Our daughter had a Gerberit and as you say James it retained her dignity and had “lady functions “ and she loved the independence it gave her Another top tip is see if you can get a “real” hospital style bed when it becomes difficult to sleep with a partner as her OT was able to source one and again it made life a lot more comfortable as her time in bed became extended or she just felt like having a lazy day ..that combined with a good air mattress again supplied via the OT .Top tip when having a wet room created is make sure there is enough space to get a reclining shower chair in the shower area , you can never not have enough space both in the bedroom and the wet room. Another great video 👍👏👏
@@johannrugby3811Hi! I came across with your conversation with with James, ALS and motor neuron disease or Lou Gehrig’s disease is just the same, in UK they usually use the term MND.😊
@@DiagnosedDad I’m still walking and able to use my arms. 2.5 years since diagnosis. Still can swallow and grip my hands. Carpal tunnel in both arms due to nerve damage. Fingers clawing. Hard to wipe. I go through a roll of toilet paper every few days. I need a bidet
