Discussing the mental mind games we play with ourselves, and how other people perceive the cause of our issues.

We talk about the reintroduction of prescription charges and how its increasing the costs of chronic illness on families.

We get riled up about the grim stories about Parkinson's that charities use to attract donations, and how difficult hearing them can be for people trying to live positively with Parkinson's. Are we just being difficult? Or are these contradictory things both true - that it is hard living with Parkinson's AND possible to live positively with it?

Is it a good idea to fess up that you have PD to your boss or prospective employer? What happens if you do and they discriminate against you?

Is honesty the best policy when it comes to opening up to others about your diagnosis? And can you deal with the whispers of sympathy?

How do you cope when you realise that your life is not going to follow the direction you imagined? Emma and Kitty discuss 'self-grief' - their term for this agonising situation. They express their feelings and explain how grief can turn to anger and other emotions.

#kittyandemma #emmaandkitty #kittyd

Inspired after watching a drama that implied that all drugs are bad, Kitty and Emma chat about attitudes towards medication and taking many pills. Is it really acceptable to question if people need the medication they are prescribed? What alternatives are there?

Kitty Fitton is on a mission to prove that disability and illness doesn’t mean the end of life as we know it. She writes about hating exercise, coping with blended families, Parkinson’s, and trying to reach the bottom of the laundry basket.

In this episode the girls talk about the senses and how they may be affected when dealing with Parkinson's.