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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.
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Community |
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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.
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Helping to prevent
suicides
and for someone to talk to
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Site Highlights |
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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.
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Donations |
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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 |
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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. |
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Use the Links below to shop online
and earn a few pennies commission for the IPRS at no extra cost to you.
UK Sites
For more UK sites and sites abroad go to the
Palindromic Rheumatoid Arthritis, Palindromic
Arthritis palendromic rhumatism
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Founded 2005.
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