normed on a national sample of 1,832 children (Pearson Assessments, 2020). The format of the
DAYC-2 assessment allows multiple ways for the administrator of the text to obtain the
information for each of the five tests (See Appendix C). The assessment administrator can use
direct assessment, which would be asking the child a question, observation of the child in their
natural environment, or an interview of the parents, caregivers and teachers of the child (Ford,
2015). Each domain can be assessed individually, however it is best practice that all five
domains are assessed (Ford, 2015), because this will help to create a whole picture of the child.
The chronological age of the child should be determined prior to administering the test in order
to obtain accurate results (Ford, 2015). Each domain observation or interview takes anywhere
from 10 to 20 minutes to complete (Pearson Assessments, 2020), and the assessment is meant
to be administered by a professional, but the family may join in the assessment and present the
materials for the child to show their skills (Ford, 2015). Once the assessments have been
administered, they will be scored and interpreted by providing standard scores, percentile
ranks and age equivalents for the child in their areas and domains (Pearson Assessments,
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2020). Age equivalents are the least reliable scores, and standard scores are the most reliable
Goals/Purpose of DAYC-2. The goals and purpose of this assessment is to determine the
child’s present level of skills in each of the domains which are adaptive behavior, cognitive,
DAYC-2 assessment allows for a multitude of benefits. The assessment helps to obtain
information about a child’s abilities through observing their skills, interviewing the primary
caregivers of the child and by assessing the child directly. The assessment also allows for a child
to be assessed on only the domain that is needed or all five domains if needed (Pearson
Assessments, 2020).
Cons of DAYC-2. The assessment does come with a small number of disadvantages. The
administer the test. Someone with a qualification Level B has a master’s degree in psychology,
that is closely related to the field in which the assessment is intended for. The alternatives to
having a master’s degree for Level B is having a degree to practice medicine or having a
Association for the Education of Young Children (NAEYC) (Pearson Assessments, 2020). Another
disadvantage to this assessment is that there is no materials kit available to order from the
complete DAYC-2 kit, so any toys, games or materials beside the test themselves must be
measures how well children with hemiplegic cerebral palsy use their most affected hand when
using both hands together during play. The Kids AHA offers three different versions of the test
depending on the child’s age. The different assessments are the Mini AHA which is for infants
ages eight to 18 months, the Small-Kids AHA which is for children ages 18 months to five years,
and the School-Kids AHA which is for children ages six years to 12 years (Cerebral Palsy Alliance
(CPA), 2018). This part of the research paper will cover the Mini-AHA and the Small-Kids AHA.
The assessment is administered by a qualified therapist and is observation and play based. The
assessment bases the child’s performance on 20 items which are later scored on an electronic
spreadsheet which calculates the raw score (CPA, 2018). The Kids-AHA assessment has good
evidence for construct validity, which is whether the test measures the characteristics that it is
supposed to measure, and has an excellent inter-rater, intra-rater and test-retest reliability
which is the tests ability to measure the child’s characteristics accurately under different
interventionists to use Kids- AHA is to describe how a child with hemiplegic CP uses their
affected hand, it allows for the interventionist and IFSP team to plan intervention around the
child’s level of ability, and the measure whether the intervention has been effective (CPA,
2018). The Kids- AHA has many benefits. For infants, the assessment occurs during an enjoyable
play session between the interventionist and the child, so the child is having fun, playing with
toys and also being assessed. The session is recorded so the interventionist can be present with
the child and re watch the video later to score the interaction. For young children, the child is
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presented with a series of toys in a play session, and the toys are carefully selected to provoke
the child to use both hands together while playing in order to get an accurate reading of their
abilities. Like the infant session, this one is also recorded so the interventionist can be present
with the child during the session and record it at a later time (CPA, 2018).
