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Ice Bucket Challenge Progress

 

More Information for Attorneys

Please use the following correct legal name when assisting a client in making a gift through his or her will, living trust, or other estate plan: The Amyotrophic Lateral Sclerosis Association Oregon and SW Washington Chapter.

A sample provision might read as follows

"I bequeath (here state the specific dollar amount, percentage, residue, or description of real or personal property) to The Amyotrophic Lateral Sclerosis Association, Oregon and SW Washington Chapter, currently headquartered in Portland, Oregon, to be used or disposed of as The ALS Association Oregon and SW Washington Chapter in its sole discretion deems appropriate."

The Amyotrophic Lateral Sclerosis Association Oregon and SW Washington Chapter's federal identification number is: 68-0516066.

To inform The ALS Association Oregon and SW Washington Chapter of your client's intent, to receive a copy of The Association's IRS determination letter, or for all other requests for information, please contact our main office using the information below.

The ALS Association
Oregon and SW Washington Chapter
Attention: Stephanie Rudeen, Director of Donor Engagement
700 NE Multnomah St.
Suite 210
Portland, OR 97232
Phone: (503) 238.5559 ext 116
Email: Stephanie.Rudeen@alsoregon.org 

Prior Addresses for The ALS Association

The Headquarters Office of The Amyotrophic Lateral Sclerosis Association Oregon and SW Washington Chapter has been located at the above location since January 2014. Previous headquarters addresses were 310 SW 4th Ave, 1221 SW Yamhill and 3316 NE Clackamas - all in Portland, Oregon.

If you are administering an estate gift that specifies a different address then what is above, please change your records to reflect The Association Oregon and SW Washington Chapter''s current address listed above.

Thank you for helping to facilitate a gift in support of The ALS Association's mission which is to lead the fight to treat and cure ALS through global research and nationwide advocacy while also empowering people with Lou Gehrig’s Disease and their families to live fuller lives by providing them with compassionate care and support.