# Losing IVIG covered insurance

**URL:** <https://forum.livingwithpolyneuropathy.org/t/losing-ivig-covered-insurance/576>\
**Category:** General CIDP Discussion\
**Created:** [April 1, 2014, 8:34pm UTC](https://forum.livingwithpolyneuropathy.org/t/losing-ivig-covered-insurance/576 "2014-04-01T20:34:09Z")\
**Posts on this page:** 1\
**Showing post:** 19

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**Author:** ![juliebug1947](https://sea1.discourse-cdn.com/flex019/user_avatar/forum.livingwithpolyneuropathy.org/juliebug1947/32/1047_2.png) [@juliebug1947](https://forum.livingwithpolyneuropathy.org/u/juliebug1947)\
**Post date:** [July 14, 2015, 9:09pm UTC](https://forum.livingwithpolyneuropathy.org/t/losing-ivig-covered-insurance/576/19 "2015-07-14T21:09:58Z")

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Rich, Are you saying that Medicare Part B is paying 80% and your medigap Plan F covers the other 20%? I am so curious because I will need to go on Medicare soon. I have a CIDP diagnosis and have been getting IVIG for about 12 years, about twice per wk. I have been getting at home, and I understand I will no longer be able to do this, but will have to go to outpatient or infusion center. But I have been told by some that my meds will fall under Part D. If so, that will be a killer for me, since the cheapest I can find will cost at least $26,000 per year. Any info will help. Thanks!

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