IPFR in Wales - who’s had one approved for lupus ... - LUPUS UK

LUPUS UK

31,743 members28,102 posts

IPFR in Wales - who’s had one approved for lupus services or treatments?

Wendy39 profile image
5 Replies

Hello!

I’m just reading the WHSSC NHS Wales Policy on making decisions on IPFR - or Individual Patient Funding Request.

As most of you know, myself and others in Pembrokeshire under Hywel Dda UHB have had IPFR applications turned down, using the fact that lupus patients can be looked after adequately by a General Rheumatologist under the health board current provision.

My argument is that this policy is unfair, it’s a post code pottery, as if we lived in England we would firstly have the right to a second opinion and secondly be able to chose to get that opinion from a lupus expert or a LUPUS UK Centre of Excellence.

We don’t have either of those rights in Wales and there are no Centres of Excellence here either. So we are automatically at a disadvantage for lupus treatment because we live in Wales.

Our health board will only let you out of Wales currently, to a Centre of Excellence if you have kidney involvement and/or they are considering Rituximab (as indicated to do so under the NICE Approved BSR Guidelines for Lupus.

I have found in the Policy a clause that says a Health Board needs to give careful consideration to certain circumstances which include 2.2,

“When other Health Boards may have used their discretion to make a different decision on a specific topic.”

2.3 says that Health Boards can lawfully exercise it’s discretion and to allow for exceptions to it in specific clinical circumstances.”

So, my question is, has anyone in Wales been “allowed out” of Wales for lupus care and/or treatment. What health board are you under?

If you would rather not say here in public, please send me a personal message.

Thank you!

Wendy x

Written by
Wendy39 profile image
Wendy39
To view profiles and participate in discussions please or .
Read more about...
5 Replies
Wendy39 profile image
Wendy39

You have made me giggle! Great analogy! We are totally trapped! Xx

CecilyParsley profile image
CecilyParsley

My God Wendy what a complex and bureaucratic process. If you had not have told me I would not have known that it was not my right to seek a second opinion. The biggest issue I have encountered is that a second opinion is often provided by a colleague of the consultant you are expressing misgivings on. I don’t know when this rule came into being but I was referred to St Thomas’s in 2013. Thank you so much for your fight and tenacity in getting better treatment for so many. I have now been downgraded to UCTD again but if there is anything that I can do to help you I will be glad to xx

misty14 profile image
misty14

A glimmer of hope maybe Wendy? Do hope you get some interesting responses. Its more than time you patients in Wales were treated much better!. Xx

Wendy39 profile image
Wendy39 in reply to misty14

Thank you Misty! For all of your support, encouragement and friendship. Fingers crossed 🤞 xx

misty14 profile image
misty14

Look forward to your update wendy. Fingers tightly crossed for you all. Xx

You may also like...

Campaign for Access to Specialist Lupus Care for People Living with Lupus in Pembs, Wales

Have you all signed? Thank you Wendy xx...

Please help people living in Pembrokeshire, Wales access Lupus Centres of Excellence in England

Lupus patients living in Pembrokeshire are being denied access to Lupus Centres of Excellence in...

North Wales Lupus Information Day - 12th May 2018

The North Wales Lupus Information Day will take place on Saturday 12th May 2018 at The Imperial...

Query re Rituximab and being licensed treatment for lupus?

working and her lupus isn’t under control. She is suffering very badly from lupus related...

Please sign this petition - Help support people living with lupus in Wales get access to specialist care.

people living with lupus in Wales by signing this petition started by the Pembrokeshire Lupus...