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Multiple System Atrophy (MSA) Awareness Month

This March, Fight Parkinson’s is recognising Multiple System Atrophy Awareness Month by busting myths, providing support and resources, and sharing personal stories of those in the Fight Parkinson’s community who are living with MSA.

What is MSA?

Multiple System Atrophy (MSA) is a rare and progressive neurological condition that affects multiple parts of the brain. The gradual loss and shrinkage (atrophy) of nerve cells affects multiple systems in the body and symptoms can be many and varied.

The symptoms worsen over time as the condition tends to advance rapidly over the course of 5 to 10 years. The person will experience progressive loss of motor skills, eventually being confined to bed. There is no remission from the condition and there is currently no cure.

 

What are some common myths about MSA?

Though MSA is a form of Atypical Parkinson’s–meaning that its symptoms are similar to those experienced by people with Parkinson’s–there are still some misconceptions that surround the condition. Read on below to test your own knowledge of MSA.

Myth: MSA is the same thing as Parkinson’s

Truth: MSA is different from Parkinson’s and effects multiple and different areas of the brain. MSA and Parkinson’s may have similar symptoms initially as it progresses, but MSA symptoms are more severe and appear earlier

 

Myth: MSA is contagious

Truth: MSA is not infectious or contagious–you cannot “catch” it from someone who has been diagnosed or is showing symptoms

 

Myth: Everyone receives the same treatment to manage the symptoms of MSA

Truth: Just as no two people with Parkinson’s will experience the exact same symptoms and therefore receive the exact same treatment, the same goes for MSA. This means that no one’s journey with MSA will look alike and each person will receive the treatment that is most suitable to manage their specific symptoms

 

Myth: MSA is a single condition

Truth: MSA encompasses multiple conditions, including olivopontocer cebellar atrophy, Shy-Drager syndrome, and striatonigral degeneration

 

Where can I learn more about MSA and how can I receive support?

Please visit Multiple System Atrophy (MSA) – Symptoms, Causes, Treatment and Support to learn more about MSA. Remember that you are not alone–Fight Parkinson’s has a dedicated commitment to research, education, and support to help people with MSA live full and active lives for as long as possible.

 

Contact our friendly team today:

Free confidential information line – 1800 931 031

Open 9am-5pm Mon-Fri AEST

Email – [email protected]

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Please note: Fight Parkinson’s uses the phrase Parkinson’s rather than Parkinson’s Disease to reflect the community’s preference. Parkinson’s Disease is used only when necessary such as in medical, research or government contents, or in direct quotes.