Hi there,
I have Connective Tissue Disease with Scleroderma. I was on the high dose Golimumab 100mg for a few months before I started getting Thunder Clap headaches and my hair started to fall out. In January I was put onto 50mg but have felt so rotten I am about to go back on the higher dose again but was wondering if anybody else out there had the same side effects and how they coped.