Support Services

Walter Boughton Foundation Patient and Family Services Grant Program

Walter Boughton lost his battle with ALS in 1993. In his memory, friends of Walter created a foundation in his name to raise funds to be donated to various ALS organizations, including the Les Turner ALS Foundation. The original Walter Boughton Foundation raised money and paid tribute to Walter through an annual golf outing until 2003.

More than 20 years after Walter’s death, his teenage granddaughters, Kathryn and Lauren, re-launched the Foundation, sending solicitation letters to friends, family and longtime customers of their grandfather’s former company. In addition, the Walter Boughton Foundation partners with Blackberry Oaks Golf Course in Bristol, Illinois, to host the annual Wally Boughton Open every September. Since reviving the Foundation, Lauren and Katheryn have raised more than $175,000 for the Les Turner ALS Foundation.

As a testament to their long-term commitment to the Les Turner ALS Foundation, Kathryn and Lauren have established the Walter Boughton Foundation Patient and Family Services Grant Program, in honor of their grandfather’s legacy. This program offers financial awards to people with ALS to help defray the cost of equipment, home modifications and other related items. Grants are awarded annually based on need.

For more information, to apply or for eligibility requirements on any of these programs, contact Judy Richman, Director of Patient Services or call 847 679 3311

Pictured: Kathryn and Lauren Maly

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Services Offered:

Home & Community Services

Home & Community Services Team

The Foundation’s Home and Community Services — which include telephone and in-person support, educational resources and patient and family advocates —  are available at no cost to ALS patients, their families  in the Chicagoland area and portions of northwest Indiana.

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Support Group & Education

Lois Insolia ALS Clinic

At the multidisciplinary ALS clinic, trained specialists use a team approach to provide comprehensive treatment. They are dedicated to the total care and support of people with ALS, their families and caregivers. During a visit, patients meet with several members of the team, and each provides input regarding assessment, care planning, education and other health care needs.

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National ALS Registry

National ALS Registry

The Les Turner ALS Foundation is a partner with the National ALS Registry, a program to collect, manage and analyze data about people with ALS and to provide clinical trial information to people living with ALS. It is important to include as many people with the disease as possible to get the most accurate information. Be part of changing the future of ALS.

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Hope and help for people with ALS.

Your contribution helps support nearly 90% of the Chicagoland ALS population.