Do you receive IVIG at home?
Good morning LEMS friends!
Last month during my infusion a patient care advocate from my health insurance company reached out to me with some exciting news! She was checking to see if I would like to change my infusions to in-home instead of going to an infusion center.
For me, this is big! I was given this option in the past, however, my neuro wasn’t too keen on it and I was told my copay would be higher so we did not pursue it. The advocate that gave me a call said she would work with my previous neurologist and my new one to devise a plan so I can begin the transition to home infusions! I was also promised that my co-pay would be equal to or less than what it is currently!
I am really excited about this opportunity; we are still working out the kinks and I will be posting more in the future about the process if you guys are interested!
For those of you who receive infusions, do you get them at home or in an infusion center? How was the transition from the infusion center to home if you receive home infusions?
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