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Welcome to the Oregon & SW Washington Chapter! |
Our Chapter Headquarters: 310 SW 4th Avenue, Suite 630, Portland, OR 97204 * 800-681-9851 * info@alsa-or.org For your local services contact information, please click here. We serve the entire State of Oregon and the 6 counties in SW Washington: Clark, Skamania, Klickitat, Cowlitz, Pacific, and Wahkiakum.
In honor of November being National Caregivers Month, please take a moment to reach out to a caregiver in your life and let them know how much they mean to you and your loved ones.
RECENT VICTORY for VETERANS and their FAMILIES affected by ALS! Click here for more information and call Lance Christian, Services Director, at 800-681-9851.
Who is affected by ALS? Click here to find out...
Below are three of our many local chapter programs and services. We hope these help our PALS & their families know what is available to them and we also hope this helps our DONORS know what amazing work they support.
Our Support Group Program - http://alssupport.thestorychannel.tv/ Our Respite Care Program - http://alsrespite.thestorychannel.tv/ Our Assistive Technology Program - http://alsassistive.thestorychannel.tv/
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 Join us in supporting the Portland Trail Blazers on Friday January 2nd, 2008 - click here for more details!
 Order Verizon top-rated FiOS Services & they will donate up to $65 to our local chapter. To learn more, download this flyer!
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 Thank you for being our 2008 Year Round Partner!
 Order yours today! Email info@alsa-or.org.
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National Family Caregivers Month: A Time to Honor Those Who Make a Difference |
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By Gary Wosk, Staff Writer
During National Family Caregivers Month in November and throughout the year, The ALS Association recognizes the most important resource in the lives of people living with ALS are their spouses, children and friends who love them the most.
Resources as precious as these also need to be treated with tender loving care or they too can become ill and at the very least exhausted.
“They are there day and night for their husbands and wives, moms and dads and best friends and we at The ALS Association need to be there for them,” said Gary A. Leo, the president and CEO of The Association.
One of the toughest jobs in the world is taking care of someone with a disease such as Lou Gehrig’s Disease, an around-the-clock responsibility that often exacts a steep emotional and physical toll on these dedicated men, women and children whose lives have suddenly been turned upside down.
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Make a general gift to our chapter. Your donation supports The ALS Association's mission. | Donate Now >> |
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