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NAMI Nevada County We help individuals and families learn about mental illnesses-provide support, educate, and advocate.

11/02/2026
11/01/2026

What a great story!!! He’s quite an actor….really…..

Caregivers matter!!!!!
11/01/2026

Caregivers matter!!!!!

Kicking off National Family Caregivers Month this November, TAC staff members Leslie Carpenter and Jerri Clark shared lived experiences and professional expertise at a two-day conference in Norwalk, Connecticut.

The conference brought together advocacy leaders from across the United States to consider vital work that uplifts families while moving the system toward reform.

Thank you to the Center for the Treatment and Study of Neuropsychiatric Disorders at Silver Hill and Dr. Michelle Sherman for hosting this important event and to the attendees for their perspectives and insights. We are so grateful to be a part of this movement for better care!

Excellent
10/31/2026

Excellent

WHY CRISIS SYSTEMS MUST UNDERSTAND ANOSOGNOSIA

How can a crisis system effectively help someone with a serious brain disorder if it does not understand that the illness itself may prevent that person from recognizing they are sick?

Imagine a mother calling crisis services because her adult son is experiencing severe psychosis. He has stopped taking medication, barely sleeps, talks to people who aren't there, and believes his family is conspiring against him. He has stopped caring for himself, and his condition is deteriorating.

When crisis responders arrive, they ask him whether he needs help.

He calmly replies, “No. There's nothing wrong with me.”

He may even appear composed during the brief evaluation. He answers simple questions, knows his name and where he is, and insists that his family is exaggerating.

The responders leave.

The mother is devastated because she knows what happens after they are gone. She has witnessed the sleepless nights, the delusions, the inability to function, and the gradual deterioration. Yet her son's statement that he does not need treatment may carry more weight than the history of serious symptoms she is trying to communicate.

This is why understanding anosognosia is so important.

Anosognosia is an impairment in a person's ability to recognize their own illness. It can occur in individuals with schizophrenia, bipolar disorder, and certain other serious brain disorders. It is not simply stubbornness, ordinary denial, or a deliberate refusal to acknowledge the truth.

A person experiencing anosognosia may genuinely believe they are healthy, even when their symptoms are severe.

If crisis responders do not understand this, they may mistake a symptom of the illness for evidence that the person does not need help.

That misunderstanding can have devastating consequences.

Families may repeatedly call for assistance, only to be told that their loved one is refusing treatment or does not meet the legal criteria for involuntary intervention. Meanwhile, the person may continue deteriorating, lose housing, become increasingly vulnerable, or eventually experience a crisis requiring emergency hospitalization.

We must recognize that anosognosia does not automatically mean someone lacks decision-making capacity, and it does not by itself justify involuntary treatment. Individual rights, legal safeguards, and careful clinical assessments are essential.

But a person's statement that they are not ill should not automatically end the evaluation when credible evidence suggests otherwise.

Crisis systems should be trained to recognize anosognosia and understand how it may affect a person's perception of their condition. Responders should consider documented treatment history, changes in functioning, basic self-care, previous crises, and information provided by family members or other people who know the individual well.

Families can generally provide relevant information to healthcare professionals even when privacy laws limit what professionals may disclose in return.

A brief conversation cannot always reveal the full extent of a serious brain disorder. Someone may appear calm during an evaluation yet experience severe symptoms at other times.

This is why we need meaningful crisis assessments—not simply a few questions followed by a decision that nothing can be done.

The Brett M. Staples Brain Disorder Awareness Coalition believes crisis-response systems should include:

Training on anosognosia for emergency responders, law enforcement, hospital personnel, and crisis professionals.

Meaningful consideration of family observations, including documented changes in behavior, functioning, and safety.

Comprehensive clinical assessments that examine more than whether someone verbally agrees that they need help.

Earlier access to appropriate treatment, including intensive community services and legally safeguarded interventions when eligibility criteria are met.

Clear follow-up plans when a person does not qualify for immediate involuntary intervention but continues to show signs of serious deterioration.

Understanding anosognosia will not solve every crisis. But failing to understand it can leave some of our most vulnerable citizens without appropriate care.

We should not confuse an inability to recognize illness with an absence of illness.

And we should not require families to wait for tragedy before their concerns are taken seriously.

OUR MESSAGE TO POLICYMAKERS AND CRISIS-RESPONSE PROFESSIONALS:

If you work with people experiencing serious brain disorders, understanding anosognosia should be an essential part of your training.

Because recognizing the illness is often the first step toward providing effective treatment.

Related free Coalition guide: Understanding Anosognosia Without Shame

Visit brettstaples.org to explore our educational guides.

Serious no fault brain disorders are not a choice.

Anosognosia is not simply denial.

Better understanding can lead to better intervention.

Share to spread awareness.

Presented by the Brett M. Staples Brain Disorder Awareness Coalition

🌐 brettstaples.org
📧 [email protected]

10/31/2026

🍂 The Future Begins with a Conversation

As October comes to a close, we've recognized the importance of estate planning, and special needs law for individuals with disabilities.

But one important message connects them all:

Planning ahead creates opportunities for a more secure future.

For parents, siblings, grandparents, and caregivers, questions about the future can sometimes feel overwhelming.

Who will help manage financial resources?

How can we protect essential benefits?

What happens when a caregiver can no longer provide the same level of support?

A Master Pooled Special Needs Trust can be an important part of answering these questions.

At Proxy Parent Foundation, we believe families should have access to information and options that help them make informed decisions about their loved one's future.

You don't need to have every answer today. Sometimes, the most important first step is simply beginning the conversation.

💙 Plan today. Protect tomorrow. Preserve peace of mind.

📅 Schedule a complimentary informational meeting:

https://calendly.com/clarkin-proxyparentfoundation/ppf-info-call

10/29/2026

Good pound!!

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