SMASAC Working Group Post Polio Syndrome - Scottish Health On ...
SMASAC Working Group Post Polio Syndrome - Scottish Health On ...
SMASAC Working Group Post Polio Syndrome - Scottish Health On ...
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<strong>Scottish</strong> Medicines and Scientific Advisory Committee <strong>Working</strong> <strong>Group</strong><br />
<strong>Post</strong> <strong>Polio</strong> <strong>Syndrome</strong>/Late Effects of <strong>Polio</strong><br />
among polio survivors and health professionals, were considering the<br />
development of UK-specific guidance in some form, and were looking to<br />
improve the processes by which polio survivors are referred, or self-refer, to the<br />
services appropriate to their specific needs.<br />
Other organisations<br />
The Pain Association Scotland runs staff-led monthly self management groups<br />
throughout Scotland, in many cases as part of a service agreement with NHS<br />
Boards. Clinicians caring for those with PPS/LEOP should bear in mind the<br />
benefits which might accrue from referral to such a group.<br />
Pain as a symptom of PPS/LEOP should benefit from the work currently being<br />
undertaken by the <strong>Scottish</strong> Government’s Lead Clinician for Chronic Pain in<br />
developing a service model for pain management in Scotland, linked closely to<br />
the work on musculo-skeletal services being taken forward as part of the<br />
process of implementing the Framework for Adult Rehabilitation.<br />
Assist UK, also known as AIMS, leads a UK wide network of locally-situated<br />
Disabled Living Centres. Each centre includes a permanent exhibition of<br />
products and equipment that provide people with opportunities to see and try<br />
products and equipment and get information and advice from professional staff<br />
about what might suit them best. Assist UK also offer training courses linked to<br />
services provided by members. There are five disabled living centres in<br />
Scotland (in Dundee, Edinburgh, Elgin, Paisley and Stirling) providing specialist<br />
information on aids and equipment as well as other disability related enquiries.<br />
In view of the importance to people living with PPS/LEOP of maintaining their<br />
independence, information should be made available to them, either from<br />
healthcare professionals or through the SPPN, about the availability of self<br />
directed support. That funding allows people to determine their own care<br />
package and, if they so wish, to employ people to deliver it.<br />
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