AmandaL's Stelera Journey

[jiml]

Thank you  I'm starting to run out of options if this doesn't work.  I've already tried methotrexate, cyclosporine, humira, uvb, infliximab.  I was surprised that they don't let you take the medication home meaning I have to go back every time for my injections.

Hi Amanda
Was wondering if you have noticed any changes to your psoriasis yet. I know it's still early but are you feeling any better in yourself, and is there any improvement to your skin.
I'm not a stelara user so I don't know how often you have your shots and have you discussed yet the possibility of doing it yourself ( after training)