New Diagnosis - Now What?

Tips for Parents / Guardians of a Child with a New Diagnosis

One Step at at Time…

Learning for the first time that your child has a developmental delay, disability, or other condition that may affect their intellectual and / or physical development can be very overwhelming. Parents and guardians who have been through this before often say, “if only I knew then what I know now, things would have be a lot easier.”

The information below is a compilation of recommendations and helpful tips from parents and professionals to help you navigate the systems of support, know what to do next, and connect with beneficial services.

Helpful Tips

  • You are your child’s biggest advocate and sometimes only advocate so speak up and let your voice be heard. Knowledge is power so be prepared to be an active participant in your child’s care, services and school.
  • Don’t put limits on your child. When you receive new medical diagnoses, you will often hear the worst- case scenario for outcomes but that doesn’t paint your child’s picture.
  • You always have options and choices when it comes to the care of your child so don’t be afraid to find a new provider if you aren’t pleased with the one assigned to your child.
  • Go up the “chain of command” when you aren’t getting the information or answer that you need. Ask for a supervisor. There are all levels of experience and clout within the human service provider system so seek out an experienced veteran to help you if you get stuck.

 

Next Steps:

Below are possible next steps for you to consider to get started in identifying services and support for your child. Don’t feel like you need to call each one right now. Read through these suggestions and start with the one that seems most appropriate for your needs. Each organization on this list will have information that can help guide you through this process.

Contact South Carolina Department of Disabilities and Special Needs

South Carolina Department of Disabilities and Special Needs (SCDDSN). SCDDSN is the state agency that plans, develops, oversees and funds services for South Carolinians with severe, lifelong disabilities of intellectual disability, autism, traumatic brain injury and spinal cord injury and conditions related to each of these four disabilities. Call 1-888-DSN-INFO (376-4636) and visit http://ddsn.sc.gov,

To request eligibility determination over age three, call 1-800-289-7012.

Contact South Carolina Department of Health and Human Services (SCDHHS)

Contact South Carolina Department of Health and Human Services (SCDHHS) about South Carolina’s Medicaid program, called Healthy Connections, a health insurance program that pays medical bills for eligible low-income families and individuals whose income is insufficient to meet the cost of necessary medical services. “Katie Beckett” TEFRA is managed by Healthy Connections and provides benefits to certain children with disabilities who would not ordinarily be eligible because their parents’ income and/or resources exceed the limit. Visit healthcare.gov or call 1-800-318-2596 and visit https://www.scdhhs.gov/ for more information.

Contact South Carolina DHEC’s Children with Special Health Care Needs

DHEC’s CSHCN division serves “children and youth who have or are at risk for chronic physical, developmental, behavioral or emotional conditions and who also require health and related services of a type or amount beyond that required by children generally.”  Services include information and referral; care coordination and financial assistance with payment for medical services, supplies and equipment.

CARELINE at (800) 868-0404 (8am-6pm M-F) (864) 372-3064  http://www.scdhec.gov/Health/ChildTeenHealth/ServicesforChildrenwithSpecialHealthCareNeeds/

Call Family Connection of South Carolina

Call Family Connection of SC, a statewide nonprofit organization that connects families of children with special healthcare needs, disabilities or chronic illnesses with resources, support and education. Family Connection provides support to parents with a child or family member with any special healthcare need and is a family-to-family network with statewide offices to educate, inspire and empower families and their children to live rich, fulfilling lives in spite of many challenges. Contact 1-800-578-8750 and visit http://www.familyconnectionsc.org.

Call SC Autism Society (SCAS)

If your child received an Autism Diagnosis, contact the SC Autism Society (SCAS). SCAS provides information to parents and professionals about autism and available services and offers Case Management to individuals with autism spectrum disorders. Visit http://scautism.org/ and call (800) 438-4790.

Cerebral Palsy?… Check out the CP Tool Kit

The CP Tool Kit was designed to help you better understand and cope with the diagnosis of cerebral palsy. Created by parents of children with CP and leading experts in the CP field, this tool kit guides you through the initial diagnosis period, offering practical advice and relating first hand experiences to help you during this time. We know this time is difficult for you and your family. You are not alone. You may download a free digital copy of The CP Tool Kit by going to the CP NOW website and signing up for our mailing list: www.cpnowfoundation org. You may also purchase printed copies via Amazon: https://www.amazon.com/Cerebral-Palsy-Tool-Kit-Understanding/dp/1523496614/ref=sr_1_1?ie=UTF8&qid=1470752984&sr=8-1&keywords=the+cp+tool+kit