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For Caregivers

The ALS Association is proud of its tradition of leadership in providing comprehensive programs and services for ALS caregivers. Along with those programs and with the assistance of the National Family Caregivers Association, our continuing partner in recognition of November as National Family Caregiver's Month, we are pleased to present to you the following information for caregivers.

Facts About Family Caregivers

Family Caregiving Statistics
Compiled by the National Family Caregivers Association
  • More than one quarter (26.6%) of the adult population has provided care for a chronically ill, disabled or aged family member or friend during the past year. Based on current census data, that translates into more than 50 million people. Source: National Family Caregivers Association (NFCA) Random Sample Survey of 1000 Adults, Funded by CareThere.com, Summer, 2000.

  • Caregiving is no longer predominantly a women's issue. Men now make up 44% of the caregiving population. Source: National Family Caregivers Association (NFCA) Random Sample Survey of 1000 Adults, Funded by CareThere.com, Summer, 2000.

  • The value of the services family caregivers provide for "free" is estimated to be $257 billion a year. Source: Peter S. Arno, "Economic Value of Informal Caregiving," presented at the American Association of Geriatric Psychiatry, February 24, 2002.

  • Virtually one half of the US population has a chronic condition. Of these 41 million were limited in their daily activities. Twelve million are unable to go to school, to work, or to live independently. Source: Chronic Care in America (Institute for Health & Aging, Univ. of CA/SF for the Robert Wood Johnson Foundation) 1996.

  • People over 85 years of age are the fastest growing segment of the population. Half of them need some help with personal care. Source: US Bureau of the Census Statistical Brief, Sixty Five Plus in the United States, May 1995.

  • Elderly caregivers with a history of chronic illness themselves who are experiencing caregiving related stress have a 63% higher mortality rate than their non-caregiving peers. Source: Journal of the American Medical Association, December 15, 1999, Vol. 282, No. 23.

  • The pool of family caregivers is dwindling. In 1990 there were 11 potential caregivers for each person needing care. In 2050 that ratio will be 4:1. Source: Chronic Care in America - as above.

  • Sixty-one percent (61%) of "intense" family caregivers (those providing at least 21 hours of care a week) have suffered from depression. Some studies have shown that caregiver stress inhibits healing. Source: National Family Caregivers Association/Fortis Long Term Care (Caregiving Across the Life Cycle) 1998; Lancet 1995; 346 (Slowing of Wound Healing by Psychological Stress - Kiecolt-Glaser, JK et al).

  • Family caregivers who provide significant time and effort in caring for a loved one, especially spousal caregivers, do not get consistent help from other family members. One study has shown that as many as three fourths of these caregivers are "going it alone." Source: Caregiving Across the Life Cycle - as above.

  • Approximately 80% of home care services are provided by family caregivers. Source: US General Accounting Office (GAO/HEHS 95-26, "Long-Term Care: Diverse, Growing Population Includes Millions of Americans of All Ages") 1994.

  • A recent study calculated that American businesses loses between $11 billion and $29 billion each year due to employees' need to care for loved ones 50 years of age and older. Source: National Alliance for Caregiving/Met Life (Met Life Study of Employer Costs for Working Caregivers).

  • Fifty nine percent of the adult population either is or expects to be a family caregiver. Source: National Family Caregivers Association (Random Sample Survey of 1,000 Adults Sponsored by Aleve).

The National Family Caregiver's Association has also compiled state-by-state statistics on the economic impact of family caregiving. Click here to view the statistics in Adobe Acrobat format. For more information, please visit http://www.nfcacares.org/.

The National Alliance for Caregiving and AARP have released "Caregiving in the US," an update to the 1997 National Caregiver Survey. The research report and supporting documents are available on the Alliance web site at http://www.caregiving.org/.

