Saving Lives Through Education                   And Awareness

  WE Need Your             Help

 Please Consider

    

 

 

       Or text  70070 followed by LSUK15 £5 or £10

                                                         ( In that format )

LSUK is determined to promote and raise awareness about Lynch Syndrome and push it into the national spotlight.  We also aim to support those affected and their families as best we can. We have drawn up an action plan in order to achive our objectives. We really need your help on this because we can't do it on our own!

♦ To organise our second annual conference with ticket prices heavily subsidised through charity funding to enable as many people as possible to attend and gain valuable knowledge to help protect themselves and their families.

 

 

 We are designing a range of leaflets for clinics across the country about LS, which will be also available on our site in PDF format. These will also be produced in Braille and translated for people where English is not a first language if requested.

 

♦ We plan to subsidise patient days across the country and assist with their running. LSUK intends to target relevant conferences with charity stands throughout the UK and continue raising awareness of LS. We will network with medical professional, other charities and patients alike to promote our cause. This will help save lives by patients questioning their family history for signs of potential LS


 We plan in the future to provide educational courses for medical professionals. To assist and continue to raise the profile for LS patients within all sectors of our healthcare system.

 

100% of donation goes to Lynch Syndrome UK

      THANK YOU!

© 2019 Lynch Syndrome UK

Site Created By Mark Cooper

Photography by Chloe-Louise Smith <INFO>

                     

Registered Address: Linden House. 9/11 Main Street. Ingleton. Carnforth. Lancs. LA6 3EB United Kingdom team@lynch-syndrome-uk.org