Guest guest Posted October 27, 2006 Report Share Posted October 27, 2006 Hi All I haven't posted for several months but I have been reading most of the e-mails. This nasty desease has been progressing in Mum and we have reached a stage where her NH is recommending a wheelchair. Mum's mobility is much worse and she has fallen several times. 90 percent of the time Mum cannot manage to get out of bed or her chair but 10 percent of the time she will have a short burst of mobility that gets her up and she then trips over her feet. The Nursing supervisor is going to arrange for someone to come and access Mum and give us advise on what sort of chair etc. but I wondered if you experienced people had any advise, caveats etc. to offer. I suspect that Mum's wheelchair needs will be constantly changing from here on in. Even though the Government pays 75% of the cost of the wheelchair I don't think we want to be trading it in every couple of months. I don't also think we necessarily need a new wheelchair. There must be all kinds of places that have used wheelchairs - I'm just not too sure where to look. We have taken Mum off the Seroquel so she is only on Aricept for the LBD now. Mum sleeps off and on most of the day. I know Mum has lost weight - she has difficulty eating even if someone is helping her. I thinks she is worried that she will choke on something. It is really tough to see this once vibrant woman just shrivelling up before my eyes. from Cresswell ON Canada Long distance CG to Margaret (Mum) aged 76 Lives at The Briton House, Memory Floor, Toronto DX Early Onset AD & PD approx. 2002 DX LBD 01/2005 Current Meds: Aricept, LD ASA, Levothyroxin, Calcium Suppl. Was on: Sinemet, Excelon, Seroquel Was given Risperdal in NH for a few weeks (Feb '05) Haldol several times in Hospital Jan 05 Quote Link to comment Share on other sites More sharing options...
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