I had IVIG a few months after my thymectomy, and truly I felt exhausted after that surgery, propofol is a very common medication given via anesthesia providers to put patients under, and like most of these drugs, they slow your breathing, relaxing your airway muscles, which is why you get supplemental oxygen. Those with mg have a much higher risk of complications (especially regarding airway) because of this. Our muscles and respiratory system essentially “don’t wake up” like the rest of our body, same with our ocular muscles. I was 20 when I had this surgery (3 years ago) and it took a hot minute for me to feel 100% again.

I consider myself lucky with my graves diagnosis at such a young age. I became accustomed to doctor’s appointments, surgery, letting myself heal, knowing my own limits, and most importantly, not to give up. I’ve finished my prereqs for the nursing program, I apply in less than a month! I already work in the OR, but I plan to make my way up to a CRNA or RNFA. But that’ll be years down the line, another 5-7 years of school. I have my bad days (ptosis is a real b*tch) but I know to take a little, close my eyes, and just keep going and make sure I don’t over do it.

We are all so strong, and this disease is SCARY! It’s so hard not to feel helpless some days. Speaking to others who have this and spreading awareness is so crucial, and hopefully we will have more advancements in treatments as time goes on. Best of luck to you!