States Cover Respite Care and Adult Day Services in Medicaid Managed Long-Term Services and Supports (MLTSS)
/in The RAISE Act Family Caregiver Resource and Dissemination Center Featured News Home, Maps State Resources, The RAISE Family Caregiver Resource and Dissemination Center Respite Care /by Kimberly HodgesState Respite Care Spending Is Low in Most Home and Community-Based 1915(c) Waivers
/in The RAISE Act Family Caregiver Resource and Dissemination Center Featured News Home, Maps State Resources Respite Care /by Kimberly HodgesState Caps on Respite Waiver Services Vary Greatly
/in The RAISE Act Family Caregiver Resource and Dissemination Center Featured News Home, Maps State Resources, The RAISE Family Caregiver Resource and Dissemination Center Respite Care /by Kimberly HodgesNational Family Caregivers Month Twitter Chat hosted by NASHP
/in The RAISE Act Family Caregiver Resource and Dissemination Center Chronic and Complex Populations, Council Meeting Materials and Resources, Long-Term Care, State Resources, The RAISE Family Caregiver Resource and Dissemination Center The RAISE Family Caregiver Resource and Dissemination Center /by NASHP StaffThe National Academy for State Health Policy (NASHP) is hosting a Twitter chat to recognize National Family Caregivers Month. Across the nation, state health programs depend on caregivers who provide critical support to help relatives, friends, and neighbors stay safely in their homes while contributing $470 billion in unpaid health care services each year. Family caregivers reduce the need for home health services and can delay hospitalizations and nursing home care. This Twitter chat will explore how states can provide flexibility, support, and resources to address caregiver needs through effective policy changes.
Please join us at 2 p.m. (ET) Thursday, Nov. 19, 2020 to discuss:
- Challenges/barriers that family caregivers face;
- Family caregiving during the pandemic;
- State innovations to support family caregivers;
- How policymakers can improve education, training, and counseling for family caregivers; and
- Opportunities for the RAISE Family Caregiver Center and Council.
How to Participate
- Follow @NASHPhealth on Twitter.
- Join us on November 19 at 2 PM EST and follow the conversation using #RAISEchat.
- Share your thoughts and ideas on policies and support resources.
- Use links to your website, programs, initiatives, and partners in your tweets to promote the good work you, your organization, and/or state are doing!
- Include #RAISEchat in all of your tweets so chat participants can easily follow you and others during this event.
How it Works
- Each question will be numbered Q1, Q2, Q3, etc.
- Start your responses with A1, A2, A3 etc. to correspond with the question.
- You only have 280 characters per tweet but you’re not limited to only one tweet per question. Use A1a, A1b, A1c, etc. to indicate either a multi-part answer or multiple responses to a given question.
The Questions
- Q1: It’s National Family Caregivers Month. How is your organization better supporting family caregivers, and do you have new resources to share?
- Q2: What are the main challenges family caregivers face when taking care of a relative?
- Q3: Given that the RAISE advisory council will be creating a national strategy for family caregiving, what do you think the strategy should include to help family caregivers address these challenges?
- Q4: What steps can states take to better support family caregivers? Share state examples.
- Q5: How are your organizations supporting family caregivers during the pandemic?
- Q6: What can states do to bring awareness to caregivers’ contributions?
This chat is an excellent opportunity to highlight some of your exciting initiatives, innovations, and resources!
Webinar: Family Caregiving Policies and Innovations
/in The RAISE Act Family Caregiver Resource and Dissemination Center Webinars Chronic and Complex Populations, Council Meeting Materials and Resources, Long-Term Care, State Resources, The RAISE Family Caregiver Resource and Dissemination Center The RAISE Family Caregiver Resource and Dissemination Center /by NASHP StaffFamily caregivers provide an estimated $470 billion per year in unpaid care and are a critical component for states seeking to support older adults and individuals with complex needs stay in their homes and communities.
Funded by The John A. Hartford Foundation, NASHP’s RAISE Family Caregiver Resource and Dissemination Center hosts a webinar to discuss state and federal policies and initiatives to support family caregivers. The webinar provides an overview of the Recognize, Assist, Include, Support and Engage (RAISE) Family Caregivers Act and features leaders from Tennessee and Washington State who share their policies and innovations to support family caregivers.
Speakers include:
Moderator Wendy Fox-Grage
NASHP Project Director, RAISE Family Caregiver Resource and Dissemination Center
Rani Snyder
Program Vice President, The John A. Hartford Foundation
Greg Link
Director, Office of Supportive and Caregiver Services, US Administration for Community Living
Bea Rector
Director, Home and Community Services Division, Aging and Long-Term Support Administration, Washington State Department of Social and Health Services
Stephanie Gibbs
Director, System Transformation and Innovation, Long-Term Services and Supports, Division of TennCare
Thursday, Feb. 20, 2020
2-3 p.m. (ET)
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For individuals living with complex, often chronic conditions, and their families, palliative care can provide relief from symptoms, improve satisfaction and outcomes, and help address critical mental and spiritual needs during difficult times. Now more than ever, there is growing recognition of the importance of palliative care services for individuals with serious illness, such as advance care planning, pain and symptom management, care coordination, and team-based, multi-disciplinary support. These services can help patients and families cope with the symptoms and stressors of disease, better anticipate and avoid crises, and reduce unnecessary and/or unwanted care. While this model is grounded in evidence that demonstrates improved quality of life, better outcomes, and reduced cost for patients, only a fraction of individuals who could benefit from palliative care receive it. 























































































































































