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Submitted by naezee on Sun, 02/26/2017 - 14:24My husband was diagnosed with ALS 2 years ago. He can no longer stand and has lost most of his hands/arms function. He can still talk and eat, which we are very thankful for. He uses a Bi-Pap when lying in bed. He has a Permobil power chair and we have a Hoyer lift, that I use to transfer him. We use a full body sling with a commode cutout. We have a hospital bed. I am his primary caregiver.