The straight-talking parenting podcast in which we shine a light on the particular highs and lows of raising disabled children, acknowledge our triumphs and our mistakes and embrace all of our beautiful differences.
Because really, what the f**k is normal anyway?!
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EPISODE 22 - transition to adulthood with Julia Marsan
In this episode, Rina and Lauren talk with Julia Marsan about her experience in supporting her disabled daughter Nicole in the transition to adulthood. Julia shares how she fought to find the right solutions to both enable Nicole to live as independently as possible outside of the care of her parents into supported living where she now lives "the best life, in her own way", as well as the way to maintain balance in her and her husband's own lives.
Episode 6 - Couple Relationships
In Episode 6, we discuss Couples Relationships, with Clare and George, who are parents to Ada and Ivo and the impact that having a disabled child has on their relationship.
An eye-opening, heart-warming and hilarious account of this fabulous couple’s story. Covering everything from finding out you’re pregnant after the second date, moving in together after three months, to being told your child’s autism diagnosis, whilst pregnant with your second child.
Hello from your Hosts
A quick hello from our hosts to say thank you and remind you how to connect with us.
We want this podcast to be about connection and building community. So please get in touch with your feedback and ideas. Please tell us what you want to hear from us... Or answer the question we have posed - "What's your F**king Normal?" and share with us any unconventional, unique, beautiful or humorous examples of your daily parenting experience.
Episode 5 - Advocacy
In episode 5 Lauren and Rina talk about a skill we have all had to develop as parents of disabled children – advocacy - with Mum of two and lawyer Caroline MacPake (Withers professionally).
Systems of support aren’t always automatically in place for disabled children and their families, and the world simply has not been designed for disabled people. As parents of disabled children, we have to champion, persuade and shout loudly on our kids behalf.