The story of Rob Burrow: My year with MND shown on BBC TV has helped promote MND awarenesses well as a special documentary about sport stars with MND and their families going through the suffering caused this debilitating disease.
South London MNDA are there to support all those who live locally who develop this dreadful disease, something that has been even more difficult over the last few months.
Normally Furzedown FACE, through its various local events and sales, raises thousands of pounds for the South London branch - providing a stairlift, living aids, respite, research help - as well as helping other local causes.
We only managed to have our PLANT SALE events - but we've heard they're really struggling during this crisis. So we are asking our Furzedown friends and neighbours’ help by donating to South London MNDA.
FACE understand we are in strange times and money is tight, but any amount will be much appreciated!
You can donate to our JustGiving page by clicking here: Thanks!
To help us through these difficult times during the Covid-19 lockdown, local Furzedown artist Sue Pearson, has created this charming #NewNormal story to share with children.
Please feel free to print the pages out so they can be coloured in - a PDF version can be downloaded HERE - and consider making a small donation to Furzedown FACE who will pass it on to local charities who are struggling to cope. Thank you
To donate please visit our #justgiving page:
Or please make a bank transfer to Furzedown FACE (Furzedown Annual Charity Events)
Account number 91519395; Sort code 40-03-19 (ref: NewNormal)