Date: April 22, 2026Attorney: Richard I. Miller

Talking about end-of-life care is never easy. Many families avoid the topic altogether, even though most people understand how important these conversations are. According to The Conversation Project, while 92% of Americans believe discussing end-of-life wishes is important, only 32% have actually had the conversation.

For families who care for a loved one with an intellectual or developmental disability (IDD), these discussions can feel even more complicated. Parents, siblings, and caregivers often want to protect their loved one from distress or worry that the person may not fully understand the subject.

But individuals with IDD deserve the same opportunity as anyone else to express their wishes, ask questions, and participate in decisions about their own lives, including their medical care and end-of-life preferences.

As special needs planning attorneys, we often remind families that these conversations are not about focusing on death. They are about respecting autonomy, protecting dignity, and ensuring a person’s voice is heard in the decisions that matter most.

Why End-of-Life Conversations Matter

Honoring Autonomy and Dignity

Every individual has the right to participate in decisions about their body and medical care. Organizations such as The Arc and the National Down Syndrome Society emphasize the importance of person-centered planning throughout a person’s life, including during serious illness or at the end of life.

Even when a guardian or caregiver helps make decisions, understanding the individual’s preferences allows families and professionals to honor their values.

Reducing Fear and Uncertainty

Many individuals with IDD are highly perceptive and may sense when something is wrong. Avoiding conversations about illness or death can sometimes create more anxiety than the discussion itself.

Open, honest communication can help reduce fear and allow the individual to ask questions in a supportive environment.

Improving Medical Decision-Making

When families know their loved one’s wishes, they can make more informed decisions during medical emergencies. These conversations can help:

  • Align treatment with the person’s values
  • Avoid unnecessary hospitalizations
  • Reduce stress for caregivers during difficult moments

Supporting Healthy Grief and Emotional Preparation

People with IDD experience grief just like everyone else. When they are included in conversations about illness, loss, and death, they often cope better when those experiences occur.

Providing space for questions and emotions helps build emotional resilience and understanding over time

When Should These Conversations Begin?

Start Before a Crisis

Ideally, discussions about end-of-life care should begin long before a serious illness or emergency arises.

Starting early allows families to:

  • Introduce topics gradually
  • Revisit conversations over time
  • Reduce the pressure of making urgent decisions

For individuals with IDD, having multiple conversations over months or years can make complex topics easier to understand.

Use Natural Life Moments

Certain events may naturally open the door to discussions about illness and death, such as:

  • The death of a family member or pet
  • Transitions to adulthood
  • Estate planning or guardianship discussions
  • A new medical diagnosis
  • Changes in living arrangements

These moments can help introduce conversations about treatment preferences, funerals, or grief in a way that feels more natural.

Listen When They Bring It Up

Many individuals with IDD are aware of aging and illness and may ask questions about these topics. When they do, it may be a meaningful opportunity to start the conversation in an age-appropriate and supportive way.

How to Talk About End-of-Life Care

Use Clear and Direct Language

While it may feel uncomfortable, using clear and honest language is important. Euphemisms like “going to sleep” or “passing away” can sometimes be confusing.

Instead, use simple and direct terms such as “dying,” “death,” or “serious illness.”

Explain one idea at a time and check for understanding by asking the person to explain the concept in their own words.

Adapt to the Individual’s Communication Style

Every individual communicates differently. Families and caregivers can make conversations more accessible by using:

  • Pictures or visual aids
  • Social stories
  • Communication boards or devices
  • Body diagrams
  • Short, repeated discussions instead of one long conversation

Breaking the topic into smaller conversations can make the information easier to process.

Offer Concrete Choices

Abstract questions can be difficult for anyone, especially individuals with IDD. Instead, offer specific and relatable options, such as:

  • “If you were very sick, would you want to be at home or in a hospital?”
  • “If a machine helped you breathe, would you want it only to help you get better, or not at all?”
  • “Who would you trust to help make decisions if you couldn’t speak for yourself?”

Providing clear choices helps individuals express their preferences in meaningful ways.

Include Trusted Supporters

These conversations often benefit from the involvement of trusted individuals, including:

  • Family members
  • Long-term caregivers
  • Direct support professionals
  • Case managers
  • Health care providers familiar with IDD

Supporters can help explain medical concepts and reinforce understanding.

Give Time, Reassurance, and Patience

These discussions rarely happen in a single conversation. It is normal, and healthy, to revisit them multiple times.

Families should allow time for emotions, answer questions honestly, and reassure their loved one that they will always be supported.

Once an individual’s preferences are understood, it is important to formally document those wishes.

Depending on the situation, this may include:

  • Advance directives
  • MOLST or POLST forms (depending on the state)
  • Guardianship arrangements
  • Supported decision-making agreements

These legal documents ensure that a person’s wishes are respected even if they cannot communicate them later.

A Compassionate, Person-Centered Approach

Planning for end-of-life care is not about expecting the worst. It is about respecting the individual, protecting their dignity, and ensuring their wishes are understood.

For individuals with intellectual and developmental disabilities, thoughtful conversations can create a sense of safety, trust, and empowerment.

When families approach these discussions with compassion, patience, and openness, they help ensure that their loved one’s voice remains at the center of every decision, throughout every stage of life.

The Special Needs team at Mandelbaum Barrett PC is here to help families ensure the proper legal protections are in place while honoring the individual’s voice. Contact us today to speak with one of our attorneys.

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