Hello everyone,
I am new to the boards but have been lurking on the site for years. Always a good source of information and encouragement.
I am almost 9 years into my official battle with this disease but, like many others, have probably had it for years. My diagnosis came quickly after a loss of function in my right arm, but I had had a mysterious loss of hearing in my right ear the year before.
Since the diagnosis it has been a daily battle with fatigue, weakness, vertigo,etc etc. Some days are better than others but definitely rarely any good days.
I miss working, being active, being spontaneous, and so many other things. I hate the struggle to remain positive but I do it for my family.
I am glad to have a place to express my real feelings and chat with people who understand.
I am new to the boards but have been lurking on the site for years. Always a good source of information and encouragement.
I am almost 9 years into my official battle with this disease but, like many others, have probably had it for years. My diagnosis came quickly after a loss of function in my right arm, but I had had a mysterious loss of hearing in my right ear the year before.
Since the diagnosis it has been a daily battle with fatigue, weakness, vertigo,etc etc. Some days are better than others but definitely rarely any good days.
I miss working, being active, being spontaneous, and so many other things. I hate the struggle to remain positive but I do it for my family.
I am glad to have a place to express my real feelings and chat with people who understand.
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