# Pp vs cell cept vs IVIG
**URL:** https://forum.livingwithpolyneuropathy.org/t/pp-vs-cell-cept-vs-ivig/769
**Category:** General CIDP Discussion
**Created:** [October 21, 2014, 5:59pm UTC](https://forum.livingwithpolyneuropathy.org/t/pp-vs-cell-cept-vs-ivig/769 "2014-10-21T17:59:09Z")
**Posts on this page:** 2
**Page:** 1
### Author:  [@Ethel](https://forum.livingwithpolyneuropathy.org/u/Ethel)
#### Post date: [October 21, 2014, 5:59pm UTC](https://forum.livingwithpolyneuropathy.org/t/pp-vs-cell-cept-vs-ivig/769/1 "2014-10-21T17:59:09Z")
. Because of my age, I have made a decision that the treatment I have is the best for me. The information that I received from everyone about plasmphersis and cell cept vs ivig helped me make that decision.. Medicare has been paying for IVIG infusions but when I start home infusion they will not pay for it . I have been accepted by a company that will pay for the IVIG. All the details have not been finalized. I have been told that all my expenses will be covered.Thank you for your help. Ethel
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### Author:  [@Jeff](https://forum.livingwithpolyneuropathy.org/u/Jeff)
#### Post date: [October 23, 2014, 1:41am UTC](https://forum.livingwithpolyneuropathy.org/t/pp-vs-cell-cept-vs-ivig/769/2 "2014-10-23T01:41:02Z")
I’m glad you’ve made your choice and found coverage for it.
Good health to you!