How does FA affect your significant other?
What is one thing that makes Friedreich’s Ataxia tough on your spouse or significant other? One thing that my husband, Justin struggles with is that I strive to be independent when things are becoming harder on me, For example, yesterday I worked, ran an errand, helped make dinner and then exercised on my stationary recumbent bike. I ended up having a bad fall last night because I did too much. He wants to help more to take things away from me to make things easier. But I am too stubborn to lose my independence. Does this happen to you too?
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