Early Intervention ("EI") is an integrated developmental service, offering both evaluation and therapeutic services to children birth to three years of age for whom there are developmental concerns due to biological, medical or environmental factors. EI services are provided individually in the home, in small integrated groups at our center and in a range of community settings. A variety of parent support, educational and resource referral services are also provided.
The First Early Intervention Program works in collaboration with community resources such as center based day care, family day care, Family Network services, schools services, Head Start, and private therapy services in the area. We provide individualized services to families, attempting to meet their scheduling and therapeutic needs. Service plans are individualized and flexible in order to meet the changing needs of the child and family.
Evaluations for all infants and toddlers;
Service Coordination;
Individualized therapeutic services in speech, occupational, and physical therapy, developmental education, social work, and counseling;
Transportation
Referrals to specialty providers including low vision, hearing impairment, and autism services
Transition planning with special education providers and private pre-schools
Training for community child care providers
For more information, please contact First Early Intervention at 781-331-2533 or email to First Early Intervention Email
The following is a list of items that are generally needed year-round by First Early Intervention. Any donations of these items would be greatly appreciated.
Thank you for your generosity!
| Various sizes of zip lock storage bags | Preschool painting smocks |
| Portable tunnels | Velcro play food |
| Bingo Daubers | Pens |
| Beans, oatmeal, and rice | Cozy Coups |
| Clorex wipes | Non toxic finger paints |
| Tissues | Vinyl gloves |
Plants for outdoor landscaping |
|
Thanks.
First Early Intervention Staff
Autism Consortium Phenotypic & Genetic Factors Study
What are we studying?
We hope to learn more about possible genetic causes of ASDs. We want to better understand the behaviors of individuals with ASDs and their family members. We think that it is important to examine behavior and genetics together to learn more about ASDs
Who can participate?
To be eligible participants must:
• Have an ASD diagnosis
• Be at least 24 months old
Parents and some siblings will also be asked to participate in the study.
What does participating in this research study mean?
The study will involve providing a blood sample.
Each participant will also have an assessment that may include IQ tests, medical/family history forms, questionnaires, and behavioral observations. Some of the testing can be done in the family's home, if preferred. Agreeing to participate in this study will also give study researchers permission to view participants' medical records.
How will participants be compensated?
• Participating families will receive:
• Gift cards for each child
• Lunch vouchers for onsite visits
• Free parking
At the conclusion of participation, the results of the testing performed on the child with an ASD will be summarized in a report. The report will be reviewed with the family by a psychologist.
The Goals of this Study Are:
To discover new genes involved in ASDs
To establish a comprehensive and efficient assessment battery for improved evaluation of individuals with ASDs
To better understand characteristics of the whole family, such as medical history, to determine if there is a correlation between these family characteristics and any genetic differences so that we may better understand the gene(s) involved in ASDs.
The study is being conducted at all of our clinical sites in Massachusetts, including UMass Medical School, or can be performed at the family’s home. At the conclusion of the study, a detailed report of the assessment results for the family member with an ASD will be provided. The report will be reviewed with the family in-person or by phone if preferred. This valuable report and consultation is provided at no cost to families participating in this study.
For more info contact:Jean A. Frazier, M.D. or Carol A. Hoffman, Ph.D., M.S., LGC, Principal Investigator Genetic Counselor/Research Psychologist, Vice-Chair of Child and Adolescent Psychiatry Child and Adolescent Psychiatry UMass Medical School, UMass Medical School Worcester, MA 508-856-5055
Autism Speaks
www.autismspeaks.org
Keeping Pace with Multiple Miracles
www.keepingpace.org
Zero to Three Magazine
www.zerotothree.org
Massachusetts Early Intervention Consortium
www.maeic.com
Federation for Children with Special Needs
www.fcsn.org
Family Ties of Massachusetts
www.famties@fcsn.org
Massachusetts Down Syndrome Congress
www.mdsc.org