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Dear Families, It is with sadness that we are writing to announce that our dedicated colleague Sian Fisher left her role as the Head of family support at the BDFA. Sian’s last day was on Friday last week. We are…
For Awareness day this year, Alison wanted to share her poem about her son Joshua. Smile Last night I watched you sleeping and I wondered what you saw. Do you dream in colour? Are you running? Singing your favourite songs?…
Aimee is mum of Issac who has CLN2, she tells us about the daily fight against Batten disease. 🧡 Together we WILL make a difference 🧡 #battenday2023#showusyourorange#battenawareness#bdfa#battendisease@bdsra @bdfabattendisease
This is Harry! He has CLN3 Batten disease. His mum Cheryl shares about his diagnosis. #battendiseasebattenday2023
Our journey with Batten disease started 9 years ago when after months of trying to fathom why our daughter Isabel who was 3 at the time was struggling with a whole host of minor issues with speech and language, coordination,…
Meet the Rich family. Daughters Nicole and Jessica have CLN2. #battenday2023
A poem about home, written by 10 year old Scarlett Evans, sister to Sam and Alice both with CLN3 and baby brother George. Here Scarlett shares how special home is with Mum Natalie, Step dad Dave and her family. We…
Beautiful Monnay has CLN6 and her mum Kelly shares her words to help raise awareness of Batten disease on awareness day. #battenday2023
Meet Kaycee and her contagious smile! #battenday2023 #showusyourorange #battenawareness #bdfa #battendisease