Adapt and go on

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Loss. Everyone with Dupuytren's deals with it. For me, I can't clap any more. Hurts if I do. So I fake clap instead. And I'm not the only one. Someone told me that she does, too. 

"Or I use my right hand to slap on my leg or a chair/table next to me," she posted.

Someone can't open water bottles any more. I'm getting there. On Thanksgiving Day, I had to ask my son to open a can of corn with a can opener. Couldn't do it myself. 

Someone can't high five his grandson any more. Because his grandson likes to high five as hard as he can. 

Handshaking is also a challenge for some with the disease. Especially if the hand shaker squeezes too hard. So some fist bump instead of shaking hands. 

So, yes, we're all learning to adapt to get on with life and co-exist with Dup. 

 

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