We asked Ms. Theresa Morris-Brown if she could reflect and offer advice to other parents from her lived experience. What would she do differently. Also, if she could advocate for system change for other families who struggle with trying to help their children, what would she tell others in North Carolina. Here’s what she said:
These are some of the things I would I do differently…
- Get a FASD diagnosis earlier
- Question and/or challenge each diagnosis received
- Insist on more thorough testing and follow-up regarding behavior issues
- Obtain more appropriate services earlier
Here are suggested changes in systems to help increase better outcomes for children and youth with suspected FASD…
Education system:
- Screen for FASD in Kindergarten
- Train school counselors regarding FASD and suspected behaviors
- Provide services other than Special Education
Social Services:
- Screen all children as they enter foster care
- Develop services for older FASD clients (jobs, housing )
- Encourage faster clearing of waiver wait-list
- Work with Vocational Rehab
- Make it easier to qualify for financial assistance
Mental Health:
- Educate service providers that FASD is NOT a mental illness
Criminal Justice:
- Train probation officers in FASD and behaviors
- Educate lawyers and judges
- Develop more community corrections options (other than probation)