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Author: Marta

Posted on 18. January 202316. January 2023 by Marta

The last decision

I’ve been writing this post forever. By the time you read it, I most likely won’t be around. I am publishing this post with timing. Yes, it is a concern … >>>>>>>

Posted on 16. December 202216. January 2023 by Marta

Tabula Rasa

It was at the beginning of December four years that Santa Claus gave me the diagnosis. I must have been terribly naughty. I will never forget the shock of that … >>>>>>>

Posted on 21. October 202230. October 2022 by Marta

Journey

Now I have not written anything for a long time. There are several reasons for this: firstly, writing is very exhausting for me. I have become very slow. And instead … >>>>>>>

Posted on 18. August 2022 by Marta

When words fail

I found out this morning that Marion has passed away. I know that she is now redeemed, but I am sad and stunned. It happened so fast…

She was my … >>>>>>>

Posted on 27. April 2022 by Marta

This demand for happiness and gratitude is annoying

Being dissatisfied or unhappy is totally taboo. Negative thoughts and feelings in general. We have to deal with the most devastating disease, our lives, and often the lives of our … >>>>>>>

Posted on 17. April 202220. April 2022 by Marta

How are you?

Currently I am dealing a lot with pain. Primarily out of my own need and distress. Almost daily people ask me how I am and I have several problems with … >>>>>>>

Posted on 25. March 2022 by Marta

About breathing

Lately I have noticed a change – among others – in myself. In the evening, when I lie on the couch, I have unusual breathing. I have to take deep … >>>>>>>

Posted on 8. March 20228. March 2022 by Marta

What does MSA mean for (care) relatives?

 

(Guest article from Silvia)

In 2017, my husband had the first symptoms – slight balance problems and speech was sometimes a little slurred. At that time he was still … >>>>>>>

Posted on 24. February 202228. September 2022 by Marta

Do what is possible

For about two weeks now lives the sports group. That’s me, and a handful of participants from our online group. We do one hour of sports every day, each as … >>>>>>>

Posted on 2. February 202211. March 2022 by Marta

Dentist visit

I recently had a visit to the dentist. It is never a pleasure and as the disease progresses it becomes more and more difficult.

My dentist had MSA in the … >>>>>>>

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Young Alliance Against Multiple System Atrophy (YAMSA) e.V.

Recent Posts

  • Pain in people with multiple system atrophy (MSA) – a web-based survey 16. February 2023
  • Wenn die Worte fehlen 19. January 2023
  • The last decision 18. January 2023
  • Tabula Rasa 16. December 2022
  • Impressions of a vacation at the foot of the Olympus Mountains 2. November 2022

Recent Comments

  • Kevin on The last decision
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  • 1 Marion
    • The long farewell to my voice and the stadium
    • My sister not my nurse
    • Oh well, it’s just always something or Colonel Hati
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    • The last decision
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    • Journey
  • 1 Nicola
    • Impressions of a vacation at the foot of the Olympus Mountains
  • 1 Silvia
    • Pain in people with multiple system atrophy (MSA) – a web-based survey
    • Wenn die Worte fehlen
    • Between hope, anger and despair

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Top Beiträge

Winter – eine Hommage an die Angehörigen von MSA-Patienten
Was bedeutet MSA für (pflegende) Angehörige?
Als mein Partner ging, kam die "Herbstzeit"
Notaufnahme
Leben mit MSA - Der Stammtisch I.
Ich kämpf, weil ich bin....
Tabula Rasa
Erstens kommt es anders......
MÖGLICHE, WAHRSCHEINLICHE , SICHERE MSA und wie spende ich mein Gehirn
Ein Märchen für Kinder, das Papas Krankheit erklärt
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