Back in April I announced my mom had MG (Myasthenia Gravis) per her neuro. Since then she's had more seizures due to her brain tumor and removal and nothing but trouble getting her Dilantin dose under control.

She decided to switch up neuro's per her GP. She was nervous, scared and not sure what to do. We encouraged her to go and just check him out. Turns out he's a VERY good neuro, highly recommended and she liked him a lot.

He said based on her records and various lab, eeg and xrays from the GP he does not feel she has MG. He said her symptoms are from the tumor and surgery, not from MG. He said he did not want the records from the other neuro because he had what he needed from the GP. He said any doctor who dx's a patient with MG would start some form of treatment immediately rather than wait for more symptoms which the other neuro was doing. She's going to send her records to him from the other neuro anyway just in case. She was so happy to hear she doesn't have MG.

He also started her on Keppra in addition to her Dilantin to help stop the seizures. He said she was having big seizures and not little ones like the other neuro said. This explains why she's having more and more memory loss and damage to her body. He promised her he will get them under control and not to worry. He's a Dr. House type and Mom is OK with that. He's to the point, no coddling or pats on the shoulder. She said she doesn't need a therapist, she needs a neuro.

So you will no longer see "mom dx'd with MG" on my siggy! Thanks to everyone who walked with us through this. Mom is still sick but not having the added dx of MG makes it so much better. To those suffering from MG I pray for all of you.