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.
International petition to fight lymphedema ignorance around the world without frontieres to bring awareness and Real treatments.
Any advice on osteoporosis treatment with lymphoedema? Prolia and cellulitis
Sock it to lymphoedema challenge
Writing to mp, starting a petition?
Cellulitis Concern 36M
