Hi A little introduction from myself and my husband.
We've been with the group for nearly a year now but this is the 1st time We've posted anything. My husband was diagnosed with MSA P & C early last year after years of thinking it was cerebellar ataxia .We find the group's posts very helpful and a lot of the post we identify with . ( it helps to feel like we're not alone ) not to say we don't have a fantastic family network supporting us . My husbands condition has deteriorated rapidly over the last couple of months and it's a scary place to be at times so your posts do really help thankyou.
Involuntary nasal dripping when eating
Temperament changes 
My dad
Frequent blocked catheters