Cons of Kids Assisting Hands Assessment. The Kids-AHA does have a few cons. One of
the disadvantages to this assessment is that there is training needed for a health professional to
earn a certificate in order to administer, score and interpret any of the versions of the Kids-
AHA. In order for a professional to become qualified, they may take a training and receive the
considerations that they must follow surrounding assessment strategies in Family Centered
Early Supports and Services. The main ethics that are followed in early childhood and in special
education connect with recognizing the individual values, culture and belief that families and
their children have, recognizing diversity, and understanding that people achieve their full
potential in life when they are met with a trusting and respectful relationship, as well as
respecting the family’s autonomy when it comes to making decisions about their own children
(NAEYC, 2011; DEC, 2009). The two assessment strategies above consider two different types of
growth and development. The DAYC-2 can be used with any child to determine their
development in each of the five domains, however, the Kids-AHA will most likely only be used
for children with CP or a similar disability. Practitioners in early childhood and special education
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need to understand that families can make their own decisions on their own child, even if it
The Division of Exceptional Children’s Code of Conduct (2009) explains that practitioners
must rely upon evidence-based research and interventions to inform the practice with children
and families, while also using every resource to assure high quality services are available to
families. Many of the DEC and NAEYC ideals and principles connect with the Family Educational
Rights and Privacy Act (FERPA) as well as the Health Insurance Portability and Accountability Act
(HIPAA). Both FERPA and HIPAA protect the privacy of students and patients under the law. DEC
and NAYEC connect in the NAEYC Code of Ethical Conduct (2011) under section 1 Ideal I-1.9
which states “to advocate for and ensure that all children, including those with special needs,
have access to the support services needed to be successful”, and DEC Code of Conduct (2009)
under Enhancement of Children’s and Families’ Quality of Lives number 4 “we shall advocate
for equal access to high quality services and supports for all children and families to enhance
their quality of lives”. This is an important connection to make because both organizations want
what is best for children. What is best for children, is for their families to be a part of the
assessment process, to make that connection with their FCESS and IFSP team (CPA, 2018).
Evidence-Based Interventions
Early intervention services are supports that are given to children with disabilities or
developmental delays that are ages birth to three and their families. Early intervention services
support the growth and development of children by finding the evidence-based interventions
that will work best for their development. Evidence-based interventions are a practice, strategy
or curriculum that is implemented in a home, classroom or caregiving setting that is created for
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an individual child or group of children to target a specific need (PRIME, 2020). This section of
research will cover evidence-based interventions for improving hand function in children with
CP, social skills training for young children, and the Lovaas Model of Applied Behavior Analysis
(WWC, 2010; WWC, 2013; Basu et al., 2014). Region M mainly focuses on the family coaching
model for early intervention, but some children with CP may need more intensive intervention
when it comes to hand function improvement and behavior strategies (Program Y 1, 2020, Basu
et al., 2014)
Children with hemiplegic cerebral palsy often have difficulty with hand involvement and
limited wrist extension from the time of infancy, but early intervention can help to break the
cycle of soft tissue and bone changes in early childhood that lead to contractures in later life
(Basu et al., 2014). The nature of the intervention must be carefully considered when deciding
how to continue with the therapy. The Kids-AHA is a great place to start when determining the
intervention needed for children with hemiplegic CP (CPA, 2018). Evidence-based approaches
to intervention for hemiplegic CP allow the child to be an active participant when participating
in play-based intervention which allow the child to have fun while participating in the
intervention (Basu et al., 2014; Brilliante, 2017). Some of the interventions that take place are
video game playing or virtual reality games for children who are older. This therapy allows a
child to use the controller to deliver upper limb therapy in a fun and engaging way (Basu, 2014).
Other play-based interventions for hemiplegic CP include playing with toys that involve problem
solving, and goal centered games that can also involve daily activities for very young children.
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Families and interventionists can work together with very young children to hold a spoon and
There are some challenges that come with early intervention therapy for infants, as it is
harder to keep their attention, and they have little understanding that they are receiving
therapy and why. Additionally, there is only one validated assessment for upper limb function
in infants which is the Mini-AHA, and this covers the youngest age of infants that can be
assessed properly for assisted hand therapy needs (Basu et al., 2014; CPA, 2018). In conclusion,
early intervention can be challenging for the upper limb in hemiplegic CP, but validated
assessments for young children and infants are available, and they offer important information
about what interventions the child will need to be successful later in life (CPA, 2018, Basu et al.,
2014).
Social skills training is not one specific curriculum, instead, it is a collection of practices
that use a behavioral approach to teaching young children social skills (WWC, 2013). After the
DAYC-2 assessment is scored, it may be identified that a child with CP will receive supports for
social intervention. Often times, children who have CP will have behavior problems (CDC, 2020).
This is when the social skills training will come in. This form of intervention targets the idea that
children who often act in a way that is looked at as misbehaving need to learn the proper skills
to react in a different way than they usually do. The social skills training intervention shows
caregivers a new way to look at behavior. This intervention gives four different reasons for why
children with disabilities may be misbehaving. (1) they don’t know another way to act other
than their present pattern of behavior, (2) they know cognitively other ways to behave but have
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not yet had enough practice to display them properly, (3) they tried another way, but it did not
work the first time, so they assumed it didn’t work, and (4) tension and anxiety interfere with
the ability to perform practiced behavior well in real life (WWC, 2013).
Often times, children with CP will act out because of their tension and anxiety in their
household (Schulze, 2020). With the social skills intervention, the children will learn about
positive interaction with others, appropriate classroom behavior, better ways to handle
frustration and anger, and acceptable ways to resolve conflicts with others (WWC, 2013).
