Living with FASD
People with fetal alcohol spectrum disorders (FASDs) may have neurological damage. Changes in the brain can be subtle to severe. There may be no physical damage. Seeing FASDs can be impossible!
People with fetal alcohol spectrum disorders (FASDs) may have difficulties processing information, with memory, focusing attention, impulsivity, etc. These issues can make living with FASD confusing and complicated not only for the person, but also for caregivers. Gaining a better understanding of the disorder and caregiver tips can help.
Since our best resources often lie in those with similar experiences, another useful tool is connecting with other caregivers.
Being a primary caregiver can be hard work! It is vitally important for the person with FASD that caregivers have breaks. Some caregivers might qualify for Respite Care, a program that strengthens families by helping make these breaks possible.
For additional resouces on helping families of children with developmental disabilities connect with services and benefits, please see The Arc of the US Family Resource Guide.
When concern exists about a possible FASD and no formal assessment has been completed, a medical evaluation may prove useful. A good starting point is always the primary physician.
