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In 1988, when Anne Fadiman met Lia Lee, then 5, for the first time, she wrote down her impressions in four spare lines that now read like found poetry:.

barefoot mother gently rocking silent child ¶ diaper, sweater, strings around wrist ¶ like a baby, but she’s so big ¶ mother kisses and strokes her ¶ The story of Lia, the severely brain-damaged daughter of Hmong refugees who had resettled in California, became the subject of Ms. Fadiman’s first book, “The Spirit Catches You and You Fall Down,” published in 1997. ¶ Its title is the English translation of the condition known as qaug dab peg (pronounced “kow da pay”), the Hmong term for epilepsy, from which Lia had suffered since infancy. ¶ In traditional Hmong belief, qaug dab peg, like many illnesses, is spiritual in origin, caused when the soul becomes separated from the body. A traditional cure might entail visits from a shaman, who would attempt to reunite body and soul.¶ A work of narrative nonfiction, Ms. Fadiman’s book is a cautionary tale about the cultural chasm between Lia’s family, with its generations-old animist beliefs, and her rationalist American doctors.

The health care bill emerging from a key Senate committee now includes expanded independent living options and autism insurance coverage, both of which are good news for people with disabilities, advocates say. The Senate finance committee agreed last week to include an amendment mandating insurance coverage for behavior treatments used with those who have autism. Similar legislation has passed in many states, but advocates say a federal mandate is key.

The governor\'s office is proposing $40.5 million in budget cuts.  $17 million would come from the Department of Public Health and Human Services.  The biggest cut would be $6 million in planned provider rate increases for doctors, child care and foster care providers, disability services and children\'s mental health services.

This Directory can help you find summer camps or programs for children with special needs and their siblings. The camps are listed alphabetically by sponsoring organization If your child is interested in going to a camp not specifically for children with special needs, call the camp for more information about including your child.Click here to download the Summer Camp Directory

What: Training to develop leadership and advocacy skills   Who: For parents/caregivers of youth diagnosed with mental illness willing to use their new skills to advocate for children with mental health needs beyond the needs of their own child.  When: Starts: ~3:00pm, Friday June 11th till ~3:00pm Saturday 12th  Where: Fairmont Hot Springs by Anaconda  Why: There needs to be a parent/caregiver voice in the system of care for children’s mental health. Parents/caregivers that have been through the experience of raising a child with a mental illness are the experts in what treatments and services are effective for recovery. Therefore parents/caregivers are key to improvement of the SOC for mental illness. In order to get parent/caregiver voice into the system of care, a leadership and advocacy training will empower parents by giving them the tools and skills to be involved in the SOC. 

Click here to register for this webinar About our series: The impact of violence, abuse, neglect, disaster, war, and other harmful experiences continues long after the traumatic event has ended. Exposure to trauma is a pervasive issue that has significantly impacted the health and well-being of millions of Americans and nearly everyone seeking services in the public health and social services systems. Understanding how trauma affects the emotional, behavioral, cognitive, social, and physical functioning of the people we care for can improve our services. When: March 17, 2011 12:00 - 1:00pm Mountain Presented by: Bruce Perry MD, PhD Senior Fellow at the ChildTrauma Academy Adjunct Professor at Northwestern University After participating in this webinar participants will: Understand the effect of trauma and neglect from a neurodevelopmental perspective Identify signs and symptoms of trauma and neglect in young children Learn new strategies for care, program development and policy as related to developmental trauma

Greetings and a warm welcome to the Fathers Network web page. Our mission is to celebrate and support fathers and families raising children with special health care needs and developmental disabilities. Please utilize the superb resources on this site. We appreciate your feedback and your support.

Our mission is to to empower all Children & Young Adults with Chronic Medical Conditions and Disabilities, and their families, to obtain Quality Health Care by building on the unique perspectives of Physician-Parents.

Nearly four-dozen health care professionals have embarked on a campaign to increase the number of southwest Montana children being immunized against disease.

Every week an average of 10 children with serious mental illnesses are admitted to Billings Clinic Psychiatric Center and about the same number are discharged. Most young psychiatric patients stay less than a week. “We try to stabilize them in two or three days,” said Terry Smith, a clinical social worker who cares for kids at Billings Clinic. The kids come from the Billings area, the Hi-Line, Eastern Montana and beyond. Billing Clinic is the only psychiatric hospital in the eastern half of the state that cares for children. It serves all children who need its services, but two-thirds of them depend on Medicaid — the state-federal health program — to pay their medical bills.

Families will soon have the opportunity to enroll in health care plans, renew their plan, or change to a new plan in the Marketplace.  Open enrollment is from November 15, 2014 through February 15, 2015. Please note that families can enroll anytime if there have been “life changes” (e.g. lost employment and insurance) or if they are eligible for Medicaid or CHIP.

HELENA, Mont. – Commissioner of Securities and Insurance Monica J. Lindeen today announced her office's new guide to health insurance, an everyday handbook for common insurance questions and problems.

The U.S. Department of Education announced today that its Office for Civil Rights has reached a resolution agreement with the Memphis, Tenn., City Schools on aids and services to students with disabilities. The agreement resolves a compliance review initiated by the department to address whether the district is appropriately evaluating students with food allergies, asthma, diabetes, and other health impairments who have Individual Health Care Plans (IHCPs) to determine if the students are qualified students with a disability as defined by Section 504 of the Rehabilitation Act of 1973 (Section 504) and Title II of the Americans with Disabilities Act of 1990 (Title II). OCR also investigated whether there was a difference in the provision of services to health impaired students on the basis of race.