Linda Faga

First post: Mar 10, 2019 Latest post: Mar 21, 2019
Welcome to our CaringBridge website. We are using it to keep family and friends updated in one place. Linda's journey with her disease started in June of 2015 when she woke up feeling dizzy. That dizziness steadily got worse and then she began to have difficulty moving her limbs. After seeing doctors in Waterloo, and after several trips to Mayo Clinic, the neurologists determined /undetermined/re-determined that she has a type of Parkinson's. Her current neurologist suggested that it may be Multiple Systems Atrophy.  It is hard to make a conclusive diagnosis for MSA; however, her symptoms are indicative of MSA so we believe that to be accurate. There is no cure for MSA so we are cherishing the time we have. The good news... Linda is not in pain and her cognition is still great. Thank you for your continued love and support. ❤🙏🏼 We appreciate your support and words of hope and encouragement. Thank you for visiting her page.

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