Teachers can use targeted instruction with 3-5 children in small groups and teach them about
these acceptable practices while allowing them to practice and watch other children at the
same time (WWC, 2013). This strategy works not only with young children, but also older
children as well. One way that family coaching could be used with this type of model is by the
interventionist showing family members of a child way to speak to a child so that they learn
about feelings and correct ways to react throughout the day, and not only when a child is
The Lovaas Model of Applied Behavior Analysis (Lovaas Model) is a type of behavior
intervention that is used as brief one-on-one instruction in the home, in an inclusion classroom
and natural environment of the child. During this intervention strategy, there are periods of
one-on-one instruction where the teacher cues a behavior, prompts the appropriate response,
and provides reinforcement to the child (WWC, 2010). This program consists of about 35 to 40
hours of intervention per week and typically lasts about three years (WWC, 2010). The studies
done on this intervention strategy considers the evidence to have an impact on the cognitive
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development, communication and language development, and social-emotional development
(WWC, 2010). This intervention strategy may be helpful for children with CP, as it targets three
domains of development and could be helpful for a child who needs support in any of those
three domains. This can be used with infants and toddlers in a natural way. Interventionists can
modify it in a way that it is less intensive and more play-based while showing the family
appropriate ways to cue a respond to the behaviors when using a coaching model (Rush &
Shelton, 2008).
Progress Monitoring
Progress monitoring is the monitoring of the child’s development to see that they are
showing movement toward their goals in their IFSP (Brilliante, 2017). Progress monitoring can
happen in different ways. Every IFSP has a six-month review where the team will determine if
the child is getting the services that they need, and whether they should make new goals.
States are required under IDEA Part C to re-evaluate the IFSP once a year and review the
document even 6 months (Brilliante, 2017; IDEA, 2004). During this time, the child may be
assessed using the same assessments that were used when the child was being evaluated for
services. The DAYC-2 assessments can be used to re-assess the child and see if they need more,
less, or different services (Pearson Assessments, 2020). The Kids-AHA assessment can be used
to monitor the use of the affected hand every six months during an IFSP review by reassessing
the child. The rating scale of the Kids-AHA is on a scale of 1 point which means that the child
has not used their affected hand at all, to 4 points which means that they used their hand
effectively throughout (CPA, 2018). By completing the assessment over again, the IFSP team can
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determine if the child has made progress with their affected hand or if they should continue
School S is a local public school that is located in City K. School S teaches about 290
children and families from Kindergarten to Fifth grade. There are three sections of
Kindergarten, 2nd Grade, 3r Grade, 4th Grade, and 5th Grade, and two sections of 1st Grade
(School S, 2020). The public-school employs about 51 teachers and faculty members (School S,
2019). City K is city that houses four public elementary schools, one public middle school, one
public high school and a public vocational school as well as one public preschool (K School
District, 2016).
School S is a public school that is one of the for elementary schools located in City K.
School S’s mission (School S, 2020) is to provide a positive, caring and academic climate for
children where every individual child is given the opportunity to realize their potential (See
Appendix D) (School S, 2019). The mission statement further explains that the school works
with students, parent and staff to create a sense of community throughout the school while
also recognizing the cultural diversity, uniqueness and creativity that each child has to ensure
that each student in their own way can build the confidence to meet the challenges of being a
lifelong learner (School S, 2019). School S also holds a schoolwide philosophy that intends to
provide educational opportunities where students can create a positive self-image, and respect
for others to ensure that each child becomes a contributing member of our local and global
The kindergarten classrooms follow a play based; theme integrated curriculum for each area of
the curriculum such as science, social studies, mathematics, and social and emotional learning
(School S 1, 2020). The first-grade classrooms follow a curriculum that assists children in how to
build independent work habits for language arts, mathematics, science, and social studies
(School S 2, 2020). The second-grade classrooms follow a curriculum that incorporates the
Responsive Classroom approach where the curriculum blends social and academic curricula
throughout the day such as language arts, math, science and social studies (School S 3, 2020).
The third-grade classrooms start to shift to an academic curriculum with reading to learn,
spelling in cursive, multiplication, division, and learning about global cultures. In the third-grade
year, student start to use Next Generation Science Standards (School S 4, 2020).
Children and families at School S are provided with a large scope of resources ranging
from free or reduced lunch, specials that include physical education, art and music (School S,
2019). The school also offers special education services that include speech therapy, physical
therapy, occupational therapy and psychological services. The school provides a reading
specialist, intervention services, a learning center or resource room and the Attachment,
Regulation and Competency (ARC) program that provides services to students whose emotional
conditions may interfere with their ability to thrive academically and socially (School S, 2019).
