Portland, April 3rd, 2013. After a nationwide search and rigorous interview process, the board of Portland Children’s Museum is pleased to announce Ruth Shelly of Madison Children’s Museum as its new executive director.
board of Portland Children’s Museum is pleased to announce Ruth Shelly of Madison Children’s Museum as its new executive director.
“We are pleased to introduce and welcome Ruth as we look forward to an exciting new chapter in the life of the Portland Children’s Museum,” said Board President Shawn DuBurg. “Ruth is a lifetime advocate of locally focused organizational development, museum education, and outdoor play. She is enthusiastic about leading Portland Children’s Museum into its next decade of community service, and we are thrilled to have her as our next leader.”This announcement is the result of a thorough search, led by committed community leaders and board members. Interim Executive Director Carrie Hoops has led the organization since November 2013, and will facilitate the transition. Shelly will officially assume her new duties in mid-May, and friends and supporters of the Museum will have a chance to meet her on Saturday, May 11, at the Museum’s Be a Kid Again gala.“Portland Children’s Museum, the Opal School, and the Museum Center for Learning create a powerful combination that has the potential to demonstrate a new model of education for lifelong learners,” Shelly said. “The Museum’s location in beautiful Washington Park, enhanced by the prospect of its new Outdoor Adventure exhibit area, provides exciting opportunities to get kids outside for healthy physical and cognitive development. I look forward to working with the board, staff, and volunteers as we take this beloved community resource to its next level of excellence.”
Shelly is a lifelong museum professional who has worked as an exhibit director and administrator in museums across the country. In 2003, she returned to her native Wisconsin to serve as executive director for Madison Children’s Museum, where she led the museum’s move from small rented quarters to a donated 1929 department store building. Shelly and her staff exceeded the $10 million capital campaign goal.
Since opening in 2010, that museum has more than doubled its annual attendance, and nearly quadrupled its membership. With a fully accessible green roof, the museum is anticipated to be the first LEED-certified Wisconsin museum, and in 2011 won the National Medal for Museum and Library Service for its exemplary contributions to the community.
ABOUT PORTLAND CHILDREN’S MUSEUM Portland Children’s Museum is the museum that doesn’t act like a museum. You won’t find any velvet ropes inside, and playing with and touching our exhibits is strongly encouraged. Our main exhibit is the imagination of the children who play here. Every activity from permanent to travelling exhibits is designed to encourage children to play and wonder while they learn about themselves and the world around them. For more, visit portlandcm.org.
Portland, March 15th, 2013. A “dinner + play” fundraiser was the 3rd in Self Enhancement Inc.’s Salon Series. The event featured Chris Coleman, Artistic Director of Portland Center Stage. After dinner, guests like Tony Hopson, Sr. and Russell Hornsby attended the Portland Center Stage production of the post-civil war drama, Whipping Man. Self Enhancement Inc. supporters had an insiders view of the production while supporting one of their favorite causes: supporting at-risk urban youth. (Photo credit, Antonio Harris)
Chris Coleman, Rukaiyah Adams and Rodney Hicks
Dinner Guests
Vanessa Morgan and Bob Quillin
Tony Hopson, Sr. and Chris Coleman
About PCS’s Whipping Man:
In the post-Civil War South, three men are tied to each other by history and faith, but are also bound by secrets. A badly wounded Jewish Confederate soldier returns home at war’s end to find that his family has fled to the countryside. Remaining in the city mansion are two former slaves, also raised by his family as Jews. With Passover upon them, the three men unite to celebrate the holiday, even as they struggle to comprehend their new relationships at a crossroads of personal and national history.
The Whipping Man, which premiered in New York in 2011 to great acclaim, is an extraordinary tale of loyalty, deceit and deliverance.
Portland, March 14, 2013. Night at the Museum was the theme for Lines for Life’s (formerly Oregon Partnership) annual Gala Dinner & Auction. Judy Cushing, CEO Lines for Life; Mayor Charlie Hales, Nancy Hales, Sharon Smith and Senator Gordon Smith attended the 20th Anniversary Gala at the Portland Art Museum. (Photo credit, Andie Petkus) Organizers say the evening was a tremendous success, raising more than $285,000 for lifesaving programs.
Each year Lines for Life (formerly Oregon Partnership) continues to advance its mission of preventing substance and suicide. Through a 24-hour crisis services and prevention education programs it has seen many lives changed for the better. The anonymous Military Helpline is unique in the country and YouthLine offers confidential teen-to-teen counseling on bullying, substance abuse, self harm and suicide.
Event co-chair Anne Naito-Campbell and Nancy Hales
Ballroom at PAM filled with generous Lines for Life supporters.
Gala Emcee Kerry Tymchuk with auctioneer Johnna Wells
(Heroes for Hope Tom Cook of Taco Bell and Mark Ganz of Cambia with (center) Lines for Life Board Chair Dan McMillan of The Standard.
