General: 07354 486 586   |   Fundraising: 07511 821 181   |   Support: 0800 046 9832  

Mimi and Andrew Petty have set up Bertie’s Helpers to honour their son Bertie, who died of CLN1 Batten Disease, aged 4.  Bertie loved his bunny toys so Mimi and Andrew knew they had to use the Bertie Bunny in the logo!

Bertie’s Helpers want to be able to provide practical help to families with a child with Batten Disease by providing food gift deliveries, so that families can spend more precious time together and not have to worry about getting to the shops.  The food delivery will be focused on high quality, quick meals and treats to make a difference at a difficult time.

Having a family member with Batten Disease is not easy but Bertie’s Helpers will focus on families who are facing a particularly challenging time.  For example, they may be facing a marked deterioration in their child’s condition, be looking after their child at end of life, have a new diagnosis, be in hospital or other difficult family circumstances. 

If you would like more information or a nomination form please contact Support at support@bdfa-uk.org.uk  Our nurse at GOSH and other parents will be also able to nominate a family for this extra special help using the same contact.

The BDFA think this is a very special project which we hope will have a hugely positive impact on the families it supports.  Mimi and Andrew are truly inspirational to think of others in this way at a very challenging personal time.  They are seeking some support to meet the long-term costs of providing Bertie’s Helpers food gift deliveries through a new appeal:  https://www.totalgiving.co.uk/appeal/Berties_Helpers

Donate to the work of the BDFA

With your support we can help support families living with the devastating diagnosis of Batten disease

The BDFA receives NO funding from Government and are only able to carry out our work because of the strong commitment of our volunteers and fundraisers.

Thank you so much for your support

How your donation can help

£5 a month
provides a support and information
folder for a newly diagnosed family

£20 a month

helps to run our family support services

£50 a month
enables us to run training workshops
for professionals to educate them on
Batten disease