The School S handbook (2019) offers families and children the resources that they need to get
started with special education services for their children and what steps they should take when
wanting an evaluation.
23,000 people (NHES, 2018). City K offers four public elementary schools, one public preschool,
one public middle school and one public high school. The median family income in City K is
$78,298, and a poverty rate of 14.7% (NHES, 2018). This city has a median property value of
$187,900 (DATAUSA, 2017). The city’s poverty rate is slightly higher than that of Region M’s
which is 10.2%, and the median property value is slightly lower than that Region M which is
$188,700 (DATAUSA, 2017). Within City K, 33.1% of students use the free or reduced lunch
School S serves a population of approximately 290 children and families. Based on the
demographic information of the city that School S is located in, the students may have potential
financial needs based on the 14.7% poverty rate and the school districts 33.1% free or reduced
lunch rate.
School S meets the needs of the community by offering a multitude of services for each
child and family based on their individual support need. School S is a public school that
emphasizes Part B of IDEA in their parent and family handbook (School S, 2019). School S (2019)
states that children with disabilities should be educated in their least restrictive environment,
and not discriminated based on their disability, race or culture. This school offers many services
for students with disabilities including speech therapy, physical therapy, occupational therapy,
psychological services, a reading specialist, intervention services for students who are not
eligible for special education, a learning center or resource room, and the ARC program for
students with trauma who need extra social and emotional supports in order to succeed
Needs (McLeod, 2018). The hierarchy of needs is a psychological model that shows the five tiers
of human needs. From the bottom of the hierarchy to the top, the needs are physiological
needs, safety needs, belongingness and love needs, esteem needs, and self-actualization
(McLeod, 2018). Physiological needs consist of food, water, warmth rest. Physiological needs
along with safety needs are the basic needs in human life. Belongingness and love needs consist
of intimate relationships and friends. Along with esteem needs which are the feeling of
accomplishment and prestige, these two tiers are the psychological needs. Lastly, self-
actualization is the top piece of the pyramid. This tier is when one achieves their full potential,
and builds their own creative needs, which connects with self-fulfillment needs. Together, these
five tiers make up the hierarchy of needs (McLeod, 2018). School S’s special education
programs connect to this hierarchy because they offer so many services to help children to feel
secure, build upon their social and emotional needs in order to create intimate relationships,
and achieve their full potential in life by having each of these services available to them (school
S, 2019).
IDEA (2004) is a law that has four connected parts: Part A, Part B, Part C, and Part D. Part
A sets the foundation for the entirety of the law by outlining provisions for Parts B through D.
Part B states that children with disabilities from the ages of 3 to 21 are entitled to a free and
appropriate public education, and the safeguards that are guaranteed to families in IDEA Part B.
Part C states that children ages birth to three with disabilities are entitled to early intervention
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services. Lastly, Part D covers the national activities that are meant to improve education for
children with disabilities and states the federal government’s obligation to support those
activities financially (IDEA, 2004). Part B of IDEA connects to School S with their explanation in
the parent and family handbook about the IDEA laws, how to be eligible and the ways in which
a student and family can begin the evaluation process (See Appendix E) (School S, 2019). Part B
of the IDEA law states that children with disabilities are entitled to receive special education if
they are between the ages of three and 21 (IDEA, 2004). The special education team, the child,
their family and other members of the team will get together to determine if the child needs to
be evaluated for special education, and what testing will be needed for the evaluation process
(Parent Information Center on Special Education, 2017). School S outlines in their handbook
(2019) the disabilities that are represented in the IDEA law which are developmental delay,
visual disability, hearing disability, speech and language impairment, emotional disturbances,
physical disabilities, learning disabilities, and other health disabilities (IDEA, 2004; School S,
2019).
The special education process in Part B is a series of steps that is called the
Individualized Education Program (IEP) process. This process is a series of six steps that include
(1) the referral, (2) the interdisciplinary evaluation in all areas of the suspected disability, (3)
eligibility determination, (4) the development and implementation of the IEP, (5) annual
reviews, (6) transition planning for postsecondary school (Brilliante, 2017; Parent Information
Center on Special Education, 2017). Children who are involved in Part C early intervention
services will often transition into Part B services by going through this process with the local
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public school and possibly some professionals from the IFSP team. Children ages three to 21
who have never received any IDEA services before may be referred by a family member to the
local public school or by a teacher (School S, 2019; Brilliante, 2017). School districts are
required to identify, locate and evaluate all children who have suspected disabilities to ensure
that all children with disabilities are referred and provided with special education services if
they are eligible. This process is called Child Find and it is outlined under IDEA Part B (IDEA,
The referral process begins with a family member or professional who suspects that a
child may have a disability. This person will write a referral, preferably with the date, child’s
name, and why they suspect the child may be eligible for services under IDEA (Parent
Information Center on Special Education, 2017). This letter will be sent to the superintendent,
the special education director, the school principal, and the classroom teacher as well as
anyone else who should know about the referral. The next step is the evaluation process.
