With reference to bluedolffin's post about campaigning for change in access to Lymphoedema treatment, I have now set up a UK government e-petition about this.
The petition can be viewed and signed via the link below:
epetitions.direct.gov.uk/pe...
In addition to signing the petition I would ask that people write to their individual MP's and ask friends and family to do the same. Also contact your local council Health and Well-being Board and tell them about the difficulty you have had. LSN have letter templates for this.
Best wishes to you and your families this Christmas.
Has anyone had an IFR accepted to pay for liposuction for secondary lymphoedema?
Lymphedema clinics/MLD massaging in Bedfordshire 
Leg pump?
Travelling abroad with lymphoedema 
Wraps
