It’s been over a year since my diagnosis now, a lot of things have changed into “habit”. After the diagnosis I was in shock for about three months, badly eaten, … >>>>>>>
The new life
A night out
I know that many people have their hair stood on end from the idea of going to a concert with multi system atrophy, with several thousand others – especially not … >>>>>>>
The black dog – the unpleasant conversation
With diagnosis he moves in with you and will not leave you again so quickly. You will be told: It is ALS, lung cancer, MSA or another pestilence that you … >>>>>>>
On the way to a new life
Like I said earlier, I live alone. Well, living alone has its advantages, but it’s becoming more and more difficult. I am becoming more and more handicapped, some things I … >>>>>>>
The difficulties of pain therapy
Eventful days lie behind me and I almost managed to stay on the ground for 7 days. Unfortunately it did not work out. But in contrast to the last but … >>>>>>>
The villain in the head
Often I was already in the situation to try to explain to my fellow beings – and also to try to understand myself – what kind of illness MSA actually … >>>>>>>