During this step, the IEP team will come together to review the child’s educational history and
decide which interdisciplinary team of experts will evaluate the child (Brilliante, 2017). These
evaluations must be done in the child’s native language (Parent Information Center on Special
Education, 2017). Once the child is determined eligible, the IEP development step will begin.
The IEP meeting must happen within 30 days of the determination of eligibility (Brilliante,2017).
The IEP will specify the child’s Present Level of Academic Achievement and Functional
Performance (PLAAFP), the goals that will be addressed in the annual review, and the supports
and services that will be needed for the child to make progress toward their goals (Brilliante,
2017).
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Lastly, the IEP team meets once a year to review the IEP and determine if progress has
been made toward the child’s goals and develop new goals for the following year (Brilliante,
2017). When the child is 16 years old, the transition planning for postsecondary school will
begin. During this time, the student and family will develop goals that will help prepare the
student for adult life outside of Part B services. This planning includes preparing for skills
needed for a job, living independently, and being a productive and contributing member of
Speech and language impairments are communication disabilities that can range from
spoken language (speech) and comprehending words which can either be written, spoken or
expressed (language) (Kolso, 2020; NIDCD, 2017). Childhood Apraxia of Speech (CAS) is a speech
and sound impairment that affects a child’s ability to say what they want correctly (NIDCD,
2017). CAS is present from birth and is different from a language delay. Some symptoms of the
impairment are difficulty pronouncing words correctly, possibly because of incorrect tongue
placement when speaking, difficulty finding the correct sound when trying to speak, and/or
making errors in the tone, stress or rhythm of the voice (NIDCD, 2017). CAS has a difficult
definition, as CAS has no diagnostic differentiation from other speech impairments, however,
professionals who have researched and studied CAS have expressed that children with CAS
have typical characteristics such as inconsistent phonemic errors, difficulties sequencing speech
movements and increasing errors in speech when words becomes longer or more complex
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(Martikainen & Korpilahti, 2011). Children who have CAS may experience difficulty with oral
motor skills and physical coordination, cognitive functions, or reading, writing and spelling
CAS and other speech impairments. However, the CAS technical report from the American
characteristics that are consistent with an impairment in speech motor planning and
programming that are specific to CAS. The three characteristics are (1) inconsistent errors on
consonants and vowels in repeated productions of syllables or words, (2) lengthened and
disrupted coarticulatory transitions between sounds and syllables, and (3) inappropriate
prosody, especially in the areas of word and phrase stress (ASHA, 2007; Terband et al., 2019).
Furthermore, a speech-language pathologist (SLP) or the child’s primary care doctor would
make the diagnosis of CAS, which would then allow a child to be referred for special education
services under Part B of IDEA to begin the evaluation process to determine if the child is eligible
for services other than speech-language therapy (Brilliante, 2017; Nijland et al., 2015).
Assessment Process
Children with CAS may show signs as early as 18 months old, as this is when children
begin to speak. CAS may be suspected as early as 18 months, but most children begin to
produce more speech between the ages of two to four. This is when a child may be clinically
diagnosed with CAS by a doctor or an SLP (Mayo Clinic, 2020). Once a child with diagnosed CAS
turns three, they will transition to Part B services under IDEA, or may begin the evaluation
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process if they had not previously received services under Part C (IDEA, 2004). Once the
transition or referral happens, the team working with the child will begin the evaluation process
and develop an IEP for the child with CAS (Brilliante, 2017).
During primary school and Part B services under IDEA (2004), typically family members
will refer the child for services, but with CAS, children will most likely already be eligible for Part
B services and may possibly be eligible for services other than speech and language therapy.
When determining if the child is eligible for other services, the IEP team will conduct an
interdisciplinary evaluation in all areas that the child could be eligible for services in (Brilliante,
2017). Once the assessment in each interdisciplinary subject have been conducted, the child
will begin services that may be unique compared to other children who are receiving Part B
services (Hammer, 2009). SLPs play a huge role in working with children with CAS. The SPLs in
the school systems who work with children with CAS face a unique job. These professionals will
complete assessments with the child and keep the family up to date for each change in the
work that is being done with the child with CAS so that the family can continue the work at
home, as the work done at home with the family will make a larger impact on the child’s
The Dynamic Evaluation of Motor Speech Skill (DEMSS) is an assessment that was
developed to help diagnose children with speech motor planning difficulties, such as CAS.
