Support Services for People Living with ALS and Caregivers
Support Services Team
Cara Gallagher, MA, LCPC
Licensed Clinical Professional Counselor
Anne Marie Doyle, MA, CCC-SLP
Speech and Language Pathologist
Karen Steffens, RN, CHRN, CCM
Registered Nurse
Easton Stevenson, LCSW
Licensed Clinical Social Worker
Michelle Shaker, MSW, LCSW
Licensed Clinical Social Worker
Rochelle Walwer, LCSW
Licensed Clinical Social Worker
Lauren Webb, LCSW
Licensed Clinical Social Worker
How can the Support Services Team help me?
Collaborate with your ALS care team at the Lois Insolia ALS Clinic to address your needs
Provide ongoing disease education and address specific concerns
Discuss educational resources regarding clinical trials, treatment and research
Provide emotional support to you, and can aid in finding support for your family.
Assess needs and collaborate with other agencies to provide resources and care
Offer solutions for challenges of activities of daily living, home safety and equipment
Provide guidance on Social Security Disability Insurance, Medicare and Medicaid
Assist with advance directives including medical power of attorney and end-of-life planning
Guide and identify care needs including caregiver assistance, facility options, palliative and hospice care
Discuss and refer to need-based financial grant programs
How do I connect with the Support Services Team?
During your visit to the Lois Insolia ALS Clinic at the Les Turner ALS Center at Northwestern Medicine, you will have an opportunity to meet with a Les Turner ALS Foundation representative to learn more about our free support services.
Once you’ve completed the authorization for services, you will be assigned to an ALS Support Services Coordinator who will set up a personalized, virtual care visit that meets your communication needs. If you need an authorization form, please email [email protected].
Your ALS Support Services Coordinator will work with you to determine your goals and values that support the best quality of life for you and your loved ones. While we encourage check-in visits with your support coordinator every 6-12 weeks, we understand that you may need or prefer more or less interaction from your ALS Support Services Coordinator. We are here to help.
What other services are available from the Les Turner ALS Foundation to support me and my loved ones?