Good post. I know that caring is stressful on the caregivers but I am sure that it is really hard to have to need help. You seem to have a lot of grace about that but it must be really hard for someone who appears to have been fiercely independent before ALS.
My dad, who has ALS and FTD always took pride in his physical strength. Part of me hopes that the dementia he has is minimizing his awareness of his loss of strength and independence.
I wish so much that you and the others profiled on your blog didn’t have to go through this. My heart really hurts for you. If I can do anything to help raise awareness by talking about our family’s experience, please let me know.
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