Saturday, April 6th
I believe my experiences have been pretty typical for anyone unfortunate in being diagnosed with dermatomyositis and lupus...
When diagnosed with DM...I was told by my dermatologist that I would no longer have a social life, I was shocked...I came to the realization that I would live my life as normally as possible on my terms, not the terms of DM or lupus...this mindset has been extremely liberating and has guided me as I take on each challenge or obstacle that DM and lupus has directly or indirectly thrown in my way...I will not restrict the paths I take...
I'm taking as much time as I can to enjoy as much as I can on my so-called bucket list...I have no regrets...I have been blessed...
Another great day!
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