# R e l a x -- User Help is Here!

**URL:** <https://forum.livingwithpolyneuropathy.org/t/r-e-l-a-x-user-help-is-here/5379>\
**Category:** General\
**Created:** [November 24, 2020, 2:47am UTC](https://forum.livingwithpolyneuropathy.org/t/r-e-l-a-x-user-help-is-here/5379 "2020-11-24T02:47:08Z")\
**Posts on this page:** 3\
**Page:** 1

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**Author:** ![Bens\_Friends](https://avatars.discourse-cdn.com/v4/letter/b/838e76/32.png) [@Bens\_Friends](https://forum.livingwithpolyneuropathy.org/u/Bens_Friends)\
**Post date:** [November 24, 2020, 2:47am UTC](https://forum.livingwithpolyneuropathy.org/t/r-e-l-a-x-user-help-is-here/5379/1 "2020-11-24T02:47:08Z")

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Handy user help for our new layout is ready for you, and it’s where you can always find it: in the “New User Help” section. Just tap on the New User Help button at the top of your screen. (You may need to scroll down just a wee bit.)

 ![](https://us1.discourse-cdn.com/flex019/uploads/ben_polyn/original/2X/d/df2279a3b5628b71c47b92583d4c5aa53e5721e9.png)

Please let us know below what you think of it. Your comments and suggestions are welcome! Just tap “Reply”.

A printable version of the help document is in the works for those of you who like a hard copy.

Stay safe and well!

**Seenie and the ModSupport Team**  
_(Sharon, Merl, TJ, Seenie)_

**BEEN AWAY FOR A WHILE?**  
Drop by and admire our easy-on-the-eyes new look! If you haven’t logged on for a while, go to [your community,](http://bensfriends.org/community-list/) tap on LOG IN, enter your email address, then “Forgot my Password”. You’ll receive instructions about what to do next.

[@trust\_level\_0](https://forum.livingwithpolyneuropathy.org/groups/trust_level_0)

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**Author:** ![ModSupport](https://sea1.discourse-cdn.com/flex019/user_avatar/forum.livingwithpolyneuropathy.org/modsupport/32/2610_2.png) [@ModSupport](https://forum.livingwithpolyneuropathy.org/u/ModSupport)\
**Post date:** [November 25, 2020, 2:51am UTC](https://forum.livingwithpolyneuropathy.org/t/r-e-l-a-x-user-help-is-here/5379/2 "2020-11-25T02:51:12Z")

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**Author:** ![pdic](https://avatars.discourse-cdn.com/v4/letter/p/ecae2f/32.png) [@pdic](https://forum.livingwithpolyneuropathy.org/u/pdic)\
**Post date:** [January 29, 2023, 6:18pm UTC](https://forum.livingwithpolyneuropathy.org/t/r-e-l-a-x-user-help-is-here/5379/3 "2023-01-29T18:18:07Z")

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I dont know who wrote the article but I hope it is seen. I have had a red itchy rash for over 2 years. It covers my face, head, neck back and chest. It itches. My ears are covered also, If I dare to touch any part of it, I am digging and itching until MY body is pleading. STOP STOP. CIDP is part (I say cause) of it. I read something in one of thiese section.The person descriped my condidtion perfectly. He also had a REMEDY for it. I went to get a paper and pencil and when I came back the page had disapeared. I have had it for two years He had a remedy that took a few months to eradicate. YES I want the conversation to continue. I don;t know what section I say it in. I just saw the remedy. to day 1/29/23… My remedys are not removing the disease or even calming it down,.I have spent a fortune for remedies and still awake in the middle of the night clawing at my body.