I just got diagnosed with MMN. Which in my view is a good thing I had been very worried about having ALS due to my symptoms.

I was told I needed 20k infusions regularly and unfortunatly I am in the state of being uninsured and far from rich.

Can anyone point me towards good aid for treatment costs. Has anyone had success with medical or SSI?

please let me know.


TO the previous poster, I was told by my neurologist 80% of people respond with in weeks to the treatment, and often get back a huge amount of strength. I wish you luck. I will be starting mine as soon as I figure out hot I can pay.