DEMSS was created for children who have a severe speech impairment, as articulation nor
phonology assessments have the ability to differentially diagnose CAS from any other speech
impairment (Strand et al., 2012). The DEMSS assessment includes nine subtests and 66
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utterances that the child will be asked to imitate while the clinician directs eye contact with the
child. The assessment offers results in 171 judgements that are related to the overall
articulatory accuracy, vowel accuracy, prosodic accuracy and consistency (Strand et al., 2012).
The child is asked to imitate the clinicians’ utterances using different levels of cues that can be
visual or tactile. The assessment may be scored on site during the administration of the
assessment, or afterward if recorded by video. The DEMSS is scored by four sub scores that sum
validity based on the probability of correct classification based on the ability to discriminate
children with or without CAS (Strand et al., 2012). The DEMSS must be administered by a
clinician, preferably an SLP with experience and training in DEMSS administration (Strand et al.,
2012).
Goal/Purpose of The Dynamic Evaluation of Motor Speech Skill. The goals and purpose
of this assessment is to determine the child’s diagnosis of CAS (Strand et al., 2012). The
assessment is criterion referenced which means that the assessment is measured based on a
fixed set of predetermined criteria (Wortham & Hardin, 2016). The administration time is
estimated to be seven to twenty-five minutes based on the child and how many levels will be
Con of The Dynamic Evaluation of Motor Speech Skill. The DEMSS assessment does
come with a small number of disadvantages. The assessment has an 89 percent test-retest
reliability, which means that there is an 11 percent chance that the child may be retested and
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receive different results. This can also connect to the disadvantage that some children who
have more mild symptoms of CAS may be missed by DEMSS (Strand et al., 2012).
The Differential Ability Scales-II (DAS-II) is an assessment tool that gives insight into how
a child cognitively processes information in the classroom so that a child’s IEP team can
determine what interventions would be best for the child in the classroom and at home (Elliot,
2020). This assessment can be used for children with CAS as they may exhibit delays or
impairments that are related to cognitive abilities (Gildersleeve-Neumann, 2007). The DAS-II
includes 20 cognitive subtests that are organized into early childhood and school aged children
based on the age and grade of the child taking the test (Elliot, 2020). The assessment
administrator required a Level C qualification which means that the administrator must hold a
doctorate degree in psychology (PhD), education (EdD) or a related field (Pearson Assessments,
2020).
strengths and weaknesses in their learning and cognitive abilities in order for the IEP team to
create appropriate IEP interventions, goals and progress monitoring for the child (Elliot, 2020).
The assessment is created in multiple languages and can predict achievement on the basis of
different cultures and background of children (Elliot, 2020). Clinical studies have been done
disorders such as CAS, ADHD, limited English proficiency and children who are deaf and hard of
disadvantage that is connected to the assessment is the qualification level needed for the
administrator. The qualification level for this particular assessment is Level C (Elliot, 2020). This
means that unless an administrator has a PhD, EdD, or a state licensure or certification to
administer this assessment, it may not be bought or administered (Pearson Assessments, 2020).
Another disadvantage to this assessment is that it is scored from the administrator’s computer
that uses software that is not compatible with Mac OS computers (Elliot, 2020).
considerations when it comes to special education and assessment strategies that are used with
children who follow an IEP. Ethical philosophy is a large part of early childhood and special
education (NAEYC, 2011; DEC, 2009). Children who have been diagnosed with a disability by
their doctor such as CAS or even CP will have confidential information that should be shared on
a need-to-know basis, and their records are held confidentially using HIPAA (HIPAA, 1996).
Children who are students at public schools will have their right to privacy under FERPA (FERPA,
1974). General and special educators have the ethical responsibility to hold themselves
accountable when it comes to keeping children and family educational and medical information
private (FERPA, 1974; HIPAA, 1996). Each of the assessments that are mentioned above should
be done lawfully and appropriately with the child’s family knowingly consenting to the
assessment and IEP evaluation. Although some educators may believe that they know what is
best for a child who has a disability, it is still the family’s decision on if they would like the child
to receive services and intervention (DEC, 2009). The DEC and NAEYC code of conduct help
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early childhood teachers, general and special educators to have something to fall back on if
Evidence-Based Interventions
Special education supports and services for children in the primary grades facilitates
growth and development for children with (dis)abilities. Special education services are supports
that are given to children with disabilities who are the ages three to twenty-one under Part B of
IDEA (2004) law. School S (2020) that has been written about above works with children who
have disabilities within their learning center and the classrooms as they believe that learning is
social. This section will cover evidence-based interventions to help children reach their IEP goals
in speech, literacy and cognition by using integral stimulation, early intervention in reading, and
self-regulated strategy development for cognitive awareness (Strand, 2005; WWC, 2008; WWC,
2017).
