Ask Me Anything ALS – Caring for a Spouse or Partner
When you are a caregiver to a spouse or partner with ALS, the impact on your relationship can feel especially difficult. For some couples, going from mutual reliance to patient and caregiver results in shifting dynamics that are felt on both sides. You are not alone in experiencing relationship changes! Join this community conversation on August 25th at 5:30 p.m. ET to ask questions and learn from to people who currently are, or previously were, navigating this difficult experience.
At this Ask Me Anything ALS – Caring for a Spouse or Partner, I AM ALS community members will share how they have adapted themselves, their relationship and their shared dreams and goals. They will also spend time answering questions submitted during registration and at the event.