I just listened to a webinar tonight (see resources for webinars). It happened tonite w/ 4 doctors from Ortho, Mental Health, Rheumatology & ?... They mentioned sleep conditions so maybe check that out...

I can relate to the limitations this disease puts on us. My children are older than your son, but i am also limited in how i can interact with them. Im unable to sit, comfortably, at a table to play a game. Often the brain fog gets in the way as well. Ive taken methotrexate (often an insurance required 1st treatment), Otezla, Humira and now Enbrel. It seems to be working, but only in terms of slowing the damage-not helping the day to day issues. There are a lot of kind folks on this site with info they will happily share. Know you are not alone and this group is here to help support folks like us. Please keep us posted. Or come back even if only to vent. 🌷

Hello Rajones and welcome to the group. Lots of us here understand what you are going thru. I, too, struggle with fatigue. There are many days I’m only ready for interaction with humans in the afternoons. Body fatigue, brain fog, joint stiffness. What treatment are you on now and what have you taken in the past?

There are a few things like sleep apnea that can have that same effect. Having recently completely misdiagnosed myself, I would caution you to be sure of causative agent.