What would you say are the pros and cons? What tips do you have for newly diagnosed “couples?”1 Member · 0 Replies ALS resources Caregivers living with ALS relationships Sorry, there were no replies found.Log in to reply.Log In to Reply ...
Resources : A new book about living with amyotrophic lateral sclerosis is a must-read for people with the disease and their caregivers.doi:10.1097/01.NNN.0000520745.37806.38MaryOvid Technologies (Wolters Kluwer Health)Neurology Now
In Gratitude for Caregivers this Thanksgiving. A Reflection on National Caregiver’s Month A Recipe for Caregiving: Love, Loss, and Lessons from My Mom’s ALS Battle for Family Caregivers Month Stay connected by learning about upcoming events, and how we are helping those living with ALS by ...
In Gratitude for Caregivers this Thanksgiving. A Reflection on National Caregiver’s Month A Recipe for Caregiving: Love, Loss, and Lessons from My Mom’s ALS Battle for Family Caregivers Month Stay connected by learning about upcoming events, and how we are helping those living with ALS by ...
This forum is a place for ALS caregivers and family members to talk with each other, share tips,… 2 months ago Navigating ALS Challenges This is a space for discussing daily life and...
In Gratitude for Caregivers this Thanksgiving. A Reflection on National Caregiver’s Month A Recipe for Caregiving: Love, Loss, and Lessons from My Mom’s ALS Battle for Family Caregivers Month Caregiving and Marriage: How ALS Has Transformed Our Lives –“Rom & Tobin” ...
Together we provide hope, information, support, help, and friendship. ALS support staff, individuals, mothers, daughters, brothers, sisters, patients, caregivers and friends alike. We've already made a big difference, help us do even better by joining and getting involved today. ...
It can be very beneficial for both of you to attend these meetings together and to be among those who are experiencing similar challenges in their lives. Not only can they support you mentally, they will have access to resources that you may not know exist that can be helpful, such as ...
patients with ALS or other neurodegenerative diseases lose their ability to speak. We want to refer you to these services so that you can preserve your voice for later use with speech generating devices should you need them. Some examples can be found here:https://simplihere.com/resources/. ...
Once you’re ready to learn more, ask your doctor or social worker how to find resources in your area. Let them know if you’re looking for practical help or emotional support. Informational websites and social groups can help you connect with other people who have amyotrophic lateral scleros...