3: At the Doctors: A List of Suggestions for Medical Practitioners

For autistic adults, the barriers to accessing health care can be substantial. Not only are autistic adults more likely to live in poverty and less likely to have access to quality medical care, they may face practical barriers such as lack of transportation to appointments and difficulty in navigating a healthcare system that relies heavily on verbal communication.

Those of us who do have access to health care often discover that our health care providers, including those in the mental health field, are unfamiliar with the needs and challenges specific to autistic patients. While each autistic adult has a unique set of needs, there are some accommodations that could address common challenges faced by many adults on the spectrum.

The suggestions that follow are divided into two categories: improving access to care and improving the quality of care. The access section focuses on reducing communication barriers between health care providers and their autistic patients while creating richer sources of information for both parties. The quality section focuses on practices that providers can use to accommodate differences in communication and sensory processing that autistic patients experience.

Improving Access to Care

Provide text-based communication options. Many autistic people have difficulty using the telephone. Some of us have Central Auditory Processing Disorder, a condition that makes it difficult to process speech, especially over the phone. Some of us are nonspeaking or have difficulties with speaking fluently to strangers. And some of us just find the telephone to be a challenging means of communicating. Text-based options for making appointments, asking follow-up questions and obtaining test results can increase accessibility and improve the quality of interactions with health care providers.

Provide longer appointment slots. Many autistic adults need additional processing time, particularly when communicating with people they don’t know well. Some experience difficulties with speech when they feel rushed or pressured. Others use AAC, typing to communicate, which can be a slower process than spoken communication. By setting aside longer appointment blocks for those autistic adults who need a slower-paced visit, providers can improve communication and ensure that their autistic patient’s needs are being addressed.

Create databases and directories of autistic-friendly providers. Within the medical system, there is still a great deal of stigma and misinformation about autism and autistic adults. Some health care professionals are willing to work with autistic adults to make care more accessible while others are less accommodating to neurodivergent patients. Identifying providers across all specialties who provide accessible and sensory-considerate care and creating a clearinghouse of this information via autistic-run nonprofits could reduce the number of negative experiences that autistic adults have with accessing appropriate treatment. The Autism Women’s Network has an initiative to identify sensory-considerate women’s health providers that could serve as a model for grassroots, crowdsourced directories of other types of providers.

Use personalized accommodations reports. AASPIRE is developing an interactive online tool that creates a detailed, personalized list of accommodations applicable to health care situations. When the interactive tool goes live this fall, Autistic adults will be able to complete the interactive questionnaire, compiling information about their sensory sensitivities, communication preferences and other key topics, and then receive a personalized report to share with their doctors. The AASPIRE website also has a wealth of healthcare-related information and resources for autistic adults and providers who work with autistic individuals.

Improving the Quality of Care

Use visual aids as well as verbal explanations. Many of us are visual thinkers or prefer to have visuals to support verbal communication. By using visual aids such as models, photos, drawings, videos or other graphics, health care providers can ensure that their autistic patients have a more complete understanding of procedures, tests and other medical information.

Always speak to the autistic person directly. If an autistic patient attends an appointment with a caregiver, loved one or support person, this does not necessarily mean that the autistic patient is unable to communicate their needs or make decisions about their health care. Providers should presume competence by speaking directly to autistic patients and allowing them to decide what role their support person will play. Similarly, if an autistic person communicates by typing, health care providers should address them directly and wait for them to reply using their AAC device. Because a person is nonspeaking does not mean that they do not understand speech.

Ask specific, concrete questions. Open-ended or vague questions can be challenging for autistic individuals. Concrete questions such as “When did your pain begin?” and  “Is your pain constant or does it feel more or less painful at certain times of the day or night?” are more cognitively accessible than open-ended prompts like “Tell me about your pain.”

