Hi Everyone!
I am new to the boards and wanted to introduce myself. I am 21 and live in Wi. I am not good at writing poems, but wanted to share my story with you anyway.
It started out as a few and then a few more,
Just looking like a little red sore.
I finally decided to the doctor I must go,
She knew it was best to send me to the dermo.
The dermo did some testing and diagnosed me with p,
I was dazed and confused at the news she just gave me.
It's a chronic skin disease with not yet a cure,
I could feel my eyes welling up for a tear.
I listened as she went on to say,
Let's sign you up with npf today.
They will send you newsletters and panflets all year through,
You can access a message board and chat with others like you.
I left that appointment feeling sad and angry,
How can this really be happening to me?
I've been doing some research to find out more,
And on this message board there's info galore!
There's venting, crying, and needing advice,
Everyone here seems really nice.
From treatments, tips, and techniques too,
There are so many you can chose to do!
Here anyone can find great support from their family,
Not related by blood, but united from P.
I can't wait to get to know everyone!