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Check out our Walk Home Page for Updates and Team Photos
Will you help us reach the finish line?
 Click the logo above to find out more.
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For more info, contact Robin Hartman robin@alsa-ec.org 1-866-STOP ALS
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Click the button to visit the DoubleDay Page site to make your donation |
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ATTENTION SHOPPERS!
Remember, you can support the Evergreen Chapter even when you’re shopping online!! IGive.com is a great place to shop online. You’ll find many, many of your favorite stores that offer a percentage of your purchase to the charity of your choice. Just enter the store of your choice through IGive.com, it’s that easy! You’ll also receive a notice of your donation to our Chapter. |
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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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Click the button to view items presently available for purchase |
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~~~~QUICK LINKS~~~~ Click the arrows to access the links |
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December 13, 11:30 AM at Luciano Ristorante Click HERE to view the complete invitation. |
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| Click the graphic above to send an eCard today |
| Announcing a new workplace giving campaign |
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National Family Caregivers Month: A Time to Honor Those Who Make a Difference |
|
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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