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Advice on DLA appeal please
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I have been involved in setting up a new Scottish Charity for SPD(Symphysis Pubis Dysfunction) called Pelvic Instability Network Scotland (PINS) We would be interested to hear from anyone who has SPD and what their experiences have been of treatment, applying for DLA etc Our website www.pelvicinstability.org.uk is in its early stages with a lot more information still to be added including a forum but we would welcome feedback on it generally and what you would like to see included in the future.
Many thanks0
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