General: 07354 486 586   |   Fundraising: 07511 821 181   |   Support: 0800 046 9832  
Mums Group Peer Befriender Advert 2023 AUG

🚺 The BDFA are hosting a MUM’S CHAT 🚺

(for mum’s of children and young people of all CLN variants)

⭐️ Tuesday 22nd August 8pm ⭐️

This will be held once a month on Zoom and is a chance for mums from the BDFA community to come together, get to know one another and talk about specific topics. It will be hosted by our trained BDFA Peer Befrienders Holli Longley and Lisa Hover. Holli is mum to Albert who has CLN7 and Lisa is mum to Annabelle and Robbie who have CLN3.

It will alternate each month between evenings and meeting during school hours, to ensure as many mums as possible can come.For now we will just be running a Mum’s Chat for mums with children and young people of any CLN variant, but other groups might develop on from this in the future.

For more information or to be sent the Zoom link please email Mimi Petty, Peer Befriending Coordinator mimipetty@bdfa-uk.org.uk

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