Pulse Center for Patient Safety Education & Advocacy Marks Autism Awareness Month with Advice About Doctor and Hospital Visits           

By Arlene Reith
Parent / Patient Safety Advocate                                                                                                                                                                              April 2018 (Re-posted 2019)

April is Autism Awareness Month, and Pulse Center for Patient Safety Education & Advocacy asked patient safety and parent advocate Arlene Reith for her advice about helping a person with autism — especially a child

— have a successful visit to the doctor or hospital.

Reith’s insights were gained the hard way, by personal experience. “I’m the parent of two children,” she says, “both diagnosed with Down syndrome and autism, who are non-verbal. In addition I spent 4 and a half years in and out of a hospital with our son who was diagnosed at age nine with A.L.L. leukemia and

died at age 13. We were told that our son was given the wrong chemotherapy only days before he passed, but were assured it should be without consequences. That is the reason I have dedicated myself to teaching parents, family members, care- givers, and staff about the importance of Patient Safety.”

Dealing With Sensory Disorders in a Doctor’s Office or Hospital Setting.

The very first thing you want to share with your child’s/family member’s health care providers in a doctor’s office or hospital setting is, “Just because my child/family member doesn’t speak, does not mean that his/her hearing is not outstanding.  Please do not speak of our child in the third person.  We are all in the same room!”

First, we must concentrate on the patient’s abilities:

• I can’t speak. But, I can hear — Talk to the patient.
• Finding the patient’s strength — Take the time to learn what works.

Communication, Hearing and Speaking:  Remember the patient may only hear pieces of words or sometimes nothing at all because of:

• Too many sounds around; therefore, keep yourself or a trusted aide close by.
• Let the patient find their own words, even if they’re not words you would use.
• Use pictures.

Consider the surroundings (environment) such as:

• Too many lights/flickering.
• Too much noise.
• Smell sensations.
• Moving too fast.

Consider Visual, Taste and Smell:

• Distracted by visuals
• May become disorganized
• Rigid about what to eat
• Texture of foods
• May crave sharp tastes and smells

Tactile System:  Inform your health care providers with the following if they apply to this patient.

• Touches people and objects constantly, needs heavy compression (eg. weighted blanket, weighted vest) to localize.
• Pica (bites nails, pencils, shirt, etc.)
• Self-imposed isolation, distractibility, hyperactivity, negative response to light touch.
• May not register pain.
• May not feel it at all.

Reith concludes, “I stress the importance of preparing an “All About Me” booklet, folder, or computer file with much of the above info and giving it to your child or other family member’s health care providers.”

“We are their VOICE, we owe it to those we hold dear to share our understanding with others.”