Children with CAS require intervention most of the time, and although SLPs are the
professionals who decide which evidence-based intervention is the best for the child, the family
of the child plays an even more important role in the development of speech for the child with
CAS because they spend the most time with them (Hammer, 2009). Integral stimulation is an
intervention that uses a bottom-up approach, which means that is starts with short, phonetic
utterances and graduates to longer more phonetically difficult stimuli (Strand, 2005). Integral
stimulation involves cueing and an SLP or family member asking the child to listen, watch and
stimulation and is adapted from intervention for adults with apraxia to children with apraxia.
The child approach has the SLP speak an utterance and the child will try to imitate the
utterance. If they are unsuccessful, then they will simultaneously say the utterance together
slowly while the SLP makes sure that the child’ lip and jaw position are correct (Strand, 2005).
This intervention strategy would be done in a separate room than the general education
classroom and it would be direct one on one work with an SLP and a family member can
Early intervention in reading is a program that is used for children who may be at risk for
difficulties in reading (WWC, 2008). Some children with CAS may be at risk for reading
difficulties, and others may be on track for reading for their grade level. Assessments like DAS-II
can help to determine if a child with CAS needs intervention in reading. This intervention is
used in the primary kindergarten through fourth grade classes. In grades K-2, the program is
used during whole-class instruction with picture books to stress phonemic awareness, phonics,
contextual analysis and repeated reading and writing. Within these grades, struggling readers
can have additional small group instruction for 20 minutes, four days a week (See Appendix F)
(WWC, 2008).
Within the kindergarten setting, the early intervention in reading program focuses on
the children listening to stories, and learning about print, rhyme, and phonemic awareness,
letter and sound recognition (WWC, 2008). In the first and second grade classrooms, the
program focuses on repeated readings of stories, coached reading with stories that the children
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have not read before, and phonemic awareness with phonics instruction (WWC, 2008). This
who have a specific disability like CAS who need extra help with their cognitive surroundings
and completing tasks. Some children with CAS may need extra help with completing tasks,
while others may be on tract cognitively. Assessment tools like the DAS-II may help the IEP
team determine if the child needs an intervention for cognitive awareness. SRSD is similar to
integral stimulation (Strand, 2005) in that it is a bottom-up strategy where special educator or
general educator will work one on one with a child to discuss the strategy, model the strategy,
help the child memorize the strategy, support the strategy and then watch the child complete
the task (WWC, 2017). In the realm of early childhood, this intervention tool can be used with
children who are in second and third grade who are learning about self-regulation strategies for
Progress Monitoring
Progress monitoring is something that is done throughout a child’s IEP and can be done
in different ways. Specifically, with integral stimulation, the progress is constantly being
monitored, because of the nature of the intervention strategy. The child must have completed
simple utterances, the child will move onto more difficult stimuli within the program (Strand,
2005). Within intervention in reading, because it can be done as a whole class or in smaller
groups, the child(ren) may be monitored by taking data throughout each season (fall, spring) to
determine if they have improved (WWC, 2008). Similarly, the child’s IEP team will hold a review
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one a year or more if needed to determine if the child has improved in each of the subjects that
are being worked on (Brilliante, 2017). Lastly, with SRSD, the child’s progress will be monitored
throughout the development of each task that they are working on. The IEP team will work
together closely throughout the time that the child is using interventions, and assessments that
monitor developmental progress can be used with children throughout their schooling.
Educators and SLPs can use assessment strategies that can be used to monitor a child’s
progress and score them throughout the year to determine if the child is making progress in
Reflection on Learning
Overview
Early childhood is a time where a lot of development happens, and children with
(dis)abilities can make a lot of progress when they have a team of professionals working
together on their IFSP or IEP to help them gain lifelong skills (Brilliante, 2017). Early childhood
ranges from birth to about eight years of age and a lot of development happens through those
years. Children who have (dis)abilities can take advantage of early supports and services and
special education in order to learn from professionals who use assessments and evidence-
based interventions.
