An open, supportive monthly bereavement group for anyone (family, friend, etc.) who has lost a loved one to ALS within the past year. This group will provide a place to connect with others who have experienced the loss of a ...
*Meets the fourth Saturday of each month from 10:30am-12pm Support group meetings are open to patients, family members, caregivers and friends. Each facility is wheelchair accessible and offers free parking. We request that you RSVP if you are planning to ...
Meets the Fourth Saturday of each month from 10:30am-12:00pm Facilitator(s): Rochelle Walwer, LCSW RSVP: Click here to register *Meetings will be held over Zoom and a Zoom invitation will be sent via email once you register for the group.*
LOCATION Guaranteed Rate Field 333 W 35th St, Chicago, IL 60616 DATE AND TIME 6/2/23 5 PM Tailgate Area Opens – Parking Lot E, just outside of Gate 2. Pick up your official shirts and be a part of the ...
Meets the Second Saturday of each month from 10:30am – 12:00 pm Facilitator(s): Karen Raley Steffens, RN, CHPN, CCM RSVP: Please email us at supportgroup@lesturnerals.org to RSVP *Meetings will be held over Zoom and a Zoom invitation will be sent ...
An ALS diagnosis is difficult to process. People often feel shocked and isolated by the news, whether the diagnosis was for themselves or a family member. It’s hard to move forward or figure out what comes next. This summer, the ...
The Caregivers Only group offers a time to talk about all the issues caregivers face in a non-judgmental, accepting atmosphere without their loved one, who is living with ALS, being present. Caregivers share a common experience; life has become so ...
Every summer, Major League Baseball celebrates Lou Gehrig Day at ballparks across the country. Whether you're loyal to the Chicago Cubs or White Sox, we'd love to meet up, honor the Iron Horse, and have a great time together at ...
The Caregivers Only group offers a time to talk about all the issues caregivers face in a non-judgmental, accepting atmosphere without their loved one, who is living with ALS, being present. Caregivers share a common experience; life has become so ...
Not everyone with ALS will need or choose to have a tracheostomy, but there may come a time when it’s necessary for continued breathing. You may have respiratory weakness that can no longer be treated with a mask and non-invasive ...
