Excessive Sleeping: My husband was... - Multiple System A...

Multiple System Atrophy Trust

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Excessive Sleeping

binnyrox profile image
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My husband was diagnosed in early 2020 with MSA. The decline was rapid - he is now on PEG for feeds, intermittent urine catheter, flatus tube for bowel movement, and a tracheotomy with ventilator on at night

He has speech therapy, physiotherapy, occupational therapy that fills up his days

However in the past week, he has had very few waking hours. He was awake for just 50 minutes today.

Could anyone please help with any feedback? I know his disease is at an advanced stage; however his parameters and bloodwork are all stable.

Would anyone be familiar with end stage MSA - is excessive sleeping a common symptom

Would really appreciate your input

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binnyrox
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TK-67 profile image
TK-67

yes - it can be part of the end-of-life process, it is normal. I posted this link a while ago as my mum entered the final weeks. It helps to normalise what is happening. It's common for obs/bloodwork to appear normal. My heart goes out to you, reach out for any help you can get, it can take time and you may want to discuss the support you and your husband now need. Mum had made the decision long before she was ill that she didn't want any interventions so it was just about keeping her comfortable as things progressed. We found surrounding mum with conversation helped so she knew we were there. I hope this helps a bit, it's hard often to share the process. youtube.com/watch?v=ayMhA1p...

binnyrox profile image
binnyrox in reply to TK-67

Thank you very much for writing. It truly helps and I’m deeply appreciative that you’re here sharing

I am sorry to hear of his decline, my wife passed away in December and the Physiotherapy helped keep her mobile to the end. We had a Neuro physio twice a week doing a number of specialised exercises which enabled her to walk a short distance as well as eat unaided, sit up in bed etc

binnyrox profile image
binnyrox in reply to Morganthreewheeler

Thanks much for your note. I’m immensely grateful for the information.

FredaE profile image
FredaE

yes..it is one of the few meriful things about this merciless disease

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