Throughout this semester and writing this research, I have a newfound love for special
educators and the work that they do. While doing research, I learned all about speech-language
pathologists and the important work that they do to help children learn about speech and
language. One piece of this research that was meaningful and important to me was the idea
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that speech and language are similar, yet different. Although I had a small understanding, once
learning about the difference, it became clear to me that I want to learn even more about the
This research has given me a lot of new understandings. I learned about how hard work
IEP and IFSP processes can become, yet how important assessments are for determining the
child’s development. One that especially connected with me was the DAYC-2 assessment
(Pearson Assessments, 2020). This assessment measures so much about a child and can tell a
practitioner a lot just by watching a child play and interviewing their caregivers. I also think that
this research has given me a different perspective on children with (dis)abilities. Having never
quite worked with children with (dis)abilities, I think I can have a deeper understanding of the
IEP and IFSP process and if I am a part of a team one day I can look back on my knowledge from
this class and this research and reflect. Although I do not have any remaining questions from
this research, I do think that although I never was able observe in the field, my research from
this paper has given me a deep understanding of the two disabilities of cerebral palsy and
Research Process
different way from how I had learned it in past coursework. Learning about it in this way has
shaped my understanding to know that the IDEA law is there to help families get the
information and support that they need when their child us in school and early supports. It
helped me to understand the IFSP and IEP process by writing each step and reflecting on how
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the steps are used in processes for children with (dis)abilities. When engaging in this work, I
was mostly challenged by finding reputable sources to fall back on. However, once I found the
resources that are true and accurate based on the peer edited work, I felt great knowing that
what I am learning about is shaping my knowledge of early childhood and special education for
references that are reputable versus those that are not. Through the semester I used time
management skills so as to not become overwhelmed with the amount of work that I had set
up for me.
Advocacy
In my opinion, advocacy is one of the most important pieces of early childhood. Children
are some of the most vulnerable people, and when they have a (dis)ability, professionals who
understand the ins and outs of special education and early supports and services are there to
advocate for that child and their family. The DEC code of Ethics and the NAEYC Code of Ethical
Conduct (NAEYC, 2011; DEC, 2009) are two important documents that give professionals a leg
to fall back onto if there is ever a question of advocacy. In the future, I hope to enter the special
education field and become an advocate for children and families. I can become an advocate
for them by becoming as educated as I can and understanding the laws so that families can feel
comfortable asking me any question and I can help them reach the goals that they need for
This semester has been unique for every student everywhere, and I think as a person
and a professional, I have grown. I have gained new skills of how to manage my time under
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difficult circumstances, and specifically working diligently to achieve success (Keene State
College Education Department, 2007). The work overall from this course has helped me grow as
a writer. I have reflected on the legal and ethical obligations of not only early childhood, but
also special education and the laws that back up the profession. Lastly, I have become
committed to professional growth and development with the finding and completing of
Conclusion
and student. As I continue my work in education, I will have a better sense of special education
and early childhood alike. My newfound knowledge of special education has helped shape me
Albertson-Grove, J. (2020, February 16). Report: 3.5% of NH babies monitored for opioid or
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http://web.a.ebscohost.com/ehost/pdfviewer/pdfviewer?vid=5&sid=16fc6a3d-cada-
4543-ae40-ec0e28e9191c%40sessionmgr4006
https://my.doe.nh.gov/profiles/profile.aspx?d=279&year=2017&tab=student
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Assessments/Cognition-%26-Neuro/Comprehensive-Ability/Differential-Ability-Scales-
II/p/100000468.html?tab=product-details
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case study. Child Language Teaching and Therapy, 27(1), 9-20. DOI:
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This artifact is a detailed description of the children’s services that Program Y offers. This
artifact explains the programs evaluation process and the services that are available to children
(Program Y, 2020)
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Appendix B
This artifact is a screenshot of the main points of Subchapter I, also known as Part A of
IDEA (2004). This elaborates on the different topics covered in Part A of the IDEA Law. The first
subchapter has many points and there are too many to fit in the Description of IDEA Law in this
paper.
(IDEA, 2004).
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Appendix C
scoring sheets. It shows what type of questions are asked for this assessment and how it is
scored. It is scored by putting a 1 next to an action that has happened and putting a 0 or blank
(Ford, 2015).
Appendix D
This artifact is the mission statement from School S (2020) that explains deeper what
the mission statement of the school is and each of the skills that the school is working toward
each of the children learning so they can become contributing members of the community.
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(School S, 2020)
Appendix E
This artifact is the special education statement from School S (2019) that explains the
IDEA law and how the school works with the law, how a child is referred, evaluated, and how
the family is involved within the IEP process. This artifact explains the learning centers and how
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they are used at School S, as well as documents that are available to families to understand the
process and their legal rights that are written in the document.
(School S, 2019)
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Appendix F
This artifact is a deeper description of the Early Intervention in Reading program. This
program is a simple intervention that requires teacher training that had many more parts to it
(WWC, 2008).
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Appendix G
Dispositions Assessment
This artifact is the dispositions given by the Keene State College Education Department
that is written briefly about under growth as a professional and educator. The explanation is
brief, so the artifact is included to give the reader an understanding of what the dispositions
are.
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