New Website

Hello everyone. I am starting a new website. There is going to be tons of relevant info. We are going to do fundraiser for people that can not afford Doctors or meds. Lets finally cure HS.

New website




I suffer from Hidradenitis Suppurativa. I am trying to build a community with other HS sufferers to create awareness of how serious this disease is.

One thought on “New Website

  1. Hey dude. I just found your website. You are not alone. I’ve been dealing with HS for a while and I know exactly what you are dealing with – I’ve had the whole blood and pus deal too for a number of years. Let me tell you this, I got on Humira and Methotrexate (a drug that impacts immune system). This has helped a LOT with reduced flare ups. Apparently HS is immune system related.

Leave a Reply

Fill in your details below or click an icon to log in: Logo

You are commenting using your account. Log Out /  Change )

Twitter picture

You are commenting using your Twitter account. Log Out /  Change )

Facebook photo

You are commenting using your Facebook account. Log Out /  Change )

Connecting to %s