Hello all!
My father (74) has MSA. We know since last november.until then we thought it was Parkinsons disease. We think the first symptoms showed up as early as 10years ago…
Fast forward 10 days ago, he was admitted into hospital for early stages pneumonia. For a moment, we feared we might lose him, but after a change of antibiotics he got better. Meaning the pneumonia got better.
We are still VERY worried bc even though his blood tests show he is better, his overall situation seems bad. One day he can ‚talk‘ as before (hard to understand for strangers, but my mom and us daughters understand him), wants to watch tv, and is longing to drink…
The speech therapist and nurses have put him on ‚no oral nutrition‘ for now bc his swallowing is so bad, he kept getting stuff into his lungs.
The next day he is unable to communicate, his breathing sound like a bubble machine and stops for up to 5seconds…
Nobody seems to know about MSA, there is no neurologist in the hospital and my dad seems so unhappy!
Has anybody some ideas what might be ahead for us? Is he dying? Will his swallowing get better again?
Btw, we are in Germany…I feel there is dimply NO INFORMATION on MSA over here!!😩
thanks in advance!