by Funmi Fashina | May 16, 2023 | Articles
Can you tell us a bit about yourself and your mum? My Mom and I were extremely close. She was a single mother when I was growing up so it was just the two of us for a long time. Later on, she remarried and I loved my step-dad very much. I was also happy to get a...
by Funmi Fashina | Mar 13, 2023 | Articles
Receiving a diagnosis of Multiple System Atrophy (MSA) can be a difficult and emotional experience. It can be hard to come to terms with the fact that you have a rare, progressive neurological disorder that has no cure. However, accepting the diagnosis is an important...
by Funmi Fashina | Mar 13, 2023 | Articles
While there is no cure for MSA, there are treatments available that can help manage the symptoms and improve the patient’s quality of life. Here are some of the common treatments for MSA: Medications Medications can help manage the symptoms of MSA. For example,...
by Funmi Fashina | Feb 9, 2023 | Articles, News
Hi Reader, if this is your first time here, we are pleased to have you and would like to introduce ourselves. We are a registered Nigerian Non-Profit Organization set up in 2013 in memory of the late Mrs. Funmi Fashina whom we lost to Multiple System Atrophy (MSA)....
by Funmi Fashina | Dec 21, 2022 | Articles
Living with multiple system atrophy (MSA) can be a challenging and difficult experience. MSA is a rare and progressive neurological disorder that affects the central nervous system, leading to a decline in various functions such as movement, balance, and autonomic...
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