Recognize that autistic people have atypical sensory processing. Many autistic individuals perceive pain and other interoceptive (internal) sensations in atypical ways. This may lead to an autistic patient not feeling an expected degree of pain for a condition, feeling a great deal more pain than is typical, or not being able to accurately describe the type or amount of pain they are experiencing. Autistic people may also have difficulty with sensing other typical physical sensations such as elevated heart rate or abnormal body temperature. This can create an apparent lack of certain key symptoms, potentially resulting in misdiagnosis.

Communicate in advance before touching a patient. Tactile sensitivity is common in autistic individuals and can be a significant source of stress and discomfort. Health care providers can lessen the stress of patients with tactile sensitivities by explaining where and how they will touch a patient and working with patients to minimize the impact of procedures that might trigger tactile sensitivities. For example, firm touching is usually less likely to trigger a negative reaction than light touching. In some cases, a patient may be able to mitigate the impact of touch by stimming or assuming a comforting position on the exam table (such as curling up tightly in the fetal position). However, most autistic adults will only use coping strategies like this if they have a high level of trust with their health care provider and are actively invited to do so.

Be aware that some medications can affect autistic individuals in atypical ways. Anecdotally, many autistic adults report experiencing unusual side effects of medications–including the side effects listed as “less common” or “rare”. This lived experience is backed up by research on the effects of psychotropic drugs in autistic children (Santosh and Biard, 2001). It has also been observed by some clinicians that autistic people respond differently to drugs than typical people do or that autistic individuals may require lower than usual dosages to obtain the expected results. By communicating with patients regarding the expected effects of a new prescription and following up to identify any unexpected outcomes, doctors can optimize the effectiveness of medications for autistic individuals.

Provide sensory-considerate care. Sensory sensitivities can make medical visits uncomfortable or even unbearable. This discomfort can be lessened by asking autistic patients about sensory sensitivities that may be affected during their examination, procedures or tests. A cold speculum may be uncomfortable for a typical patient but feel unbearably painful to an autistic patient with a sensitivity to cold. The scent of a cream or medication may be inoffensive to most people but make an autistic patient nauseous or dizzy. Sensory sensitivities can be managed but they aren’t something that an autistic patient simply “get over” or ignore. It is important for health care providers to take sensitivities seriously and work with patients to minimize or mitigate any sensory challenges that may arise during their appointment.Implementing accommodations that make health care more accessible to autistic patients can create a win-win situation by improving the effectiveness of care and enhancing quality of life for adults on the spectrum.

 

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Author: health matters for aspergers syndrome women

Based in New Zealand. As a senior woman now aged 69, I grew up in an era when professional and public ignorance of Asperger's Syndrome was total, and people on the ASD spectrum were often misdiagnosed and badly treated because doctors did not understand the ASD is a neurological condition, a neurodiverse difference, not a psychological illness. I am interested in the lived experience of AS people. ASD is not a set of tickboxes in some diagnostic manual of dubious validity which change every few years. ASD is as fundamental a part of people on the spectrum as neurotypicality is to neurotypicals. I live in the hope of better outcomes for all people on the spectrum, while speaking from the Asperger's Syndrome part of it.

One thought on “3: At the Doctors: A List of Suggestions for Medical Practitioners”

  1. Since posting the article by Celia Lim, I have found the best workaround (so far) for facilitating good communication during a GP consultation was to begin the session by stating how the consultation would work better for me. Basically it came down to sharing this:
    “I wonder if you would mind if we do thinks a little differently from now on. You see, the rapid question and answer back and forth interview style doesn’t really work for me, and triggers anxiety which makes it harder for me to provide the information you need. It would be much more helpful if I could share the information that I need to communicate while you listen, and then we switch to your input while I listen. After that we can discuss any need further exploration by you. Would you be willing to do that?”

    The GP immediately agreed, let me speak for five minutes while he listened attentively without interjections, and then we swapped over. It worked extremely well, my medical needs were heard and met and his time and information needs were met, and this was the least stressful medical encounter I have ever had.

    Liked by 1 person

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