# Second opinion

**URL:** <https://forum.livingwithpolyneuropathy.org/t/second-opinion/982>\
**Category:** General CIDP Discussion\
**Created:** [August 16, 2015, 12:58am UTC](https://forum.livingwithpolyneuropathy.org/t/second-opinion/982 "2015-08-16T00:58:05Z")\
**Posts on this page:** 1\
**Page:** 1

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**Author:** ![laurie1](https://sea1.discourse-cdn.com/flex019/user_avatar/forum.livingwithpolyneuropathy.org/laurie1/32/922_2.png) [@laurie1](https://forum.livingwithpolyneuropathy.org/u/laurie1)\
**Post date:** [August 16, 2015, 12:58am UTC](https://forum.livingwithpolyneuropathy.org/t/second-opinion/982/1 "2015-08-16T00:58:05Z")

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Saw my regular dr and he was wondering how long I should be receiving IVIG treatments. It will be a year for me next month. He believes it is all about money. He suggests getting a second opinion from a research hospital like Boston's Brigham & Young. However, I believe the treatments have helped w/my strength. Not sure what to do. Suggestions?