Aspiration Pneumonia: My friend, 7... - Multiple System A...

Multiple System Atrophy Trust

1,717 members1,357 posts

Aspiration Pneumonia

K8chris profile image
3 Replies

My friend, 75, was diagnosed recently with MSA. Diagnosis took weeks despite a long history of orthostatic blood pressure and swallowing problems. He was moved into a local rehab hospital 6 weeks ago with the aim of getting him wheelchair mobile. However, he keeps getting aspiration pneumonia. He is PEG fed, allowed only small sips of water. Must sit up in bed. He has twice daily nebulisers but always sounds a bit chesty. Any advice on how to prevent this frequent occurrence of aspiration? Has anyone any thoughts on the nutrition he receives? Currently vanilla fortisips. Thank you.

Written by
K8chris profile image
K8chris
To view profiles and participate in discussions please or .
3 Replies
SilentEchoes profile image
SilentEchoes

Tucking the chin when drinking helps protect the airway. Unfortunately a person can aspirate saliva too. There is no real way to prevent this - it's the progression of the disease.

SE

esj20 profile image
esj20

I too have aspiration problems, speach and lanuage therapists have given me help with food etc but i see you metioned PEG. i use a swallowing app with alerts me to swallow my saliva.

hope this helps

K8chris profile image
K8chris in reply to esj20

Thank you

Not what you're looking for?

You may also like...

midodrine

Hi everyone my husband has hypertension one of the symptoms of MSA and been taking fludrocortisone....

I've lost my deepest love and soulmate

It’s with huge sadness I'm letting you know that after a severe bout of pneumonia Jackie, my...

I don’t understand

hi My husband was diagnosed with Parkinson’s in 2021 after a few years of dizziness and balance...

Newbie

Hi, just introducing my self and hoping for some to understand this MSA. I am a retired Senior...

MRI Scan not showing up MSA

Husband had a mri scan doctors are saying results not clear for MSA is this normal! He had an...