Sometimes the best pain reliever can just be a scream when the pain hits...to just scream at the top of your lungs and let out the frustration. One of the hardest parts about HS is no one can see it. All sores are hidden under my clothes and bandages. I dont look "sick" I just look like another fat lazy woman but people dont feel the pain I have, they dont even see the sores. People may judge me because of it all but they have never had to walk in my shoes or bandages. The only ones who understand are the others who have HS. In everyday life I just smile and say Im fine when I am falling apart inside. The pain is like scratching/digging/ raking a bad burn/sore over and over and nothing can fix it just the air touching hurts it. Some of you may be wondering why I share this info...well my number 1 answer is people keep it secret because its embarassing but that doesnt help the word getting out,it doesnt produce research. I am tired of suffering in silence.
Posted on: Thu, 27 Jun 2013 01:12:32 +0000
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