This has not been my week.
I’m hanging in there a little bit. Thursday night I watched one or two specials on the State of the Union. and I had … >>>>>>>
Our daily life with Multi System Atrophy
This has not been my week.
I’m hanging in there a little bit. Thursday night I watched one or two specials on the State of the Union. and I had … >>>>>>>
The current situation is very challenging. I’m lucky to be able to tolerate the ghosting relatively well. I live in complete isolation for a week now, what about those who … >>>>>>>
Now we’re in for a big shock, all of us. Now take a deep breath again, we have to somehow endure this situation, bear it, and we can’t do more … >>>>>>>
Today is World Down’s Day. To draw attention to it, one should wear two different socks. Actually, I should be sitting in the Müngersdorfer Stadium with my 2 different socks … >>>>>>>
We all go through special times. We’re all concerned. The difference is that this situation makes our situation with MSA, even more difficult. For a human being, the probability of … >>>>>>>
I’m a little overwhelmed with this Corona madness. Of course one should not take it carelessly – especially we MSA-sick people – but also not fall into hysteria. Somehow I … >>>>>>>
Can anything be positive in this misery? I try to list the “pro’s”, although I’d like to be without all that, and the list “cons” is much longer. But as … >>>>>>>
In my previous life, I was very fond of shopping. So not shopping, but shopping. I was always up to date on what was new in the candy department. … >>>>>>>
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, … >>>>>>>
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 … >>>>>>>