|
|
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.
|
|
 |
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
|
| |
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)
|
|
 |
 |
| |
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
For more UK sites and sites abroad go
to
the
Palindromic Rheumatoid
Arthritis, Palindromic Arthritis palendromic
rhumatism
|
Founded
2005.
|
