JohnHMich
Active member
- Joined
- Feb 17, 2020
- Messages
- 58
- Reason
- Lost a loved one
- Diagnosis
- 4/2020
- Country
- US
- State
- MI
- City
- Ann Arbor
It has been about three months. The big change is that we had the door to the first floor powder room widened and replaced with a barn door. This makes it a straight shot into the bathroom and easy for caregivers to maneuver. We also replaced the sink with a wall mount so the wheelchair fits under it. Still no vent during the day. Swallowing like a champ. The right hand grip and her voice are flagging. I think we will be feeding her in the next month or so. The speech therapist mentioned an eye gaze device, but I don't know when that will go into use. And we are still waiting to hear about the PEG.