update:
I got on new meds because I have chronic migraines and my old meds stopped working. well the new meds make it really hard to eat and since I've been on them I actually haven't though about my ed much so that's interesting. I was originally really nauseous and that's why I couldn't really eat on the meds but that's gotten better but it's still just like hard to eat on them. they are really helping my headaches though so I'm hoping my neurologist doesn't take me off them when I go back. they were almost concerned that I lost 10 pounds between my last visits and were apprehensive to put me on meds with a side effect of weight loss
but yeah I'm still alive guys, I'm still here. a bit less active because my brain chemicals took over Ed for a while lol












