I feel the same way about ER visits. Ours used to be so good too. Such a shame to see quality care go down the drain and we're the ones who suffer!!!

Geez alit if us have problems with ER
It's scary because what can we do? Sometimes I feel like im dying but still refuse to go there after 3 times and no help or very little.
Today I was bad I thought my heart was going to give out....I struggle to decide what to do. I rode it out and now its almost midnight and im feeling a bit better. (That's how much I DO NOT like ER)

Blessings to you all 😇🫶🙌

Pray you get fortunate and find a good doctor , that will address your health problems , this is just plain crazy on the part of the medical field🙏🙏🙏🙏

I definitely know what you mean Roberta. I'm waiting to see my neurologist in December as well. It makes me nervous having to wait 6 months or more for just a 15-minute office visit.......things can happen so fast with MG. Wishing you good health and a really good visit with your neuro when you see him or her. Let's keep in touch! ❤️

I feel the same way about going to the ER. They just don't know enough about MG and that scares me. When I had surgery last December, the surgical team was great and took the time to make sure I would be okay from a Myasthenia standpoint but it was a totally different story when I was out on the floor in a regular room. If I had not been alert enough to know, they would have given me meds that I cannot take because of the MG. They almost gave me muscle relaxers. One of them was a doctor. I just pray that I am never in a position where I cannot speak for myself.