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I am also new to the posts. I've been on a week or so and am not

regular about checking in.

These people are amazingly honest and forthright about sharing their

stories. This is a hard pill to swallow no matter which " flavor " of

fibrosis with which we happen to be afflicted, and there are many.

Take delight in the good days and lean on your support system on the

bad days. I joined in because I could not find information on

questions I needed answers for. Like for instance, why do my calves

hurt? Is that a normal part of my disease or just something else

failing in my body? Those kinds of things. I made the statement to

my doctor that I was just trying to figure out what normal is now. He

said " , there is nothing normal about this. " So here we are.

Life just changed.

S, Lubbock, Texas

NSIP w/PF

Celiac Disease

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