IPRS logo International Palindromic Rheumatism Society IPRS logo

 

   

 

What is "PR"

Symptoms And Diagnosis 

Photos Of My PR

Medication and Treatment 

Prognosis For PR

PR FAQ

It Makes PR Worse...  It Makes PR Better...

PR Stories

Impact of The IPRS

PR Forum

PR Articles

How You Can Help The IPRS 

IPRS Publications

Helpful Guides

DLA (UK) Guides

Useful Links

Contact Us By Email 

Disclaimer and Terms Of Conditions

 
 

 

Palindromic Rheumatism

Hello and welcome to the IPRS website. This website is for people interested in or suffering from Palindromic Rheumatism. The IPRS has grown with so many members in such a small time as it is the only place offering a place to find advice, help and support for people with PR. The IPRS was created by a sufferer of PR who has had PR for well over 20 years. We also have a great bunch of volunteers that work very hard for the IPRS themselves having PR or now RA. So it is run by people who understand what it is like to live with PR. I hope this website, the information and pictures help and inform you. We have now been going for a number of years and we are glad that we have helped, supported and informed so many. We are even inspiring others to create there own websites and hopefully spreading awareness.

 

 Information

  The International Palindromic Rheumatism Society is a voluntary group made up of people who know the most about PR, that is the people who have PR. The aim of the The IPRS is to reach and bring together as many people affected by PR, to help inform, give advice and offer a place of support. The goal is to have every Dr aware of PR and every sufferer of PR access to an online support and advice group. We hope to have all the information you will ever need to know about PR. As the IPRS is privately funded we welcome donations. We are also glad others have been inspired to start their own website and spread the awareness of PR. However if you do copy our information for your own website please ask first.  
   

Community

 

If you want to ask questions about your own experiences and symptoms, or just want further information about anything PR related then the best place to do so is to use one of our three online social networks, where there are lots of friendly people ready to share their advice and experiences with you:

1. The IPRS Forurm
    www.palindromic.org/pr
2. Using our Facebook page
    www.facebook.com/palindromic.rheumatism
3. Using Twitter.
    www.twitter.com/TheIPRS

 

We continue to work on, and update this website whenever we can. We hope to continue to include everything you will ever need to know regarding PR. If you come across any news, or articles regarding PR and PR Medication that isn't included on this site etc please let us know. 

Also we need you to get involved so we can have more example photos and stories on how PR affects you. Particularly if you work and look after a family or have an interesting or unusual situation.

 


Helping to prevent suicides
and for someone to talk to

 

 
   
     
 

In
Memory
Of

 
 
 

Site Highlights

 

The only web site to have PR Photos.

'Podcast' (Audio Recording) added to 'What is PR' page.

Join The IPRS Forum -  Speak to others that understand what you are going through.

Check out 'Medication and Treatment' to find out the latest information on the medication you are using

Read our members own PR Stories to find out how PR affects them.

The ipad compatible "Quick Links" at the top of the page which should make it easier to visit your most frequently visited pages.

 
 

Donations

 

To help maintain this website, forum & leaflets
All donations gratefully received:-
 Click the Paypal button below to make a secure payment online.

 (No Paypal Account Needed - Just pay by card)

 


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 Thanks

 

Since we started this site we have received hundreds of messages thanking The IPRS and congratulating us on a fantastic site. These messages mean a lot to the IPRS. This site is receiving thousands of hits a week now and with new forum members joining every day. We try to reply to each and every message however with PR and a limited amount of resources we may not get round to replying straight away. We tend to reply first to the urgent emails and sometimes don't get around to thanking everyone. We would like to take this opportunity to thank each and everyone of you that has thanked The IPRS via email.

We also thank all of you that have supported and enjoyed this site, and hope that you will continue to in the future.

 

 

   

 

 

Use the Links below to shop online and earn a few pennies commission for the IPRS at no extra cost to you.

UK Sites

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Thorntons
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         For more UK sites and sites abroad go to the
Palindromic Rheumatoid Arthritis, Palindromic Arthritis palendromic rhumatism

 

Founded 2005.