We know it's been a minute since we released an episode - but we're still here.
If you are a newly diagnosed family, you can find loads of information regarding Rett syndrome on our website (linked below), including links to various foundations and support groups worldwide. And, of course, feel free to reach out to us; we love connecting with new families!
Subscribe today so that you never miss an episode. And we'll see you next time!
Podden och tillhörande omslagsbild på den här sidan tillhör
Sarah and Sam. Innehållet i podden är skapat av Sarah and Sam och inte av,
eller tillsammans med, Poddtoppen.