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FOR MORE INFORMATION OR FURTHER ASSISTANCE:

Sonja Zimmer
Patient Services Director
King County, and in support of All Regions
1-866-STOP ALS
Fax: 425-656-1649
email: sonja@alsa-ec.org

South Sound Region
Wes Cauthers
Patient Care Coordinator
Phone: 1-866-786-7257
Fax:425-656-1649
email: wesc@alsa-ec.org
Central Washington Region
Nina Maltos
Patient Care Coordinator
Phone:(866) 236-7442
email: ninam@alsa-ec.org
North Sound Branch
Mary Rebar
Patient Care Coordinator
Phone:  360-733-5222
Fax: 360-733-5376
email:  maryrebar@alsa-ec.org

Greater Inland Empire Region
Including Spokane,  Northern Idaho, Western Montana
NaDean Watkins
Patient Care Coordinator
Phone:  877-201-3610
Fax: 877-219-1032
email:  nadeanw@alsa-ec.org

SUPPORT GROUPS:

Bellevue Caregivers Support Group
Highland Community Center

Second Saturday 9:30 am - 11:30 am
14224 Bellevue-Redmond Road in Bellevue.
425-452-7686 for directions only

Bellevue Support Group
Highland Community Center

Fourth Thursday 6:30 pm - 8:30 pm
14224 Bellevue-Redmond Road in Bellevue.
425-452-7686 for directions only

Bellingham Support Group
St. Luke's Community Health Education Center

Second Thursday  12:00 noon - 1:30 pm
3333 Squalicum Way
Bellingham, WA
360-733-5222  for more information

Central Washington-Yakima Support Group 

Open to PALS and Caregivers

First Saturday  10:00 am - 12:00 pm
5111 Lyons Loop 98903
866-236-7442

Coeur d'Alene, ID Support Group
Hospice of North Idaho

Second Tuesday 5:30 - 7:30pm
9493 N. Government Way
Hayden, ID.
877-201-3610 for info

Edmonds Support Group 
Stevens Hospital

Second Monday 10:00 am - 11:30
Cafeteria East Room, Stevens Hospital
21601 76th Ave. W
Edmonds, WA 98026
For more info, call 360-733-5222

Kent Support Group
Home of Carl & Merilyn Moore

Second Sunday 3:00 pm - 5:00 pm 
13209 SE 236th Place
Kent, WA 98042
253-631-7986 for info/directions

Missoula Support Group
Community Hospital Cancelled indefinitely

Last Thursday 5:30 pm - 7:00 pm
2825 Fort Missoula Rd
Missoula, MT
(use Rehabilitation Institute Door)

Peninsula Support Group
Silverdale Community Center

Third Wednesday 12 pm - 2:00 pm
Silverdale Community Center 
Coho Room
9729 Silverdale Way NW
Silverdale, WA 98383-9445
For directions call 360-337-5700

Spokane PALS and CALS Meeting
Valley Hospital & Medical Center 

Fourth Thursday 3 pm - 4:30 pm New Time
12606 E Mission Ave
Spokane WA 99216
877-201-3610

Sequim Support Group (now North Peninsula Support Group)
The home of Sandra Smith

Second Tuesday 1 pm - 3 pm
3400 Snow Creek Road
Quilcene, WA 98376

Tacoma Support Group
The Village Assisted Living Community

Third Tuesday 2:00 pm - 4:00 pm
4707 South Orchard St - Assembly Room
Tacoma, WA 98466
For directions please call 253-475-4707

Tri-Cities and SE Washington PALS
and Family Support Gathering

Neurological Resource Center, Richland

Open to PALS and their family members/friends
Current Information about ALS and treatment options

Fourth Wednesday 6:00 pm - 8:00 pm
712 Swift Blvd #1
Richland, WA 99352
P866-236-7442

 Wenatchee Support GroupNew

Second Wednesday 5:00 - 7:00 pm
Wenatchee General Hospital Room E
Call Nina for more info, if needed:
866-236-7442

Online Chatroom Support Group for PALS
First Wednesday 2 - 3 pm
Link
(go to WA support in the Room Menu)

Online Chatroom Support Group Chat-for-All
Updated: Our chat is now open to all ages! Please join us next time :-)
First Tuesday 7 pm
Link
(go to WA support in the Room Menu)


Virtual Support Group for PALS & Caregivers
(using webcam and virtual meeting software - webcams ARE available)
Fourth Monday 4 pm
Contact Sonja Zimmer: sonja@alsa-ec. for more info.

This list was updated 23 September 09
If there are typos, please don't hesitate to email Dede!
dedes@alsa-ec.org

We send out monthly email reminders to Support Group members.
We also encourage people to have their own unique email and
not use a family member's email. This cuts down on expensive duplicate records 
and helps us track email snaffus with our email provider.

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