Be counted, and help us fight DADA2
We want to learn as much as we can about our patient community, so that we can more effectively advocate for new research and help families facing DADA2 find the support they need.
We're asking for a lot of information here, but we understand that you may not want to share all of these details about yourself or your child. Please answer as many questions as you feel comfortable answering — any information will be helpful.
We will never share any identifiable information with anyone without your explicit permission. But please give us an email address so that we can contact you. We'll be in touch soon with more thoughts on how we can work together to advocate for our families.
Thank you for joining us!