Whether you’ve just received a lissencephaly diagnosis, have been on this journey for years, or simply want to connect, we’d love to hear from you.
The Oliver Effect was created so that no family has to face lissencephaly alone. We know how overwhelming those first days can feel, and sometimes the most comforting thing is talking to someone who truly understands.
If you have a question, would like to share your story, need support, or simply want to say hello, please get in touch. We’ll always do our best to reply as soon as we can.
Together, we can build a community where every family feels seen, supported and never alone.
Share at your own pace
Our parent matching team reads every single note with gentle guidance and unspoken understanding. We remember the heavy silence of the early days, and we are here to help you navigate it.