Our youngest supporter Ellen McMillan joins in the fun
Senator Gordon Smith raises his paddle high for Lines for Life
From Lines for Life:
We are dedicated to preventing substance abuse and suicide because they touch so many families in our society.
Lines for Life (formerly Oregon Partnership) is a non-profit dedicated to preventing substance abuse and suicide. We have served thousands of people with addiction, mental health and suicide intervention services, treatment referral and drug prevention education.
Lines for Life Crisis Lines receive approximately 35,000 calls per year. We are able to de-escalate 98 percent of the 17,000 suicide calls we receive. The Military Helpline offers free, anonymous assistance 24/7/365 to active duty service members, veterans and their families.
Our YouthLine offers a confidential teen-to-teen phone line and texting to help youth deal with bullying, depression, substance abuse or other issues that can make those years especially painful.
The Lines for Life staff works closely with schools, parents, treatment professionals, law enforcement and the military. We train and support community anti-drug coalitions. We lead public awareness campaigns on underage drinking, youth access to alcohol and reducing illegal drug use.
Portland, March 9th, 2013. Over 300 guests gathered at the Governor Hotel for Thomas Edison High School’s Brilliance Benefit. The gala raised over $220,000 to support financial aid, technology, and professional development at the school. Thomas Edison supporter Scott Gardner, Debbie Maguire, school director Pat Maguire, and MaryLynn Gardner were busy at the silent auction. (Photo Credit, Andie Petkus) All proceeds benefit Thomas A. Edison, the only high school in Oregon and southwest Washington dedicated to students with complex learning differences.
Edison student volunteers gathered onstage to support the Brilliance Benefit student speaker, who shared her story and encouraged guests to donate to financial aid at Thomas Edison High School.
The Brilliance Benefit’s silent auction, featuring over 200 items, kept guests bidding until the last minute.
Edison student volunteers show their school spirit at the silent auction portion of the Brilliance Benefit.
The benefit was chaired by Walt and Kim Weyler.
Located in Portland, Oregon, Thomas A. Edison is a private high school dedicated to meeting the special education needs of Learning Disabled (LD) teens. Our students’ learning differences include Dyslexia, ADD, ADHD, Asperger’s Syndrome, Tourette’s Syndrome, Dysgraphia, Dyscalculia, Visual Perception and Nonverbal Learning Disorders.
Portland, March 9th, 2013. The ALS Dinner & Auction Gala was an upbeat affair. The ALS Association Oregon and SW Washington Chapter benefit raised $300,000 to support local care services for families living with the progressive changes of Lou Gehrig’s Disease and provide funding for ALS specific research and public policy efforts. (Photo credit, Michael Keo Photography)
Lance Christian, Executive Director, received a standing ovation and well deserved recognition from board president, Dr. Lou Libby, in honor of his 10 years of service to The ALS Association.
Bo Stern, a sought-after author and teaching pastor from Bend, Oregon gave an eloquent and heart felt address to the crowd about the realities of living with ALS as she and her family provides care and support to her husband, Steve, who is living with the disease.
Tracy Barry, news anchor with KGW, was the Mistress of Ceremony for the evening.
About Our Chapter
Since its inception in 2002, our local chapter of The ALS Association is the central source for services and education for people with ALS, their families, caregivers, and health care professionals in all of Oregon and the six counties of SW Washington. The progression of ALS varies significantly from one person to another. Responding to each person’s individual needs, our local chapter is available to provide vital services and reliable information.
A sampling of services provided free of charge:
One-on-one consultations to assess the needs of those living with ALS, suggest equipment and help families plan for the future.
A Medical Equipment Loan Program that provides mobility equipment when insurance and other programs cannot fund needed items.
A comprehensive Alternative Communication and Assistive Technology Program.
Caregiver support groups, Share the Care™ guidance, and respite care grants to relieve stress and “caregiver burnout.”
Monthly support groups for people with ALS, family members, caregivers and friends.
Partnerships in ALS multidisciplinary clinics staffed by professionals with ALS expertise.
Outreach to the local medical community with updates on current ALS needs and solutions.
The ALS Association is the only national not-for-profit health organization dedicated solely to the fight against ALS. The ALS Association covers all the bases — research, patient and community services, public education, and advocacy — in providing help and hope to those facing the disease.
The ALS Association (National Office and The ALS Association Oregon and SW Washington Chapter) operates under a shared mission: to help people living with Amyotrophic Lateral Sclerosis and to leave no stone unturned in search for the cure.
We work together to accomplish our mission. The ALS Association Oregon and SW Washington Chapter focuses primarily on helping local families living with ALS while the National Office focuses primarily on research and advocacy. The Chapter supports the National Office through revenue sharing and research contributions. The National Office supports the Chapters by providing up-to-date information, materials and hands-on support.
Our chapter receives no government or insurance funding – we rely solely on our events, corporate and personal gifts, and local foundation grants.
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