# New member

**URL:** <https://forum.livingwithpolyneuropathy.org/t/new-member/593>\
**Category:** General CIDP Discussion\
**Created:** [April 22, 2014, 12:02am UTC](https://forum.livingwithpolyneuropathy.org/t/new-member/593 "2014-04-22T00:02:24Z")\
**Posts on this page:** 1\
**Page:** 1

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**Author:** ![BobF](https://sea1.discourse-cdn.com/flex019/user_avatar/forum.livingwithpolyneuropathy.org/bobf/32/802_2.png) [@BobF](https://forum.livingwithpolyneuropathy.org/u/BobF)\
**Post date:** [April 22, 2014, 12:02am UTC](https://forum.livingwithpolyneuropathy.org/t/new-member/593/1 "2014-04-22T00:02:24Z")

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# New Member

- Posted by [BobF](http://www.livingwithcidp.org/profile/BobF) on April 21, 2014 at 6:53pm in [General](http://www.livingwithcidp.org/forum/categories/general/listForCategory)
- [View Discussions](http://www.livingwithcidp.org/forum/topic/listForContributor?user=3m427u5veex62)

Hi! I am a CIDP patient in remission (hopefully permanently). In the Spring of 2013, my legs started getting weak and then I started to fall down, which put me in the emergency ward. In the hospital they diagnosed me with CIDP, gave me IVIG, kept me for 5 days and then sent me to hospital rehab for 3 weeks. Both my legs and my arms were quite numb and tingly. After rehab, I was sent home with no follow-on CIDP meds and have had none since. Progress at home (walking, stair climbing, getting out of chairs, etc) was quite slow and depressing. Then after about 2-3 weeks, there was a rapid change and things started improving much faster (don't know the reason for this). My arms and hands got back to about 98% recovery but the legs were a little slower, but I can now walk 2 miles, climb 100 stairs and have removed all the "blocks" we used to raised the chairs so I could get out of them. I can pretty much do everything I did before the onset, only at a slower speed! Where I was really lucky was that during this entire time I had ZERO-NO pain, just tiredness in my legs. Looking at the discussions, I know I got off easy and have this little black cloud over my head called "possible relapse". I was hoping I could get some insight into that possibility but looking at the discussions it seems it is very patient specific, with no real guidelines. I go to the gym to strengthen my arms, shoulders to help the legs (which don't seem to improve too much with the gym work)-- anyway, I'll be happy if I can just stay where I am at now. Glad I found this site, a wealth of information!

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