Skip to content

Living with MSA / A blog

Our daily life with Multi System Atrophy

  • What is MSA?
  • Blogs
  • Useful links
  • Shop
  • About Marion
  • About Marta
  • Team
  • Unforgotten
  • English
  • German

Category: Caregivers

Caregivers

Posted on 2. November 20223. November 2022 by Nicola

Impressions of a vacation at the foot of the Olympus Mountains

From September 10 to 24, 2022 I was in Greece, more precisely, in the north (Macedonia). Of course, I did not travel alone, but with my husband and my caregiver … >>>>>>>

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 … >>>>>>>

Zusammen sind wir stark

Melde dich an zum Stammtisch


Trete der Whatsapp-Gruppe bei

Search Blog

Categories

  • Caregivers (2)
  • General (184)
    • Aids (15)
    • Bureaucracy & paperwork (16)
    • Diagnostics (10)
    • Everyday life (98)
    • Exception (8)
    • Habits (33)
    • MSA & other diseases (15)
    • Nutrition (7)
    • Psyche (73)
    • Rehab (10)
    • Speech therapy (9)
    • Sports & Exercise (24)
    • Studies & Research (20)
    • Symptoms (58)
    • Travel with MSA (13)
    • What is MSA? (14)
  • Guest article (3)
  • Life despite MSA (5)

Contact us

info@leben-mit-msa.de

Archives

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
  • Henrike on Marta’s journey to Bavaria
  • Kevin on Marta’s journey to Bavaria
  • Darrell Meekcom on How are you?
  • Monika on A man goes when he wants to go

Writers

  • 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
  • 1 Marta
    • The last decision
    • Tabula Rasa
    • 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

Subscribe to blog via email

Enter your email address to subscribe to this blog and receive notifications of new posts via email.

Community

  • agileloudly89311fe39e
  • maximum134dea16a9
  • Nina
  • Maik
  • Anja
  • Closed Account
  • Silvia
  • sharkbriefly8fe71b45f8
  • Heike Klauser
  • Susanne Dinse-Wendt

Top Beiträge

Was bedeutet MSA für (pflegende) Angehörige?
Erstens kommt es anders......
Treffen am Ammersee
Flyer Leben mit MSA zum Download
Anfangen mit Aufhören?
The last decision
Erster Ausflug mit dem Rollstuhl oder „ Wie man wieder zum Kleinkind wird“
Travel with MSA
Erwin und die Wohlfühlmomente im Tageshospiz
Homeland
Privacy & Cookies:
Diese Seite benutzt Cookies. Mit Fortfahren erklären Sie sich einverstanden. / This site uses cookies.By continuing to use this website, you agree to their use. Cookie-Richtlinie / Cookie Policy
  • Imprint
  • Privacy Policy
Datenschutzerklärung Proudly powered by WordPress